Sep 102026
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

With apologies that this has been posted with such late notice due to illness.

On the 11th of September, MPs will vote on whether to legalise assisted dying in England and Wales. If the vote passes, the bill will undergo edits at the Committee and Report stages, then MPs will vote again on the amended bill.

Take action

What you need to know before MPs vote on Assisted Dying – Disability Rights UK

Write to your MP

Join our protest

This is a flyer with a picture of the UK Parliament on it. In big red at the top are the hashtags 'Vote No' and 'No To A D'.

Text asks people to join disabled people against cuts at a protest against the Assisted Dying (AD) Bill on Friday 11 September 2026. Assemble at 8.30am for 9.30am start, at Parliament Square Westminster, London, SW1P 3BD.

The flyer advises to bring water, hat, power bank for phones, medication.

 

Poster for Disabled People Against Cuts protest against the Assisted Dying (AD) Bill.

#VoteNo #NoToAD. “Our lives are not up for a vote.”

Friday 11 September 2026 at Parliament Square, Westminster, London SW1P 3BD. Assemble at 8.30am. Protest begins at 9.30am.

Attendees are asked to bring water, a hat, phone power bank and any required medication.

“No to Assisted Dying. Fund social care, palliative care, pain management, give us dignity in life.”

The event is for disabled people, families, friends and allies. Step-free access is available.

“Together we fight for dignity, rights and a life worth living.”

Aug 242026
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Welsh disability campaigners reject invitation to be “glorified doorstaff” in controversial DWP review.

DPAC Cymru statement

On Friday, the Timms Review Steering Group wrote to Disabled People Against Cuts Cymru (DPAC Cymru), inviting us to “co-host” one of the upcoming ‘shaping recommendations’ workshops looking at changes to the PIP disability benefit.

This put us in a difficult position. DPAC Cymru has consistently fought against the failings of the Timms Review. We have been clear that the review has repeatedly failed us as disabled people, and as Welsh people. We are clear that it is not the ‘co-production’ that was promised by Sir Stephen Timms to parliament last year – which even review co-chair Dr Clenton Farquharson acknowledges.

We did not want our name used to legitimise a review that was entirely unfit for purpose. But we also did not want to miss an opportunity to make it better.

Most importantly, we have consistently argued that we need an independent review, democratically led by disabled people and our organisations including our trade unions, that invites the views of non-disabled carers, volunteers, and workers in health, social care, housing, transport, education, and welfare.

Being ‘appointed’ by the DWP as co-hosts would take us no nearer to the independent review we need.

However, the briefing attached to the document made the decision easier for us. It explained what the DWP meant by “co-hosting.”

It said plainly that we would not be “deciding or designing workshop content” or “facilitating discussions during workshops” as these were “out of scope.”

Instead, this would be done by Public Service Consultants (PSC) facilitators and a West-England disabled people’s organisation.

We would also “not be part of the workshop participants in an organisational capacity” and would “not be expected to provide feedback on recommendations.” In other words, we would have even less input as co-hosts than as attendees.

Instead, our role on the day would be to “welcome participants to the venue and help them settle in”, “set the scene” at the start, and “thank participants at the end”, for which we would be paid £37.50 per hour.

What the Timms Review have described as an invitation to “co-host” a workshop, is instead a request for glorified doorstaff.

We are not boycotting the review. We responded to the Call for Evidence. Our members want to attend the workshops and have our say on the record. We also intend to simultaneously protest outside the workshops, as we did in high-profile protests last year during the sham Pathways to Work consultation.

But we will not be there to smile and take people’s coats.

Press queries to dpac.cymru+press@gmail.com

Nov 182025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

A vector graphic with an arm holding a wine-coloured megaphone. A spikey speech bubble points to the microphone and says, in all caps, "protest the budget"

 

Saturday 29th November

1pm @ Swansea Castle

With Disabled People Against Cuts Cymru (DPAC Cymru) and others.

No disability cuts.

Hands of Motability.

Living wages.

Pension justice.

Rent control.

Trade union rights.

No to hate & division.

Make the rich pay.

 

The budget is being written by the Swansea West MP.

A photo of a mobile billboard featuring the face of the Torsten Bell MP. Text, in black on yellow, says: "Swansea West: £4,500 disability cuts backed by your MP." Text, in white on black says "11,592 disabled people here rely on that support. Torsten Bell supports these cuts. Protest disability support." At the bottom-right is the Amnesty International logo, which is black on yellow.

Disabled people defeated his Spring Statement & PIP disability cuts. Now he’s back with another anti-working-class budget. We will defeat him again.

First Bus workers are on strike over low pay.

65 student nurses have been told there are no vacancies when they graduate.

£25 million of job cuts at Swansea University.

Disabled people are still fighting cuts and Swansea women are still fighting for pension justice.

Politicians try to divide us by blaming migrants, low-paid workers, trans people & disabled people.

“An injury to one is an injury to all”

 

We want to co-organise a protest with everyone affected by the budget.

Contact Disabled People Against Cuts Cymru (DPAC Cymru)

Swansea – Protest the budget (PDF for printing)

A graphic of the DPAC Cymru logo. There is the main DPAC logo to the left, which is a red, pink, blue, and green circle being held by four hands of different skin tones, with the words "disabled people against cuts" surrounding it, and an upside-down black traingle in the middle bearing the letters D P A C. On the right is the word Cymru (pronounced cum ree) (C Y M R U) in large letters, and the background of the letters are cutouts of the Welsh flag. Above Cymru (pronounced cum ree) is written the words Disabled People Against Cuts. Below Cymru (pronounced cum ree) are the words Rights, not charity, and the equivilant phrase translated into the Welsh language.

This is a graphic advertising a protest in Swansea on the 29th November.

There are striped green and red corners with the text "Swansea" along the diagonal.

A speech bubble that says "protest the budget" is exiting a megaphone.

There are three clasped hands of different skin tones and the text "an injury to one is an injury to all" curves around them.

Large text says "Saturday 29th November. 1pm at Swansea Castle, S A 1, 1 D W." Smaller text says "With Disabled People Against Cuts (D P A C) and others."

Beneath, with a ripped paper effect, is text that says "no disability cuts. Hands off motability. Living wages. Pension justice. Rent control. Trade union rights. No to hate & division. Make the rich pay."

This is a graphic advertising a protest in Swansea on the 29th November.

There are striped green and red corners with the text "Swansea" and "Protest" along the diagonals, and the text "budget" in the center.

Beneath, in all-caps, is the text "Sat. 29 November. 1pm @ Swansea Castle."

In the centre of the leaflet is text that starts in bold with "The budget is being written by the Swansea West MP."

The text continues: "Disabled people defeated his Spring Statement & PIP disability cuts. Now he’s back with another anti-working-class budget. We will defeat him again."

There are then five bullet points that say: "First Bus workers are on strike over low pay. 65 student nurses have been told there are no vacancies when they graduate. £25 million of job cuts at Swansea University. Disabled people are still fighting cuts and Swansea women are still fighting for pension justice. Politicians try to divide us by blaming migrants, low-paid workers, trans people & disabled people."

At the bottom, with a ripped paper effect and a pink background, is the D P A C Cymru logo - a red, green, blue and pink wheel being held by four hands of different skin tones. To the right is a blue box that asks "Your org's logo here?" and text that says "We want to co-organise a protest with everyone affected by the budget", the email D P A C dot C Y M R U at gmail.com and the website "D P A C hyphen C Y M R U dot C A R R D dot C O."
Oct 302025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Contents

DWP’s plans ‘in tatters’ as McFadden scraps white paper on further disability cuts 1

Shocking’ figures show parents linked to DWP service face death rates up to three times higher 3

Former detective exposes culture of disability discrimination within ‘institutionally disablist’ Met 6

Committee calls cuts bill ‘discriminatory’, even though all its Labour MPs voted for it 10

Disabled people warn of ‘severe’ consequences if chancellor removes Motability VAT exemption 13

Disabled people face ‘systemic’ barriers in accessing community equipment, parliamentary inquiry finds 16

Regulator’s annual report shows impact of social care crisis on disabled people 18

Other disability-related stories covered by mainstream media this week 19

 

 

DWP’s plans ‘in tatters’ as McFadden scraps white paper on further disability cuts

Ministers have dumped plans for a major white paper containing a swathe of further cuts and reforms to disability benefits, following months of activism by disabled people and allies that forced the government into a major U-turn this summer.

Work and pensions secretary Pat McFadden, who only took on the role last month, confirmed the move in a meeting with representatives of disabled people’s organisations (DPOs) earlier this month.

One DPO said yesterday (Wednesday) that the admission was a “major success” for disabled people who fought the summer cuts bill.

But DPOs also warned that activists would need to keep up the pressure on ministers because McFadden had made it clear that, despite abandoning the white paper – which is likely to have significant political implications for the Labour government – individual measures would be taken forward.

He insisted in the meeting – first revealed this week by Greater Manchester Coalition of Disabled People – that further reforms would go ahead, but they would be introduced individually rather than all together in a white paper.

The white paper was set to be based on many of the measures outlined in the Pathways to Work green paper, and responses to a subsequent public consultation.

The results of that consultation should be published before the end of this year.

The decision to bin the white paper means that many of the reforms suggested in March’s green paper – including removing the health element of universal credit for those under 22; reform, and possibly cuts, to Access to Work; a time-limited replacement for contributory employment and support allowance; scrapping the work capability assessment; and changes to the safeguarding, conditionality and sanctions regimes – are likely to be announced separately over the coming months.

Some – but not all – of the reforms will still require legislation.

McFadden’s admission that he had dumped the white paper was made in a meeting on 14 October with Fazilet Hadi and Svetlana Kotova from umbrella organisation DPO Forum England.

Hadi, head of policy for Disability Rights UK, told Disability News Service (DNS): “I definitely think that the amazing campaigning from disabled people and our allies against the PIP cuts has left the government feeling very bruised.

The change of heart in publishing a DWP white paper, and the delay in launching the SEND white paper, bear this out.

Having said this, Pat McFadden has been moved to DWP to drive through cuts to social security, so the lack of a white paper doesn’t mean that there won’t be further threats to the benefits of disabled people.

It just means that those threats won’t all come at once.”

Kotova, director of campaigns and justice at Inclusion London, agreed.

She said: “There is a pause, but it does not mean reforms won’t be coming.

And we need to keep the pressure and persuade or force the government to switch its focus from cutting benefits or ‘fixing us’ to be more work ready to putting resources and its attention to making workplaces more inclusive.”

Among their arguments in the meeting, she said, was for the government to move money from employment support towards the Access to Work scheme.

Steve Darling, the Liberal Democrat work and pensions spokesperson, has lodged a parliamentary question about the “deeply disturbing” situation after being alerted by DNS.

He said: “At the time of a cost-of-living crisis, it is concerning that the secretary of state could be moving away from a more thoughtful, considered approach, to one more driven by cuts than by strategy.

This will only add to the stress and uncertainty that disabled people are facing with the threat of more cuts to disability benefits next year.

I have therefore asked the secretary of state a named day parliamentary question to find out when (if at all!) the white paper will be published, to try to shed some light on this fraught situation.”

Rick Burgess, from Greater Manchester Coalition of Disabled People, who first revealed publicly that the white paper had been dumped, told DNS: “They are not confident that they will get a big piece of legislation through parliament anymore.

It shows we really scared them. It’s a huge embarrassment for them. All their plans are in tatters, and they are afraid of losing another showdown in parliament.

A Starmer government couldn’t survive another drubbing.”

But he said he did not think ministers had changed their attitudes towards welfare reform, only that they were not confident they could push a large bill through parliament.

And he said it would be much harder for disabled people to stop a stream of smaller reforms, and that “keeping track of them is going to be really tricky”.

Linda Burnip, co-founder of Disabled People Against Cuts, said the government’s move to drop the white paper was “obviously a major success for disability rights activists and the many months of campaigning”.

But she said it appeared likely that ministers would use secondary legislation to “sneak things through in dribs and drabs and hope changes won’t be noticed”.

McFadden told Fazilet Hadi and Svetlana Kotova at the meeting that no decisions had yet been taken on barring under-22s from the health component of universal credit, and that it was a priority of his to get more young people into work.

They said he seemed to indicate that time-limiting contributory benefits would be taken forward relatively soon.

Hadi said: “We emphasised the need for government to join up its policies on disabled people and to coproduce solutions with us.

We urged him to move funding to the Access to Work scheme from the additional money being spent on employment support.”

Reforms – and almost certainly cuts – to personal independence payment are expected to follow next autumn, following a review being headed by Sir Stephen Timms, the minister for social security and disability.

Sir Stephen today (Thursday) launched the review, and announced his disabled co-chairs – Dr Clenton Farquharson and Sharon Brennan – as well as a recruitment process for the 12 members of a steering group that will jointly lead the review.

He said the majority of this steering group would be disabled people or representatives of DPOs.

DWP had not commented on McFadden’s admission by noon today (Thursday).

30 October 2025

 

 

Shocking’ figures show parents linked to DWP service face death rates up to three times higher

Parents who pay to support a child through the Department for Work and Pensions (DWP) and its Child Maintenance Service (CMS) face death rates up to three times higher than others the same age, according to “shocking” and “deeply troubling” new figures.

Analysis by Disability News Service (DNS) has shown that, for every age group between 20 and 54, those who use the service – known as “paying parents”* – face a much higher rate of death than those of the same age who do not have to deal with the CMS.

DNS carried out the analysis using figures obtained from DWP through a freedom of information request.

The request followed concerns raised by campaigners who have called for an inquiry into the deaths of parents driven to take their own lives by DWP’s refusal to correct errors in child support demands.

The figures, which are particularly exaggerated for younger age groups, have been passed to the Commons work and pensions committee, which is at the early stages of an inquiry into concerns about CMS.

Among the inquiry’s aims will be how to “improve the way it deals with families”, and concerns over how CMS calculates payments, and enforcement of its decisions.

The DNS analysis shows that, for all those aged 20 to 24 in England and Wales, the rate of deaths in 2024 was 0.04 per cent, compared with 0.13 per cent for CMS paying parents (more than three times higher).

For those aged 25 to 29, the rate of death was more than twice as high for paying parents, and for those 30 to 34 it was twice as high (0.12 per cent versus 0.06 per cent).

The difference in death rates narrows for older age groups, but there is still a substantial difference for every group analysed by DNS, with CMS paying parents aged 50 to 54 facing a death rate of 0.46 per cent in 2024, compared with 0.34 per cent for all adults in that age group.

Results for 2022 and 2023 show similar, striking differences.

Over those three years, there is not a single age group between 20 and 54 – the only groups examined in the analysis – where the death rates are not higher for paying parents than for all adults in England and Wales.

Although the figures do not show how many of these deaths were suicides, they do add strong evidence to the claims of campaigners who believe the higher rates of death for paying parents are at least partly caused by errors by CMS and its toxic culture, including its refusal to correct its mistakes. 

DWP said this week that it was carrying out reforms aimed at streamlining CMS but that it did not “recognise” the DNS figures or any suggestion of a causal link between the actions and culture of CMS and the deaths of paying parents, although it did not point out any errors in the DNS calculations.

Ian Briggs, from research and campaign group STOPS (StopSuicides UK), which focuses on the harm caused by CMS, said: “I, and many others, have long known that the CMS and the DWP have been responsible for driving many parents to suicide.

For years we have tried to highlight this to the DWP, yet every attempt is met with the same denial – that there is no link between the CMS and suicides.

Even when presented with clear and credible evidence gathered by the STOPS group, the official response from ministers has remained one of outright dismissal.”

His son Gavin took his own life five years ago.

The coroner at Gavin’s inquest refused to investigate his father’s claims that the actions of the CMS had contributed to his decision to take his own life, even though the agency had wrongly claimed he owed £16,000 in support payments, after claiming his income was £76,000 rather than the £26,000 it was in reality.

Ian Briggs said this week: “The mortality rates recently revealed through John’s** research and exposed by Disability News Service cannot all be explained away as coincidence.

While not every death may be due to suicide, these figures reveal a deeply troubling pattern that demands urgent scrutiny.

At some point, there must be a full and independent public inquiry into these disturbing facts and the systemic failures within the CMS and DWP that continue to destroy lives and families.

I would like to personally thank John and Disability News Service for… exposing these shocking mortality rates, and for giving a voice to the countless families – like mine – who have suffered unimaginable loss.”

Craig Bulman, who was left with PTSD after the Child Support Agency mishandled his case – the agency, the predecessor of CMS, eventually paid him a £5,000 consolatory payment – said the figures uncovered by DNS were “shocking”.

He told DNS: “Even allowing for statistical margins, the death rates you’ve calculated are deeply disturbing and point to something seriously wrong within the Child Maintenance Service.”

The Child Support Agency’s failings left Bulman homeless, triggered a mental breakdown, and caused the loss of his job.

He said this week: “These figures confirm what families have been warning for years – that the Child Maintenance Service is operating without proper oversight or duty of care.

Death rates among paying parents are up to three times higher than the national average, and yet the DWP has failed to investigate or publish these findings. 

This now warrants an independent inquiry under the Inquiries Act 2005.”

In January 2023, during the final session of a previous inquiry into CMS by the Commons work and pensions committee, Labour MP Debbie Abrahams told of a paying parent whose arrears had been inaccurately assessed “and the frustration that he found ultimately led to him taking his life”.

She said his mother had previously written to DWP “expressing real concerns about mental health” but there had been no reply.

She added: “This is not the first time. We had a panel before Christmas that also provided data about the suicides of paying parents who were inaccurately assessed in terms of the arrears that they owed.

This is tens of thousands of pounds that they said that they owe, leaving literally pounds for them to exist on.”

She asked Tory work and pensions minister Viscount Younger at the time if DWP collected data on suicides of paying parents.

He told her: “Could I just say that, being new into the department, I am already aware, having seen some of the correspondence that I have had to look at and sign off on, of some absolutely tragic cases?

It is absolutely appalling that cases can lead to people taking their own lives.

That is dreadful and we must look at all ways in which we can avoid that or have systems and processes that do not lead to that.”

Despite those comments, a DWP spokesperson said this week: “Over 780,000 people engage with the Child Maintenance Service, many of whom are experiencing a difficult time in their lives, and all staff are trained to support vulnerable customers.

We do not recognise this data or suggestions of a causal link between the CMS and deaths among parents.”

*Child maintenance covers how a child’s living costs are paid when one of the parents does not live with the child

**DNS editor John Pring

***The following organisations are among those that might be able to offer support if you have been affected by the issues raised in this article:  MindPapyrusRethinkSamaritans, and SOS Silence of Suicide

30 October 2025

 

 

Former detective exposes culture of disability discrimination within ‘institutionally disablist’ Met

A culture of institutional disability discrimination within the Metropolitan police is exposed today by the former head of its disabled staff association.

Dave Campbell, who retired this year after serving 32 years as a police officer, has told Disability News Service (DNS) that he believes disability discrimination within the force is rampant and that the Met is institutionally disablist.

He believes this “corporate culture” impacts how the force engages with disabled members of the public.

Campbell was chair of the Met’s Disabled Staff Association (DSA) for six years, and he was also vice-president of the Disabled Police Association of England and Wales.

His disclosures come only days after DNS revealed that prosecutions of disability hate crime across the country were continuing to plummet, with police forces in England and Wales passing on just a tiny proportion of recorded cases to prosecutors.

For six years, Campbell repeatedly tried to persuade the Metropolitan Police Service (MPS) to act on his concerns, before his retirement earlier this year.

It was his intervention that ensured the recent Casey review of the force’s internal culture and standards of behaviour examined the treatment of disabled people, when its initial focus was on racism, sexism and homophobia.

He believes the review provided an “alarming insight into how disabled people feel about their place in the organisation”, as he told Met commissioner Sir Mark Rowley in a letter last year.

He has told DNS that the upper levels of the Met have made it clear through their actions and inflexible policies – which he says marginalise disabled staff, and stem from outdated attitudes – that they do not want people who become disabled to continue serving as police officers in the force.

He says several disabled officers and staff have left the force because of their disability-related treatment and have written directly to the commissioner expressing their “despair and concerns”, without receiving any acknowledgement.

Over the four years between 2019 and 2023, he says, more than 200 disability discrimination employment tribunal claims were taken against the Met, including a significant number which included claims of race or gender discrimination.

The Casey review found an even higher number – 358 – in the five years between 2017-18 and 2021-22, but it was criticised by disabled campaigners for concluding that MPS was institutionally racist, sexist and homophobic, but not that it was institutionally disablist.

Campbell believes the number of disability discrimination tribunal cases increased after the Casey review by up to 60 per cent in 2023-24 compared to the previous year, while the DSA received hundreds of emails from distressed colleagues about the way they were being treated by their managers.

He has told Sir Mark that disability-led internal grievances are also at a high level, while many of his members had “no confidence or trust in the grievance management process” or in the ability of the Culture, Diversity and Inclusion directorate – set up after the Casey review – to produce change.

In the wake of Casey’s report, Campbell – as DSA chair – commissioned an independent review of disability inclusion and workplace adjustments in the force, by the Business Disability Forum (BDF), which reported its findings in September 2024.

Disabled colleagues in the DSA were asked if they had witnessed or personally experienced unfair treatment at work through disability-related harassment, bullying or discrimination, and 358 of the 775 who responded to the survey said yes (46 per cent), and another 123 (16 per cent) said maybe, a total of 62 per cent.

Of 504 police officers, 49 per cent said yes, and 15 per cent said maybe, a total of 64 per cent.

Of the 775 responses from disabled officers and civilian staff, less than 20 per cent (160) agreed with the statement: “MPS is an organisation that recognises and values disabled people.”

And just 65 (eight per cent) agreed that “feedback and complaints are listened to”.

One respondent said: “If you treated any of the other protected characteristics as you did disability then there would be uproar and heads would roll.”

Campbell believes the BDF report supports the view that MPS is institutionally disablist.

He told Sir Mark in last year’s letter: “In my experience Disability discrimination in the MPS is viewed less significantly and addressed differently in comparison to Race, Homophobia, Gender or any other type of Discrimination…”

In an earlier letter to Sir Mark, in 2022, Campbell told him: “There needs to be a change in attitudes [towards disabled officers] and an end to conscious labelling, as sick, lame, lazy, shirker, which are all derogatory terms yet seemingly acceptable…”

He has yet to receive any “tangible” response to the concerns he raised in last year’s letter and the survey report.

Campbell, a detective sergeant before his retirement, has himself twice taken successful action against the Met for disability discrimination, winning the first case at tribunal and then securing an MPS settlement before the start of a tribunal for the second case.

He describes himself as a person of ethnic origin, and has experienced intersectional discrimination, which he says is widespread in the Met.

He said the same complaints are being made “time and time again” at tribunal and through the force’s internal grievance process, which shows there is a “systemic” problem and failure to address these issues through an absence of “corporate memory” and a lack of “morality”.

Currently, about 3,500 police officers have adjustments made for them to allow them to continue in their roles, he said, out of about 36,000 officers in total across the force.

Campbell believes the number of MPS disabled officers and civilian staff may be as high as 10,000 – almost a quarter of the workforce – because many staff do not share their impairment with the force “due to concerns of how they will be treated”.

The Met’s DSA has more than 6,500 members and has 37 peer-to-peer support networks for disabled staff.

Campbell says he has increasingly been coming across incidents where the force’s occupational health department is making recommendations for adjustments to be made for officers who become disabled – often caused by their duties – but managers are refusing to agree to these adjustments.

Instead, officers are often told: “If you cannot do the job then you should just leave,” or: “This isn’t the right job for you.”

He told DNS: “We are just hitting a brick wall. This is about holding the police to account for systemic behaviour both internally and externally.

If these attitudes exist towards disabled people in the workforce, what hopes do disabled people have when they become victims of crime?”

Louise Holden, Inclusion London’s senior policy officer for disabled people and crime, said: “I admire Dave Campbell and his tireless work within a disablist organisation.

I share Mr Campbell’s concerns about how the Met treat disabled victims when their attitude to their own disabled staff is so appalling.

Things have gotten worse since the A New Met for London plan following the Casey review.

The work Inclusion London was involved in stopped and the new structure is a closed shop.

Community confidence is at an all-time low.

There has been no follow-up to the Casey review and with the Met decision to stop investigating non-hate crime incidents, without any consultation, it’s clear the Met is just not interested in disability issues.

There has been no radical reform, only half-baked gestures and platitudes that amount to nothing.

We are calling for renewed engagement with us, so we can support the Met with our expert knowledge on these issues.

I hope the Met is ashamed of how they have behaved since the Casey review and want to work with us again.”

Commander Simon Messinger, the Met’s professionalism and senior lead for disability, said: “We are fully committed to driving positive change across the Met and fostering a culture of inclusion, and have taken significant steps to improve how we support disabled colleagues.

This progress has helped us to achieve Disability Confident level three status, the highest level of recognition within that scheme, which reflects our determination to improve how we recruit, retain, and support our staff.

We know there is much more to be done and will continue to work with the Met police Disabled Staff Association, and partners such as the Business Disability Forum, to drive further progress.”

A spokesperson for the mayor of London said: “The mayor is clear there is no place for harassment or discrimination in the workplace and is committed to working with the Met police to deliver a New Met for London where everyone can thrive.

Since the Baroness Casey review in 2023 the Met has implemented a number of improvements for disabled employees, including the introduction of disability passports, Disability Smart assessments and the force is now a Disability Confident employer, improving how they recruit, retain and develop disabled staff.

But there is more to do and the Met is working closely with the Disability Independent Advisory Group and the new chair of its Disabled Staff Association to listen and act on concerns to deliver a fairer and more inclusive Met.”

*If you have information about a police officer or member of staff who works for the Met and is corrupt or abusing their position and power, you can call the force’s anti-corruption and abuse hotline anonymously on 0800 085 0000

30 October 2025

 

 

Committee calls cuts bill ‘discriminatory’, even though all its Labour MPs voted for it

A Labour-led committee of MPs has called the government’s universal credit cuts act “discriminatory” and warned that it will push disabled people into poverty, despite every one of its Labour members voting for the legislation in July.

The Universal Credit Act will see the health element of universal credit halved for most new claimants from 6 April next year, from £105 to £54 a week.

All seven Labour MPs on the committee* voted for this cut in July.

But Labour’s Debbie Abrahams, who chairs the committee, said this week: “This is not only discriminatory, but without mitigations, will potentially push more people with disabilities and health conditions into poverty, exacerbating their condition and pushing them further away from the labour market.”

She was commenting on the publication of the government’s response to the committee’s report on the Pathways to Work green paper.

Her committee’s report had called on the government to delay the cut to the health element until it had carried out an “independent and comprehensive assessment of the impact the change could have on disabled people”.

But in this week’s response, the Department for Work and Pensions (DWP) dismissed those concerns.

Instead, it pointed to the “sustained, above inflation increase” to the standard allowance of universal credit (UC), which will also be introduced through the bill.

It said that this, together with the cut to the health element, would address “perverse incentives in the UC system and better encourages those who can work to enter or return to employment”.

Asked why she had voted for the cut to the health element when she thought it was discriminatory and would push more disabled people into poverty, Abrahams told Disability News Service (DNS) in a statement: “I worked very hard to secure major concessions on removing the cuts to PIP and people currently on UC health in the welfare bill.

The bill isn’t perfect, and that was reflected in the work and pensions Pathways to Work report and its recommendations.

However, voting against the bill would have meant that the increase in the standard allowance wouldn’t have gone ahead, and that was seen as a major positive aspect of the bill.

This increase is not just for this year, but for each year until the end of this parliament.

I am still continuing to work hard on securing mitigations around the reduction in support for newly disabled people from April next year and I remain committed to ensuring disabled people across the country have access to the support they need.”

Meanwhile, DWP has refused to explain to the committee what assessment it made of the bill’s impact on safeguarding, before the legislation was introduced to parliament earlier this year.

The bill had originally included steep cuts to personal independence payment (PIP), before a backbench Labour rebellion – following three months of activism from disabled people and allies – led to those measures being removed.

But there has been almost no discussion in parliament – and little or no information from ministers – on the bill’s potential impact on safeguarding claimants.

In its response to the committee’s report, DWP has made no mention of safeguarding, although it said that it had carried out an equality impact assessment for the bill.

But the impact assessments published on parliament’s website make no reference to safeguarding.

Asked by DNS why it failed to respond properly to the committee’s recommendation to release its assessment of the bill’s impact on safeguarding, and whether it did assess the safeguarding implications of the original bill, DWP said it was looking to improve its safeguarding approach, which included a review of the green paper consultation responses.

A DWP spokesperson said: “Our welfare reforms package was appropriately advised and numerous protections were baked into our plans.

We are shifting our focus from welfare to work, skills, and opportunities, so more people can move out of poverty and into good, secure jobs as part of our Plan for Change – backed by £1 billion a year for employment support by the end of the decade.”

Grassroots groups of disabled people, such as Black TriangleDisabled People Against Cutsthe Mental Health Resistance Network, and the Spartacus network, spent years highlighting deaths linked to DWP’s actions.

Concerns have also been raised by relatives who have called for action after the deaths of their family members.

Some of the evidence linking DWP with the deaths of benefit claimants has come through prevention of future deaths reports written by coroners, several of which only emerged years after they were written.

Other evidence of persistent DWP safeguarding flaws has emerged through freedom of information requests to the department, which have revealed how hundreds of recommendations for improvements have been made by DWP’s own secret reviews into the deaths of claimants.

Some of these reviews showed DWP staff continuing to make the same fatal errors, year after year.

The evidence collected by DNS and others, stretching back more than a decade, has shown how DWP repeatedly ignored recommendations to improve the safety of its disability benefits assessment system, leading to countless avoidable deaths.

It also shows how DWP hid evidence from independent reviews, and how the department failed to keep track of the actions taken in response to recommendations made by its own secret reviews.

Evidence also demonstrates that the cultural problems within DWP extend far beyond the assessment system, touching all aspects of its dealings with disabled people in the social security system.

The evidence, compiled over the last decade by DNS and other journalists, academics and activists, shows systemic negligence by DWP, a culture of cover-up and denial, and a refusal to accept that the department has a duty of care to those disabled people claiming support through the social security system.

Much of that evidence has been brought together in a detailed timeline, as part of the Deaths by Welfare project headed by Dr China Mills and supported by Healing Justice Ldn, which works with marginalised and oppressed communities.

*Debbie Abrahams; Johanna Baxter; Damien Egan; Gill German; Amanda Hack; Frank McNally; and David Pinto-Duschinsky

**The Department: How a Violent Government Bureaucracy Killed Hundreds and Hid the Evidence, DNS editor John Pring’s book on the years of deaths linked to DWP’s actions and failings, is published by Pluto Press

30 October 2025

 

 

Disabled people warn of ‘severe’ consequences if chancellor removes Motability VAT exemption

Disabled people have warned of “severe” consequences if the chancellor goes ahead with reported plans to remove the Motability car scheme’s VAT exemption in next month’s budget.

Disability News Service (DNS) reported last week how the company that runs the scheme, Motability Operations, had warned that removing the VAT tax break entirely could impose an upfront cost of at least £3,000 on even the cheapest cars it offers.

There is no certainty that the chancellor will go ahead with removing the tax exemption entirely – which was revealed by the Times – and she may abandon the plans completely.

But the minister for social security and disability, Sir Stephen Timms, failed to deny plans to target the VAT exemption when asked by disabled Labour MP Emma Lewell on Monday about potential cuts to the scheme.

Instead, Sir Stephen said again that there would be no changes to personal independence payment until next autumn.

Yesterday, a Reform UK press conference on the party’s plans to slash disability benefits – particularly personal independence payment (PIP) – saw the party target the Motability scheme.

The party’s work and pensions spokesperson in the Commons, Lee Anderson, said the scheme had “got completely out of hand” and was “an absolute scandal”, and he suggested that all those receiving Motability cars should only be able to secure a “blue three-wheeler”*.

He said: “What’s wrong with that? Let’s go back to that.”

Meanwhile, disabled people who rely on Motability to maintain their independence have told DNS this week of the drastic impact that increased costs could have on their ability to afford a car through the scheme, and how this would affect their ability to work, enjoy leisure opportunities, and attend medical appointments.

Julia Dalton, a Motability customer for more than 40 years, relies on an adapted vehicle, which she says has allowed her “to work for over four decades, contribute taxes, and live independently” in east Yorkshire.

As an electric wheelchair-user, she needs a large vehicle with a hoist to lift her wheelchair into the car.

She said: “Without Motability, I could never have afforded a suitable vehicle.

It is not possible for me to use a cheap second-hand car because if it breaks down, I cannot simply use a hire car that is not adapted for my needs.

Without a reliable vehicle I would not have been able to get to work and would likely have lost my job.

This scheme has protected my independence, wellbeing, and ability to contribute”.

She says that advance payments – on top of contributing the enhanced rate mobility component of PIP every month – have risen significantly in recent years.

Her latest vehicle in March cost her £4,000 in an advanced payment as well as £1,500 for essential adaptations.

She said: “I am managing financially, but even I would struggle to pay thousands more on top.

If someone like me is at risk of coming off the scheme, what happens to those with less support?

The consequences are severe: disabled people stuck at home; people losing work because they cannot travel; missed medical appointments; isolation.

Motability is not a luxury. It is a lifeline.”

She added: “If exemptions are removed or costs continue to rise, we risk destroying a system that enables disabled people to live, work, and participate fully in society.

I am deeply grateful for Motability. I want to see it protected for the future, so others can have the same opportunities that I had.”

Emma, from Leicester, told DNS that her Motability wheelchair-accessible vehicle (WAV) – which needed an advance payment of £4,500 – had made “a huge positive difference” to her life, and allowed her to continue to visit her dad after he had a stroke, firstly while he was in hospital, and then at home.

She said: “WAV taxis are expensive and difficult to arrange, and using public transport would have been impossible for me health-wise.

Without that access, he might have declined further or needed residential care.

The scheme has literally kept our family connected and independent.”

She said the knock-on effects of removing the VAT exemption – and the insurance premium tax, which is reportedly also being considered – would “make it even harder for disabled people to stay mobile”.

She said: “The knock-on effects would be huge — more reliance on carers, increased pressure on health and social care services, and greater difficulty getting to appointments or even maintaining social contact and contributions to society.

If the tax relief were removed, I simply wouldn’t be able to afford a vehicle and would be stuck in my house even more.”

Richard, a Motability-user for 30 years, from the West Midlands, told DNS that the scheme was vital as a wheelchair-user living in inaccessible housing, and that he and many others would be forced to leave the scheme because it would become unaffordable if its VAT exemption was removed.

He has a progressive, neurological muscle-wasting condition and uses his Motability car to drive to a pool to swim, which allows him to keep the strength in his shoulders that he needs to pull himself up and down the stairs of his home.

Without the car, he would not be able to use the stairs and would end up in expensive extra care housing or a nursing home.

He said: “Being stuck at home would be very detrimental to my mental health.

It will have similar effects on many, especially those who would have to give up work due to unaffordable initial payments.”

April, who has been a Motability customer for 15 years and lives in Lancashire, said the scheme has allowed her to maintain her independence and job and “gets me to and from my workplace safely and stress free”.

She has a small automatic hatchback which now requires a £1,000 advanced payment, when previously there was no advance payment required.

She said: “I fear these government proposals will make Motability pass these costs on to the scheme users – to the detriment of those struggling on low incomes and those needing larger adapted vehicles.

The scheme must be preserved for those of us that need it to maintain our independence, to work, attend appointments, and to live decently, with dignity and safety.”

Michael Newbold, from Staffordshire, a Motability customer for more than 20 years, said the scheme was “essential” for him and his disabled wife.

He said: “I need a car for appointments and shopping, also for leisure.”

They have already had to cope with the council stopping paying for a personal alarm, and for the insurance on his stairlift.

He said: “It’s like little by little they are taking all the things that make life easier.

Most people, in my opinion, will not be able to afford the VAT rise if they are in a similar position as me.”

Another customer, Phil, told DNS that he and his wife Kath would be “totally screwed” without their Motability vehicle.

They are both disabled, but it is Kath who is the Motability customer as she uses a powerchair following a spinal stroke, so she needs a WAV.

Phil said: “We had to find a £4,000 down payment for our WAV and when it has to go back [at the end of the lease] we’ll have to find the same if not more for the next vehicle.

Adding VAT on top would make it unaffordable for us.”

Without the car, he said, they would be “totally isolated”, and they already both struggle with their mental health.

He said: “I can only believe others in the disabled community will be affected in the same way.

My wife and I are from Bristol and it’s a city with an awful bus service so another reason the Motability scheme is so vital for us.”

*A reference to the Invacar that was provided by the government to disabled people up until the late 1970s, when it was replaced by the Motability scheme

**Motability Foundation, the charity that oversees the car scheme, is a DNS subscriber

30 October 2025

 

 

Disabled people face ‘systemic’ barriers in accessing community equipment, parliamentary inquiry finds

A cross-party group of MPs and peers has called on the government to draw up a national strategy to address the “deeply troubling” and “systemic” barriers that prevent disabled people accessing the equipment they need to live independently.

Hundreds of disabled people and professionals across the UK fed into the inquiry by the all-party parliamentary group for access to disability equipment, which found an “inconsistent” community equipment system that was in crisis due to fragmentation, underinvestment, and a lack of leadership.

The inquiry heard of disabled children missing school because the correct hoists had not arrived; disabled adults unable to live independently and forced out of their jobs because repairs to equipment were taking months; and carers driven to “physical and emotional exhaustion”.

It found too many disabled people faced long delays, unsuitable equipment and “a lack of joined up support” within the system, which provides equipment such as grab rails, hoists, wheelchairs, ramps, specialist mattresses, and assistive technology.

The group’s report includes findings of a survey from more than 600 users of equipment, carers, professionals and equipment-providers.

More than half of equipment-users who took part (55 per cent) said they believed services were worsening.

The same proportion said they did not have access to the equipment they needed.

One equipment-user told the inquiry that the support offered “barely scrapes the barrel of what people actually need to live their everyday lives.”

More than a fifth of those surveyed (22 per cent) said they had waited more than two months to receive their equipment once it had been approved.

The report heard of the experience of Rhys Porter, who has cerebral palsy, and went without essential equipment, including a hoist and home adaptations, for two years.

His parents had to help him use a commode seat in his bedroom and drag him into the family bathroom on a towel once a week.

He was only able to go ahead with vital surgery because the charity Newlife provided him with a portable hoist.

The report calls for a “cohesive” national strategy; funding reform of the current “fragmented” model; action to address lengthy waiting-times for assessments and equipment; improved communication with equipment-users and between local authorities, health bodies, and government departments; a national advisory board with service-user representation; and action to improve reuse and recycling of equipment.

Labour MP Daniel Francis, chair of the all-party group, said: “Across hundreds of testimonies, one message came through loud and clear: the system designed to support disabled children and adults is failing them.

It is failing to deliver equipment on time, failing to provide the right support, and failing to listen to the very people it exists to serve.

Under the current system we’re seeing children missing school, adults being forced out of work and carers injuring themselves.

It’s failing patients, carers, and the sector alike, and it’s high time for the government to get a grip.

Access to community equipment is not privilege, it’s a daily necessity.

We need a national strategy for community equipment and clear leadership and accountability in its delivery.

Ensuring everyone is given the right support at the right time is simply a matter of political will and commitment.”

The Department of Health and Social Care was unable to comment on the report by noon today (Thursday).

30 October 2025

 

 

Regulator’s annual report shows impact of social care crisis on disabled people

An annual report by the care regulator has highlighted how the continuing social care crisis is impacting disabled and older people who need support in their own homes.

The Care Quality Commission said in its annual State of Care report that the health and social care system remained “fragmented and under severe strain”.

It said that demand for local authority-funded support had continued to rise, while the job vacancy rate in adult social care was still three times higher than in the wider employment market.

And it said that more community services were “urgently needed” to support people to stay in their own homes for longer.

The report includes evidence from members of CQC’s Experts by Experience group, which has come from their own experiences of care and support and from talking to other service-users during CQC inspections.

Living in a rural area can particularly affect alternative options if a homecare agency is providing poor care, the report says.

One of the Experts by Experience told CQC: “The only other agency down the road hasn’t got any space for me. Where do you expect me to go?

I’m telling you what’s wrong and the things I’m not happy with, but I don’t feel like I’ve necessarily got a choice to change that.”

CQC’s Experts by Experience said disabled people had told them how they had been “left to sit or lie in soiled or wet clothing for hours while waiting for their care worker to arrive”.

The report says: “As local authorities around the country increasingly look to make savings, it seems likely more will signpost people to support in the community, ration the care they do provide, and reduce the provision of other statutory and non-statutory services.

As well as negatively affecting the health and wellbeing of those in need of social care support, this could increase the pressure on the health and care system and the voluntary, community and social enterprise sector, and further increase the burden on unpaid carers.”

As CQC only began implementing its new single assessment framework in January 2024, it is not possible to directly compare the latest ratings from its inspections with previous years.

Inspections have been focused on services where CQC information suggested people might be at risk.

The ratings produced through the framework for about 3,000 adult social care services (out of a total of about 20,000 services across England) show four per cent were rated inadequate, another 26 per cent were seen as requiring improvement, 67 per cent were rated good, and two per cent were seen as outstanding.

Professor Sir Mike Richards, CQC’s chair, said: “The Casey Commission will be an important step in reforming social care – but it won’t solve the core funding problem.

We continue to call for long-term, sustainable funding for adult social care.”

30 October 2025

 

 

Other disability-related stories covered by mainstream media this week

Reform UK’s draconian plans to scrap the personal independence payment (PIP) for people with anxiety were last night labelled “cruel, heartless and reprehensible”. At a press conference in London, the party vowed to end PIP for claimants with “non-serious anxiety disorders” and introduce more regular reassessments for those who qualify: https://www.mirror.co.uk/news/politics/reform-uks-plans-rip-up-36150700

Journalist and former BBC presenter Mark Mardell was left feeling “humiliated” after he was told he could not board a Turkish Airlines flight due to having Parkinson’s disease and no doctor’s report. The broadcaster was unaware of this requirement and was shocked when he could not board his flight home from Istanbul to Gatwick: https://www.bbc.co.uk/news/articles/ce9dx4zgzjzo

30 October 2025

News provided by John Pring at www.disabilitynewsservice.com

 

Oct 222025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net
The words "We want an Independent PIP Review" in bold and black text, with Independent highlighted in red. On the left there is a tear-out effect of a greyscale photo of a disability protest, and a red-tinted photo of Stephen Timms, the disability minister.
Disability campaign group Disabled People Against the Cuts Cymru pose for a group photo outside the Senedd (Welsh parliament) with Sioned Williams MS. Sioned is holding up the DPAC Cymru letter. There are 15 people in the photo. Two people are wearing DPAC t-shirts. Four people are using wheelchairs. Two people are wearing face-masks. One person is holding a flag showing a Welsh dragon with a disability equality colour background. Behind everyone is the DPAC Cymru banner. It is very large, and has five people holding it. It says Disabled People Against Cuts and then the word Cymru with a Welsh dragon background effect on the text. It has the DPAC logo which is a red, green, purple, blue wheel being held by four arms with different skin tones. At the center of the logo is an upside-down black triangle bearing the letters D P A C and the word Cymru. Behind the campaigners are various tall buildings in Cardiff. The nearest building is made of a striking orange brick.

On Tuesday 14th October, members and supporters of Disabled People Against Cuts Cymru (DPAC Cymru) met outside the Senedd (the Welsh Parliament) to protest the disability cuts and hand over a letter to Senedd members. The letter, co-signed by over 700 individuals and organisations, outlined DPAC’s request to the Welsh Government to support an independent review of Personal Independence Payment (PIP). The letter calls for a PIP review that is truly led independently by disabled people and our organisations, to allow our lived experience to influence the policies and decisions that will ultimately affect us.

We are grateful to the members of the Senedd who met with us or wrote to us about this matter, and we hope that all members will take into consideration what the letter said.

The lobby happened on the same day that the Minister for Social Security and Disability, Sir Stephen Timms, declined an invitation to meet with the Senedd Cross Party Group on Disability due to “diary pressures”. Timms is currently responsible for the PIP review, and we feel that his response highlights how disabled people and Disabled People’s Organisations (DPOs) are being excluded from the review and decision-making process.

Timms’ promise that the PIP review would be a genuine co-production with disabled people is not being upheld, and the Senedd lobby was part of an ongoing campaign to ensure that disabled people’s voices are being heard.

As a new member of DPAC Cymru, it was wonderful to see so many people at the Senedd to support what DPAC is working to achieve. Given the current situation, it is vital that disabled people’s voices are amplified in a way that is accessible, impactful, and authentic. We will continue to campaign for the rights of disabled people and to push for a fairer, independent PIP review to create a system that truly supports the needs of disabled people across the UK.

Briallen Symons-East
Disabled People Against Cuts Cymru (DPAC Cymru)

 

Disability campaign group Disabled People Against the Cuts Cymru pose for a group photo outside the Senedd (Welsh parliament) with Sioned Williams MS. Sioned is holding up the DPAC Cymru letter. There are 15 people in the photo. Two people are wearing DPAC t-shirts. Four people are using wheelchairs. Two people are wearing face-masks. One person is holding a flag showing a Welsh dragon with a disability equality colour background. Behind everyone is the DPAC Cymru banner. It is very large, and has five people holding it. It says Disabled People Against Cuts and then the word Cymru with a Welsh dragon background effect on the text. It has the DPAC logo which is a red, green, purple, blue wheel being held by four arms with different skin tones. At the center of the logo is an upside-down black triangle bearing the letters D P A C and the word Cymru. Behind the campaigners are various tall buildings in Cardiff. The nearest building is made of a striking orange brick.

Photo: Disability campaigners from Disabled People Against Cuts Cymru outside the Senedd in Cardiff.

 

A photo of a disability lobby at the Senedd (Welsh parliament). Lee Ellery, who is a wheelchair user, is handing over pack of documents to the Welsh politician Sioned Williams. Lee is smiling and in the middle of talking. In the background is the Disabled People Against Cuts Cymru (DPAC Cymru) banner.

Photo: Lee Ellery hands a pack of documents to Sioned Williams MS.

 

Sioned Williams MS talks to campaigners from Disabled People Against Cuts Cymru (DPAC Cymru) outside the Senedd. There are about 20 people in shot. Four people are users of powered wheelchairs. One person is wearing a yellow medical face mask and is draped in a Welsh flag with disability equality colours. Another wears a black medical face mask. People are standing around chatting, while Sioned is at the center of the photo. At the right of the photo is the DPAC Cymru banner being held by several people. The banner says "rights not charity." One person wears a hat that says PCS. One has a copy of the Socialist newspaper.

Photo: Lee Ellery hands a pack of documents to Sioned Williams MS – from another angle!

 

Disability campaigners from Disabled People Against Cuts Cymru at the Senedd (Welsh Parliament) talk with the politician Jenny Rathbone MS.

Photo: DPAC Cymru talk with Jenny Rathbone MS outside the Senedd.

 

Disability campaigners Lee Ellery and Joshua Reeves, who are both wheelchair-users, are conversing. Around them are other campaigners from Disabled People Against Cuts Cymru.

Photo: Disability campaigners Lee Ellery and Joshua Reeves BEM conversing.

 

Lee Ellery, Ben Golightly, John Williams from Disabled People Against Cuts Cymru are talking to Sioned Williams MS. In the background is the Senedd building. Lee is using a powered wheelchair. He is wearing smart clothes. Sioned is holding a pack of documents and smiling and looking at Lee attentively. Ben is wearing a DPAC t-shirt and is holding a small placard with text. John is holding a copy of the Socialist newspaper and looking at Ben.

Photo: disability campaigners converse with Sioned Williams MS.

 

Darren Millar MS and staff converse with disability campaigners outside the Senedd. In the background are trees and the sea. It is picturesque, although overcast.

Photo: DPAC Cymru spoke with Darren Millar MS and his staff outside the Senedd.

 

Lee Ellery and Ben Golightly from Disabled People Against Cuts Cymru (DPAC Cymru) pose for a photo with Sioned Williams. Lee Ellery is a wheelchair user and is in smart clothes. Ben is wearing a DPAC t-shirt. Ben is holding a sheet of paper with the DPAC Cymru logo that says "No disability cuts! Disabled people want to run our own independent PIP review!" Sioned is holding a sheet of paper with the same message translated into Welsh. She is also holding up the DPAC Cymru letter with 700 signatures. In the background, John Williams is standing to their leftwith a copy of a newspaper called the Socialist. On the cover of the newspaper, it says: "Your party: let's build a party to fight labour's war and austerity. defend the right to protest."

Photo: We posed for photos with Sioned Williams MS holding bilingual (English and Welsh) signs that said:
“No disability cuts! Disabled people want to run our own independent PIP review!”

Oct 092025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Contents

Tory trio mislead party conference on disability benefits as they stir up hostility towards disabled claimants 1

Government ‘has lost its way’ on accessible housing, after new towns report ignores disabled people 3

Alarm over government’s choices to lead ‘over-diagnosis’ review that could help ministers cut benefits 5

Coach firm to pay thousands to accessible transport activist after driver lied that he threatened violence 8

Access to Work dossier of evidence shows ‘real harm’ and job losses caused by DWP cuts and failings 10

Greens show contrast with other major parties on disability cuts and refusal to stir up hostility to claimants 13

New film celebrates 10 years since ‘moment in time’ victory over care charges in London borough 14

Other disability-related stories covered by mainstream media this week 16

 

 

Tory trio mislead party conference on disability benefits as they stir up hostility towards disabled claimants

A trio of leading Tories have used misleading and offensive statements at their annual conference in Manchester to scapegoat disabled people who rely on support from the benefits system and whip up hostility towards them.

The Conservative party made it clear this week that it would go further and faster than the Labour government in cutting disability benefits, and said it would cut £23 billion from social security spending if it won back power.

Some of these savings would be used to pay for the abolition of stamp duty on residential property sales*, which would only benefit the better-off.

The most offensive line may have come from Tory leader Kemi Badenoch, who told the conference yesterday (Wednesday): “I stand for a society where… the vulnerable are supported, but where freeloaders are told where to get off.”

She said a Conservative government would “restrict benefits to those with more severe mental health conditions, not anxiety or mild depression”**.

Disability News Service (DNS) reminded the party this week how government-funded research found that when a Conservative-led government tried to slash the number of people on out-of-work disability benefits and force them into work in the post-2010 austerity years, it led to 590 suicides in three years.

The party had not responded to these concerns by 11am today (Thursday).

Badenoch also told the conference that “after Covid, 2,000 people a day were being signed onto out-of-work sickness benefits”, which she said was “a national tragedy”.

There was no suggestion in the former engineer’s speech that she had connected the impact of a deadly and disabling pandemic with this increase in the number of people being unable to work due to sickness or disability.

Badenoch also appeared to suggest that she supported allowing disability hate speech to pass unpunished, telling Tory members: “I stand for a society where free speech trumps hurt feelings.”

Mel Stride, the former work and pensions secretary and now his party’s shadow chancellor, had spoken earlier in the week of the “spiralling welfare bill”.

DNS has now told the party’s press office on at least three occasions that figures from the Office for Budget Responsibility*** show clearly that social security spending as a proportion of GDP**** is predicted to remain at or close to 11.1 per cent for the next five years, and that it is lower than it was in 2015-16.

Again, the party had not responded to these concerns about Stride’s misleading comment by 11am today.

The party also announced plans to prevent anyone other than British citizens from receiving social security support, if it regains power.

It appears that this would apply to disabled people with significant support needs and those who have legally worked in the country for years through “indefinite leave to remain”.

The third shadow minister to mislead the conference on cuts to disability benefits was shadow work and pensions secretary Helen Whately.

She told Tory members: “Millions are getting benefits for anxiety and ADHD, along with a free Motability car.”

A disabled person can only qualify to join the Motability scheme if they receive the enhanced mobility component of personal independence payment (PIP) or similar benefits.

In fact, DWP figures showas highlighted by the Benefits and Work website – that only about 190,000 PIP claimants have ADD, ADHD, anxiety or anxiety-related conditions as their “main disabling condition” and receive an enhanced mobility component.

And many of this group will not have exchanged their PIP mobility component for a Motability vehicle.

It is possible that Whately was referring to all those disabled people with anxiety and ADHD who have a Motability vehicle (ie including those with a different main disabling condition in addition to a mental health condition or being neurodivergent), but – if so – her statement was still highly misleading.

And even if that had been her intention, Motability Operations, the company that runs the scheme, says it has only a total of 860,000 customers, and many of those use their allowance to hire a powered wheelchair or mobility scooter.

Whately’s comments also suggest that PIP claimants receive a “free” car in addition to that benefit, when in fact a claimant usually has to exchange all their mobility allowance to lease a Motability vehicle, and must also often make a non-refundable advance payment.

Once again, the Conservative party had refused to comment by 11am today on Whately’s figures.

*It is believed this would apply to primary residences in England and Northern Ireland

**Although she said she wanted to “restrict benefits”, it is unlikely that she meant that people with anxiety or “mild” depression would be prevented from accessing mainstream benefits such as the standard universal credit allowance

***See chapter five of OBR’s Economic and Fiscal Outlook – October 2024, chart 5.2

****Gross domestic product, the size of the country’s economy in a particular year

9 October 2025

 

 

Government ‘has lost its way’ on accessible housing, after new towns report ignores disabled people

The government has been accused of losing its way on accessible housing, after refusing to explain why a report by its “taskforce” on delivering a series of new towns across England does not include a single mention of disabled people.

The independent report – commissioned by the government – recommends 12 potential locations for new towns across England, with at least 10,000 new homes in each location.

But the 135-page report contains only two brief references to the need for accessibility, either with the new homes themselves or the built environment surrounding them, and there is no mention of working-age disabled people.

One reference in the report says new towns should “include homes for older people, as well as specialist housing built to accessible and adaptable standards”.

The other says the mix of homes in new towns should include “homes for market sale, private rent, affordable housing, and specialist accommodation for students, families, and older people, all within a single coherent masterplan”.

Disabled people’s organisations that have been campaigning for action to solve the accessible housing crisis were critical of the latest failure by the Ministry of Housing, Communities and Local Government (MHCLG).

Mikey Erhardt, policy lead for Disability Rights UK, said: “It is unacceptable that, in 2025, a plan to deliver thousands of new homes, to tackle the housing crisis, will do nothing to improve the lives of disabled people.

Relegating the needs of millions to a classification as ‘specialist’ shows just how entrenched ableist views are within the department.

What is specialist about creating places that millions can actually call home, instead of the less than 10 per cent that disabled people can currently even visit?

Yet again, we see a government department that has lost its way in trying to triangulate policy in favour of big developers and landlords, with disabled people as ever missing out.

Talk about a missed opportunity; they’ve not even chosen to commit to a minimum number of accessible or wheelchair-accessible homes, let alone ensuring DDPOs* are included in the planning process.

If our newest towns can’t be accessible, which ones will be?”

Last week, housing secretary Steve Reed announced that the government would build 12 of the new towns across England, but he and his party failed to make any pledge that accessibility would be central to their design.

More than 15 months after the general election, disabled people are still waiting for the new government to say whether it will introduce stricter minimum accessibility standards for new-build homes in England, three years after a pledge by the last Conservative government – which was never fulfilled – to take action to address the critical shortage of accessible housing.

Laura Vicinanza, senior policy and stakeholder engagement manager for Inclusion London, said: “The taskforce talks about accessible ‘specialist housing’, but accessible and adaptable standards must apply to all housing, so we’re not cut off from our communities.

Housing with a baseline level of accessibility benefits us all – it allows us to stay in our homes longer as our needs change and we age.

Three years ago, the Conservative government committed to raise the minimum accessibility standards for all new-build housing to the M4(2) accessible and adaptable standard, but they didn’t follow through.

It’s time for Labour to commit to M4(2) accessibility for all new-builds, and for 10 per cent of new housing to be M4(3) wheelchair-accessible, focused in social housing.

This is the opportunity to ensure that this wave of new housing and new towns doesn’t lock us out of safe housing for another generation.”

This week, Disability News Service (DNS) asked the government why the taskforce and its report had almost completely ignored disabled people’s housing needs, and the opportunity to build in accessibility across the new towns from the beginning; and why there was nothing in the taskforce report that sets a minimum level of accessible homes, including how many wheelchair-accessible homes should be built in the new towns.

DNS also asked for reassurance for disabled people that the government’s new towns plans would build in accessibility right from the start and from the ground-up, in co-production with disabled people and their user-led organisations.

MHCLG declined to explain why the taskforce report contained so few references to accessible housing and built environment in the new towns and failed to mention disabled people.

And it once again said it would set out its policies on accessible new-build housing shortly.

At last year’s Labour party conference, in September 2024, after DNS questioned the party on the failure of ministers to mention the accessible housing crisis, a Labour spokesperson promised the government would “set out its policies on accessible new build housing shortly”.

An MHCLG spokesperson said in a statement this week: “Everyone deserves to live in a decent home that is suitable for them and meets their needs.

We will create New Towns that work for everyone, including disabled people, and we welcome recommendations from the taskforce that they should include specialist housing built to accessible and adaptable standards.

We’re committed to working with disabled people and their organisations to shape these new communities together.”

*Deaf and disabled people’s organisations

9 October 2025

 

 

Alarm over government’s choices to lead ‘over-diagnosis’ review that could help ministers cut benefits

The government’s decision to commission a review of alleged “over-diagnosis” of mental health conditions and neurodivergence has caused alarm among many disabled people, with fears that it will allow ministers to justify further sweeping cuts to disability benefits.

There is also concern that health and social care secretary Wes Streeting has commissioned two high-profile mental health figures with controversial backgrounds to lead the review.

Although the government has not yet confirmed the review will take place, it will reportedly examine the prevalence of mental illness and neurodivergence, “with a particular focus on whether some conditions are being overdiagnosed”.

But disabled activists believe its authors have been chosen because they will “help to slash the social security bill”.

The review will apparently be chaired by Professor Peter Fonagy, while the vice-chair will be Professor Sir Simon Wessely.

Fonagy is a highly-decorated clinical psychologist and psychoanalyst but he has also been closely associated with the Serenity Integrated Mentoring (SIM) programme, which was described as unethical, unlawful and unsafe and “a national scandal” that had put people in severe mental distress at risk of being denied vital support.

He was lead author of an article (PDF) whose co-authors included Paul Jennings, the former police officer who founded SIM, and which examined how SIM was working in London and concluded six years ago that it was “promising”.

Jennings described Fonagy in one presentation as a “senior supporter” of the programme.

Campaigning by the StopSIM Coalition later exposed SIM as discriminatory, coercive and punitive, and eventually persuaded NHS England to admit it was wrong to endorse SIM without applying “sufficient scrutiny” and to accept that this had harmed service-users.

Wessely’s appointment is likely to prove even more divisive.

He helped recruit patients onto the notorious, and later discredited, PACE trial – part-funded by the Department for Work and Pensions – and he was hugely supportive of the PACE research (PDF) into the use of controversial treatments such as cognitive behaviour therapy and graded exercise therapy for those with ME.

In 1993 (PDF, page 17)*, Wessely had written to the then Department of Social Security to argue that the only difference between “chronic fatigue syndrome, or ME as it is sometimes known” and “the major psychiatric disorders” was “the existence of a powerful lobby group that dislikes any association with psychiatry”.

Wessely argued in his letter that any suggestion that ME was a neurological condition would “discourage any sensible efforts at rehabilitation” and lead to an “ever increasing stream of claims for permanent benefits in people who might otherwise have had a chance of recovery”.

The view – shared by Wessely – that it was the attitudes of people with ME that were preventing their recovery, and the impact of this belief among many doctors and scientists on the treatment of many thousands of people with ME, was described by the Guardian’s George Monbiot last year as “the greatest medical scandal of the 21st century”.

Wessely also led a review of the Mental Health Act, which was criticised for falling “significantly short” of recommending full human rights for people in mental distress, but was a blueprint for Labour’s much-criticised mental health bill.

Although the Fonagy review has yet to be officially confirmed by the Department of Health and Social Care (DHSC), its existence was revealed by the well-connected Health Service Journal (HSJ).

Linda Burnip, co-founder of Disabled People Against Cuts (DPAC), said: “I think the choice of these two people shows how little regard the government, and Streeting and Timms** in particular, have for the fears of disabled people.

It seems likely that they have deliberately been chosen to help to slash the social security bill.”

The grassroots, user-led mental health group Recovery in the Bin (RiTB) said both appointments were “safe establishment” figures with troubling backgrounds, such as Wessely’s links to the ME “forced exercise programmes” and Fonagy’s links to SIM, which suggested “a very low probability that this will be an open and fair investigation”.

RiTB said: “We expect it will return findings the government will find useful to deny people benefits.

The issue that should be investigated is the thousands of deaths covered up by the DWP.

Instead, they want to cause more death.”

A spokesperson for DPAC Cymru said it was “alarmed” at the decision to appoint Fonagy and Wessely, whose backgrounds were “a clear signal” of a “politically-motivated review that has had its outcome decided in advance.

In the context of an NHS starved of funding, disability welfare cuts, and the UK government’s demonisation of disabled people, it is obvious why these two men have been selected.”

A DPAC Cymru member added: “Normalising mental health and neurodiversity normalises seeking help and clarity which makes diagnosis more accessible.

We’ve always existed, we’ve always been different, we just didn’t have the ability to seek help or diagnosis.

This whole ‘autism is new’ and ‘over-diagnosed’ argument is just another load of rubbish to demonise young people, make disability a taboo, exclude disabled communities, and save rich people pennies on providing help to people who really need it, and it frustrates me so incredibly much.”

Bethan Edwards, co-founder of the Stop SIM Coalition, which has now been disbanded, told Disability News Service (DNS) this week: “Professor Fonagy led an evaluation of SIM during its implementation in London in 2018 and 2019. 

SIM involved withholding care from people in extreme mental distress and involved the threat of criminalisation for attempting to use statutory services to meet significant mental health needs. 

It should not have taken a group of service-users to bring this to the public and professional bodies’ attention in 2021, leading to SIM’s demise. 

The alarm could and should have been raised sooner, including by Professor Fonagy himself. 

I, therefore, have very little confidence that the DHSC’s review will put the well-being and safety of people with mental health needs ahead of the Labour governments agenda – to cut welfare spending and to continue underfunding mental health services.”

And Kate Skinner, a neurodivergent campaigner, psychology student and academic research assistant, told DNS: “In my mind, the government’s potential reasons behind this review are straightforward: if fewer people qualify for diagnostic labels (such as ADHD), then fewer people will qualify for benefits, accommodations, and specialist services, as so many places lock the provision of support behind these labels.

Reviews like this one feel like their real purpose is redefining who counts as being ‘deserving’ of support, as evidenced by the wider media, which has been chipping away at the ‘validity’ and ‘deservingness’ of neurodivergence for a while now.”

She said: “I understand why many disabled people, particularly those who are neurodivergent, are deeply concerned about this review.

Psychology and psychiatry have a long history of researchers deciding what is ‘best’ for others, while ignoring the lived experiences of the people they study.

This history of exclusion and paternalism already makes it difficult to trust that this new review, commissioned in such a negative light, will be conducted with genuine openness or ethical integrity.”

Skinner added: “One of the professionals leading this review [Wessely] has previously argued that greater awareness of mental health conditions may not be ‘beneficial’, and has warned against ‘over-professionalising’ or ‘medicalising’ certain conditions.

Therefore, it is difficult not to feel that the government is seeking to use ‘experts’ to push through a harmful, ideologically-driven agenda.

Until reviews like this are shaped and conducted by those they claim to represent, any talk of ‘overdiagnosis’ will continue to sound less like healthy, scientific investigation and more like deep, cynical suspicion.”

DHSC declined to comment on the HSJ article.

*This document was obtained from the National Archives through the efforts of disabled barrister Valerie Eliot Smith, who has ME

**Sir Stephen Timms, minister for social security and disability

9 October 2025

 

 

Coach firm to pay thousands to accessible transport activist after driver lied that he threatened violence

A coach operator that passed on defamatory lies about a well-known disabled activist who exposed the inaccessibility of one of its coaches will have to pay him substantial damages, and make a humiliating apology in open court.

A driver for Bolton-based Tyrers Coaches fabricated claims about Doug Paulley, alleging he had threatened a Network Rail coordinator with violence and that he hurled swearwords at him over an access failure at Rochdale train station 13 months ago.

Tyrers had passed on the allegations to the Driver and Vehicle Standards Agency (DVSA), and another transport company, Arriva.

The incident occurred after Tyrers – which was one of the companies providing a rail replacement service on behalf of government-owned Northern Trains – had been unable to accept Paulley onto its vehicle because the relevant door was not working.

Coaches from two other companies were also not able to accept Paulley on board, with one driver not trained to operate the accessibility equipment, and the other vehicle not wheelchair-accessible.

Tyrers later told DVSA and another transport company, Arriva, that Paulley had threatened violence, was physically threatening, called its driver “a d**khead” and told him he didn’t know what he was “f***ing doing”.

Paulley later discovered by accident – when his solicitor submitted a subject access request to DVSA in connection with another discrimination case – what Tyrers had said about him.

The coach company was unaware that Paulley – who has spent years exposing access failures across the transport industry – had recorded the incident on a camera attached to his wheelchair.

He was able to use the recording to show that none of the claims made by the Tyrers driver had been true.

He decided to launch a defamation claim in the high court because of the risk of serious damage to his reputation, and – he told Disability News Service – because he wanted to address the “reprehensible”, discriminatory and dishonest behaviour of transport companies and coach drivers, and their “horrific, hateful, ableist behaviour”.

Tyrers has now agreed to pay him £7,500 in damages and a further £1,000 for a breach of data protection law.

The company will also have to write to DVSA and Arriva, making it clear that the allegations it shared were false.

And it will have to apologise in open court for the false claims it made, and for the distress and damage caused to Paulley’s reputation.

Tyrers had not commented on its actions by 11am today (Thursday).

Train company Northern has also apologised to Paulley, after one of its managers claimed in an email that he “goes around Railway Stations and tries to find fault at each location”.

The email had been sent out after Paulley complained about the Rochdale incident, in which he had been “simply trying to travel and encountered genuine accessibility barriers” with the rail replacement bus service.

He told Northern in a complaint: “When I documented these experiences, it was as part of my legitimate role as a nationally recognised transport accessibility advocate, not as malicious troublemaking.

The suggestion that I ‘go around’ railway stations looking for problems fundamentally misrepresents evidence-based documentation of accessibility failures as some form of personal vendetta.”

He said the language used showed “a concerning institutional prejudice against disabled passengers who exercise their legal rights to document accessibility failures and hold operators accountable”.

And he said it had “contributed to the toxic atmosphere” that enabled the discriminatory behaviour by Tyrers, and the subsequent “inaccurate, defamatory allegations” that were made about him.

Paulley said Northern’s actions had created “chilling effects that may deter other disabled passengers from reporting legitimate concerns”.

Northern has now apologised in an email for the distress caused by its manager’s comments and told Paulley his campaigning was “invaluable” and “helps us learn from our mistakes” and that his work over the years “has been greatly appreciated and has played an important role in helping us improve”.

Paulley’s data protection case against another transport company is ongoing.

A Northern spokesperson said the company had no further updates to the apology issued to Doug Paulley.

But he added: “As referenced [in the emailed apology], the work that campaigners including Mr Paulley do is invaluable.

The comments in the email about which the complaint was received are not reflective of Northern’s views, and we are truly sorry for any distress caused by these comments.”

9 October 2025

 

 

Access to Work dossier of evidence shows ‘real harm’ and job losses caused by DWP cuts and failings

The Access to Work scheme is failing Deaf and disabled people, and its “decline” in the last two years has caused them “real harm”, with some support packages cut by 80 per cent, according to a detailed dossier of evidence prepared by a user-led organisation.

The 33-page report was put together by London-based Action on Disability (AoD), which said its evidence shows “systemic administrative failure, lack of transparency, and potential breaches of equality and human rights obligations” by the Department for Work and Pensions (DWP). 

The evidence has been sent to the National Audit Office (NAO) as part of its ongoing investigation into how DWP is addressing “challenges” in the operation of the Access to Work (AtW) scheme.

NAO launched its investigation earlier this year following concerns that increased demand for AtW support, and other factors, had “adversely affected DWP’s administration of the scheme”, with “growing backlogs of people waiting for their applications to be processed or their claims to be paid”.

Much of the AoD report is based on its experience assisting disabled people with their AtW applications, renewals and appeals, in which their awards were “reduced, delayed, or rendered unusable due to unimplementable conditions”.

Between January 2023 and July 2025, it says, average support hours per week for more than 35 work placements it monitored have fallen from 22.5 to just four, while the average waiting time for an AtW case manager to be allocated has risen from eight weeks to 30, the job retention rate has halved from 88 per cent to 43 per cent, and the progression to paid work for those on supported internships has fallen from 72 per cent to 28 per cent.

Employers working with AoD say the deterioration of the scheme since 2023 has led to “job losses, reduced hours, and withdrawal from inclusion programmes that were previously successful”, with a significant decline in confidence in AtW among employers.

The dossier was shared with Disability News Service (DNS) this week, just days after DNS reported how disability minister Sir Stephen Timms admitted signing off on a directive that led to widespread cuts to disabled people’s AtW support packages.

Sir Stephen admitted to DNS last week that he had signed off on an order for AtW staff to apply guidance more “scrupulously”, after civil servants submitted a “proposal” to him to approve.

Among its concerns, the AoD report says changes to the way the scheme operates have made it harder for disabled people to contact their AtW case manager, while leading to inconsistency around quotations, inconsistent decision-making, and delayed or unclear pathways for appeals.

The effect of the changes has been to exclude disabled people from employment, destabilise supported internships, and undermine employers’ commitment to inclusion.

This has left AtW no longer operating “as a transparent, accountable, or lawfully administered scheme”, says the report.

The impact of changes over the last two years has been “a significant reduction in awards, increased administrative delays, and a breakdown of communication between AtW and service users, reversing years of progress in inclusive employment”.

And it says its evidence suggests that DWP has refused to publish internal policy instructions; denied claimants procedural fairness; obstructed transparency; and failed to ensure economy, efficiency, and effectiveness in public spending.

The report particularly highlights what AoD calls a “systemic policy shift”, with many applications that would previously have been awarded 100 per cent of a disabled person’s support needs in the workplace now being awarded about 20 per cent of their assessed needs.

This occurs when AtW categorises the assistance requested as a “job aide”, meaning the support worker is viewed as performing part of the job on the claimant’s behalf, rather than helping the disabled employee to overcome barriers related to the work.

AoD says AtW’s “rigid” approach fails to recognise the “legitimate” support that many disabled people need to complete their work independently, such as prompting and structured guidance.

It says AtW’s lack of recognition of such an approach to support has led to significant funding reductions of up to 80 per cent, disproportionately affecting people with learning difficulties, autistic people, those with acquired brain injury, or people with sensory processing impairments.

The report says the 20 per cent award policy “is like handing someone a plank that only stretches a fifth of the way across a river and then blaming them when they fall in”.

The NAO said its report was likely to be published early next year, and its team was still “gathering evidence through different methods”.

A government consultation on the future of Access to Work closed on 30 June, and DWP says it is now reviewing those responses and the scheme and working with disabled people and others on its proposals.

A “collaboration committee” on Access to Work – whose members have remained anonymous – concluded its work this month, and DWP says its views and concerns will now help shape the department’s policymaking.

DWP continues to insist that no changes have been made to AtW policy.

David Buxton, chief executive of AoD, said: “Access to Work should be a bridge into employment.

Instead, thousands are being left stranded mid-way.

The scheme’s decline is costing jobs, damaging wellbeing, and wasting public money.

We hope the NAO’s inquiry restores transparency, fairness, and trust.”

A DWP spokesperson said: “We inherited an Access to Work scheme that is failing both employees and employers, which is why – as part of our welfare reform – we consulted on how it could be improved.

We are reviewing all aspects of the scheme and will develop future policy with disabled people and the organisations that represent them.”

Meanwhile, disability consultant Alice Hastie, who specialises in providing AtW advice, warned this week that DWP had now shut down the AtW complaints email address, which she said “seems like a bizarre (and barely legal!) way of reducing the number of complaints they have to deal with”.

DWP said last night (Wednesday) that its policy is that email is not a valid contact method for complaints unless this has been agreed as a reasonable adjustment.

It is believed that the complaints email may have been shut down because it was for internal use only and its existence was not supposed to have been leaked to claimants.

9 October 2025

 

 

Greens show contrast with other major parties on disability cuts and refusal to stir up hostility to claimants

The Green Party is set to continue to contrast its policy approach on disability with other political parties by supporting disabled people who rely on benefits and have already experienced years of austerity cuts.

The newly-elected leader of the Green Party of England and Wales, Zach Polanski, told members at their annual conference in Bournemouth that the party would fight for the many disabled people “who have found themselves at the sharp end of brutal government cuts”.

His speech was focused on reducing the cost-of-living and addressing “rip-off Britain”, demanding more from “the very wealthiest”, tackling climate breakdown, attacking the “alarm bells of authoritarianism” within the Labour government, supporting the NHS and community cohesion, protecting “rights” and “liberties” through a “politics of hope”, and supporting migrants.

But there was almost no mention of how the party would fulfil these pledges, other than a repeated emphasis on wealth taxes, although its general election manifesto last year pledged a five per cent increase in the level of disability benefits, free personal care for adults, and more money to support disabled children in mainstream schools.

The difference in emphasis from the Liberal Democrat conference – where party leader Ed Davey spoke in an interview of targeting disability benefit fraud – and particularly the Labour, Reform and Conservative party conferences (see separate story), was clear.

There were no attacks on disabled people claiming benefits in Polanksi’s speech, and no calls for cuts to spending on supporting disabled people, or complaints about the “over-diagnosis” of mental distress or neurodivergence.

Instead, he said his party would fight for hard-pressed families, renters who live in “shoddy accommodation” and are wary of further rent increases, and “thousands and thousands of disabled people in the UK who have found themselves at the sharp end of brutal government cuts”.

In his speech, Polanski mentioned meeting a disabled man and his carer while knocking on doors with another Green politician, and how they spoke about “how hard everything is and how it just didn’t feel like a single person was representing them”.

Despite his words, there was still no clear picture of what Polanski and the Green Party would do to change that, other than “focusing day-in, day-out on the cost of living”.

One of the party’s co-deputy leaders, Rachel Millward, had told the conference of her experience of physical impairment and associated “horrendous” pain in her 20s, when she had a blue parking badge and an adapted vehicle.

But she said: “Far worse than that was the pain of separation from my community and from nature.

Conference, please let us always make it a priority to find ways to give people with disabilities much better access to both.”

The contrast with the four main UK-wide parties continued this week, when the Green Party’s other co-deputy leader, Mothin Ali, attacked the “divisiveness and hatred” of the Conservative party and its announcements at its conference in Manchester this week (see separate story).

He said: “The package so far – turbo-charged welfare cuts, draconian anti-migration measures, and axing life-saving foreign aid – would leave few but the wealthiest unscathed.

These measures are a cruel attack on the sick and disabled, migrants and asylum-seekers, and some of the poorest communities in the world.”

9 October 2025

 

 

New film celebrates 10 years since ‘moment in time’ victory over care charges in London borough

A new film released to celebrate 10 years since activists won a campaign to stop their local council charging for care shows how disabled people can achieve important victories by taking collective action, say campaigners who fought for that success.

The film* highlights the eight years of campaigning by Hammersmith and Fulham Coalition against Cuts (HAFCAC), which led eventually to their London borough scrapping home care charges in April 2015.

The campaign began in 2006 when the new Conservative-led council introduced a policy that imposed charges for home care.

HAFCAC was set up to fight the “discriminatory policy”, and it spent eight years lobbying councillors, holding protests and pushing the council to change its policy.

Tara Flood, one of the HAFCAC steering group members, says in the film: “There’s something particularly awful about receiving, through the post or via email, a document, an invoice, that sets out how much you have to pay to enable you to live at home with the support that you need to participate in your community, to be a friend, to be a family member, to be a parent, to get to work.

No-one else is experiencing that.”

HAFCAC also backed a judicial review legal action against the charges brought by three disabled people from the borough who received home care.

Although they lost the case, one of the high court judges described the policy as sacrificing home care services on the altar of council tax reductions.

The film describes how the coalition raised much of its funding with pub quizzes, at which disabled activists such as Flood, Kevin Caulfield and Debbie Domb – all members of HAFCAC’s steering group – began to build relationships with politicians, including Labour’s Steve Cowan.

Cowan, who would go on to lead Hammersmith and Fulham council, says in the film: “The crucial thing was what Debbie, Tara and Kevin were able to do, was educate me and my colleagues on the need for the social model of disability to be right at the heart of our Labour administration’s approach.”

Months after Labour won back control of the council in May 2014, Cowan announced that Hammersmith and Fulham would be scrapping all home care charges in May 2015.

It remains one of only two councils in England that do not charge for home care, after Tower Hamlets council in east London scrapped adult home care charges from April this year.

Caulfield says in the film: “That moment [in 2014] was a real moment in time to show that campaigning does work, that disabled people getting together and collectively taking action can really have an impact.”

David Webb, a fourth member of the HAFCAC steering group, who ran the fund-raising pub quizzes, describes in the film how having personal assistance has completely changed his life.

He says: “It has given me a measure of choice and control that I didn’t have before.”

Victoria Brignall, who has benefited from scrapping care charges in the borough, says in the film: “People don’t choose to be disabled.

It’s a tax on disability and we would like disabled people to be treated in the same way as other people.

You don’t charge people to send their children to school, or to use parks, or to collect your rubbish, so why charge disabled people for their care?”

She says she hopes other councils will now be inspired to abolish home care charges.

Last year, Disability Law Service published research which showed that disabled people across England were continuing to face unlawful discrimination and inequality on an “unparalleled” scale due to “unjust” social care charging policies.

Caulfield points out in the film that tens of thousands of disabled people every year are taken to court for non-payment of care charges.

That’s just a disgrace,” he says.

He and his fellow HAFCAC veterans say the film serves as both a celebration and a rallying cry, and that they hope their success “will inspire more disabled people to take action”.

The film, launched on Tuesday, is dedicated to Debbie Domb, “a fearless freedom fighter for disabled people’s rights”, who died in 2018.

*The film, ‘£12.40 an Hour for a Shower: The Story of Disabled People’s Struggle to Abolish Home Care Charging in Hammersmith & Fulham’, was directed, edited and produced by disabled film-maker, journalist and author Richard Butchins, and can be accessed with BSL and subtitles only, or with added audio description.

**Inclusion London is campaigning to persuade the government to scrap all social care charges.

9 October 2025

 

 

Other disability-related stories covered by mainstream media this week

Thousands of sick or disabled people will be helped into work through a major push to place job advisers in GP surgeries, the DWP has claimed. Work and pensions secretary Pat McFadden is announcing a £167.2 million expansion of the Connect to Work programme to nine further areas across England, including Cumbria, Oxfordshire, and West Sussex and Brighton: https://www.mirror.co.uk/news/politics/dwp-change-affect-gp-surgeries-36033854

Jobcentre work coaches say they are struggling to find employers who can accommodate disabled people and get them into work. The BBC spoke to two work coaches, who said opportunities are hardest to come by for those with long-term health conditions who may require a level of flexibility or additional support. It comes as new data obtained by the BBC from the Department for Work and Pensions suggests that the number of jobseekers finding work each month is falling: https://www.bbc.co.uk/news/articles/c4gz9njvj43o

9 October 2025

 

News provided by John Pring at www.disabilitynewsservice.com

Oct 082025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

4pm to 4.15pm

Tuesday 14th October

Outside the Senedd (Welsh Parliament) in Cardiff

 

The words "We want an Independent PIP Review" in bold and black text, with Independent highlighted in red. On the left there is a tear-out effect of a greyscale photo of a disability protest, and a red-tinted photo of Stephen Timms, the disability minister.

The Disability Minister Stephen Timms was forced to promise UK parliament that there would be no more PIP disability cuts until a review had been co-produced with disabled people.

He has broken this promise.

Disabled people want to run our own, independent, and democratic PIP review.

Disabled People Against Cuts Cymru (DPAC Cymru) will be handing in our open letter with 700 signatures from individuals and organisations. We are calling on the Welsh government to do its part and practically support Disabled People’s Organisations to carry out the review.

Placards, in English and Welsh, with the Disabled People Against Cuts Cymru logo, will say:

“No disability cuts! Disabled people want to run our own independent PIP review. We’re asking the Welsh Government to do its part!”

 

If you are able to, would you consider…

Joining us at the lobby in person on Tuesday 14th.

This will involve: being outside for 15 minutes with placards and possibly a megaphone.

Ask your Senedd member to meet us there.

Let people knowour Google Drive has bilingual social media graphics and placard text, as well as alt text for social media graphics accessibility.

We welcome all support!

 

Access requirements

Is there anything that would help you take part? Is there anything we can do better? Do you have any access requirements? Let us know! Email <dpac.cymru@gmail.com>

A limited number of PPE masks will be available for free.

 

 

Social media graphics

This is a graphic advertising a protest. The top half of the image is a picture of the Welsh Government building (the Senedd) with a blue tint, and the bottom half is a ripped paper effect. Text on the top half, in big letters, says: “Protest (Senedd Disability Lobby)”. On the bottom half, text says: “We will be handing in 30 pages of signatures. No disability cuts! Disabled people want to run our own, independent, PIP review.” In bold, it says “We’re asking the Welsh Government to do its part. Tuesday 14th October 2025.” Next to a red map pin, it says: “Cardiff, outside the Senedd, 4pm to 4:15pm”. To the right is the Disabled People Against Cuts Cymru logo, which is a red, pink, blue, green wheel being held by four hands of different skin tones. At the center of the logo is an upside-down black triangle bearing the letters D P A C and the word Cymru.
A graphic of the DPAC Cymru logo. There is the main DPAC logo to the left, which is a red, pink, blue, and green circle being held by four hands of different skin tones, with the words "disabled people against cuts" surrounding it, and an upside-down black traingle in the middle bearing the letters D P A C. On the right is the word Cymru (pronounced cum ree) (C Y M R U) in large letters, and the background of the letters are cutouts of the Welsh flag. Above Cymru (pronounced cum ree) is written the words Disabled People Against Cuts. Below Cymru (pronounced cum ree) are the words Rights, not charity, and the equivilant phrase translated into the Welsh language.
Sep 262025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

A graphic on a black background, using white and mint green text. At the top, in a large font, is the text “hashtag No Sham Panel. Online Disability Protest.” This is followed by text that says “The government says it’s setting up a group of disabled people to give advice. They are calling this the Independent Disability Advisor Panel. But we are worried because it looks like the panel won’t be fair. The government only wants a panel that will agree with them.”

A graphic on a black background, using white and mint green text. There are two headings in mint green that ask “when” and “how.” Underneath “when” is the text “Saturday 27th and Sunday 28th September 2025.” Underneath “how” is the text “follow our guide at: bit.ly/panel-protest for instructions.” Below, in a large font, is the text in white and all-caps “then spread the word!”, followed in green by “hashtag No Sham Panel.”

A graphic on a black background, using white and mint green text. At the top, in a large font, is the text “hashtag No Sham Panel. Online Disability Protest.” This is followed by a speech bubble containing the text “I’ve send in my application to the sham government disability panel. I’m letting them know that I refuse to accept their unfair rules. You can do it too!” Underneath is the Disabled People Against Cuts Wales logo and the Disability Rebellion logo. There are two headings in mint green that ask “when” and “how.” Underneath “when” is the text “Saturday 27th Sunday 28th September 2025.” Underneath “how” is the text “follow our guide at: bit.ly/panel-protest for instructions.”

 

Take part at bit.ly/panel-protest

 


 

Plain text:

 

#NoShamPanel Online Disability Protest:

The government says it’s setting up a group of disabled people to give advice.

They are calling this the Independent Disability Advisory Panel.

But we are worried because it looks like the panel won’t be fair.

The government only wants a panel that will agree with them.

 

When?

Saturday 27th and Sunday 28th of September 2025.

 

How?

Follow our guide at bit.ly/panel-protest for instructions.

 

Then spread the word! #NoShamPanel

Tell everyone:

I’ve sent in my application to the sham government disability panel.

I’m letting them know that I refuse to accept their unfair rules.

You can do it too!

You can also share our social media graphics with Alt text from our Google Drive folder.

 

Organised by

Disabled People Against Cuts Cymru (DPAC Cymru) and Disability Rebellion

Sep 252025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Contents

Davey stirs up hostility towards disabled claimants, as Lib Dem spokesperson links similar attacks to far right 1

Lib Dems want to use new Hillsborough Law to force DWP to release secret reports into deaths 3

Darling accuses DWP of ‘absolutely shameful’ cover-up over Access to Work changes 4

Disabled activists working with peers to address serious flaws in ‘dangerous’ assisted dying bill 5

UN calls for human rights assessment of government’s benefit cuts bill and mental health reforms 8

DWP is ‘dysfunctional’ and needs major review, says Lib Dem Steve Darling 11

Lib Dems insist they are still focused on social care, despite leader concentrating again on carers 13

New publications ask how disabled people and allies can hold the state to account for welfare state killings 15

Mother left ‘disgusted’ by DWP’s silence over secret report into Jodey Whiting’s death 17

Anger and frustration after DWP’s latest jobcentre announcement and McFadden’s ‘incentives’ comment 19

Other disability-related stories covered by mainstream media this week 21

 

 

Davey stirs up hostility towards disabled claimants, as Lib Dem spokesperson links similar attacks to far right

Liberal Democrat leader Sir Ed Davey has whipped up hostility towards disabled people by suggesting there is widespread fraud among claimants of personal independence payment (PIP), despite his own work and pensions spokesperson linking similar unfounded attacks to the far right.

In an interview with Times Radio at the Liberal Democrat party conference in Bournemouth, Sir Ed suggested the reduction in face-to-face assessments had led to “quite a lot of fraud” among the recent increase in PIP claimants since the start of the pandemic.

But the latest figures from the Department for Work and Pensions (DWP) estimate that just 0.4 per cent of PIP spending in 2024-25 was due to fraud, while the previous year’s estimate had been zero per cent.

Despite these facts, Sir Ed said: “There’s a real suggestion in those numbers, by the way the Conservatives managed the system, that there’s quite a lot of fraud there and surely everyone can agree we should go after the fraud to make sure that people who need the benefits that people who are really disabled can still get them.”

But Sir Ed’s comments came on the same morning (Sunday) that his own work and pensions spokesperson, disabled MP Steve Darling, told Disability News Service that far-right activists were launching similar attacks on disabled claimants using dubious figures on economic inactivity.

Darling said: “My real fear is that in our now Trumpian world, [the far right] don’t need the facts to add up to make outlandish claims.”

He said it was disturbing how “the far right will just make up narratives for their own purposes, and demonising others is part of their playbook and sadly people with disabilities and quite often people with hidden disabilities are in their crosshairs.

It’s part of that push back against the far right [and what] we need to be doing is unpicking that, because otherwise that half-truth will be built on by the far right to demonise people with disabilities.”

Sir Ed also mirrored claims by right-wing politicians when he claimed in the Times Radio interview that it was vital to reduce spending on social security, despite widely-available official figures showing that expenditure is stable as a proportion of GDP*.

His comments on PIP were particularly embarrassing because he focused in his main conference speech on Tuesday on attacking Reform UK and its leader, Nigel Farage, warning repeatedly of the “Trump-inspired country Farage wants us to become”.

Asked about his leader’s comments, Darling declined to say if he agreed with them, but yesterday (Wednesday) he issued a statement through his party’s press office.

He said: “Liberal Democrats are proud champions for the most vulnerable in society.

We led the charge against the government’s ill-thought welfare cuts bill and played an instrumental role in defeating plans to slash PIP.

We will always stand up for disabled people and their carers.

Ed rightly pointed out that the Conservative party’s move to telephone assessments has damagingly undermined public trust in the welfare system.

A fair system of in-person assessments, where possible, is vital to make sure this crucial support is there for people who need it.

More broadly, Liberal Democrats have long argued the best way to reduce welfare spending is to tackle the root causes of the rising welfare bill – by seriously investing in health and care, and making it easier for disabled people to access the world of work.”

Sir Ed’s speech to the conference included just two mentions of disabled people, but neither in relation to his own party’s policies.

Instead, he mentioned family carers like himself 10 times in Tuesday’s speech, without once mentioning the adult social care charging crisis, which sees tens of thousands of disabled people falling into debt every year because of those charges (see separate story).

*Gross domestic product, the size of the country’s economy in a particular year

25 September 2025

 

 

Lib Dems want to use new Hillsborough Law to force DWP to release secret reports into deaths

The Liberal Democrats are set to try to use the government’s new Hillsborough Law to force the Department for Work and Pensions (DWP) to release secret reports into the deaths of disabled benefit claimants.

For years, the department has refused to hand bereaved relatives the internal process reviews (IPRs) it carries out into deaths that have been linked to its actions and failures.

It releases reviews only when ordered to do so by a coroner, or a court, or very rarely on other occasions – there is no record of it doing so in such circumstances – because it insists they are intended for learning purposes within the department.

This week, Disability News Service (DNS) has reported DWP’s latest refusal to release an IPR – or even to say if such a review was carried out – to a family, this time following the death of Jodey Whiting (see separate story).

Her mother, Joy Dove, is in her ninth year of campaigning for justice for her daughter, who took her own life in February 2017.

In a letter to Dove, DWP said IPRs were “internal retrospective investigations focused on organisational learning” and “often contain sensitive personal information about claimants” and so “could be considered a breach of privacy”, even though the claimant is dead.

The letter, from the Government Legal Department, said DWP was “working towards a more open approach to sharing findings and learning from IPRs”, but this is believed to refer only to anonymised recommendations made by the reviews rather than the facts they uncover.

DNS reported in June that a DWP director who gave evidence at the second inquest into Jodey Whiting’s suicide claimed she didn’t know whether an IPR had been carried out and would have to ask colleagues.

The minister for social security and disability, Sir Stephen Timms, came into his post last year pledging to increase transparency within the department.

But he has so far refused to change the department’s position, even though adult safeguarding reviews – sometimes examining the same deaths as IPRs – are released to relatives, and are published anonymously.

Now Steve Darling, the Liberal Democrat work and pensions spokesperson, has pledged to use the government’s new public office (accountability) bill, otherwise known as the Hillsborough Law, to force DWP to publish IPRs and release them to families.

This is because the new bill includes a legal duty on public authorities and public officials “to act with candour, transparency and frankness”.

In an interview with DNS at his party’s annual conference in Bournemouth, Darling said he wanted the bill to produce a “culture change” within DWP and the whole of Whitehall, and that he intends to ask parliamentary questions about how the release of IPRs should be part of that.

He said it should be the same approach as in the aviation industry when there are near misses and “things have gone wrong”.

Otherwise, he said, “how can you expect the rest of the organisation to learn from it and the rest of society to learn where things have gone wrong?”

*The Department: How a Violent Government Bureaucracy Killed Hundreds and Hid the Evidence, DNS editor John Pring’s book on the years of deaths linked to DWP, is published by Pluto Press

25 September 2025

 

 

Darling accuses DWP of ‘absolutely shameful’ cover-up over Access to Work changes

The Department for Work and Pensions (DWP) has been accused of an “absolutely shameful” cover-up, after refusing to release documents that should show why disabled people across the country have faced cuts to their Access to Work support.

Disabled campaigners have been warning for the last 18 months of DWP cuts and inconsistent decisions on their Access to Work (AtW) claims.

But when social security and disability minister Sir Stephen Timms was challenged on these apparent cuts this summer, he insisted that no guidance had been issued to reduce support, and he said: “No changes have been made to Access to Work policy.”

In his response to a written parliamentary question from Liberal Democrat work and pensions spokesperson Steve Darling in July, he said instead that guidance was “now being more consistently applied” and that “work has been underway to improve [AtW] decision-making by applying the guidance with greater consistency, to provide a fairer process”.

He said: “This may mean that some awards change at the point of renewal, but there has been no change in Scheme policy, or instruction to reduce support levels.”

But Sir Stephen added: “Any updates to operational guidance are reflected through the published version available online at GOV.UK.”

Disability News Service (DNS) subsequently submitted a freedom of information request for DWP to provide all the changes to AtW “operational guidance” in the last 24 months.

But DWP has now replied to say that, although it holds this information, it would take more than three-and-a-half working days to determine “whether the Department holds the information, and locating, retrieving and extracting it”, so it is not obliged to seek the documents under freedom of information laws.

The DWP freedom of information team said this was because “the time period you have chosen is very wide and the topic you ask about is very broad” and suggested instead that DNS should “narrow your request to the latest version of a specific section of a particular topic within Access to Work that you are interested in”.

Speaking to DNS at the Liberal Democrat conference in Bournemouth this week, Darling said this lack of transparency from DWP was “absolutely shameful”.

He said: “We need to have that transparency about what is going on, because the evidence we have has demonstrated that there have been significant changes [to people’s AtW support packages].”

He said he was convinced that cuts were being enacted by DWP even if they were coming through operational changes rather than alterations in policy.

He told DNS that he has heard from disabled people made redundant from disability charities who have been offered much lower levels of support when they applied for AtW support with their new job.

He said: “What was taken as a given with their previous employment, [AtW] are shrinking it down, whether it’s travel to work or the level of support workers, or the way support workers are employed.

It is just absolutely perverse.

I’m sure there are cuts; there are cost savings happening there and I’m sure the Treasury are delighted with it being sucked back into the system.”

A consultation on the future of the AtW scheme has now closed.

Work and pensions minister Baroness Sherlock said, in a written answer to the disabled Liberal Democrat peer Baroness [Celia] Thomas earlier this month, that DWP was now “reviewing all aspects of the Scheme now that the consultation has closed”.

25 September 2025

 

 

Disabled activists working with peers to address serious flaws in ‘dangerous’ assisted dying bill

Disabled activists who are working with sympathetic peers to address the serious risks posed by the assisted dying bill believe there is also still a chance that the legislation could eventually be thrown out by the House of Lords.

Not Dead Yet UK (NDY UK) said there were grounds for “hope” after the completion of the first two days of debate on the terminally ill adults (end of life) bill in the Lords.

Friday’s debate saw speakers opposed to the bill outnumbering supporters by about two to one.

NDY UK said the campaign was “in the best place it could have been, because we can’t kill the bill at this stage.

While NDY UK continues to oppose the bill in principle, it recognises the need to engage with the legislative process to help ensure, if the bill does pass, it contains the strongest possible safeguards to protect disabled people.”

Almost two-thirds of peers who spoke during the debate on Friday (19 September) were opposed to the current version of the bill, while a little over a third were in favour, a similar proportion to the first day of the debate the previous Friday (12 September).

Of 15 Labour peers who spoke on 19 September, nine were in favour, five were against, and one – speaking for the government – was neutral.

But of 29 Conservative speakers, just seven were in favour and 22 were opposed to the bill in its current form.

Liberal Democrat peers were split, with two on each side, while of 11 crossbench speakers, five were in favour and six were against, while seven non-affiliated peers spoke against the bill and just one in favour.

George Fielding, a member of NDY UK’s coordinating group, who watched both days of the second reading debate from the floor of the Lords – as he is a wheelchair-user – said he was “genuinely moved by the quality of the debate, by the nature of the debate”.

He said NDY UK and other opponents of legalisation had formed “a hotchpotch alliance” among cross-party and crossbench peers.

He said: “We are building a network and a consensus across the Lords and I think that is emblematic of the fact that this bill will touch pretty much every corner of our society, and every corner of the House of Lords has people we have found are sympathetic to our views.”

Fielding said NDY UK was convinced that the bill would be “significantly amended” by peers “because the consensus is, at the very, very least, that this is a dangerous bill, it will foreshorten lives.

At the very least, this is going to be one of the most significantly-amended bills in parliamentary history.”

He said NDY UK was “working closely with cross-party peers and allies to propose amendments aimed at closing loopholes and reducing risks, especially around coercion, eligibility, and judicial oversight.”

Fielding said there was an “incredible effort going in the Lords” – with input from NDY UK – to make the bill safer through amendments, because it was currently “unworkable”.

NDY UK welcomed the decision on Friday to set up a select committee of peers that will take expert oral evidence from ministers, professional bodies and legal experts, which Fielding said would be “another public opportunity” for peers to probe the bill’s weaknesses and to “demonstrate how dangerous this bill is”.

He added: “NDY UK plans to contribute evidence and research to inform the committee’s understanding of how disabled people may be affected by the bill.”

This committee will hold six evidence sessions over three weeks, beginning in the week of 20 October.

The committee stage will then follow, with its clause-by-clause examination of the bill.

Among those who spoke in Friday’s debate was disabled Conservative peer Lord [Kevin] Shinkwin, who said the bill would “prise open” a “Pandora’s box” that would be “the stuff of nightmares”.

He said the bill “gives the state a licence to kill the wrong type of people.

I am the wrong type. This bill effectively puts a price on my head.”

He told fellow peers that, if the bill’s scope was expanded over time, he faced “the realistic possibility, as a severely disabled person, of being killed as a result of legislation passed by [the House of Lords]”.

And he pointed out that no organisation of or for disabled people supported the bill.

Another disabled Conservative peer, Lord [Craig] Mackinlay, who became disabled in 2023, said he had found the “joyous, tear-flecked celebrations” by some MPs when the “unwholesome” bill was passed in the Commons to be “quite bizarre and chilling”.

Among his concerns was the risk of coercion, and he told peers: “I am professionally trained and licensed to do probate work through the Institute of Chartered Accountants; believe me, post-death battles over inheritance can get very ugly.

I am fearful of the coercion of the elderly and the vulnerable. It is so obvious.”

Baroness [Luciana] Berger, a former Labour MP and minister, recalled her shock when hearing a constituent speak of wanting their family member dead.

She said she had also not forgotten “the words and realities of too many former constituents: people isolated and abused in their own homes, sometimes for decades, in fear for their own lives; people who felt like a burden because of long-term illness or serious mental health conditions, especially the elderly; and people treated as though their lives were worth less because they had a disability.

Many were from low-income backgrounds, facing not only poor health but the crushing stress of unaffordable care costs.”

She was another peer to point out that there was “no organisation of or for disabled people in this country that supports the bill”, and she added: “In considering who the bill might benefit by giving them more autonomy, we must equally consider who it may harm by taking their autonomy away.”

The former Conservative minister for disabled people, Lord [Mark] Harper, told fellow peers that many of the disabled people he had met as minister and shadow disability minister were “profoundly concerned by what the bill will do to society’s view of people who have challenges thrown in front of them”.

He said the bill was “not supported by a single organisation in this country that represents disabled people – not a single one – and we should listen to their views and take them very seriously”.

The Liberal Democrat peer Lord Beith said: “I have this fear – this instinct – that this is one of those big decisions that society may one day regret. There will be no way back.”

Lord Falconer, the Labour peer sponsoring the bill in the Lords, told fellow peers: “One of the features of this debate was the personal experience that so many people have had of how, had that option been available, it would have ended terrible suffering.

That suffering is not often about the pain but about the lack of dignity and the profound desire to keep control, because that is what people want.

I believe, from my own experience and from talking to so many people, that having that option is important.”

NDY UK argues instead – with many other disabled-led organisations – that the bill risks embedding discrimination into end-of-life law, “especially at a time when many disabled and terminally-ill people still struggle to access basic care and support”.

Lord Falconer also apologised for not declaring in the first day’s debate that he had benefited from an assistant funded by Bernard Lewis – founder of high street retail chain River Island and a supporter of legalisation of assisted suicide – to support him with his work on the bill, and that literature he had sent to fellow peers had been funded by the pro-legalisation organisation Dignity in Dying.

25 September 2025

 

 

UN calls for human rights assessment of government’s benefit cuts bill and mental health reforms

Disabled experts from the United Nations have told the UK government to carry out a “comprehensive” assessment of the human rights impact of its universal credit cuts bill, further plans to reform disability benefits, and its mental health reforms.

The UN’s committee on the rights of persons with disabilities (CRPD) had previously raised concerns about the impact on disabled people of the Universal Credit Act, the mental health bill, and further reforms laid out in March’s Pathways to Work green paper.

It wrote to the government after being alerted to the implications of its plans by DPO Forum England and the user-led, rights-based organisation Liberation.

Now, after assessing the government’s response, and evidence provided by disabled people’s organisations, the committee has called on the UK government to act.

It says it should assess the impact of its reforms, and ensure – in “close consultation” with disabled people – that its future plans do not cause any further “retrogression” in their rights, following years of attacks by successive governments.

The UN committee calls for a comprehensive human rights assessment of both the Universal Credit Act and Pathways to Work, before implementing the cuts and reforms to disability benefits expected in this autumn’s white paper.

And it calls on work and pensions ministers to take measures to “eliminate and reduce” the negative impact of the Universal Credit Act on disabled people, and to carry out a full assessment of its impact after its measures have been implemented.

It should then – again, in close consultation with disabled people – set out a plan to mitigate the impact of the act to ensure disabled people have access to the support they need to fulfil their rights to live independently, be included in the community, obtain work and have an adequate standard of living.

And it says that government plans to scrap the work capability assessment must be “designed and implemented” with the “close consultation and active involvement” of disabled people, and that they should not lead to any further assault on disabled people’s rights.

It calls for action to ensure, after months of concerns about Labour’s plans to force banks to carry out mass surveillance of claimants through its “Orwellian” public authorities (fraud, error and recovery) bill – currently approaching its final parliamentary stages – that those banks are not able to access claimants’ personal and private information.

The committee also calls for a comprehensive human rights assessment of the government’s mental health bill, which has been approved by the House of Lords and reaches the report stage in the Commons on 14 October, to ensure it is “fully aligned” with the UN Convention on the Rights of Persons with Disabilities (UNCRPD).

And it says the government should improve its procedures for measuring the impact of new laws on the rights of disabled people.

Rick Burgess, co-chair of DPO Forum England, said: “We are grateful to the UN for recommending the UK government make a full human rights assessment of the impact of its social security policies, introduce mitigations to protect us from further harm, protect us from bank spying, and remind the government they should be consulting closely with disabled people and our organisations.

It illustrates again that the UK government remains hostile to disabled people, and evades its treaty and legal obligations, but we will not relent in defending our rights and lives.”

Dorothy Gould, Liberation’s founder, said she was “absolutely delighted” that the committee’s response “cuts right through” the government’s attempts to justify its mental health bill, and she praised its “vital” intervention and “refutation of the government’s stance”.

She said the government’s earlier response to the committee had “utterly failed either to acknowledge the continuing, highly discriminatory nature of this bill, or to set out any plans for the fundamental changes that are needed” and had “misleadingly claimed” the bill was compatible with UNCRPD.

And she said it was a “complete disgrace” that the government had “yet again tried to justify the bill’s continuing treatment of people in acute mental distress and people with learning difficulties, or autistic people, as second-class citizens”, and had “again tried to argue that involuntary hospitalisation and forced treatment are not disability-based discrimination”.

Gould said the government was also still failing to make the committee’s Deinstitutionalisation Guidelines “its baseline for ensuring that we can instead live independently in the community, just like anyone else”, while also claiming it was making good use of consultation with user-led groups and individuals with lived experience “in the teeth of contrary evidence”.

Asked if the UK government accepted the committee’s recommendations, and if it would act on them, a DWP spokesperson failed to mention the recommendations in its statement, although it insisted the government was committed to implementing the convention.

In its statement, DWP said: “We’re changing the welfare system so sick or disabled people have the opportunities to move into good, secure work and out of poverty as part of our Plan for Change.

The views of disabled people remain at the heart of our decision making, including through the consultation earlier this year and the Timms Review, which will be co-produced with disabled people and their organisations.

Our reforms will rebalance the rates of universal credit to reduce the perverse incentives that trap people out of work, while giving people the genuine support they need through our £3.8 billion employment support package.”

Asked if the Department of Health and Social Care (DHSC) accepted the committee’s recommendations, and if it would act on them, a DHSC spokesperson also failed to mention the committee in its statement.

Instead, it said: “The Mental Health Act is there to protect people when they are at their most vulnerable, and in many cases, it has saved lives.

But it is hugely outdated and has not kept pace with evolving understanding of mental health, learning disability and autism.

Through our mental health bill, this government is now one step closer to bringing forward the essential reforms that will transform the care of some of our most vulnerable people, providing them with more dignity, choice and voice.

The 10 Year Health Plan sets out ambitious plans to boost mental health support across the country so people can access the right support at the right time in the right place.

This includes ensuring more people get the support they need in the community, closer to where they live.”

25 September 2025

 

 

DWP is ‘dysfunctional’ and needs major review, says Lib Dem Steve Darling

The Department for Work and Pensions (DWP) is “dysfunctional” and needs to be the subject of a major review, according to the disabled MP who speaks for the Liberal Democrats on work and pensions.

Steve Darling said his first year as an MP and as the party’s spokesperson had convinced him of the major problems within DWP and the “broken” social security system.

He said a review would need to engage with disabled people and others with lived experience of the benefits system, and academics, because the benefits system should be co-designed with claimants.

In an interview with Disability News Service at his week’s Liberal Democrat party conference in Bournemouth, Darling also raised concerns about the new work and pensions secretary, Pat McFadden.

He said McFadden appeared to be a “take no prisoners” and “driven” politician and an “enforcer”, and he raised concerns about his past comments about financial support for people with mental distress.

McFadden told Times Radio in March that he wanted benefit claimants with “mental health and depression and anxiety” to be “given support but not financial support”.

Darling also said that McFadden appeared to be a career politician who was lacking in “empathy and engagement and passion for people”, and that he seemed to be “a bit of a SPAD*-spawned apparatchik” who would “probably take no prisoners in driving forward with Starmer’s plans”.

He said he believed that the right-wing Reform UK was “worrying [the government] massively and I fear that they may lose their humanity for fear of Reform”.

Darling also said he had serious concerns about DWP forcing its disabled advisers to sign non-disclosure agreements (NDAs).

He said he and his wife had been forced to sign an NDA after winning a disability discrimination legal case and he said: “I really hate NDAs. They are meant to be there to protect intellectual property of commercial interests.

One of the things that we need to see change on is the culture of DWP and having a more open and transparent approach.”

He said that “slapping NDAs on those who they are engaging with” sends a “negative” message.

Darling also called for the Commons work and pensions committee to investigate the unreliability of DWP statistics on “economic inactivity”.

DNS reported last week that the proportion of working-age disabled people in England who are “economically inactive” was not “spiralling” and may even have fallen over the last nine years, according to new official government statistics.

The new figures came from the Office for Health Improvement and Disparities, just as a leading expert, Professor Ben Baumberg Geiger, from King’s College London, published a blog which showed that DWP’s “raw statistics” on all out-of-work benefits – not just relating to disabled people – were “wildly misleading”.

Darling said he was “keen to suggest” an inquiry by the work and pensions committee into the use of these statistics.

He said an investigation would “either debunk” the figures used by DWP or prove their accuracy.

He said: “My real fear is that, in our now Trumpian world, [the far right] don’t need the facts to add up to make outlandish claims.

The far right will just make up narratives for their own purposes and demonising others is part of their playbook and sadly people with disabilities and quite often people with hidden disabilities are in their crosshairs.”

He said that “unpicking” the claims and counter-claims behind the figures on economic inactivity should be “part of that push back against the far right that we need to be doing” because “otherwise that half-truth will be built on by the far right to demonise people with disabilities”.

*A SPAD is a ministerial special adviser

25 September 2025

 

 

Lib Dems insist they are still focused on social care, despite leader concentrating again on carers

Senior Liberal Democrat MPs have insisted they are still committed to social care reform and want to move towards eliminating all care charges, despite the party saying little or nothing about the issue during its annual conference this week.

Liberal Democrat leader Sir Ed Davey focused again on improving support for “family carers” – he is one himself – but said nothing in his main speech about disabled people who rely on care and support, other than saying he wanted to see a country that “properly values care” and one “where we take care seriously”.

He mentioned family carers like himself 10 times in Tuesday’s speech, without once mentioning the adult social care crisis, which sees tens of thousands of disabled people falling into debt every year because of care charges.

Last year, Disability Law Service published research which showed that disabled people across England were continuing to face unlawful discrimination and inequality on an “unparalleled” scale due to “unjust” social care charging policies.

Earlier in the conference, Dr Danny Chambers, the party’s mental health spokesperson, told Disability News Service (DNS) that he was in favour of moving towards free social care.

He said disabled people were “inadvertently sort of being punished for having a disability because of the changes in personal independence payment and all that kind of stuff, so if it ends up giving people more independence and allowing them to live a much more fulfilling life, it actually ends up costing the taxpayer less anyway.”

At last year’s general election, the party promised to offer free personal care to all adults, although it would not scrap charges for other support such as housework, shopping, laundry and engaging with the local community.

During a Health Foundation and Ipsos fringe event, Dr Chambers said the party was “absolutely focusing” on social care.

The Winchester MP said that, at any one time, the Royal Hampshire County Hospital in Winchester had between 160 and 200 people “who would be better off cared for with a social care package than stuck in a hospital bed”.

But, he said, it costs more than £850 a night to keep someone in a hospital bed and only a fraction of that to fund a social care package.

This may save a council money from its social care budget, he told the meeting, but “as a tax-payer, you don’t care which silo it comes out of, it’s costing us £850 a night to keep these hundreds of people in a hospital bed that don’t need it.

Our mantra has been, ‘You can’t fix the NHS without fixing social care.’”

He said his party had been “genuinely disappointed and quite annoyed” that the new Labour government had so far placed “so little emphasis on social care”, including in the NHS 10 Year Health Plan for England, and the NHS workforce plan, due this autumn, and extra funding provided to the NHS.

He said: “None of it is focusing on social care.

They are pouring money into a leaky bucket, and if you do not plug those holes it doesn’t matter how much money or how much you try and reform other parts of the NHS, it means there’s always going to be this huge drain that means you cannot unblock these huge problems.”

At a question-and-answer session, also attended by Dr Chambers, the party’s health and care spokesperson, Helen Morgan, told DNS that she came away from a cross-party roundtable meeting on social care reform feeling “reasonably optimistic”.

The long-awaited meeting was held to discuss the work of the government’s Independent Commission on Adult Social Care, which is chaired by the crossbench peer Baroness [Louise] Casey.

It was attended by senior representatives from the Labour, Conservative, Liberal Democrat, Green and Reform UK parties, including health and social care secretary Wes Streeting.

Asked by DNS whether she was encouraged by the attitudes of the other parties on social care, Morgan said on Monday that she came away feeling “reasonably optimistic”.

But she said she made clear in the meeting that the Liberal Democrats believed that the timetable set by the government, which will not see the commission produce a final report until 2028, was “too late”.

But she said: “At least we had that first discussion, and we had that opportunity to point out the urgency of delivering.

It was an introductory discussion; it was trying to find the points of similarity between the different manifestos.

I wouldn’t say there were any particular breakthroughs in the first discussion.

At least we had that first discussion, and we had that opportunity to point out the urgency of delivering.”

Dr Chambers said earlier in the week that the government’s decision to wait until 2028 for the commission’s final report suggested it was “playing for time”.

He said: “We don’t need to wait until 2028 to say something needs to be done and then start the process of implementing something.”

At another fringe meeting, hosted by the Liberal Democrat Disability Association (LDDA), Dr Katharine Macy, LDDA’s chair, called for the party to do more to focus on social care.

They wrote the young carers motion to the party conference in 2019 which kickstarted Davey’s focus on carers.

And they told the fringe meeting that the party’s public statements on care can sometimes suggest that disabled people are “a burden”.

Dr Macy, a disabled person and carer themself, said: “There are times when it has crossed the line. There are times when it very much skirts the line.”

They said their party needed to be aware that there were more disabled people than carers, although the emphasis in its public statements also reflected a culture where caring is seen as noble and being disabled is seen as being a burden “and that is where we can start to change things”.

Dr Macy said the party needed to address its focus on caring rather than social care, but that the Liberal Democrats needed to do that by saying more about social care rather than less about caring.

25 September 2025

 

 

New publications ask how disabled people and allies can hold the state to account for welfare state killings

A new series of resources examines ways in which disabled people and allies can find ways to hold the state to account for the deaths of hundreds – and probably thousands – of claimants it has killed through welfare state violence.

The three resources are being released as part of the Deaths by Welfare project at Healing Justice Ldn, which has previously created a timeline charting 30 years of evidence linking the systemic violence of the Department for Work and Pensions with the killing of countless disabled claimants of benefits through state violence.

The Deaths by Welfare project has also produced an exhibition, podcasts, and more than 50 interviews with disabled activists and bereaved family members.

Healing Justice Ldn hopes the new resources* – written by Dr China Mills – will inspire activists to find new ways to secure welfare justice and work towards new, “life affirming” systems of support.

The first resource to be published, Deaths by Design, asks whether the social security system was actually “deadly by design” rather than being a system riddled with flaws and mistakes by DWP staff.

It points to the coroner who concluded at the end of an inquest into the death of Philippa Day that there were systemic flaws in the personal independence payment system.

As disabled activist and author Ellen Clifford said in one of the Deaths by Welfare podcasts: “They created a system that’s deliberately designed to push people into poverty because our lives are worth less to them than other people’s.”

And it quotes fellow disabled activist Rick Burgess, in another Deaths by Welfare interview, who said: “We’re now 14 years into this process; that’s not an accident, that’s not a passing fad – that’s a cultural democide against a demographic, that demographic being disabled people benefit claimants.”

Deaths by Design asks the question: “If systems are harmful by design then we need to campaign beyond ‘cuts’.

If we only mobilise around ‘cuts’ to welfare, we might overlook how harmful the foundation of welfare can be.”

And it concludes: “People want to build a different welfare system but it’s hard to get specific about what we want… when all we’ve known is a violent bureaucratic system.”

Another of the resources, Evidence, examines how disabled people and bereaved fam­ilies have produced evidence of state harm; how to use that evidence in ways that do not dehumanise disabled people; and how disabled people have used direct action to alert the public to this evidence.

It points out that constantly being asked to provide evidence of the harm the system is causing “mirrors the violence” of claimants being forced to prove they are disabled so they can receive the support they need to survive.

One of the questions it asks is: how many people must die through DWP violence before those in power listen and act?

The third resource, Accessing Justice, co-written by Dr Mills and Imogen Day – whose sister took her own life due to DWP’s actions and failings – examines how families bereaved by DWP killings have sought justice.

It looks at the experiences of relatives Joy Dove, Alison Burton and Imogen Day – each of them disabled people themselves – after the deaths of their daughter, father-in-law and sister through DWP violence.

It also hears from the mothers of Seni Lewis and Komang Jack Susianta, who were both killed by non-DWP state violence.

While Accessing Justice accepts that some activists want to see those guilty of complicity in the state killings face criminal justice, HJL also questions whether justice for those killed can ever be secured through the criminal justice system, and whether there are other ways of holding those responsible accountable.

*DNS editor John Pring was involved in editing the resources and was co-editor of the Deaths by Welfare timeline

25 September 2025

 

 

Mother left ‘disgusted’ by DWP’s silence over secret report into Jodey Whiting’s death

The Department for Work and Pensions (DWP) has refused to release any information about a secret report into the death of a disabled woman, despite a coroner ruling that its actions had been the “trigger” for her suicide.

DWP has even refused to tell lawyers for the family of Jodey Whiting whether it carried out an internal process review (IPR) into her death.

It claimed in the letter that releasing an IPR to her family could breach her privacy, even though she died more than eight years ago.

It said IPRs were “internal retrospective investigations focused on organisational learning, not public accountability” and that they “often contain sensitive personal information about claimants, including health, benefit history, and interactions with DWP staff”.

It added: “The disclosure of such information, even to close family members, could be considered a breach of privacy.”

Disability News Service (DNS) reported in June that a second inquest into Jodey Whiting’s death – which only happened because of her mother’s eight-year campaign for justice and accountability – found that her “deteriorating” mental health had been “precipitated” by the withdrawal of her out-of-work disability benefits after she missed a work capability assessment.

But DNS also showed in June how DWP hid the truth from the coroner about its role in Jodey Whiting’s suicide, including by failing to confirm if an IPR was carried out.

Joy Dove, Jodey Whiting’s mother, told DNS this week that she was “really disgusted” by DWP’s refusal to release the IPR – or even to say whether one was carried out – after campaigning for more than eight years to discover the truth about DWP’s role in her daughter’s death, and for justice for her and countless other disabled people whose deaths were caused by DWP.

She said: “We were forced to give documents to the coroner, we had to do what we were told, so why the heck can’t they?

What’s the problem? We know she’s dead because of them. What are they hiding?

They don’t care. To them, Jodey is just a number. It’s not personal to them. They are not bothered.”

In the letter, a solicitor in the Government Legal Department – writing on behalf of DWP – made it clear that DWP “fully accepts the coroner’s conclusions” in the second inquest, and “accepts that the withdrawal of Jodey’s Employment and Support Allowance precipitated her deteriorating mental state”.

But further anguish was caused to the family by the Government Legal Department mis-spelling Jodey’s name in a brief one-line apology included in the letter, saying: “Please do pass on this heartfelt and sincere apology from DWP to Jodie’s family.”

Dove said she was annoyed at this lack of care and respect and said she did not consider it a “proper apology”.

She is now considering a complaint to the Parliamentary and Health Service Ombudsman over DWP’s actions and its role in her daughter’s death.

The letter came as Steve Darling, the Liberal Democrat work and pensions spokesperson, told DNS that he was hoping to use the government’s new Hillsborough Law to force DWP to release IPRs to relatives.

This is because Labour’s public office (accountability) bill includes a new legal duty on public authorities and public officials “to act with candour, transparency and frankness”.

In an interview with DNS at his party’s annual conference in Bournemouth, Darling said he wanted the bill to produce a “culture change” within DWP and the whole of Whitehall, and that he intends to ask parliamentary questions on how the release of IPRs will be part of that.

The solicitor for Jodey Whiting’s family, Merry Varney, from Leigh Day, said yesterday (Wednesday): “Joy has fought for many years to secure recognition that Jodey’s death was caused by DWP failings.

The second inquest into Jodey’s death confirmed that earlier this year and during the hearing the DWP witness was unable to confirm whether an internal process review had been competed following Jodey’s death.

Joy had hoped that a full and frank apology, together with disclosure of information about any internal process review, would come from the DWP.

The response indicates a continued unwillingness of the DWP to be fully transparent and to admit, in clear unequivocal terms, that their acts and omissions cause deaths.”

A DWP spokesperson said: “We continue to offer our sincerest condolences to Jodey Whiting’s family and are deeply apologetic for the misspelling of her name.”

The Department: How a Violent Government Bureaucracy Killed Hundreds and Hid the Evidence, DNS editor John Pring’s book on the years of deaths linked to DWP, including Jodey Whiting’s, is published by Pluto Press

25 September 2025

 

 

Anger and frustration after DWP’s latest jobcentre announcement and McFadden’s ‘incentives’ comment

Sick and disabled people have raised serious concerns about the latest Department for Work and Pensions (DWP) announcement on its strategy to persuade more claimants receiving out-of-work sickness and disability benefits to consider moving towards employment.

Many reacted angrily to DWP’s announcement that every jobcentre in England, Scotland and Wales now has “specialist” Pathways to Work advisers who will offer skills and employment support to claimants receiving out-of-work disability benefits.

DWP said it has redeployed 1,000 existing jobcentre staff to provide voluntary help to people on universal credit who have “no requirement to look for work or engage with job help because of their condition”.

Disabled people highlighted concerns this week about safeguarding and the lack of evidence for such a strategy, and they questioned why a Labour government did not do more to focus on cutting NHS waiting-lists and addressing barriers in the workplace.

Their anger and frustration only increased when new work and pensions secretary Pat McFadden claimed in an interview that there were currently “incentives” in the system for people to declare themselves unfit for work so they can “double their money”, and also claimed that people were “declaring themselves long-term sick”.

McFadden will have been aware that claimants cannot declare themselves “long term sick” but instead must go through the harsh work capability assessment process in order to be found not fit for work, and he should also have been aware that this system has led to countless deaths.

Researcher and writer Sue Jones responded on X/Twitter: “Progressive, incurable illnesses are not ‘perverse incentives’ you vicious man, and no amount of lying about people and inventing ‘incentives’ and motives will change the fact that many of us can no longer work, simply because we are too ill and disabled.”

DWP said it hoped its Pathways to Work advisers would help 65,000 people found to have limited capability for work and work-related activity (LCWRA) by the end of 2025-26.

DWP claimed this kind of “additional work coach support” was “proven to help people into work” and that research had found LCWRA claimants who accepted this support were a third more likely to be in work a year later.

However, the research it referenced, published by DWP in March*, showed the proportion of those in the LCWRA group in work rose from just eight per cent to 11 per cent, a year after the provision of “additional work coach support”.

The department said more than 10,000 people had taken up the voluntary offer and had had at least one appointment since April 2025.

It said it would not contact claimants with “the most severe and lifelong health conditions” – which DWP later confirmed will match the “severe conditions criteria” described in schedule one of the new Universal Credit Act – or those who receive support through the “special rules” for those with less than 12 months to live.

But there was significant concern among sick and disabled people on social media after the announcement.

Disabled People Against Cuts said on its Facebook page: “The question that’s in the back of our minds is, how long before it’s mandatory?”

Many warned that even a voluntary approach would cause serious safeguarding issues.

The anti-cuts grassroots group Disability Rebellion said on X/Twitter: “Here we go again – DWP are now going to ask thousands of UC claimants with no requirement to look for work to attend ‘work conversations’.

No thought given to safeguarding or how unwell this could make people.”

Another grassroots group, Recovery in the Bin, said: “We don’t need f*****g skills. We need healthcare, housing, enforceable legal rights.

Want to improve disabled people’s access to work? Make legal aid more widely available for disability discrimination cases.”

Others pointed out that such initiatives “barely make a dent in employment rates”, because the reasons sick and disabled people are not in work are not “lack of coaching, confidence, etc”.

Many suggested that the government would do better to focus on improving access to NHS services and investing in treatment for conditions such as long Covid and ME, and addressing discrimination by employers.

Similar points were raised by those who said the barriers they faced were not those that could be addressed by DWP Pathways to Work advisers.

One of those who responded to the announcement said: “I worked for Goldman Sachs, UBS, Deutsche Bank, Standard Chartered, etc over the course of my career.

I do not need more skills or experience. I am TOO ILL to work.”

Another said: “I’m chronically ill and mostly bedbound. I’m a fully skilled plater/welder.

I also have qualifications in carpentry, hedge laying, dry stone walling, and also have chainsaw licence to fell medium sized trees.

My problem isn’t skills. It’s illness.”

*DWP did not provide a link to this research in its press release

25 September 2025

 

 

Other disability-related stories covered by mainstream media this week

MPs have warned the Government of a “showdown” over reforms to the special educational needs system they fear will cut support for disabled children. Labour members say they are gearing up to vote against any changes that “take away services” or “reduce support, financial or otherwise” for pupils with special educational needs and disabilities. Backbenchers say their red lines would also include children losing their legal rights to funding and provision – currently set out through education health and care plans: https://inews.co.uk/news/education/starmer-collision-course-mps-send-reforms-austerity-3930632

Trafford Council’s new council tax reduction scheme must be quashed after a high court judge ruled it unfairly discriminated against two “vulnerable” residents who discovered they had to pay the full bill when previously they had to pay nothing because they were on benefits. A judge ruled the council’s working-age local council tax reduction scheme for 2025-26 was both unlawfully adopted and discriminatory against disabled people and carers on certain benefits: https://www.manchestereveningnews.co.uk/news/greater-manchester-news/high-court-slams-obviously-unfair-32514179

More than 1,000 disabled children across the UK are waiting for wheelchairs and mobility equipment that could transform their lives, according to charity Whizz Kidz. The charity, which helps wheelchair-users up to 25 years old, has been forced to close its specialist wheelchairs waitlist for the first time in its 35-year history. It says escalating costs and squeezed NHS budgets are creating a “huge demand” for its service, leading to long delays: https://www.bbc.co.uk/news/articles/cm2zwm8m41mo

25 September 2025

News provided by John Pring at www.disabilitynewsservice.com

 

Sep 132025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Calls for an independent PIP review with UK minister under fire

A Welsh disability group is calling for an independent review of Personal Independence Payments (PIP).

Disabled People Against Cuts Cymru (DPAC Cymru) has accused the disability minister Stephen Timms of failing to properly lead his own review into the disability benefit, saying that “co-production is not taking place as promised.”

Speaking exclusively to LBC’s Welsh Correspondent Caitlin Parr, the group’s comments follow the Minister of State for Social Security and Disability, Sir Stephen Timms MP, meeting with the Welsh Government Disability Equality Forum on Tuesday 2nd.

LBC news reported that DPAC Cymru had long fought for disabled people’s voices to be heard in changes to welfare reforms, but were concerned that the minister, despite promises to engage widely over the summer, had so far left Welsh disabled people out of discussions around the review, outside of those forum meetings.

DPAC Cymru claims that Timm’s attendance at those recent forum meetings is “far too little and far too late for Welsh disabled people after months of stonewalling from Timms,” and said they were frustrated by “more promises but no action.”

Ben Golightly, from Swansea, is a coordinator for DPAC Cymru. He told LBC, “he [Timms] agreed in that meeting that it was important for Welsh disabled people and Welsh disabled people’s organisations to be heard. He was meant to talk about how he was delivering co-production. It was his job to do it. And he had no real update, because he hasn’t been doing that job.”

Despite promises from government ministers, DPAC Cymru say that co-production has not taken place, and they are “back to square one.”

Ben said, “We had hoped that after a major defeat in parliament that when he [Timms] promised co-production with disabled people, that we wouldn’t have to go through all of this again. There is so little trust in the way the government has treated disabled people that we need an independent review, led by disabled people, and Stephen Timms and the government should turn up and listen, but they should have no say over how it’s run because they’ve shown, throughout several months, that they’re unable to do it.”

Lee Ellery, an independent disability activist and lead press coordinator for DPAC Cymru, who has Cerebral palsy quadriplegic, agreed, telling LBC news it’s time more Welsh voices were heard.

Lee said, “people with disabilities, particularly in Wales, are left to the bottom of the pile so to speak, and we should be at the forefront of everything. I’m worried about what the result of the [PIP] review might come out to say, if the person who’s leading it doesn’t understand the whole process.”

LBC news reported that “the Timms review into PIP assessments is expected to conclude in Autumn 2026, when changes already decided on for new PIP claimants will come into force.”

DPAC Cymru’s calls for an independent review, made in an open letter released last Monday, has already received wide support, collecting 600 signatures and the support of representatives of more than twenty-five organisations.

Comments collected from respondents talk about their feelings of hurt, being “belittled,” “completely disregarded and isolated,” and the “harm and loss of trust” caused by Timms and the government.

Signatures on the open letter are open until the end of September.

Sign here

A notice graphic with a red tinted photograph of Stephen Timms as the background. Title text to the left of him reads: "We want an independent PIP review" with emphasis on the independent. A divider then separates the next header text that reads: "Nothing about us, without us!", followed by another divider. Body text then reads: "Please sign and share our open letter!" with an arrow pointing to a link: "bit.ly/independent-pip-review". The DPAC Cymru logo sits at the bottom of the screen.
Sep 062025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Trade unionists look after people at work and in the community. There are 1.4 million disabled trade unionists. There is a big trade union meeting starting Sunday and ending Wednesday called the TUC (Trades Union Congress)

That meeting is discussing lots of different things (motions) and voting on them. If you are a member of a trade union you might know someone who is going, called your delegate. You might want to talk to them about the following:

 

Sunday 7th, 1pm

National Shop Stewards Network lobby – The Old Ship Hotel, Brighton, BN1 1NR.

One of the speakers is from Disabled People Against Cuts and the lobby is asking the TUC to support disability motions. More info.

 

Tuesday 9th (scheduled late morning)

Motion 38 – Disabled workers oppose welfare reforms

from the

TUC Disabled Workers Conference

 

Tuesday 9th (scheduled late morning)

Motion 39 – Oppose disability benefits cuts emergency

from the

TUC Trades Councils Conference

 

See what’s being discussed

https://www.tuc.org.uk/Congress2025/programme-business-congress-2025

 

Watch live or recorded sessions

https://www.tuc.org.uk/Congress2025/congress-live

Sep 012025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

The words "We want an Independent PIP Review" in bold and black text, with Independent highlighted in red. On the left there is a tear-out effect of a greyscale photo of a disability protest, and a red-tinted photo of Stephen Timms, the disability minister.

This is an open letter from DPAC Cymru, produced with feedback from six Disabled People’s Organisations.

Disclaimer: DPAC Cymru didn’t have time to reach 100% agreed wording with DPAC UK, as we would have liked to. Even within DPAC Cymru, the letter wording is somewhat of a compromise. However, for important tactical reasons in Wales, we felt it was important to publish without delay. DPAC have therefore agreed to share the letter with this disclaimer.

Click here for the Easy Read version.

To:

The Welsh Government,

The Scottish Government,

The Northern Ireland Executive,

The UK Government,

1st September 2025

After a major, if partial, defeat in parliament over disability cuts, the disability minister Stephen Timms promised MPs that the PIP benefit review would be co-produced by disabled people and their organisations.

There is widespread skepticism if this will genuinely be the case. Promises to “engage widely over the summer” have not been met, and there has been no transparency over Timms’ plans for “ten people” to have “a lot of sway”. His comments reveal that he does not understand what co-production means. Timms has also repeatedly declined to acknowledge the many serious failures of the Pathways to Work green paper consultation process, particularly felt in Wales.

We counterpose this to the Disability Rights Taskforce, initiated in partnership with the Welsh Government, which brought together 350 stakeholders and 200 policy experts, as a model of what co-production can look like. However, many Taskforce participants were frustrated that much of their work was ultimately missing from the Welsh Government draft plan. This is a lesson that even co-produced policy will fall flat without accountability. Disabled people’s organisations must be given the necessary resources and powers to carry out the implementation and monitoring of decisions.

[Some of us] cautiously welcome[d] the announcement of the Government’s new Independent Disability Advisory Panel. This panel is separate to, but will feed into, the Timms review of PIP. However, trust remains very low, and the terms – of “up to 10” people – have already been set for us. [See update, below]

We the undersigned demand that:

• The new Independent Disability Advisory Panel must be genuinely independent, representative, transparent, and have real powers of oversight.

• The UK government must acknowledge its failures in delivering the Pathways to Work consultation and legislative process, as a precondition to rebuilding trust and ensuring those mistakes are not repeated.

• The PIP review must be independently led by disabled people and our organisations, inviting the views of carers, volunteers, and workers in health, social care, housing, transport, and welfare.

• Any review of welfare reform must also, in a process led by disabled people, involve trade unions as democratic organisations representing 1.4 million disabled workers as well as representing the workers responsible for the day-to-day delivery of services that disabled people rely on.

• The scope of the PIP review must be widened to all aspects of welfare and employment for disabled people, guided by the principle: from each according to their ability, to each according to their need.

• Dedicated funding must be provided to Disabled Peoples Organisations to support outreach, accessible engagement, and the collection of views from disabled people, including those without internet access or digital skills.

• The devolved governments of Wales, Scotland, and Northern Ireland, and councils, should recognise and support this independent review even if the UK government refuses to.

• The UK government must immediately halt all cuts to disability and incapacity benefits for the duration of the review, and urgently fix Access to Work.

• Parliament must be given time to properly scrutinise any new legislation.

• The UC bill should be repealed. It is flawed, and was rushed through in an abnormal and undemocratic way.

 

[Update 4th September] Statement from DPAC Cymru regarding the “Independent Disability Advisory Panel”:

“The recently published terms for the so-called Independent Disability Advisory Panel, including the requirement to sign a non-disclosure agreement, are completely unacceptable. We are going to go back to a full consultation with all of our members and allies and take time for discussion to correct the weakness in our compromise wording of ‘cautiously welcome’ and come back united, realigned on the strongest possible response. We hope you will continue to support the demand for an independent PIP review, led by disabled people, and support this letter with your signature.”

 

For a full list of signatures and footnotes, see here.

To add your support to the letter, add your signature here

Here are short URLs for sharing the letter:

Non-Easy Read: Bit.Ly/independent-pip-review

Easy Read: Bit.Ly/easy-read-independent-pip-review

Aug 222025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

From Merseyside DPAC:

 

Join Disabled People Against Cuts to protest against the Labour policies killing disabled people outside the Labour Party conference in Liverpool 29/09/2025 at 12pm. We will assemble near the Wheel of Liverpool on Keel Wharf L3 4FN.

We encourage those who can to a mask in order to protect immunocompromised members of our community and will have some masks available for those who do not have their own. We ask that political parties do not bring branded placards.

#GenocideAbroadDemocideAtHome #WelfareNotWarfare

 

"Text over a dark background with the disability pride colours. Text reads "Genocide abroad, democide at home is Labour policy. 12:00 September 29th, the Wheel of Liverpool L3 4FN"

Beneath the text is an inverted black triangle with the text "DWP stop killing us" and a black and white photo of a group of protesters with a Merseyside DPAC banner.

Jul 032025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

A poster about a protest. On a marble blue background with black bold text. It says: Disabled People Against Cuts Cymru. Disability Protest. Swansea - Cardiff. Below that is an image of three women protestors. One is in a wheelchair. They have a red flag, a red sheet, and a purple placard. They are dressed in red and purple. To the right is a red megaphone graphic. To the left is the DPAC logo. It is a red, pink, blue, green wheel being held by four hands of different skin tones. In the center is an upside down black triangle bearing the letters D P A C. Below, the text says: Cardiff - Monday 7th July. Meet 4pm outside Cardiff Central Library Hub. Swansea - Tuesday 8th July. Meet 4pm at Castle Square, Swansea. Organiser: 07410 303 652.

Disabled people in Wales will be protesting in Cardiff on Monday 7th, and in Swansea on Tuesday 8th.

We will be meeting at 4pm.

In Cardiff, meet outside Cardiff Central Library Hub.

In Swansea, meet at Castle Square.

All support is welcome! Bring friends and banners etc.

This is ahead of the vote on the bill on Wednesday 9th.

We want to defeat the Labour disability cuts bill entirely.

 

Why we are still protesting

⚫ The victory on changes to PIP is temporary. It’s a bad bill that will mean MPs voting to approve the results of a review in advance, before it happens.

⚫ We do not trust Stephen Timms to lead the PIP review. He has not acknowledged our concerns about the failures of the original consultation process.

⚫ Under 22s still face loosing Universal Credit health component – an injury to one is an injury to all and we won’t leave anyone behind!

⚫ The bill still contains cuts to Universal Credit for new claimants.

⚫ It’s very uncertain what the bill will mean for people on ESA.

⚫ It is a rushed bill and the government is acting undemocratically.

⚫ The government must stop and listen to disabled people and carers, and consider our consultation responses.

⚫ The bill must be withdrawn and time taken to get it right!

⚫ We have gone beyond “co-production”. This government is incapable of doing it. Disabled people must lead the process of welfare reform, involving carers and the workers delivering the welfare system. Not clueless ministers seeking short-term cost savings.

 

Swansea and Cardiff protest graphics for social media

A graphic of the DPAC Cymru logo. There is the main DPAC logo to the left, which is a red, pink, blue, and green circle being held by four hands of different skin tones, with the words "disabled people against cuts" surrounding it, and an upside-down black traingle in the middle bearing the letters D P A C. On the right is the word Cymru (pronounced cum ree) (C Y M R U) in large letters, and the background of the letters are cutouts of the Welsh flag. Above Cymru (pronounced cum ree) is written the words Disabled People Against Cuts. Below Cymru (pronounced cum ree) are the words Rights, not charity, and the equivilant phrase translated into the Welsh language.
Stop the Cuts This is our last chance! Date: Tuesday 8th July 2025 Time: 4:00pm Meeting point: Castle Square, Swansea, SA1 3PP what3words: ///bunny.extend.error MPs final vote for the Bill is 9th July so this is our last chance to take action against it. Labour want to cut disability benefits that people rely on to survive – we say stop the cuts! Listen to disabled people! Join us to tell Labour to kill the cuts, not disabled people. @DPAC_CYMRU #WelfareNotWarfare
Stop the Cuts This is our last chance! Date: Monday 7th July 2025 Time: 4:00pm Meeting point: Cardiff Central Library Hub, The Hayes, Cardiff, CF10 1FL what3words: ///rounds.unions.salsa MPs final vote for the Bill is 9th July so this is our last chance to take action against it. Labour want to cut disability benefits that people rely on to survive – we say stop the cuts! Listen to disabled people! Join us to tell Labour to kill the cuts, not disabled people. @DPAC_CYMRU #WelfareNotWarfare

A poster about a protest. On a marble blue background with black bold text. It says: Disabled People Against Cuts Cymru. Disability Protest. Swansea - Cardiff. Below that is an image of three women protestors. One is in a wheelchair. They have a red flag, a red sheet, and a purple placard. They are dressed in red and purple. To the right is a red megaphone graphic. To the left is the DPAC logo. It is a red, pink, blue, green wheel being held by four hands of different skin tones. In the center is an upside down black triangle bearing the letters D P A C. Below, the text says: Cardiff - Monday 7th July. Meet 4pm outside Cardiff Central Library Hub. Swansea - Tuesday 8th July. Meet 4pm at Castle Square, Swansea. Organiser: 07410 303 652.

A poster about a protest. On a marble blue background with black bold text. It says: Disabled People Against Cuts Cymru. Disability Protest. Swansea - Cardiff. Below that is an image of three women protestors. One is in a wheelchair. They have a red flag, a red sheet, and a purple placard. They are dressed in red and purple. To the right is a red megaphone graphic. To the left is the DPAC logo. It is a red, pink, blue, green wheel being held by four hands of different skin tones. In the center is an upside down black triangle bearing the letters D P A C. Below, the text says: Cardiff - Monday 7th July. Meet 4pm outside Cardiff Central Library Hub. Swansea - Tuesday 8th July. Meet 4pm at Castle Square, Swansea. Organiser: 07410 303 652.

Jul 032025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Contents

Disastrous’ cuts bill that leaves legacy of distrust and distress ‘must be dropped’ 1

Four disabled Labour MPs stand up to government over cuts to disability benefits 4

Silence from MP sister of Rachel Reeves over suicide linked to PIP flaws, just as government was seeking cuts 7

Disabled people receiving care were ‘ignored by design’ during the pandemic, Covid inquiry hears 9

Disabled activists warn Labour MPs who vote for cuts: ‘The gloves will be off’ 12

GB News says it has nothing to apologise for, after guest suggests starving disabled benefit claimants 15

SEND inspections find services in just one in four areas usually lead to ‘positive’ outcomes for disabled children 17

Other disability-related stories covered by mainstream media this week 19

 

Disastrous’ cuts bill that leaves legacy of distrust and distress ‘must be dropped’

Disabled activists have called on the government to scrap its “dangerous” and “disastrous” disability benefits bill, despite forcing ministers into last-minute changes that scrapped all their planned cuts to personal independence payment (PIP).

Chaotic events in parliament on Tuesday, and three months of activism since the publication of the Pathways to Work green paper, have left disabled people’s organisations (DPOs) appalled, shocked, and struggling to trust the government.

Their activism, together with the efforts of a small group of backbench MPs, forced ministers into a series of U-turns and concessions on the universal credit and personal independence payment bill.

The lack of trust in the government, and in the minister for social security and disability, Sir Stephen Timms, now creates a significant barrier as he begins a year-long review of personal independence payment (PIP), including an examination of its eligibility criteria and assessment process.

A chaotic few hours in parliament on Tuesday led eventually to ministers withdrawing all their proposed cuts to PIP, at least until the end of the review next autumn.

The bill passed its second reading by 335 to 260 votes, and it will return to the Commons on Wednesday (9 July) for its committee stage, with significant cuts to the health element for most new claimants of universal credit from next April remaining in the legislation.

Disabled people’s organisations were united yesterday (Wednesday) in their call for the “sham of a bill” to be dropped, with many expressing distrust in the government.

And there was little celebration that their successful activism – led by Disabled People Against Cuts (DPAC) and other grassroots groups such as Taking the PIP – had forced the government into gutting its bill.

DPAC described the bill as a “complete and utter mess”.

Paula Peters, a member of DPAC’s national steering group, said the process had done nothing but “cause more anxiety and more distress for disabled people”. 

She told Disability News Service (DNS) that she did not trust Sir Stephen as he had “shown time and again he doesn’t listen to charities, DPOs or disabled people”.

And she pointed to the concerns – expressed also by some MPs – that the government will merely introduce a new series of cuts to PIP at the end of the review, through a parliamentary mechanism that means they will not need to be approved by MPs.

Svetlana Kotova, director of campaigns and justice at Inclusion London, was also distrustful of the government’s motives.

She said: “The social security system needs reform, but not like this.

It is clear that this was never about reform, it was about balancing the books at the expense of disabled people.

Removing PIP cuts from the bill is a positive step, but there is no guarantee the government will be open to true co-production; more likely, they will want us to engage in ‘co-producing cuts’.

The bill still includes deeply harmful cuts to universal credit.

The government should admit they made a mistake, drop this harmful bill and go back to the drawing board.”

National Survivor User Network (NSUN) said the decision to gut the bill was “the direct result of tireless campaigning by disabled people and their organisations in recent weeks”.

But it said that the chaotic and confusing way it was passed showed “callous disdain for the lives of disabled people”, while the bill “should have been withdrawn in its entirety”.

An NSUN spokesperson said: “It is vital that co-production through the Timms review meaningfully involves disabled people, putting power in the hands of those whose lives will be most impacted.

We have seen the violence of the government’s rubber-stamp consultations so far and demand genuine co-production rather than inadequate and tokenistic consultation on an already-decided course of action.”

And it said the refusal to remove the cuts to the health element of universal credit for most new claimants from the bill showed the government “remains willing to attack disabled people” and was “a shameful attempt to divide the disabled community and stifle solidarity”.

The NSUN spokesperson added: “We will continue to organise with DPO allies, push for the rights-based reform which our deadly social security system needs, and ensure there are electoral consequences for those who go after disabled people in this way.”

Disability Rights UK (DR UK) said disabled people would be “enormously relieved” that the PIP cuts had been dropped from the bill, although “serious concerns” remained about the cuts to the health element of universal credit for most new claimants, which would make hundreds of thousands of the poorest people in the country even poorer.

A DR UK spokesperson said: “We’ve known all along that the public, disabled people and our organisations have found this bill to be unjust and unfair.

Yet the government has used every tool in its arsenal, every procedural trick, to push this dangerous bill through.”

DR UK said the government’s “floundering and chaos” was “a direct result of the steadfast work of disabled campaigners and our allies, who have made it clear that this bill is unworkable.

Despite attempts to silence us, through our collective campaigning, we made them drop billions of pounds worth of cuts, and we will continue to resist this disastrous bill.”

Rick Burgess, campaigns lead at Greater Manchester Coalition of Disabled People, said Tuesday’s events had demonstrated the “arrogance and disrespect” of the government, and he also called for the bill to be scrapped.

He said the bill still contained cuts to the health element of universal credit, and it imposed “extremely restrictive” criteria on those who will be offered some protection through the “severe conditions criteria”.

He said disabled people would seek to stop these elements of the bill through amendments.

Burgess added: “The PIP review must be to a specified standard of coproduction agreed with our organisations and be subject to statutory public consultation.

Given our experience to date, however, we have low confidence in the government.

However, it must also be said, while we lost the vote, we won a victory in gutting the bill and exposing the utter shambles of Starmer’s administration.”

The grassroots, user-led mental health group Recovery in the Bin (RITB) delivered a bleak assessment last night of the impact of the government’s actions.

An RITB spokesperson told DNS: “The whole sequence of events from the announcements, to constant vilification in the media, and from ministers, especially Kendall and Timms, has caused such distress that Labour have ended any hope of support.

They are loathed and despised, and we have no trust whatsoever in them not to attack us.”

AJ Le Brun, a disabled activist with DPAC Cardiff and Valleys, said the bill had been “rushed through” with no thought for disabled people.

She said: “The changes and promises made in the final hours before the vote may have soothed the consciences of some MPs, but we see through these shaky promises.

The changes to universal credit will push more of us into poverty, when we are already struggling with the rising costs of aids and support needed to live with dignity.

I do not trust Stephen Timms and his department to conduct a fair PIP review.

They have shown us they are not listening to disabled people by only providing one face-to-face consultation for Wales, and holding the vote the day after the consultation formally closed.

What confidence can we have that this review will be any better?”

Because of the number of changes to the original bill, DNS asked DWP to confirm exactly what the bill would now do.

Here is the list provided by the department (edited for clarity by DNS):

  • The bill will make changes to universal credit (UC) from April 2026
  • It will not bring forward any changes to the PIP eligibility criteria

From April 2026:

  • The standard allowance of UC will rise above inflation in each of the next four years
  • The health element of UC for new claimants will be reduced to £50 per week
  • Existing claimants of the health element and those new health element claimants meeting the severe conditions criteria (SCC) or considered under the special rules for end of life (SREL) will see their UC standard allowance combined with the UC health element rise in line with inflation in the next four years
  • People in the SCC group will be exempt from future UC reassessments

3 July 2025

 

Four disabled Labour MPs stand up to government over cuts to disability benefits

Four disabled Labour MPs stood up to their government’s attempts to reduce vital disability benefits, despite ministers’ chaotic last-ditch concessions to rebels that removed a significant chunk of their cuts bill.

Marsha de Cordova, Marie Tidball and Emma Lewell all voted against the universal credit and personal independence payment bill, and each of them delivered powerful speeches in the House of Commons on Tuesday.

Another disabled Labour MP, Marie Rimmer, also voted against the bill.

But a fifth disabled Labour MP, Vicky Foxcroft – who had played a key role in the rebellion that forced a series of government concessions – voted for the bill and its significant cuts to the health element for many new claimants of universal credit.

She and many other Labour MPs who had previously opposed the cuts bill voted with the government after the minister for social security and disability, Sir Stephen Timms, suddenly announced at 5.25pm on Tuesday – nearly four hours after the debate began and just 95 minutes before MPs voted – that there was to be another concession.

Ministers had already announced that existing PIP claimants would not now be subjected to new rules that meant they would have to be awarded at least four points on at least one “activity” to qualify for the PIP daily living component, which were to be introduced from November 2026.

Work and pensions secretary Liz Kendall had also announced the previous day that the government would no longer freeze the health element top-up for existing claimants of universal credit, and that they and new claimants who were terminally-ill or were placed in the “severe conditions group” would instead see the combined value of their universal credit standard allowance and health top-up “rise at least in line with inflation”.

But in a dramatic intervention, Timms then also announced at 5.25pm that no cuts at all to PIP would go ahead until his own review into PIP – which Kendall said would be “co-produced with disabled people, their organisations, clinicians, other experts and MPs” – was completed in the autumn of 2026.

This final concession ensured that the bill passed by 335 to 260 votes.

The committee stage of the bill will take place in just a few days, on Wednesday (9 July), but without any measures to cut PIP.

Marsha de Cordova, a former shadow minister for disabled people, was one of the few MPs in the debate to warn how previous Department for Work and Pensions (DWP) cuts and reforms had led previously to the deaths of many disabled people.

Speaking before the final concessions were announced, she pointed to the many internal process reviews into deaths linked to DWP actions, and the long-delayed second inquest into the death of Jodey Whiting, which found last month that DWP’s decision to wrongly stop her benefits after a string of safeguarding failings was the “trigger” for her to take her own life.

De Cordova told fellow MPs: “I set that out because it is important that we understand that disabled people’s lives have not been valued or respected for the last 14 years.”

She also pointed to the findings of the UN committee on the rights of persons with disabilities, which last April found successive Conservative-led governments had made “no significant progress” in the more than seven years since a finding of “grave and systematic” violations of the UN disability convention.

Marie Tidball delivered an emotional speech, in which at times she appeared close to tears, in which she told MPs she would be voting against the bill “with a heavy, broken heart”.

She said she had been in discussions with ministers since April, “making clear that I could not support the proposals on PIP”.

She added: “PIP is an in-work benefit designed to ensure that disabled people can live independently.

Low-level support such as PIP helps to build the bridge to the deinstitutionalisation of disabled people, keeping us out of the dark corners of hospitals, prisons and social care settings.”

Tidball voted against the bill despite the late concession from Sir Stephen Timms that ruled out all PIP cuts until the end of his review.

Emma Lewell also voted against the bill, despite the late concession.

She had told MPs that past Conservative social security reforms had not led to any cost savings but instead to “an increase in poverty, an increase in suicides, strain on the NHS and other public services, and, in the long run, higher welfare spending and reduced growth”.

But two other disabled Labour MPs, Liam Conlon and Jen Craft, voted for the bill, although they did not speak during the debate.

Steve Darling, the disabled Liberal Democrat MP and his party’s work and pensions spokesperson, voted against the bill, as did the rest of his party.

He had told MPs: “We all know that rushed bills are poor bills, and the law of unintended consequences will come to haunt the government if this bill goes through.”

Rachael Maskell, who was among leaders of the rebel Labour MPs – and proposed an amendment that would have killed the bill, but was defeated by 328 to 149 votes – told MPs in another passionate speech that she was voting against the bill because it was “a matter of deep conscience, as it should be and will be for us all”.

She was another MP who highlighted the harm caused by previous cuts and reforms to disability benefits, pointing to the 600 suicides between 2010 and 2013 that were linked to the programme to reassess incapacity benefit claimants.

Maskell said: “When they are managing discomfort, despair, pain and prejudice, are isolated and lonely, or their life has spiralled out of control, disabled people want anything but this bill.

They are already discriminated and dehumanised, so I plead that we do not leave them desperate, too.”

There was disappointment among many disabled people that among those voting for the cuts to the universal credit health element was Labour’s Debbie Abrahams, chair of the work and pensions committee, who had been outspoken about her concerns about the “dog’s breakfast of a bill”.

She had told MPs that “too many people relying on social security support to survive have died through suicide, starvation and other circumstances exacerbated by their poverty” in the last 15 years as a result of the “punitive, even dehumanising, social security system in which not being able to work has been viewed with suspicion or worse, with devastating consequences”.

But she still voted for the bill, despite its significant cuts to the rate of universal credit that will be paid to most new recipients of the health element of universal credit from next April, who will see the health element nearly halved and then frozen.

Asked last night (Wednesday) why she had voted for the bill, despite the significant cuts to disabled people’s support that it still contains, Vicky Foxcroft referred Disability News Service to a statement on her website.

She did not mention those cuts in the statement, but she said that securing the concessions was “a huge victory for Labour backbenchers” and that she voted for the bill because it was “now in a much better form than it was two weeks ago”.

She said she would only vote for the bill at its final Commons stage “if the final proposals reflect the commitments ministers have made”, and that she would be “looking for ministers to take these commitments forward and ensure we have co-production right across government”.

Because of the number of changes to the original bill, DNS asked DWP to confirm exactly what the bill would now do.

Here is the list provided by the department (edited for clarity by DNS):

  • The bill will make changes to universal credit (UC) from April 2026
  • It will not bring forward any changes to the PIP eligibility criteria

From April 2026:

  • The standard allowance of UC will rise above inflation in each of the next four years
  • The health element of UC for new claimants will be reduced to £50 per week.
  • Existing claimants of the health element and those new health element claimants meeting the severe conditions criteria (SCC) or considered under the special rules for end of life (SREL) will see their UC standard allowance combined with the UC health element rise in line with inflation in the next four years
  • People in the SCC group will be exempt from future UC reassessments

3 July 2025

 

Silence from MP sister of Rachel Reeves over suicide linked to PIP flaws, just as government was seeking cuts

Labour’s chair has refused to answer questions about a disabled constituent whose suicide was closely linked to flaws in the personal independence payment (PIP) system, just as her government was trying to cut PIP spending by billions of pounds a year.

Three months after an ombudsman found that failings within the Department for Work and Pensions (DWP) and its PIP system were a factor in the death of Tracie, from south London, her MP, Ellie Reeves, is still refusing to comment on that report’s findings.

Reeves is chair of the Labour party and a Cabinet Office minister, but she is also the sister of chancellor Rachel Reeves, who many disabled people blame for the government’s decision to attempt to slash spending on PIP and other disability-related benefits.

The ombudsman’s ruling was delivered to Tracie’s husband, Mustapha, just five days after Rachel Reeves announced, at the spring statement, that she would be making cuts to PIP spending of £4.5 billion a year by 2029-30.

It was Ellie Reeves, the MP for Lewisham West and East Dulwich, who referred the case to the Parliamentary and Health Service Ombudsman in December 2021, when Labour was still in opposition, and her office has supported Mustapha for nearly five years.

But since the ombudsman finally produced its report in March, Mustapha has not yet been able to discuss its contents with his MP.

He was originally told that Reeves was happy to discuss the report but had not yet received a copy, so he visited her office last month and posted a hard copy through the letterbox after an emailed copy apparently did not reach her.

Her office claims it did not receive a copy of the report until 18 June.

The ombudsman has apologised for not sending her a copy on publication, as it usually would; it finally emailed her a copy this week, but it is not clear why her office did not attempt to secure a copy of such an important report herself.

A member of her casework team has now told Mustapha that she – although not the MP – would be happy to discuss the report with him.

Mustapha has provided permission to Ellie Reeves to discuss the case with Disability News Service (DNS).

But the MP has so far failed to respond to questions from DNS, including what conclusions she has reached about the safety of the PIP system, in the context of the billions of pounds her sister has been trying to cut from PIP spending, and whether she would be taking any action on her constituent’s behalf.

Reeves has also refused to comment on the possible harm that could be caused to other disabled people like Tracie if the billions of pounds of cuts to PIP had gone ahead.

DNS first put the questions to Reeves on 7 April, nearly three months ago.

The ombudsman had concluded that DWP’s failings in dealing with Tracie’s PIP claim were a “significant contributing factor” in her decision to take her own life in March 2020.

Tracie’s mental health had been stable, but she “spiralled into a deep depression” after DWP removed the daily living part of her PIP following a review of her eligibility in July 2019.

The ombudsman concluded that DWP – which eventually admitted that its decision on her claim had been wrong – failed to consider the relevant evidence properly.

The ombudsman is now looking at whether DWP needs to make “wider changes to its service and the way it considers benefit claims”, as part of a broader piece of work which includes an investigation into the death of another disabled claimant.

Asked for an update on this work, a spokesperson for the ombudsman said: “This work involves an ongoing investigation.

By law we investigate in private so we cannot comment further on this.”

DWP eventually decided – after her death – that Tracie should have been entitled to the enhanced daily living rate of PIP.

DWP accepted that Tracie had needed help from another person to get in and out of the bath; couldn’t wash all her body herself; relied on incontinence pads; needed assistance to take her medication; had paranoid thoughts and felt anxious when others were around; rarely left the house; avoided mixing with other people; and experienced significant mental distress and suicidal thoughts.

But despite her significant support needs, the report shows that someone with Tracie’s level of impairment would not have qualified for even the standard rate of the daily living part of PIP if the chancellor’s cuts had been implemented from November 2026.

This is because to qualify for PIP daily living, a new claimant would have needed at least four points in at least one “activity”, and the most Tracie qualified for in any single activity was three points.

The ombudsman’s findings have therefore been posing a political headache for Ellie Reeves, although that eased this week when a chaotic parliamentary debate saw ministers withdraw all cuts to PIP from the universal credit and personal independence payment bill, with future cuts not to be considered until after a ministerial review (see separate stories).

The ombudsman finally sent Reeves a copy of the report on Monday, three days after DNS had asked when the MP had received the report.

A spokesperson for the ombudsman said: “The usual procedure after a parliamentary investigation is closed is that the report would be sent to the referring MP on the same day as the complainant and organisation involved.

In this case, human error meant the report was not sent to the MP.

We have apologised to the complainant and MP for this error.

We will learn from this mistake to prevent it from happening again in the future.”

*The following organisations are among those that could be able to offer support if you have been affected by issues raised in this article:  MindPapyrusRethinkSamaritans, and SOS Silence of Suicide

3 July 2025

 

Disabled people receiving care were ‘ignored by design’ during the pandemic, Covid inquiry hears

Four national disabled people’s organisations (DPOs) have told the Covid inquiry that people who receive care and support were “ignored by design” during the pandemic.

The inquiry heard on Monday that there were more than 43,000 deaths involving COVID-19 in care homes across the UK between March 2020 and July 2022, although there were no figures given for how many disabled people died in their own homes while receiving care services.

The inquiry also heard that, during the first two peaks of the pandemic, before vaccines became widely available, people with learning difficulties were seven to nine times more likely to experience a COVID-19-related death than people without learning difficulties.

And more than a quarter of all deaths from COVID-19 in 2020 were in people with dementia, even though they only made up two per cent of the total adult population.

Disability Rights UK (DR UK), Disability Action Northern Ireland, Disability Wales and Inclusion Scotland have together been granted “core participant status” in module six of the UK Covid-19 Inquiry, which is examining the impact of the pandemic on the adult social care sector across the UK.

Their opening statement for module six was delivered on Monday by barrister Danny Friedman, from Matrix Chambers.  

He told the inquiry that the pandemic saw care settings become life-threatening, while “care services to sustain everyday basic quality of life were withdrawn”.

He highlighted how the Scientific Advisory Group for Emergencies (SAGE), which provides advice to government during emergencies, stated in May 2022 that no UK country was able to “routinely identify who is resident in care homes, who is receiving social care at home, and who works in or visits a care home or a person’s home”.

These data weaknesses meant the “recipients of care, the way they live, and the way that many of them died, was ignored by design”, said Friedman.

The DPOs’ opening statement said that care staff were allowed to move from care setting to care setting, spreading the virus, because those in charge knew the system would “collapse” if staff were forced to work only in one location.

Friedman said: “Care homes would go under. People would be abandoned. It was decided that the lesser of evils was hazardous movement of staff.”

The DPOs also highlighted how the “very first thing” the UK government did in the pandemic was to “legislate to take their rights away” under the Care Act.

But Friedman said that only eight local authorities in England lodged reports to show they were operating under these emergency care laws, even though the evidence showed there were “vastly reduced services across the country”, which meant local authorities must have “embarked on mass violations of the law”.

He said: “Some local authorities reduced their services to basic life and limb protection, social contact services were drastically cut, leaving people with dementia, learning disabilities and learning difficulties and mental ill-health totally isolated for long periods.

The singular benefit of easements was that the law required reasoned, recorded, and open decision-making about withdrawal of services and disclosure of that fact to central government, but across the system, that is the one thing that local authorities near uniformly appear not to have done.

Government then helped to misrepresent the human cost by finding false consolation that only eight reports were made.

Rather than taking steps to enforce the law, the result is one of the singularly worst failures of accountability, and indeed illegality, across the period.”

The DPOs also highlighted that the government had focused on care homes and not domiciliary or supported care settings when it thought about issues such as providing personal protective equipment, testing for the virus, and getting hold of food.

Friedman said: “All these things were afterthoughts, grafted on to government responses far later than for hospitals and residential settings, if at all.”

The inquiry had heard earlier that its module six investigation had gathered more than 200,000 pages of evidence.

The hearings will last five weeks, and about 55 witnesses will give oral evidence.

Nearly 47,000 people have shared their experience of the care sector during the pandemic with the inquiry’s Every Story Matters listening exercise, the inquiry heard.

After the hearing, Georgia Bondy, who is working for DR UK on the inquiry, said: “The government needs to take responsibility for the fact that its lack of planning, consultation and care is part of the reason so many disabled people receiving care died and suffered during the pandemic.”

Rhian Davies, chief executive of Disability Wales, said: “Curtailing disabled people’s rights under the Social Services and Wellbeing (Wales) Act (2014) was one of the earliest decisions taken by Welsh government at the outset of the pandemic and paved the way for Wales experiencing the highest death rate from Covid-19 amongst disabled people in the UK.”

And Nuala Toman, head of accessibility at Disability Action Northern Ireland, said: “The pandemic exposed a brutal truth: disabled people were not only forgotten, they were disregarded through planning and service design failures.

The UK and Northern Ireland’s fragmented and underfunded care system, combined with institutional ableism, led to preventable deaths and trauma.

Unless our governments act now, we are knowingly walking into the next crisis with the same failures.” 

Heather Fisken, chief executive of Inclusion Scotland, said: “If there was ever any emergency planning around these vital services and supports, disabled people were unaware and not involved.

As a consequence, tens of thousands of disabled people lost vital support, often overnight, and were put at increased risk of contracting COVID.

Today, some still don’t have the support they had prior to the pandemic.

Governments need to take this learning forward and work with our organisations to ensure social care support is invested in and systems around it are strengthened and people-led so that this never happens again”.

3 July 2025

 

Disabled activists warn Labour MPs who vote for cuts: ‘The gloves will be off’

Labour MPs were given their final warning by disabled activists at a sweltering rally outside parliament on Monday that, if they vote for cuts to disability benefits, the “gloves will be off”.

Ellen Clifford, one of the key organisers of the rally and award-winning author of The War on Disabled People, warned MPs of the consequences if they voted for the cuts.

She told the #WelfareNotWarfare rally, which took place a day before MPs voted on the cuts in the universal credit and personal independence payment bill (see separate stories): “I know that disabled people will fight to the end.

We are not going to let this through without one hell of a fight. And if it does, we are not going to forgive any Labour MPs who either vote for it or abstain.”

Paula Peters, from Disabled People Against Cuts (DPAC), said any Labour MPs who voted for the cuts would be forced from their seats.

She said: “Let’s tell these MPs: the gloves come off. We turn the anger into action and we’re not going to back off.”

John McArdle, co-founder of the Scottish grassroots group Black Triangle Campaign, warned Scottish Labour MPs – including his own MP, Ian Murray – that disabled people would “wipe the floor” with them at the next general election if they backed the cuts.

Any of these MPs that vote for this bill… if you vote to push us into the most appalling poverty and despair, we will wipe the floor with you at the general election, we will boot you out of Scotland.”

Among the speakers was Joy Dove, who has fought for justice for eight years for her disabled daughter Jodey Whiting.

She took her own life in February 2017 after the Department for Work and Pensions (DWP) wrongly removed her out-of-work disability benefits following five missed chances to save her.

Dove read out part of the ruling given by the coroner at a long-awaited second inquest last month, which concluded that her daughter’s benefits had been “wrongly” withdrawn.

And she warned that other disabled people could die if the cuts went ahead.

She had a message for the department: “DWP, you killed my daughter, and I don’t want it to happen to anybody else.”

Dr Natasha Hirst, disabled activist and former president of the National Union of Journalists, also spoke of the harm the cuts would cause.

She said the bill would take money from disabled people “who are already struggling to survive.

We know this will harm them, we know this bill will kill people.

MPs need to listen to their disabled constituents. Take the money from those who can afford to pay, not those who can’t.

We will not forget how you vote.”

Welfare rights adviser Emma Cotton told the rally of the damage already caused by 15 years of austerity.

She said: “I have seen the damage that austerity has done. I have been a witness to a near-total degradation of the UK social security system.”

Fazilet Hadi, from Disability Rights UK, was among those who mentioned the government’s pledge that it was now going to start co-producing policy with disabled people.

She said: “That is absolute rubbish. If they had wanted to co-produce with disabled people, they should have talked to us a year ago… they should have put these proposals in the green paper… they should have stopped rushing this bill through.”

She said earlier: “It is absolutely shameful what this government is doing to disabled people, and it will be shameful for Labour MPs if they vote with the government.

Successive governments have made us poor, successive governments have put the NHS on its knees, successive governments have taken away social care, successive governments have made us a society where disabled people are becoming sicker and new disabled people are coming on stream because of homelessness, poverty, and lack of food.”

There were regular outbursts of anger among speakers, including from Mac, from Crips Against Cuts, who told the rally: “Tax the wealthy, instead of killing the crips.”

Several disabled speakers – including Clifford – also spoke of their pride in a disability community that continues to fight, despite 15 years of battling against austerity cuts.

The rally was led by DPAC, and supported by the Taking The PIP campaign and Crips Against Cuts, as well as mainstream campaign groups Stop the War Coalition, The People’s Assembly, The Trade Union Coordinating Group, and We Demand Change.

There were several speeches from members of the disabled people’s Taking the PIP anti-cuts campaign, including actors Cherylee Houston, Lisa Hammond and Cerrie Burnell.

Houston said: “How dare they try to reduce our futures, how dare they try to infer that we are of less value, a lesser part of society.

We need to stand up and hold firm. They cannot strip away years of legacy within our community.

I’m here alongside everyone else to say stop this bill, stop it now before more people die.”

Hammond said the concessions made by ministers were “nothing more than political spin.

They are designed to buy off rebellion, not to protect our rights.”

Among others who warned of the consequences of the cuts was Angela Grant, president of the DWP group of the PCS union, who said: “Many of us, including me, depend on PIP to keep us in work.

I would not be able to work if they came after PIP.”

She added: “They do not care, they are not listening, until we make them listen.

We stand together because if we start letting them divide us, divide us in our communities, they will break us down one by one.”

Hamza spoke of the impact on fellow disabled asylum-seekers, and he told the rally: “We are here today to fight for our fundamental human rights.

We fight to win, or we die fighting.”

The rally was temporarily disrupted by protesters from a rival rally who supported the right of Israel to continue its genocide in Palestine and to continue bombing Iran, and supported the son of Iran’s former Shah and want to see regime change in Iran.

They had edged closer and closer to the disabled people’s rally, and several of their supporters appeared intent on antagonising and intimidating disabled activists, with several reports of aggressive disablist abuse.

When disabled activists saw this begin to happen, they linked arms with allies to protect disabled people and their rally and continued to chant “welfare not warfare” until the pro-Israel protesters eventually melted away.

Although police officers had been seen dragging away at least two members of the pro-Israel rally, the Metropolitan police said afterwards that they were not aware of any arrests.

Several of the pro-Israel supporters refused to talk to Disability News Service, but one of them claimed they were opposed to Stop the War Coalition, which was supporting the anti-cuts rally, and he criticised the argument that cutting spending on bombs would allow increased spending on social security.

The disabled people’s rally also included songs from disabled activist and singer-songwriter Sophia Kleanthous, who minutes earlier had been part of the human barrier.

Her songs included a new anti-cuts anthem written for the rally: Cut Us Until We Bleed.

As she introduced the song, she told the rally: “We will not allow people to divide us.

We will not support war, and we will not support these cuts.”

At the end of the song, activists displayed a huge new banner, which said: “You Cut We Bleed.”

A string of MPs spoke at the rally to express their solidarity with disabled people, including Labour’s Ian Lavery, Andy McDonald, Richard Burgon, Lorraine Beavers and Brian Leishman, former Labour leader – and now an Independent MP – Jeremy Corbyn, and fellow Independent MP Adnan Hussain.

Burgon told the rally: “You’re saying, and we support you, that enough is enough.

Let’s be clear: this bill was brought to save money. This bill was brought to do that by making things worse for disabled people in this country.”

And he sent a message to fellow Labour MPs: “Certain votes in parliament define you, certain votes in parliament will be remembered not only for the rest of your political career, but probably for the rest of your life.

It’s about time that my colleagues got an inch of the guts, an inch of the courage of disabled people outside here today, and did the right thing.

Don’t talk to me about agonising over the vote – the people agonising are disabled people across the country who are worried about the future.

Don’t talk to me about agonising on £93,000 a year, do the right thing for God’s sake.”

3 July 2025

 

GB News says it has nothing to apologise for, after guest suggests starving disabled benefit claimants

A British news channel has said it has nothing to apologise for after a right-wing commentator and comedian suggested the best way to cut the number of disabled people claiming benefits was to starve, or even shoot, them.

It is just the latest example of disability hate speech broadcast and published by mainstream media organisations over the last 35 years that have run in parallel with government attempts to cut spending on disability benefits.

GB News presenter Patrick Christys had told viewers that “welfare needs to be cut” – while ignoring the evidence that working-age social security spending is stable as a proportion of GDP* – before claiming that the prime minister was not “doing much” to cut disability benefits.

He then asked his guest Lewis Schaffer how he would “get them off their backside”.

Schaffer replied: “Just starve them, that’s what people have to do, that’s what you’ve got to do to people, you can’t just give people money.”

He then added: “What else can you do? Shoot them? I mean, I’d suggest that, but I think that’s maybe a bit strong.”

Christys then replied: “Yeah, it’s just not allowed these days.”

On his X/Twitter profile, Schaffer describes himself as a “virologist, cardiologist, climatologist, historian”, but elsewhere he is described as a “comedian and broadcaster”.

One of the earliest commentators to pick up Schaffer’s comments was “Maximilien Robespierre”, who described the comments on his YouTube channel as “dangerous rhetoric”.

GB News originally refused to comment, but it eventually produced the following statement for Disability News Service (DNS): “Having reviewed the comment, which is clearly comedic, GB News does not consider there is anything that requires an apology, or further explanation.”

But Dr Natasha Hirst, disabled members’ representative for the National Union of Journalists, told DNS: “It is appalling and unacceptable for an Ofcom-regulated broadcaster to encourage and allow discriminatory and harmful commentary about disabled people.

Suggesting violence towards disabled people is no joke and has real-life consequences by emboldening hate speech and harassment.

We expect Ofcom to do its job as a regulator and investigate the complaints raised with a recognition of the wider context of exclusion and abuse that disabled people experience in their daily lives.”

Disabled campaigner Ben Scott called for GB News to be shut down by the broadcasting regulator Ofcom because of the “astronomically shocking” and “appalling” rhetoric.

He said Schaffer’s comments reminded him of Nazi “useless eater” rhetoric from the 1930s, which eventually led to the targeted killing of hundreds of thousands of disabled people in Germany through the Aktion T4 programme.

After Scott criticised him on X, Schaffer repeated some of his comments, posting: “I’m suggesting ‘starving’ or and then ‘shooting’ the disabled, to lower costs!”

This week, Schaffer’s website appeared to have been taken off-line, but Wikipedia describes him as “an American comedian and broadcaster” who is also a GB News presenter.

The comments come just three months after the Department for Work and Pensions drew horrified comments after publishing figures that showed the total cost to the economy of disabled people who cannot work, which was described as a “chilling” echo of the propaganda of 1930s Germany.

Ofcom confirmed that there had been complaints about Lewis Schaffer’s comments, but because there were less than 50, it was unable to say how many.

An Ofcom spokesperson said: “We are assessing complaints about this programme against our broadcasting rules before deciding whether or not to investigate.”

*Gross domestic product, the size of the country’s economy in a particular year

3 July 2025

 

SEND inspections find services in just one in four areas usually lead to ‘positive’ outcomes for disabled children

Only one in four inspections of local services for disabled children in England last year concluded that they usually lead to “positive experiences and outcomes” for those young people, the education regulator has announced.

The findings from Ofsted showed that 28 inspections of special educational needs and disabilities (SEND) services in local areas were carried out in 2024, but only seven led to a positive report.

Six of the inspections – which do not involve inspections of schools – concluded that there were “widespread and/or systemic failings” in local services which led to “significant concerns”, while the other 15 concluded that there were “inconsistent experiences and outcomes” for children and young people with SEND.

The inspections are carried out jointly by Ofsted and the Care Quality Commission, a process which began in January 2023, with every area supposed to be inspected at least once every five years.

Only about a third of 153 local areas have been inspected so far.

Dr Edmore Masendeke, policy and research lead for The Alliance for Inclusive Education, said the figures were “not surprising” and reflected the continuing segregation and exclusion of disabled children and young people within the education system.

He said: “What ALLFIE sees is a growing investment in segregation and deliberate dismantling of any progress made towards inclusive education.”

He said this was happening in areas such as Newham, in east London, where Sir Stephen Timms, the minister for social security and disability, is MP for part of the constituency.

In January 2024, there were 576,000 children and young people aged up to 25 with an EHC plan, and another 1.2 million pupils receiving SEN support in school. 

The worst-performing area since the inspections began in January 2023 is the East Midlands, where four areas were found to have “widespread/systemic failings” and just one was found to be “typically positive”.

The North West has also performed poorly so far, with four failing areas, three inconsistent, and one positive.

The best was North East, Yorkshire and the Humber, with four positive, five inconsistent and none found to be failing; London is not far behind, with three positive, six inconsistent, and just one failing.

Masendeke said: “For years, ALLFIE has repeatedly warned that disabled children and young people are being harmed by all forms and practices of segregated education, which continue across all areas of learning but does not lead to inclusive education experiences, where all students are taught together in the same classroom and settings alongside their peers.”

He added: “ALLFIE is also deeply concerned that just a third of local areas have been inspected so far.

How many more disabled children and young people are enduring the same poor educational experiences, or worse?”

He said the findings came at a time when there were serious threats to the legal protections provided by education, health and care plans.

And he said there appeared to be a “wider move by government to disrupt inclusive education by reducing disability provision and support, redirecting funding from mainstream settings to expand segregated provisions, including building more units within mainstream schools and increasing the number of segregated schools”.

An Ofsted spokesperson said: “These statistics highlight that the outcomes and experiences of too many children with SEND are not as positive as they should be.

We recognise the SEND system is under significant pressure; however, it is vital that improvements are made so children get the support they need.”

The inspections evaluate arrangements for all children and young people with SEND aged up to 25, including those who have an education, health and care (EHC) plan and those who receive special educational needs (SEN) support.

They examine the education, social care and health services provided to disabled children and young people in the local area, including the structure of the local education system, school attendance figures, school transport, employment data for those who have left education, provision of short breaks, transition into adult social care, and performance data on health services.

As part of the inspections, they visit schools and other settings and services, and gather the views of parents and carers, children and young people. 

CQC had not commented by noon today (Thursday).

The Department for Education had also not commented by noon today.

3 July 2025

Other disability-related stories covered by mainstream media this week

Discharging untested patients from hospitals to care homes during the Covid pandemic was the “least worst decision”, the former health secretary Matt Hancock has told a public inquiry. In his testimony to the UK Covid-19 inquiry, Hancock defended the decision – which was later ruled illegal in a high court judgment – to move hospital patients into care homes during the early weeks of the pandemic to free up space: https://www.theguardian.com/uk-news/2025/jul/02/matt-hancock-covid-inquiry-care-homes-hospital-discharge-policy

3 July 2025

 

News provided by John Pring at www.disabilitynewsservice.com

 

Jun 292025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

1st July 15:00 to 17:00. Bedford Square, Exeter.

This is a poster for a protest in Exeter.

At the top is the DPAC logo, a red, pink, blue, green wheel held by four hands of different skin tones, with an upside-down black triangle in the center bearing the word Exeter.

Underneath, on a red and white stripe design, is large text that says Kill the Bill Before it Kills Us. Above and below it says: Bust Cards, chants, satements for Starmer, Myth-busting, speeches, community first.

Underneath are two QR codes. The one on the left is labelled Email templates for your MP and the speaker of the house. The one on the right is labelled Facebook event page.

Underneath is large text that says 1st July 15:00 to 17:00. Bedford Square.

In medium text, it says that Masks are requried for those who are able to use them, limited spare masks and bottles of water provided.

Kill the Bill Before it Kills Us!

Bust Cards, chants, statements for Starmer, Myth-busting, speeches, community first.
Masks are required for those who are able to use them, limited spare masks and bottles of water provided.

Links

Facebook event

Email templates for your MP and the speaker of the house.

Jun 272025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net
Coventry TUC is organising a protest on Tuesday, 1st July, at 5 PM in Broadgate, Coventry, coinciding with the discussion of the welfare cuts bill in Parliament.
They have also contacted the three Coventry MPs to voice their opposition.
If anyone would like to speak at the demo, they would be most welcome.
A poster with a white background and red text and graphics. It says, in very big letters: stop. Disability benefit cuts. Tuesday, 1st July, 5 PM. Broadgate, Coventry (to oppose Labour's Welfare Cuts Bill due to be voted on at 7pm). Hashtag Welfare not Warfare. There is then a poster of protestors holding placards. Several placards say Welfare Not Warfare. One says no genocide, no cuts, no war. One says They Say Cut Back We Say Fight Back. Underneath, in black, says: Organised by Coventry TUC and local campaigning organisations - further info 07970 294 237.
Jun 222025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net
A graphic of the DPAC Cymru logo.

There is the main DPAC logo to the left, which is a red, pink, blue, and green circle being held by four hands of different skin tones, with the words "disabled people against cuts" surrounding it, and an upside-down black traingle in the middle bearing the letters D P A C.

On the right is the word Cymru (pronounced cum ree) (C Y M R U) in large letters, and the background of the letters are cutouts of the Welsh flag. Above Cymru (pronounced cum ree) is written the words Disabled People Against Cuts. Below Cymru (pronounced cum ree) are the words Rights, not charity, and the equivilant phrase translated into the Welsh language.

The first vote in parliament is 1st July. Here’s a helpful guide to some things people in Wales can do NOW to help defeat the welfare cuts bill.

These actions are specifically customised for people in Wales, and includes lobbying the Welsh government. However, people not living in Wales might still find the resources useful with small adaptations.

Print out a window poster

Stick it in your window, or on workplace or community noticeboards.

Ready-made

Make your own!

Send yours in!

Contributions welcome! Please send it in to swaneadpac@gmail.com and/or dpaccardiffandvalleys@gmail.com

 

  1. Write to ALL of your elected representatives.

Follow each link for instructions and template letters.

 

  1. Write to the press

 

  1. Get involved!

Here are some ideas (there are many more ways to get involved in addition to those listed here):

  • Share this resource!

    • Bit.Ly/DPAC-Cymru-Defeat-The-Bill
  • Research joining a political party that aligns with your views.

 

Jun 182025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Protest outside Cardiff disability cuts consultation

Cymraeg (Welsh) : Protest tu allan ymgynghoriad toriadau anabledd Caerdydd

 

Important update

The DWP have rescheduled their consultation on the disability cuts. The venue is now much more accessible and has better transport links.

This was the result of disabled voices calling out the injustices of the previous event.

The consultation is still unfair with the most controversial proposals not up for discussion.

Protest information

Outside Ty William Morgan, 6 Central Square, Cardiff, CF10 1EP

12:45 – 16:00 *

Monday the 23rd of June

* Please do not feel you have to stay for the full time.

It’s important that those wanting to attend the consultation are not prevented from doing so.

 

Protest outside Cardiff consultation Breaking - important update The DWP have rescheduled their consultation on the disability cuts. The venue is now much more accessible and has better transport links. This was the result of disabled voices calling out the injustices of the previous event. The consultation is still unfair with the most controversial proposals not up for discussion. Protest information Outside Ty William Morgan, 6 Central Square, Cardiff, CF10 1EP 12:45 - 16:00 Monday the 23rd of June Please do not feel you have to stay for the full time. It’s important that those wanting to attend the consultation are not prevented from doing so.

Protest! Disabled People Against Cuts Wales

The government want to take money and help away from disabled people.

Disabled people are worried and angry.

The government have a meeting with us in Wales.

Not many people are allowed to go to the meeting.

It is an unfair meeting.

We want people to protest outside the meeting.

A protest will give us hope.

The protest is on Monday 23rd June 2025 in Cardiff.

The protest starts at 12:45 and ends at 4pm. You don’t have to stay the whole time. You can join at any time.

The protest is outside Ty William Morgan, 6 Central Square, Cardiff, CF10 1EP.

 

Protest! Disabled People Against Cuts Wales The government want to take money and help away from disabled people. Disabled people are worried and angry. The government have a meeting with us in Wales. Not many people are allowed to go to the meeting. It is an unfair meeting. We want people to protest outside the meeting. A protest will give us hope. The protest is on Monday 23rd June 2025 in Cardiff. The protest starts at 12:45 and ends at 4pm. You don’t have to stay the whole time. You can join at any time. The protest is outside Ty William Morgan, 6 Central Square, Cardiff, CF10 1EP.

 

Cymraeg (Welsh) version

Protest tu allan ymgynghoriad toriadau anabledd Caerdydd

Newydd – diweddariad pwysig

Mae’r DWP wedi aildrefnu eu hymgynghoriad ar y toriadau anabledd. Mae’r lleoliad newydd yn llawer haws i’w gyrraedd ac efo cysylltiadau trafnidiaeth gwell.

Mae hyn oherwydd bod pobl anabl wedi galw allan anhegwch y digwyddiad.

Mae’r ymgynghoriad dal yn anheg gan fod yr awgrymiadau mwyaf dadleuol dal ddim yn cael eu trafod

Gwybodaeth protest
Tu allan Tŷ William Morgan, 6 Sgwâr Canolog, Caerdydd, CF10 1EP

12:45 – 16:00

Dydd Llun Mehefin 23

Plȋs peidiwch a teimlo eich bod yn gorfod aros am yr amser i gyd.
Mae’n bwysig bod y rhai sydd eisiau mynychu’r ymgynghoriad ddim yn cael eu stopio rhag gwneud hynny.

 

Protest!

Pobl Anabl Yn Erbyn Toriadau

Mae’r llywodraeth eisiau cymryd arian a help o bobl anabl.

Mae pobl anabl yn poeni ac yn flin.

Mae’r llywodraeth yn cael cyfarfod efo ni yng Nghymru.

Does dim llawer o bobl yn cael mynd i’r cyfarfod.

Mae’r cyfarfod yn anheg.

‘Da ni eisiau pobl i brotestio tu allan i’r cyfarfod

Bydd protest yn rhoi gobaith i ni.

Mae’r brotest ar ddydd Llun 23 Mehefin 2025 yng Nghaerdydd.

Mae’r brotest yn dechrau am 12:45 ac yn gorffen am 4yp. ‘Da chi ddim yn gorfod aros am yr holl amser. Gallwch ymuno ar unrhyw adeg.

Bydd y brotest tu allan Tŷ William Morgan, 6 Sgwâr Canolog, Caerdydd, CF10 1EP

 

Social media:

UK:
 
X/Twitter: Disabled People Against Cuts
Facebook: DPAC (Disabled People Against Cuts)
Instagram: disabledpeopleagainstcuts
Wales:
Facebook: Disabled People Against Cuts – Cymru
Instagram: dpac_cymru
Bluesky: @dpac-cymru.bsky.social
Jun 122025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Save the date. Protest the disability cuts.

The government is expected to introduce the disability cuts bill on the 18th of June, and vote on it as soon as July 1st.

They are not even waiting for the sham “consultation” to end on 30th of June.

Disabled People Against Cuts and allies are organising a mass Protest of Parliament on June 30th and a national day of action on July 1st when the second reading of the bill will occur.

More details to follow but it is essential that as many people as possible attend these events.

Some funding is available for travel and other essential costs. Email mail@dpac.uk.net

If you are able to arrange a local protest on July 1st please send us details of your event.

A drawing of the politician Rachel Reeves in a robber's outfit and a sack that says Disability Benefits

Welfare Not Warfare

End Labour’s War on Disabled People

Tax the Rich, Not Crips.

The Government are lying about cuts.

  • Total planned disability benefit cuts are at least £9 billion and not the £4.8 billion being reported.

  • Number of households to be plunged into poverty by the PIP cuts alone is at least 350,000 – 4000,000 including 50,000 children.

  • 1.5 million Deaf and Disabled people will be badly impacted by the changes to PIP, not just the 800,000 being reported.

  • MPs will be forced to vote on the cuts without having all the information and based on the misleading figures that have been reported.

 

Image of a person at the top of a cliff pushing someone out of a wheelchair. The Labour party logo. The Department for Work and Pensions logo.

What can I do as a disabled person?

  • If you’re not already a member – join DPAC!

  • Set up a DPAC group in your area if one doesn’t exist!

  • Participate in DPAC Actions to Scrap the Benefit Cuts

  • Organise locally with other Disabled People to mobilise support for our campaign

  • Contact unions, trades councils, Labour party branches, and build a broad based movement to reverse these austerity cuts.

For more details of local groups and actions, keep checking this page!

 

 

Jun 032025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

The DWP have cancelled the only in-person consultation event on the disability cuts for the whole of Wales, and do not plan to run another.

They did this after announcing an inaccessible venue at the last minute, in what we believe to be a clear example of disability discrimination.

The consultation was always going to be unfair, given half the proposals – the most important half – were off the table for discussion on day one.

We are demanding that there must be no vote in the House of Commons on disability cuts until a full and genuine public consultation has been carried out in Wales.

Please sign our open letter, and ask your MP or Member of the Senedd (Welsh Parliament) to sign too. You can sign, and ask your MP to sign, even if you don’t live in Wales.

Below is a template letter for contacting your MP or MS.

Find your MP or MS using WriteToThem, Find your MP, and/or Find a Member of the Senedd (in Wales)

 

Template letter

[Please use this template as a starting point and use your own words as much as possible.]

Dear [MP or member of the Senedd]

 

I am writing as your constituent to ask that you support an open letter demanding that there must be no disability benefit cuts vote in the House of Commons until Wales has had a full and genuine consultation – #NoVoteWithoutWales

The DWP have now cancelled the only in-person consultation event on the disability cuts for the whole of Wales, and have communicated that they do not plan to run another. Instead they are suggesting an online-only event at the end of the month, probably after any vote has already happened. This isn’t good enough.

The DWP cancelled the consultation after announcing an inaccessible venue at the last minute, in what could only be described as a clear example of disability discrimination.

Given the DWP’s failures, any consultation must now be run independently by Welsh disabled people’s organisations.

Please read and sign here:

https://Bit.Ly/No-Vote-Without-Wales

No vote without Wales! #NoVoteWithoutWales

Kind regards,

[Name]

[Postcode]

[Phone number]

May 302025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Welsh disability cuts consultation cancelled

The only face-to-face consultation for the whole of Wales has now been cancelled, after blatant and unlawful disability discrimination by the DWP in arranging such an inaccessible venue at the last minute.

The Cardiff disability cuts consultation on the 3rd was always going to be unfair, with half the proposals, the most important half, completely off the table for discussion.

 

Disabled people in Wales denied a voice

According to DWP email communications, there will now not be any in-person consultation on the disability cuts in Wales.

We demand that any house of commons vote on the proposals must not go ahead until we have had a full and genuine public consultation in Wales.

The DWP are now only offering an online-only event at the end of June. This is not acceptable. It is possible that MPs will already have voted by then.

Join us for a protest in Cardiff on the 3rd June

DPAC are sticking with our existing plans to protest.

Meet us outside the front of Cardiff Central train station at noon on the 3rd.

The DWP have shown themselves to be incapable of organising a fair consultation. Disabled People Against Cuts will hold our own.

Fortunately, we no longer have to worry about transport to an inaccessible location, and we will hold our protest at our original meeting point.

We invite everyone to join us and have their say. We demand that the DWP turn up and listen.

Updated plans for the day are available on our LinkTree: LinkTr.ee/SwanseaDPAC

Labour Minister dodges debate

A poster on a lamppost in Swansea. It says "Missing: have you seen our MP?" and has a picture of Torsten Bell MP.
Missing: have you seen our MP?

The Swansea West MP, Torsten Bell, a DWP minister, who defends the cuts, has insulted us and has refused to debate with us. His excuse was that a public consultation is taking place. Now that there is no public consultation taking place for the whole of Wales, Torsten must stop dodging and finally accept our invitation to debate his policies with Swansea Disabled People Against Cuts. We have written to him once again to ask for a fair and respectful public debate.

Dear Torsten Bell MP,

As you are aware, Disabled People Against Cuts (DPAC) members in Swansea have repeatedly invited you to publicly debate with us on the issue of disability benefit cuts, which you have defended on Newsnight.

The only face-to-face consultation for the whole of Wales has now been cancelled, after blatant and unlawful disability discrimination by the DWP in arranging such an inaccessible venue at the last minute.

At 6pm on Friday 25 April, responding to our request for a debate, and after press attention over your lack of reply, you told us that you “have to politely decline given the Department is carrying out a public consultation with public events on this issue.”

Given your stated reason for declining, and given (according to the DWP) that there will now be no Wales in-person consultation, Swansea DPAC expect you to now “politely accept” our invitation, as supported in an open letter signed by more than 250 individuals and organisations, including a national Labour-affiliated trade union. (bit.ly/swansea-dpac-debate-invite)

We would ensure that the debate is carried out fairly, respectfully, and in an orderly fashion. Please let us know when you are available and we will book a venue.

We also seek a public retraction and apology for your repeated public accusations of dishonesty against Swansea Disabled People Against Cuts. We robustly defend claims we have made about your language and refusal to engage with us as asked. Given your accusations, we are putting this letter on the record, copying to journalists, and we will publish any reply, so that the public can judge.

Kind regards,

Swansea Disabled People Against Cuts

 

Stop Labour’s disability cuts

The proposals are fatally flawed, and the “pathways to work” green paper must be retracted.

The government must start again on welfare reform, listening to disabled people and carers in a genuine process of co-production. It cannot be an excuse for short-term budget cuts.

A photo of people protesting in Swansea city centre. They are holding a homemade banner that says "Disabled People Against Cuts" with the DPAC logo, which is a pink, purple, blue, green circle being held by four hands of varying skin tones. In the center is a triangle bearing the letters D P A C. Above the banner is a homemade placard that says "Betrayed and ignored by the Labour party". Beneath the banner is a placard in trans pride colours with a Welsh dragon and a DPAC logo. It says "Stand together". A young man and a young woman are holding the banner. To their left is a woman in a wheelchair holding a socialist party placard that says "stop benefit cuts". In the background is a man handing out DPAC leaflets.

Above: Swansea Disabled People Against Cuts protesting

Notes:

Disabled People Against Cuts (DPAC) Cymru is a group of disabled people from across Wales. It is made up of Swansea DPAC, Cardiff and Valleys DPAC, and individual members in West, North, and Mid Wales. We are affiliated to Disabled People Against Cuts nationally.

Disabled People Against Cuts Cymru are releasing a full press statement on Monday morning. Press queries can be sent to swanseadpac@gmail.com

We also invite anyone interested in coming to our fortnightly meetings, or receiving our meeting minutes and email updates, to please get in touch.

May 272025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

A mock-up 'missing' poster for Rachel Reeves, Member of Parliament for Leeds West and Pudsey and Chancellor of the Exchequer. There are two photos of Rachel Reeves, below a heading of 'missing' in white text on a pink background. The text below the photos reads, 'Rachel, aged 46, has not been seen by any disabled constituents for several weeks. Rachel, we are here for you, any time you want to talk about your addiction to cuts, imaginary fiscal rules, discredited austerity economics and expensive corporate gifts.' 'Please email mail@dpac.org.uk if you see this member of Parliament. To help democracy please remind your MP that they must listen to you and not cut what you need to live

Picture shows image of Rachel Reeves with following text: Dear Rachel ... ACTION Leeds DPAC and Leeds, Wakefield & York Unite Community will be sharing the concerns of disabled people in West Leeds about the proposed cuts outside of Rachel Reeves MP's constituency office. Come and join us to offer your solidarity and support. Further information about the event to follow. SAT 31 MAY, 10AM-11:30am BRAMLEY CENTRE LS13 2ET

Missing – have you seen Rachel Reeves MP?

Join our action on 31st May

Leeds DPAC and Leeds, Wakefield & York Unite Community will be sharing the concerns of disabled people in West Leeds about the proposed cuts outside of Rachel Reeves MP’s constituency office.

1. we are collecting letters from people in Leeds and surrounding areas. We will be reading these out on video, and sharing them on social media on the week leading up to the action.
2.  for the action itself we will be reading out the letters (via a sound system) and holding a stall.
Come and join us to offer your solidarity and support.
Saturday 31 MAY, 10AM-11:30am
Bramley Centre LS13 2ET
Facebook event page: https://fb.me/e/2KE3gkXJh
We will be sharing the videos and other information on our Instagram account (@leedsdpac) and on facebook https://www.facebook.com/DPACLeeds
“Rachel, aged 46, has not been seen by any disabled constituents for several weeks. Rachel, we are here for you, any time you want to talk about your addiction to cuts, imaginary fiscal rules, discredited austerity economics and expensive corporate gifts.”

“Please contact Disabled People Against Cuts if you see this member of Parliament. To help democracy please remind your MP that they must listen to you and not cut what you need to live.”
May 272025
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Summary of the Leeds DWP Consulta-sham 

Leeds, Marriot Hotel   Wednesday May 21st

A photo of a disability protest outside a Marriott hotel in Leeds. In the center is a large Disabled People Against Cuts banner that says 'Rights not charity'. Other placards say 'Hands off PIP', 'Welfare not warfare', 'Blood on DWP' (with two red hand prints) and 'Benefit cuts kill'. There are seven protestors in the photo. On the left in purple is a protestor in a wheelchair. On the right is a protestor with red hair and red boots and a red outfit in a wheelchair. In the background is a security guard looking stern.

6 Leeds DPAC members made their way to the Marriot Hotel to protest against the Labour Government and DWP Pathways to Work Consultation, that has now received the nation-wide moniker of Consulta-sham. One of our member was (un)lucky enough to have been given a ticket to enter the sham and the other 5 of us, made our way to the hotel steps to unfurl our banner and begin our chants. We were met by the DWP lead organiser of the event and 2 security guards who informed us we were on Hotel property and that we would have to stand in front of the steps. The DWP spokesperson tried to be polite whilst we asked why a paltry 20 people had been offered tickets to get in. He said rather confusing that if there was spare space he’d come and invite us in – this never happened although only 15 people turned up for the con-sulta-sham. 

We began our chants, “welfare, not warfare, you say cut-backs, we say fight-back!” Trevelyan Square is a busy square so plenty of people were witness to our protest. We gave out flyers about the Green Paper and explained it’s likely effects on our community. People in general were very supportive. 

We had the pleasure of being joined by activists in Unite the Union and Crips Against Cuts, who raised the volume and energy. A heartfelt thanks to them!

Our comrade inside the meeting stated:

“There were as many DWP staff as consultees in the meeting – clearly not a question of space then. We asked if our comrades could come in as there was spare space but were told that the hotel ‘security’ had blocked the entry of anyone else! The hotel said it contravened their risk assessment. We were asked pre-scripted questions. We were told that we couldn’t comment on proposed changed to the PIP scoring system despite this being the most impactful proposed change. I pointed out it was misleading to call this event ‘Pathways to Work’ given that PIP isn’t an out of work benefit. We explained that DLA and PIP are not lilke4-like so moving 16-18 years olds to PIP may lose their entitlement. I expressed concern about this group were supposed to do without life-supporting benefits, especially those no loner able to live at home or leaving care. The questions were ostensibly focused on getting people into work but I pointed out that without addressing Access to Work or any commitment from employers to step-up their reasonable adjustments the support is not fit for purpose. I stressed that DWP work coaches aren’t knowledgeable enough to understand the range of health conditions they are charged with assessing.”

Ultimately, we all felt this consultation was not fit for purpose. Only asking pre-selected questions about the less impactful changes and only consulting a tiny minority of those affected renders the process toothless. Solidarity to those fighting these poorly thought out proposals

Next action in Leeds on 31st May

Leeds DPAC are running a stall in Rachel Reeves constituency with the Unite Community Leeds, Wakefield & York Branch
1. we are collecting letters from people in leeds and surrounding areas. We will be reading these out on video, and sharing them on social media on the week leading up to the action.
2. the action itself will be
10am – 12pm
Bramley Town Centre
31st May
We will be reading out the letters (via a sound system) and holding a stall.

More info: https://www.facebook.com/events/4069198743403992/