Aug 092018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Sano Physiotherapy markets itself as a professional service offering sports massage and rehabilitation but has a murky side business renting out its rooms to controversial disability assessor ATOS. 

 

ATOS has recently changed the name of its benefits assessment arm to ‘Independent Assessment Services’ with the words “delivered by ATOS” written in tiny letters underneath. You will not see ATOS branded in big letters across any of Sano Physiotherapy commercial premises despite renting spaces to the much discredited benefits assessor in Pudsey and Castleford.

 

You will find a picture of Tory MP, Stuart Andrew shaking hands with Matthew Taylor, clinical lead for Sano Physiotherapy LTD outside the companies new premises in Pudsey. Stuart often promotes himself as a community champion in Pudsey with photoshoots like these whilst voting for welfare cuts and benefit changes in parliament that affect his constituents.

 

The Independent newspaper recently put in a freedom of information request which found the Department for Work and Pensions (DWP) paid Independent Assessment Services and Capita nearly £255m last year to perform Personal Independent Payment assessments. How much has Sano Physiotherapy LTD made from this windfall whilst local residents are having to use foodbanks?

 

Sano Physiotherapy LTD is facilitating controversial disability assessments which potential private customers need to be made aware about so they can choose a more ethical physiotherapist firm that doesn’t have a murky side-line in profiteering from the suffering of benefit claimants.

Please let us know of any other firms involved in aiding Atos or Capita with details of who and where they are. You can email us at amil@dpac.uk.net

 

 

 

 Posted by at 19:11
Jul 212018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

 

Our Festival of  Resistance highlighting the hypocricy of the UK and Kenyan governments hosting a Global Disability Summit kicks off in ernest today/Saturday as our overseas activists arrive in the UK to join in with our fun.

On Sunday we are holding our own global summit which is very over subscribed with guest speakers including -:

Rose Achayo from the National Union of Women with Disabilities of Uganda (who will be talking about the particular barriers disabled women in Uganda face, the work of her organisation including its work with disabled refugees)

John Clarke from Ontario Coalition against Poverty (who shares DPAC’s concerns over universal basic income as a proposed solution to the future of social security)

Antonios Rellas from a disabled campaign group called Zero Tolerance in Greece (who campaigns against institutionalisation of disabled people and recently testified against Golden Dawn). https://dpac.uk.net/2016/09/greeces-shocking-secretthe-work-of-zero-tolerance/

Bolivian campaigners who were involved in this: https://www.theguardian. com/news/2017/may/05/the- fight-disability-rights- protestors-in-bolivia-on-the- barricades

And successfully forced their government to introduce disability payments for people. Although not yet at a high enough rate to enable an adequate standard of living.

We will be live streaming this conference using our facebook page https://www.facebook.com/disabledpeopleagainstcuts/

And tweeting with the hashtag #Disability&Resistance

Unlike the summit arranged by DfID we will not be having anyone from any large corporations hyping expensive equipment which is beyond the reach of many disabled people to fund.

On Monday and Tuesday follow us on twitter @dis_ppl_protest and please use  hashtags #NowIsTheTime and #disability summit

Tweet to any or all of the following saying why the UK government is unfit to host a disability summit.

@DFID_UK

@IDA_Forum_CRPD  gate keepers for who was allowed to come to the summit, to be kind possibly due to ignorance of the UK violation of disabled people’s rights.

Speakers at Tuesday’s summit event

@SophMorgan a disabled model

@Lenin  Lenin Moreno (president of Ecuador)

@gabimichetti  (vice president of Argentina)

More to follow shortly re-tweets.

And remember watch out for any surprise events happening in the very near future after all no-one ever knows quite where and when DPAC will pop up unexpectedly.

 Posted by at 12:55
Jul 202018
 
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To:

Lenin Moreno, President of Ecuador

Gabriela Michetti, Vice President of Argentina

Sophie Morgan

20 July 2018

We are writing this open letter to you on behalf of Deaf and Disabled people across the UK concerning your involvement in the global disability summit being co-hosted by the UK government in London on 23 and 24 July.

We are strongly in favour of international support that improves the lives of Deaf and Disabled people across the world and welcome co-operation between States that lead to stronger human rights laws and protections. We particularly support the building of international solidarity and links directly between Deaf and Disabled People, our organisations and campaigns.

However, we have the following concerns regarding the July summit:

  • The role of the UK government in co-hosting the event. Following an unprecedented investigation carried out by the UN disability committee under the United Nations Convention on the Rights of Persons with Disabilities (UN CRPD), the UK was found responsible for grave and systematic violations of Disabled people’s rights due to welfare reform. The findings of their investigation, published in November 2016, were and continue to be entirely dismissed by the UK government. In August 2017 the UK government was routinely examined under the UN CRPD and again the UN disability committee expressed their deep concerns regarding the UK government’s failure to understand the Convention, the impact of their policies and failure to recognise them. Again the UK government said they disagreed with the findings of the Committee. The involvement of the UK government in co-hosting the summit therefore undermines any aims of the summit linked to strengthening Deaf and Disabled people’s rights under the UN CRPD. Instead it provides a platform for them to showcase to other States how it is possible to get away with ignoring those rights when it comes to your own citizens.

 

  • The UK government’s use of its international work to cynically deflect from criticisms of their disability record in the UK. On a number of occasions when government ministers have been criticised for implementing policies with an adverse impact on Deaf and Disabled people, they have cited the poorer conditions of Disabled people in other countries. This represents a misunderstanding of the UN CRPD which is about the progressive realisation of rights. The UN disability committee have such concern about the situation in the UK because it represents a serious and dramatic retrogression of rights, described by the Chair as a ‘human catastrophe’. In deflecting attention from their record in the UK, the Government clearly intend to more easily continue their punitive policies targeted at Disabled people and the poorest members of society. There is now overwhelming evidence, evidence which the UN disability committee considered, that prove the brutal impacts of these policies. It would be a betrayal to all those suffering under them not to raise concerns about attempts such as use of the global summit to divert attention and opposition to those policies.

 

  • The suitability of the Government of Kenya as co-hosts given their abuse of the rights of LGBTQI+ people, many of whom develop lifelong impairments as a result. LGBTQI+ people in Kenya are routinely banished from their families, denied work and accommodation, imprisoned and persecuted. They face severe barriers to forming and maintaining relationships and to living as a couple, the ‘Right to Family Life’ that every human is promised. This results in widespread damage to their mental and physical health, creating impairments where none previously existed. This is reflected in the high level of asylum applications to the UK from LGBTQI+ asylum seekers from African countries. Despite their experiences, the majority are then refused asylum in the UK and forcibly returned home, where many disappear or are murdered. Just this April, President Kenyatta said that LGBT rights are “not acceptable” and not “an issue of human rights”. The Kenyan Government has also claimed this is a non-issue for Kenyans, and no doubt would argue that it has nothing to do with the Summit. However, if you are Kenyan or Ugandan and are lesbian, gay, bisexual, trans, queer or intersex, it is an issue that completely dominates and dictates your life. For many Disabled people from Kenya, it is the reason they developed an impairment in the first place. Under the UN CRPD, the Kenyan government also has an obligation to protect the rights of disabled people who are LGBTQI+.

We appreciate that you may not have had this information when you agreed to involvement in the summit and would be happy to meet to discuss our concerns. Please do not hesitate to contact us with any questions or for further information.

 

Yours sincerely,

Disabled People Against Cuts

Sisters of Frida

Alliance for Inclusive Education

Inclusion London

Mental Health Resistance Network

Reclaiming Our Futures Alliance

Recovery in the Bin

 

 

 Posted by at 20:12
Jul 192018
 
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A minister has been asked why the benefits of hundreds of sick and disabled claimants are apparently being sanctioned, even though they should not have to meet any of the strict conditions imposed by the government’s new universal credit system.

Department for Work and Pensions (DWP) figures show that more than 1,100 claimants of universal credit were being sanctioned in February this year (1,108), even though they had been moved into the “working enough” or “no work-related requirement” group.

They have usually been moved into these groups because they have been found not “fit for work” or are not expected to look for jobs.

The figures also show a striking increase in the number of claimants in these two groups who were being sanctioned from January 2017 (649) to February 2017 (1,109).

The concerns have been raised by the Commons work and pensions committee, after it was sent the figures by employment minister Alok Sharma.

In a letter to Sharma, the committee’s chair, Frank Field, says: “What is the point of applying sanctions to people who cannot work and are not expected to look for jobs?

“The DWP have yet to make the case that benefit sanctions work to get people into employment and it’s difficult to see how they can have that affect for people who are ‘working enough’ or cannot work.

“Benefit sanctions are the only major welfare reform this decade to have never been evaluated, and the picture DWP paints of the policy doesn’t match the troubling stories we’ve heard.”

The committee also raised concerns with Sharma that DWP’s figures “consistently understate” the number of benefit claimants being sanctioned, particularly those on the out-of-work disability benefit employment and support allowance (ESA), where there is a high rate of successful appeals.

In Field’s letter, he says that DWP removes a sanction decision from its statistics if it is overturned at an appeal.

This had been pointed out by Dr David Webster, a leading researcher on unemployment and sanctions at the University of Glasgow, when he gave evidence in May to the committee’s inquiry into the benefit sanctions regime.

Webster had told the committee that the only reason DWP had not abandoned ESA sanctions when the National Audit Office reported in November 2016 that their use led to a fall in the time claimants spent in work was because of “embarrassment”.

Field asks Sharma in his letter to publish pre-appeal sanction figures so that “the true picture can be understood”.

In one month, in December 2016, the pre-appeal figures would have been 57 per cent higher (1,173) than the figures published by DWP (749).

By January 2018, the pre-appeal figures were still 30 per cent higher (544 rather than 420).

Asked to respond to the points raised by Field in his letter to Sharma, a DWP spokeswoman declined to explain why disabled people were apparently being sanctioned when there were no conditions attached to their universal credit.

She did not dispute the universal credit sanction figures but said that “where someone’s situation changes and they have different conditionality, we can adjust an ongoing sanction amount”.

And she claimed that “only a small proportion of sanction decisions are appealed and in the cases where they are overturned, the claimant’s payments are backdated”.

19 July 2018

 

 

McVey’s U-turn means DWP will pay at least £100 million more to disabled claimants

Disabled people will be paid more than £100 million extra in backdated benefits owed by the government, after a U-turn by work and pensions secretary Esther McVey on the eve of a court hearing.

The Department for Work and Pensions (DWP) had previously only agreed to offer a partial backpayment to an estimated 70,000 disabled people who for years did not receive the correct level of out-of-work disability benefits.

The underpayments were caused by the botched migration of former claimants of incapacity benefit and other benefits to the new employment and support allowance (ESA) from 2011 onwards.

The department failed to realise that many of the claimants were entitled to income-related ESA – and therefore to associated disability premiums – rather than just the contributory form of ESA.

Although DWP had previously agreed to pay back as much as £340 million to those affected – with average payments likely to be about £5,000 – it had said it would only backdate arrears to 21 October 2014, the point at which the upper tribunal ruled that DWP should have assessed claimants for both income-related and contribution-based ESA when deciding their entitlement.

DWP had been refusing to pay back another £100 million to £150 million in arrears that dated from before 21 October 2014.

But yesterday (Wednesday), McVey announced that claimants would receive arrears backdated to the date they moved onto ESA, with some claimants now likely to receive up to £10,000 more in arrears.

It is just one in a series of major errors by DWP senior civil servants relating to disability benefits, with the department now believed to be carrying out six separate trawls through the records of disabled people unfairly deprived of benefits.

In a written statement to MPs, McVey said that individuals contacted about their backpayments could expect to receive the “appropriate payment” within 12 weeks after the “relevant information” has been gathered.

Those who have already received arrears payments from 21 October 2014 will have their cases looked at again, with additional arrears paid dating back to the date they were moved onto ESA.

The announcement came as DWP was about to face a court hearing in a judicial review case taken by the Child Poverty Action Group on behalf of a claimant who was underpaid from 2012.

Meg Hillier, chair of the Commons public accounts committee, welcomed McVey’s announcement, which came hours after a report by her committee had attacked DWP’s “culture of indifference”, which saw it take six years to start to address its ESA error.

She said: “I was appalled by the department’s apparent indifference to correcting its mistakes.

“Today’s statement, coming so soon after publication of our report, indicates DWP finally intends to treat this problem with the seriousness it deserves.”

Hillier had said earlier, in publishing her committee’s report, that DWP “simply didn’t listen to what claimants, experts, support organisations and its own staff were saying.

“Its sluggishness in correcting underpayments, years after it accepted responsibility for the error, points to weaknesses at the highest levels of management.

“Indifference has no place in the delivery of vital public services. It must be rooted out wherever it is found.”

19 July 2018 by John Pring, Disability News Service

 

 

 Posted by at 21:19
Jul 192018
 
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A regulator has been told there are “issues of concern” about the way it deals with complaints against health and care professionals, including those who write dishonest benefit assessment reports.

The Professional Standards Authority (PSA) agreed in January to look at concerns about the way regulators deal with complaints about nurses, physiotherapists and paramedics who carry out personal independence payment (PIP) assessments for the outsourcing giants Capita and Atos.

It agreed to act after being contacted last year by disabled activist Mark Lucas, who has twice appealed successfully against the results of what he believes were dishonest PIP assessments.

Hundreds of disabled people have come forward over the last 18 months to tell Disability News Service (DNS) how assessors working for Atos and Capita wrote dishonest PIP assessment reports on behalf of the Department for Work and Pensions.

Many also raised concerns about the apparent refusal of the Health and Care Professions Council (HCPC) and the Nursing and Midwifery Council (NMC) to take their complaints about these assessments seriously.

Only this week, Lucas received an email from HCPC, explaining that it would not take any further action over his complaint about an occupational therapist who had assessed him for PIP.

He believes the assessor deliberately downplayed the seriousness and frequency of his seizures, but HCPC told him it did not believe this had happened and even if it had, “it would be considered a minor error, which would not be capable of amounting to an allegation of impaired fitness to practice”.

Lucas has twice been found ineligible for PIP following assessments, but on both occasions was later awarded eligibility for the PIP standard daily living rate after appealing to a tribunal.

Frustrated at HCPC’s failure to take another complaint about a PIP assessor seriously, he contacted PSA – which reviews the work of the regulators of health and care professionals – last year.

PSA incorporated Lucas’s concerns into its annual review of HCPC, which found this month that the regulator was meeting only four of the 10 required standards for the way it deals with complaints against healthcare professionals, including those who carry out PIP assessments.

Last year, before Lucas contacted the regulator, PSA had reviewed 100 complaints made to HCPC, including a small number relating to PIP assessments.

David Martin, PSA’s concerns and appointments officer, said the 2017-18 review “concluded that there were issues of concern about the HCPC’s process across all of its activity”, in relation to fitness to practise.

These concerns include the way it deals with the initial stages of the fitness to practise process, and how it determines if there is a “case to answer” against a health and care professional.

Among PSA’s concerns are that HCPC makes it too difficult for complaints about a healthcare professional to be accepted into the fitness to practise process, while other cases are closed at the initial stage instead of being referred to an investigating committee panel.

Martin said HCPC had confirmed that PIP assessment work “should be considered in the same way as any other professional activity of its registrants” and that its procedures “require it to fully consider the concerns it receives about PIP assessors”.

He said: “The HCPC was clear that it considers registrants, acting as PIP assessors, are exercising their professional judgement.

“It therefore considers that allegations of misconduct or lack of competence when carrying out PIP assessments could constitute a fitness to practise concern to be investigated in accordance with its usual process.”

He said HCPC was now “undertaking an action plan” to address the concerns PSA has raised about its fitness to practise processes, and that PSA would probably review further HCPC cases in detail over the next couple of years.

A similar annual review by PSA of NMC is due to be published later this year.

An HCPC spokesman said: “The PSA audited a sample of 100 of our cases as part of their review of our yearly performance review in 2016-17.

“While a small number of these cases related to PIP, the audit was not specifically looking at HCPC’s handling of PIP cases.

“HCPC registrants who are employed in assessor roles are recruited because of their skills and experience as registered health professionals. Therefore, their work and conduct needs to comply with our standards.

“If in the course of conducting a PIP assessment a concern is raised regarding a registrant’s fitness to practise, ie lack of competence or misconduct, then this will be investigated following the same robust and thorough processes and applying the same tests as concerns raised in relation to any other area of a registrant’s practice.

“We have also provided input into the PSA’s review into how regulators approach fitness to practise concerns in relation to PIP assessments and have confirmed our view that the PIP assessment process requires the registrant to employ their professional competencies.

“This year we continued to meet the majority of the PSA’s Standards for Good Regulation.

“Although we did not meet all the standards relating to fitness to practise, the PSA has acknowledged our on-going work to improve our performance in this area and stated that we have made ‘significant progress during this review period’.

“We continue our programme of improvement work to address the issues that were previously identified.”

But Lucas was heavily critical of PSA’s efforts to address his concerns.

He said PSA was “a joke” and a “toothless quango”.

He said: “I am not happy with the way PSA have treated me and it is behaviour that I have been subjected to on many occasions over the last few years.”

Lucas said that complaints processes are “designed to abuse” disabled people because they first “promise the earth”, then “forget” the complaint, and finally “communicate the result from the complaint in a letter with preapproved techniques of neutralisation and consolatory phrases like ‘we realise you will be disappointed’”.

He said: “This experience of the last few years has given me anxiety over making complaints.

“I have spent much time and written many letters, but it is all for nothing because organisations like the PSA are just for show.”

19 July 2018 by John Pring Disability News Service

 

 Posted by at 21:15
Jul 192018
 
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Four opposition parties demand DWP answers over WCA deaths ‘cover-up’

Two opposition parties are writing urgent letters to work and pensions secretary Esther McVey – while a third is demanding an investigation – about a possible cover-up over documents linking the “fitness for work” test with the deaths of benefit claimants.

Senior figures from both Labour and the Liberal Democrats said this week that they were writing urgently to McVey to ask whether the Department for Work and Pensions (DWP) had shown the documents to the independent expert the government commissioned to review the work capability assessment (WCA) in 2013 and 2014.

The Green party’s co-leader, Jonathan Bartley, said the failure to be clear about what happened with the documents had “all the hallmarks of a deliberate cover-up”. He has called for an independent investigation.

The SNP also said it would be seeking answers from DWP.

Dr Paul Litchfield was commissioned by DWP to carry out the fourth and fifth reviews of the WCA but has so far refused to say if he was shown letters written by two coroners and a number of secret DWP internal “peer reviews” into deaths linked to the WCA regime.

Litchfield, who was recognised by the prime minister with a CBE in last month’s birthday honours, published the two reviews in December 2013 and November 2014, but neither of them mentioned the documents, all of which link the WCA with the deaths of claimants.

A spokesman for Marsha de Cordova, Labour’s shadow minister for disabled people, said she would be writing to McVey “as a matter of urgency”.

Stephen Lloyd, the Liberal Democrat shadow work and pensions spokesman, said: “I will be writing directly to the secretary of state, Esther McVey, to seek clarification whether or not her department, the DWP, ever showed [Litchfield] the documents linking the WCA to the deaths of benefit claimants.

“The public has a right to know, particularly now he’s been awarded a gong.”

Neil Gray, the SNP’s social justice spokesman at Westminster, added: “This issue has thrown up a number of questions for the DWP and we need a clear and definitive statement on what people knew and when. We will be seeking those answers.”

Even though DWP possessed all the coroner’s letters and peer reviews, it has claimed in a freedom of information response that it holds no information in its records on whether they were shown to Litchfield while he was reviewing the WCA.

Since Disability News Service (DNS) revealed the existence of the documents in the years after Litchfield’s final report was published, concerns have grown that DWP and its ministers deliberately covered-up evidence of the fatal impact of the assessment on sick and disabled people.

The coroner’s letters followed the deaths of two men with mental health conditions in 2010 and 2013 and each warned of further such deaths if changes were not made to the WCA.

The call for evidence for Litchfield’s second review was issued on 10 June 2014, five months after coroner Mary Hassell had written to DWP following an inquest into the death of Michael O’Sullivan, who had had significant, long-term mental health problems.

Hassell had told DWP that the trigger for O’Sullivan’s suicide had been the conclusion by civil servants that he was fit for work, but she said that neither DWP nor the Atos doctor who had assessed him through the WCA process had asked his GP, psychologist or psychiatrist for information about his mental health.

Hassell told DWP that it needed to take action “to prevent further deaths” like Michael O’Sullivan’s.

But despite that urgent call, Litchfield’s second review failed to mention Hassell’s letter or a similar letter sent to DWP by another coroner in 2010 following the suicide of Stephen Carré.

Litchfield’s two reviews also failed to mention the peer reviews.

Peer reviews – now known as internal process reviews – must be carried out by civil servants into every death “where suicide is associated with DWP activity”.

One of the aims of these reviews is to “determine whether local and national standards have been followed or need to be revised/improved”, so DWP would find it hard to explain why they would not have been shown to Litchfield, whose job it was to review how the WCA was working.

DWP has admitted that at least seven peer reviews written in 2012 mentioned the WCA, and there are almost certainly more that were written by the time Litchfield wrote his final report in late 2014.

Litchfield has so far refused to comment about the documents.

But Professor Malcolm Harrington, the independent expert who carried out the first three reviews of the WCA in 2010, 2011 and 2012, has already told DNS that he believes he was shown neither the first coroner’s letter (the second letter had not yet been written by the time he completed his third review) nor any WCA-related peer reviews.

Bartley said this week: “If the Department for Work and Pensions failed to show Dr Litchfield vital documents linking the work capability assessment with the deaths of benefit claimants, DWP are clearly implicated in a cover-up.

“If he was shown them but didn’t mention them in his reports, then so was he.

“This has all the hallmarks of a deliberate cover-up over the fatal impact of the assessment on sick and disabled people.

“There is no justification for secrecy, it is clearly in the public interest for the truth to be told and there should be an independent investigation of what happened.”

A DWP spokeswoman said: “As we’ve previously said, this was an independent review, and DWP provided information alongside other stakeholders – on request.

“Any evidence used was referenced in the review.”

19 July 2018 story by John Pring Disability News Service

 

 Posted by at 21:10
Jul 192018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Next week DfID will be jointly hosting a Disability Summit with the Kenyan government. While we fully support all and any initiaitives to improve the lives and circumstances of disabled people in other countries we can only say that the UK government’s choice of partner for this summit seems shameful and inapprpriate. Of course there is nothing new in that and no-one who has endured the never ending attacks against disabled people’s human rights in the UK will be surprised.

You can see more about the summit

https://www.gov.uk/government/ news/uk-government-to-host-its -first-ever-global-disability- summit [NB this announcement came out the same day as they snuck out the much criticised and long awaited command paper “Improving Lives” through which conditionality was extended to all groups of disabled people]

And here:

https://www.gov.uk/government/ topical-events/global-disabili ty-summit-2018

So what of their partner country Kenya?

The Government of Kenya criminalises and persecutes LGBTQI+ Disabled people

It is hard to imagine a less suitable partner to co-host a Global Disability Summit than the Government of Kenya — apart from its neighbor, Uganda. It is illegal to be gay in both countries, and as a result many LGBTQI+ people develop lifelong impairments.

LGBTQI+ people in Kenya are routinely banished from their families, denied work and accommodation, imprisoned and persecuted. They face severe barriers to forming and maintaining relationships and to living as a couple, the ‘Right to Family Life’ that every human is promised. This results in widespread damage to their mental and physical health, creating impairments where none previously existed.

This is reflected in the high level of asylum applications to the UK from LGBTQI+ asylum seekers from African countries. Despite their experiences, the majority are then refused asylum in the UK and forcibly returned home, where many disappear or are murdered.

Just this April, President Kenyatta said that LGBT rights are “not acceptable” and not “an issue of human rights”. The Kenyan Government has also claimed this is a non-issue for Kenyans, and no doubt would argue that it has nothing to do with the Summit.

However, if you are Kenyan or Ugandan and are lesbian, gay, bisexual, trans, queer or intersex, it is an issue that completely dominates and dictates your life. For many Disabled people from Kenya, it is the reason they developed an impairment in the first place.

Regard, the UK’s LGBTQI+ Disabled People’s Organisation, says: “The involvement of the Government of Kenya discredits any debate that takes place at the Summit. Whatever the political reasons for involving Kenya in co-hosting the Summit, the rights and welfare of Disabled people seem to have had very little to do with it.”

 

 Posted by at 18:54
Jul 172018
 
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Edge Fund is recruiting for the post of Regional Organiser and Administrator. If you are committed to activism, systemic change and creating a world free of injustice and inequality, we want you to apply. If you’re unsure, feel free to contact us on jobs@edgefund.org.uk

The Edge Fund is a grant-making body with a difference. We support efforts to achieve social, economic and environmental justice and to end imbalances in wealth and power – and give those we aim to support a say in how money is distributed. For more information visit www.edgefund.org.uk

We are a membership based organisation, run through a non-hierarchical structure, with a Facilitating Group overseeing the strategic running of the organisation. The day to day runnings are overseen by the two Regional Organisers who work closely together. We already have someone in post for the Regional Organiser and Communications post, who is based in London. We are looking to recruit a Regional Organiser and Administrator who will preferably be based in North England or Scotland and we welcome applications from people based in Ireland or Northern Ireland.

Key information:

  • Flexible location
  • 3 days per week (21 hours)
  • Salary £25,750 pro rata

We would like to encourage applications by people from minoritised and racialised communities, people underrepresented in similar roles and people without university degrees. Deadline for applications has been extended to 5pm, Friday 20th July.

 

 Posted by at 13:17
Jun 232018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Info here about regional actions for the stop trump day of action

Three asks for Stop Trump

Last year we – as Stop Trump Coalition members – committed to making the resistance against Trump and everything he stands for one of the biggest and most visible demonstrations in British history. With Trump’s visit just three weeks away we need you to help make that happen by using your power and influence to mobilise on and offline.

Do these three things:

ONE: Populate and share the carnival of resistance map which is now LIVE.
Actions happening regionally and coaches to the London march and rally are being plotted on the carnival of resistance map. Add yours and encourage your followers to do the same. Share the map as widely as you can.

https://stoptrump.us15.list-manage.com/track/click…

TWO: Let people know why you’re joining the carnival
Record a one-minute clip like these:
Send them to us (mail to: info@stoptrump.org.uk ) or post them on your own social media using #CarnivalofResistance #Resist #StopTrumpism

THREE: Follow and engage with us on social media
Follow and share the Stop Trump Coalition on social media – we’re posting daily on Facebook, Twitter and Instagram so stay up to date on the latest and help get more people involved. Use #carnivalofresistance #resist #stoptrumpism as often as you can!

More soon.

Stop Trump Coalition

#carnivalofresistance #resist #stoptrumpism

Image may contain: sky, cloud, night, text and outdoor
 Posted by at 21:13
Jun 182018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

DfID and DPAC Global Summits

In response to the UN disability committee findings and criticism of their record on disability rights, the Tories have been using international comparisons. The previous Minister for Disabled People used her time up in a debate on the UN CRPD that the SNP had tabled talking about how when she was in the navy she had liberated all these poor starving neglected disabled orphans from “the socialist republic of Romania.”

The implication is always that disabled people in the UK are over-privileged and should be grateful for what we get here. This shows a misunderstanding of the UN Convention as a progressive tool for rights implementation.

The same day as a much criticised government strategy on disability, health and work was published, the previous Minister for Disabled People, Penny Morduant, made an announcement in her new role as Minister for International Development that the UK would be holding a global summit on disability at the end of July 2018. This has proved a very popular initiative with international organisations falling over themselves to be involved and the Tories are using it to its maximum to validate their self-proclaimed status as “world leaders in disability”.

https://www.gov.uk/government/news/uk-government-to-host-its-first-ever-global-disability-summit

It is also linked to a 27m international disability development support programme and you can see from the announcement about the focus on technology companies (and opening up new markets).

We obviously support better rights for all disabled people regardless of where they live but cannot let the Tories continue to pass themselves off as world leaders in disability rights when they have been found guilty of the grave and systematic violation of those rights and their policies have been called a ‘human catastrophe’ by the UN Disability Committee.

Therefore we will be holding our own summit on Sunday, July 22nd with input from disabled activists from the global South. This will be near the Olympic Park although the venue is still to be confirmed.

On July 24th the actual day of the summit please join us for some on-line activism.

Further details to follow shortly.

 

 

 

 

 Posted by at 18:49
Jun 182018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

ShareAction are running a training on shareholder activism aimed specifically at disabled people. There are SO many companies which could do with a sharp reminder of their access responsibilities – not least some of the big high street names which still lock out disabled people from their premises.

 

Details are below – but please do (a) sign up online if you can make it and (b) forward this email to any other disabled campaigners you know who may be interested.

 

P.S. This training is focused around disability rights, but lots of opportunities to campaign at AGMs around Living Wage, climate change and other issues.

———————————-

Date:

10 July

Time:

6-8pm

Address:

Christian Aid

35-41 Lower Marsh

Lambeth

London

SE1 7RL

 

The venue has stepfree access and accessible toilets and is a short walk from Waterloo station which has stepfree access.

Register attendance here >> https://bit.ly/2sWTE9h

Outline:

AGM activism is a unique campaigning strategy that gets you in a room with the CEO’s of the biggest companies. You ask a question to the board and they take action.

 

It’s a winning tactic. Intertek – a huge global company that tests and certifies products accredited to the Living Wage Foundation in June and said it was the direct result of our AGM questions. Since we started campaigning on the Living Wage at AGMs in 2011, the number of FTSE100 companies paying a fair wage has jumped from 2 to 36! And 3 years ago, bus company National Express changed its unfair wheelchair policy as a result of an AGM question.

Any campaign issue that is geared towards company action can use AGM activism as a tool. Come along to this training for disability rights campaigners to:

 

  • Learn about what AGMs are
  • Learn about what AGM activism is and why it’s so powerful
  • Get trained to be an effective AGM activist
  • To plan using AGM activism at upcoming AGMs for disability rights and access campaigning

Please contact Michael from ShareAction on Michael.kind@shareaction.org to let him know about any access requirements.

In the meantime, check out this short video introducing AGM activism >> https://bit.ly/2JznniS

 

 Posted by at 18:00
Jun 122018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Call for Submissions

Are you an artist, sculptor, film maker working around disability issues? 

Would you like your work to play a part in building a Global Resistance Movement of disabled people?  

Then here’s how

In July 2018, DPAC will be holding a public event around building a Global Resistance Movement of disabled people.

We need your creativity and energy to help make this happen.

We want to create an event which celebrates our shared experiences and aspirations; and which connects our struggles and campaigns. As a backdrop to this, we would like those attending on the day and taking part from afar to do so in a space filled with creative expressions of our lives and our politics.

We are calling for contributions, large and small to exhibit at the event. Artists can come and be part of our activities or can simply give us access to their material. We will store and exhibit your material and return it to you after the event.

We are asking for:

  • Imagery such as
  • Pictures
  • Prints
  • Collages
  • Photographs
  • Paintings etc

 

  • Ceramics
  • Carvings
  • Glass work
  • Metal work

 

  • Digital Art
  • Film
  • Animation
  • Video Art

 

If your work has supporting materials such as mounts, plinths, frames, description or requires these materials for exhibition, please let us know.

 

If you would like to find out more or contribute please email. mail@dpac.uk.net

 Posted by at 20:44
Jun 082018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

https://www.parliament.uk/business/publications/written-questions-answers-statements/written-statement/Commons/2018-06-07/HCWS745/

There has been some significant changes announced by the government concerning Universal Credit.  In a parliamentary statement yesterday Esther McVile says that the government intends to make the following changes-

The timetable for managed migration has been extended by 1 year.  It is now due to run from July 2019 – March 2023. Yet another delay on top of the years and many, many millions of pounds it has already taken

And transitional protection and the severe disability premium- some good news ahead of the court verdict which is expected shortly.

The Government has already made a commitment that anyone who is moved to Universal Credit without a change of circumstance will not lose out in cash terms. Transitional protection will be provided to eligible claimants to safeguard their existing benefit entitlement until their circumstances change.

Today I am announcing four additions to these rules to ensure that Universal Credit supports people into work, protects vulnerable claimants and is targeted at those who need it.

“In order to support the transition for those individuals who live alone with substantial care needs and receive the Severe Disability Premium, we are changing the system so that these claimants will not be moved to Universal Credit until they qualify for transitional protection. In addition, we will provide both an on-going payment to claimants who have already lost this Premium as a consequence of moving to Universal Credit and an additional payment to cover the period since they moved.

Second, we will increase the incentives for parents to take short-term or temporary work and increase their earnings by ensuring that the award of, or increase in, support for childcare costs will not erode transitional protection.

Third, we propose to re-award claimants’ transitional protection that has ceased owing to short-term increases in earnings within an assessment period, if they make a new claim to UC within three months of when they received the additional payment.

Finally, individuals with capital in excess of £16,000 are not eligible for Universal Credit. However, for Tax Credit claimants in this situation, we will now disregard any capital in excess of £16,000 for 12 months from the point at which they are moved to Universal Credit. Normal benefit rules apply after this time in order to strike the right balance between keeping incentives for saving and asking people to support themselves.”

The above changes will be brought in by new regulations in the Autumn (Universal Credit Managed Migration and Transitional Protection Regulations).

 Posted by at 21:29
Jun 062018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

On June 29th help us honour the memories of Kamil Ahmad and others who have been failed by the system. We are holding an event as part of Bristol Refugee Festival to:

  • bring together the disability and the asylum/immigration sectors
  • get the voices of disabled asylum seekers / refugees better heard
  • build awareness of policies and practices that currently divide us
  • challenge divisions and develop solutions

Our event is in honour of Kamil Ahmad a disabled Kurdish man who came to Britain seeking sanctuary, after having been imprisoned and tortured in Iraq. He was murdered in his supported accommodation in Bristol on 7th July 2016.

Kamil never gave up his loving nature and sense of justice, despite the horrific experiences he had been trough. It seems fitting that one of the ways of honouring his memory, together with others who have been failed by the system, is to create a stronger movement for positive change.

All welcome. Help us honour Kamil and build a stronger movement for justice. 

To book go to: https://www.eventbrite.co.uk/e/honouring-kamil-exploring-disability-and-migration-tickets-45856613365

Programme for Fri June 29th

14.30 – City Hall – (College Green, Bristol BS1 5TR)
We will install a copy of the mural which Kamil helped to create in the foyer of City Hall, as a memorial to him and other disabled asylum seekers and refugees who have been failed.
15.30 – Procession from City Hall to We the Curious – please bring banners, musical instruments.
16.00 – We the Curious (Anchor Rd, Harbourside, Bristol BS1 5DB)
Talks, discussion, workshops, film, learning from disabled asylum seekers.
What is the Problem? What needs to change?
Followed by food and music from LARA and others – (musicians include asylum seekers, refugees, disabled and non-disabled)

Please contact mail@dpac.uk.net with any access requirements when booking.

The event is supported by: Bristol City Council, City of Sanctuary, Disabled People Against Cuts, SARI (Stand Against Racism and Inequality), Bristol Defend Asylum Seekers, Bristol Disability Equality Forum, Bristol Hospitality Network, Bristol Refugee Rights, SW Region of the FBU, TUC SW, SW Doctoral Training Partnership, University of Bath, Unison, Bristol West Constituency Labour Party, Bristol National Education Union: NUT section, Aslef.

For more information please contact r.a.yeo@bath.ac.uk

Tickets are free but donations to help cover the costs of the event are welcome. To donate go to:https://www.justgiving.com/crowdfunding/disabilitymigration

Please visit our Facebook page for the latest updates.

 Posted by at 20:45
Jun 032018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

BEING THE BOSS 

National Information Gathering Survey 

INTRODUCTION – Who we are and why we are doing a survey

“Being the Boss” is a national network of disabled people who employ their own personal assistants (P.A.s)/support workers or carers. Our central role has been to support disabled people who employ their own Personal Assistants by providing peer support and a coherent voice for them in the wider community. The website and Facebook page are for disabled people who employ PAs no matter how they are funded – it is NOT just for disabled people who are receiving Direct Payments or Personal Budgets from the local authority. See: https://beingtheboss.co.uk/

Since 2010 when the Coalition government introduced Austerity measures we have seen many changes in assessment procedures, funding regimes, criteria, the closure of the Independent Living Fund and an overall undermining of Independent Living.

Given the current climate Being the Boss believe it is essential to establish ourselves as the advocate for disabled people who employ their own personal assistants because all forms of living independent lives is under threat. Alongside maintaining Being the Boss’s existing service/role, we want to build on our experience by making our advocacy role more visible and proactive and extend it to other disabled people facing difficulties with benefits and other areas which impact upon their ability to live independent lives.

To be able to play this advocate role we need to fully understand the national picture on the ground and to establish what are the key issues for those who employ their own personal assistants (P.A.s)/support workers or carers and are currently finding it difficult to live independent lives. To this end we have decided to launch a National Information Gathering Survey and are asking you to participate in it.

We can provide the Survey as a download from our website/Facebook page. Please feel free to be as detailed as you believe to be necessary or simply answer as much or as little as you feel able. Thank you for your time and support.

 https://goo.gl/forms/axbdtUnWOiUmL2sH3

 Posted by at 20:09
Jun 032018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

sadly neither Welsh Labour not the national DPO – Disability Wales whose funding of course comes via Welsh Labour are supporting this vital campaign.

 

Please find below an important Thunderclap that we should all get involved in to help save the Welsh Independent Living Grant, #SaveWILG. 

This grant allows disabled people with high care and support need to live independently and was introduced by the Welsh Government following the closure of the ILF. 

Unfortunately, the Welsh Government have decided to follow England’s lead and pass all responsibility for social care to Local Authorities. This cannot be allowed to happen as we all know the problem this has caused to our friends in England. This fight is important to disable people across the UK as if we manage to win the battle in Wales, it will add strength to the arguments for three tier support in England.

This is a vital and easy way for  people to get involved with the campaign. Please encourage everyone you know, to take part and spread the message that we all want to save WILG, and deserve to have our voices heard.

The more pressure we can put on the Welsh Government, the better. On June 5th, when the thunderclap is activated, I will  be in Cardiff  at the Senedd, meeting with the Petitions Committee, Minister for Children, Older People and Social Care, Huw Irranca-Davies, Mark Drakeford AM and Julie Morgan AM.

We want to flood social media, and hope you will be able to spare one minute to help us achieve this aim. If this action succeeds, there will be future thunderclaps held.

Unfortunately, Thunderclap no longer allows targeted messages to prevent individual accounts being bombarded unfairly.

The message that will be shared across Twitter and Facebook reads as follows:

Welsh Labour need  to listen to their members and Save WILG for those with high care and support needs across Wales.

Anyone wishing to add memes or postcard photos to their social media accounts, can find plenty via my website or by simply contacting me via the contact page or on social media. I can’t make it much easier for you 

Many thanks for your support, and please do not hesitate to click on the following link:

https://www.thunderclap.it/projects/70260-savewilg

***

According to Wikipedia, Thunderclap is a platform that lets individuals and companies rally people together to spread a message. The site uses a model similar to crowdfunding sites such as Kickstarter, in that if the campaign does not meet its desired number of supporters in the given time frame, the organizer receives none of the donations. This is referred to as “crowdspeaking”, as Thunderclap and its rival site Daycause use the same terminology. [2][3] Backers are required to copy the original message in tweets or social media posts.[4]

 Posted by at 20:05
May 112018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Annie has high support needs and was diagnosed with secondary progressive Multiple Sclerosis in  December 2009 and has become increasingly impaired.

After suffering excruciatingly painful spasticity in 2011 she spent 2 ½ months in Rehabilitation and on discharge in February 2012 was assessed by her Local Authority for care and was awarded 23 hours a week.

At the end of 2016 she collapsed and spent months last year in hospital.  They have said she will never walk again, and pain in her right arm since April has left her using a hoist since then.

But when she was reviewed on leaving hospital in May last year, her care package remained at a completely inadequate 23 hours a week and she was told she was lucky.  This despite the fact that in her current condition it scarcely gets her up in the morning.

She is now completely reliant on human support to live independently, unable to move, clean, toilet, dress, feed herself – or do anything.  She uses a hospital bed and wheelchair, and needs to be moved with a hoist by two people.

She is in constant pain, has spasms and severe spasticity yet she has been unable to access the extra hours of help she now needs.

She has no money and has had to borrow heavily from friends and family to survive and get some of the extra care she needs. This won’t continue to be possible.

Social services continue to fail to assess her needs, and have not provided her with a proper care plan since 2012. Like many others Annie has been stripped of her entitlement to legal aid due to the changes made by the Tories.

Thank you for taking the time to read this.  Any amount you can spare to help us pay for a legal opinion for Annie would help her and possibly others enormously. Any money donated and not used will go to Disabled People Against Cuts. (DPAC).

Please donate via GoFundMe or by paypal on the website. Mark any website donations for Annie.

https://www.gofundme.com/share/link/annie-needs-care-help-her-get-it

 

 

 Posted by at 20:53
May 112018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Disability News Service (DNS) has been investigating claims of dishonesty in the personal independence payment (PIP) assessment process for the last 18 months.

Now a leading discrimination lawyer has said he may be able to take legal cases on behalf of PIP claimants who believe that the healthcare professionals who carried out their face-to-face assessments did not honestly report the results of those assessments.

The cases would be taken under the Equality Act, but crucially the assessment must have happened in the last six months, for legal reasons.

If there are any PIP claimants who have had an assessment in the last few months and want to consider legal action, please contact DNS – with some brief details of the dishonesty and when it took place – either by phone or email.

If you’re interested in potentially taking a legal case, contact DNS editor John Pring by phone (weekdays only, please: 01635 228907) or email: john@disabilitynewsservice.com

Read the background here https://www.disabilitynewsservice.com/comment-seeking-claimants-to-take-legal-cases-over-pip-dishonesty/

 

 Posted by at 18:15
Apr 042018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

As we’re being asked more and more often to endorse candidates standing for various political positions we feel that it is important to re-iterate that DPAC remains completely independent from supporting any particular political party.

Nor can we guarantee to endorse someone just because they are a disabled person – after all some disabled people vote Tory or even UKIP and we could not under any circumstances endorse anyone who supported such policies. However we will consider endorsing people seeking office in any other reputable political parties.

We will only be able to support candidates who contribute to DPAC’s aims and are prepared to support #StopandScrap Universal Credit and our manifesto demands from politicians.

Overall this means that while we might endorse someone to stand for a political party that does not in any way negate our independence or our right to criticise that party and its policies when ever we deem it necessary.

 

 Posted by at 18:00
Apr 032018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

The Public Law Project (PLP) is an independent, national legal charity which aims to improve access to justice for those whose access is restricted by poverty, discrimination or other similar barriers. It represented RF in the recent High Court case where the DWP’s changes to the PIP regulations were found to unlawfully discriminate against people with mental health conditions. PLP is representing another individual client, who is bringing a case concerning the DWP’s “workaround” communications system for people with disabilities who receive DLA/ESA/IB/PIP.

 

The DWP has a policy that it communicates with (non-UC) benefits recipients by post. However, its policy allows them to agree to email as a reasonable adjustment (the “workaround”), for example where a recipient has a disability.

 

The case is that the workaround is not satisfactory because it puts people using it at a disadvantage, including because there is a risk of letters being lost and there is no provision for two-way communication.

 

PLP needs to gather evidence of examples of problems caused by the workaround to support its client’s case. If you have had difficulties with the DWP’s communications system because of your disability, in particular if you have had difficulties getting the DWP to agree to email you as a reasonable adjustment, or have had information lost,  and are willing to discuss this further then please email Ollie Persey (o.persey@publiclawproject.org.uk).

 

 

 

 Posted by at 21:13
Mar 252018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

All over Britain we’re holding locally based protests against universal credit to support the DPAC demonstration in London. Obviously everyone can’t get to London so this is going to open up the event and make it easier for more people to access and take part.

Sheffield

Anyone is welcome to come and speak at the demo, just inbox the DPAC Sheffield page or email DPACsheffield@gmail.com
So far we have: Labour sheffield, Women’s lives matter campaign Yorkshire, Sheffield Green party, Momentum Sheffield disability officer, and DPAC.

Birmingham

Meet New Street, Time to be confirmed

Brighton

Information table 10.30am Meet at the Clock Tower

Ceredigion

We will be outside Cardigan job centre on the 18th at 11.00

Edinburgh

Edinburgh Coalition Against Poverty
STOP AND SCRAP UNIVERSAL CREDIT – DAY OF ACTION WED 18 APRIL
High Riggs jobcentre 12.30
Leicester
Wednesday 18th April, 12- 2 pm at the Clocktower, Unite Community and friends supporting DPAC.

Manchester

St.Peters Square, 13.00-15.00 joining together with Greater Manchester Law Centre and Acorn Tenants Union to say no to evictions

Norwich

12.30-14.00

Meet City Hall steps from 12.15 pm

Truro 

11am – 13.00 pm April 18th Lemon Quay 

https://www.facebook.com/events/1638152956261713/

York

The York Unite Community Branch  is supporting the Disabled People Against Cuts national day of action against Universal Credit by holding a gathering on and adjacent to the footpath outside The Jobcentre Plus (one of our local Department of Work and Pensions buildings), 11-17 Monkgate, York YO31 7JZ  between 10 and 12 on Wednesday April 18th 2018.

 Posted by at 15:29
Mar 202018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

A report coming out tomorrow shows that since 2011, the Department for Work & Pensions has underpaid an estimated 70,000 people who transferred to Employment and Support Allowance (ESA) from other benefits.

The ‘error’ related to people who may have been entitled to income-related ESA but were instead only awarded contribution-based ESA, and therefore may have missed out on premium payments.

The average underpayment is likely to be around £5,000 but some people will be owed significantly more. A review of a sample of 1,000 cases suggests that 45,000 claimants  entitled to the enhanced disability premium only may be owed around £2,500 and that around 20,000 claimants who are entitled to the severe disability premium may be owed around £11,500 each. A small number could be owed around £20,000.

 

If you think you might be affected by this complete botch up by DWP then BBC  and ITN news would like to speak to you. Please contact Camilla Horrox – Camilla.horrox@bbc.co.uk

Telephone – 02036143166 or Amie Stone amie.stone@itn.co.uk telephone – 020 74304551

 

 Posted by at 15:56
Mar 192018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net
NHS facing court action over unlawful policies

Published: 19 Mar 2018

NHS organisations are facing legal action over discriminatory Continuing Healthcare policies, the Equality and Human Rights Commission warned today.

The Commission has taken its first steps in judicial review proceeding by issuing legal letters to 13 Clinical Commissioning Groups (CCGs).This follows an initial warning issued by the Commission, which highlighted concerns about NHS Continuing Healthcare (NHS CHC) policies being unlawful and breaching the human rights of patients.

If the CCGs fail to provide evidence to demonstrate that their policies are lawful, or do not take steps to review them, they will be taken to court.

The Commission has raised significant concerns about blanket NHS CHC policies having arbitrary caps on funding and failing to consider the specific needs of individual patients, such as living location and family life.

This is a serious breach of the Human Rights Act, the Public Sector Equality Duty and the Department of Health and Social Care’s own NHS CHC framework.

Rebecca Hilsenrath, Chief Executive at the Equality and Human Rights Commission, said:

‘It is utterly unacceptable that anyone should be forced into residential care when they are healthy enough to live independently and with their families. And it doesn’t make sense for individuals or communities.

‘A “one-size fits all” approach will never properly address every single individual’s healthcare needs, and NHS CHC policies are no different. This is another example of individuals being disabled by society, and prevented from living as full and independent lives as possible, as is their right. We will use our powers to ensure that the NHS thinks about this again.’

The Commission first aired concerns over discriminatory NHS CHC policies in October 2017, when it wrote to 43 CCGs demanding more information on their approach.

Following this warning, almost a quarter of those contacted are now reviewing their policies and the Commission will be writing to the others whose policies are of less concern.

It will use its formal legal powers to initiate judicial review proceedings against 13, who it determines have not considered their human rights and equality responsibilities in the way they operate their policies.

NHS CHC provide funding for care outside of hospital, either in a care home, nursing home, hospice or a person’s own home, funded by the NHS to meet physical, mental health and associated social care needs.

The letters have been sent today (19 March 2018) and the CCGs have 14 working days to respond, after which decisions about starting court proceedings will be made.

Notes to editors

The Commission will be writing to the following 13 CCGs across England:

  • Brent
  • Coventry and Rugby
  • Dudley
  • East and North Hertfordshire
  • Eastern Cheshire
  • Harrow
  • Hillingdon
  • South Cheshire
  • Vale Royal
  • West Cheshire
  • Warwickshire North
  • Lincolnshire West
  • Redditch and Bromsgrove
 Posted by at 18:38
Mar 192018
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

 

March 15th

Stroud, Rising Up! organised an action in solidarity with Disabled People Against Cuts this week. Read the Stroud News and Journal report: “Protesters spray ‘human rights abuse’ on Stroud Job Centre” https://www.stroudnewsandjournal.co.uk/news/16090675.

“Campaigners said that this afternoon’s action was intended to show the disgust at what the group sees as the latest attack on the social security of people living in the UK.”

“Simon Bramwell who took part in this afternoon’s protest said “We spoke to people on the streets and there was much support for our action, including from claimants who are deeply affected by Universal Credit.

“One woman told us she was about to get evicted as a result of the policy and another man said delays in his payments and left him struggling to make ends meet.

Watch a live-streamed video of the Jobcentre protest on via Rising Up!’s facebook page.

https://www.facebook.com/RisingUpUK/videos/412214735885083/?hc_ref=ARSUH4Pk9Acg_o9Nq9wyoM-K5mAn4oCtIjhMJY2T8rF-JbUOTqbhyK6zpSSgKFmHEfA

 

 

17 March  Ceridigion/Cardigan

A group of members and supporters of Disabled People Against the Cuts (DPAC) Ceredigion were on the streets again today, talking to passers by, leafleting, collecting petition signatures and bearing witness to the cruel injustices being imposed on the vulnerable people in our communities by the cruel Westminster Tory Government in the name of ‘austerity’.

The slogan was STOP The Rollout of Universal Credit. The Rollout of Universal Credit is due in Ceredigion later this year.

Organised by DPAC Ceredigion with the support of the Ceredigion Peoples’ Assembly.
More actions are planned.

for pictures and videos see facebook

https://www.facebook.com/groups/1853022925010117/?ref=bookmarks

 

 

 

 Posted by at 18:02