Aug 112012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Please find below an open letter from staff working at the Equality and Human Rights Commission (the Commission) to Baroness Margaret Prosser who chairs the Commission’s Resources committee. This committee approved proposals in June this year that would see the Commission reduce its staff headcount to 150. These proposals are now the subject of a 90 day statutory consultation with the trade unions representing staff at the Commission.

 

The Resources committee arrived at this new headcount by assuming that the Government will reduce the Commission’s budget to £18 million by the financial year 2014/15. However, the committee has recommended that these staff cuts should be implemented by the end of 2012. This assumed budget of £18 million represents an additional 30% cut to the budget already announced in the 2010 Comprehensive Spending Review when the Government said that the budget would be reduced from its original budget of £70 million to £26 million by 2014/15. The Equalities Minister, Lynne Featherstone MP, confirmed the £26 million budget as recently as March this year in answer to a parliamentary question https://www.theyworkforyou.com/wrans/?id=2012-03-27a.100388.h&s=speaker%3A11641#g100388.r0

Over 200 skilled and experienced staff have already left the Commission in the past year and if these proposals are implemented a further 100 staff will leave. More staff will be lost when the Commission’s helpline is outsourced to Sitel in the autumn because Sitel has only one site based in Stratford-upon-Avon. Staff do not believe that the Commission will be subjected to yet more draconian budget cuts given that it has already had its budget reduced by 62%, a hugely disproportionate cut compared to those imposed on other public bodies. Indeed, we would expect stakeholders, parliamentarians and the UN International Coordinating Committee of NHRIs to vigorously oppose any Government plans to make further cuts to the Commission’s budget.

 

Staff believe that the Resources committee should withdraw these proposals and commence a meaningful consultation based on the actual budget of £26 million. Following the statutory consultation period the proposals must be approved by the full Board of the Commission in early October before they can be implemented. So the time to take action is now.

 

What you can do:

Write to Baroness Prosser, EHRC, 3 More London, Riverside Tooley Street, London SE1 2RG

Write to members of the Commission’s Board at 3 More London: Stephen Alambritis, Kaliani Lyle, Sarah Anderson, Meral Hussein Ece, Simon Woolley, Kay Carberry, Ann Beynon, Trevor Phillips, Professor Geraldine Van Beuren, Baroness Sally Greengross, Dr Jean Irvine, Angela Mason and Michael Smith

Ask your MP to lobby the Chairs of the following Parliamentary Select Committees requesting an inquiry into the Commission’s restructuring plans: Home Affairs, Joint Committee on Human Rights and the Public Accounts Committee

Join our Facebook Group – Save the Equality and Human Rights Commission

Follow us on twitter #savetheehrc

Prosser Final 23 07 12

 

 

 
 
Jul 252012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Re-thinking disability equality policy and practice in a hostile climate’

 

Advance notice of a national event for the UK disabled people’s movement

 

When: Thursday 27 Sept 11am to 4.30pm

Where: Coin St Neighbourhood Centre, 108 Stamford Street South Bank, London SE1 9NH

Who is the event for: Places available for 80 representatives from disabled people’s organisations (DDPOs) and disabled activists from across the UK .

Aims of event:

1. ‘Take stock’ of the achievements and challenges
disability equality policy and practice has created over
last 15 years

2. To explore how we can best defend our achievements
and rights in a climate of austerity and free market/
anti Welfare state ideology.

3.     To identify areas of consensus that the movement can
mobilise around and take action on to influence the
political and policy agenda

 

Speakers include: Jenny Morris, author of Re-Thinking
Disability Policy published by the Joseph Rowntree Foundation

Booking details to follow soon. To register an interest in
attending email: info@inclusionlondon.co.uk

 

 

 Posted by at 13:47
Jul 162012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

The dangers of throwing several thousand people from paid work into unemployment should be obvious to anyone. The fact that a majority, although not all, of the Remploy workers are disabled people should signal a further problem: Disabled people who want to work, are more likely to be unemployed than non-disabled people in all official statistics since records began. For example in 2011 the employment rate was 48.8% for disabled people compared to 77.5% for non-disabled people[1].

It is dangerous, misguided and completely ludicrous to claim that all disability organisations and the disability movement have decided that a new perverse way of supporting disabled people is to make them unemployed and subject to the ravages that disabled people must endure under this government, as the Sayce report suggests. See for example https://www.dpac.uk.net/tag/guardian-newspaper/

For those of us that have spent years arguing for an equality agenda for disabled people the arguments put forward in the Sayce report are: dangerous, misguided and wrong.

Dangerous Partners

The Sayce report (‘Getting in, Staying in and Getting on’) and the Tory desire to seemingly make the poorest most excluded people further excluded and even poorer are a strange partnership, throw in Miller, Unum and ATOS and we have a list of known enemies of disabled people-some might wonder what Sayce is doing in such unpleasant company.

The Sayce/ Tory partnership produced a report rumoured to have cost over 2 million pounds to:

1. Explain how to save money

2 Improve disabled Remploy workers lives’ by closing their factories and seemingly removing their jobs.

3. Ensure that if factories are sold off to buyers at knock down prices, buyers have no enforcement in place to re-employ disabled workers

The basis of these ‘improvements’ are predicated on the notion that disabled people need to be included in society- who would disagree? However, inclusion for disabled people and many non-disabled people in society now often means being included in the growing army of the unemployed –for those disability organisations that sign up to this notion, unemployment prevents segregation- well that’s true, but maybe they should re-examine that particular version of inclusion vs segregation. Maybe we need examine the other partners in this game? Is it a surprise that Unum were involved in the Sayce report for example? See here for an explanation of why Unum have satisfied the status of an enemy of disabled people and co-conspirators in welfare reform or the cuts agenda. One organisation that needs no introduction is ATOS. ATOS own the company KPMG. KPMG were contracted by the Department of Works and Pensions too (cost currently unknown) – they produced a report of their own in March 2012. The report was titled: Analysis of Remploy Enterprise business and Employment Services’ A copy of the report summary can be found here

However, the validity of this report may be in doubt to the general reader as page two is filled with a list of disclaimers. These include:

●Nothing in this report constitutes a valuation or legal advice.

●We have not verified the reliability or accuracy of any information obtained in the course of our work.

●In preparing our report, our primary source has been Remploy’s internal management information and representations made to us by Remploy Senior Management during the project. We do not accept responsibility for such information which remains the responsibility of Management. Details of our principal information sources are set out on page 4 and we have satisfied ourselves, so far as possible, that the information presented in our report is consistent with other information which was made available to us in the course of our work in accordance with the terms of our Service Order. We have not, however, sought to establish the reliability of the sources by reference to other evidence.

Maybe Les Woodward’s analysis, which the DWP didn’t pay millions for, might be more credible

Closing Remploy factories will not save disabled workers from ‘Victorian-era segregation’. It will wreck lives[2]

An interesting postscript is that one of the directors of Remploy is also a director of RADAR: ‘all in it together’? Labour, (who incidentally closed a number of factories in 2008 so let’s not get too teary eyed), have urged the Government to start the whole consultation again, some claiming that it is a shambles. While Phil Davies, secretary of the GMB accused the Government of turning the consultation into a

good old-fashioned Klondyke gold rush”[3].

But there’s more, as argument after argument presented in the Sayce report is knocked down and proved to have a false or questionable basis.

 Misguided Arguments

The ‘Independent’ Sayce Report of June 2011 and the consultation that followed apparently showed that a group of  individuals, organisations, charities (and the insurance company Unum) felt that segregated workplaces were outdated and as a result disabled workers should be made redundant (see appendix for those involved in consultation).

 

 However, the process of redundancies was underway as early as January 2011 six months before the estimated 2 million pound plus Sayce report began. On 14 January 2011 Remploy HR Director, Sue Butcher phoned the GMB National Secretary and informed him that an announcement was to be made on 18 January 2011. No other information was given.

On 18 January 2011 the company met with the trade unions and informed them that they were opening up a voluntary redundancy programme and that consultation would start on 24 January 2011. The company had already informed the employees by letter that it was opening up a Voluntary Redundancy scheme. No consultation had taken place with the trade unions. Seems they were not important enough to be invited[4].

The Sayce report found people working at Remploy factories who were quoted as saying they wanted ‘real’ jobs and the report ‘team’ claimed to have consulted in-depth with workers

 

The GMB union cannot seem to find these quotees in the factories who wanted ‘real’ jobs, for some reason. It has, however found 4 people who took part in what was presented as an in-depth consultation with Remploy employees[5].

The closure of the Remploy factories is because they are segregated workplaces isn’t it?

 This is one simplistic argument popularised by the Sayce report, however the Remploy factories do not employ disabled people exclusively. In 2008, 29 factory sites geographically based from Scotland to Cornwall closed with over 2,500 Remploy employees becoming unemployed. Of these, 1,700 employees were disabled. The 2012 closures will affect around 80% of employees who are disabled.

Given the other players in the partnership –it all points to a ‘cuts agenda’ rather than any supposed moral high ground on inclusion.

The workers will find alternative jobs in the open workforce?

 

In 2008, 29 factory sites geographically based from Scotland to Cornwall closed with over 2,500 Remploy employees becoming unemployed. Nearly 1,700 of these employees were disabled and most of them have not worked since and remain on benefits.

From the last round of Remploy closures  85% of disabled ex-employees remain unemployed[6]. This was in a better economic climate than that of today. Some committed suicide, many threatened suicide and many experienced mental health issues, for those that already had mental health issues these were exacerbated.

The workers will be supported when the factories close

 

 During 2007 and the early part of 2008 the company gave promises of support for those leaving in the round of closures carried out under the Labour government but history has shown that very few of the 1,700 disabled people received even a phone call from Remploy let alone any practical support[7].

In 2012 there is a community pot of 1.5 million offered to charities and disabled peoples’ organisations (DPOs) to support the workers into jobs by the DWP. This may explain the keenness of the illogical ‘equality into unemployment arguments’ that some were producing but it is unlikely that DPOs and the usual list of disability charities or voluntary organisations can find jobs for ex-Remploy workers where they do not exist, despite taking their 30 pieces of silver. However, some are running the much maligned mandatory work programs-so maybe that will the grand plan, sanctions and all.

The full criteria for this fund has been laid out in a Freedom of Information Request on the purpose of the Community Support Fund (CSF)  [8]

The CSF will offer financial and non financial support to local disabled people’s user led organisations (DPULOs) and voluntary sector organisations to deliver support and services designed to meet the specific needs of
disabled Remploy employees affected by the announcements on the future of Remploy factories.

The intention is that the fund will help to support affected Remploy staff to re-engage with their local communities and help their transition from segregated sheltered employment to mainstream employment. It will be focussed around the geographical areas where affected Remploy employees live and used to build the capacity of local DPULOs, 3rd sector and voluntary organisations and to develop a range of activities and projects to help the move from sheltered to main stream employment.

As well as a modest amount of money being available to support projects to help ex-Remploy employees, and other local disabled people, get into work, training or volunteering funding will be made available to help create learning and development activities to improve employment
opportunities.

 Not really that impressive. But impressive enough for emails asking organisations to ‘put their applications in’ to go out to selected disability organisations and charities 24 hours after the closures were formally announced. These emails say nothing about jobs but give examples of film clubs and other types of support , none of which offer a paid job which is what the factories offered. One option is to offer support in ‘choice and control’ where was the choice and control for those workers that wanted to stay in their paid jobs in the Remploy factories?

The Remploy workers will be better supported by Access to Work Schemes- money will be better spent on Access to Work

 

First, to qualify for Access to Work you need to have a job or a documented firm offer of one: first hurdle. The problems with Access to Work, including cost cutting under this government are too numerous to go into here, but even the hallowed Access to Work cannot match the percentage of support that was already being provided at the Remploy factories. This is particularly the case with learning difficulties and mental health issues.

Another point made in the Sayce report is that access to work may be able to benefit disabled people with a mental health conditions.  Out of the 32,680 helped in the current year only 460 have a mental health conditions.  This is only 1.4% of all those helped.  Compare this to 131 employees in Remploy who have a mental health conditions out of 2,692 employees which is 5% or 4 times higher.

When you look at another major disability which is learning disability, out of the 32,680 helped by access to work only 1,680 with this particular disability have been helped into employment.  This is just over 5% compared to the 462 disabled people out of 2,692 who have a learning condition working in Remploy (17.2%) again over 3 times as high[9].

Never the less, its all been a useful exercise to set up an expert panel on Access to Work run by the CEO of Essex Coalition of Disabled People and to extend access to Work to young disabled people enduring workfare type schemes[10]

The workers in the factories cost too much

 

GMB argues that voluntary redundancies increased the cost of each worker by £1,000 per worker. Management has remained top heavy, apparently ineffectual and overpaid- and the continued use of consultants such as KMPG have added to costs. These costs were lumped together along with running costs to produce a misleading amount per worker[11].

Further: There are 3238 employees most of whom are disabled and who earn less than £16,000 per year. The cost of travel for all employees has escalated to £2m, the cost of company cars to £2.4m and the cost of car allowances to £1.1m; a total cost of £5.5m.

The figure of £138m losses for the factory network is not true. We believe that if all the measures outlined in the trade unions document are taken on board and implemented then the cost of the factory network would be approx £35m per year.

Put another way when the profit from sales is considered and taken into account the cost per disabled worker to the State could be as low as £7,000.

When you also take into account the fact that tax and insurance is being paid in and benefits are not being paid out this figure could be substantially lower[12]. Alternatively: the cost of unemployment which for a disabled person could be as much as £25,000 to £30,000 per year for each disabled person not working when you take into consideration the revenue lost in tax and national insurance contributions the cost could be higher. A disabled person who is not working will probably receive higher benefits than a non disabled person. Housing benefits and careers allowances are only the tip of the iceberg.

The unseen and unmonitored costs start to mount up when you consider that a large number of disabled people who were made redundant when Remploy closed 29 factory sites now have severe health problems and the use of the NHS has greatly increased. We would estimate that this cost could be as high as £20,000 for some disabled people.

Figures in the Sayce report show that factories never profit

 

 In May 2012 Profits were up -Sally Kosky said: “According to the management’s own figures, the cost to government is down by £16.5 million on the previous year – £2.5 million better than budget”[13].

Also from May: A letter sent to Remploy employees shows the business is doing well, Plaid Cymru has claimed. The letter congratulates workers on a 12.2 per cent growth in sales and a 17 per cent reduction in costs. The Remploy factory in Swansea is one of seven sites in Wales which has been earmarked for closure.

Plaid Cymru’s equalities spokeswoman, Lindsay Whittle AM, said: “These figures prove that the UK Government’s intention to close Remploy factories is a thinly veiled attack on the welfare state. It shows that there is absolutely no justification for the government’s plans, except as a continuation of its attack on welfare recipients.”[14] 

So it looks like they did profit! The Swansea factory will be closed along with the others despite 12.2% in growth and a 17% reduction in costs. It was never about profits or costs was it?

But Remploy wasn’t getting Contracts was it?

 

The more worrying aspect of the company’s strategy on sales is the outsourcing of work and the lack of tendering for public procurement contracts.

Letters from the NHS Forth Valley and Stirling Council to the Minister show it is clear that Remploy has not shown interest in tendering for large contracts that the company could have won.

It is also apparent that the senior managers work within a very nice comfort zone; no aggressive sales strategy exists and no stretching targets exist. The trade unions believe this is part of the conspiracy to fail and the failure of the sales team is the responsibility of the Chief Executive and the Board.

We understand that because of the previous reduction in manpower that large amounts of work is being turned away or outsourced. Birmingham factory and Healthcare are prime examples[15].

 

DPAC seems to be saying that disability Charities and some DPOs are involved in some way that is not in line with the principles of disability rights- this does not make sense

 

It depends on your idea of disability rights; the old chestnut that keeps being trotted out is that closing the factories is all about the right of disabled people to be included. We ask what are the ex-Remploy workers going to be included in exactly? Film clubs?

Where was their choice and their rights in where they wanted to work and in keeping their paid jobs in the worst recession since the 1930s?

So who Gains?

 

 Cleary not the Remploy workers, they are merely the collective sacrificial lamb on the altar of profit and gain by others or those with vested interests if you prefer.

These include:

The beneficiaries in the invited team that made up the Sayce report.

The director who was on the board of Remploy and RADAR (now DRUK: chief executive Liz Sayce) simultaneously–there’s got be some gain there.

Those disability charities and organisations who may gain from the community pot to support the Remploy workers in their unemployment

KPGM (and ATOS who own KPGM) whose report has so many disclaimers making it another gross waste of tax payers’ money

UNUM, but we are not sure how they gain yet-their inclusion in the Sayce consultation team must serve some purpose for them.

Remploy senior managers’ beneficiaries of a 1.2 million bonus payment in 2012 when it was clear that factories were earmarked for closure

Those companies and disability charities running work programs such as work for your benefits ‘work programs’ such as workfare.

Those that will further their careers (and income) by sitting on ‘expert’ panels discussing Access to Work (rather than paid jobs) in the wake of the closures

Remploy itself by winning contracts to deliver Access to Work for mental health users for every area tendered before the closure deal was complete[16]

Doesn’t all that show a conflict of Interests?

 

 Yes, but this is Tory Britain- who cares about other peoples’ lives anymore when they can make a few quid?

Debbie Jolly co-founder DPAC

twitter: @redjolly1


[1] Source: Labour Force Survey, Quarter 2, 2011

 [4] Written evidence submitted by the GMB May 2011

 [5] Sayce Report Analysis July 20th 2011 GMB,UNITE, Community

 [7] Written evidence submitted by the GMB May 2011

 [9] A new strategy for the employment of disabled people: a new concept in the field of employment – by Phil Davies, GMB National Secretary for Manufacturing Section on behalf of the Consortium of Trade Unions

 [11] Written evidence submitted by GMB May 2011

 [12] A new strategy for the employment of disabled people: a new concept in the field of employment – by Phil Davies, GMB National Secretary for Manufacturing Section on behalf of the Consortium of Trade Unions

 [15] Written evidence submitted by the GMB May 2011

 

Appendix

 List of those involved in Sayce Consultation NB we are still waiting for a list of those involved in the report itself.

The following organisations submitted evidence to the review. Source: appendix 3 of Sayce report

1. 104 films Limited
2. A4e
3. Acquired Brain Injury Forum for London
4. Action Group
5. Asperger’s Inc
6. Barnsley Metropolitan Borough Council
7. BASE
8. Birmingham City Council
9. British Assistive Technology Association
10. Bradford Council
11. Bristol and South Gloucestershire People First
12. Bristol City Council
13. British Psychological Society
14. Camden Society
15. Cardiff and Vale Coalition of Disabled People
16. Centre for Mental Health
17. Centre Point
18. Changing Faces
19. Cheshire East Council
20. Choices and Rights Disability Coalition
21. Elcena Jeffers Foundation
22. Employment Services at Westminster Centre for Independent Living
23. Enham College (RTC)
24. ERSA
25. Finchdale RTC
26. Foundation for People with Learning Disabilities
27. Hands Free Computing Ltd
28. Hao2.eu Ltd
29. Headway
30. Hertfordshire Action on Disability
31. Hillcrest Branch
32. Hudson Interpreting Services
33. Inclusion
34. Indigo Dyslexia
35. Ingeus
36. Kent County Council
37. Key Ring
38. KM Furniture Ltd
39. Lancashire County Council
40. Leicestershire Centre for Integrated Living
41. Low Incomes Tax Reform Group
42. Mencap
43. Mental Illness
44. Mind
45. Monmouth People First
46. National Association of Deafened People
47. NASUWT (teachers union)
48. Newco Employment and Training
49. North Bank Forum
50. Nottinghamshire Deaf Society
51. Papworth Trust
52. People First
53. Pluss
54. Queen Alexandra College (RTC)
55. Queen Elizabeth’s Foundation (RTC)
56. Reed in Partnership
57. Rethink
58. Royal British Legion Industries
59. Royal College of Nursing
60. Royal College of Psychiatrists
61. Royal National College for the Blind (RTC)
62. RNIB
63. RNID
64. Scope
65. Scottish Association for Mental Health
66. Scottish Autism Service
67. Scottish Independent Advocacy Alliance
68. Sense
69. Shout Out
70. Signature
71. Slough Council
72. Social Firms FRC Group
73. St. Annes (social firm)
74. St Loye’s (RTC)
75. St Mungo’s
76. Sustainable Hub of Innovative Employment for People with Complex Needs (SHIEC)
77. The Association of National Specialist Colleges
78. The Coalition of RTC Providers (covers all nine residential colleges)
79. The Small Business Consultancy
80. Transition Information Network
81. Travel Matters UK
82. UNITE
83. UNUM
84. Vangent
85. Visibility
86. Vocational Rehabilitation Association
87. Welsh Assembly Government
88. Woman at Wish
89. Work Fit

Liz and the review team met with people from a wide range of other organisations including, among others, People First, National Centre for Independent Living, Disability Wales, Inclusion Scotland, the Employers’ Forum on Disability, Remploy, the TUC, GMB, Social Policy Research Unit, Centre for Mental Health, Disability Alliance, Sense, UNITE, RNIB, Mencap, the Scottish Union for Supported Employment, a range of central government departments, Essex Coalition of Disabled People and many more.

N.B we do not suggest that those appearing on this list are all in favour of closure of the Remploy factories, but the list is telling, more so because DPAC also responded to this consultation and don’t seem to get a mention. The DPAC consultation response can be found here

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Jul 032012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

DPAC now has a volunteer run legal referral service with solicitors based in London. Please read the information below. If you feel after reading the information below you may still need legal advice please contact us at info@hafcac.org.uk or on 07899 752877. This is run by DPAC volunteers so you may not get an immediate reply.

Frequently, the most effective way of resolving a community care/ social services, health authority (public bodies) related dispute will be through informal contact with the local authority, NHS body, MP or a local councillor.

You may be able to get advice from a local advice agency or law centre first which may be more accessible to you.

www.citizensadvice.org.uk

www.legalservices.gov.ik

www.lawcentres.org.uk

However, the law permits a person to apply to the High Court to have a decision made by a public body reviewed under Human Rights Act 1998 s7.

You will generally be expected to give the local authority or NHS body that you are unhappy with the opportunity to remedy the issue before the ombudsman (a person who is there to represent the interests of the public by investigating and addressing complaints reported by individuals) or a court or will be prepared to consider a complaint.

In certain situations, (such as where a person is facing a deterioration of his or her health as a result of a decision taken by a public body), it may be possible to challenge the decision quickly in the Court or make a direct approach to the ombudsman.

 Posted by at 13:06
Jun 302012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

We’ve been involved in 3 major direct actions, plus several more minor protests this year all of which have been instrumental in raising the profile of the attacks against disabled people: the first was with UKUNCUT when we blocked Regent Street for several hours and the second saw 2 groups of disabled people blocking Trafalgar Square causing a massive backlog of traffic into the centre of London. The most recent joint action with Transport for All didn’t quite work out as planned but was very effective nevertheless and took place opposite parliament.

We protested in leafy Leamington Spa, outside DWP offices and supported the Big 6 Energy Bash with Climate Justice Collective with on-going campaigning against fuel poverty and for an accessible and sustainable public transport system we can all use.

We’re further involved in numerous anti-Olympic events being planned over the summer. These are particularly targeted at many of the less acceptable sponsors of the Olympics such as ATOS, Dow and Rio Tinto Zinc.

Many disabled people joined in with the Great British Street Party organised by UKUNCUT when we all partied outside Nick Clegg’s house. Disabled people from Islington blocked and held the road until other activists could get there.

We’ve continued to campaign against the WCA and ATOS in particular and were given an award earlier this year for nominating ATOS as the least appropriate sponsor of the Olympics by War on Want. We also have a French speaking supporter who now tweets regularly o the French media about ATOS.

Together with Inclusion London, Disability Hate Crime Network and others we made a joint-submission to the Leveson Enquiry about the negative media portrayal of disabled people. This is still being followed up as we want to be able to give oral evidence to the inquiry which is being refused. Most of the hard work for this was done by Inclusion London following on from the research they commissioned fromGlasgowUniversity. Failing this we plan to perform our own version of the Leveson Enquiry.

We collected with Anne Novis signatures from over 400 disabled people and DPOs against the loss of ILF funding. We took this to DWP and asked to see Maria Miller which was refused. We were very pleased to have Jamie Bolling from ENIL join us for this lively protest. Correspondence with Maria Miller has since been on-going over this and we expect the consultation to be launched shortly.

We have prepared two lengthy reports which we’ll be finalising and publishing shortly on the importance of ILF and cuts to care and support funding. We will be using these in our on-going campaigning around these issues.

We’re helping with two pieces of undercover research although can’t say more about that as it’s undercover.

At an international level we’ve been involved with lobbying in the European Parliament and with a working group onEurope, Disabled People and Austerity. We were also part of a European working group on disability hate crime and had the research undertaken by Anne Novis from Disability Hate Crime Network donated to us to disseminate more widely which we’ve done.

We’ve also made links with Danish activists and are helping with a Spanish research project into disability activism. Debbie has also travelled toBulgariato support a direct action against lack of funding for independent living.

We seem to be very much in demand still to speak at a wide range of events both nationally and locally. There are too many to mention each individually but a few in the past few months include having people speak at British Youth Council,  PCS, TUC disabled members conference, Right to Work AGM , Sussex LRC and GMB congress fringe meeting on ‘Defend Welfare and Pensions’, and CoR conferences. A few local events include Islington DPAC skills day and Deaf Access Bromley, and in the future SHP residential home for mental health survivors inWestminster, West Midlands Against the Cuts and Birmingham Against the Cuts.

Unfortunately we weren’t able to find anyone to speak at RMT AGM or at an NUT fringe meeting which we were also invited to speak at. Both of these were in Torquay so if anyone in Devon orCornwallcan help in the future please get in touch.

We’ve also done workshops at various events on benefit cuts and particularly on planned changes to Universal Credit. Fortunately the number of people who are willing to speak on DPAC’s behalf has increased as otherwise it would be impossible to respond to all the requests we are getting.

We also had a motion passed against WCA and welfare reform at NUT conference and NUT affiliated to DPAC.

We had a stall to advertise our work at NASWUT disabled members’ conference and have been asked to have another stall at the West Midlands NASWUT regional conference in October. We also shared a stall we were given at TUC disabled workers’ conference with allies from Transport for All and ALLFIE, and were represented at the NUS disabled students conference inManchester. We’ve also been invited to take part in a TUC conference fringe meeting with the Peoples’ Charter.

The number of local DPAC groups continues to expand and we now have 12 local groups around the country. The newest group in theEast Midlandsis being set up with input from the steering group.

We’re working with Inclusion London and  NCoDP on the launch of rethinking disability policy, a key national conference on the way forward for disabled people  and in the meantime are stimulating debate within the disabled people’s movement, eg interviews with a range of disabled people.

We’ve continued to build links with solicitors and are shortly launching a legal referral service set up with help from Inclusion London and HAFCAC. We have already been involved in supporting a landmark legal ruling on Housing Benefits and size criteria.

We’ve also been actively involved in helping to support Remploy workers whose jobs have been threatened by factory closures, including running a national meeting to build support from among disabled people and our organisations for the Remploy workers, wrote a letter in support of the workers in partnership with Inclusion London which was signed by 50+ organisations and individuals, we set up a Remploy campaign steering group bringing together the unions with the disabled people’s movement, we made a solidarity visit to the Barking factory, we continue to publicise arguments in support of the workers to counter the myths and distortions about the need to close the Remploy factories being put around by government and some disability organisations.

We’re still involved with the Right to Work steering committee, and generally try to ensure that disabled people’s rights are defended in the wider context of the welfare state but also raise awareness of disabled people’s issues within the mainstream cuts movement at every opportunity. We’re also working to ensure disabled people’s access issues are taken on board in building for the forthcoming TUC demonstration in October.

We’ve also planned and made funding applications for a disability, art and protest exhibition and are starting conversations with the disability arts movement about joint working.

Vitally we’re trying to work with people in Worcestershire to oppose the moves of the local council there to slash care and support funding and once again warehouse disabled people in care homes rather then fund independent living.

We’ve also between us written a range of articles and briefing notes available on the website or produced for specific events. We’ve also responded to numerous requests for articles for publication elsewhere.

Dutifully we’ve made submissions to a range of consultations although we are not convinced that the Coalition take much if any notice of the results of these.

One area we want to do much better in but have problems due to lack of financial resources is the inclusion of the Deaf community. We’d like to be able to provide interpreters, and BSL clips on the website. So if anyone has any suggestions about how we can do this more effectively please let us know by emailing us at mail@dpac.uk.net

As always we’ve lobbied MPs and Lords, tweeted lots and generally raised the problems people face wherever we can.

 

 

 

 

 

 

 Posted by at 11:29
Jun 292012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

As the Olympic torch arrives in Birmingham tomorrow, June 30th, we were asked to write a short piece about ATOS sponsorship of the Olympics. Here is what we wrote.

One might be forgiven for wondering just why and how ATOS  ( ‘Licensed to Kill Disabled People’ by the Condems) and the corporate butchers of Bhopal Dow are two of the most prominent Olympic sponsors. How can such odious corporations be given worldwide publicity and credibility?

In exchange for lucrative payments from the government ATOS happily continue to hound and harass disabled people into even further poverty and to drive many to suicide.

Over 1 million disabled people, many too ill to work face losing their benefits or have already lost them.  If you become ill or disabled in the future this could happen to you, even if you’ve worked and paid National Insurance contributions most of your life.

People with life-threatening illnesses, some with terminal cancer, and mental health conditions live in fear of their forthcoming ATOS assessments acknowledged as totally flawed by CAB, McMillan Cancer charity and a host of others. The tick-box computer assessment system takes no account of real life problems people face or the complexity of many long-term illnesses and disabilities. Yet within minutes this process which violates the fundamental medical principle of ‘first do no harm’ can strip disabled people of essential benefits and rob them of their lives.

Real-life horror stories of assessments and outcomes now abound and can be read in papers on an almost daily basis yet still the government refuse to halt or change these vicious tests. Some of the reports are little short of torture. A woman forced to try to walk to prove she couldn’t who fell onto the ground and had to be helped up again crying by her mother. Another woman forced to try to walk down a long corridor also to prove she couldn’t walk. People waiting for major heart surgery or those who have had numerous heart attacks killed by the stress of the assessments and being told they are fit to work.

A Grimsby Fisherman suffering from horrendous blood clots and open ulcers and struggles to walk who has been told by specialists at two hospitals he would be risking his life if he went back to work lost his disability benefits.

A more recent case is that of aDundeeman found fit to work who is deaf, blind and tube-fed and who needs 24 hour care. How could anyone with such profound impairments be found fit to work?

Yet this is how ATOS treats disabled people.

The BMA Local Medical Committee Conference recently voted unanimously for an end to these notorious Work Capability Assessments as Scottish GPs did earlier this year.  Dr Stephen Carty has likened the UK Government’s welfare reform crackdown on disabled people to the “barbarism” of the Nazis.

The cost of these sometimes murderous assessments to the taxpayer are enormous as appeals rocket costing a predicted £50 million in tribunal costs in 2012 alone. The backlog of cases has reached epidemic proportions with tribunals sitting even on Sundays to try to reduce the 10 month backlog of cases. Yet even if a claimant wins their appeal against their assessment, and most do, the treadmill experience of  being retested can start again immediately for no justifiable reasons.

As the blood of disabled people continues to drip steadily from the hands of our Olympic sponsors they should hang their heads in shame at the terror they are causing to those who deserve support not victimisation from our welfare state.

If you would like to join us in expressing your disgust at ATOS and its sponsorship of our Olympics then please email their CEO at  Thiery Breton at  thierry.breton@atos.net (https://www.ceoemail.com/se.php?id=10159)

 Posted by at 19:05
Jun 242012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

What follows is a personal account of the experience of one person and what it is like to be unemployed and disabled in Tory Britain. It shows the contempt that people are treated with by some so-called work program providers engaged by their Tory friends and paid for by the taxpayer.

This example shows quite clearly what we all knew: that people are not being supported under this Tory regime, rather they are being belittled humiliated and having legal rights under the Equality Act ignored. At the same time they are being driven towards new or further mental health issues resulting in suicidal tendencies for some.

The fact that this example features the A4e Company run by disgraced multimillionaire Tory darling Emma Harrison speaks volumes.  Ministers ended the A4e contract for the Welfare to Work scheme in May this year under the shadow of a range of accusations, arrests and resignations within the company.

Karen wrote to DPAC so that her story could be shared –we believe this inhuman treatment and worse is happening to many people under this Tory regime. She says:

Background

I finished University in 2002 and was sent toQueenAlexandraCollege. I signed on in 2004, before that I had long term problems with health and eyesight. I had specialist help from Action for Blind People who were instrumental in getting me a voluntary placement at aBirminghamCollege. Although it was two years before I got a paid contract there. I was supported in furthering my skills and gaining more qualifications as well as experience. In 2009 government cuts meant I was unemployed again. Action for Blind People got me some courses under the advisors discretionary fund. However, I was summoned to the jobcentre and informed I was to be put on flexible new deal with A4e in 2010. I was stopped from seeing Action for Blind People and the placement they were arranging fell through as a result.

A4E and the constant threat of sanctions

I informed A4e that I needed large print documents, but they continued to send out small print documents which were illegible to me. The first contact given for at A4e was not contactable so I went to my job centre and asked for someone else. A4e said they’d send someone out but I had already arranged a lift to their offices. When I got in the office they presented me with a form to fill in, in small print. I told them I couldn’t see it and asked them to photocopy it, but they didn’t enlarge it. I was then taken to a very public area where there were other clients and I was asked humiliating personal questions. For example: are you a drug user? What medication do you take? and so on, at no time was I informed that I didn’t need to answer these questions.

I was then called over to see a woman, let’s call her Ms Harris. The first thing she said was:

If I were you I’d go on the sick.

This would have meant that I was off their books. I told her I wanted to work, at which point she became very rude and then refused to reimburse my travel costs. I explained that I needed large print documents, Ms Harris and her manager barked at me that they didn’t need to provide me with anything! Then they amazingly proceeded to threaten me with sanctions.

Three months passed. I decided that if they couldn’t provide reasonable alterations, equipment etc.   I wasn’t going to sign it or do it. They threatened me with their sanctions again and put me through a psychometric test. Once again, no attempt was made to provide for my reasonable alterations. In the end I showed the A4e worker how she could enlarge the screen this for others that might need it, after I’d worked it out for myself-they didn’t have a clue nor care. I think I skewed the results so badly that they didn’t bother me for a while, until I received a call from Ms Harris, she informed me about a teaching job. However, when I told her that I didn’t have a teaching qualification, she got aggressive. I later learned that she had immediately got in touch with the benefits office in an attempt to impose sanctions again. To be fair they did provide training in CV writing-that was great as they told me to leave my degree off the CV! In the end they submitted the CV I had done while at Action for Blind People and claimed credit for it.

More months passed and I was transferred to Beacon Centre for the Blind. It was not taken into account how I would get there, I got lifts mostly, but trying to get travel costs reimbursed was still made as difficult as possible. At this time my mental health issues had been worsened by the treatment at A4e. I told A4e I couldn’t use buses (I had had some training before going to A4e but it was a bad experience and really didn’t work). A4e thought this was an opportunity to belittle me and humiliate me, telling me I was missing out. By the next meeting they made their contempt even clearer:

Look you’ve been sent here, you’re better off than others: stop complaining!.

If you don’t like it, don’t sign on-nobody is forcing you to claim JSA are they!

I was then sent to the Job Centre. They told me to sign for the work program, if I didn’t …then – you guessed it: I would be sanctioned.

I am now with Action for Blind People again, the people I have had a ten year relationship with, they saw the mess I was in and helped me loads. I am also now seeing a specialist mental health nurse and psychiatrists for the suicidal feelings.  I avoid signing anything and am terrified of going to the job centre now, after my experience.  In fact, I am starting to be scared of going out at all. Sometimes, I’ll pretend to be sick so I don’t have to go out of the house. For example I live with my parents and they often go to see my nephew-I just can’t face leaving the house. It’s the same when I have the chance to go to my brothers.

Complaint

I put a formal complaint in to the Independent case examiner. They believed that it was acceptable for A4e NOT to provide large print documents, despite the Equality Act. The job centre still doesn’t provide large print documents. I have to ask each time and explain again and again. I’m close to the end of my tether with it all. I finally got my travel expenses 12 months after that first meeting with A4e, after my formal complaint. They were paid on the 1st April.

 

Jun 142012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

John McDonnell, MP who has always been very supportive of DPAC and who we work closely with has asked for help to try to get legislation through parliament to allow job-sharing for MPs.

For many disabled people being an MP full-time would never be a viable option and the only way more disabled people with a range of valuable life experiences, and knowledge of disability could contemplate becoming an MP would be for there to be a job-share system for MPs.

The UNCRPD article 29 is specific in stating that persons with disabilities should have the right to participate in political and public life on an equal basis with others. Unless job-sharing for MPs is introduced this is yet another area of the UNCRPD where the government continue to fail to adhere to the convention.

This would of course not just encourage more disabled people to become MPs but would also be an advantage to women especially those with children and so would facilitate also encouraging another under-represented minority group to take amore active role in politics.

Please could we ask people to email John to say they would be interested/more likely to consider standing as an MP if they could job-share. He needs to be able to say he’s been contacted by lots of disabled people about this to try to make it a reality.

His email address is john.mcdonnell.mp@parliament.uk  

If your email bounces back please resend it another time.

Please watch the videos at www.disabilitypolitics.org.uk – John’s
asks for people to contact him if they can be a job share MP and Caroline’s asks people to write to their MPs in support. There is also the e-petition on the site too.

 

 Posted by at 20:26
Jun 082012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

The closure of the Remploy factories has ignited a wealth of media attention and strong feeling as well as differences of opinion between disabled people, and Disabled Peoples’ Organisations (DPOs) on the position of disabled Remploy factory workers. The now infamous Sayce report called for closure of the factories in the ironically titled: ‘Getting in, staying in and getting on: disability employment support fit for the future’. This was followed by a consultation exercise in July 2011 to which DPAC responded outlining the impact of the closure of the factories and urging that they remain open.

Since then, DPAC, DPOs, Unions, disabled workers, disabled and non-disabled people have been active on the proposed closures in a number of ways which have been publicised on the DPAC site. DPAC have invited Liz Sayce to comment, but she has not responded to our request.

Most recently the Sayce report has been accused of doing the Governments ‘dirty work’, as elitist and a part of the cuts agenda at the TUC Disabled Peoples’ conference. 

There was overwhelming support at the annual TUC Disabled Workers’ Conference for the campaign to fight the planned closure of the Remploy factories.

The government announced in March that 36 of the 54 remaining Remploy factories across the UK would close by the end of 2012, with the loss of more than 1,500 disabled people’s jobs, while there would be further consultation over the future of the other 18 factories.

The announcement was part of the government’s response to a consultation on last year’s review of employment support by Liz Sayce, chief executive of Disability Rights UK (DR UK).

Sayce called in her report for funds currently used to subsidise the factories to be ploughed into more personalised forms of employment support for disabled people, including the Access to Work (AtW) scheme.

But Mandy Hudson, from the National Union of Teachers, told the conference that the Sayce report had “gone about doing the government’s dirty work”.

And she criticised “the completely cavalier way that Liz Sayce’s report sets adrift a whole set of disabled workers”.

The disabled peer Lord [Colin] Low also criticised Sayce’s report, and said its “highly individualised approach… seems to smack of elitism”.

Read more of the article by John Pring including the Remploy protest outside the offices of DR UK by Remploy workers and UKUncut here  

 Opening up the debate

Since the government announced the closures, some DPOs have backed its plans, arguing that the move was one towards the inclusion of disabled people.

But Tracey Lazard, chief executive of Inclusion London, said:

This is a cut. It isn’t about inclusion. We shouldn’t let the government justify this in the name of inclusion.

She accepted that the disability movement has been divided on whether to support the closures, but she said:

What we need is a dialogue. This is us putting an alternative view forward which hopefully will get a debate going. That’s what we need. Read more

Letter to the Guardian

The publication of a letter against Remploy closures was published in both on-online and print versions of the Guardian on May 10. The letter was composed by Inclusion London, DPAC and unions. Many DPOs and disabled people signed in support of the Remploy workers. The letter was shortened and some names and DPOs were reduced due to space restrictions by the Guardian. This link  will take you to the letter with a link to the original letter’s wording. DPAC will be updating the names and DPOs that were left off the printed and online versions shortly. We asked Liz Sayce to comment, but she did not respond.

However, a response article to the letter was issued by DPO Breakthrough UK claiming that while they agreed with many aspects of our letter they could not join other DPOs in signing it and wanted to open up debate on the Remploy issue.

We agree with opening the debate, and provide a link to the thoughtful piece by disabled activist and comedian Laurence Clark published in the Independent: Remploy Closures: right in theory but where does it leave disabled employees?

Sean McGovern a former Remploy factory worker responded directly to the Breakthrough article

and Les Woodward a GMB convener and worker at the Swansea Remploy factory said of the Breakthrough article:

This article, unfortunately is typical of the “Politically Correct” brigades attitude to Supported Employment and the language they use to try and justify their positions…

Another unfortunate slant of this article is that it totally fails to take into account the effect on the workers themselves or indeed other disabled workers who given the present economic climate would give their eye teeth for a job any job. They would sell their soul for a job in Remploy that can provide skilled work, training and other support that employment in Remploy offers.

 I have said it many times and I will say it a lot more. No-one ever forced a gun to my head to work in Remploy, over the 28 years I have been employed by the Company, I have been free to leave at any time I wanted, just like any other worker in any other workplace.

 Of course whether or not I exercise that choice to leave is dependant not least on economic circumstances that I have found myself in and whether or not the alternative employment was viable in terms of remuneration or terms and conditions. No employment opportunities that can match those that I am on in Remploy have presented themselves as yet.

 No one would disagree with the aspirations of a fully inclusive society, and I for one would absolutely love to see the day when Remploy really was old fashioned and there would be no need for Remploy because we would have a fully inclusive society that caters for everyone. Unfortunately we live in a rather different world which is going further and further away from inclusion and equality of opportunity over the last 18 months or so rather than moving more towards inclusion and equal opportunity. The reason for this is that we are now governed by the rich for the rich and of the rich, while we get poorer and poorer.

 The ultimate shame in all this is that organisations such as the one who authored this article are wittingly or unwittingly collaborating with this Government in implementing cuts in the living standards of some of the very people they purport to support.

 Thanks a million to everyone that signed the letter, we really appreciate it and appreciate the support that you give us.

 Les

 We will provide more responses soon….

Previous pieces from DPAC and others

DPAC has always been transparent in its connections, actions and thoughts on the Remploy closures, which have been published on the DPAC web site, some of which we list here. We also include pieces by other groups

Remploy Closures: no segregated employment translates to unemployment for up to 2000 workers

DPAC Remploy Workers meeting London March 20th

Right to Work Pledges Support for Remploy workers

London meeting unites resistance to Remploy Closures

Furious workers hit out at Boss whose report led to Remploy factories getting the Axe

Demo for Remploy workers April 20th

Independent: Betrayed Disabled Workers protest against Remploy Closures

Fight the Remploy Closures

Remploy Public Meeting Thursday 26th April

Government accused of Hijacking Disability Equality Language to Justify Remploy Closures

The closure of Remploy factories is about cuts and cannot be justified by a misguided language of inclusion in a time when disabled people are facing the worse attacks on their inclusion, human rights and equality in UK history. Disabled people and DPOs need to support the Remploy workers rather than engaging in forms of ideological bullying that refuse to take into account the impacts on disabled peoples’ lives. Nor should they be so arrogant as to suggest that these workers shouldn’t have choice in where they chose to work. Less than 5% of Remploy workers in the last set of closures found alternative jobs, with some committing suicide-is this really something that we want to support for up to 2000 more disabled people under a flimsy Tory rhetoric of inclusion?

 

Jun 052012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

JUBILEE: It has been exposed that the Queen’s Jubilee was staffed by
security and stewarding staff on workfare in the worst imaginable
conditions: https://www.boycottworkfare.org/?p=1039

You might like to write to the CEO of the security firm involved and
circulate the email address here: molly@close-protectionuk.com

ARGOS: We’ve also heard from someone made to work at Argos without pay
that his store was taking workfare on a massive scale. Read his story
here: https://www.boycottworkfare.org/?p=1049

And join the people giving Argos a really hard time on their Facebook
page: https://www.facebook.com/argos

IT WORKS! Last week we exposed Body Shop as profiting from workfare and by
the end of the week they had pulled out!
https://www.boycottworkfare.org/?p=1025

Help uncover more workfare exploiters on your high street! Top tips here:
https://www.boycottworkfare.org/?p=1017

GROWING A UK-WIDE NETWORK: On Saturday 26th May, Brighton Benefits
Campaign hosted a meeting to bring together all those actively fighting
workfare. Lots of action plans came out of the day including:

A regular online forum for groups and individuals to share ideas and
co-ordinate. The first meeting is this Thursday 7th June at 7.30pm on
Skype. Download instructions for how to take part here:
https://www.boycottworkfare.org/wp-content/uploads/2012/06/Setting-up-a-Skype-account.doc

A week of action on 7-14 July kicking off with a day of action against
Holland & Barrett. More to follow as plans develop but put the date in
your diary!

ALSO COMING UP THIS WEEK:

* Combat Workfare action in Liverpool this Saturday 9th June, 12.30pm:
https://www.facebook.com/events/241340275974402/

* Come along to the London Boycott Workfare meeting on Wednesday, 7pm, 11
Goodwin St, Finsbury Park, N4 3HQ.

Our campaign is growing and gaining support – congratulations everyone!

Boycott Workfare

P.S. Don’t forget you’re welcome to take part in the UK-wide skype
discussion this Thursday evening. It’s easy to set up skype if you don’t
already have it. Details here:
https://www.boycottworkfare.org/wp-content/uploads/2012/06/Setting-up-a-Skype-account.doc

Care Quality Commission lie about their competence

 All Posts, Disability Rights, Social Model  Comments Off on Care Quality Commission lie about their competence
May 312012
 

With thanks to https://www.kingqueen.org.uk/archives/70

For letting us repost- pop over for some more brilliant stuff!

The Care Quality Commission (CQC) has come in for somewhat of a bashing recently. But I didn’t think they would lie as well.

In response to a recent documentary exposing care home abuse, CQC said the following in their media statement:

CQC carries out an unannounced inspection of every care and nursing home in England every year – more often if we believe people may be at risk. This system of regulation can and does identify poor care which CQC then takes action to tackle.

What?!

A quick look at the five care homes I’d stayed in in the last year revealed last inspection dates as follows:

  • Summer 2010 (in response to a specific incident, last “proper” inspection November 2007)
  • January 2009
  • November 2009
  • February 2011 (in response to specific allegations)
  • December 2009

Not one was inspected in the past 12 months. 0%.

Personal experience with looking for care homes for a relative confirmed the impression that most care homes have gone well beyond 12 months without an inspection.

I smelled a rat. So I asked CQC how many homes it had indeed inspected. The response came. Answering a slightly different question, CQC admit they did 13,082 inspections of care homes over the last 12 months. There are 17,756 care homes. So at least 26% of homes didn’t get inspected. I say “at least” as where CQC identifes problems at a care home they conduct more than one inspection. (hence why I think their FoI response is disingenuous.)

Let’s look at these once again.

  • “CQC carries out an unannounced inspection of every care and nursing home in England every year – more often if we believe people may be at risk.”
  • Of the 17,756 English care homes, CQC did 13,082 inspections over the last 12 months.

Is it me, or do the figures not add up?

Where did this come from?

The sad thing is we always knew CQC would be an appalling, incompetent mashup.

It was formed from a merger of the Healthcare Commission, the Commission for Social Care Inspection (CSCI) and the Mental Health Act Commission a couple of years ago. Having worked with CSCI, who were at least trying to do things right, me and other service users raised the concern that it would follow the sad precedent of the subjugation of disabled people’s rights following the Disability Rights Commission being subsumed into the Equality and Human Rights Commission. Sadly, we were right. Our concerns that social care would always be lower priority than healthcare were realised.

It didn’t help that the new body was given new, overarching registration standards. These same standards applied to all bodies registered – from acute hospitals, to dentists and care homes. The result being the emphasis on residents rights was lost, and the regulations simply weren’t specific enough for the situation. We lost rights in the change.

Then CQC sacked 70% of its inspectors so that it could register dentists. They adopted what they acknowledge as light touch regulation. They ceased grading care homes, and largely stopped inspecting them. The majority of care home reviews became based on self-declaration by care home managers. Inspections became very rare. Now, precisely which poorly performing care homes would state this to the regulator do you think?

Abuse

All this came to a head during the very sad and distressing Panorama documentary of the systemic abuse of people with learning difficulties at Winterbourne View. CQC became a very public whipping boy, held accountable for a lot of what happened. Much criticism resulted, including a select committee and the PM criticisng CQC for reducing inspections. Many made a comparison with the seminal Silent Minority documentary exposing the “care” of people with learning difficulties in institutions in the early 1980s. (Documentary available to view online – very distressing too.)

Meanwhile, there’s been blood on the carpet and accusations of gagging orders on staff etc. CQC has become a toxic brand. It’s been desperately attempting to reinvent itself, so far (in my view) failing miserably.

Consequences

If it wasn’t so serious, this would be funny. The reality is, though, that people are suffering as a result of this disgusting shambles. Care home residents are some of the most vulnerable, most disadvantaged, most disempowered people in this country. Abuse is the norm, not the exception in my experience; it just varies in degree. Without an effective regulator, the thousands of people in care homes up and down the country suffer even more abuse, poor treatment, curtailment of life opportunities.

CQC are ineffective, stuffed up, an ineffective regulator who lie about themselves to try and stop the torrent of legitimate criticism aimed their way. They are beyond redemption and need replacing.

(With grateful thanks as always to the wonderful Crippen for his inciteful cartoon

 

 

May 272012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

While there always seems to be plenty of money for some from disability sadly, the trickle-down effect never seems to reach as far as disabled people themselves. We still seem to be being exploited as cash cows for others. Below tells how charities are exploiting disabled people through the evidence of a whistleblower from one of the charities.

 Scandal of charities that bully people off benefits

by Dave Sewell

Charities and voluntary organisations that claim to be helping vulnerable people are instead enforcing government plans to throw them off benefits, Socialist Worker can reveal.

Over 270 voluntary organisations signed up to the government’s Work Programme, which pays contractors to bully unemployed people off benefits.

Sometimes this involves “workfare” schemes—herding unemployed workers into mandatory unpaid work at supermarkets, fast food restaurants and even NHS hospitals (see below).

An “employment advisor” at one of the charities spoke to Socialist Worker anonymously about the practice. “It’s disgusting,” they said. “We get letters from people who are really ill asking why their benefits have been taken away.

“I remember one client with severe psychosis. He didn’t know what day of the week it was—but he was about to lose his benefits because he had missed his appointments.”

The charities claim they are providing a service to help vulnerable people into jobs. But the jobs simply aren’t there.

Last week St Mungo’s became the latest charity to pull out of the Work Programme. It hadn’t made the revenue it expected. And it failed to put a single homeless person into work.

“Charities signed up naively,” the advisor told Socialist Worker. “They thought—we already work with vulnerable people, so why shouldn’t we do the same for a contract?”

Factories

In practice this has meant charities turning into factories designed to process unemployed claimants. And if claimants can’t jump through the government’s impossible hoops, their benefits can be removed.

“There is so much pressure to get results—either by getting people into work, or by getting their benefits sanctioned,” the advisor said.

Around one in ten of those that the charity recommends to be stripped of their benefits are later found to have been sanctioned wrongly, the advisor added.

Their caseload includes people who are claiming Employment Support Allowance and are not obliged to seek jobs, as they are not considered fit for work.

But the advisors are not trained to tell them this. Nor are they trained to help claimants who miss appointments for health reasons—and then find they have lost their benefits as a result.

The voluntary organisations involved in the Work Programme are subcontractors of private sector training firm Seetec. They include charities that work with disabled people, homeless people, single parents, young people and ex-offenders.

But the Work Programme is in a mess over its use of contractors. One prominent firm, A4e, is so mired in fraud allegations that it has had to be axed from the scheme.

And last week the House of Commons’ Public Accounts Committee called for payments to Work Programme contractors to be frozen. The advisor welcomed this move, saying, “It’s an obscene system. Let’s hope it falls apart soon.”

Originally posted at https://www.socialistworker.co.uk/art.php?id=28575 nice pic of DPAC protesters there too blocking the road

 see also: https://johnnyvoid.wordpress.com/2012/02/18/shame-of-the-third-sector-how-charities-got-it-wrong-on-workfare/

https://johnnyvoid.wordpress.com/2012/05/28/workfare-isnt-working-so-grayling-plans-more-workfare-this-time-its-for-charity/

 According to DWP charities involved are set out in the following table by area: find your charity here-we’ve kindly highlighted the disability ones for you- let us know if we missed any-for full excell sheet email us at mail@dpac.net.uk

 Btw Disability Works UK includes SCOPE, Leonard Cheshire, Mind, MENCAP, Action for Blind People (or RNIB) Disability Works UK has a turnover value of £654.4 million and a surplus of £15.6 million Recession? What recession?

Work Programme Supply Chains

 
The information contained in the table below reflects updates and changes to the Work Programme supply chains and is correct as at 30 January 2012.
It is published in the interests of transparency. It is limited to those in supply chains delivering to prime providers as part of their tier 1 and 2 chains. Definitions of what these tiers incorporate vary from prime provider to prime provider. There are additional suppliers beyond these tiers who are largely to be called on to deliver one off, unique interventions in response to a particular participants needs and circumstances.
The Department for Work and Pensions fully anticipate that supply chains will be dynamic, with scope to flex and evolve to reflect change within the labour market and participant needs.
The Department intends to update this information at regular intervals dependant on time and resources available.
In addition to the Merlin standard, a robust process is in place for the Department to approve any supply chain changes and to ensure that the service on offer is not compromised or reduced.
 
 
 
 
 
 
 
 
 
   
Comparison between the August 2011 stock take and the January 2012 figures shows a small net increase in the overall number of organisations in the supply chains. Both the public and private sector shows slight increases, while the voluntary and community sector shows a small net decrease.
The table below illustrates these changes
 
 
 
 
   
Sector Number of organisations in the supply chain    
Private As at 30 January 2012 – 306 / As at 12 August 2011 – 295*  
Public As at 30 January 2012 – 137 / As at 12 August 2011 – 133*  
Voluntary or Community (VCS) As at 30 January 2012 – 412 / As at 12 August 2011 – 420*  
Totals As at 30 january 2012 – 855 / As at 12 August 2011 – 848*  
   
*Note  These figure have been amended due to organisations being incorrectly recorded in the earlier stock take, which has now been rectified. This included two strategic partners being listed as a tier 2 sub contractor when no contractual relationship was in place; one organisation being incorrectly categorised as voluntary sector when they were in fact from the private sector, and a voluntary sector organisation being recorded under two different names, thus decreasing the voluntary sector count and increasing the private sector.

East of England              
Papworth Trust              
Action for Blind People              
Royal Mencap Society               
East Midlands              
Disability Works (UK)              
Disability Alliance              
Action for Blind People               
Royal Mencap Society              
West London              
Acton for Blind People              
Hammersmith & Fulham MIND              
MENCAP              
Disability Works UK              
East London              
Disability Works UK              
Mencap              
North East              
Action for Blind People              
North West – Merseyside, Halton, Cumbria and Lancashire              
Disability Works UK              
Eden Mencap              
Action for Blind People              
Royal Mencap Society              
North West – Greater Manchester, Cheshire & Warrington              
Disability Information Bureau              
Action for Blind People              
Leonard Cheshire Disability              
RNIB              
Royal Mencap Society ( Mencap )              
Scotland              
Action for Blind People              
Scottish Association for Mental Health (SAMH)              
Scottish Mental Health Co-operative              
South East – Thames Valley and Hampshire and Isle of Wight              
Disability Works UK              
MENCAP              
South East – Surrey, Sussex and Kent              
Disability Works              
Action for Blind People              
Disability Works UK              
RNIB              
Royal Mencap Society ( Mencap )              
South West – Devon and Cornwall, Dorset and Somerset              
NIL              
South West – Gloucestershire, Wiltshire and West of England              
Shaw Trust               
Swindon Mind              
Action for Blind People              
Wales              
Action for Blind People ( RNIB )              
West Midlands – Birmingham, Solihull and Black Country              
Action for Blind People              
Disability Works UK              
Birmingham Disability Consortium              
West Midlands – Coventry and Warwickshire, Staffordshire and the Marches              
Mencap               
Shaw Trust              
West Yorkshire              
Action for Blind People              
South Yorkshire              
Disability Works UK              
Disability Works UK              
North East Yorkshire and the Humber              
Leonard Cheshire Disability              
RNIB              
Royal Mencap Society ( Mencap )              
The Mind Consortium              
               
 
 
 
 
   
May 252012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

 Deadline for signatures: 30th May 5pm-releasing to press day after

Posted on Social Welfare Union

 Dear Sir/Madam,

 We the undersigned are deeply angered and concerned with the way sick and disabled people are being portrayed by the press and wider media as well as the distinct lack of fair and accurate reporting in relation to disability benefits.

The use of defamatory language is being used in a totally irresponsible and callous manner by a steadily increasing number of newspapers and other media providers.

We believe that the press and the wider media are blatantly using this language as a means of labelling all disabled benefit claimants as ‘cheats’ and ‘scroungers’, yet most are genuine sick and disabled people who are in many instances unable to work and are asking for only the very basic levels of support.

Such support is in no way over generous as some newspapers are claiming with administrative error and miscalculations at 0.5%. In fact disability benefits like Disability Living Allowance have some of the lowest levels of fraud of all forms of social security benefits and it is estimated that billions remain unclaimed in benefits every year. A significant fact that news provider’s and even the coalition government are neglecting to inform the public.

We also believe that whilst many claimants are now being found fit for work through the use of new assessment processes, most often the press and wider media are shirking in their responsibility to report from both sides and about the large number of sick and disabled people who are being wrongfully found fit for work and who are later having those decisions overturned in their favour by a social security tribunal. They also fail to report on people found ‘fit for work’ by Atos Healthcare, the private health firm contracted to carry out work capability assessments on behalf of the Department for Work and Pensions. Those people then find that they cannot claim Job Seekers Allowance (JSA) because they are ‘unfit for work’ as deemed by the JSA qualifying criteria. These people often have to rely upon handouts and food parcels and become lost statistics unseen by the public.

The signatories of this letter are greatly concerned that the way the press and wider media are portraying sick and disabled people will continue to fuel a growing hatred and discrimination, adding to increasing reports of hate crime towards disabled people and the potential for suicides already being reported by some news providers.

Whilst we support the democratic idea of a free and open press we feel that they have a moral and social duty. We ask that they refrain from the use of language and/or defamatory terms which is fuelling the growing and unjust public hate and disdain of sick and disabled people and benefit claimants. We also ask that they honour and obligate to report all stories related to disability and disability benefits in a manner that best informs their readers and viewers which is balanced, accurate and fair.

To add your signatures go to: Social Welfare Union

May 232012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

DPAC are delighted to hear this news which is a further important condemnation of the WCA carried out by ATOS. Together with other allies we will be continuing our fight against these assessments which are leading to thousands of deaths of disabled people.

The United Kingdom Local Medical Committees Conference of the British Medical Association has voted today to carry the following motion:

22nd May 2012 12.10 pm

103 HAMPSHIRE AND ISLE OF WIGHT & 103a SCOTTISH CONFERENCE OF LMCs

That conference, in respect of work capability assessments (WCA) as performed by ATOS Healthcare, believes that the:

(i) inadequate computer based assessments that are used have little regard to the nature or complexity of the needs of long term sick and disabled persons

(ii) WCA should end with immediate effect and be replaced with a rigorous and safe system that does not cause avoidable harm to some of the weakest and most vulnerable in society.

The motion was carried UNANIMOUSLY

The motion originated with Black Triangle’s Dr. Stephen Carty who put it forward to the Lothian Local Medical Committee who then put it to the Scottish LMCs Conference inClydebanktwo months ago where it was carried (almost) unanimously. It was then put forward to today’s UK LMCs Conference inLiverpoolboth by the Scottish Conference and Hampshire & Isle of Wight LMC. It was voted on by GPs representing all the LMCs in theUnited Kingdomand carried unanimously. The voice ofBritain’s doctors has spoken. It is time to end the DWP/AtoS Work Capability Assessment régime “with immediate effect” Black Triangle

 

 Posted by at 13:26
May 192012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

An application has been made by members of the Mental Health Resistance Network for permission to have a Judicial Review of the Work Capability Assessment (WCA) and a judge has decided that there should be a hearing to decide whether to grant us the Judicial Review.

The hearing will happen at the Royal Courts of Justice in the Strand in London on Friday 29th June. We won’t know until the day before what time it will be heard. 

With thanks to MHRN for letting us publicise this. It is MHRN who have pushed this through, not any big charity -remember most activism is coming from grassroots groups-rather than well funded charities who like to try to claim the credit.

Lets support MHRN as much as we can with this great achievement on 29th June-hopefully the first of many challenges to the corrupt WCA…..

 

 

May 162012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

July 7th to 14th – at sites across London
Applications due Monday, June 11th

If you are aged 16 – 30 and see injustice, pollution, racism, poverty in your community and want support in how to effectively tackle these issues, or know someone who is, then read on! ‘So We Stand’ Summer School is an intensive 1-week introduction to community organizing and social change.

The School exists to harness our anger at economic, environmental, racial and social oppression. The School exists to catalyse self-organisation + self-mobilisation into building strength in our communities to defend and confront oppression over the coming years. The School is chiefly dedicated to building the skills of young women, young people of colour, working class people, and queer people and those with different mental and physical abilities as the next generation of leaders in the social justice movement. Limited places welcome to people all across the UK – please email sowestand@gmail.com for an application form ASAP.

The School aspires to turn marginalisation and isolation into politically powerful support systems, ideas for actions and long term strategic organising. We will be challenged with new ways of thinking, provocative speakers, inspiring mentors and fascinating guests with a deep understanding of engaging with the head, heart and hand. Youth affected by economic inequality understand oppression because it is daily life – you don’t need to read it in a textbook. The School exists to harness our anger at oppression and turn our anger into political organising against it. The School exists to encourage self-determination and self-mobilisation into building positive communities who can defend and confront oppression over the coming years. We’re looking for advice or involvement in any of those areas. Join us for a week of experiences and ideas, and help us change things.

SWS provides a transformative framework to develop your organising skills, methods for empowerment and political education. SWS Summer School is organised around 3 pillars:

1. COMMUNITY ORGANISING + EMPOWERMENT LEARNING – to deepen the context of power and resistance in the UK. The educational tools will strengthen knowledge for our community based projects work within working class communities and communities of colour, fighting alongside people for their rights along with examples for global fights for hands on, effective community power. We shall look into how to turn marginalisation and isolation into politically powerful support systems, ideas for actions and long term strategic visions. Participants will be challenged with new ways of thinking, provocative speakers, inspiring mentors and fascinating guests from a range of communities facing injustice. Together, we will develop ideas for hands-on, effective, community projects.

2. EMPOWERMENT ORGANISING MENTORS –  to build long-term relationships with those who participate, through mentoring with activist elders, peer support, more frequent workshops and through participation in events within the local community, at youth centres and social nights to deepen the practice of critical community organising. The mentor programme will continue relationship building between front-line activists and supporters to deepen transformative possibilities for greater positive change and strategic visioning for movement building today.

3. SKILLS TRAINING – to learn the tools to build power and excitement in your community to tackle injustice. The trainings will be a building block to deepen within your organising internships. You will develop skills such as popular education, storytelling, building connections across cultures, radical education, direct action, monitoring police brutality, reclaiming space, spoken word and creating conscious music, anti-oppression organising, anti-racist and environmental justice training.

SWS Summer School is ideally a week-long full-time commitment. You’ll spend at least 25 hours in the week in our political education + skills training sessions. SWS intends to provide practical support you may need and expenses will be covered. Everyone involved in the School – organisers, volunteers, attendees, speakers and facilitators –  are active participants and will build the curriculum to sort all our needs.

In the meantime we need mass involvement to enable the School to reach its full power. If you have a little or a lot of time and want to gain experience in organising empowering and action orientated education programmes for our people on the frontline of injustice then please simply email sowestand@gmail.com or call 0044 (0) 7514326539. If you have further questions about SWS Summer School into social justice and community organising, please get in contact ASAP.

So We Stand – stand shoulder to shoulder with communities on the front-lines of social, racial and environmental injustice.
 

By dan glass
15th May 2012

 reposted from: https://www.campaigncentral.org.uk/opinion/so-we-stand-summer-activism-school-introduction-community-organising-and-social-change-2012

May 132012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

DPAC UNIVERSAL CREDIT CAMPAIGN

 

www.dpac.uk.net

 

Universal Credit: What it means

The coalition government and New Labour before them agreed that a reform to the current benefits system was long overdue. In November 2010 the Coalition published a white paper on Universal Credit. It is claimed to be the biggest overhaul of the benefits system since the 1940s when what was known as the welfare state began.

The Government White Paper, ‘Universal Credit: welfare that works’ was published on 11 November 2010 laying out the first steps of the overhaul of the welfare process. The Welfare reform Bill through which this will be introduced was forcibly passed through the Commons and Lords earlier this year by the Coalition government.

This paper deals with Universal Credit. It examines what it means, what it may mean for disabled people and what the key changes will be.

What is Universal Credit?

The coalition notes that there are over 30 different social payments or benefit systems in place. They think this is confusing and too complex for people to understand. They believe that by combining social payments/benefits into one universal payment things will be easier and better for people. Universal credit is intended to be a new benefit which will replace:

  • child tax credit
  • housing benefit
  • income related employment and support allowance
  • income based jobseekers allowance
  • income support
  • social fund budgeting loans
  • working tax credit

Universal credit is a proposed system that will see many social payments or benefits merged into one single payment. The coalition claims that nobody will be worse off under this system. However, the rhetoric of a fairer system is coached in terms of welfare dependency which suggests that this strategy main aim is to reduce welfare spending.

The white paper begins by saying:

The Government is committed to reforming the welfare system to make it fairer, more affordable and to tackle poverty and welfare dependency, whilst continuing to support the most vulnerable in society

The scheme is estimated to cost 2 million to set up. First steps towards the coalition’s vision included strategies introduced in the budget and spending review of 2010. These included:

  • capping household benefit payments so that families do not receive more in welfare than median after-tax earnings for working households;
  • withdrawing Child Benefit from families with a higher rate taxpayer;
  • measures to control the cost of Tax Credits, Housing Benefit and Council Tax Benefit; and
  • time-limiting contributory Employment and Support Allowance for those in the Work Related Activity Group.

The capping of housing benefit payments is likely to hit disabled people particularly hard at a time of rent increases in social housing and the private rented sector.

Whilst withdrawing child benefit from families with a higher rate tax payer may suggest making things fairer, it actually undermines the principle of universality in built into child benefit to ensure that it was not means tested but a benefit to aid mothers bringing up children. The removal of higher rate tax payers is in effect removing that safeguard and the first step towards to means testing.

Employment and Support Allowance (ESA) replaces incapacity benefit for all disabled people from 2014. Those in the work related activity group are deemed to be ‘fit for work’ and will have their benefit limited to 12 months retrospectively from the date of the comprehensive spending review or the award if the award was made after the 20 October 2010. There are other categories of the Employment and Support Allowance such as the support group, these will be unaffected by the time –limits. Those in the work related group will be expected to sign up for job seekers allowance a lower amount compared to ESA.

At the time of the White paper Universal credit did not include:

  • bereavement benefits
  • contributory jobseeker’s allowance
  • contributory employment and support allowance
  • disability living allowance
  • child benefit
  • industrial injuries disablement benefit
  • maternity allowance
  • statutory maternity pay
  • statutory sick pay
  • pension credit

However, since this time clear proposals to abolish Disability Living Allowance (DLA) and replace it with Personal Independence Payment (PIP) have been put forward with the reasoning that 20% needs to be cut from the case loads of DLA.

The paper says universal credit ‘will consist of a basic personal amount’ with additional amounts for ‘disability, caring responsibilities, housing costs, and children’.

When will Universal credit begin?

The white paper stated that universal credit would be rolled out in October 2013. Pilots are due to begin in May 2013.

Claiming and accessibility

Claims are set to be made online and on the basis of households, rather than individuals

Claims will be made on the basis of households rather than individuals and both members of a couple will be required to claim Universal Credit. Claims for Universal Credit will normally be made through the internet and we expect that most subsequent contact between recipients and the delivery agency will also be conducted online. People will be able to obtain all elements of Universal Credit through a single application, ending the excessive form filling of the current system, reducing scope for error and reducing administration costs p.25

Two issues arise for disabled people; the first is that claims made on behalf of a household will exacerbate some disabled peoples’ feelings of dependence as opposed to independence and independent living. The second is that access to computers and to the internet is known to be lower for disabled people and those with lower incomes. Although the paper mentions ‘ These changes will enable the targeting of resources to support vulnerable people with additional needs’ (p.25) which we assume is disabled people, no further method of the method or how this will be achieved is given.

Payment Periods

The paper states that the coalition is considering both payment and assessments on a monthly basis. This would seem to suggest that entitlement will need to be re-registered and hence re- assessed on a monthly basis.

Critiques of universal credit

The coalition claim that nobody will be worse off under the new universal credit, however current proposed changes suggest that this may not be the case for disabled people or others on low incomes. Universal credit appears to be focused on getting people into work and away from benefits. It is laudable that the coalition accept that some people may be worse off in work than on benefits and are attempting to adjust the discrepancy.

At the same time as assessment s for ESA have come under constant and increasing criticism for being unfair[i] it is unlikely that disabled people declared as ‘fit for work’ under the Work Capability Assessment will benefit from this change. The WCA shows that ‘target driven’ simplified tests do not work. It is likely to be the same with one single benefit system –how will this be able to address the complexities of different impairments, multiple impairments, and the multitude of disabling barriers that disabled people face?

Sanctions

In addition, the universal credit and welfare reform will bring in ‘a commitment’ for those who fail to ‘apply themselves’ to proper work seeking activities to tougher sanctions. Once again this will not address the complexity of employment related barriers that disabled people face, even if they really are ‘fit for work’.

Page 21 of the white paper states:

We will require every Income Support, Jobseeker’s Allowance and Employment and Support Allowance recipient to have a claimant commitment. The commitment will set out our general expectations of recipients, and the requirements placed upon them; it will also be clear about the consequences for the recipient of failing to meet these agreed standards. This will be carried forward into Universal Credit.

 

 

DPAC say that Disabled People and Disabled Children should not be penalised in this way when £25 billion in unclaimed taxes remains uncollected, bankers continue to receive massive bonuses, and MPs spend £40,000 for trees in Portcullis House plus thousands more for their personal expenses.

 

Summary of key points of the bill

  • The introduction of a Universal Credit to replace existing means-tested benefits and tax credits for people of working age from 2013.

 

  • The introduction of Personal Independence Payments to replace Disability Living Allowance with a stated aim of reducing the number of claimants by 20% and replacing the current 3 bands of the care component with only 2. Half a million disabled people will lose their entitlement to DLA which in many cases is what allows them to work.

 

  • At the moment anyone getting the mobility component of DLA before the age of 65 continues to receive it once they reach 65 but with PIP proposals they will not be able to continue to claim PIP once they reach 65 and there is no mobility component of Attendance Allowance.

 

  • Limiting of contribution based Employment and Support Allowance payments to 12 months for those in the Work Related Activity Group. This is what people think they are paying National Insurance contributions to be entitled to if they need it.  100,000 people will lose out at the beginning of April 2013 and another 100,000 will lose out  the following April after 12 months on the benefit.

 

  • Removal of ESA entitlement from young disabled people under 25 years of age. Non-disabled young adults are treated as such from the age of 18 yet you will no longer be treated as an individual adult if you are disabled. At the same time Income Support is being abolished as well so it remains unclear what if any money younger disabled people will be entitled to.

 

  • Caps on the total amount of benefit any claimant can get, for both housing needs and living expenses. The suggested total amount is £350 for a single person and £500 per week regardless of family size, or costs of housing. This will particularly affect those living in areas such as London where rents are higher than average. Currently 7 out of 8 people who get Housing Benefit are in low paid jobs, so having a living wage might well reduce the overall benefit bill more effectively than demonising benefit claimants further.

 

  • Much has been made of the figure of £26,000 as the maximum annual cap but the vast majority of claimants will in fact get far less then £26,000. Only 1% of claimants will be affected by this cap level but that will still be 67,000 families. In Brent alone 3,300 families are due to lose benefits because of the cap. Social cleansing of poor families has already started in boroughs like Westminster.

 

  • Half of all household affected by the cap on benefits has a disabled person living in them. Moving is often not an option as care packages are not transportable across local authority boundaries, and continuity of other services is often essential.

 

  • Social housing tenants with a spare bedroom will no longer get funding for the extra room. Most will lose £12 a week. The National Housing Federation estimate 180,000 social tenants are underoccupying 2 bedroom homes but there were only 68,000 1 bed social homes to rent in 2009-2010. Even the DWP EIA said there were not enough 1 bedroom properties.

 

  • This is unlikely to reduce housing costs as a couple with one child having to move from a 3 bed social house in Crawley and rent a smaller property in the private sector would be able to get £66 a week more in Housing Benefit.

 

  • It will link Local Housing Allowance rates to CPI index, which excludes housing costs.

 

  • The resulting increase in homelessness will lead to local authorities paying out millions more in costs.

 

  • Not excluding child benefit from the cap levels will mean anyone having a child will not get any extra money to care for them. This will increase child poverty rates and child benefit for a first child is currently about £1,000 per year.

 

  • With the scrapping of Income support single parents with a child over 5 years of age must work or be available for work to receive Job Seekers Allowance.

 

  • The Severe Disability Premium currently part of Income Support will disappear and there are no details about what if anything will replace this. This amount makes up one-third of some severely disabled people’s incomes.

 

  • Claims will be made on the basis of households rather than individuals and both members of a couple will be required to claim Universal Credit. If couples have savings over £6,000 or one of them receives an income then the other will not be able to claim anything else.

 

  • As income support is being abolished carers entitled to benefits will be reduced to 40% of current claimants. Those carers who are also disabled will lose about half of their income as they will only be able to claim one Universal Credit premium either as a carer or a disabled person.

 

  • Removal of the Social Fund which has previously given grants to enable people to buy essential items or to allow women fleeing domestic violence to move. Some of this funding will now go to local authorities but will not be ring-fenced in any way.

 

  • Withdrawing Child Benefit from families with a higher rate taxpayer will affect many families adversely and takes women’s rights backwards.

 

  • Many families with disabled children will face a cut to the financial support they receive from tax credits. The new system will result in these children losing up to £1,400 per year The Government estimates that 100,000 disabled children would lose out under this change.

 

  • Changes to Tax Credits will also affect families caring for disabled children as claimants of these will need to work at least 24 hours rather then 16 hours per week so many families will lose tax credits.

 

  • To access the Child support Agency single parents will have to pay a fee reduced from a suggested £100 down to £20 plus 7-12% of any maintenance collected for them.

 

  • All claims are to be processed via the internet which is not accessible for many disabled people.

 

  • In addition, the universal credit and welfare reform will bring in ‘a commitment’ for those who fail to ‘apply themselves’ to proper work seeking activities to tougher sanctions. Once again this will not address the complexity of employment related barriers that disabled people face, even if they really are ‘fit for work’.

Sanctions proposed include:

  1. a.   Failure to meet a requirement to prepare for work (applicable to jobseekers and those in the Employment and Support Allowance Work-Related Activity Group) will lead to 100 per cent of payments ceasing until the recipient re-complies with requirements and for a fixed period after re-compliance (fixed period sanctions start at one week, rising to two, then four weeks with each subsequent failure to comply).

 

  1. b.   Failure to actively seek employment or be available for work will lead to payment ceasing for four weeks for a first failure and up to three months for a second.

 

  1. c.   The most serious failures that apply only to jobseekers will lead to Jobseeker’s Allowance payment ceasing for a fixed period of at least three months (longer for repeat offences). Actions that could trigger this level of penalty include failure to accept a reasonable job offer, failure to apply for a job or failure to attend unpaid Mandatory Work Activity.

 

  1. d.   Some types of recipient, such as lone parents with young children, are only required to attend work-focused interviews and their failure to attend is more often due to challenging circumstances than wilful evasion of the rules. However, financial sanctions where necessary will be applied.

 

 


 

May 132012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

 

 

DISABLED PEOPLE AGAINST CUTS

 

www.dpac.uk.net

 

HOUSING AND HOUSING BENEFITS- BRIEFING NOTES

 

The future prognosis for disabled people’s housing is grim

 

  • Already 30% of disabled people live below the poverty line and 1 in 4 families with disabled children can’t afford heating.

 

  • The Chartered Institute of Housing has calculated that the cumulative effects of the coalition’s proposals mean that by 2020 every tenants’ Housing Benefit will be too low to cover their rent.

 

Changes to Housing Benefits from April 2011

 

The size criteria will be adjusted to provide for an additional bedroom for a non-resident carer ( ie not a member of your family who shares your home) where a disabled customer has an established need for overnight care. This must be claimed for and will not be awarded automatically.

 

While this is a very small positive change it still totally fails to address the lack of an extra room for disabled children who need an extra bedroom, pensioner and other couples who need an extra room due to their medical needs, and a wide range of other disability related factors which mean disabled people need extra housing space including the need for space for dialysis, room to store equipment, room to use a wheelchair, ground-floor and level access accommodation. The recent DWP Select committee into LHA said that these factors were posing considerable barriers to independent living and should be addressed urgently but still have not been. In essence the overall proposed changes to LHA will simply increase these barriers.

 

From January 2012 – Under 35s

 

Any single  person under 35 years of age renting in the private rented sector who is disabled but not in receipt of middle or higher rate DLA care component will not be able to claim for more than a shared room rate. As DLA is now being scrapped we currently have no idea of the full impact of these 2 changes together.

 

The difference between the LHA for a one-bed property and single room rate is almost 50% and inEdinburghthe one bed rate is £114.23 per week compared to £66.92 per week. It is generally agreed that there are not enough houses in multiple occupancy for everyone who needs to move to be able to do so. ssac’s own report estimated this move alone to change Housing Benefit could lead to 11,000 people becoming homeless.

 

Disabled people who are most likely to be disproportionately affected by these changes are those who most need to live in peaceful surroundings such as those with Mental Health and Neuro-Diverse impairments.

 

From October 2011

 

The Local Housing Allowance has been set at the 30th percentile rent in each Broad Market Rental Area, rather then the 50th percentile as before. Disabled people will only be able to afford to rent in the cheapest properties in an area, which are more than likely to be inaccessible.

 

This will also increase the difficulties disabled people face in finding suitable accommodation to live independently , increase homelessness amongst disabled people and push disabled people further into poverty especially if DLA recipients are cut by half a million as planned by DWP.

 

The proposed changes to the 30th percentile, rather then the median, rent being used to calculate LHA from October 2011 will only make these matters worse than they already are and will constitute serious breaches of UNCRPD particularly article 28, article 19,and article 7. New changes to our legislation should not be allowed to contravene these convention rights.

 

Longer term reforms

 

These required primary legislation

 

from 2013-14 Local Housing Allowance and Housing Benefit rates will be upgraded in line with CPI ( Consumer Price Index)  rather than on the basis of local rents. CPI does not include any account being taken of housing costs so this will result in the amount of money people can get to help pay their rents being even lower. At the same time this will apply to increases in other benefit rates and an estimate I have seen is that disabled people will be £300 per year worse off because of this.

 

Social Rented Sector

There are plans to remove any security of tenure from social housing tenants and to increase rents to 80% of market values. Together with the caps on Housing Benefits this will make renting in the social housing sector unaffordable in many higher priced areas  of the country.

 

The Bedroom Tax

From 2013 housing benefit for working age social rented sector customers will be restricted for those who are occupying a larger property than their household size would warrant. This is something that the Labour government and DWP tried to introduce in Welfare Reform bill 2007 but were forced to drop by pressure from Housing Associations. It means that if you are living in an adapted property which may have cost thousands of pounds to adapt then if you also have an extra bedroom you have no apparent need for you will only get HB paid at the one bedroom rate.

 

Evicting disabled people from adapted properties when there are few other accessible and adapted ones available seems an act of lunacy and an unnecessary expense to taxpayers as well as causing untold misery to disabled people who will be affected by all of this.

 

Social housing tenants who no longer get funding for an extra room will mostly lose £12 a week. The National Housing Federation estimate 180,000 social tenants are underoccupying 2 bedroom homes but there were only 68,000 1 bed social homes to rent in 2009-2010. Even the DWP EIA said there were not enough 1 bedroom properties.

 

This is unlikely to reduce housing costs as a couple with one child having to move from a 3 bed social house in Crawley and rent a smaller property in the private sector would be able to get £66 a week more in Housing Benefit.

 

Discretionary Housing Payments

 

Recognising the chaos their HB reforms are going to make the sum allocated by government has increased by £10 million in 2011 and by £40 million in 2012. This will apparently give more flexibility to local authorities but DHPs are not supposed to cover long term housing costs and have to be applied for every 13 weeks. There is no right of appeal if they are refused although you can seek a Judicial Review.Leicesterfor example has now introduced a policy where they will only pay for a maximum of 13 weeks during which time disabled people getting a DHP are harrassed to move to a cheaper property, regardless of their independent living needs.

 

Less important changes for disabled people who live outside ofLondon, but disastrous for anyone living inLondonor other high priced areas of the country. Planned introduction postponed until 2012.

 

Local Housing Allowance levels have been restricted to the 4 bedroom rate. The 5 bedroom rate has been scrapped.

 

Caps have been introduced which are

 

A new upper limit will be introduced

£250 a week for a one bedroom property

£290 a week for a 2 bedroom property

£340 a week for a 3 bedroom property

£420 a week for a 4 bedroom property

 

According to government figures about 3-3,500 disabled people rent privately in centralLondon. DPOs in London however have raised concerns that as the centre of London becomes unaffordable to most disabled people then there will be additional pressures on local councils for example in Brent where there is already a 10 year waiting list for re-housing as more people are forced to move.

 

Half of all household affected by the cap on benefits has a disabled person living in them. Moving is often not an option as care packages are not transportable across local authority boundaries, and continuity of other services is often essential.

 

Universal credit will introduce caps on the total amount of benefit any claimant can get, for both housing needs and living expenses. The suggested total amount is £350 for a single person and £500 per week regardless of family size, or costs of housing. This will particularly affect those living in areas such asLondonwhere rents are higher than average. Currently 7 out of 8 people who get Housing Benefit are in low paid jobs, so having a living wage might well reduce the overall benefit bill more effectively than demonising benefit claimants further.

 

Much has been made of the figure of £26,000 as the maximum annual cap but the vast majority of claimants will in fact get far less then £26,000. Only 1% of claimants will be affected by this cap level but that will still be 67,000 families. In Brent alone 3,300 families are due to lose benefits because of the cap. Social cleansing of poor families has already started in boroughs likeWestminster.

 

Mortgage Interest changes

Changes to the amounts paid to mortgage interest for disabled claimants have been estimated to potentially lead to an additional 64,000 disabled people becoming homeless.

 

Cumulative Impact

The resulting increase in homelessness will lead to local authorities paying out millions more in costs.

May 132012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

 

Employment and Support Allowance (ESA) is the benefit which is replacing Incapacity Benefit. ATOS healthcare are currently making £100 million a year processing both new claims and re-assessing those who are in receipt of Incapacity Benefit.

There are 2 types of ESA, one contributory ESA which disabled people are entitled to based on having paid National Insurance contributions and Income based ESA which is awarded to those on low incomes who are not in a partnership.

People claiming IB plus new claimants have to undergo a WCA (Work Capability Assessment) to claim ESA. There are 3 things that can happen from WCA

  • People can be found fit for work and have to claim JSA and register or work and meet lots of requirements about looking for work. If they don’t or they are late for appointments etc they are likely to have their benefits sanctioned ie stopped for 13-26 weeks. (This means that they only get an emergency payment of  £30 pw to live on plus Housing and Council Tax benefit stop being paid automatically and if they don’t know that and don’t make  new claim can end up with rent and CTB arrears.)

 

  • Second group of people get put in WRAG group ( Work Related Activity Group)

that is they get ESA( a lower rate) but this entitlement to Contribution based ESA for those placed in the WRAG has now been limited to 12 months and 700,000 claimants will be affected by this cut.

Disabled people in the WRAG have to jump through lots of hoops and make themselves work ready. Again if they don’t sanctions/ reduction of benefits will apply.

  • Third group is the support group- those  disabled  people who are considered unable to work due to their level of functional impairments.

 Overall the Coalition plan to remove 1 million disabled people from being able to claim ESA and declare them fit for work and force them to claim JSA (Job Seekers Allowance instead) Financially this is a loss of about £30 a week, but as well as losing entitlement to Incapacity Benefit many are also losing entitlement to DLA ( both components so in total people may lose a further  minimum £34 a week from an income which is there to meet the extra costs of being disabled). 

WCA assessment has been criticised by CAB, many DPOs, disabled people, Cancer support groups, a GP

Paul Gregg who originally devised it but now says it isn’t working.

Basically measures physical functional ability so fails massively anyone with non-physical or fluctuating impairments. New WCA assessment is even worse then what was in place and eg someone with a visual impairment is likely to be found fit for work unless they need an actual person guiding them. Someone who has agoraphobia would be fit for work and the fact that they physically can’t get to a place of work is ignored.

Totally ignores any of the barriers disabled people face in the labour market i.e. attitudes, physical access, environmental access, the reduction in Access to Work funding.

At the moment 70% of those who fail the WCA with representation win at appeal and have benefit reinstated, 40% who don’t have representation win. Waiting time often up to 12 months due to backlog in Tribunal service.

Another problem is that if you win your appeal ATOS can just start all over again re-testing you which is what happened to one of our supporter’s uncles. When he got papers for 2nd tribunal hearing he killed himself as he couldn’t face going through it all again. ( he won 1st appeal then had to have a second WCA,  and  failed that again )

 

 

 

 

 

 

 

 

May 132012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

 

 

  Disabled people feel their lives are under threat and many of them are living in fear.

 

Data from Family Resources Survey and the National Equalities Panel Research (2010) found that:
· 75% of disabled women and 70% of disabled men are already at the bottom end of Britain ’s income distribution scale living in poverty.


· A tenth of disabled woman have disposable incomes below £31 per week and a tenth of disabled men have incomes below £59 per week including earned income and benefits.

 

· Already 30% of disabled people live below the poverty line and 1 in 4 families with disabled children cannot afford heating·

 

– The median level of total wealth for households headed by an employee is £217,500 compared to only £21,100 for households headed by someone who is sick or disabled.

 

– Under the coalition government’s austerity drive disabled people are set to lose at least £140 per month through direct cuts to disability benefits (initially devised to pay the extra costs of being disabled) alone.

 

  • Care and Support funding. Funding from the Independent Living Fund for care and support has now ceased to all new claimants and any additional needs cannot be met by them. From 2015 the ILF will cease to exist cutting £330 million from funding for care and support. For the 20,000 of the most severely disabled people this is a total betrayal by the coalition government and will prevent independent living.

 

Social Services budgets are under extreme pressure and nearly all Social Services departments have been told to reduce their budgets by 25% which has an obvious knock-on effect to their provision of support and the amount people need to pay towards this. Local authorities all over the country are cutting the amount of care funding available, tightening eligibility criteria, and increasing charges for those who are still eligible for care. In Warwickshire it is anticipated that one-third of people who currently receive free care will no longer be eligible. InBirminghamthe council are trying to remove care from over 4,000 people and move to providing care to those deemed critical only.

 

In many local authorities charging for care services has rocketed. One woman has told us that although she has had free care for the last 7 years she is now paying over £50 a week for the same level of service. We also know that in Dudley and Warwickshire charges have risen steeply. Are there any other local government services that people have to pay for twice, once through council tax and again through charging policies?

 

 

  • The Coalition are scrapping Disability Living Allowance and replacing it with a new benefit Personal Independence Payments. An arbitrary figure of removing 20% of claimants from entitlement to PIP has been decided regardless of need. Many disabled people use this benefit to help make up the shortfall they have in paying their rent or for care costs.

 

  • The mobility component of DLA may no longer be removed from disabled people living in residential care homes who do not pay for their own fees. However many people who live in residential homes still face losing mobility funding due to the abolition of DLA.  This will leave many more residents with only £22 a week to pay for clothes, travel costs, outings, and basics such as toothpaste, soap, etc.

 

Many disabled people use this mobility component to pay for wheelchairs, mobility scooters and travel to meet friends and family. Losing DLA will leave disabled residents effectively trapped in these homes, and denied any right to a family life.

 

 

  • Other Benefits Employment and Support Allowance (ESA)  and work capability assessments (WCAs) have been criticised by CAB, disability charities and Disabled People’s Organisations. Even people with terminal cancer have been declared fit for work and removed from Incapacity Benefit. The government have now said that from October 2010 they will speed up the re-assessment of everyone currently claiming Incapacity Benefit so that 10,000 claimants a week are ‘processed. Their overall aim in this is to remove a 1 million disabled people from higher paying Incapacity Benefit onto lower paying Job Seekers Allowance.

 

  • These assessments which ignore GP and consultant views are earning Atos healthcare £100 million a year.

 

  • Contribution based ESA has now been time-limited to 12 months and this will remove 700,000 from receipt of this benefit for any longer than that even though people may have paid National Insurance contributions for years.

 

  • At the same time as the government claim they want to help disabled people back into work they have slashed Access to Work funding which meets the costs to employers of any reasonable adjustments needed in a workplace. Yet only 20% of people with Autism and 25% of those with a mental health condition are in employment. They are not workshy, but excluded by physical and attitudinal barriers.

From Guardian letters page June 3rd 2011. Letter from Claire Debenham, Brighton

The government says it is committed to a ‘fair and accurate’ work capability assessment. The distress and injustice caused by this new system needs to be publcised far and wide.

My brother died last week of kidney cancer. He was disgnosed a year ago and at Christmas was told he had about four months to live.In the spring he was summoned for a work capability assessment (by this time he had two brain tumours) and found fit for work. In addition to everything else, he bacame anxious about losing the small amount of money he was living on. He was aked to go in to the job centre for an interview but was too ill at the time. On May 19th he received a letter from Jobcentre plus telling him he was to be trested a shaving limited capability for work. The medical officer overseeing his case had advised that “death within six months is unlikely to occur due to the client’s cancer” and there would be no “sunstantial risk to his mental or physical wellbeing if he were found capable of work-related activity.”

He died six days later, having been unable to get out of bed for ffour weeks. What work were they suggesting he wa scapable of? He asked:”What have I paid tax and national insurance for if not help to pay the bills and feed me at ateim like this?”

 

  • Changes to Housing and Housing Benefits

 

These changes will affect everyone living on a low income who rents either in the social housing or private rented sectors. The majority of people who get Housing Benefit and Council Tax benefit are in work.

 

There are 1.8 million households on social housing waiting lists. Last year in Birmingham there were almost 19,000 applicants on the homeless person’s register. Last year in Leicester 500 people needed an accessible property and only one was available. Currently 1 million children live in overcrowded households, changes to social housing tenure and housing benefits will only increase these numbers.

 

  • The Chartered Institute of Housing has calculated that the cumulative effect of the coalition’s proposals mean that by 2020 every tenant’s Housing Benefit will be too low to cover their rent

 

There are plans to time limit people’s right to live in their social rented homes and it has been suggested that they will have to reapply every 2 years. If they have improved their lives by getting a higher income they may then be forced to move out of their homes. This will apply to new tenancies or if anyone moves to a smaller/ larger property. As well as removing the right to life-time tenancies it is proposed that rents in the social rented sector should rise to 80% of market value rents- a 30% increase in rent for most tenants. Together with the caps on Housing Benefits this will make renting in the social housing sector unaffordable in many higher priced areas of the country.

 

 

Local Housing Allowance, Housing Benefit for those renting in the private sector, will be reduced for the 2 million disabled people living in private rented accommodation. The Local Housing Allowance has now been set at the 30th percentile rent in each Broad Market Rental Area, rather then the 50th percentile as before. Disabled people will only be able to afford to rent in the cheapest properties in any area, which are more than likely to be inaccessible.

 

This change will also increase the difficulties disabled people face in finding suitable accommodation to live independently, and increase homelessness amongst disabled people. The caring Condems have said people will have to move to cheaper areas yet that may be impossible for disabled people as care packages are not transportable from one local authority to another. As each local authority has its own rules and regulations the care someone has in one area may not be the same as the care they can have if they move. It also means that disabled people will lose their trained Personal Assistants.

 

Disabled people with learning difficulties or those with visual impairments often need several years to be able to find their way around an area and need consistency in services like GPs, nursing services and so forth to be able to survive.

 

Due to the size criteria for LHA parents of disabled children are also unable to get an extra bedroom for a disabled child regardless of their needs as the number of bedrooms you can get benefit for is restricted simply by the age and gender of your children.

 

Already one in four homes in the social rented sector are inaccessible and often disabled people are unable to get into and out of their own homes.

 

  • Housing Benefit levels have now been capped and will be capped again under Universal Credit plans.

For families renting in the private rented sector Local Housing Allowance levels is now restricted to the 4 bedroom rate regardless of the size of your family. New upper limits will be introduced which are scarcely likely to cover rent levels in many parts of London and the South East. According to government figures about 3-3,500 disabled people rent privately in central London. DPOs in London however have raised concerns that as the centre of London becomes unaffordable to most disabled people then there will be additional pressures on local councils for example in Brent where there is already a 10 year waiting list for re-housing as more people are forced to move.

 

  • From 2013 housing benefit for working age social rented sector tenants will be restricted for those who are occupying a larger property than their household size would warrant. This is something that the Labour government and DWP tried to introduce in Welfare Reform bill 2007 but were forced to drop by pressure from Housing Associations. It means that if you are living in an adapted property which may have cost thousands of pounds to adapt then if you also have an extra bedroom you have no apparent need for you will only get HB paid at the one bedroom rate. I know 2 local disabled people who have 2 bedroom council flats – one who is blind and who needs to be able to live in a location and property that he knows well, and another who has had adaptations made to his flat who from 2013 will only get Housing Benefit for a one bedroom property which will either force them to move or push them into further poverty.

 

  • Under 35s

Anyone under 35 years of age who is disabled but not in receipt of middle or higher rate DLA care component will not be able to claim for more than a shared room rate if renting in the private rented sector. Yet these are exactly the same people who cannot get onto waiting lists for social housing so they have no choice other then to rent from private landlords. As DLA is now being scrapped we currently have no idea of the full impact of these 2 changes together. However for anyone with Autism or a mental health condition being forced to live in a multiple occupancy house can be very difficult. The difference in benefit payable for a one bedroom and shared room rate is an average of £47 per week  and it has been estimated by housing charities that there are 11,000 too few multiple occupancy properties so we had all better get used to seeing increasing numbers of young, homeless disabled people on our streets.

 

Discretionary Housing Payments

 

Recognising the chaos their HB reforms are going to make the sum allocated by government has increased by £10 million in 2011 and by £40 million in 2012. This will apparently give more flexibility to local authorities but DHPs are not supposed to cover long term housing costs and have to be applied for every 13 weeks. There is no right of appeal if they are refused although you can seek a Judicial Review. Leicester for example has now introduced a policy where they will only pay for a maximum of 13 weeks during which time disabled people getting a DHP are harassed to move to a cheaper property, regardless of their independent living needs.

 

  • Benefits will be linked to the Consumer Price Index (CPI) instead of the Retail Price Index, so claimants will lose £300 a year as the CPI ignores any housing costs you might have.
  • VAT increased to 20% will hit those on the lowest incomes the hardest – it is estimated this rise will increase each household’s costs by £500 per year

 

What disabled people say about these changes

.“I am in receipt of DLA, without which I could not survive. I have severe allergies, home bound, mostly bedridden.  I have carers, and have to pay for extra hours not subsidized by social services. My utility bills are extremely high, and I have to contribute to the rent, which is not met by housing benefits. I also suffer from malnutrition!! Being chronically ill is costly, being depending on carers for everything.
Cutting DLA would mean that I have to find housing within the Housing Allowance which is much, much lower than rental market. There are pockets of housing, in undesirable areas, with mould and cockroaches, and no amenities, no lift, or if on the ground floor, simply not safe.
I could go on and on, about the misery it would cause, to remove DLA.
It would lead to a slow death painful death. Worth adding here, I have spoken to many in my situation, who are discussing mass suicide, rather than suffer more health miseries, for which there are no cures! They are not depressed, but pragmatic about what awaits all.”

 

 

May 132012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

DISABLED PEOPLE AGAINST CUTS (DPAC)

www.dpac.uk.net

Briefing Notes DLA Abolition.

 

Background to the Abolition of Disability Living Allowance  

Disability Living Allowance was introduced in 1992 to provide support with the extra costs of living that disabled people face.

In the Budget (June 2010) and Comprehensive Spending Review (October 2010) the new Condem government announced its intention to arbitrarily cut spending on Disability Living Allowance by 20 per cent or remove eligibility from half a million disabled people.

In December 2010, government then published its detailed plans to abolish Disability Living Allowance (DLA) and introduce Personal Independence Payment (PIP), for those of working age from 2013-14. This is in spite of the fact that the fraud rate is only 0.5%.

The government said that the changes to the assessment and eligibility would be the means through which a 20 per cent cut in spend and recipient numbers would be achieved. By 2016 this cut was intended to amount to savings of £2.6bn annually.

The government has said that it wants a more ‘objective’ assessment a statement driven by the political goal of lowering the spend on DLA, as there is little evidence of unnecessary payments:  fraud rates for DLA are low at only 0.5%[1]. This indicates there is sufficient rigor and objectivity under the present DLA assessment system. In addition only about 50% of DLA claimants are successful and in 2008 49% of appeals were turned down, which also suggests that the assessment is rigorous.

“The new benefit will have two components, linked to a range of activities that will be considered in the new assessment. One will be awarded on the basis of the individual’s ability to get around (the mobility component), the other on their ability to carry out other key activities necessary to be able to participate in daily life (the daily living component).”

The government continue to echo the notion that support should go to those “who face the greatest need”. However they do not justify how they intend to equate ‘greatest need’ with enabling disabled people to fully participate within society and DPAC has concerns that any such false distinction will simply further  the notions of the ‘deserving’ and ‘undeserving’ disabled.

The policy goal which frames the PIP assessment criteria DPAC  would argue is totally flawed. We believe that the proposal for PIP is driven by a cost cutting agenda and a predetermined goal of cutting spend by 20 per cent, rather than any kind of objective assessment of need of support to cover disabled people’s extra costs of living.

Maria Miller has once more stated that the cost of supporting disabled people is unsustainable but that “The Coalition Government is committed to helping disabled people to exercise choice and control over their lives and ” “We have been absolutely clear that our welfare reform plans are designed to protect people in the most vulnerable situations, including disabled people.”

However in reality both the work capability assessment for ESA and the proposed planned changes of replacing DLA with a Personal Independence Payment are simply designed to reduce the number of people whose disability is recognised by this government.

We further believe that government ministers have continually created confusion over DLA by linking it to a goal of encouraging people to be in work. DLA is not an out-of-work benefit and people can receive it whether in or out of paid work. For many disabled people DLA is what allows them to be able to work and without it they will no longer be able to continue in employment.

Assessment development group

The government formed an ‘Assessment Development Group’ to design the assessment, comprising The government’s ‘Assessment Development Group’ which drew up the draft assessment has ten health and social care professionals plus government officials, yet only one person representing disabled people. Since the numbers of health professionals and officials heavily outweighed the number of disabled people present, it is not surprising that the group was able to come to a ‘broad agreement’ on the proposed assessment.

If more disabled people had had been present it is doubtful that such a medicalised/ functional ability type of assessment would have been agreed on.  Disabled people should have been fully involved in this decision making process at the early stage of discussion, i.e. as members of the Assessment Development Group in at least an equal number of disabled people representing disabled people’s organisations as government and other officials.

Article 4 of the UNCRPD states; the general obligation on government to consult with disabled people, before not after decisions or policies are changed.

This lack of early involvement is compounded by the government  ignoring the concerns raised by disabled people and their organisations via consultation responses by refusing to amend the Welfare Reform Bill sufficiently to address these concerns.

PIP components and eligibility assessment 

PIP Components

Personal Independence Payment will have two components:

  • daily living component
  • mobility component

Each component has two rates rather than the existing three rates:

  • daily living component standard rate
  • daily living component enhanced rate
  • mobility component standard rate
  • mobility component enhanced rate

PIP Eligibility Assessment

 Activities for daily living and mobility

The new assessment will cover activities for daily living and mobility. To qualify for PIP disabled people will need to score enough points in the following daily living and/or mobility activities:

Daily Living Activities:

  1.  planning and buying food and drink
  2. preparing and cooking
  3. taking nutrition
  4. managing medication and monitoring health conditions
  5. managing prescribed therapies other than medication
  6. washing, bathing and grooming
  7. managing toilet needs or incontinence
  8. dressing and undressing
  9. communicating with others

The mobility activities:

  1. planning and following a journey
  2. moving around

The number of points scored will dictate whether a claimant is assessed as having a ‘limited ability’ or ‘severely limited ability’ to carry out daily living activities and/or mobility activities. The score will also dictate whether a claimant will receive the standard or enhanced rate of the Daily Living component.[2]

PROBLEMS WITH PIP

  • In order to receive PIP disabled people must be aged between 16 and 65 years and satisfy the daily living and/or mobility activities test for 3 months prior to claiming and be likely to continue to satisfy this test for a period of at least 6 months after claiming.

 

  • It remains very unclear what will happen to anyone who becomes 65 and is in receipt of the mobility component of PIP as they would have to claim Attendance Allowance which has no mobility component. (currently anyone in receipt of DLA mobility component who becomes 65 continues to receive this). DPAC is therefore concerned that any older disabled people will lose their independence simply because they have reached the age of 65.

 

  • There is also no clarity about what will happen when someone is admitted to hospital for any length of time but with the proposals for PIP as they now stand it would seem that even a very short stay in hospital could result in someone losing their mobility cars, plus any equipment such as wheelchairs or hoists and other essential equipment they may be using PIP to pay for.

 

  • Government guidance on DLA states that ‘Disability Living Allowance (DLA) is not based on your disability but the needs arising from it’. This is not reflected in PIP and the assessment involves a rigid and crude set of questions which examines what a disabled person cannot or can do from a prescribed list that only covers basic mobility activities and daily living activities.  This method of assessment follows the medical model of disability.

 

  • The Work Capability Assessment was described by Professor Harrington as ‘impersonal and mechanistic’ [3] and has resulted in many flawed decisions, which have been over turned on appeal. It is deeply worrying that the government appears be adopting a similar rigid assessment for PIP.

 

  • The estimate for ESA tribunal appeals for 2012-2013 is £50 million and the backlog of cases is so long that tribunals are sitting even on Sundays so the logic behind also adopting a similarly flawed assessment process for PIP remains unclear to DPAC.

 

  • The cost of changing from DLA to PIP has also been estimated to be £65 million and on top of that there are plans to regularly re-assess even claimants whose condition will never improve. Not only does this seem a waste of money but it will add unfair additional stress to the lives of people who are already struggling to overcome the disabling barriers put in their way on a daily basis.

 

  • DLA acts as a passport to other welfare benefits and concessions such as the Blue Badge, loss of which will increase the impact of losing DLA. We feel the government have failed to consider how these passporting functions will be replaced if PIP is introduced.

 

  • Higher rate care component of DLA has passported disabled people to eligibility for funding for care and support from the Independent Living Fund although this is also now closed to new applicants and due to close completely by 2015.

 

  • Being in receipt of higher and middle rate care components of DLA has also passported disabled people to additional disability premiums in both Income Support and Housing Benefits. These premiums are now also planned to be abolished with no clear guidance on what these additional amounts of funding will be replaced by or how people will become eligible for any additional amounts of basic benefits.

 

  • Many disabled people will live in increased poverty because of the new assessment.  The government has not sufficiently tested what the impact on those losing DLA will be. In particular the cumulative impact of benefit changes remains unknown.

 

  • By depriving disabled people of a much needed benefit we believe the government is failing in their duty under the Equality Act and its responsibilities under the UN Convention on the Rights of Persons with Disabilities.

 

  • The assessment of mobility impairment is ridiculously crude and neither allows for cumulative impact, fluctuation in factors such as stiffness and pain, nor for factors such as steps. A person may be able to walk 50 or 200 metres on one day but none on another. They may be able to walk short distances on a flat surface but be unable to walk up and down steps to access buses and tube trains safely. An assessment of these factors is needed.

 

  • Many claimants with Neuro-diverse and Mental Health conditions also say that while they can plan a journey the stress and anxiety involved in making such a planned journey has simply been ignored and that they can physically only carry out the planned journey if they have support from another person to do so. This is another group of disabled people whose real needs will be ignored by changes to PIP>

 

  • Claimants with conditions such as arthritis or osteoporosis may be able to complete a one off physical task, but completing several tasks over the course of a day can have a cumulative effect and increase pain and immobility to totally debilitating levels.  Additional consideration of the impact of pain and fatigue is essential.

 

  • Again many claimants with Neuro-diverse and Mental Health conditions can physically cook a meal but find that to do so is stressful and exhausting for them so in reality they are not able to prepare and cook a meal.

 

  • Disabled people are already twice as likely to live in poverty as non-disabled people. Far from the intention to ‘improve the support for disabled people and better enable them to lead full, active and independent lives’, these proposals will lead to an increase in disabled people’s poverty and isolation.   Therefore DPAC is strongly opposed to the introduction of PIP and the eligibility assessment.

 

  • The government’s work and pensions select committee recognised that many more disabled people need to be lifted out of poverty and recommended a DLA awareness campaign.

 

  • DLA supports disabled people to become more equal and independent.  Instead of attacking DLA, which supports independence (including helping to overcome barriers that prevent some people taking up employment), government should be doing more to stimulate demand in the economy so that jobs are available and to tackle discrimination by employers by vigorously enforcing the Equality Act 2010.

 

 

 

 


 

 

 

Disabled Peoples’ organisations support saving Remploy Jobs: letter published in print and online versions of Guardian

 Action, All Posts, Disability Rights, media, News, Politics, Welfare reforms  Comments Off on Disabled Peoples’ organisations support saving Remploy Jobs: letter published in print and online versions of Guardian
May 112012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Please see below for published letter in Guardian put together by Inclusion London, DPAC and allies including unions. The final letter needed to be shortened for publication, as a result we apologise to any signatories who may have missed as the Guardian also insisted on individual names representing each organisation. The text of the original full letter with our recommendations can be seen at: https://www.dpac.uk.net/2012/04/sign-up-to-support-the-remploy-workers/

The strength and number of signatories that were published makes a mockery of the assertion in the Sayce report that 100% of disabled organisations support the closure of Remploy factories- this is simply not true!

DPAC, Inclusion London, listed organisations, unions and individuals will continue to support the Remploy workers against the loss of their jobs and will not be taken in by the spurious ‘disability inclusion’ argument being used to advocate more disabled people losing their jobs in a time of economic disaster for disabled people.

Please help support the Remploy workers by leaving comments to the letter at:  https://www.guardian.co.uk/society/2012/may/10/disabled-works-fight-remploy-jobs

Disabled workers fight to save Remploy factory job

Thursday 10 May 2012 21.00 BST

As a group of disabled people’s organisations, run by and for disabled people, we – together with other individuals and organisations – believe the government’s decision to make 1,518 disabled workers unemployed by August, and a further 1,282 unemployed next year, by closing the Remploy factories is wrong (Report, 12 April). We do not believe these job losses constitute a victory for inclusion in the workplace. We have fought long and hard for an inclusive society where disabled people have the same employment chances, choices and opportunities as everyone else. Our goal and demand for inclusive employment must not be used to justify job cuts that will push these workers into poverty, exclusion and isolation.

This decision will effectively put these disabled workers on the scrap–heap at a time of recession when there is little to no hope of finding alternative employment, when eligibility for benefits is being slashed, and when support services for disabled people are being destroyed.

True equality and inclusion will be achieved through development of a plan of investment and support to transform the Remploy factories into viable social enterprises controlled by disabled employees, rather than their closure; investment to increase and expand the access to work scheme; investment in high-quality employment support services that enable disabled people to find employment and stay in employment; the right to inclusive education and accessible training and apprenticeships for all disabled people; and commitment to tackle discrimination in the workplace through better understanding and enforcement of Equality Act duties.
Deaf and disabled people’s organisations and groups:
Tracey Lazard CEO, Inclusion London, Linda Burnip Disabled People Against Cuts, Bill Scott Manager, Inclusion Scotland, Rahel Geffen Interim CEO, Disability Action in Islington, Lucy Byrne CEO, Richmond AID, Michelle Baharier CEO, Cooltan Arts, Caroline Nelson Director, Choice in Hackney, Roy Benjamin Chair, Merton Centre for Independent Living, Mark Harrison CEO, Norfolk Coalition of Disabled People, Alan Kerr CEO, Artsline, Dr Ju Gosling Chair, Regard, Rosemary Nicholson Visually Impaired in Camden, David Stock CEO, Southwark Disablement Association, Joanne Munn Director, Greenwich Association of Disabled People, Pat Bhabha Director, Disability Action Waltham Forest, Sharon Schaffer London Visual Impairment Forum, Mary Hick deafPLUS, Caroline Jones Chair, Norfolk Association of Disabled LGBT People, Ellen Clifford Bromley Experts by Experience CIC, Gill Goble Brighton DPAC, Andy Greene Islington DPAC, Roger Lewis Lambeth DPAC, John McArdle Black Triangle Anti-Defamation Campaign in Defence of Disability Rights, Kevin James Atos Victims Group

Individuals:
Bill Holmwood, Richard Sturgess , Stephen Lee Hodgkins, Mo Stewart, Dr Stephen Hall, Caroline Richardson, Calum McLean, Pam Tinsley, Valerie Lang, Geoff Dewhirst, Sandra Dooley, Rubbena Aurangzeb-Tariq, Mik Scarlet, Isabel Ros López, Caroline Jones, Liana Lloyd, Alan Woodward, Diane Lucas, Ralph Pettingill, Alexandra Stein, Brid Fitzpatrick, Sasha Callaghan, Beverley Woodburn, Keith Hodgson, Ben Samuel, Julia Cameron, Ellen Clifford, Elane Heffernan, Vicky Ayech, Teresa Rayner, William Nutthall , Merry Cross, John Collings, Derek Kelter, Kaliya Franklin, Richard Lumb, Derek Stevens, John Newman, Maureen and Martyn Stagg, Stephanie Cadd, Jayne Linney, Liaquat Hussain, Ian Parkhill (a member of Worcester Coalition for Independent Living), Pat Onions, Rosemary O’Neill, Jean Ashlan, Jonathan Toye, David Steele, John McArdle , Paul Smith, Deborah King, Alison Morgan, David Brown, Mark Thomas, Danka Gordon, Les Seavor, Sue Brassey, Maureen Armstrong, Iyiola Olafimihan, Eleanor Firman, Gail Jeynes, Rosemary Iddenden, Dora Kostiuk, Bronwen Williams, Roger Lewis, Rob Murthwaite, Andy Greene, Beverley and Robert Stevens, Paul Farrelly MP, John McDonnell MP, Lisa Nandy MP, Peter Beresford, Karen Wild, Ellen Goodey

 

Other organisations/groups:
Jonathan Bartley Co-director, Ekklesia, Dr Artemi Sakellariadis Director, Centre for Studies on Inclusive Education, Jo Claire CEO, Three Cs Support, Martin Rathfelder Director, Socialist Health Association, Alison Blackwood Head of policy and knowledge, London Voluntary Service Council, Peter Corbett CEO, Thomas Pocklington Trust, Margie Arts Barrow and Furness Pensioners’ Association, Stefania Rulli-Gibbs Communications manager, Brandon Trust, Gordon McFadden Director of policy, Limbcare, Bahir Laattoe Barnet Alliance for Public Services, Marie Lynam The Kilburn Unemployed Workers Group

Unions:
Sean McGovern Unite executive council disability representative, Ivan Hickman Secretary, Stoke-on-Trent NUT, Steve Roberts Chair, Warwickshire Fire Brigade Union, Rob Crowther Unite (UCU branch), Ray Smith Secretary, Newcastle Central Unite 1901, Dr Helen Groom GP, Gateshead Medical Practitioners Union (part of Unite), Gavin Dudley GMB workplace rep, Helen Winterburn Branch chair, Unison Darlington LG branch, Barrow Trades Union Council, Chris Youett NUJ rep on TUC Midlands, David O’Tooe Branch development organiser, UCU Exeter office, Doug Oxer RMT Union, David Lowdon GMB member, SWP member, Martin Bove Unite member, John Lea Unite, Matt Brierley on behalf of PCS Ofsted branch committee, Rugby Trade Unionist and Socialist Coalition, Neil Smith GMB branch secretary

May 102012
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Lord Freud – The Benefit Fraud

With thanks to the ever brilliant Johnny Void for letting us repost this– for more of The Void go to https://johnnyvoid.wordpress.com/

Lord Freud, the toff banker, will be defending the Government’s savage welfare reforms at a conference called by the National Housing federation on May 23rd.  Freud has been one of the chief architects of the vicious Welfare Reforms as both a Labour and then a Conservative Party member.

Freud was asked by Tony Blair to review the benefit system way back in 2006, despite Freud saying he knew nothing about it.  This didn’t stop him from leaping at the opportunity to claim that single parents should be sent to work, lay the foundations for the Atos shambles and encourage the use of fraudulent bastards like A4e to run huge chunks of the Welfare State.

The great welfare rip off has seen companies paid billions of tax payers’ money to provide barely existent training courses or claim huge fees every time someone unemployed finds a job.  The likes of the now disappeared Emma Harrison formerly of A4e have awarded themselves multi-million pound dividends whilst their staff, under enormous pressure from above, have ended up cooking the books to pay for them.  Like all the best scams, the companies involved don’t even have to break the law to make off with the cash.  Training providers on the Government’s flagship Work Programme can be paid up to £13,000 for claiming to have helped someone get a job who has barely even met them. 

Private sector sharks have also been brought in to carry out assessments for sickness and disability benefits, another of Freud’s ideas.  The Atos assessment system has turned out to be a disaster, costing a fortune in appeals against their flawed decisions, whilst being devastating for those forced to undergo the stressful and demeaning tests. This hasn’t stopped Atos creaming £100 million a year off the tax payer.  And Atos, along with prison companies like G4s and national joke Capita, are set to pick up huge contracts for re-creating the exact same shambles to re-assess over three million people currently claiming Disability Living Allowance.

With George Osborne promising up to £5 billion in cash to Work Programme contractors, it seems the gravy train for private sector sharks infecting the Welfare State is far from over.  Meanwhile millions of people face poverty and homelessness due to ideas generated on the back of an envelope by Lord Freud and his chums.

Lord Freud is a member of the pervy Freud dynasty and went to Whitgift Public School and then Oxford.  On leaving university he just happened to be offered a job at the Financial Times.  After a few years he ditched financial journalism to begin work as a professional crook for stockbrokers Rowe & Pitman (later to be taken over by SG Warburg).  His first job was to compile research on companies he was also taking money from, a practice which was made illegal after analysts were found publicly backing clients whilst slagging them off behind closed doors.

During his career Freud cost the tax payer a fortune when he botched the Eurotunnel flotation in a deal he describes as a ‘shambles’ and claims he ‘sold the market a pup’.  He did a similar thing with the Eurodisney flotation, costing investors millions.  Asked to handle the flotation of doomed company Railtrack, Freud priced the shares at £3.50 despite them being worth over four times that figure.  Freud remained a senior figure at SG Warburg helping to oversee the collapse of the investment bank in 1995 when it was taken over by the Swiss Bank Corporation.

David Freud’s omni-shambles career is best summed up by himself:

“Nearly everything I’ve done has been total chaos. I cannot believe it’s just because of me.”

This is typical of arrogant little posh boys like Freud.  Believing they are born to rule, their old school chums will prop them up as they fail time and time again.  In return they offer kickbacks, like the multi-billion pound give away to the private sector that Freud has overseen whilst involved in welfare reform.  They really are all in it together.  A self-serving smug elite sharing around power and money like pass the fucking parcel whilst the rest of the country gets on with doing the real work that keeps them rich.

When Freud saw which way the wind was blowing under the Labour Government he jumped ship to the Tories where he was immediately made a life peer and given a Baroncy.  As Minister for Welfare Reform he has wasted no time in continuing the incessant lies about benefit claimants he began telling under Blair.  The man who’s worth millions is outraged that single mums should be paid a pittance to feed their children, or large families in cities should have somewhere to live.

If the fraud Freud had been born on a council estate he’d probably be banged up by now for flogging fake Armanis or nicked ipods down the boozer.  Instead he picks up huge sums of tax payers’ cash he doesn’t need to advise the Government on something he knows nothing about.  All that’s required for the rich to succeed is the old school tie and a commitment to staying on the right side in the class war.  Brutality and incompetence is the hallmark of the English ruling class and there has rarely been a better example than Lord Fraud and his chinless cabinet cronies.

Freud will be speaking at the National Housing Federation’s Welfare Reform Conference on the 23rd May.  Join protesters at 9.15 to tell him what you think outside the Commonwealth Club, 25 Northumberland Avenue,
London, WC2N 5AP

See also: ‘A Tale of Two models: disabled people vs Unum, Atos, Government and Disability Charities’ for more on Freud’s doings and the sell out of welfare https://www.dpac.uk.net/2012/04/a-tale-of-two-models-disabled-people-vs-unum-atos-government-and-disability-charities-debbie-jolly/