Sep 102014
 

Posted on September 10, 2014 by johnny void

Poundland have seen dozens of protests outside their stores over their use of unpaid workers.

Poundland have seen dozens of protests outside their stores over their use of unpaid workers.

In a bizarre move, several companies known to use unpaid staff on workfare schemes have teamed up to write a letter to The Guardian singing the praises of the disastrous Work Programe.
The list of employers – which includes Homebase who are known to have used workfare is the past, and Poundland, who were at the heart of the successful legal challenge against workfare – say that the government’s support for schemes like the Work Programme ‘must continue’.  Otherwise they might have to start actually paying their staff instead of exploiting unemployed people coerced into unpaid work by sanction-happy Jobcentre busy-bodies.
It is not known whether all the companies on the list, which include Ocado and Gap, are involved in unpaid work, although it is difficult to see why they have signed otherwise.  In fact it seems a strange thing for these businesses to be bothered to do at all.
The last signatory on the list may reveal one explanation for how this strange initiative came about.  Kirsty McHugh is the Chief Executive of the Employment Related Services Assocation, or ERSA for short.  This is the trade body established to lie on behalf of the welfare-to-work parasites like A4e and G4S who run the Work Programme.  Just last week they published a breath-takingly dishonest report making wild claims that no-one believed about how much money the Work Programme is saving the country.  It seems likely that this letter was co-ordinated by ERSA as part of a shabby PR campaign designed to convince the DWP to keep giving welfare-to-work firms billions of pounds of our money.
Labour have hinted that they might bring in local councils to run forced work schemes.  The Lib Dems are caling for a policy change and may yet hold the balance of power again come the next election.  More importantly, no-one know better than the welfare-to-work sector that the latest ‘Help to Work’ scheme is set to be a disaster and that they will be the ones that get the blame when it all goes wrong.  The future does not look so assured for ERSA and their welfare-to-work cronies who  have made hundreds of millions out of bullying and exploiting unemployed people.  They will fight as dirty if they have to keep Brtain’s biggest benefit scam alive.

Expect more bollocks like this.
join the Week of Action Against Workfare beginning on October 4th.  Please spread the word.
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with thanks from DPAC for allowing us to reblog

Sep 082014
 

Response
(1) The Work Capability Assessment is a much more rigid test & cannot be compared with former Personal Capability Assessments.  It is inconceivable that a conclusion can be reached that the more rigid Work Capability Assessment has become easier to negotiate than the previous Personal Capability Assessment which had a lower threshold.
It is not accepted that there has been any form of significant improvement in the claims process surrounding the Work Capability Assessment.
Never before has one benefit assessment process attracted so much adverse publicity and negativity as the Work Capability Assessment.
It stands to reason that if the test is set as high bar as the Work Capability Assessment is, it logically follows that qualifying for entitlement will be far more difficult than qualifying for the previous Incapacity Benefit via the Personal Capability Assessment process used to determine eligibility for Incapacity Benefit & Income Support on the grounds of incapacity for work.
It is not accepted that any accurate comparison with Incapacity Benefit can be drawn without full regard to analysing similar cohort factors such as the ages, ICD coding, duration of claim, gender, and regions of the claimants being taken in to consideration.

(2) No comparisons can be drawn between Incapacity Benefit & Employment & Support Allowance without a proper scrutiny of a more complete set of statistics
Before drawing any analysis between Incapacity Benefit and ESA, the numbers of claimants used in the comparison including on and off flows would need to be carefully scrutinised. This is especially important where the flow rate is mixed with ib/ESA migration cases and where it can no longer be safely concluded that new ESA claimants are not in fact older claimants who have since submitted a fresh claim.
Between October 2008 and September 2013 the ESA regime has involved a total departmental case-load (across all cohorts) of 6,440,000 cases involving 4,396,400 Work Capability Assessments of which 1,198,700 were a repeat.  A case load of this magnitude requires considerable analysis across all cohorts before any accurate comparisons can be drawn between the older incapacity benefits and ESA.  The former was far less complex in cohort terms.
Between October 2008 and September 2013, 1,407,400 claimants have been placed in the Work Related Activity Group (453,300 at repeat assessment) and 1,437,300 in the Support Group (479,800 at repeat assessment).  These figures are considerably higher than those relating to the new ESA claim group in which 484,900 have been placed in the Work Related Activity Group and 445,400 have been placed in the Support Group. Far more information is required as to not only the numbers allocated to the groups but also what happens to the claimants after they have been assessed in to a placement.

(3) The DWP needs to produce statistics on appeals & reconsiderations before any reliance be can be placed on the Work Capability Assessment statistics.  Well over a million claimants have disputed the findings of Work Capability Assessments and the full dispute outcomes are as yet still unknown.
From April 2009 to December 2013, HMCTS figures confirm 1,054,541 ESA appeals have been lodged with Tribunals of which an average of 40 + % of those already heard have been overturned in the claimant’s favour.  These figures are far in excess of any related to the previous Incapacity Benefit and are an obvious indicator of significant numbers of claimants having a lack of confidence in the decision reached at initial assessment.
The DWP’s WCA statistics are inherently unreliable and cannot be read in the context of isolated quotations from quarterly releases without proper reference being made to the more specific and overall totals available.  The overall (cumulative) ‘qualifying’ rates for claimants are (up to September 2013):
-New ESA claimants 47%
-New ESA claimants at repeat assessment 78%
-IB/ESA migrated claimants 80%

Whilst it may be helpful to look at quarterly shifts in the figures, it is the overall cumulative rate which needs to change before it can be safely concluded that any material change has taken place.

The DWP’s WCA statistics are rendered inaccurate by way of the DWP’s inherently slow update of information from the inputting of the number of formal appeals lodged with HMCTS together with a total lack of explanation as to the number of initial decisions overturned informally following DWP reconsideration. This is particularly important in respect of monitoring the effects of mandatory reconsideration since October 2013.

(4) Employment & Support Allowance is an entirely different regime to that of Incapacity Benefit making any comparison unreliable.  Delays with the DWP & Atos Healthcare have resulted in a chronic backlog of 750,000 cases awaiting assessments from which no conclusions can be drawn.  The WCA statistics are made additionally complex by the influx of a case load of 1,354,800 claimants assessed from the Incapacity Benefit migration programme.
The claims process involving ESA is entirely different to that of Incapacity Benefit.  ESA involves the claimant initially being subjected to what should be a 13 week assessment phase before the Work Capability Assessment decision is decided upon by the DWP.  It is only once the assessment phase has been completed that a proper decision can be made as to whether the claimant can move in to the main WRAG/Support Group phases of ESA entitlement.  Chronic delays have built up to a point where the backlog awaiting assessment had recently reached over 750,000 claimants.  It is a clear sign that the DWP was earlier ‘over reassessing’ claimants leading to a substantial lack of residual data on outcomes and the possibility that the Department is now making less rigid placement decisions in order to get though its chronically stretched backlog.
Claimants who have undergone ib to ESA migration do not in any event claim ESA, their claim is merely converted (providing they qualify at the point of WCA conversion) and thus no comparison can be drawn between this cohort and those making a new ESA claim from scratch.

(5) Statistical manipulation
Between October 2008 and September 2013, the Work Capability Assessment statistics record that 1,551,500 claimants have been found fit for work and 1,500,900 claimants have ended their claims without completing their Work Capability Assessment. In total the overall number of claimants who seemingly should have exited Employment & Support Allowance is therefore in excess of 3 million claimants. However the DWP off flow figures for the period October 2008 to August 2013 show the numbers exiting from Employment & Support Allowance to be 2,288,980.

The number of claimants leaving Employment & Support Allowance who closed their claims is a fixed statistic, whereas the number found fit for work is reversible if the claimant appeals or requests a reconsideration.
It is hard to understand how an apparent ‘exodus’ of some 3 million plus Employment & Support Allowance claimants as shown in the assessment statistics is not matched by statistics showing a rise in the numbers claiming Jobseeker’s Allowance.
In addition to the exodus related to assessment, there are also claimants who will have died, transferred to other benefits or ended their claim through time limiting imposed upon contributory claimants in the Work Related Activity Group who cease claiming where there are no grounds upon which to continue claiming income based Employment & Support Allowance.
DWP figures, related to on-flows, show that of October 2008 to August 2013, 636,410 Employment & Support Allowance claimants made a second or more claim for Employment & Support Allowance. This will add substantially to the number of on flows and may therefore give a distorted perception over more claimants claiming as well as ‘clouding’ the influx of what may appear to be new Employment & Support Allowance claimants who are in fact previous claimants who have simply made another claim.

(6) Mistrust
Media articles including those relating to the deaths of ESA claimants such as Graham Shawcross (63), Mark Wood (44), Neil Groves (46), Lee Robinson (39), Elenore Tatton (39), Linda Wootton (49), Brian McCardle (57), Karen Sherlock (44), Trevor Drakard (50), David Groves (56) and others have created a massive mistrust in the Work Capability Assessment as a valid measure of a claimant’s ability to work.  The DWP has failed to produce any up to date statistics upon which any reliable conclusions can be drawn as to the number of deaths & whether they can be ruled out as being directly or indirectly related to the Work Capability Assessment process.
The Work Capability Assessment remains condemned by disability groups, the BMA, National Charities, senior judges and Parliamentary Select Committees. The process has been identified as unfit for purpose and of such toxicity that major re-work is required. There clearly remains widespread concern that the WCA has not improved, customers have no confidence in it in, employers are clearly not convinced by it as an accurate measure of fitness to work as evidenced by the appalling Work Programme Job Outcomes valid to March 2014:
In the New ESA claimant group, out of 484,900 in the ‘Work Related Activity Group’, just 10,760 ended up with a Job Outcome (2.2%)
In the Incapacity Benefit to ESA conversion group, out of 469,200 claimants placed in the ‘Work Related Activity Group’ just 980 ended up with a job outcome (0.2%)
In the Incapacity Benefit to ESA conversion group, out of 249,300 claimants found ‘fit for work’ just 3,160 (1.4%) ended up with a job outcome.   Whilst this appalling result is shocking in itself, it should be remembered that the DWP’s figures only point to people on JSA who have been on incapacity benefits.  These figures may therefore relate to claimants who have ended their older incapacity claims and taken up a JSA claim voluntarily without being tested for ESA.
In the overall ‘voluntary participation group’ where there is no mandatory requirement to take part (unless a claimant has agreed to participate) out of 957,500 claimants placed in the Support Group (from both new ESA and incapacity to ESA claim groups) 3,350 claimants (0.4%) ended up with a job via the Work Programme. This group does better than the mandatory groups in incapacity to ESA conversion cases.

(7) Summary
It is unsafe to draw any conclusion that it is any easier for a claimant to make a claim for Employment & Support Allowance than it was for previous range of incapacity benefits. It is not possible to make a valid comparison on the basis of comparing numbers/success. A full explanation as to how claimants made their claims and how they were assessed is required before an accurate comparison can be made.  There is simply not enough information currently available to conclude that the Harrington reviews have led to any identifiable improvement.
A rise in the numbers being placed within the Support Group and Work Related Activity Groups may be more related to the greater number of claimants involved, the appeal/reconsideration results beginning to filter through after data lag, more claimants re-applying after being turned down, less capacity within the Work Programme to handle the larger numbers involved and a reduction in the number of repeat & ib/ESA migration assessments following the announcement that Atos Healthcare were withdrawing from the contract to conduct assessments for the DWP.
For these reasons any claim that it is easier to make a claim for Employment & Support Allowance than it was for Incapacity Benefit is strongly refuted.
By Nick Dilworth.
For and on behalf of New Approach.
New Approach are committed to working with other individuals & groups, please add your signature to this statement by emailing newapproach_uk@outlook.com or in comments.

follow new Approach on twitter @newapproach_uk

website: www.http://newapproachuk.org/

Aug 262014
 

Thursday 11th September 2014

End Bedroom Tax; No Sanctions for Claimants – No Targets for Staff

On 11th September the Anti-Bedroom Tax and Benefit Justice Campaign is holding a day of protest: say no to claimant sanctions, bedroom tax and benefit cuts

Government attacks on benefits mean hunger, debt and fear. Ex-soldier David Clapson died hungry and destitute after his benefits were stopped, the latest in a string of deaths and suicides related to sanctions and benefit cuts.  The overwhelming majority of referrals to food banks are due to  claimants being sanctioned.

Sanctions cutting benefits of disabled people on Employment and Support Allowance, rose by nearly 580 percent between March 2013 and March 2014, and total sanctions rose to over a million last year, from 100,000 in 2010 (DWP figures).
PCS union is supporting the 11 September protests.  Research by PCS members working in the DWP revealed that 82% of members felt ‘pressured’ into sanctioning claimants, and 62% said they had made ‘inappropriate’ sanctions decisions.Protests have forced Government to promise changes: see Review report. But sanctions remain a vicious plank of the Government’s punitive welfare reforms, and are still supported by Labour in parliament.

Join us on one of protests below or organise your own.  Demand an end to the Bedroom Tax and link it to the slogan: ‘No sanctions for claimants, No targets for staff’. Build links with local PCS members – contacts for local PCS in DWP and PCS regions.The Bedroom Tax is almost dead – we will demand MPs kill it now  and up the pressure to beat the sanctions regime too. Let us know any actions you are planning so we can promote them.

End Sanctions, Bedroom Tax and benefit cuts11am Old Palace Yard Westminster SW1P 3JY
and 1pm DWP HQ Tothill St SW1

Other protests planned in
Leeds, Sheffield, Oxford, Manchester/Liverpool, Birmingham, Glasgow


Aug 192014
 

 

A second court case against the DWP on the closure of the Independent Living Fund (ILF) will take place at the Royal Courts of Justice on the 22nd and 23rd of October. It is expected to last one and half days.

There will be a vigil outside the courts from 12.30 on the 22nd to support the ILF users taking the case and to support our right to independent living as enshrined in the UN Convention on the Rights of Persons with Disabilities- article 19

Article 19: “Living independently and being included in the community”, states that “disabled people have a right to live in the community; with the support they need and can make choices like other people do”.

Please join with us to show your support!

The closure of the ILF  has obvious implications for the UK’s chances of meeting such obligations. Most importantly for those disabled people who will lose this financial support they will lose any independence and choice in their lives. You can listen to how this vicious attack will affect disabled people at these links.

http://www.dpac.uk.net/2013/02/a-nasty-cut-people-affected-by-the-closure-of-the-independent-l5142/

 

https://www.youtube.com/watch?v=OMElPk0pq6I

 

We will be posting further updates

 

Aug 162014
 

 

(Report from workshop at national meeting of Anti Bedroom Tax and Benefit Justice federation)

Fighting Benefit Sanctions

 

The government has a policy  of increasing sanctions to force people off benefits. 

 

More than 800,000 people have been sanctioned in the last year. Referrals to food banks are mainly due to claimants being sanctioned. 

 

Martin Cavanagh is the PCS Group Exec member for civil servants working in the DWP.  The PCS union resolved at their recent conference to oppose both Workfare and Benefit Sanctions. He explained the three central reasons behind the Tories policy of increasing sanctions; Further demonisation of the poor, financial savings for the government, and driving a wedge between claimants and workers. 

 

PCS survey of members working in the DWP revealed that 82% of members felt ‘pressured’ into sanctioning claimants, and 62% said they had made ‘inappropriate’ sanctions decisions. 

 sanctions

The Kirklees Axe The Tax group have used a banner : No Sanction for Claimants! No Targets for Staff! This attracted claimants and some staff to their stall outside a job centre.

 

Roger Lewis speaking for DPAC said that ‘more needed to be done by the PCS.’ But, he insisted, ‘we will not allow the government to divide us. Those working for the DWP alongside claimants have a common interest, we are locked together in a common fight against the Tories.’ 

 

‘More will be done from our union the PCS over the sanctions,’ explained Martin. 

 

‘Advice for claimants on how to challenge sanction decisions has now been agreed between our union, the PCS, Unite the Union Community branches, and campaigners against sanctions. That advice will be issued shortly.’

 

Research has shown that only 1 in 50 claimants who are sanctioned appeal the decision. Of those 90% win their appeal. Forthcoming advice will explain to claimants how they can appeal. 

 

To launch the joint advice and joint campaign, we agreed a day of action against benefit sanctions for Thursday 11th September. 

 

Protests will be organised in every region outside key DWP headquarters or similar high profile government offices.

Fighting Workfare

Public campaigns work! 

 

With just a few protesters the Boycott Workfare actions have ‘shamed’ many employers into withdrawing from the Workfare scheme. Companies and businesses don’t want to be exposed as employing ‘slave’ labour. Only when a company signs up to the Boycott Workfare pledge are they removed for the Boycott Workfare website listing. 

 

Protests outside flagship venues of those companies still in the scheme will continue until the schemes are scrapped.

 

Reblogged with thanks from http://antibedroomtax.org.uk/2013-05-29-04-42-41/latest-news/110-stop-sanctions-11th-sept-day-of-action

 

 

Jul 202014
 

Rob prepared this statement for the recent Disability Rights UK conference (18th July) He was not allowed to give his statement- we publish it here so people can understand why all voices should be heard and listened to.

The Fight for Our Lives

 My name is Robert Punton I am a disabled person and an Independent Living Fund (ILF) recipient I come here today to oppose Disability Rights UK stance on the closing of the ILF.

I have been a disabled activist for over 30 years both in a paid and unpaid capacity.  The money I have received through ILF funding has in no small part enabled me to achieve this, I have employed the same two guys as my Personal Assistants Mike Orme and Darren Harrison for over 25 years and now I am employing their son Daryl Harrison-Orme in the same capacity.  If the closure goes ahead this puts our partnership (family) in serious jeopardy.

I make no bones about the fact that as a person with high support needs without this extra funding I would be languishing in a Scope home or one run by some other likeminded establishment.  In saying this I am not in anyway denigrating the lives of anyone living there but I much prefer my lifestyle and will fight to my last breathe to save it.  Make no mistake everyone using ILF is in the same boat and none of us want to sink.

I am a member of DPAC and Co Director in Community Navigator Services with Clenton Farquharson MBE and Jack Nicholas it is a Community Interest Company we all identify as disabled; we aim to build capacity within communities to allow them to participate within society to their fullest n need or want.  We all agree the closure of ILF will severely destroy the advances that disabled people that achieved in last 3 decades.

Disability Rights UK and Simon Stevens advocate that when they close ILF it will make it a level plain field when they pass on funds to local authorities and everyone will be treated equally, equality only works when you use the highest possible denominator, in other words no one wants to be treated like their neighbour if they are being treated badly.  The term we like to use now is fighting for social justice for all, hence wanting the best standard of living (in this case support plans) for everyone.

Simon Stevens and his supports say that the ILF has made users of their scheme elitists in their communities.  I can’t argue that this may be perceived in that light. However, I would argue this two-tier system in society cannot be blamed on the independent living fund or its users; it was the Conservative government who closed the ILF in 2010 under the guidance of Maria (Killer) Miller, and in doing so cut off thousands of possible or probable new users of ILF, Con-Demning them to the level of substandard support given by most Local Authorities.

This substandard support shows the priority most local governments, and therefore National Government accord to people requiring high support – they are more than willing to leaving wallowing in our own shit!

Anyone following the campaign to SAVE the ILF led by DPAC and Inclusion London must know that we the major goal is to reopen the ILF to all people who fit their criteria.  In doing so raising the standard of those people’s support.  We believe this is the only solution not butchering the funding  of the so called “lucky” ones it in all honesty won’t help anyone.

I would love to know where the advocates of this Don’t Save ILF think the monies to raise everyone’ standards of support will come from. The money release from ILF we be swallowed up by incompetent politicians looking after their powerful votes, not us the people they view as worth less. In Authorities like Birmingham who have amassed debts of £600m you think the money given up by ILF will not even make a drip in their ocean of debt.

While I disagree with Simon’s argument I support his right to voice his opinion.  However, it is an understatement to say I am flabbergasted to hear Disability Rights UK supports this argument.  I thought you represented disabled people not the establishment!

What really exasperates me though is that we never learn from our mistakes.  Once more we are doing the governments work for them fighting between ourselves while they sit back laughing at us.  We must stop fighting and work together to defeat the Con-Dem coalition

I will finish with message to the camp supporting shut ILF.  If you can’t support don’t fight us.

Today we fight for our lives, if we lose today there will be no Tomorrow just an eternity of marginalisation and isolation either trapped our own homes or corralled in Care(less) Homes run by unscrupulous privateers only interested in profit not people

 

Thank you for listening  I hope you hear me!

 

see also: http://www.internaldpac.org.uk/DPACClone/2014/07/disability-rights-uk-independent-living-or-new-visions-in-neo-liberalism/

 

Jul 032014
 

 Hello comrades 

ALLFIE  (the Alliance for Inclusive Education) would like to put together some short and snappy videos on disabled peoples experiences of having Disabled Students Allowance and the impact it has had in helping them benefit from higher education on our lovely website – 

In particular we would like to focus on inclusion and participation whilst recognising that for some disabled students having the DSA means the potential of getting higher grades or getting a qualification whilst studying at university.  Also it be great to hear how DSA has supported disabled students who benefited from higher education even if they have not ‘passed’ their course.  

We would like to interview disabled people (young and old!) who  are thinking twice about going to university as a result of Government’s DSA reforms.

If anyone wants to know more about the DSA reforms please follow the link – http://www.allfie.org.uk/   Please scroll down to ALLIFE’s june briefing. 

If you are going to be around for the ILF tea party on Friday  – please let me know as I will have a small video camera to do the interview with.    I will be wearing an ALLFIE teashirt.     If you want to have a chat please ring me on 0207 737 6030 during Tuesday and Thursday.

 See u there, Simone Aspis.

Jul 012014
 

Urgent – Legal Challenge to PIP 20 metre descriptor to be held in Birmingham Administrative Court, Bull Street next week on July 9th and 10th.

 

The solicitors have asked for a room for observers to the case and are waiting for confirmation of that. They would like anyone who can to attend to show how important this case is to disabled people.

 

There will also be a vigil outside the court from 1- 2pm on July 9th. Bring placards, banners and friends and supporters.

 

To get updates on room availability and to check the case will not be affected by strike action on July 10th please email

birminghambenefitjustice@gmail.com

 

 

 

 Posted by at 21:30
Jun 172014
 

DWP ministers said only 9% of ESA decisions were wrong.  Our research reveals the DWP have been quoting from figures which state 151,800 appeals have succeeded.  Our evidence shows the true figure to be at least 567,634 – casting serious doubt over 43% of 1,302,200 ‘fit for work’ decisions. 
 

ilegal Press Release – 16th June 2013


DWP’s internal figures reveal a much higher number of successful ESA appeals than have been made publicly available.

article-2520639-19FD00E400000578-512_634x330

DWP reply on 13 June 2014 to a Freedom of Information Act request made as part of an investigation in to DWP figures relating to the controversial Work Capability Assessment by ilegal.org.uk has revealed that of 1,287,323 ESA appeals, at least 567,634 claimants have had the original DWP decision overturned in their favour.

Government’s key defence of the assessments has been that around 9% of all decisions are incorrect.  The most controversial of which are those where a claimant is found fit for work.  DWP figures (for new claims) show that betweenOctober 2008 and September 2013 a total of 1,306,200 fit for work decisions have been made.

It is with considerable disappointment noted that the DWP’s latest publicly available statistics confirm that only 151,800 successful appeals have been recorded out of a total of 410,400 appeals (for new claimants only).  Our investigations reveal evidence of three times as many appeals being ‘internally recorded’ of which
567,634 have been successful.  The DWP have revealed to us figures which show nearly quarter of a million internal reconsiderations have led to decisions on new ESA claims being overturned in favour of the claimant; we have added these to figures from HMCTS tribunals which provides us with a much higher figure than the DWP seems to be prepared to admit to in their publicly available figures.

Our intensive research into the assessment of claimants for the DWP’s Employment & Support Allowance (ESA) has, following a freedom of information request to the DWP, provided one of the final pieces of the jigsaw needed to unpick the Department’s overly complicated statistics. We now have the final clue which has enabled us to identify that no less than 567,634 ESA claimants have in fact had their initial ESA refusals overturned in their favour.

It is a startling revelation that the government department has apparently been keeping a lid on a set of statistics that clearly shows between May 2010 and June 2013 no less than 820,356 decisions were looked at again by the DWP after claimants had been assessed by the controversial private contractors Atos Healthcare. These ‘internal’ statistics show that a very substantial 232,782 (28.5%) decisions were then subsequently overturned in the claimant’s favour.

What makes this all the worse is that these reconsideration statistics come on top of separate figures that show us that of those claimants who did not have the decisions overturned in their favour by the DWP, 817,102 went on to appeal to tribunals arranged by Her Majesties’ Courts & Tribunals Service where a further 332,607 were then overturned in the claimant’s favour by the tribunal.

These figures completely negate all of the DWP’s claims that it is getting the majority of its decisions right

These figures completely negate all of the DWP’s claims that it is getting the majority of its decisions right. Government ministers in conjunction with the DWP’s Press office have been telling us that a million claimants have been found fit for work whereas these figures show that in reality this is only a small part of the true story and that huge numbers have gone on to successfully appeal decisions which were wrong.

These new figures highlight the dubious practice of using the unchallenged assessment results, which only encourage media sensationalisation, with headlines such as those appearing in the Daily Express in July 2011 stating that ‘75% on sickness benefits were faking’. The same article goes on to say that out of ‘…2.6 million on the sick, 1.9 million could work’ before receiving an endorsement from the Prime Minister with an assurance that his government was “producing a much better system where we put people through their paces and say that if you can work, you should work”.

DWP and Ministers know the truth, they just aren’t telling anyone

These figures have been available to the DWP and its ministers since April 2010 from their ‘Decision Making & Appeals Case Recorder (DMACR) – ESA Management Information Statistics’. The DWP confirms this to be unpublished information which is for internal department information only, yet our research notes that the Right Hon Chris Grayling was using the same information in answer to Parliamentary questions on the 10th January 2012. 

We question then why the DWP has consistently ‘over promoted’ only the results of Work Capability Assessments relating to ‘initial’ decisions (including the opinions of Atos Healthcare in the absence of a statutory DWP decision) when it could instead have come clean and declared how hundreds of thousands of their incorrect decisions have since been overturned in favour of the person appealing.

These revelations seriously undermine the DWP’s contention that the initial Work Capability Assessment outcomes are a valid measure of the claimant’s ability to work. The DWP has consistently defended its assessments by giving an impression that only a relatively low number of decisions have been overturned whereas the reality is that well over half a million have resulted in a successful outcome for the claimant.

And this DOES NOT include the 712,000 people awaiting assessments BEFORE they can appeal

This news must have come as cause for grave concern when considered in the light of a recent revelation by DWP Minister Mike Penning which revealed that in addition to the figures we have highlighted, a further 712,000 Employment & Support Allowance claimants are awaiting assessments without which they cannot yet appeal.

This hugely unacceptable backlog of cases means people with disabling medical conditions are left hanging for months and months on a basic allowance way below what they are entitled to. This is leaving hundreds of thousands deprived of the support they require and means having to scrape by on money which is wholly insufficient to meet their needs due to disability and illness. It also means many claimants affected by severe and complex mental health conditions are facing prolonged torment as they wait month upon month for their decision to be overturned before they can even lodge an appeal.

Face up to reality: it doesn’t work. Scrap the WCA

These findings add considerably to the pleas of disabled groups all over the country to scrap the Work Capability Assessment (WCA) and to find a better way to assess their needs.

It is simply appalling that the DWP, along with Ministers and other government spokespeople appear to be feeding the media with misleading statistics that are unrepresentative of the real story and instead encourage headlines vilifying the disabled and the genuinely ill. These figures clearly show the DWP has evidence in their possession which shows how in far too many cases the decisions it is making are dead wrong and they know they’re dead wrong.

Editorial notes

Please contact the author of this article Nick Dilworth for verification of any of the figures quoted.  We welcome sharing our findings on social media and allow this information to be produced providing credit is given to the
i-legal website with links to the article produced.

We apologise for the slight delay in publishing this release.  This was due to a need to align the figures to ones recently produced by the DWP in their Work Capability Assessment figures released on the 12th June 2014 which relate to the most recent statistics up to September 2013.

A full supporting explanatory memorandum will be published very shortly.

The Reconsideration statistics relate to new ESA claimants only (excluding incapacity benefit to ESA conversion cases) whereas HMCTS figures refer to all ESA claimants.  It is our contention that had the DWP supplied all of the information we had requested, the figures for reconsiderations would have been considerably higher.

We acknowledge that not all appeals will be against fit for work findings for new claimants but given the DWP’s emphasis on this claimant cohort and the lack of information to the contrary we are of the contention that other appeals relating to claimants being moved from the Work Related Activity Group to Support Group are likely to be of a much lower volume and more likely to be contained within the cohort relating to incapacity benefit/ESA assessment.

We would like to express our thanks to Anita Bellows an i-legal member for her cooperation and for making the freedom of information request upon our guidance and our thanks extend to the DPAC organisation with whom Anita is also a member.

http://ilegal.org.uk/thread/8640/release-staggering-numbers-overturned-secrecy?page=1&scrollTo=21759

with thanks as ever to Nick  @Mylegalforum

Jun 062014
 
Boycott Workfare is a UK-wide campaign to end forced unpaid work for people who receive welfare. Workfare profits the rich by providing free labour, whilst threatening the poor by taking away welfare rights if people refuse to work without a living wage. We are a grassroots campaign, formed in 2010 by people with experience of workfare and those concerned about its impact. We expose and take action against companies and organisations profiting from workfare; encourage organisations to pledge to boycott it; and actively inform people of their rights.

PCS need to ballot for non-cooperation on workfare and sanctions!

dpac-logo-3-amendment-1-smallblack-trianglebw logoMembers of PCS union work for the DWP and job centres so are involved in the day to day delivery of workfare and sanctions. Members have shown they oppose it by voting for national policy against workfare and sanctions. Now Disabled People Against Cuts, Black Triangle and Boycott Workfare are asking them to use their power to help put a stop to these punitive measures. 

Disabled People Against Cuts, Black Triangle and Boycott Workfare joint statement on PCS Union and non-cooperation:

1. We note that motion A81 that recently passed at the PCS conference makes reference to the PCS Union working with Disabled People Against Cuts and Black Triangle. (1)

2. We note that motions E340-E342 submitted by DWP branches also called for the PCS to work with Boycott Workfare, but that references to Boycott Workfare were dropped by the NEC from motion A81. (1)

3. Black Triangle and Disabled People Against Cuts wish to express their solidarity with Boycott Workfare who we believe have organised a broad based and successful campaign against workfare and sanctions.

4. We note that the legal advice received by the PCS in 2013 accepted that the tactic of non-cooperation could be used as part of a campaign of industrial action consisting of action short of a strike. (2)

5. We note that the PCS currently have a live mandate for industrial action and will be consulting members on 12th June about coordinated strike action. (3)

6. Disabled People Against Cuts, Black Triangle and Boycott Workfare therefore call on the PCS NEC to consult members on adopting a tactic of non-cooperation with workfare and sanctions.

References:

(1) http://www.pcs.org.uk/download.cfm?docid=3FBA9F5E-D8B1-4164-AA1B7CF5C50F3E33
(2) http://www.pcs.org.uk/download.cfm?docid=C20641E2-9DE4-4FFE-8E11590CCB7E0F51 (Motion A533)
(3) http://www.pcs.org.uk/en/news_and_events/pcs_comment/index.cfm/vote-yes-in-pcs-ballot-for-fair-pay

 Posted by at 22:48
Jun 042014
 

Disabled people’s experiences needed

Please send me short descriptions of disabled people’s experience on 3 employment related issues.   I can tidy the case studies up and make sure they are anonymous so you don’t need to spend too much time writing them up –  I just need proof of the points I’m making!  See details below:

·       If you have examples of Jobseeker’s Allowance (JSA) or Employment Support Allowance (ESA) claimants where the loss of £40/50 will have a serious impact on the ability to pay for food and other essentials please let me know. There’s a consultation on the increase of ‘waiting days’ for Jobseeker’s Allowance (JSA) or Employment Support Allowance (ESA).  Claimants will lose, on average, £40 or £50 respectively.  More information is at: http://ssac.independent.gov.uk/news/press-releases/23-05-14.pdf http://ssac.independent.gov.uk/consultations/

·       I also need examples of disabled people that have experienced difficulties either obtaining or maintaining Access to work e.g. cuts in their budget etc., changes to BSL interpreters conditions for the Access to work inquiry at: http://www.parliament.uk/business/committees/committees-a-z/commons-select/work-and-pensions-committee/inquiries/parliament-2010/access-to-work/

·       Lastly I would welcome recent examples (i.e. from beginning of Sept 2013) of difficulties caused by the WCA/ESA including issues around difficulties in paying bills due to benefit delays as above as well inaccurate assessments, lack of mental health champions or recording equipment or any other issues for the 5th and final review of the Work Capability assessment (to be announced shortly, see information below).   

 

Henrietta  Doyle

Policy Officer

Inclusion London

 

henrietta.doyle@inclusionlondon.co.uk

www.inclusionlondon.co.uk

Twitter: @inclusionlondon

 

 Posted by at 13:59
May 182014
 

ocap_logo_biggerDPAC_coloured_Logo_2__normal

If you’ve been following this on twitter and face book, you’ll know what a great success the first international #dpactour has been. The excellent Ellen Clifford of DPAC travelled to Canada at the invitation of John Clarke of Ontario Coalition against Poverty (OCAP).

John and OCAP have been great allies to DPAC, supporting us since 2012 ATOS Games protests, and DPAC was happy to return that support. We want to thank all for inviting us to share the knowledge of #dpac campaigns and actions, and the history of the unelected coalition Government’s appalling treatment and stripping of rights from disabled people.

The terrifying model of the coalition is spreading with punitive, harmful and potentially murderous regimes being taken up by other Tories at international and European levels. Canada have an election coming up and already plans similar to those carried out in Britain are starting to take shape. The Canadian people wanted to hear from #dpac on how they could increase campaigns and what was happening here to disabled people. Ellen and John did a tour letting people know what could be done, what has been done and how to fight it.

Remember: #internationalsolidarity, ‘fight to win’, ‘austerity is global so is our resistance’

With thanks to everyone involved we reproduce below some pictures from the #dpactour- more on the #dpactour to come..so watch this space

 

johnBm_SC6NCMAAhiZDBnEZ0Z8IEAApL5gBnKNjYeIcAASqw3BnjRGT0IIAAGlRKBnjSpx8IAAA8DE1BnjWpUlIQAA3AdPBnoVYa7IgAAIGtMBnrPXbnCMAAeNw8

May 132014
 

I went to the Work and Pensions Select Committee meeting in Newcastle today at the Newcastle FC in the Bobby  Moncur  Suite. Access to the building was fine although parking was a fair distance from stadium, but the best they could get. Signers and induction loop were available. I enquired with Sheila Gilmore MP the terms of reference for the meeting.

Dame Anne Begg opened the meeting which was to gather information from people on personal ESA/WCA experiences only. The meeting was well attended by individuals and also charities with case studies which were presented to the committee in report form. The horrors I listened to made me cry openly which is pretty hard I can tell you, as I’m not one for showing my emotions in public or private easily, and those who know me personally know this to be the case. The committee were also struggling to remain composed.  The committee had come to Newcastle because it had the highest complaints across the entire system, so decided a one off trip to hear from people was appropriate.

Many cases of failure were given and it was brought up time and again of fabricated reports, people being humiliated by HCP’s which we have known about for years. Many cases of suicide were mentioned , many cases of where the claimant was terminally ill yet denied what they were rightfully entitled to in their time of need and that documentation from GP’s /consultants were being ignored as ‘they know better’.

I mentioned the fear of ‘brown envelope syndrome’ and that disabled peoples’ voices were not felt to be heard and our human rights were being abused on a daily basis. I called the WCA a ‘wicked regime’ which has targets even if they deny so, and is cost cutting exercise and nothing more. I also brought up as did others the fact most people would work if they could but many cannot, as getting through a day by day basis was as much as many could cope with. I also asked where the jobs were for those  who wish to work and why those meant to help like Shaw Trust/Action for the Blind were also vilified by claimants for failures when they are supposed to help? Whether they could help as the claimants’ impairments mean that employers wont take  them on  so they are abandoned to their own devices.

It was mentioned frequently during the meeting about JCP disability advisors being no use and they also, didn’t understand conditions either; often bullying the claimant into jobs they can’t perform, and that education for those who needed to gain skills was being denied .

Decision Makers are trained by ATOS I found out today  so that is a conflict of interest  which I found disgusting  given the level of control they have over peoples’ lives and the  cumulative impact on a disabled person’s well being. I mentioned that this model used is flawed and didn’t take into account those with fluctuating conditions and the cost of tribunals and re-assessments of those with long term progressive illnesses , was a waste of taxpayers’ money unless changes had occurred .

I explained how we are demonised and treated as liars and criminals when, in actual fact all we are, is disabled or have a long term health condition. I asked why shouldn’t we be afforded the same rights as non-disabled people such as holidays which we have to save for, or have a pet , or go to the supermarket without the fear of being seen as a potential fraudster, when actual fraud was 0.8% including deptartmental error. I brought it up that many claimants have had support needs, financial and other, refused saying it wasn’t available.

On a lighter note the committee  were understanding, listening and attentive and genuinely DO CARE  and were encouraged by the turnout and assured us that those who sent in personal  stories were not being ignored by them and that they were ploughing through each and every one of them, but they would encourage any further submissions of case studies by groups or individuals.

I have to say I found today harrowing as much as I do daily on facebook the horror stories that people are suffering. It has to stop!

 

 Posted by at 21:17
May 042014
 

I’m at rock bottom right now and unable to go through writing it again. I have an appointment to see my MP tomorrow. I have copied and pasted an email I sent to his secretary earlier today. Dear Mary, I was going to write a brief summary of the main issues I’m facing right now and send them to you to save some time tomorrow, but it looks like all my benefits have just been stopped. I was due a DLA payment yesterday (Thursday 27th March) but it’s not been paid into my bank account. I signed on at the Job Centre in Stevenage on Tuesday, but the staff (My Adviser/Coach) doubt that I’m fit for work and think I should be on ESA.
I’ve done everything they’ve asked, searched for work everyday, applied for Jobs, even worked on a business plan to start my own business from home, I don’t know what more I could have done. DWP arranged an appointment for me with PLUSS a few weeks ago and after going there I felt quite optimistic, but when I went to sign on following that, their feedback was that they couldn’t help me because my health problems are too severe. I went to DAS (Depression and Anxiety Service) on 16th March, they can’t help with my Mental Health problems because they are too severe and complex.
Unless I say “I’m going to kill myself” I can’t get any help because local Mental resources are too underfunded and their caseload is too big. I DO NOT WANT TO GO INTO HOSPITAL and I would be extremely uncooperative if I was forced!!! Do you think this is Fair or Just??? What am I supposed to do??? My health problems are hard enough to deal with, without all this!!! I went from mid July last year up until a few weeks ago with nothing other than my £40 a week DLA to live on. I had £500 savings and a good credit rating before then, and a £950 overdraft which I never used until I lost my ESA at Tribunal. I got a statement from my bank this afternoon, I’m £921.12 overdrawn with an available balance of £6.20 (I don’t know how they do their maths?) I have £96 of overdraft charges being taken out of my account on 1st of April. I had come to an arrangement with housing people to pay back the outstanding rent arrears I owed when I started to receive JSA a few weeks ago and had promised a payment of £70 by tomorrow (28th March). DNRS have already tried to send the Bailiffs to my flat to take possessions for outstanding council tax arrears.
I’ve been to CAB numerous times recently. If this is how my life is going to be then what’s the point??? I can’t sleep at night because I’m so stressed out all the time, my health mental and physical are getting worse by the day. Everybody I’ve seen, my Job Centre Coach, CAB, My COPD Nurse and the Doctor I last saw (Dr Roper), PLUSS, DAS and my family ALL SAY I SHOULD BE ON ESA. I have an appointment tomorrow morning with my GP. I need immediate help, no more forms, no more appointments, NO MORE BULLSHIT!!! I refuse to live like this any longer, I can’t take anymore of the daily stress and injustice!!! I SHOULD NEVER HAVE BEEN IN THIS SITUATION FROM THE START!!! I’ve always been a fighter, I’ve had to survive but I’m totally exhausted now, mentally and physically… I HAVE TAKEN AS MUCH AS I CAN –
My appointment with my MP went well. I was already so angry to begin with made sure I made the most of my 15 minutes. I had written my main issues before hand so that I did not forget anything. To be fair I came away feeling he had listened to me and understood my situation. I was fluent in my arguments and never had any denial from him that what this government are doing to the most vulnerable people in this country is totally wrong. Since then I have applied for ESA again, all done over the phone this time, with help from my local CAB. My MP has also liaised with my GP so that I get to see the same doctor each time.

I have been to my local surgery twice since my meeting and the way I have been treated is 100% better. DWP asked me to get a letter from my GP to inform them of how many hours a week I was capable of working while claiming JSA. My COPD and mental health conditions have worsened considerably over the past few months and my GP signed me off sick saying in his opinion I wasn’t well enough to work, hence the claim for ESA. It’s like a merry go round and so frustrating and stressful it just makes my health and life in general suffer as a result. I stated strongly to my MP that I should never have been in this situation, and far from what Iain Duncan Smith claims to be doing. that he is helping people. My MP agreed.
I am due to receive my first ESA payment this coming Tuesday and looking forward to being able to eat properly again.

If I could give any advice to someone in a situation like mine it would be to get mad, make yourself heard with the right people. I am a fighter but fighting battles everyday to survive is tiring and wears you down. It either that or give in, I wasn’t prepared to give in with the injustices I had to face and wasn’t going to go without a fight.

Update: I received a letter this week from the DWP saying they were investigating my case. We will see what comes of it. I am still angry because of all the debt all this has got me into just trying to survive.
I will never forgive nor forget what this government has done to me and tens of thousands of others.

This is an edited version of a set of emails received by DPAC- all names and places have been changed and the author has given DPAC permission to use this to publicise the inhumane situations many are finding themselves in under the Condem regime

 

Apr 272014
 

Please support Obi and team to continue live-streaming direct actions and events for #dpac, #ukuncut and others. Live-streaming is important for disabled people that cannot always get to events and protests because none of us should be left out of our fight for our rights

It is also important in these times ruled by the right-wing press to get a record of our news and events-its time to fight back and ensure that our voices and protests are heard, recorded, documented and visualised -live-streaming does that- lets support it to continue the  real and uncensored news is seen and heard! Please donate if you can at http://www.gofundme.com/8nzi68

see some of the events live streamed for DPAC

JohnMcDonnell MP Praises DPAC at DPAC conference April 2014

August 5, 2012 Akira: update on ATOS. Paralympics sponsor

August 29, 2012 #ATOS #REMPLOY #ParaOlympics #2012 #Protest by previous gold medal winners

August 31, 2012 #ONN #OLSX covering anti #ATOS #ATOSkills #dpac event at Triton Square, Camden

October 28, 2012 Akira and experiencing Public Transport for a Wheelchair user.

September 3, 2013 DPAC AND BLACK TRIANGLE DIRECT ACTION. BBC PORTLAND PLACE, LONDON

September 5, 2013 DPAC FREEDOM DRIVE.

June 4, 2013 DPAC Bromley Benefit Justice second Meeting

September 26, 2013 10,000 Cuts and Counting

October 5, 2013 SOLIDARITY ACTION WITH UKUNCUT AND DPAC #ROADBLOCKS4JUSTICE

Oct 20, 2013 The DPAC action in Marble Arch . TUC March 2012.

September 28, 2013 DPAC DIRECT ACTION: 10,000 CUTS AND COUNTING. SCRAP ATOS

@Obi_Live
@OccupyNN

https://twitter.com/Obi_Live
https://twitter.com/OccupyTTIP
occupylondon@lists.riseup.net

 

Apr 212014
 

DPAC would like to thank everyone for making last week’s (April 12 2014) National Conference such a huge success. There was a huge turnout with over 150 disabled activists from all over the UK including many new DPAC members attending, but just as important there were hundreds of members and supporters beyond the venue taking part through social media – watching the video live-stream, tweeting and sharing comments, views and sending messages of support. This was fantastic work by everyone and a truly inspiring collective effort.

DSC_1030 con

Here’s a brief outline of how it went.

Programme
The day was timetabled into sections beginning with practical reports and voting on policy motions. This was followed by two workshop sessions and then a closing session for everyone to feedback on the day. Four workshops were available to choose from in each Workshop session. Detailed reports on these will follow later.

John McDonnell MP, a longstanding friend and supporter of DPAC, gave a rousing opening speech to encourage everyone and remind us of the victories achieved so far. He congratulated disabled people and DPAC for fighting back, along with our sister organisation Black Triangle and WoW Petition initiators

As he finished he mentioned his own recent health condition which he said he felt brought him closer to our movement. Ellen reacted quickly by giving him a DPAC t-shirt and declaring him a full DPAC member to instant applause and cheers.

photo1jm tshirt

Finances
The Finance Report showed a healthy state of affairs for the time being thanks to individual donations, t-shirt and badge sales plus grants from the Edge Fund, the Network for Social Change, Trust for London  and the Andrew Wainwright Trust. More fund-raising is necessary going forward.

Motions
1. Government Honours
This proposed that any future candidates for the DPAC Steering Group could thwart the network and collective ethos of DPAC if they had received a national honour like an OBE or MBE. The ‘BE’ refers to the imperialist British Empire which is still celebrated despite what we know of the suffering and oppression this caused. The motion conversations also suggested that any media attention would be focused on those with honours and titles, rather than on the collective network ethos that DPAC ascribes to. The motion was put forward as a rejecting of this possibility and that of the honours system more generally. This was defeated.

2. Discrimination
This motion stated DPAC opposition to discrimination on the grounds of gender, sexuality, age, faith, disability, ethnicity or status. It also empowered the Steering Group to terminate the membership of anyone who supported a party which holds discriminatory policies, like UKIP. This motion passed based on an appeals process being put in place

3. Steering Group Size
This motion sought to expand the Steering Group from 8 members to 12 in order to respond to increased activity and maintain a broad, diverse and inclusive profile. This was passed.

Steering Group
There were 11 nominees for the Steering Group. Conference took a vote on whether to vote for accepting all 11 nominees, or vote for them one by one. Conference voted to accept all 11 nominees. The new steering group are currently reviewing co-opted places and will get back to the additional people that applied past the deadline as soon as possible

Steering Group:
Andy Greene
Bob Ellard
Ciara Doyle
Conan Doyle
Debbie Jolly
Eleanor Firman
Ellen Clifford
Linda Burnip
Paula Peters
Roger Lewis
Sabina Lahur

It was highlighted that the working groups are important in taking DPAC forward. The co-chair said she hoped those who did not stand for the Steering Group but were still interested in getting involved would join these as soon as possible.

Finally, a big thank you to the Conference Organising group and Workshop leaders who worked so hard to make this wonderful event a reality.

Links to videos from the day are here with thanks to Occupy for live streaming on the day to make the conference inclusive to all are here

Links to pictures can be found on DPAC flicker here
Thanks to Pete Riches, Szucs Gabriella and Rob Peters

The powerpoint on highlights of the last year can be found DPAC Report
A link to 2013 and some of the things DPAC did is here

See you on the streets!

DPAC www.dpac.uk.net
Twitter: Dis_ppl_protest
Also find us on Facebook with a group and open page under ‘Disabled People against Cuts’

contact: mail@dpac.uk.net

 

Apr 182014
 

We read with interest the piece in the Independent by Rachel Reeves and Kate Green regarding Labour’s response to the Work Capability Assessment [1]

Labour should realise that disabled people are deeply distrustful of any Labour reform of a Work Capability Assessment system, which Labour introduced in the Welfare Act of 2007 with the stated aim of removing 1 million claimants from the benefit system [3].

Our position has been and will be that the Work Capability Assessment is deeply flawed in its basic concept, not just in terms of the details of its delivery, and inclusion in the workplace for disabled people cannot simply be achieved by a ‘back to work’ test.

manifesto

In the Reclaiming Our Futures, Disabled People’s Manifesto [4], we state that a priority demand from government is that:

A comprehensive and strategic plan of action is developed with disabled people and our organisations to tackle the discrimination and exclusion disabled people face in work and employment including: increasing quality and range of personalised support available to disabled people, strengthening disabled employees rights and tackling employer discrimination and poor practice

Other key demands include that:

Economic productivity must not be the only measure of people’s worth and value, volunteering offers as much value to society as paid employment. While we recognise that volunteering can offer additional skills, it should not be the default option for disabled people because of our exclusion from paid work

There must be policy and media recognition that there will always be disabled people who are unable or too ill to work. These individuals must be supported by a publically funded system. They should not be penalised or demonised as they are currently.

For true inclusion in the workplace for disabled people a wider approach is necessary including but not limited to:

• Will Labour commit to the restoration of Disabled Student’s Allowance,
• Will Labour commit to the restoration of the Independent Living Fund,
• Will Labour commit to the extension of Access to Work (AtW) to include unpaid voluntary positions,
• Will Labour commit to the reversal of the reduction of people who currently receive DLA, but will not receive PIP and also lose their Motability access,
• Will Labour commit to the reinstatement of the requirement for councils to produce equality schemes on employment and access
• Will Labour commit to the provision of accessible transport.
• Will Labour commit to the reinstatement of “day one” protection from unfair dismissal in employment law
• Will Labour commit to the provision of Employment Tribunals enforcing mandatory organisation-wide measures on preventing disability discrimination
• Will Labour commit to the provision that all government contracts, at a national, regional and local level, are only awarded to companies that are fulfilling measurable equality targets for the employment of disabled people

(for further points see reference 2)

These currently are some of the barriers to inclusion in the workplace for disabled people, and they will not be fixed by simply amending the WCA. The issue must be seen within the context of the wider interconnected system of barriers in place. It must be seen in terms of what a large majority of disabled people have already identified as key problems.

In terms of inclusion we also need from Labour, a recognition that for many disabled people to be able to work there has to be a nationally transportable social care system with a guarantee that people would keep the same levels of funding wherever they needed to move to work.

We need recognition that there is an onus on government and employers to fully accept the spirit of the Equality Act 2010 [4] with its requirement to the opening of work opportunity to disabled people. Without this, no “fit for work test” aimed at cutting disability benefits will make any impact whatsoever on the numbers of disabled people who can attain and sustain employment.

We also need from Labour a stronger recognition that there are many disabled people who cannot enter the work place and should not have to live in fear of being pressured into doing so.

There is much that the article leaves out and that leaves us with a number of serious concerns and questions.

While we are not yet prepared to endorse in any way Labour’s new approach to the Work Capability Assessment, we do see the article by Rachel Reeves and Kate Green as a helpful starting point for discussions on the future of inclusion of disabled people, who want and are able to work, in the workplace and we would welcome an opportunity to meet with them and discuss this further. We would like meet with Kate Green and Rachel Reeves to ask the following questions:

1. Will Labour commit to stop spending public money on private
contractors and return any assessments of disabled people back to GPs
with medical evidence taken into account as well as give a commitment to
look at the barriers to work for disabled people who can and want to
work (in line with the social model of disability)?

2. Will Labour commit to a time and date to talk with DPAC, My Legal,
the Mental Health Resistance Network, Black Triangle, Deaf activists,
those with learning difficulties ( with an outreach of ½ a million
disabled people) to listen to the views of the largest network of grass
roots disabled people on the WCA and ESA?

3. If Labour are committed to scrapping the WCA when will Deaf and
disabled people, and those with mental health issues have sight of the
detail of any alternative Labour is proposing?

4. If Labour accepts the harm, devastation and premature deaths that have
been an outcome of the WCA why have they chosen to suspend their
prospective parliamentary candidate for St Austell and Newquay, Deborah
Hopkins for speaking out in public about the harm caused by the WCA.

5. Will Labour address the disproportionate harm that the WCA and
sanctions on ESA and JSA are causing to all disabled people, in
particular those with mental health issues and learning difficulties?

6. We along with many others insisted that a centralised Independent Living Fund
for Scotland be established and it has been done. They have also promised to re-open ILF to new users, with a commitment of additional funds and recognition of its importance to independent living and obligations to article 19 of the UN Convention on the Rights of Persons with Disabilities. Why has the Labour
Party not promised to re-establish it south of the border?

Many of the Statements included in this response are taken from the UK Disabled Peoples’ Reclaiming our Futures Manifesto and are endorsed by a UK network of disabled people and Deaf and Disabled Peoples Organisations, including: ALLFIE, Inclusion London, Equal Lives, DPAC, Inclusion Scotland, Disability Wales and the TUC Disabled Workers Committee [2], who between them reach several million disabled voters.
References
1. How Labour would reform the Work Capability Assessment http://www.independent.co.uk/voices/comment/how-labour-would-reform-the-work-capability-assessment-9265479.html
2. The Reclaiming Our Futures, Disabled People’s Manifesto http://disability-studies.leeds.ac.uk/files/library/UK-Disabled-People-s-Manifesto-Reclaiming-Our-Futures.pdf
3. The Green Paper: The new deal for welfare: Empowering people to work. 2006 http://webarchive.nationalarchives.gov.uk/+/http://dwp.gov.uk/docs/a-new-deal-for-welfare-empowering-people-to-work-full-document.pdf
4. Equality Act 2010 http://www.legislation.gov.uk/ukpga/2010/15/contents

 

Apr 142014
 

Are you interested in challenging the government’s huge increase in court fees?

We need people eligible for legal aid to get in touch with Karen before the 22nd April

Don’t let them get away with it without challenge!

The fee hike – coming in later this month – will affect people bringing a wide range of civil cases, including consumer claims, family cases, personal injury claims, landlord-tenant disputes, and private discrimination cases. It means that only those with deep enough pockets to afford these expensive new fees will be able to take cases to court to uphold and protect their rights.

If you think you might be eligible for Legal Aid and are interested in acting as a claimant in a judicial review challenge to the new fees then please contact me directly karenpassmore@hotmail.com

With your contact details

Thank you, Karen

 

Apr 072014
 

DPAC_coloured_Logo_2__biggerWe are very much looking forward to seeing everyone who can come to our national conference on Saturday but it is also important that those of you who can’t get there in person are able to take part. There are a number of ways you can do this:

  • Send messages of support and your ideas for what DPAC should focus on over the next year to mail@dpac.uk.net or @dis_ppl_protest.These will be put up on the graffiti wall at the conference and included in the notes from the day.
  • Watch the conference live on:

http://bambuser.com/channel/OccupyLondon and http://bambuser.com/channel/DPAC

  • Live tweet your questions and contributions to @dis_ppl_protest

  Or email: mail@dpac.uk.net

 The program for the day is at DPAC Conference 2014 Saturday 12th April – Conference Programme

Apr 052014
 

Defend Independent Living Rights

 Stop the Closure of the Independent Living Fund

 Stop Disability Cuts

 The European Network on Independent Living is calling on disabled people’s organisations across Europe to mobilise together on or near Monday 5 May 2014 through events, lobbying and protests to oppose the deep and ongoing cuts affecting disability services and benefits.

 As disabled Independent Living Fund users, close family members and allies campaigning to defend independent living rights and stop the Fund’s closure, we urge disabled people’s organisations and the broader disability movement in England, Wales, Scotland and Northern Ireland to actively support this important day.

 Even small events and public activities will help to raise awareness and act as a focal point for those who want to work together to oppose cuts to services and benefits, including the proposed closure of the Independent Living Fund in fifteen months.

 It is vital that we also use this opportunity to reflect and learn from the mistakes associated with the public service reforms of a decade ago and the policies of ‘welfare reform’ and ‘personalisation’, including the use of ‘tick-box’ processes such as the Work Capability Assessment and the Resource Allocation Systems in social care to replace the individual and detailed assessment of need.

 The fear of a ‘demographic time-bomb’ associated with growing numbers of older disabled people in their eighties and nineties, creating an age imbalance in a static or falling population, has been used to justify the raising of the pension age and the way pensions are calculated, the erosion and privatisation of the ‘welfare state’, cuts to health and social care, changes to the benefits systems, and latterly ‘austerity’.

 But a growing population associated with increasing birth rates and the immigration of young adults, improved productivity and the greater fitness and activity levels of older people means the ‘demographic time-bomb’ in Britain may be a myth.

 The political climate that has undermined independent living and disability rights, and is using positive ideas such as ‘direct payments’ and ‘individualised funding’ as vehicles for shifting financial responsibility for meeting social care needs from the state to the individual needs to be challenged.

 We should no longer ignore the needs of the tens of thousands of children who are compelled by their family circumstances to be ‘young carers’ or the four hundred thousand disabled people confined to residential care or the way new concepts such as ‘prevention’, ‘reablement’ and ‘recovery’ are used to deny hundreds of thousands of disabled people the services they need.

 Those who argue disabled people have been ‘liberated’ and the welfare state is ‘broken’ are wrong, and only do so in pursuit of a very negative agenda associated with privatisation and greater inequality between the ‘haves’ and ‘have nots’. The same people have been passive while the Independent Living Fund has been dismissed as ‘anachronistic’ and ‘paternalistic’, and the experience and wishes of the Fund’s users and their families ignored.

 The disabled people’s movement across England, Wales, Scotland and Northern Ireland has a proud history of campaigning for independent living rights, but the gains of a generation ago for disabled people of working age are now under threat, as are the social opportunities pursued by many disabled people with complex conditions.

 The innovations of the ‘independent living movement’ such as the ‘personal assistance’ approach, specialised information and training, and the self-assessment of personal needs have been marginalised. While our organisations and projects have struggled financially since the millennium, tens of millions of pounds have flowed towards those who supported the development of ‘personalisation’ and its ‘evidence base’.

 But what is perhaps worst of all is many of those severely disabled people who have assumed the demanding responsibility of organising and managing their own complex personal assistance support, and do so fifty-two weeks a year without any financial rewards, are defined as being ‘economically inactive’.

 A jigsaw of social equality has been slowly constructed since the end of slavery and the emergence of the Chartists through the right to vote, women’s suffrage, universal healthcare, the legalisation of same-sex relationships, reproductive rights for women, equal pay legislation, and the outlawing of racism and homophobia.

 Limited advances in tackling disability and age discrimination are now being reversed, with the statutory right to an individual assessment of need by local councils being replaced. Local authorities are to be given the power to restrict a disabled person’s rights or freedom of action in pursuit of a legal duty to prevent or reduce a person’s need for social care services or personal assistance.

 Social equality for all will never be achieved unless the needs of disabled children and adults are acknowledged, assessed and met as of right, and those children and young people compelled into a caring role within their family because of a lack of social services support are freed from this and allowed to develop socially in the same way as their peers. But this would require an unparalleled redistribution of wealth, and the redrawing of our society’s social priorities.

 We believe disabled people of all ages should: have the right to live in the community free of the threat of segregation; be supported to stay healthy, safe and free of distress; and be freed from the harsh means-tests that are a feature of social care. Young disabled people in particular should be supported to pursue their dreams and aspirations free of the social barriers and discrimination that impeded many in the past. And because of the vital social role played by full-time family carers, they should be paid a social wage of at least fifty percent of the average wage of a skilled worker.

 Our movement has a collective responsibility to defend the gains we have made, and renew its commitment to campaign for full civil and human rights for all disabled people and their families.

 The ‘European Independent Living Day’ is an opportunity we should not waste.

 Abi Vanes, sister of ILF user

Aine Young, family of ILF user

Alma Lunt

Andy Greene, Islington Disabled People Against Cuts

Angela Mountstephens, sister and carer of an ILF user

Ann Walawalkar, parent of an ILF user

Anne Novis MBE

Anne Pridmore, ILF user and Director of ‘Being the Boss’

Anne Rae, Chair of Greater Manchester Coalition of Disabled People

Ann Rainey, ILF user

Anne Whitehurst, ILF user

Anita Bellows

Ashleigh Myatt, personal assistant

Bill Riddall, Centre for Independent Living Northern Ireland

Brian Glaves, family carer and husband of ILF user

Brian Hilton, ILF user

Bob Ellard, member of Disabled People Against Cuts

Brenda Bayliss, mother of an ILF user

Caroline Kelly

Caroline Martin, mother of an ILF user

Cath Gibson, ILF user

Charles Rainey, brother and carer of an ILF user

Christine Pickthall, ILF user

Christine Squires, ILF user

Christine Stringer, parent of an ILF user

Clare Palmer, mother of an ILF user

Colin Griffiths, ILF user

Colm Murphy, family of an ILF user

David Vanes, brother-in-law of ILF user

Debbie Domb, ILF user

Debbie Jolly, co-founder of Disabled People Against Cuts and Board member of the European Network on Independent Living

Dessie Allen, brother of ILF user

Dolores Hannigan, ILF user

Ellen Clifford, Disabled People Against Cuts

Emma Dakin, ILF user

Fred Bayliss, father of ILF user

Gabriel Pepper, ILF user

Helen Brown, personal assistant

Ian Atkinson, Gateshead Access Panel

Ian Kenny, ILF user

Jacqui Armston, personal assistant

James Corker, carer of ILF user

Jan Turner, Project Manager of ‘Being the Boss’

Jean Allen, mother of ILF user

Jean Glaves, ILF user

Jenny Hurst, ILF user

Joe Whittaker

John Aspinall, ILF user

John Buckley, parent of an ILF user

John Gilliland, father of ILF user

John Kelly, ILF user

Juliet Marlow, ILF user since 1991

Kieran Coffey, ILF user

Kieran McCarthy M.L.A. Strangford (Northern Ireland)

Kieran Walawalkar, ILF user

Kristine Cope

Laura McCrum, ILF user

Lianne Bayliss, ILF user

Linda Burnip, parent of an ILF user and co-founder of Disabled People Against Cuts

Lise Marron, ILF user

Mandy Dexter, personal assistant

Margaret Coffey, mother and carer of ILF user

Maria Nash, ILF user

Marie Thompson, sister of ILF user

Mark Williams, ILF user

Michael Bayliss, brother of ILF user

Michelle Allen, personal assistant

Mick Hutchins, ILF user

Neil Bayliss, brother of ILF user

Niqi Rainey, sister-in-law and carer of an ILF user

Paul Taylforth, step-father and carer of ILF user

Paula Peters, Disabled People Against Cuts

Peter Coffey, father and carer of ILF user

Peter Steele

Philomena McCrory, Centre for Independent Living Northern Ireland

Rahel Geffen – CEO Disability Action in Islington

Richard Parker, ILF user since 1991

Rob Punton, ILF user, Community Navigator Services and Disabled People Against Cuts

Robert Allen, ILF user

Ronnie Allen, brother of ILF user

Rosemary Kelly, ILF user

Rosemary O’Neill, CarerWatch

Roxanne Homayoun, ILF user

Sam Whalley

Sean O’Hare, ILF user

Sophie Partridge, ILF user

Stuart Bracking, ILF user

Sue Lovett, English Campaign for a Fair Society

Surojit Walawalkar, parent of an ILF user

Theresa Murphy, family of an ILF user

Tracey Lazard, Chief Executive of Inclusion London

Ursula Corker MBE, carer of ILF user

Valerie McCarthy, sister and carer of an ILF user

Vin West, parent and carer

Wendy Mortimer, personal assistant

 

Apr 042014
 

We’ve had a great response to bookings for the DPAC conference on Sat 12th April in London, but places are now running out. Please email:  dpacfightback@yahoo.co.uk

with your details, number of places needed and any access needs.

12th April 2014 – 11am until 5pm

London Met University, Tower Building, 166 – 220 Holloway Road, London, N7 8DP

Since we started in October 2010 Disabled People Against Cuts has been at the forefront of the fight against austerity. With Atos on the run, and the bedroom tax on the ropes we are seeing the results of hard campaigning. But there is much more to do to ensure disabled people’s rights to live independently and with an adequate income.


The national conference is a chance for DPAC members to come together, to share experiences and discuss your ideas for moving forwards.


DPAC are working hard to bring to conference a surprise guest, a person who, if anyone has, has been the catalyst for the re-emergence of disability activism in the last few years, someone DPAC has enjoyed a close relationship with from visiting him at home to donating underpants to supporting his select committee appearances.


Workshops will look at: –  Where Now for the Independent Living Fund campaign,  – Developing a Social Model of Distress,  – Winning the Argument,  – Disability, Art and Protest,  – Building a National Network of Disabled People’s Organisations and Direct Action practical skills among others.

 Please note places are limited so priority will be given to DPAC members. For information about joining please contact mail@dpac.uk.net

The venue is wheelchair accessible. BSL and a note taker will be provided. For access information go to: http://www.disabledgo.com/access-guide/islington-council/london-metropolitan-university-tower-building

For access queries including booking parking please contact DPACfightback@yahoo.co.uk
To book places or for more information please contact DPACfightback@yahoo.co.uk

 

 

 

Apr 032014
 

For those of us that can’t be there at the demo on Friday at 11.00. We must support Focus E15!

Yet another example of the misery and inhumanity heaped on ordinary working-class people, women and children by the anti-welfarism agenda. An agenda that is taking and blighting lives, an agenda that sees people without any right to decent housing for their children, and ripped from their families and friends by a program of social cleansing.

Our silence is complicity and agreement- our support shows we will not accept this!

Please tweet from here http://dftr.org.uk/FocusE15

What the Newham Mothers say:

We have been told we will not be offered council housing but that we will be offered private rented accommodation from accredited landlords outside of London in places like Hastings, Birmingham and Manchester. If we refuse this offer, we will be classed as making ourselves intentionally homeless and face temporary accommodation with little protection from eviction and no guarantee of a long-term solution from the council. Also if we chose to rent privately we are not entitled to get sufficient help with deposits which we cannot afford ourselves.

We want secure and suitable housing for mothers in east London!

‘This life is stressful I understand why people take their lives. Even more stressful if we’re young. We want to work or study, we’re not lazy, we don’t want to be on benefits forever, and we want to raise our children ourselves. Children need stability, moving is traumatic, for anyone, especially children.’

‘Our children need to know their grandparents, their cousins, their families.’

‘I have stopped looking for places as I have been rejected so many times’

‘You’re not tearing us apart from our families….we are fighters’

Sign the petition here: http://www.change.org/en-GB/petitions/robin-wales-no-eviction-from-focus-e15-suitable-permanent-social-housing-in-london-not-in-the-private-rented-sector-and-all-discussions-and-negotiations-to-be-held-with-all-the-affected-mothers-present

To read more on Focus E15 see links

http://www.opendemocracy.net/opensecurity/kate-belgrave/focus-e15-young-mothers-struggle-for-universal-housing

http://falseeconomy.org.uk/blog/young-mothers-occupy-newham-council-to-fight-for-social-housing-for-all-foc

http://uclu.org/policy/up1321/focus-e15-mothers

http://anticuts.com/2014/03/19/current-struggles-focus-e15-mothers/

 

 

Apr 022014
 

We are pleased that the DPAC research team’s submission to the Work and Pensions Committee has been accepted and published. We especially want to thank Anita Bellows and Bob Ellard for all their hard work on this.

Great to see submissions from our sister organisation Black Triangle, our allies, Inclusion London, WoW, Nick and Carer Watch.

We are disappointed that no formal national organisation of disabled people claiming to be run and organised by disabled people based in England appears to have submitted any text on this important issue.

The link to see all submissions is http://www.parliament.uk/business/committees/committees-a-z/commons-select/work-and-pensions-committee/inquiries/parliament-2010/esa-wca-inq-2014/?type=Written#pnlPublicationFilter

You need to scroll down the page.

We reproduce DPAC’s submission below for ease of reading

Written evidence submitted by Disabled People against Cuts (WCA0152)

 

Who we are:

DPAC is a grass roots campaign body. It was formed by a group of disabled people after the first mass protest against the austerity cuts and their impact on disabled people held on the 3rd October in Birmingham 2010, England. It was led by disabled people under the name of The Disabled Peoples’ Protest. DPAC has over 12,000 members and supporters and works with many anti-cuts groups, Universities, Disabled Peoples’ Organizations, and Unions

Introduction

1.    This document contains the Disabled People Against Cuts (DPAC) submission to the Work and Pensions Committee call for evidence on ESA and WCA dated 21/3/14

2.    This submission contains a number of areas of ESA and WCA that we believe demonstrate why the ESA system is fundamentally flawed both in concept and implementation and should be scrapped with immediate effect.

3.    All of the statistical claims made in this document have links provided to verifiable sources

 

WCA Descriptors

 

4.   The WCA descriptors are the criteria used to assess whether a claimant has limited capability for work, in other words whether a claimant falls within the eligibility criteria for claiming ESA, or not.

5.   The descriptors define a set of functions related to work tasks, which, if the claimant can perform to an adequate standard, the claimant is considered able to perform some paid work and therefore not eligible to receive the ESA Benefit.

6.   However we believe that the criteria for ESA eligibility are disingenuous. They take into account only functional ability, NOT the ability to hold down a job in practical terms.

7.   They do not consider such issues as:

·  Is the claimant able to work for suitable number of hours a week

·  Is the claimant able to travel a reasonable distance to and from  a job, consistently, every day.

·  Is the claimant robust enough to hold down a job, without taking an unreasonable amount of sick leave

·  The cumulative effects of physical stress on claimants with physical health conditions which induce fatigue symptons

·  The cumulative effects of mental/emotional stress on claimants with mental health conditions

·  The physical/emotional/mental stress of seeking a job

8.   Nor does it consider what physical discomfort or pain, or emotional or mental pain the claimant may encounter while employed.

9.    The WCA does not represent a finding on whether or not the claimant is employable or whether the claimant will be able to find work.

 

The ‘Gap’ between ESA and JSA Criteria

 

10.               While the WCA is commonly called a “fit for work” test, it does not actually test whether a claimant is fit for (ie capable of doing) work.

11.               The WCA tests whether claimants have the ability to perform certain limited work related functions as defined by the WCA Descriptors

12.              Whereas the criteria  for eligibility for the alternative benefit Jobseekers Allowance include the clauses that a claimant must be:

·                        be able and available for work

·                        be actively seeking work

13.              Thus is stands to reason that there are many who will be found ineligible for ESA but not able to meet the practical requirements being able to find and hold down a job and are thus ineligible for both benefits.

14.We do not know how many claimants have found themselves in this position, as the government do not monitor this, and provide no statistics from which we can exptrapolate or estimate a number, but we believe that there will be a significant number of Disabled claimants who fall into this trap and are denied income from either ESA or JSA .

 

Health Care Professionals performing the WCA

 

15.              The majority of Healthcare Professionals that perform Work Capability Assessments on claimants are Nurses, Physiotherapists and Occupational Therapists, with a lesser number of Doctors and “Mental Function Champions”

16.              While we do not dispute that these Health Care Professionals are qualified and have experience as Nurses, Physiotherapists, Occupational Therapists, etc, we do dispute that this is sufficent to judge a persons’ capability to work, given the panopoly of condition types that any Healthcare professional will be required to assess.

17.              The range of condition types that an HCP will be presented with include:

·                        Stable Physical Conditions

·                        Fluctuating Physical Conditions

·                        Mental Health Conditions (ranging from mild to extremely severe)

·                        Behavioral Conditions

·                        Cognitive Conditions

·                        Learning Conditions

·                        Autism Spectrum Disorders

·                        Degenerative Conditions

·                        Physical Conditions where the claimant is expected to return to full health

·                        Terminal Conditions

18.              In addition it is not uncommon for claimants to simultaneously have multiple condition types such as a mental and physical health condition.

 

WCA and mental health

 

19.              From the start, the descriptors were recognised as inadequate at capturing the level and the complexity of mental illnesses, and the problems faced by claimants in making a claim or an appeal were already recognised by Judge Martin in his 2008-2009 Report:

20.              ‘Mental health issues are a continuing source of problems in terms of making claims and assessing the impact of mental health issues on disability. In some cases mental health issues were not fully addressed or given due weight’.

21.              Following Professor Harrington’s recommendations, DWP accepted to amend the descriptors to better capture mental health issues and to introduce Atos Mental Function Champions in each assessment Centre to ‘spread best practice amongst Atos healthcare professionals in mental, intellectual and cognitive.  Although it has led to an increase of claimants with mental health issues being awarded ESA, and especially being placed in the Support Group, the statistics tell a different story. 

22.              Official DWP figures confirm that in the 2008 quarter from June to August, two months before Employment & Support Allowance was introduced, 153,050 claimants took up a claim for incapacity benefits, around a third of them (56,730) on the grounds of mental and behavioural problems. 

23.              By the end of the November 2012 quarter, the number of claimants taking up or being transferred on to Employment & Support Allowance had spiralled to 316,950 claims with nearly 140,000 of them (135,990) making a claim on the grounds of mental and behavioural problems – nearly 3 times as many as four years previously, but also representing a higher proportion in the total number of claims (44% against 37%). 

24.In the November 2012 quarter, 25,950 of the claimants who took up a claim ESA on mental health grounds had been on the allowance on one or more previous occasions. These figures show a perpetual cycle of claimants and reclaiming, those with mental health problems being by far the most susceptible to making a re-claim.

ESA claimants with mental illness are disproportionally sanctioned

25.              The latest DWP statistics on Employment and Support Allowance published in January 2014 show in Table 7 the Outcomes at initial functional assessment split into International Classification of Diseases.

26.              The total number of ESA claimants is 834,500 (WRAG 467,400 + SG 367,100), of which 339,200 (WRAG 193,100 + SG 146,100) of them fall under the Category ‘Mental and behavioural disorders’. It means that this group of claimants accounts for 40% of all illnesses, but because 193,100 (57%) have been placed in the WRAG, proportionally, this group is already more exposed to sanctions than any other groups. 

27.              A recent response to a FOI request confirms that claimants with mental health issues are not only sanctioned disproportionally, but also exposed twice to more sanctions and hit harder than any other groups.

28.Even before the introduction of the stricter sanction regime, there were already a higher number of claimants with mental health issues being sanctioned. But the latest figures disclosed show that 5,940 claimants with mental health issues were sanctioned out of 10,210 ESA sanctioned claimants (58%) in 2013. 

29.              The figure in 2012 was 54% when these claimants only account for 40% of all illnesses.  Since October 2011, on average the rate of sanctions for claimants with mental and behavioural conditions has been exactly one third (33%) higher than for other claimants, as the graph shows[1].

index

 

30.              This is a trend, for which the Citizens Advice Bureau had already provided anecdoctal evidence,

31.              ‘Bureau experience is that vulnerable clients (e.g. those with mental health problems or minor learning difficulties) are disproportionately sanctioned.’ (http://www.citizensadvice.org.uk/citizens_advice_bureaux_foodbank_survey) but which is now confirmed by DWP statistics.

32.              This has to be seen in the context of the number of people with mental health issues placed onto the Work Programme. The latest Work Programme statistics (20th March 2014) show that this group constitutes the majority of ESA claimants on the Work Programme (65%), although as noted previously they account for only 40% of illnesses.

33.              Not only are a disproportionate number being placed in the WRAG, but an additional disproportionate number are being put onto the Work Programme, compared with ESA claimants with other illnesses or disabilities. The job outcomes for this group, as shown by the latest statistics, are very poor: only 4,2% of the 131,480 claimants referred to the programme in this group have a job outcome.

34.              Not only is the WCA failing people with mental health issues by putting a disproportionate number of them in the WRAG on a shorter prognosis, and a disproportionate number of them onto the Work Programme, resulting in very poor job outcomes, but it also seems that because of the nature of their illnesses, they are the claimants having most difficulty adhering to the conditionality regime, or that they are seen by Job Centre staff as easy targets for sanctions as documented by the CAB, leading to a disproportionate number of them being sanctioned when compared to other ESA claimants.

35.              Ultimately, they would be the very people whose health is likely to worsen as a result of the failings of the WCA and of the consequences of having been put into the WRAG. 

 

WCA Appeals

36.              The latest figures published by Her Majesties’ Courts & Tribunals Service in March 2014 show a dramatic reduction in the number of Social Security & Child Support appeals lodged directly with Tribunals. This is the result of the introduction of ‘Mandatory Reconsiderations’ which is a DWP internal dispute resolution process, aimed at reducing the number of appeals directly lodged with Tribunals.

37.              These Mandatory Reconsiderations have had a substantial effect on the number of appeals lodged against an ESA decision. Only 32,969 ESA appeals were received between October and December 2013 compared with 111,817 in the first quarter of 2013/2014 and 76,456 in the second quarter.

38.              The number of ESA appeals ‘cleared at hearings’ in the third quarter of 2013/14 has significantly increased with 83,202 being heard, of which 45% were in the claimant’s favour. This is the highest success rate for claimants ever recorded. This compares with 58,276 in the same quarter of 2012/2013 when the success rate was 42%.  The overall number of cleared ESA Tribunal hearings in 2012/2013 was 224,375 with an average success rate of 43%.  

39.              The drastic reduction in the number of appeals lodged directly with Tribunals makes it even more urgent for the government to publish statistics on the number of ESA decisions which have been overturned in claimants’favour through mandatory reconsiderations.

40.Benefit claimants are the only group to be denied direct access to a Tribunal and therefore to Justice, although the fees introduced for Employment Tribunals also had the effect of substantially reducing the number of claims
 

WCA and Legal Aid

 

41.              On 1 April 2013, the Legal Aid Sentencing and Punishment of Offenders Act(‘LASPO’) came into effect.

42.              Clause 15 of Part 2 of Schedule 1 of this Act excludes all welfare benefit issues.

43.              Welfare benefit cases no longer qualify for advice or assistance under the Legal Help scheme, not even for initial advice to identify justiciable issues under social security law, or to provide a triage role to steer cases away from tribunal and ensure that benefit claims are processed correctly.

44.              The Government’s view is that as these are matters of ‘administrative justice’ issues in which decision making, adjudication and dispute resolution systems are accessible to claimants acting on their own, and that given the underlying issues are financial, they should be of minimal priority for public funding.

45.              The government also says that legal aid is:

46.              “still available for civil legal services provided in relation to an appeal on a point of law to the Upper Tribunal, the Court of Appeal or the Supreme Court relating to a benefit, allowance, payment, credit or pension” (Point 157)

47.              But as Judge Robert Martin points out in his response to the Ministry of Justice Consultation Paper on Legal Aid (page 8, paragraph 40):

48.              ‘An appeal against the tribunal’s decision in a welfare benefits case lies to the Upper Tribunal but only for error of law ….. These limitations of further “appeal” are often not appreciated by parties without Legal Help, who may fruitlessly seek to appeal further simply because dissatisfied with the outcome’

49.              Although the government says that claimants can represent themselves, at a time when the UK’s social security system faces arguably the biggest upheaval since the introduction of the Welfare State, the Government should have recognised that the need for advice on welfare benefits has never been greater.

50.              It should also have recognised the complexity of the benefit changes affecting disabled people.

51.              Disabled people make up a disproportionate proportion of 58 per cent of those who receive legal aid for welfare benefits cases.

52.              The Government’s own Equalities Impact Assessment (page 64, paragraph 7.36) notes that:

53.              the proposals have the potential to disproportionately affect female clients, BAME clients, and ill or disabled people, when compared with the population. This is as a result of those groups being overrepresented as users of civil legal aid services’. 

54.              The removal of Legal Aid for benefit claimants needs to be seen in the context of cuts to legal aid funding with £320m cut from the annual £2bn legal aid budget and the closures of 100 of Citizen Advice Bureau offices which used to support the most people with access to legal advice and representation. 

55.According to the government’s own assessment, around 600,000 people will lose access to advice and legal representation, when CAB advisers estimate the success rate at ESA appeal where someone receives specialist CAB advice and is represented is around 80 per cent.

WCA Mandatory Reconsideration

 

56.              In October 2013, DWP has introduced changes to the appeals system; a claimant wishing to appeal a fit for work decision will no longer be able to submit their appeal to DWP, which would lodge the appeal with HMCTS (tribunals) on behalf of the claimant. 

57.              There will now be a first step known as Mandatory Reconsiderationwhich is an internal DWP process.

58.              This has serious implications for claimants:

59.              As admitted in the government response, there are no timescale for completion of the Mandatory Reconsideration process, as shown in the response to this Freedom of Information Request

60.              If someone’s claim has been disallowed completely, they will not receive payment pending Mandatory Reconsideration as was the case previously when somebody was allowed to appeal the same decision. DWP is suggesting that claimants should claim other benefits, such as Jobseeker’s Allowance, but there is evidence that some people are being refused JSA on the basis that they cannot, because of health issues fulfill all the conditions attached to this benefit.  

61.              If DWP refuses to Reconsider the case, the claimant will not be allowed to proceed to appeal

62.              There is absolutely no indication or evidence that the UK government has taken any steps whatsover to reduce the stress or anxiety inherent in the Work Capability Assessment for benefit claimants.

63.              The WCA is inherently stressful for claimants, because of the uncertainty of such a notoriously unreliable system where there are frequent media reports of incorrect decisions. Claimants are forced to wait long durations trapped in a bureaucracy that shows no compassion, not knowing if they will be judged “fit for work” and required to seek work, whether or not their medical condition makes that possible.

64.              Claimants are understandably fearful that their benefits will be stopped, at the end of a process that they have no control over.

65.              This is particularly harmful to claimants with Mental Health Conditions, especially those in the class of anxiety disorders as described in DSM-IV   .

66.The following media articles give anecdotal evidence of the stress and anxiey caused by undergoing the Work Capability Assessment, in addition, video testimony is given in this evidence session to the Scottish Parliament on the WCA

 

21 March 2014

 

 


[1]                            This graph was compiled by Dr David Webster, Honorary Senior Research Fellow, Urban Studies, University of Glasgow, based on the figures released by DWP.

Also please note that DPAC has over 20,000 members and supporters and an outreach of over 45,000 disabled people

 

Apr 022014
 

It strikes me that not enough mention is being made of the important victory in the Court of Appeal in the case of [2013] EWCA Civ 1565 Case No: C3/2013/1626/SSTRF IN THE COURT OF APPEAL (CIVIL DIVISION) ON APPEAL FROM THE UPPER TRIBUNAL ADMINISTRATIVE APPEALS CHAMBER) Mr Justice Charles sitting with Upper Tribunal Judges Jacobs and Lane Case Nos. JR/2638 & 2639/2012 CO/2385/2012.

You can download the judgement here and read about what it means here. I also consider that an important investigation called ‘Who benefits?’ in to the ‘The benefits assessment and death of Ms DE’ by Mental Welfare Commission for Scotland which you can refer to here has a relevance to the tragic consequences of what can go wrong if the right decision is not made for lack of obtaining the right evidence.

It is of paramount importance that anyone with mental health problems who is facing having to complete an ESA50 or who has had a decision which the DWP say does not qualify them for Employment & Support Allowance (particularly if it involves a transfer from older incapacity benefits) seeks specialist help from an experienced welfare benefit specialist.

Regrettably we cannot deal with cases on an individual basis on this forum, but if you have a question about the procedure then by all means ask one on this thread and I’ll do my best to answer it in due course.

An important part of the Court’s finding is the recognition of the following:

“Decision-makers should actively consider the need to seek further documentary evidence in every claimant’s case. The final decision must be justified where this is not sought.”

“41. Given the unique circumstances of their condition, particular care should be taken when the claimant has a mental, intellectual or cognitive condition as these individuals may lack insight into the effects of their condition on their day-to-day functioning.”

The drastic consequences of not seeking further medical evidence are clearly outlined in the report in to the death of a claimant allegedly affected by the Work Capability Assessment.

Fundamentally the Court of Appeal recognised the many instances where claimants may not disclose details of a mental health problem to the DWP or their contracted healthcare professional of their own accord.  The difficulties are summarised in the judgement as follows:

31. From that detailed evidence, the Upper Tribunal identified the following particular problems which MHPs as a group face, whilst recognising that the extent to which any particular MHP will suffer from these problems will vary.

“(i) In terms of filling out a form, seeking additional evidence and answering questions, claimants with [mental
health problems] as a class have the following problems and difficulties because of their [mental health problems],
some of which overlap:

a) insufficient appreciation of their condition to answer questions on the ESA50 correctly without help,

b) failure to self-report because of lack of insight into their condition,

c) inability to self-report because of difficulties with social interaction and expression,

d) inability to self-report because they are confused by their symptoms,

e) inability because of their condition to describe its effects properly,

f) difficulty in concentrating and in understanding the questions asked,

g) unwillingness to self-report because of shame or fear of discrimination,

h) failure to understand the need for additional evidence because of cognitive difficulties,

i) problems with self-motivation because of anxiety and depression which may prevent them approaching professionals for help and assistance,

j) false expectation that conditions will be understood without them needing additional help, and

k) lack of understanding that professionals named in the form will not automatically be contacted in the assessment process.

ii) in terms of further aspects of the process for the determination of their entitlement to ESA, claimants with
MHPs as a class have or have to face the following problems and difficulties because of their MHPs:

a) particular conditions (e.g. agoraphobia and panic attacks and autism spectrum disorder) make attending and/or travelling to a face-to-face assessment difficult,

b) finding the process itself intimidating and stressful, and, in some cases, that having a long-lasting negative effect on their condition,

c) a desire to understate conditions,

d) the masking of health problems as physical problems,

e) dealing with assessors who have little or no experience of mental health problems,

f) the difficulties of identifying many symptoms of a condition and its impact on what a person needs without proper training and knowledge,

g) the lack of time during a short assessment to identify a person’s needs,

h) fluctuation in condition, and

i) scepticism about the condition.”

32. It is important to note that these problems fall into two categories, although they overlap. Some of these difficulties go to the adverse experience which might be felt because of what, from the vantage point of some MHPs, will be perceived to be stressful, embarrassing or confusing features of the process, in particular the completion of the questionnaire and the face to face interview. Other difficulties lead to the decision maker having inadequate or even false information about the nature and extent of the illness thereby increasing the risk that a false functional assessment will be made which in turn may jeopardise the right to an ESA. I will call these “adverse experiences” and “outcome effects” respectively.

My note

Whilst the judgement places an emphasis on the DWP seeking further medical evidence in mental health cases, the reality is that in many cases the DWP fails to do so.  In the investigative report in to the death to which I have referred it appears for instance that the claimant’s doctor was not contacted and asked to complete what is called an ESA 113 report.

There is nothing to prevent a claimant when completing the ESA 50, especially when assisted by someone, to point out that they specifically want the DWP to obtain further medical evidence from their own doctor or clinicians.  A claimant could for instance write something along the following lines:

“I have severe mental health problems and find it impossible to describe them in this form.  Please ensure that you contact my doctor (or other named clinician) and ask them for full details of my mental health problems.  I believe this is necessary to make a proper decision on my claim.”

In long term claims it may also be relevant to state:

“You already hold details of my long term mental health problems and I am asking you to make sure these are made fully available to the decision – maker who is looking at my claim.  I believe these details to be very relevant to getting the full picture and vital to a correct decision being made.”

In Incapacity Benefit cases where you have been asked to undergo an assessment for Employment & Support Allowance, the following may be relevant (most claims have now now been ‘migrated’ according to the DWP).
 

When you receive the ESA 50, make an appointment to speak with your doctor either by phone or at the surgery.  This is particularly important where you have not seen your doctor for some time.  Tell your doctor you are being reassessed and ask for a review of the time since you were last seen by the doctor.  This allows you to update your doctor and tell him or her of any problems you have faced since you were last seen, it also means the doctor is better equipped to comment if the DWP contacts them.  It also makes it possible for you to bring matters to the attention of your doctor over which they may be unaware.  You could for instance talk to them about declining levels of social confidence and any fears you have about meeting people or facing certain situations.

The reason this is important is because in incapacity benefit to ESA cases, no medical certificate is required at the commencement of the ‘conversion phase’.  You only need a medical certificate if the DWP assesses you and finds you fit for work and you want to appeal.   The rules are different to new claims for ESA where medical certificates are required at the very start of your claim in the ‘assessment phase’.  In migration cases the ‘prompt’ to speak with your doctor about a certificate only arises once you have already been assessed.

Claimants who have been refused ESA in cases where mental health was relevant (even if the DWP did not know of this) and no attempt was made to obtain further medical evidence by the DWP should consider an appeal.

There will be more on this in subsequent posts.

With thanks to the brilliant nick at http://ilegal.org.uk

Please follow on twitter: @Mylegalforum

Mar 312014
 

Bedroom Tax demo in Swindon in conjunction with the  Swindon Tenants Campaign Group, on 5th April as part of a national campaign.

At the fountain, Canal Walk, Swindon Town Centre

10.30 am on April 5th

We will have leaflets to distribute and banners.

We also have a project collecting peoples stories about ATOS injustice in Swindon. We will be arranging a meeting with our MPs to present our concerns. People can join the face book group or email SPA  peoplesassemblyswindon@gmx.co.uk or phone 01793 522824 if they would like to be a part of this. All information will be treated with strict confidentiality.

https://www.facebook.com/SwindonAtosProject?ref=ts&fref=ts

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