Aug 252013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Disabled People turn the tables by Assessing the Assessors and find them Not Fit for Purpose.

 

Friday 6th September 11.30am til 2pm  outside  Atos Healthcare, Gladstone Business Centre, Heathfield Way off Gladstone Road, Dallington, Northampton, NN5 7QA

 

As part of Disabled People Against Cuts (www.dpac.uk.net ) national campaign to reclaim our rights Disabled People and their allies and supporters will protesting against the continued use the French private company Atos Healthcare to assess people under the governments Welfare programme.  Atos Healthcare and their infamous work capability test has been proven not fit for purpose time and time again. Through the continued use of this crude test ATOS are making Millions of Pounds from the Taxpayers by Finding People fit to Work, and then having to re-assesss them time and Time again by ATOS

According to the Government’s own figures,1,300 people have died after being put into the work-related activity group,2,200 people died before their assessment was complete, and 7,100 people died after being put into the support group. www.dpac.uk.net

Disabled People Against Cuts have used non violent direct action and creative protests to draw attention to the devastating impact cuts in services , support and welfare benefits is having on Disabled People and their families and communities.

 

*Amongst the protest at Atos Healthcare, DPAC Northants will be appealing on behalf of a  special “guest” who has been assessed fit for work.

* Undertaking our own assessment of the Assessors (Atos Healthcare)

* Highlighting to wider general public the devastating impact flawed assessments by Atos has had on Disabled People since Atos Healthcare began assessing People.

* Issuing Atos Healthcare with a Disabled People Against Cuts “Not Fit For Purpose” notice.

 

 

Aug 222013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Updated video of the excellent Condemn Love DPAC’s Anti-Atos song -with massive thanks once more to Kevin Robins for all his work on this. See Kevin perform live at Piss on Pity 31st August-part of the DPAC Reclaiming our Futures week of action.

Also watch this space for more news on how to download Condem Love and contribute to DPAC

 

Con-Dem Love!

They’re screwing up my mind , wasting my time
Keeping up the pressure on this heart of mine
They’ve got a real obsession , egos out of hand
Out to make a make a killing from their “welfare” scam.

This is Con-Dem love, Con-Dem love, Con-Dem love ,
Condemn .. … Con-Dem love.

Laid my cards on the table told their GP straight
Depressions biting hard and that’s hard to take
I showed him the scars on my arms where I’d cut
He looked me in the eye and said you’re “working fit”

This is Con-Dem love, Con-Dem love, Con-Dem love
They’re going to show you what they’re made of.

On a circle of emotion on the treadmill again
They took away my social, can’t pay the rent
What can do, so ill, I can’t fight,
I toss and turn I stay awake all night
Darkened thoughts are haunting me
I’m so afraid of this reality

This is Con-Dem love, Con-Dem love, Con-Dem love
They’re going to show you what they’re made of.

Sitting in a corner — with the lights switched off
This no win situation’s lost
Can’t make no plans for you or for me
There’s no reason to go on you see .

This is Con-Dem love, Con-Dem love, Con-Dem love
They’re going to show you what they’re made of.
They’re going to show you what they’re made of

They’re screwing up my mind, wasting my time
Keeping up the pressure on this heart of mine
They’ve got real obsession, egos out of hand
Out to make a make a killing from their “welfare” scam.

They’re screwing up my mind , taking away my life x 3

©  Robins/Clark

If you would like to know more about DPAC or make a contribution to our work please visit our website www.dpac.uk.net or email: mail@dpac.uk.net or twitter: @Dis_PPL_Protest *Special thanks to all including Rob Livingstone and Simon Gomery for some of the excellent artwork contribution on this video.

 

Aug 132013
 

 

 

 

 

DPAC Norfolk, Reclaiming Our Rights

 

 

Fri, 30th August 2013

 

12:30pm – 2pm

at

Jobcentre Plus, Kiln House, Pottergate, Norwich, NR2 1BZ             

 

This is part of the national DPAC week of action, toprotest at organizations that are creating barriers to inclusion for disabled people.

 

 

We look forward to seeing as many of you as possible at this event, please join us if you possibly can, tell as many interested/supportive friends and family to come along too. Let’s unite together in solidarity to leave this Government under no illusion that we will not rest until we get our message across about what we want and expect from them and future Governments.

Aug 132013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

dpacxx

Reclaiming Our Futures UK

 

Join this year’s week of action to protest against austerity, fight for our rights and celebrate disabled people

 

From 29th August – 4th September DPAC and other campaigns will offer a range of activities you can get involved in. These events will bring together our anger at what is happening now, and celebrate our victories won, both in the past and to come.

 

 

Our rights are being stripped away day by day, by the neo-liberal policies being imposed on us all by the Condems, leaving us without much hope for our futures – or our children’s.

 

We have been here before. Our history is littered with examples of how our community has come together when under attack to fight – and win. From the early campaigns of NLBDP (National League of Blind and Disabled People) through to the founding and manifesto of UPIAS (Union of

 

the Physically Impaired Against Segregation) and on to DAN (Direct Action Network)- Now we have DPAC leading direct action and a host of other key grass root campaigns working towards reclaiming our rights and futures.

 

We have fought our corner over 3 centuries. And those fights have brought victories; the Independent Living Movement, our early CILs (Centres for Independent Living) and early active DPO’s (Disabled Peoples Organisations) and the significant rights for disabled people (which are now under attack). They represent big victories, brought about by mobilizing in our communities around our common cause – and having the will and determination to see our demands met without compromising our rights. We have consistently united in anger and celebration.

  

Download easy read information about the week here:

DPAC easy read (2)

 

DPAC Reclaiming our Futures Action

 

This autumn, we are asking our community to come together in anger, and celebration again – and to unite around our demands

 

We will be launching the UK Disabled People’s Manifesto setting out our vision of how the resources, structures and institutions of our society today can be re-designed to empower disabled people to take part in life on our terms. Disabled people are, and always will be, the experts on our lives and our self-determination. It will be a vision and practical plan that we can take forward in our communities, workplaces and lives to reclaim our futures.

 

In the build up to the manifesto launch, DPAC is leading The ‘Reclaiming Our Futures’, seven days of action to protest against the targeting of disabled people by austerity measures, to fight for our rights for inclusion and independence as equal citizens and to celebrate the value, pride and self determination of disabled people.

 

From 29th August – 4th September DPAC and other campaigns will offer a range of activities you can get involved in. These events will bring together our anger at what is happening now, and celebrate our victories won, both in the past and to come.

 

The plan below is only half the story. We want YOU, your Deaf and Disabled People’s Organisation, your campaign group, your community, your friends to put on events and get involved too. Can’t get to our exhibition? – then put on your own. Can’t get to our direct action? – then do your own. Barbecues, debates, quiz nights, family days, picnics – whatever! ACT – in celebration or in anger! (PS don’t forget to let us know what you’re doing).

 

 

Day by Day: 29th August-4th September

 

 

Thursday 29th August – YOU launch our 7 days of action

 

A range of resources will be available for your use as we ask all supporters to start our week of action with an online blitz. You will be the ones creating the buzz and the hype sending letters and twitter messages to targets of your choice ranging from MPs to disability charities to the media. We will be producing twibbons and memes but make and circulate your own. If you haven’t got a Social Media account (such as Facebook & Twitter) set one up now, link to DPAC ( twitter: @Dis_PPL_Protest) and let’s create a cyber wave. #dpacrof

 

The launch will coincide with Transport for All’s Day of Action to make CrossRail accessible: https://dpac.uk.net/2013/07/day-of-action-to-make-crossrail-fully-accessible-thursday-29th-august-2013/

 

 

 

Friday 30th August – Local Protests

 

Last year during the ATOS Games over 30 local actions took place around the UK Local actions mean you get to choose the target of your choice. You could take the Reclaiming Our Futures manifesto to present at your local MP’s constituency office, spread it through social media, protest on the streets against segregated education, the proposed ILF closure or show solidarity at your local Remploy site (for those few factories in their last weeks of operation). Alternatively, you might want to lobby your local Council on the Bedroom Tax and cuts to local services/support. Oh, and as we know ATOS offices are still around too….we’re sure you have other great ideas to add… Remember to let us know what you are doing so we can promote your actions. We will be producing local action resource packs but any materials you develop please send us copies to share with other protests and online.

 

 

Saturday 31st – Disability, Art & Protest Exhibition and Fundraising Gig

 

An exhibition and sharing of work exploring disability, art and protest followed by a ticketed fundraising gig run in partnership with Madpride and Tottenham Chances. Come during the day and join in our banner making workshop to prepare for the big Freedom Drive on the 4th September. If you would like to nominate an artist, collective and/or piece of work please let us know (including any links) and we will try to get them involved. If you want to do a local, street or online art protest too-this could be the day to do it.

 

Venue: Tottenham Chances, 399 High Road, London, N17 6QN Times:

 

12 – 7pm Exhibition: disability, art and protest

1 – 3.30pm Banner and placard making workshop

 

4 – 6pm Work Sharing

7.30pm till late Gig

 

 

Sunday 1st September – Reclaiming the Social Model: the social model in the 21st Century

 

Anne Rae: former UPIAS and current chair of the Greater

Manchester Coalition of Disabled People (GMCDP),

 

Colin Barnes: Professor of Disability Studies at Leeds Centre for Disability Studies

 

 

As government and the private sector increasingly use a so-called ‘modern understanding of disability’ to redefine who is and who isn’t disabled it is more important than ever that we understand, defend and promote the social model of disability. This isn’t helped when the social model is not fully supported within our movement. This event will be a chance to hear from a range of speakers and to discuss why the social model is still relevant today to our lives and our futures and to map out what we need to do to fight for it. The event will be live-streamed with the opportunity for people to participate in the discussion virtually. We will also be promoting a range of resources around the social model.

 

Venue

UNITE House, 128 Theobald’s Road, Holborn, WC1X 8TN

Time: 12.30 – 4.30pm

 

 

Monday 2nd September – Direct Action

 

Despite the huge efforts of thousands of disabled people throughout the country, it is increasingly difficult to find spaces where lies, inaccuracies and mis-use of statistics can be challenged. DPAC recently released a study into how the DWP uses all of these to vilify and demonize disabled people.

 

See more at: https://dpac.uk.net/2013/06/lies-damn-ids-and-statistics/#sthash.MAk5nTiU.dpuf

 

But why is this down to us? People should be presented with both sides of the story and this isn’t happening. Disabled people are having to find ways to make sure our truths will be heard. Watch this space…

 

 

Tuesday 3rd September – ‘I Dare’ day

 

A day of online action to reinforce that we want ‘Rights not Charity’, and a society where we are able to operate on our own terms as disabled people. Dare to ask for Rights not Charity. Dare to be an activist. Dare to ask more of ‘our’ organisations. We aren’t asking for Care, we want Power: Power to write the script for our own lives, and not to be written out or written off by others. A range of actions and captions will be available for you to capture in an image and circulate online.

 

 

Wednesday 4th September – UK FREEDOM DRIVE

 

A final-day march and events in and around Parliament. Four

 

themed ‘blocks’ will meet at 4 Government departments, central to the lives of disabled people. After handing over our demands, blocks will then move towards Parliament for a lobby where we will formally launch the UK Disabled People’s Manifesto and present our demands to our

 

elected representatives.

 

Choose your ‘block’ and meet at 12.45pm at one of:

 

·        Department for Education to oppose government attacks on inclusive education and a return to segregation (Sanctuary Buildings, 20 Great Smith Street, London, SW1P 3BT)

 

·        Department of Energy and Climate Change if you’re angry about the numbers of disabled people living in fuel poverty while the energy companies rake in ever growing profits (3 Whitehall Pl, City of Westminster, SW1A 2AW)

 

·        Department for Transport to challenge inaccessible transport, the opening of new inaccessible stations for Crossrail and proposed cuts to rail staff further reducing customer assistance (Great Minster House, 33 Horseferry Rd, London SW1P 4DR)

 

·        Department of Health to defend our NHS and demand our right to levels of social care support enabling choice, control, dignity and independence (Richmond House, 79 Whitehall, London SW1A 2NS)

 

Lobby of Parliament: 5 – 6pm – launch of the UK Disabled People’s

Manifesto

 

WE WANT EVERYBODY TO JOIN US FOR THE FREEDOM DRIVE ideally in person, but also online-this is for everyone everywhere. There will be accessible transport from a variety of towns and cities throughout the country (details to follow) and there is some funding available for transport but we will need your co-operation and patience to make this work for everybody, so please bear with us and note that while DPAC members will be given priority we want to support as many people as we can. If you can’t get there send a photo or your name and you can march with us.

 

This week of action is yours. Please take part at whatever level suits you – BUT MAKE SURE YOU TAKE PART. Share our events, resources and actions as far and wide as you can.

 

 

 

Let’s Reclaim Our Futures, together!

 

 

DPAC web site: www.dpac.uk.net

 

DPAC facebook:

 

https://www.facebook.com/pages/DPAC-Disabled-People-Against-Cuts/213545112011414?fref=ts(Open Community group- including allupdates from DPAC)

 

https://www.facebook.com/groups/DPAC2011/?fref=ts(original open groupDPAC page- faster paced and more opinion driven than community group )

 

DPAC Twitter: @Dis_PPL_Protest 

 

DPAC email: mail@dpac.uk.net

 

 

Remember if you need help with funding to get to London (4th Sept) email us at mail@dpac.uk.net with details. DPAC members will get first priority but we’re hoping to be able to contribute to all that want to come along. If you are unable to come but would like your picture carried send us a photo or message. Please get in touch with any other queries as well and we’ll try to help.

Download this as a PDF Doc: https://dpac.uk.net/wp-content/uploads/2013/08/Reclaiming-Our-Futures-call-out-long-w-logos-v2.pdf

 Download this as a Word Doc: https://dpac.uk.net/wp-content/uploads/2013/08/Reclaiming-Our-Futures-call-out-long-w-logos-v2-1.doc

 

 Reclaiming our Futures is supported by The Edge Fund, Andrew Wainwright Reform Trust, Network for Social Change, Black Triangle, Mental Health resistance network, Wow Petition, Fuel Poverty Action, Occupy London, TUC, UK UNCUT, Boycott Workfare, Right to Work, Just Fair, Unite Disabled Workers, BFAAWU, European Network on Independent Living, Anti-Bedroom Tax and Benefits Justice Federation, and more…..

 rof8

Aug 052013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Hoban-Expenses-235x300

Last month (12 June), Mark Hoban said this during a debate on people’s right to ask for a recording of their employment and support allowance face-to-face assessments: https://www.publications.parliament.uk/pa/cm201314/cmhansrd/cm130612/debtext/130612-0004.htm#13061288000001

 

“The Department and Atos are in the process of amending written communications to claimants by updating the WCA AL1C form. The document is sent to claimants when they need to arrange a face-to-face assessment and will provide more information on how to arrange an audio-recorded assessment. We expect the revised form to be sent out to claimants by the end of next month, once the necessary changes have been made and the form has been cleared for use.” 

In other words – the DWP was finally going to change the documents it sends to ESA claimants to let them know that they can ask to have their Atos face-to-face assessments recorded. It’s vital that people know they have that right, because with a recording, they are able to demonstrate beyond doubt what was said and what happened at their assessments.

By “the end of next month,” Hoban surely meant the end of July – and we’ve just gone past that deadline.

 

Jayne Linney, DPAC, Black Triangle, False Economy and Public Interest Lawyers  (who, with disabled man Patrick Lynch, took a legal action against the DWP last year on people’s right to record their assessments https://www.guardian.co.uk/society/2012/dec/13/disabled-man-government-court-benefit-test ) are publishing this blog and asking you to reblog and share it to find out if the DWP has changed the documents it sends out to ESA claimants and if people have noted that. Earlier this month, the DWP sent Public Interest Lawyers this document as an example of the leaflet that claimants should receive about their face-to-face assessments. This document includes information which advises people of their right to ask for a recording. We want to know whether people are getting that document and if word is spreading that people can make that request.

 

This is important for a number of reasons. The first is, of course, that people need to know they have this right and that they can request a recording when they are called to an Atos ESA face-to-face assessment. The second is that Hoban claims that he is evaluating the demand for recordings and that he’ll be doing so until the end of summer 2013. (It will be important for people to respond to these blogs as soon as possible – by the end of August 2013 at the very latest – that being the case). https://www.publications.parliament.uk/pa/cm201314/cmhansrd/cm130612/debtext/130612-0004.htm#13061288000001

 Hoban continues to argue that the demand for recordings is not high. Campaigners have argued, rightly, that their surveys https://dpac.uk.net/2012/11/dpac-survey-responses-on-wca-what-harrington-didnt-ask/

 and calls for information show that people do want recordings – and that demand may well increase if people actually know that they can ask for a recording. Unfortunately – or intentionally – Hoban says that the evaluation of demand will finish at the end of summer. That isn’t far away and doesn’t give anybody much time to find out if the amended documentation (presuming that people are receiving it) is having an effect. The third reason that this is important is that the DWP says it has based its decision NOT to offer recordings for Personal Independence Payment assessments on the ESA experience: “the DWP has not seen evidence from other disability assessments that this would improve the quality of assessments,” Esther McVey told parliament this year. So evidence of the demand for ESA recordings is very relevant to the PIP debate. https://www.publications.parliament.uk/pa/cm201213/cmhansrd/cm130418/text/130418w0003.htm#13041838000125  The department’s whole approach to recording PIP assessments is a mess – Capita, which has a contract to carry out some of the PIP assessments, originally said it would offer recordings. McVey put a stop to that and said that it wouldn’t. Meanwhile, the DWP was telling journalists that recordings would be offered for PIP assessments.  https://www.newstatesman.com/politics/2013/07/secret-cuts-part-four-personal-independence-payments They’re making it up as they go along, so pressure needs to be applied.

 

The aim should be to get rid of the work capability assessment altogether – but while it’s there, safeguards like recordings of assessments need to be in place. Claimants and campaigners have fought hard for the right to record their face-to-face assessments. As we’ve said, people need to be able to demonstrate beyond doubt what is said at assessments. Atos is notorious for returning fit-for-work reports which ignore a claimant’s true circumstances and the details shared in face-to-face assessments. The ever-increasing number of ESA appeals  https://mikesivier.wordpress.com/2013/06/28/esa-appeals-more-than-double-and-decisions-in-the-claimants-favour-are-increasing/ prove Atos’ problems with accuracy.

https://www.guardian.co.uk/society/2012/dec/13/disabled-man-government-court-benefit-test

Campaigners have won some concessions through their hard work. These include a commitment from the DWP to offer ESA assessment recordings (on “official” dual-CD recording equipment – people still can’t bring their own recording equipment unless it can dual-produce a CD or cassette). The changed paperwork was another concession. Let’s see if they’ve done it and if people are aware of it.

Download DWP Notes Sheet on assessment

https://dpac.uk.net/wp-content/uploads/2013/08/WCAAL1C_0713-21.pdf

 

 

 

 

Aug 032013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

DPAC and Black Triangle condemn the misguided, insensitive and inflammatory comments of Dr Phil Peverley. We also want to condemn the pitch and severity of the pieces in the Mail and Telegraph (2nd August) framing Peverley’s comments, as a further outrageous abuse of the facts and issues affecting disabled people and those with diagnosed long term health issues.

 

Peverley’s words are an insult to all those that suffer the misery and anxiety of Atos within the regime designed to remove support from disabled people. His words are an insult to those that have died shortly after being declared ‘fit for work’ or before an appeal which found that, once again, Atos were wrong-something that happens with increasing regularly in a system that is chaotic and unworkable.

 

Those people may also have been within the so-called ‘proportion of punters’ that Peverley claims ‘are hell-bent on trying to prove they’re really ill, and need us [GPS] to confirm it’ or maybe they were some of the perceived ‘disgruntled unworking well’ who are ‘full of indignation at being considered reasonably healthy.’ The Department of Works and Pensions DWP own figures show deaths within 6 weeks of tests were at over 10,000. The DWP are refusing to publish up –to date statistics, so we would guess that these figures have risen significantly.

Thanks to the tireless efforts of Black Triangle on the 28th June 2012 the British Medical Association (BMA) supported a call to demand that the WCA should be ended ‘with immediate effect and be replaced with a rigorous and safe system that does not cause unavoidable harm.’ Peverley on the other hand thinks Atos are doing a great job -despite new evidence everyday that they clearly are not, despite MPs, journalists, and the public accounts committee condemnation of their conduct and the multi-million Atos contract. (See Dr McCartney’s piece in the British Medical Journal and Black Triangles’ 2013 letter of support from Drs and MPS)

 

Remarkably, Peverley declared that he considered putting a picture of Stephen Hawkings in his surgery with the caption: ‘This bloke is not on the sick!’ The comparison of Hawkings to every single disabled person is beyond bizarre. This is a man with the funds to ensure a network of P.A. support, home adaptations and technical aids- something far out of the reach of the majority of disabled people –where even a basic level of support is becoming increasingly unlikely in the current slash and burn climate. Hawkings won’t miss his ILF payments if the appeal hearing against the DWP doesn’t produce the correct verdict. Hawkings won’t need to worry about local authority cuts or the tsunami of other cuts, caps, punitive costs, sanctions and penalties being imposed on disabled people and other low income people by this Government.

 In Sept 2012 the BMA also said that GPs workloads had massively increased due to the chaotic system of the WCA and increasing numbers of appeals. Peverley also says: ‘’These fitness-to-work assessments – under Atos, and under anyone who takes the role for that matter – generate a massive amount of work in general practice’ in his column in the Pulse. However, neither the Mail nor the Telegraph wanted to pick up on the increased workloads the Atos/WCA system is causing for GPs.  None wanted to mention that people can now be charged up to 200 pounds for GP reports, to support them in an assessment, or that GPs increasingly refuse to supply reports either.- a further hurdle for disabled people and those with debilitating long term health issues in the attempt to gain the support they need in the punitive assessment process.

 The Mail and Telegraph both carried the comments of Peverley. True- they’re both right wing newspapers and tools of Tory propaganda. Yet, the pitch and severity of both pieces in framing Peverley’s comments was a clear abuse of the facts and issues facing disabled people; as are Peverly’s inflammatory comments.

The Telegraph carried the headline: ‘A GP incensed at his surgeries being full of the “disgruntled unworking well” has said he considered displaying a poster of Professor Stephen Hawking along with the caption: “This bloke is not on the sick”’.

While the Mail went that bit further with the more loaded headline:  ‘THIS bloke is not on the sick! Angry GP cites Hawking to shame hordes of patients asking him to sign them off’.

Peverley’s original Pulse piece fits the welfare ‘reform’ agenda perfectly. An agenda that incorporates the right wing media and Governments constant demonising of disabled people as feckless/workshy/scroungers  – Peverley’s original rallying cry in the Pulse was that he did not want to sign ‘sick notes. The piece headlined: ‘Save me from the unworking wellwas posted on the 29th July. Neither the Mail nor the Telegraph showed the same eagerness to publish his jaunty column of 25th April ‘A Curious Case of Missing Sick Notes’ which talks about the constant losing of sick notes by the DWP. But why would they?

Peverley has played into their hands, not only does he appear to support the discredited bio -psychosocial model, beloved of Aylward and Freud, that removes GPs and replaces them with private companies paid with huge amounts of public money- he has given them the final piece of the puzzle –privatise the sick note and remove it from any element of medical evidence. Let’s have 100% ‘fit to work’ even if a 100% drop dead in the process. Those that can afford it, like Hawkings can buy their own private back-up plan’.

In the meantime Peverley has been reported to the GMC. Twitter @gmcuk

There is a facebook campaign group at facebook.com/permalink.php?…

Peverley is on twitter @PhilPeverley

His surgery address for letters is at the link below-please do not use the surgery telephone lines!

Dr Phil Peverley 

Old Forge Surgery
Pallion Park
Pallion
Sunderland, SR4 6QE

 To Protest against this and the other attacks on disabled people join DPAC’s 7 days of Action https://dpac.uk.net/2013/07/reclaiming-our-futures-7-days-of-action/

DPAC twitter: @dis_ppl_protest

Black Triangle twitter: @blacktriangle1

 

Jul 272013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

BEDDING OUT

Exhibited beyond a red rope barrier, a woman lies in her bed for 30 hours

At Edinburgh Fringe Festival and on Twitter

9 – 10 August 2013

 

Bedding Out is a 30-hour performance by artist-activist Liz Crow that has emerged from the current welfare benefits overhaul that threatens many with poverty. A propagandist campaign that has seen a doubling in disability hate crime.

 

At set times on both days members of the public are invited to Bedside Conversations, gathering round the bed to talk about the work, its backdrop and its politics. For those who cannot visit the work in person, there will be two twitter-based conversations.

Bedding Outis a performance in which I take my private self and make it public, something I have not done in over 30 years’ says Liz Crow. ‘In a gallery, over a period of two days, I will perform the other side of my fractured self, my bed-life. Since the public me is so carefully constructed, this will be a kind of un-performing of myself. I want to make a twilight existence visible. But more, I want to show that what many people see as contradiction, what they call fraud, is only the complexity of real life.’

 

Bedding Outhas previously been performed at SPILL festival and Salisbury Arts Centre where the piece was set over 48 hours. A live feed was viewed by nearly 10,000 people in over 50 countries, generating interest and debate about changes to the benefits system. 

 

 

Bedding Out at Edinburgh Fringe Festival

Friday 9 – Saturday 10 August, starts 10.00am

At Hunt & Darton Cafe (Venue 172), 17-21 St Mary’s Street, EH1 1SU

Wheelchair accessible venue, with accessible loo

 

On Twitter

Follow @RGPLizCrow and use the #beddingout hashtag throughout the 30 hours. Join our Twitter-based Bedside Conversations on Friday 9.00pm, Saturday noon.

 

Bedside Conversations

Members of the public gather round the bed to talk about the work, it’s background and its politics.

Friday 1.00pm, 5.00pm. Saturday 2.00pm.

Free entry. Duration 45 minutes. Book at Box Office: 0131 556 6550 or www.pleasance.co.uk/edinburgh

 

BSL interpreter and notetaker available.

www.roaring-girl.co.uk   @RGPLizCrow   #beddingout

lc DSC_0160edit copylcDSC_0117edit copy

Jul 262013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

La société Atos Healthcare, filiale d’Atos Origin est chargée par le gouvernement Britannique d’effectuer des contrôles auprès des bénéficiaires d’allocations handicap, dans le but avoué de réduire de 20% ce poste budgétaire au Royaume Uni, tandis que le gouvernement mène sans relâche une campagne de diabolisation des personnes handicapées,  traitées en parasites de la société.

Ces contrôles humiliants auxquels doivent se soumettre les personnes handicapées  ont été condamnés par l’Ordre des Médecins britannique, le RCN qui représente les infirmiers et infirmières dans tout le Royaume Uni , les associations de personnes handicapées; ils ont fait l’objet de multiples débats à la Chambre des députés;  le rapport du Comité des comptes de l’état a également  vigoureusement critiqué les termes du contrat passé avec Atos qui coûte une fortune au contribuable britannique et dernièrement un médecin travaillant pour Atos a démissionné, révélant à la BBC que les dés étaient pipés, que les évaluateurs des capacités au travail, qui utilisent un système de points, se voyaient fixer des objectifs préétablis de radiation, avant même d’effectuer ces contrôles, comme l’ont révélé deux reportages télévisés et que les personnes handicapées étaient injustement privées de leurs allocations, et de ressources financières.

Mais le gouvernement Britannique continue toujours à faire la chasse aux personnes handicapées et à refuser de révéler combien d’entre elles sont décédées après avoir fait appel mais avant qu’un jugement soit rendu, certaines devant attendre parfois plus d’un an pour cela. 1,3 millions de personnes ont fait appel en trois ans, et les statistiques du Ministère de la Justice révèle qu’environ 43% d’entre elles gagnent leur procès. Ce chiffre atteint 80% lorsqu’elles sont représentées par un avocat.   Alors qu’Atos se défend en disant que la décision finale concernant le droit d’une personne handicapée à des allocations handicap est prise par un fonctionnaire sans qualification médicale du Ministère du travail, toujours est-il que les recommandations d’Atos sont suivies à plus de 90%.

Mais derrière les chiffres, se cachent des milliers de tragédies humaines.

Pour reprendre les termes de la médaillée d’or aux Jeux paralympiques Tara Flood, « le scandaleux paradoxe est que le principal sponsor de Londres 2012 [ait étéAtos, celui-là même qui détruit la vie des plus vulnérables pour le compte de l’État ».

Pour de plus amples informations :

https://www.courrierinternational.com/article/2012/09/04/la-vitrine-doree-d-une-politique-honteuse-envers-les-handicapes

 https://www.bastamag.net/article2608.html

https://www.bbc.co.uk/news/uk-22546036

https://www.telegraph.co.uk/health/9590852/Botched-tests-deny-the-disabled-their-benefits.html

https://www.guardian.co.uk/society/2013/jan/04/disability-claimants-work-assessments-atos

https://www.independent.co.uk/news/uk/home-news/atos-told-incontinent-woman-to-wear-nappy-firm-condemned-by-mps-for-pressuring-sick-and-disabled-into-returning-to-work-8456447.html

https://www.publications.parliament.uk/pa/cm201213/cmselect/cmpubacc/744/744.pdf

https://atos.net/fr-fr/accueil/nous-sommes/newsroom/communique-de-presse/2013/pr-2013_07_17_01.html

 

Disabled people are furious that Atos has again been appointed Official IT partner of the International Paralympics Committee Athletics World Championships in Lyon

 

Atos Healthcare, a branch of Atos Origin, holds the British government contract to assess disabled people’s entitlement to disability benefits, with the stated goal of a 20% reduction in costs.

 The humiliating assessments disabled people are subjected to have been condemned by the BMA, the RCN and many other official organisations and bodies which have called for them to be scrapped; there have been numerous debates in the Houses of Parliament about the way Atos carries out assessments; the Public Accounts Committee found that the British public was not getting value for money with the Atos contract. And lately an Atos whistle blower doctor explained to the BBC how the assessments, using a tickbox point scoring questionnaire, deliberately fail disabled people in order to stop their benefits. Two television programmes have also revealed that Atos assessors were given targets as to the number of claimants who should be entitled to disability benefits. 

The British government still refuses to release figures about the number of disabled people who have died while waiting for the outcome of their appeals. Over 1.3 million people have appealed in 3 years, of which, according to Ministry of Justice figures, 43% won their appeals, rising to 80% if they had legal representation. Although Atos’ answer to its critics is to say that the final decision is taken by an employee of the DWP without a medical background, over 90% of Atos recommendations are upheld. 

But behind the figures, a human tragedy is unfolding

As gold medal-winning Paralympian Tara Flood puts it: “It is a shocking irony that Atos is a main sponsor of London (Olympic) 2012 while destroying disabled people’s lives on behalf of the governmen

Jul 222013
 
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But will any ‘improvement’ plan be
just another whitewash?

Of course it will.

Government is just oh so predictable.  People will no doubt be jumping with joy over today’s ministerial statement that Atos is at long last going to be subjected to having to put in place an improvement plan.  You’ve only got to read the small print before you see how yet another corporate global giant will be offering Atos some ‘independent advice’ as to how to go about making the much needed improvements.

The DWP has engaged PricewaterhouseCoopers “to provide independent advice in relation to strengthening quality assurance processes across all its health and disability assessments. In addition, and in the longer-term, increased provider capacity will ensure that a greater focus on quality can be achieved alongside enabling the number of assessments the Department requires to be delivered.”

Independent?

PricewaterhouseCoopers are no strangers to Atos as clarified by an excerpt from yet another Atos glossy leaflet entitled “e-invoicing – speed-up your process – take cost-cutting initiatives”; it’s hardly encouraging that the accent is on even more cost cutting.  The glossy goes on to highlight the close working relationship with Atos Worldline (another Atos derivative) and PWC:

“Atos Worldline studies European and worldwide constraints from a legal and fiscal point of view in collaboration with Price-waterhouse-Coopers Tax Consultants SCCRL office who is the leader studying rules to be applied to e-invoicing and e-archiving at international level. e-invoicing covers fiscal and legal prerequisites in more than 30 countries over the world” 

And as if you couldn’t guess there’s more controversy involving the question of donations to the Tory Party

“The Electoral Commission confirmed that, since Cameron
became Tory leader, PwC has made non-cash
donations worth £545,000 to the
Conservative party in

“staff” and “consultancy services”.

It seems PWC was also called in to sort out a probe in to the death of NHS patients at a cost of £2.7 million pounds according to an article in the Daily Mirror

No doubt PWC will leave aside the need for probing questions in to the deaths of benefit claimants following Atos’s infamous health assessments.

Await the whitewash and clean bill of health to appease the select committee; after which it’ll be business as usual.  Here’s Lord Freud’s ministerial statement:


Written Ministerial Statement

 

Monday 22 July 2013

 

THE DEPARTMENT FOR WORK AND PENSIONS

 

New providers to deliver Work Capability Assessments

The Minister for Welfare Reform (Lords) (Lord Freud): The Department for Work and Pensions is committed to continually reviewing and improving the Work Capability Assessment (WCA) process, to ensure that it is as responsive to the needs of claimants as possible. As part of this and to bring down waiting times for claimants, DWP has decided to change its approach to contracting for the WCA, by procuring additional providers on a regional basis. This is in keeping with the Department’s current commercial strategy and will provide increased capacity. These arrangements are likely to be operational from summer 2014.

The WCA process is currently subject to a system of quality assurance and audits by both Atos Healthcare and DWP. A recent DWP audit identified a reduction in the quality of written reports which are produced by Atos following assessments and are then used by the Department to form part of the decision making process on benefit entitlement. This is contractually unacceptable. The Department is considering all its options under the contract and will apply all appropriate contractual remedies to ensure quality and value.

Atos has been instructed by the Department to immediately enact a quality improvement plan. Measures include retraining and re-evaluating all Atos healthcare professionals, with those not meeting the required standard of written reporting either remaining subject to 100% audit until compliant or having their approval to carry out assessments revoked by the Department.

The Department has also engaged PricewaterhouseCoopers to provide independent advice in relation to strengthening quality assurance processes across all its health and disability assessments. In addition, and in the longer-term, increased provider capacity will ensure that a greater focus on quality can be achieved alongside enabling the number of assessments the Department requires to be delivered.

Assessment reports, such as those provided by Atos, form only one part of the WCA process, which has a number of checks and balances built in to ensure the right decision is reached for claimants. After the Atos assessment DWP Decision Makers make the final decision on claimants’ benefit entitlement based on all evidence provided during the claim. If the claimant disputes the decision or appeals there is then a reconsideration process where another DWP Decision Maker will reconsider the decision. If the claimant is still unhappy about the decision made, they can appeal. It is important to stress that DWP’s audit activity showed that claimants whose reports did not meet our rigorous quality standard were no more or less likely to have been found fit for work or appeal against the Department’s decision than other claimants.

The Department also remains committed to the ongoing process of annual independent reviews of the WCA. From the three reviews already carried out by Professor Malcolm Harrington, over 50 recommendations have been, or are being, implemented to ensure the WCA is as fair and as accurate as possible. For example, we are currently carrying out an evidence-based review of the WCA descriptors with a number of major charities and we are working closely with the First-tier Tribunal to better understand the reasons for upheld appeals.

A further independent review of the WCA is currently being undertaken by Dr Paul Litchfield, a respected Senior Occupational Physician, and we expect Dr Litchfield to make recommendations before the end of the year to further strengthen the WCA.

The above measures show our commitment to continually improve the assessment, and to take decisive action when it becomes clear that there are issues which need addressing. We will come back to Parliament in the autumn with a further update.

A million thanks to the fantastic Nick at My legal Forum

Follow Nick on twitter: @Mylegalforum

See more here: https://ilegal.org.uk/thread/7790/atos-job?page=1&scrollTo=20067

 

 

Jul 162013
 
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DPAC Logo 3 amendment 1 (Small)Our rights are being stripped away day by day by the neo-liberal policies being imposed on us all by the Condems leaving us without any hope for our futures or our children’s futures.

 

DPAC say this is not fair, not acceptable and we must fight back against the continuing attacks. We will be having a week of actions nationally and virtually from August 29th and culminating on September 4th with  mass events and actions in London.

 

Thursday 29th August – launch on anniversary of coffin delivery to Atos, make Crossrail fully accessible protest, plus more….

 

Friday 30th August – local protests –go to local MPs, Atos offices, schools and colleges that are creating barriers to inclusion..plus more…

 

Saturday 31st August – disability, art and protest exhibition and gig

 

Sunday 1st September –
The Social Model In The 21st Century – Why Is It Still relevant?

 

Monday 2nd September – Media direct actions, picking up the pace as we come to the end of the week of action, despite everything we do it is getting more and more difficult to get media space to present the facts whereas there is plenty of space given to misrepresentation of stats and government lies

 

Tuesday 3rd September – ‘I Dare’ day – to reinforce that we want Rights not Charity and a society where we are able to operate on our own terms as disabled people.

Approximate time 1pm -2.30pm

 

Wednesday 4th September – Grand Finale events in London and public launch of the Manifesto ‘Reclaiming our Futures’

noon- 4pm followed by lobby of parliament 5-6pm

 

We want to get disabled people from around the UK out resisting, based on their experiences, creating disabled people’s space, raising awareness of what we are all about. But there is plenty of social media stuff too- everyone can be an ‘extremist’!

 

The Anti Atos message last year was very clear and very successful. This year we want the messaging to be broader and to be about what we want and expect from any future government including all aspects of inclusion.

 

At the Rethinking Disability Policy event last September a network of Disabled People’s Organisations agreed to develop a manifesto of demands. The manifesto is nearly ready for consultation and sign up. Let us know if you’d like a copy.

 

The Reclaiming Our Futures week will launch the manifesto and say what we want to protect our futures.

 

Last year’s ATOS GAMES protests had at least 33 separate local protests in different locations in England, Scotland and Wales over the course of the week.

 

While the Atos Games focused on demonstrating and closing things down, this year’s week of action will retain that anger and include direct action but it will also be a celebration of disability pride.

 

DPAC has some funding for the week of action and we have worked out what we have the capacity to do. We are asking other groups to think about what they can put on and contribute to the week. This needs all of us!

 

We are asking people around the UK to do things as well – debates, forums, art exhibitions, protests, to link in with this. Let us know what you’re planning and we’ll publicise it!

 

If you need help with funding to get to London (4th Sept) email us at mail@dpac.uk.net with details. DPAC members will get first priority but we’re hoping to be able to contribute to all that want to come along. If you are unable to come but would like your picture carried send us a photo or message. Please get in touch with any other queries as well and we’ll try to help.

more to come…….

Jul 072013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

DPAC Paupers Picnic: BRING LOUD VOICES TO CREATE DEMO IN CENTRAL LOBBY AT HOUSE OF COMMON AS MPs ARE IN CIA DEBATE – BRING BREAD & WATER FOR THE PAUPERS PICNIC IN THE CENTRAL LOBBY… https://www.facebook.com/events/143321692538348/

 

Plus Opposition day debate program

Commons main chamber
12pm
[ Minister’s Question Time

Ten Minute Rule Motion
Slavery – Mr Peter Bone]

>>>Debate<<<
Opposition Day (5th allotted day) (Half day) – The effect of Government Policies on Disabled People

https://wowpetition.blogspot.co.uk/2013/07/ciadisability-on-big-wednesday-july-10.html

HOC sel cmte
9.30am Education
Subject: Foundation years: Sure Start children’s centres
Witness(es): Louise Silverton, Director for Midwifery, Royal College of Midwives, Cllr Richard Roberts, Lead Member for Children’s Services and member of Health and Wellbeing Board, Hertfordshire County Council , Jane Williams, Head of Children, Young People and Family Services, Integrated and Community Care Division, South Warwickshire NHS Foundation Trust and Carole Bell, Head of Children’s Commissioning, North West London Commissioning Support Unit ; Annie Hudson, Chief Executive Designate of The College of Social Work,, Neil Couling, Work Services Director, Department of Work and Pensions, Tim Sherriff, Head Teacher, Westfield Community School and Children’s Centre, Wigan and Elizabeth Young, Director Research Evaluation & Policy, Home Start UK
Location: The Wilson Room, Portcullis House

9.30am Work and Pensions
Subject: Universal Credit: follow-up
Witness(es): Rt Hon Iain Duncan Smith, Secretary of State, Department for Work and Pensions, Lord Freud, Parliamentary Under Secretary of State for Welfare Reform , Howard Shiplee, Universal Credit Director General and Suzanne Newton, Real Time Information Programme Director, HM Revenue and Customs
Location: The Grimond Room, Portcullis House

2.30pm Work and Pensions
Subject: DWP Annual Report and Accounts 2012-13: DWP Statistics
Witness(es): John Shields, Director of Communications and David Frazer, Director of Information, Governance and Security Directorate
Location: Room 5, Palace of Westminster

HOL Sel cmte
10.45am Olympic and Paralympic Legacy Committee
Subject: Olympic and Paralympic Legacy Committee
Witness(es): (at 10.45am) evidence will be heard from Councillor Guy Nicholson, Cabinet Member for Regeneration, Hackney Borough Council and Councillor Chris Robbins, Leader, Waltham Forest Borough Council and at approximately 11.45 evidence will be heard from Patricia Yates, Director of Strategy and Communications, Visit Britain
Location: Committee Room 4A, Palace of Westminster

 Posted by at 21:45
May 292013
 
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The chair of the UK Statistics Authority, Andrew Dilnot, has responded to a complaint from Sheila Gilmore MP regarding an article published in the Daily Telegraph which implied that 900,000 people who had been in receipt of Incapacity Benefit had dropped their claims rather than undergo a face-to-face assessment for the replacement benefit, Employment and Support Allowance (ESA). The article quoted Rt Hon. Grant Shapps MP, in his capacity as Conservative Party Chairman, as saying “This is a new figure, nearly a million people have come off incapacity benefit…before going for the test. They take themselves off.”

After investigation, Mr Dilnot concluded that these statements were misleading, although he formulates his response more diplomatically, as the 900,000 persons quoted did not appear to be claiming Incapacity Benefits, but represented the cumulative total of 878,300 new ESA claims which were closed before undergoing assessessment in the period from October 2008 to May 2012. Which means these people closed their claims before receiving benefits, and this happened over a period of four years. And according to research undertaken by DWP, an important reason why ESA claims in this sample were withdrawn or closed before they were fully assessed was because the person recovered and either returned to work, or claimed a benefit more appropriate to their situation.

Regarding claimants on Incapacity Benefits, a total of 603,600 recipients were referred for reassessment as part of the migration across to ESA between March 2011 and May 2012. Of these, 19,700 claims were closed prior to a work capability assessment in the period to May 2012.

Again, the right wing press and the Conservative Party have been caught red handed manipulating the figures. This is an exercise that DWP and IDS have also mastered over the past 3 years, by repeatedly using the number of new ESA claims to boost the number of people found fit for work, and distorting the real picture. The real picture for those who can remember the media headlines fed by DWP ” 70% of Britons on ‘incapacity benefits’ found to be fit to work”, is that with a much more stringent test, over 70% of people previously on incapacity benefits are still entitled to them.

Link to PDF copy of  letter HERE

May 282013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

When I received the initial phone call, from the DWP, I was hopeful that my health would be assessed fairly. I knew nothing of Atos.

I was told that during the process, I would lose no money. That was the first inaccuracy of many to come.

I returned the completed health questionnaire and waited.

Soon after I was summoned to attend a medical assessment at Wolverhampton, to be conducted by a ‘health care professional’ (HCP). This turned out to be the strangest medical I’ve ever gone through. I was asked to squeeze the HCPs fingers; I was asked to squat, and was told that I could use the wall as balance if necessary.

What possible relevance could these exercises hold?

The HCP spent more time looking at the computer monitor than she did in eye to eye contact.

The assessment eventually ended and I left, with a feeling of impending doom.

When I received the decision from the DWP, I was a little shocked, I must be honest. I knew that I could not carry out constant functions over a period of hours. I knew how my symptoms displayed themselves.

I sought help at my local CAB centre and almost at once I felt a sense of relief that I was not on my own.

The CAB advisor spent over twice the time the HCP had done and she came up with a report which clearly explained how my health affected my ability to carry out day to day functions.

There was nothing so profound in the DWP report.

My first appeal, to the DWP, failed as was expected, and I was advised to appeal to the first tier tribunal.

I also contacted my MP, Valerie VAZ, who wrote to the DWP, arguing that the assessment had failed to consider the degenerative nature of my condition, and was therefore flawed.

Soon after I received a phone call from a Decision Maker (DM) at the DWP who, after running through the assessment findings, offered another assessment.

Subsequent I received a new date with Atos.

This was in June 2012.

Between then and May 2013 I attended a handful of appointments, all of which were either cancelled by Atos due to my falling poorly during an assessment or for some administrative reason, such as computer problems.

On one occasion I was conveyed from the assessment centre to the local AE dept., when my BP & Pulse Rate were exceedingly high, and I was experiencing chest pains.

I spent the rest of that day hooked up to a variety of machines in the hospital.

Days later I received another Atos appt., this time for 0900…there was no chance I could make an appt. so early in the morning.

They should have been aware of this. It’s mentioned in my medical notes.

These frequent journeys were taking their toll on my health. My GP was so concerned that he wrote to Atos, explaining and sharing these concerns.

The Atos response was to change my AC venue from Wolverhampton to Birmingham, which is further to travel, and to approve a taxi, for collection and drop off at the attendance centre (AC). I already had a lift too the AC. travel was NOT the issue.

Atos had, for whatever reason, misread or misunderstood the nature of the letter from my GP.

The next appt. was the first taxi journey to the new venue, Birmingham, and my appt. was for 1:15pm.

I rang Atos at 12:30 just to confirm the taxi was booked, and was told it was.

13:15 came and went with no taxi.

The taxi arrived at about 13:25, which meant I was already late.

I arrived at 1355. Almost 45 minutes late.

To add insult to injury, I had pre-arranged to meet my welfare advice rep. at Birmingham. He was not happy either.

Understandable really.

More complaints were submitted to Atos.

This time they responded, eventually, with the offer of a home assessment.

Great news? No!

By the time if my tribunal I had still received no appt. for the Atos doctor to attend my home for the assessment.

My appeal was heard by the First Tier Tribunal and I was successful.

As good as this news is, it must not be seen as a way out for Atos. They caused considerable stress and aggravated my medical conditions for over a year with the catalogue of errors conducted by their staff. Pure and simple.

This would not be tolerated in any walk of life, so why should Atos be permitted to behave in this manner?

Something needs to be done.

I am hopeful that someone reading this will be in a position to offer some advice and support.

I am very sorry for those who are still fighting Atos.

I understand how they feel and I hope that something can be done to help them.

Thank you for reading this.

If any journalists would like to follow up this story please contact mail@dpac.uk.net

May 252013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Any campaign from this Government which claims to support disabled people should be viewed with suspicion and the latest offering from the DWP is no exception.

The department yesterday put out a press release boasting: “Celebrities have joined forces with the government to help launch a campaign aiming to promote positive role models for disabled people.”

This campaign features a youtube channel where 50 videos have been posted which have “been produced with a focus on overcoming barriers”.  Many of these videos are unsurprisingly about disabled people who have high flying careers, such as Dame Anne Begg, or are stories of disabled entrepreneurs.

The accompanying press release includes a gushing quote from Emmerdale actor Kitty McGeever explaining how after becoming disabled it ‘took some time to get back into work’ but she managed it with the help of the Government’s Access To Work scheme.

This scheme provides funding for workplace adaptations, travel or some care needs for disabled people in employment.  The number of people benefiting from Access To Work has plummeted by over a third since this Government weren’t elected showing the true situation for disabled people currently seeking employment.

Whilst this campaign may be a cheap attempt to improve those figures, it comes against a background of savage cuts to benefits, services and housing for disabled people.  It is a campaign run by a government which is declaring hundreds of thousands of sick and disabled people to be ‘fit for work’ with the aim of stopping their benefits.  A government which has been only too happy to force sick and disabled claimants onto workfare as part of the Work Programme –  with no public scrutiny of where they are being sent or for how long.  A government that is set to force potentially hundreds of thousands of disabled people from their homes due to the bedroom tax, benefit cap and other measures.

And when Personal Independence Payments (PIP) fully replace Disability Living Allowance, this is a Government which will have slashed completely a vital benefit for 20% of disabled people.

This move alone is likely to mean that over 50% of disabled people are forced to leave work as funding for specialist equipment, care and transport disappears*.

Vast numbers of disabled people are set to be plunged into poverty by these measures, and it is this which reveals the true intentions of this latest DWP run project.  One of the charities involved in the campaign is quoted as saying that the “project is about showing what disabled people can do – not what they can’t”.

This is eerily similar to David Cameron’s line when interviewed shortly after the opening of the Paralympic games when he said: “It’s about the inspiration and it will change people’s minds and that’s what matters. It’ll teach people about what they can do, rather than what they can’t do.”

It is also the line used to justify the benefit-stripping Work Capability Assessment which according to the DWP focuses on “what an individual can do despite their health condition, rather than simply what they can’t.”

Minister for Murdering Disabled People, Esther Mcvey also pops up in this week’s press release, and whilst not quite so explicit, her underlying message is the same:  “young disabled people tell me they want to see more inspiring role models to show where disabled people have achieved their ambitions despite the odds being stacked against them”

For young disabled people the odds are stacked against them like never before due to this Government and in this context the true nature of the DWP’s latest campaign becomes clear.  This is not about providing role models for young disabled people or helping people fulfil their potential or even changing perceptions of disabled people as is claimed.  This Government doesn’t care about any of that.  This campaign is yet more insidious DWP propaganda attempting to give the impression that those plunged into poverty due to the ruthless cuts to disability benefits will only have themselves to blame.  If only they’d learnt to play wheelchair rugby, or been a fucking Dame, then they could afford to put the heating on.

The campaign also has a facebook page which might be a good place to share experiences of what people can no longer do due to the vicious cuts to benefits: https://www.facebook.com/Rolemodelsinspire

Dawn Willis writes well about this kind of narrative: ‘I’m not Stephen Fry, how damaging is that?’ from Dawn

*this figure comes from a survey carried out by Disability Rights UK (DRUK) which reported that 56% of those asked said they would have to leave work if they lost their DLA.  DRUK are notoriously in the pockets of the DWP, with Chief Executive Liz Sayce writing a report which recommended the closure of the Remploy factories.  The survey relating to the number of people likely to leave work due to PIP seems to have disappeared from DRUK’s website, for which there is surely an entirely innocent explanation.

Follow me on twitter @johnnyvoid

With massive thanks to the brilliant Johnny Void for letting us re-post

See more from Johnny at https://johnnyvoid.wordpress.com/2013/05/25/achieve-your-potential-or-starve/

 

May 222013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

DPAC Logo 3 amendment 1 (Small)On the day of the success of the ruling against the WCA-Activists from DPAC and disabled workers attending the TUC Disabled Workers Conference have blocked Tottenham Court Road in an unprecedented act of solidarity.

 This Government has repeatedly used the language of division, trying to divide workers and claimants, public and private sectors workers, non-disabled and disabled people. Today we strike back as one, united voice.

 The Cuts imposed by the ConDem Government under the cloak of ‘Austerity’ impact on disabled people in every area of life. The scrapping of Disability Living Allowance (DLA) and the Independent Living Fund (ILF) will tens of thousands of disabled workers, and will force many of them out of their jobs. Hundreds of thousands of disabled people both receive and deliver public services as workers in Public Service Departments, Local Authorities and the Voluntary Sector. ILF and DLA play critical roles in maintaining people in these jobs. The 1% uplift limit on Benefits, Universal Credit and the Bedroom Tax will impact on many disabled people both in and out of work.

 The removal of many of our basic rights affect not just disabled people, but all of us. For example, the removal of Legal Aid for medical negligence claims comes at the same time as every single contract within the Health Service is open to tender by private companies. This has serious and significant implications for each and every one of us who make up the 99%.

 But not everyone is being hit by austerity. While multi-nationals like Atos and Capita make fortunes, tax avoidance and evasion to the tune of tens of billions goes uncollected. The wealthiest 1000 UK residents increased their wealth by some 35 billion last year while disabled people and the poorest members of society were pushed into poverty and despair as the targets of brutal cuts.

 Disabled activists have led the fightback against this Government since the beginning, and today disabled activists and workers lead the way again in the first joint, co-ordinated direct action by campaigners and unions on the streets of the U.K.

 Shabnam O Saughnessy from DPAC said: “We are delighted to be joined on the streets today by our union comrades. This represents the first steps towards uniting resistance from communities and workplaces. It dispels the myth of disabled people as scroungers and workshy. We are not some separate group of others, we are your friends and neighbours, we work alongside you. Many millions of disabled people are being affected by cuts, and today is about getting our voices heard.”

 Sean McGovern, co-chair of the TUC disabled workers committee said: “Trade unionists would like to send a clear message to this government that trade unions, workers and grass roots disabled groups stand together against the onslaught of vicious cuts rained down upon us by the Condems.”

DPAC and disabled workers from the TUC conference block Tottenham Court Road 22nd May

Notes

1)    Disabled People Against Cuts is a national campaign led by disabled people to oppose the attacks on disabled people being carried out under austerity. www.dpac.co.uk

 

2)    The 2013 TUC Disabled Workers’ Conference takes place on 22-23 May. The TUC Disabled Workers committee recently rejected an invitation to join the government’s new Disability Action Alliance on the grounds that involvement would restrict the TUC’s ability to campaign against government policies that are affecting disabled people.

 For more information contact Ellen Clifford on 07505144371 or ellenrclifford@btinternet.com

For updates see twitter: @Dis_PPL_Protest

and Disabled People against Cuts Face book Group

We previously incorrectly attributed a quote to  Mandy Hudson that was said by Sean McGovern. This has now been corrected after we were alerted to this by Sean (26th May)

May 222013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Three judges today confirmed what DPAC and other campaigners have been saying since 2010– the benefits test used to decide whether people are fit for work, actively discriminates against disabled people and those with mental health issues

 Mental health Resistance network (MHRN) have won the judicial review case against the DWP on the clear inadequacy of the Work Capability Assessments. They supported two users who took a case against the DWP for the harm these tests do to those with mental health issues. The WCA has been severely criticised since the Condems took over the reins from the New Labour WCA inception, making the tests more and more difficult and more and more humiliating for all concerned.

 Last week Dr Greg Wood resigned claiming the tests were biased, there have been a number of high profile resignations from nurses resigning and claiming that not only were the tests unfair they were degrading. This is a subject disabled people know all too well, from the millions lavished on Atos for tests and the millions for appeals.

 The  judicial review focussed on specific issues for those with mental health issues – that of gathering supporting evidence. Under the current system, individuals are responsible for gathering their own medical evidence and sending it to the Department of Work and Pensions (DWP). If anyone fails to do this, it simply won’t be looked at, and in many cases if you do do this your papers will be brushed aside (see DPACs survey responses on the WCA HERE).

Reporting the victory DPAC’s sister group,  Black Triangle Campaign wrote:

“The judgment that the DWP is in breach of the Equality Act is a huge victory for everyone affected by severe mental illness, but it’s sad that it took a court case to force the DWP to take action”.

DPAC wants to congratulate the two people that took the case, MHRN and all others that supported this. We hope this is another step towards outlawing these tests and stopping them for the damage they are causing all disabled people as called for by the BMA and the RCN.

We note that the big Disability charities have , as usual, chosen to take the credit for this success and we say again that this success is due to MHRN a small group that chose to do something. It is due to the two people that took the case and the solicitors involved. This case was not initiated by any of the big disability charities-despite them joining in later to save face.

 The charities sat back and did nothing, but they are fast to take the credit for something that they didn’t even contribute too. We hope that the success of the MHRN actions leads to an end to this inhuman process for all and we congratulate them for their tenacity and their actions in getting someone done- to the charities we say: we know the difference between the real heroes and those that try to bask in reflected glory-if you had made the move that MHRN had or acted more vigorously we might applaud you, as it is we are, once more unimpressed by your actions.

 see also:

https://dpac.uk.net/2013/05/esa-regulations-25-and-31-campaign-black-triangle-to-meet-with-scottish-parliament-welfare-reform-committee-chief-this-thursday/

https://dpac.uk.net/2013/05/where-are-the-mental-function-champions-at-atos-and-other-atos-type-things/

https://dpac.uk.net/2013/01/dpac-press-release-wca-descriptors-fail-dwp-fails-atos-fails/

https://dpac.uk.net/2012/10/joint-statement-on-work-capability-assessment-wca-by-dpac-and-black-triangle/

https://dpac.uk.net/2012/11/dpac-survey-responses-on-wca-what-harrington-didnt-ask/

 

 

 

 

May 152013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Bromley and Croydon DPAC are holding a benefit Justice  meeting Monday 30th May at 7pm at Acts Ministries, Acts House, 30 Union Road, Croydon, CR0 2XU.

Its another opportunity for people to come together against the cuts affecting us all.

“The Bedroom Tax and the benefits cap, alongside other sweeping changes to the benefits system and the reduction in vital services supporting disabled people and parents, is hitting the poor hard – both those in and out of work,” DPAC’s spokeswoman said.

“The benefits cap on top of the Bedroom Tax will impoverish and stigmatise people who can’t move home, while driving out others to unfamiliar parts of the country, uprooting their lives and their support networks, and leaving London to the better off.”


For more information visit www.benefitjustice.wordpress.com.

Email: benefitjustice@gmail.com or mail@dpac.uk.net

May 042013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Yet another Daily Mail FAIL!!



What is it with these journalists from the Daily Mail?

Why can’t they ever get anything right when it comes to reporting something factual over the government’s callous welfare reforms.  Here’s a really ‘slack’ piece of journalism from one of the Daily Mail’s finest, strangely enough he goes by the name of James Slack; slack by name slack by nature I’d say.

Read Slack’s factually inaccurate article here



The REAL facts with all the DWP links are here

Slack makes a pathetic attempt to try and get his deluded readers to believe that it’s the ‘lefties’ who are creating the myths over the dangerously hazardous welfare reforms which government is inflicting upon thousands.  Slack headlines his article ‘ What the Left doesn’t want you to know about Britain’s £200 billion welfare bill’.  He goes on to write the usual rubbish we’ve grown accustomed to reading in the gutter press, the particular piece which got my goat was Slack’s incredibly lazy attempt to rubbish what he absurdly pitches as a left – sided myth over those on incapacity benefits. Here’s an excerpt from Slack’s article:

‘Slack fact 1’

 

“THE TRULY SICK ARE NOT BEING FORCED TO WORK”

“CLAIM: New tests to check Incapacity Benefit claimants’ inability to work are having a devastating effect on the sick and mentally ill.”

“REALITY: Incapacity Benefit, which was renamed Employment and Support Allowance, is paid to people considered unfit for work. Only 232,000 — one in eight of those tested by doctors — have been deemed too unwell to do any work.”


Actually in reality incapacity benefit was never renamed Employment & Support Allowance at all

If Slack had checked his facts he would see that the Employment & Support Allowance here is entirely separate to the incapacity benefits found here.  If one had been renamed as the other the two would not continue to exist.    

‘Slack fact 2’

“Another 837,000 who took the test were found to be fit to work immediately, and a further 367,300 were judged able to do some level of work.”


In reality Slack is miles off the mark with this little gem.  In actual fact only 700,200 incapacity benefit claimants have been tested under the much stricter Employment & Support Allowance rules of which 496,800 (71%) were found to be perfectly entitled to the allowance.  the percentage figure varies each month – figures of 78% being recorded in October 2010, 77% in March 2011 and 75% in July 2012.   

290,200 were deemed chronically incapacitated and incapable of any work related activity whatsoever and 206,600 were deemed to have a severe limitation such that they qualified for ‘support’ from the government in helping them work towards a return to work – sadly very few end up getting the Support because the DWP is seemingly too busy feeding the press with the kind of garbage which incompetent journalists like Slack writes for the Daily Fail. 

‘Slack fact 3’

“Some 878,300 people — around a third of the 2.6 million who were claiming the benefit — have chosen to drop their claims rather than face a medical.”


In actual fact the figure relating to incapacity claimants, who for any number or reasons dropped their claim, is nowhere near 878,300 – it is 24,700 as per the DWP’s most up to date figures of August 2012.

‘Slack fact 4’

“One in eight of those tested by doctors”
In actual fact the DWP under it’s private and ‘commercially sensitive’contracting arrangements with Atos Healthcare recruits an abundance of nurses as well as doctors and the chances of everyone being tested by a fully qualified doctor is zero.



‘Slack fact 5’

“Some 30 people were claiming they were unfit to work because of blisters, while 60 cited acne and 2,110 said ‘sprains and strains’ rendered them unfit for employment.”


How on earth can Slack have had access to what should be highly confidential medical records relating to 30 individual assessments to know precisely what conditions they were citing as their one and only ground for claiming they were unfit for employment?

It bemuses me how the Daily Mail can make so much fuss about footballer Wayne Rooney’s £130,000 a week sprained sprained ankle with no reference or inference to the possibility of him ‘skiving’.

I also note the gutter press draws attention in previous articles to the tragedy of a 31 year old woman who committed suicide over what they describe as a ‘minor skin condition. The article describes how the woman’s mental health deteriorated to the point where, after two failed attempts, she sadly took her own life by jumping off the Humber Bridge.

I presume James Slack would not retrospectively imply the poor woman was ‘fit for work?’

Why not email Slack and tell him what a truly useless
journalist he is is?



j.slack@dailymail.co.uk



And then complain



To the Press Complaints Commission

 

 

 

 

 


 

Unreal!  The Daily Mail prints the 

 

‘Workshy map’ 

 



 

“This map of Britain reveals the ‘workshy’ spots around the country where people claiming incapacity benefit claimants are actually fit enough to work.

The Government introduced tough new health tests for those who claimed to be too unwell to get back into employment two years ago.

Since then some 203,000, 30 per cent, out of 700,000 receiving the old Incapacity Benefit were declared fit to find work.”

“The Department for Work and Pensions (DWP) said Birmingham had the biggest number of claimants capable of work. Of 14,640 claimants, 5,180 were fit.”

Once again we are indebted to Nick at My Legal Forum-who seems to be taking over the DPAC web site but in the best possible way

For more from Nick see

https://ilegal.org.uk/thread/7616/page/1/cut-slack-quit-media-lies

twitter: @Mylegalforum

and we promise more brilliance fromNick very soon

May 012013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

The latest Work Capability Assessment figures released by the DWP yesterday (30th May 2013) attracted little of the usual fanfare which usually sounds as they trumpet the results. Perhaps they’re getting nervous with an increasing number of rebuttals over their use of statistics appearing in the press of late?

Or perhaps on this occasion they simply didn’t have too much which they wanted to shout about?

I think it’s a mixture of both.

Amongst other things the DWP’s latest Quarterly figure release’ for June – August 2012 reveals:

52% of new Employment & Support Allowance were entitled to the allowance after assessment

73% of claimants having undergone conversion from their incapacity benefit claims had qualified for Employment & Support Allowance with 38% ending up in the Work Related Activity group and 35% in the Support Group.

It’s all a far cry from the days when not so longer ago the media fuelled almost certainly by the DWP were saying 75% of claimants were skivers.

Closed claims

After being heavily criticised in a number of media articles over drawing unsubstantiated conclusions as to why 878,300 (A figure which in itself was wrong) claimants had closed their claims before being assessed, the DWP appears to mitigate its incorrect assumptions by drawing a reference to a further report ‘Unsuccessful Employment and Support Allowance claims – qualitative research. I’d encourage those following the reassessment programme to give it a close read, not least because it was prepared some time ago back in 2011 and relates to findings drawn from a survey across only 952 individuals and a further sample of just 60 claimants. It’s a meagre number of claimants upon which to draw any conclusions when looking at the many thousands who have, for a variety of unknown reasons, closed their claims prior to being assessed.

The report concludes

“An important reason why ESA claims in this sample were withdrawn or closed before they were fully assessed
was because the person recovered and either returned to work, or claimed a benefit more appropriate to their
situation”

Before accepting the conclusion, I’d look at the report and the sample size of those surveyed.

What’s missing?


A complete reference to any of the results of the claimants who have been assessed following their initial assessment is missing from the report although the information is to be found in the tables.  These are often omitted but should be included.  If you look at the accompanying tables which the report if linked to you you will see that there is a total case load of no less than 958,300 from which 340,300 claimants were placed in the Work Related Activity Group since October 2008, far fewer are found fit for work in the group with 215,100 from October 2008 to August 2012.  Both of these groups will have a propensity to appeal, some claimants may for instance at the initial assessment have been placed in the Support Group but after being assessed again may be put in the Work Related Activity Group – creating a number who will appeal.

Of these assessed in the ‘reassessed following initial assessment’ group, 78% were entitled to ESA in June, 79% in July and 79% in August 2012 – a sizeable increase when compared with the 73% cumulative total relating to the entire period from October 2008 to August 2012.  I fail to understand why so little attention is drawn to a cohort of close to a million claimants who have been ‘repeat’ assessed in this group since the programme started .

The quarterly comparison 

When comparing the overall figures for all three cohorts (new claims, claims reassessed following initial claim and ib/ESA conversions) between May 2012 and August 2012

To date total


Increase/decrease on figure to May 2012 

Per month average over quarter

Numbers assessed WCA

3,053,200

367,300

122,433

Work Related
Activity Group placements

1,028,800

134,200

44,733

Support Group
placements

715,500

139,200

46,400

Fit for work findings

1,308,700

93,500

31,167

Closed claims before assessment

1,074,200

91,800

30,600

Cases still in progress

193,200

26,000

8,667

Overall case load

4,320,600

485,100

161,700

Case load

What these figures, taken across ALL claimants involved in the assessment programme, show is that the DWP ‘case load’ increased by 485,100 over the period from June 2012 to August 2012.  The case load isn’t the number of claimants, it is the number of claim interventions made by DWP officials as part of their case load, it can be divided in to cases where an outcome has been recorded in which case the claimant will be placed in the Support Group, Work Related Activity Group or found ‘Fit for Work’.

Of the cases which have not been assessed, the claimant’s case can ‘still be in progress’ (this is not the same as the assessment phase data) or could be closed without assessment.

With usual thanks to the brilliant Nick of My Legal twitter @Mylegalforum

For a detailed breakdown up to August 2012 see Nick’s detailed work at

https://ilegal.org.uk/thread/7140/page/5/dwps-esa-reassessment-programme-chaos



Apr 252013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Man Jailed After Comments Made In Atos Assessment

atos-killsA Nottingham man has now been held in custody for two weeks after he was accused of “threatening behaviour” due to comments he allegedly made during his Atos benefits assessment.

Steve Topley is a 49 year old father with multiple serious health problemswho was required to attend a Work Capability Assessment with the notorious IT firm Atos – the company responsible for stripping benefits from hundreds of thousands of sick and disabled people.  During the process Mr Topley made some comments about someone not present at the assessment.  His family say these comments were misunderstood and were in response to questions from the assessor about his personal life.

These comments led to Atos staff calling the police and Mr Topley was asked to attend Queens Medical Centre (QMC) in Nottingham.  When he refused to do so he was arrested.  At QMC he was de-arrested and received a mental health assessment but no reason was found to detain him under the mental health act.  He was then re-arrested and taken in handcuffs to Nottingham police station where he was later charged.

He has now been refused bail twice in closed courts which his family were not permitted to attend.  His sister Gina Topley, who says the family are being kept in the dark about the legal process, has said:

“My brother has not been given any opportunity to speak and give his side of the story to a judge and he was not offered an appropriate adult to accompany him when he was arrested.”

His family have not been allowed to visit him in prison and have raised concerns that his medication may not be being administered properly.  Mr Topley will face another appearance in a closed court tomorrow (Friday 26th April) and there are major fears that he will be remanded once again pending psychiatric reports.

His family and supporters have called a demonstration outside the court tomorrow calling for his immediate release.

Meet outside Nottingham Crown Court on Friday 26th April from 9.30-11.00am – please help spread the word.  For more details and the  latest news visit:https://freestevetopley.wordpress.com/

reposeted from Johnnyvoidwordpress –  twitter @johnnyvoid

 Posted by at 16:35
Apr 212013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

this is taken from kittyjoneswordpress.com and we hope it will be useful for people to know about.

Courageous Scottish nurse Joyce Drummond, who made a heartfelt apology to Atos assessment victims, has submitted evidence to the Scottish Parliament Select Committee on Welfare Reform.
I have a correspondence with Joyce, who was the subject of this article: www.dailyrecord.co.uk/news/scottish-news/nurse-makes-heartfelt-apology-after-1340838

Joyce has submitted evidence to the Scottish Parliament Select Committee on Welfare reform, which she forwarded to me this morning. I have edited where needed, and added to the text to make it easier to read. I’ve included the contents from Joyce’s notes in full.

I knew nothing about Atos when I joined, and left as soon as I realised that there was no way to fight from the inside.
I carried out Incapacity Benefit assessments, these were the forerunner to ESA assessments. I stated at my interview for the job that I believed in social inclusion and social justice.

I went for 4 weeks training in England. The training did not prepare me for what I was expected to do in real life.

The forms that are completed prior to assessment, I have recently found out, are opened by Royal Mail Staff. They are then sent for “scrutiny” where nurses decide whether or not a face to face assessment is required. I was not involved in this and do not know what criteria are used.

It is made clear throughout training and working that we are not nurses- we are disability analysts. Also, we do not carry out ‘medical assessments’ – we carry out ‘functional assessments’. We did not even need a diagnosis to carry out assessments. I had reservations around consent, as we were expected to assess patients – sorry, we didn’t have patients, we had ‘claimants’- who appeared to be under the influence of alcohol or other substances.

We were also consistently told that we did not make benefit decisions. The final decision was made by a DWP decision maker with no medical qualification. If our assessment was overturned at appeal we never knew about it. There was no accountability for assessments overruled.
Assessment starts on the day of your appointment with the HCP reading the form you complete when you applied for benefit. Remember that every single question you are asked is designed to justify ending your claim for ESA and passing you as “fit for work”. That is what Atos are contracted to do by the Government. This is not a genuine assessment, but rather, an opportunity for the DWP to take away your financial support, which you are entitled to.Things that are noted are :-

Did you complete the form yourself
Is the handwriting legible
Are the contents coherent.

These observations are already used in assessing your hand function, your cognitive state and concentration. Next under observation:-
Do the things you have written add up.
Does your medication support your diagnosis.
What tests you have had to confirm diagnosis. For example a diagnosis of sciatica is not accepted unless diagnosed by MRI scan.
Do you have supporting medical evidence from GP or consultants. If you do, it shows that you are able to organise getting this information.

This is also a hidden cost to the NHS. I believe that if ATOS request information there is a charge levied by GP’s. However claimants are expected to source medical evidence themselves. It uses valuable NHS time for medical staff to write supporting statements.
There were no hidden cameras, at least in Glasgow, to watch people arriving for assessment or sitting in waiting room. This may not be true in other areas.

When the HCP has read your form they input some data into the computer system. The assessment properly begins when they call your name in the waiting room. At this point they assess:-
Did you hear your name being called
Did you rise from your chair unaided, did the chair have arms or not
Were you accompanied – this addresses you’re ability to go out alone.
Were you reading a paper while waiting- looks at your concentration.
Did you walk to the assessment room unaided, did you use aids correctly. Did you navigate any obstacles safely- assessing sight.
The HCP will shake your hand when inroducing herself- are you trembling, sweating- signs of anxiety. Again note the constant scrutiny. The HCP will often ask on way to waiting room:-

How long you’ve been waiting- assessing ability to sit- both physically, and looking at your mental state.
How did you get here today- ability to drive, use public transport.
Assessment begins by listing medical conditions/complaints. For each complaint you will be asked:-

How long have you had it, have you seen a specialist
Have you had any tests, what treatments have you had
What’s your current treatment. Have you had any other specialist input eg. physiotherapy, CPN.

The HCP will use lack of specialist input/ hospital admissions to justify assessing your condition as less severe. Medications will be listed and it will be noted if they prescribed or bought. Dates will be checked on boxes to assess compliance with dosage and treatment regime. Any allergies or side-effects should be noted.
A brief note is made of how you feel each condition affects your life
A brief social history will be taken – who you live with, if have you stairs in your house or outside to your house.
Employment history taken – asking when you last worked, what you worked as, reason for leaving employment.
Typical Day – this is the part of the assessment where how you function on a day to day basis is used to justify the HCP decisions. Anything you say here is where you are most likely to fail your assessment. Along side this, the HCP records their observations.
Starting with your sleep pattern, questions are asked around your ability to function.

Lower limb problems- ability to mobilise to shops, around the house, drive, use public transport, dress, shower.
Upper limb- ability to wash, dress, cook, shop, complete ESA form
Vision- did you manage to navigate safely to assessment room.
Hearing- did you hear your name being called in waiting room.
Speech- could the HCP understand you at assessment.
Continence- do you describe incontinence NOT CONTROLLED by pads, medication. Do you mention it’s effects on your life when describing your typical day.
Consciousness- Do you suffer seizures- with loss of continence, possible injury, witnessed, or uncontrolled diabetes.
HCP observations include- how far did you walk to examination room, did you remove your coat independently, did you handle medications without difficulty, did you bend to pick up handbag.
Formal examination consists of simple movements to assess limited function.Things HCP also looks out for:-

Are you well presented, hair done, make-up, eyebrows waxed.
Do you have any pets – this can be linked with ability to bend to feed and walk.
Do you look after someone else – parent or carer- if you do this will be taken as evidence of functioning
Any training, voluntary work, socialising will be used as evidence of functioning.

This is not a comprehensive list, but gives you an idea of how seemingly innocent questions are used to justify HCP decisions.
Mental Health
Learning tasks- Can you use phone, computer, washing machine.
Hazards- Can you safely make tea, if claiming accidents- must have had emergency services eg fire service. Near miss accidents do not count.

Personal Actions
Can you wash, dress, gather evidence for assessment
Manage bills.

Observations made by HCP – appearance and presentation
Coping with assessment interview, abnormal thoughts, hallucinations, confusion.
Coping with change – ability to attend assessment, attend GP or hospital appointments, shopping and socialising.

More HCP observations:-
Appearance, eye contact, rapport, any signs/symptoms that are abnormal mood/thoughts/perceptions. Suicidal thoughts.
Coping with social engagement/appropriateness of behaviour – any inappropriate behaviour must have involved police
Ability to attend assessment, engage with assessor, behave appropriately.
Again this is not an exhaustive list, merely examples.
There are some “special cases”. Off the top of my head, exemptions from assessment include – terminal illness, intravenous chemotherapy treatment and danger to self or others if found fit to work (Regulation 29.)

At present to qualify for ESA you need to score 15 points. This can be a combination of scores from physical and mental health descriptors.
To qualify for the support group you must score 15 points in one section.
As long as you are claiming income – based ESA then your award can be renewed at each assessment, if you gain 15 points.

Contribution ESA lasts for 1 year only, unless you are in the support group. After 1 year in the support group, you may only get income based ESA if your household income is below a certain threshold. It makes no difference how long you have previously paid National Insurance.

For clarity, as far as I know in the real world, doctors carry out medical assessments, nurses carry out nursing assessments and physios carry out physiotherapy assessments. In the world of Atos, each of these separate professions are employed as disability analysts, carrying out functional assessments.
Nurses are employable for these posts if they have been qualified for at least 3 years, are registered to practice with the NMC, and have basic computer skills.
My interview consisted of-
Face to face interview with medical director and nurse team leader.
A written paper assessing a scenario, in my case someone with back pain
A 10 minute basic computer test.
In order to be approved as disability analyst I had to complete 4 weeks Atos disability training, reach a certain standard of assessment reports- as decided by audit of all cases seen (don’t know what criteria was) and finally approval to carry out WCA assessments from the Secretary for Work and Pensions.
In my opinion the money given to Atos and spent on tribunals should be given to NHS GPs. They are best placed to make assessments regarding patients work capability. They have access to all medical reports, past history, specialist input and know their patients. My concern would be what criteria the DWP would impose on GPs risking the doctor/patient relationship. GPs already assess patients for “fit notes”, which have to be submitted to DWP during assessment phase of ESA.

While I worked at Atos, sessional medical staff were being paid £40 per assessment, as far as I am aware. I have no idea of wages of permanent medical staff. Nurses were on a salary, which based on 10 assessments a day (Atos target) equalled around £10 per assessment. These are approximate figures but may give a clue as to why Atos are employing nurses rather than doctors.

Further information:-

Special exemptions from the 15 points criteria: Regulations 29 and 35.

Questions you may be asked at assessment: dwpexamination forum

How to deal with Benefits medical examinations: A Useful Guide to Benefit Claimants when up against ATOS Doctors

More support and helpful advice here: How to deal with Benefits medical examinations

Previous related article: After Atos

List of conditions judged suitable for assessment by neuro trained nurses/any health care profession: –
Prolapsed intervertebral disc
Lumbar nerve root compression
Sciatica
Slipped disc
Lumbar spondylosis
Lumbar spondylolisthesis
Lumbar spondylolysis
Cauda equina syndrome
Spinal stenosis
Peripheral neuropathy
Neuropathy
Drop foot
Meralgia paraesthetica
Cervical spondylosis
Cervical nerve root compression
Cervicalgia
Nerve entrapment syndrome
Carpal tunnel syndrome
Trapped nerve
Paraesthesia
Tingling
Numbness
Brachial plexus injury
Polyneuropathy
Dizziness
Vertigo
Essential Tremor
VWF
Alzheimer’s

List of conditions judged by the DWP and Atos Healthcare as suitable only for assessment by doctors:-
Stroke
Head injury with neuro sequelae
Brain haemorrhage
Sub Arachnoid Haemorrhage
Brain tumour
Acoustic Neuroma
Multiple Sclerosis
Motor Neurone Disease
Parkinson’s disease
TIAs
Bulbar Palsy
Myasthenia Gravis
Muscular Dystrophy
Guillain-Barre Syndrome
Amyotrophic lateral sclerosis
Syringomyelia
Neurofibromatosis
Spina bifida
Polio
Fits (secondary to brain tumour)
Learning difficulties (with physical problems)
Nystagmus
Myelitis
Bells Palsy
Trigeminal Neuralgia
Paraplegia
Quadriplegia
Huntington’s Chorea
Huntington’s Disease

 

 Posted by at 17:24
Apr 162013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

If you missed it all -the Disability Action Alliance or DAA[i] has had a strange and tortured beginning. It was set up in 2012 to help with the new disability strategy. The merged organisation of RADAR, Disability Alliance and the National Centre for Independent Living (NCIL) AKA Disability Rights UK (DRUK) got the’ job’ of co-organising the DAA. This was a great surprise to all, not least the United Kingdom Disabled Peoples’ Council (UKDPC). The great surprise was that this ‘job’ hadn’t been advertised or put out for tender. After initial rumbles of shock and discontent DRUK said that they would not be paid for this ‘job’ so it didn’t matter, or words to that effect -and we all forgot about it.

Another issue was that this Alliance would include charities, presumably big disability charities as well as small ones, and private companies or corporations. This caused more rumbles of shock and discontent because some of us had been taught and still believed that any ‘disability movement’ was about disabled people leading it, was user-led and rights not charity based, we weren’t sure how to deal with this astounding corporate thing being added on either.  DRUK said DAA would be advising on government policy and would not supplant the role of disabled peoples’ organisations so it didn’t matter, or words to that effect -and we all forgot about it.

Then there was a flash new website called unsurprisingly: Disability Action Alliance. At the link if you want to have a look https://disabilityactionalliance.org.uk/ or join

A site with pictures, a bit government branded in style, but what can we expect.  The ‘About us’ section says:

During the development of Fulfilling Potential – Next Steps, the idea of a new way of working in partnership emerged and ODI agreed to set up the Disability Action Alliance.  Disability Rights UK agreed to convene the Alliance to ensure ‘nothing about us without us’ – so that disabled people’s voices and experiences drive change, locally and nationally.

The ODI or Office of Disability Issues (an adjunct to the DWP) also set up a network called the ‘Network of Networks’ in 2010 so that disabled peoples’ voices could drive change, locally and nationally’ with a pure base of 12 user-led disabled peoples’ organizations, which they then disbanded, unceremoniously, shortly after the development of Fulfilling Potential.  So the ‘nothing about us without us’ does ring a bit hollow, especially with the potential corporate business and big disability charities in the ‘us’ bit.

Maybe a more apt chant would be ‘something about us without us again’ led by Government departments, sorry ‘disabled peoples’ voices’

Alliance Declaration and Membership Agreement

There was some more shock and discontent over the DAA ‘membership agreement’ on the web site. For example the section states members must:

‘Respect the views of other members, and not represent their views unless they are given permission’

It is unclear what this means exactly, but it doesn’t sound particularly empowering to disabled peoples’ voices. Does it mean that a group cannot represent another groups views ‘unless they are given permission’? or that they cannot represent their own views? It all seems a bit defeatist to us. Also included is that members must:

‘Protect the integrity of the Alliance and not bring it into disrepute’

Again, what does this mean? Why would any group want to bring the alliance into disrepute? And what is the ‘protect’ element about?

We also see members must: ‘Not campaign or lobby in the name of the Alliance (this would not affect whether members campaign or lobby on behalf of their own organisations)’

Oh well, that’s good then and…in the spirit of incorporating others into the new world order, members must:

‘Identify existing groups/alliances/networks who may already be acting and could be engaged’

Already be acting….?

Anyway, the drive for members of the quango, sorry, new exciting network of disabled peoples’ voices was launched and anyone could join up, presumably providing they could understand exactly what the Alliance declaration and membership agreement actually meant. At the time of writing there are 102 members. As we seem to have waited so long to find out who they are let’s see if our anticipation has paid off…

Members of DAA so Far….

Members include some disability type organisations, plus: the Department for Works and Pensions, the Department of Climate and Energy Change and presumably the ODI. Also Lloyds bank is there and big charity Shaw Trust. There are a number of companies but no big names such as Atos or Capita which is reassuring, for the moment anyway; a couple of DIAL’s (taken over by SCOPE a few years ago), a regional unison, and a local council.

For those who filled out or took part in completing the consultation on the disability strategy (Fulfilling Potential), the outcome of the DAA is all slightly surreal. There we were with our disabled voices trying to affect change and here we are with a hotchpotch of unforeseen organisations who are going to talk about it-providing they get ‘permission to represent’ their? Our? the DWPs? Views-oh who really knows anything about what’s going on with this anymore?

There was more surreal stuff to come when the TUC Disabled Workers Committee were approached by the government to join the Alliance- eh? –‘approached by the government’ must have been some kind of an elongated typo on the TUC website there…but anyway they said no. Why did they say no?

TUC Disabled Workers Committee says no to DAA

According to a piece in Disability News Service and on the TUC website: the TUC disabled workers committee were approached by the Government-OK-so not an elongated typo- to join the DAA. They said no. According to the TUC web site, they said no because:

Disabled trade unionists feel very strongly that joining the DAA – an organisation recently set up by the Office for Disability issues to encourage groups representing disabled people to work together – would restrict the TUC’s ability to campaign against government policies that are affecting disabled people.

Representing disabled people? Does Lloyds bank really represent disabled peoples’ views or do the DWP or those other government departments?

No, we didn’t think so either. But Sean McGovern (chair of disabled workers committee) gets to the heart of the matter and maybe to the focus of the real disability strategy when he says:

The government has been attacking the living standards of disabled people for almost three years now and things are getting worse.

Unions are working with disabled people against these brutal and inhumane cuts, and are campaigning against the government’s unnecessary and damaging austerity drive.

The ATOS work capability assessments, the closure of the independent living fund, the switch from disability living allowance to the personal independent payment, and the bedroom tax – every single one of these changes is punishing and impoverishing disabled people and their families.

Joining this government-inspired alliance now would be to pretend that none of this is happening.

We want to see all disabled people and the organisations that represent them continuing to oppose government policy and not conned into becoming part of the problem rather than part of the solution.’

And this is exactly where any growth of a real disabled peoples’ led disability action alliance must be focused for anyone aware of what is really happening to disabled people under this government and its disability strategy

 You can join up at www.dpac.uk.net

We already have over 12,000 members and supporters, and not a government department in sight. You know it makes sense.



[i] Not to be confused with Disability Awareness in Action a user-led organisation

Mar 262013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net

Benefit appeals are on the rise….

Sickness benefit appeals up by 70%….

‘Chaos is looming’

Latest statistics from Her Majesty’s Courts & Tribunals Service (HMCTS) reveal that the DWP’s increasingly controversial Employment & Support Allowance is leading to a massive surge in the numbers of appeals lodged with independent Tribunals.  The Ministry of Justice figures can be read here and confirm that for the period July to September 2012 the number of appeals was up by 69% on the same quarter on the previous year.  Benefit appeals are now accounting for 58% of all cases received for appeals across all Tribunals – an alarming increase.

The Ministry of Justice figures exhibits all the signs of impending chaos with a staggering 813,500 tribunal cases in total; an increase on the previous year when the number had already exceeded three quarters of a million appeal cases.

The number of Employment & Support Allowance appeal receipts is of particular concern, in the year 2011/2012 a total of 181,000 appeals were received by the Tribunals. In the first six months of 2012/2013 the figure has shot up to 133,700 indicating that these appeals alone are well on track to exceed a quarter of a million by year end.

42% of DWP decisions in ESA cases are wrong!

By comparison with the second quarter of 2009/2010 when Employment & Support Allowance (ESA) appeal receipts stood at 29,000 – the same quarter in 2012/2013 has zoomed up to 73,700 – an increase of 44,700.  Of the 53,200 ESA cases cleared at an appeal hearing 22,500 (42%) were found in favour of the claimant.  These figures highlight ongoing problems with the standards of decision – making following Atos ‘Work Capability Assessments’ – the DWP is still making an unacceptably large number of incorrect decisions.  

Total number of benefit appeals now on track to exceed 600,000 by the end of the year!

The total number of benefit appeal cases for 2012/2013 has already reached a wholly unacceptable figure of 308,200 meaning that if the trend continues, and there is every sign it will, the total number of benefit appeals alone will have reached well over 600,000 by the end of the year.

Cases outstanding (all) – 813,800  – chaos!

The total number of benefit appeal case ‘outstanding’ in 2008/2009 was 53,200 in the second quarter and has now more than trebled to 158,700 in the second quarter of 2012/2013.  A comparison with the figures for 2007/2008 when the figure stood at 347,100 shows the numbers have increased to a colossal 813,800 in 2012/2013. the number of employment tribunal cases outstanding as of the second quarter stands at 570,200, benefit cases stand at 158,700 in 2012/2013 and immigration & asylum cases at 41,000 – this is absolute chaos!

Exceeding the warnings given by the judiciary….

In a report issued in February 2012 provided by the Tribunal president  the judiciary gave the following breakdown of benefit appeal cases in the first – tier Tribunal and made the following predictions for increases in the appeal load:

Annual Intake of SSCS Appeals

2008-09 – 242,800

2009-10 – 339,200

2010-11 – 418,500

(forecast)

2011-12 – 421,609

2012-13 – 483,400

2013-14 – 576,700

2014-15 – 644,000

These latest figures show we are well on track to break past the 483,400 forecast for 2012/2013 and exceed the figure given for 2013/2014.  

The full effect of welfare reform changes has yet to hit the fan, the bedroom tax, more ESA cases, JSA sanctions (standing at 700,000), Disability Living Allowance giving way to Personal Independence Payments are all in the line up and will undoubtedly lead to the Tribunal president’s forecast being considerably exceeded.

Government and the DWP has to stop pretending that there is not a perfect storm brewing here, mandatory revision before appeal is only keeping the dispute out of the public’s attention in a pretence that the people who create the problems will somehow fix it.  The DWP is assessing twice as many ESA claimants as it needs to just to claim double its dubious ‘results’.  In reality the vast majority of those who flow off ESA and incapacity benefits are flowing straight back on to them shortly afterwards – government has no other credible explanation as to why after assessing over 2.8 million claimants between 2008 and 2012 the claimant count has barely reduced by little more than 70,000 – it’s derisory and half that achieved by way of reductions under the older incapacity benefits regime.  

The fact is that we were seeing much better reductions under the older incapacity benefits.  Government is using severely disabled claimants to manipulate its figures by its recycling of what can only be the same claimants.  It stands to reason that if vast numbers were really being ‘found fit for work’ the Jobseeker’s Allowance claimant count would have rocketed up to an embarrassingly high level which this government simply cannot afford to show.  

After coming off ESA claimants are being re-directed back on to it by Jobcentres who can clearly see these claimants are no where near ready for the labour markets.

Government’s mismanagement of the ESA reassessment programme:

There’s any number of statistical charts on here which you can muse over all day long.  

In doing so just apply the logic:

(1) We start with 2.6 million on the sick in 2008

(2) Various claims are made by the DWP/media of 75%, 50% and more recently 33% being found ‘fit for work’ 

(3) In 2012 we have 488,000 claimants waiting to be assessed

(4) In 2012 we have a Jobseeker’s Allowance queue that’s hardly grown

(5) By 2012 – 2.7 million have been subjected to Work Capability Assessments

(6) By 2012 – 3.8 million is the total number ‘case loaded’ through ESA

(7) By 2012 we are on track to break all previous appeal records with more hidden from view at the DWP

(8) In 2012 there are twice as many claiming on the sick as there were in 2006 

(9) By 2012 the claimant count for those on the sick has trickled down by a mere 70K, still leaving us with…. 

                              Around 2.6 million ‘on the sick’? 

(10) This wretched scheme is rapidly emerging as an absolute farce which is being used as a vehicle to keep the long term sick numbers down; thus keeping them from the long term ‘economically inactive’ count used by the ONS to work out the numbers said to unemployed. 

They have engineered themselves a clever way of marshalling the unemployment figure to one which is more ‘commensurate’ with the chancellor’s increasingly doubtful claims that we are ‘on the way’ to economic growth.  

With everlasting thanks to the brilliant Nick-

Twitter: @Mylegalforum

See more from Nick at https://ilegal.org.uk/ and below
See ESA Customer’s journey to nowhere

See the ‘journey in to work’

See a discrepancy uncovered

See unemployment is ‘falling’

See turning back the long term incapacity clock to zero

Mar 102013
 
DPAC Logo with text underneath "Disabled People Against Cuts" and then web address dpac.uk.net
  Time for your ESA assessment?

Not for 78,000 claimants
– waiting over a year!

Only the other week we had the DWP recklessly fuelling the tabloids over its absurd claims that 15,000 Disability claimants (most of whom were pensioners and children) were seemingly breaking a leg to get their claims in before the dreaded new Personal Capability Assessment comes in to being this April for new claiments; the DWP neglected to make sure the media told everyone how the figures they were quoting were months out of date!

When challenged over the figures the DWP advocate that you should ‘dig deep’ and look beyond their damaging headlines.  When you do so it’s interesting to see what you turf up – the utterly chaotic Employment & Support Allowance ‘reassessment of the sick’ programme goes from bad to worse as it is revealed (upon digging deeper in to their figures) that thousands upon thousands of claimants remain ‘stuck’ in what the DWP term the ‘assessment phase’ of an allowance which seems to be getting its claimants no support at all in to employment.  

Read more about the DWP’s ‘customer journey to nowhere’  The DWP’s most up to date figures for May 2012 (the figures for August 2012 are apparently ‘delayed’) show that an astonishing 455,860 claimants are either waiting for their Work Capability Assessment to be completed or waiting for an appeal against a decision they believe to be wrong.  What is totally unacceptable is how a programme which is meant to be helping people back to work is seeing no less than 77,820 claimants waiting a year or more for their assessment or appeal to lead to any kind of proper decision! – in nearly 30,000 cases it’s over 2 years!

This is nothing short of a National outrage which the mainstream media have a duty to publish.

Here’s the official DWP figures…. 

Assessment Phase  

Total 

Up to 3 months 

3 to 6 months 

6 months to 1 year  

1 to 2 years

2 to 5 years

May 2012

455,860

157,940

122,180

97,910

49,040

28,780

February 2012

424,170

166,230

107,930

81,460

44,740

23,810

Change (+/-) +31,390 

– 8,290

+ 14,250

+ 16,450

+ 4,300

+ 4,970

 
 

DWPs ESA Process in Chaos?

You can check them against the official DWP tables here….

DWP figures for May 2012

DWP figures for February 2012

With thanks to the brilliant Nick at Mylegal for more from Nick see https://ilegal.org.uk/

Twitter: @Mylegalforum