The staggering rise in PIP complaints shows there’s rot in the system

It’s not just the scale of the complaints, it’s the increasing evidence that disability benefits are being removed on fabricated grounds

What happens when the system designed to help you is actually hurting you? This is the question I keep coming back to as I look at the newly released evidence of widespread failings in the disability benefit system. Complaints about the personal independence payment (PIP) assessment process rose by nearly 880% last year, according to the Department for Work and Pensions.

That translates to almost 1,400 people, who might have Parkinson’s or severe depression, put through the government’s flagship disability benefit who – after months of gruelling paperwork, assessments, and perhaps even tribunals – are so desperate that they then find more energy to put in a formal complaint. These can’t be dismissed as being unjustified either: DWP statistics also show that the number of complaints that were upheld rose by 713% in the same year (from 67 in 2015-16 to 545 in 2016-17).

For the past four years, I’ve been reporting on the radical changes to disability benefits orchestrated by Conservative governments. The lack of humanity is glaring: there’s the Open University student with agoraphobia, Asperger’s and complex mental health problems living without a washing machine, oven or television after benefit cuts left her destitute; the 14-year-old child carer listening to her disabled dad crying because he doesn’t know how he’s going to pay the bills after having his disability benefits taken. But as the DWP’s complaints show, the scandal of this goes even further: there’s increasing evidence that benefits have been removed from disabled people based on entirely fabricated grounds.

The picture that’s emerging should disturb anyone who cares about the welfare state, poverty, or basic government transparency.

The specialist disabled news site Disability News Service (DNS) has been carrying out an investigation into claims of widespread dishonesty in the disability benefit system, with more than 250 PIP claimants alleging assessors repeatedly lied, ignored written evidence and dishonestly reported the results of physical examinations. It’s a regular occurrence for disabled readers to show me the reports of their benefit assessment, point to a statement, and tell me that it never in fact happened.

Even the latest official independent review of PIPs this March found there was “inherent distrust” of the system, due to the “lack of transparency in the assessment process” and the scale of faulty decisions (four out of five cases where a disabled person is denied disability benefits are now overturned on appeal).

Almost 80% of disabled people put through the PIP test have seen their health deteriorate due to stress or anxiety, a major survey found last month. More than a third of those who have had their benefit cut said they were struggling to pay for food, rent and bills. Forty per cent had become more isolated, and more than 50,000 disabled people have had their Motability cars removed after undergoing the PIP test.

read more here: http://www.computerweekly.com/news/4500248772/Universal-Credit-costs-leap-by-more-than-20-to-158bn

Blind from birth, epileptic and unable to leave home alone – but Government says she’s fit to work

Hazel Macrae has been told by the Department of Work and Pensions that she must go back to work despite being blind from birth

Blind since birth and stricken by a string of disabilities but told she is fit to work – this is the reality of Government benefit cuts.

Hazel Macrae, who also suffers from epilepsy, Type 2 Diabetes and osteoarthritis, was claiming Employment Support Allowance (ESA) and was told she’d have to undertake a back to work assessment.

The 62-year-old filled in a questionnaire explaining she’s unable to leave her home without the help of her partner or son because she is afraid of falling, can’t use a pen or pencil, telephone, and would be unable to “move safely” in a workplace.

She was also required to meet with a health professional in Gosforth to undergo a face-to-face assessment where she was asked a series of questions about her daily activities.

Echoing the award-winning Ken Loach film I, Daniel Blake – which was shot in Newcastle – Miss Macrae has been told she has “limited capability for work” and her ESA has been moved from the Support Group to Work Related Activity Group, and reduced by £15 per fortnight.

Miss Macrae, who has artificial eyes, will now have to regularly meet with a work coach to discuss how she can get back into work.

read more here: http://www.chroniclelive.co.uk/news/north-east-news/blind-birth-epileptic-unable-leave-13737805

Former DWP ministers could face police investigation over fit-to-work tests

A complaint was made against Iain Duncan Smith and Chris Grayling

Police in Scotland are assessing whether to launch a criminal investigation into two former DWP ministers’ handling of so-called disability fit-to-work tests.

Disabled activist John McArdle of the Black Triangle campaign lodged a complaint with police in March against Iain Duncan Smith and Chris Grayling, according to the Disability News Service news agency.

He told police in Edinburgh that the two ministers had ignored a coronor’s concerns about the safety of the tests, which are used to judge whether a disabled person receives benefits.

He also produced evidence of suicides he said were related to fitness-to-work tests.

Mr McArdle says the ministers may be guilty of “willful neglect of duty by a public official”, which is a criminal offence.

According to the Crown Prosecution Service, willful neglect “can be the result of a positive act or a failure to act”.

“There must also be an element of knowledge or at least recklessness about the way in which the duty is carried out or neglected,” the CPS explains.

“The test is a subjective one and the public officer must be aware that his/her behaviour is capable of being misconduct.”

Welfare reform ‘will see £50 a week more cuts to 900,000 disabled people

About 900,000 disabled people will see their weekly incomes fall by at least £50 a week by 2020, because of the continuing impact of the government’s welfare reforms, according to new research.

The research by the consultancy Policy in Practice found that, of 7.2 million working-age, low-income households, more than two-fifths of those containing a working-age disabled person would lose at least £50 a week, compared with November 2016.

read more here: https://www.disabilitynewsservice.com/welfare-reform-will-see-50-a-week-more-cuts-to-900000-disabled-people/

Farron slams DWP over breaking promise to stop re-testing claimants with lifelong illnesses

Tim Farron has slammed the Government for lying to local people over plans to stop re-testing benefit claimants who have long-term chronic illnesses such as Huntingdon’s, MS, and Parkinson’s.

Back in October last year, the then Secretary of State at the Department for Work and Pensions, Damien Green, said that they would no longer reassess benefits for those who have long-term sickness as it is “pointless” and “only adds to their anxiety and difficulties”.

However, a freedom of information request from Tim Farron has revealed that the DWP never intended to carry out this proposal as they do not even record data which would allow them to pull out the group of claimants who have chronic illnesses.

Tim said: “The Government have let down millions of people across the country who have chronic diseases with another shameful U-turn.

“This pathetic decision to break their promise on re-testing benefit claimants who have long term illnesses will cause more misery and discomfort for many people up and down the country who continue to be dragged to medical assessments just because the DWP can’t be bothered to make records of who is chronically ill.”

An example of someone who the Government has broken their promise to is John Heaton. John has a degenerative brain disease and severe obstructive pulmonary disease of which he has a sick note to cover him from his doctors. He is also suffering from a hip injury and extreme weight loss for which his dietician nurse makes home visits.

Kath Dunning, who is John’s carer, said: “I received a letter from the DWP saying that John had missed a medical assessment. I rang the relevant authorities to tell them that I hadn’t received a letter about the assessment.

“They told me to put it in writing which I did. They then replied four weeks later after numerous phone calls from myself to say that they were upholding their decision. This meant that I would have to take it to a tribunal and John would have to apply for Jobseeker’s Allowance.

“For me the current system is a joke and doesn’t seem to care for the people who are ill.”

read more here: http://www.cumbriacrack.com/2017/09/11/farron-slams-dwp-breaking-promise-stop-re-testing-claimants-lifelong-illnesses/

Stroke sufferer may need to sell his home after being denied benefits

A Somerset man, who was left partially paralysed after suffering a stroke, may be forced to sell his house. This is because he has accumulated high levels of debt whilst waiting to receive benefit payments.

Chris Gold was initially refused the Universal Credit benefit after being told he should be working.

This was despite Chris suffering brain damage as well as paralysis following the stroke.

After a life driving a lorry around the world, in a job he loved, Chris now rarely leaves the downstairs of his house.

His current situation means that he can barely afford to live there at all.

A stroke in 2015 left Chris with brain damage and without feeling in parts of his body.

When his employment and support allowance was stopped he was told to apply for the new Universal Credit. However when he did so, he was told he should be working.

Chris said, “The doctor’s given me a sick note saying I’m unfit for work – I have to do what the doctors tell me. They’ve got the knowledge – they know how stroke victims are.”

“I just think it’s unfair that the Department for Work and Pensions can do this to people when they’re unwell. Irrespective of what they say, the doctors are saying I’m not well.”

“I want to keep the house because I’ve worked hard for thirty eight years but it just seems unfair that I’ve worked all my life to buy a house and now I’m going to end up with nothing.”

read more here: http://www.itv.com/news/westcountry/2017-06-30/stroke-sufferer-may-need-sell-his-home-after-being-denied-benefits/

UN demands annual UK progress report on correcting ‘grave and systematic violations’

A UN committee has told the UK government to produce an annual progress report on how it is implementing the recommendations of a damning inquiry that found it guilty of “grave and systematic violations” of key parts of the disability convention.

The committee of disabled human rights experts concluded last November that the government had violated the UN Convention on the Rights of Persons with Disabilities (UNCRPD) under the articles on independent living, work and employment, and social protection.

read more here: https://www.disabilitynewsservice.com/un-demands-annual-uk-progress-report-on-correcting-grave-and-systematic-violations/

Austerity has trampled over disabled people’s rights. But the UK won’t admit it

The UN has found that current policies violate both a UN convention and UK legislation. There is little hope for change when the government simply denies it

Like a lot of other disabled people, I’ve been eagerly following the progress of the United Nations’ inspection into the UK’s record on disability rights. Last month in Geneva, a UK delegation faced questioning by a UN committee based on 2,000 pages of evidence gathered during the course of its inquiry. The UN’s final report, published on Thursday, as widely expected, is a 17-page-long catalogue of shame, and highly critical of the UK’s record on almost every area covered by the UN convention on the rights of persons with disabilities (CRPD).

read the rest of this article by  Mike Lambert in the GUardian here: https://www.theguardian.com/commentisfree/2017/sep/04/austerity-disabled-people-rights-uk-un-government

 

Cruel Tory disability benefit changes strip £6million a year from people with multiple sclerosis

New figures lay bare the scale of cuts to people with the lifelong condition as claimants move from an old welfare system to a new one

Cruel Tory changes to disability benefit have stripped £6million a year from multiple sclerosis sufferers, shock research reveals today.

New figures lay bare the scale of cuts to people with the lifelong condition as claimants move from an old welfare system to a new one. Officials downgraded or denied help to nearly a third of 8,800 MS sufferers who were reassessed for PIP in the three years to October 2016.

The MS Society charity, which obtained the figures from the government, warned the cuts are having a “drastic impact” and need fixing “urgently”. The figures show MS suffers who moved from the old Disability Living Allowance onto a new system, Personal Independence Payments.

These sufferers were in the group receiving the highest payments to cope with reduced mobility. In a second group, known as ‘daily living’, 3,400 people receiving the most help were reassessed of which 800 had support downgraded or denied. The MS Society estimates this cut was worth £4.9million a year in lost benefits for the first group and £1.1million a year for the second.

Spokeswoman Genevieve Edwards said: “These staggering figures show how PIP is failing some of the most vulnerable people with MS who need the highest level of support. It doesn’t make sense that people are losing money they once qualified for, when they are living with a progressive condition that will never improve.

Read more here: http://www.mirror.co.uk/news/politics/cruel-tory-disability-benefit-changes-11082384

 

A mother took her own life after the DWP cut her disabled son’s benefits | The Canary — Britain Isn’t Eating

https://www.thecanary.co/2017/09/01/mother-took-life-dwp-cut-disabled-sons-benefits/

A mother took her own life after the government took away nearly all her disabled son’s benefits and support, a coroner has ruled.

“What have I got to do? Top myself to get help for my son?”

BBC News reported that 73-year-old Valerie Grant of Great Bridgeford, Staffordshire, “walked in front of a train” and died in April 2017. Prior to this, her severely autistic son had lost a job placement as a bin man, was not entitled to support via a day care centre, had been turned down for accommodation, had lost his Disability Living Allowance (DLA) payments, and was refused a Personal Independence Payment (PIP) by the Department for Work and Pensions (DWP).

Grant had reportedly told mental health workers:

What have I got to do? Top myself to get help for my son?

Coroner Andrew Haigh said of Grant’s death:

There were a number of agencies involved, but nobody took a lead. I do have concerns about the lack of support, but I don’t think there’s any one agency that I can write to to try to remedy this…

The inquest concluded that Grant had taken her own life while suffering from depression. And as the verdict was announced, Grant’s step-son reportedly shouted:

It is just being swept under the carpet. One agency blames another agency and they can get away with it.

 

via A mother took her own life after the DWP cut her disabled son’s benefits | The Canary — Britain Isn’t Eating