This article was written by Karen McVeigh, for The Guardian on Sunday 14th December 2014
The Department for Work and Pensions has been urged by mental health and disability charities to publish its secret investigations into suicides that may have some link to benefit changes, following revelations that it has carried out internal reviews into 60 such cases.
A Freedom of Information request by the Disability News Service has revealed that the DWP has carried out “60 peer reviews following the death of a customer” since February 2012. A peer review is triggered when suicide or alleged suicide is “associated with a DWP activity”, according to its internal guidance.
Despite growing concern over the way benefits are administered in relation to vulnerable individuals, and amid a number of reports of related deaths, the department told the Guardian it had no plans to publish the reviews.
Disabled People Against the Cuts said that, because of the way the reviews were carried out, the DWP figure was likely to be the “tip of the iceberg”.
Tom Pollard, the policy and campaigns manager at Mind, told the Guardian the figures were a concern. He stressed that suicide was a complex problem but added:
“It would be helpful for organisations to see what things could be going wrong in the benefit system that could lead to these tragic situations.”
Sue Bott, director of policy and services at Disability Rights UK, said DWP reviews should be transparent.
“There have been allegations and anecdotal evidence for a while that the benefits regime has tipped people over the edge. It should be looked into in a transparent way,”
“This is not just about the nature of the decision taken as to whether it was right or wrong. It’s also about the process and there is a lot of concern about the way benefits are administered.”
The DWP’s latest figures show that sanctions to punish disabled ESA claimants had risen by 470% in 18 months, from 1,096 in December 2012 to 5,132 in June 2014.
According to DWP figures released as the result of an FoI request, 62% of adverse ESA sanction decisions in the first three months of 2014 were made against people with mental or behavioural problems (9,851 out of 15,955).
The calls for transparency from the DWP come after a number of reports of the deaths and suicides of vulnerable individuals after adverse benefit decisions.
David Clapson, 59, a former soldier and type-1 diabetic, died in July after his benefit was cut. Clapson had no food in his stomach, £3.44 in the bank and no money on his electricity card, leaving him unable to operate his fridge where he kept insulin.
MPs are to look into his death after a petition written by Gill Thompson, his sister, gathered more than 200,000 signatures.
Thompson, told the Guardian:
“All I’ve ever asked for is lessons to be learned. I can’t bring him back but we should know what is going on. There are certain people who shouldn’t be sanctioned. People with terminal cancer, waiting for heart operations, people with diabetes. Before they sanctioned my brother, they knew his disability. He was waiting to hear from a job, he had been on work placement. He was claiming the bare minimum.”
Christine Norman, a nurse whose disabled sister, Jacqueline Harris, took her own life in November 2013 after her benefits were cut, said:
“It’s too late for my sister. Everything is stacked against you. If you’ve got a great education, if you have great health, you’re OK. But if you haven’t, you have to fight against the odds. The government want you to work. The ones they pick are the ones that are vulnerable and ill.”
An inquest found last month that Harris, 53, of Bristol, who was partially sighted, took her own life after months of constant pain and following a “fit for work” ruling that replaced her incapacity benefit with jobseeker’s allowance. Staff at a jobcentre Harris was told to attend had to call an ambulance after she blacked out in pain.
Disabled People Against Cuts said that, because the DWP’s reviews only relate to suicides or alleged suicides and were triggered by regional managers within the benefit system, the number of deaths was likely to be far higher than the 60 cases that reached review.
Anita Bellows, of Disabled People Against Cuts, said:
“The triage for advising whether a peer review is to be carried out is done by regional managers at seven regional centres, who may not have an interest in putting them forward. Also, the guidance for peer review is focused on suicide, which does not cover people like David Clapson.”
She called on the DWP to open a proper investigation into the deaths, and include evidence from medical experts.
“These should be public documents” she said. “They are also only focused on the process. There are no medical experts on it.”
The DWP said it was unable to disclose the names of individuals under review because of provisions of the Social Security Administration Act.
However, the Mental Welfare Commission of Scotland, a Scottish government-funded watchdog, published its comprehensive review of the suicide of a claimant known only as Ms DE this year. The MWCS concluded that the WCA process and the subsequent denial of ESA was at least a “major factor in her decision to take her own life”. It concluded that the work capability assessment process was flawed and needed to be more sensitive to mental health issues.
Colin McKay, chief executive of the Mental Welfare Commission of Scotland, said he was disappointed with the DWP response to the report on Ms DE, who died on 31 December 2011.
“Certainly, nothing in what they said gave us confidence that if another Ms DE was claiming benefit, the outcome would be any different,” he said. “If the number of deaths are 60, that’s a lot. You would expect any organisation experiencing deaths as the potential consequences of their actions would be seriously considering whether they needed to do anything differently.”
This year a whistleblower tasked with getting claimants out of the ESA sickness benefit told the Guardian that some of her clients were homeless, many had extreme mental health problems – including paranoid schizophrenia, bipolar disorder and autism – and some were “starving” and extremely depressed after having benefits stopped. “Almost every day one of my clients mentioned feelings of suicide to me” she said.
Mind released research on Thursday that found that people with mental illness were having their benefit cut more than those with other illnesses. It also found 83% of those with mental health problems surveyed said their self-esteem had worsened, and 76% said they felt less able to work as a result of DWP back-to-work schemes.
The DWP said: “We take these matters extremely seriously, which is why we carry out peer reviews in certain cases to establish whether anything should have been done differently. However, a peer review in itself does not automatically mean the department was at fault.
“Since its introduction in 2008 there have been four independent reviews of the work capability assessment and we have made significant improvements to make it better, fairer and more accurate.”
Source – Welfare Weekly, 14 Dec 201
A scandalous picture of suffering, trauma and destitution is painted by a former Work Programme adviser who was tasked with getting claimants off the employment and support allowance (ESA) sickness benefit.
Speaking to the press for the first time since she quit the job last year, Anna Shaw (not her real name) says:
“Some of my clients were homeless, and very many of them had had their money stopped and were literally starving and extremely stressed. Many had extreme mental health conditions, including paranoid schizophrenia, psychosis, bipolar disorder and autism.
One guy [diagnosed paranoid schizophrenic and homeless] came to see me for the first appointment and mentioned that he had not eaten for five days. I offered him my lunch, thinking he would refuse it out of pride, and he fell upon it like a wild animal. I’ve not seen a human being eat like that before.”
Shaw can only speak out anonymously, because when she resigned, after just a few months in the job, her employer made her sign a confidentiality clause.
She believed that the majority of her ESA caseload of about 100 clients were not well enough to have been on the government’s welfare-to-work Work Programme, but should instead have been signposted to charities that could support them with their multiple problems.
“Almost every day one of my clients mentioned feelings of suicide to me,” she says. Shaw says she received no training in working with people with mental health issues or physical disabilities.
Under the government’s welfare reforms, Shaw’s clients would have completed a controversial test, called the work capability assessment (WCA), currently conducted by contractor Atos, and been placed in the work-related activity group (WRAG) of ESA because they were judged capable of working, albeit with appropriate support.
Shaw’s employer was subcontracted by one of the 18 “prime providers” the government pays to implement its Work Programme to get jobless people into employment. However, Shaw says she was never given a copy of her clients’ WCA, which details their health conditions, so it was difficult to provide the support they needed.
Shaw thinks many of her ESA claimants wanted to work, but the “fundamental issues” – their physical and mental disabilities, often coupled with situations such as homelessness or domestic abuse – were not dealt with.
“Every person who came in needed specialist help on a whole range of things, and to be supported, not under imminent threat of losing their benefit the whole time.”
She believes many of her clients had been wrongly assessed as fit to work. “I had a woman with multiple sclerosis who had been domestically abused and was suffering from very severe depression and anxiety, and she had a degenerative condition and she was deemed fit for work,” she says. “I gave people advice under the radar about how to appeal … but it was absolutely not in our remit to encourage people to appeal.”
The most recent government figures (to June 2014) show that only 2% of longer-term ESA claimants find sustained employment. Independent research by the Centre for Economic and Social Inclusion has found that disabled people are about half as likely to find employment as non-disabled people. Last week, a report suggested that officials were considering cutting ESA, which is paid to around 2 million people, by as much as £30 a week as the chancellor, George Osborne, seeks a £12bn cut in the welfare bill.
Shaw says she was expected to enrol claimants on back-to-work courses.
“It was very much ticking boxes. My managers were just obsessed with compliance with the Department for Work and Pensions (DWP). We would be penalised as an organisation if we didn’t sanction people who failed to show up… but with ESA they realised there was very little chance of getting these people into work. They were kind of parked.”
In the past year, sanctions for ESA claimants who fail to turn up for interviews with their job adviser have increased more than sevenfold. In each case, claimants lost at least one week of their benefit money, even if they said they were too ill to get to an appointment.
“One minute we had to sanction and the next minute we were told absolutely not to sanction,” says Shaw. “I think this was in response to [hostile coverage to sanctions in] the press… so the advice was given that we weren’t sanctioning them but we weren’t to let them know we weren’t sanctioning them… so they would come for appointments.”
According to one of Shaw’s former colleagues who is still working for the organisation, sanctioning has intensified.
“She said: ‘It’s got a lot worse since you left and now we’re having to sanction all the ESA claimants if they don’t turn up for appointments,’” says Shaw.
Two months ago, the work and pensions secretary, Iain Duncan Smith, stated that the WP “revolutionises the way we provide support to those who are the hardest to help, supporting a move from dependency to independence and getting people into work so that they have financial security for the future”.
But Shaw’s revelations contradict the ministerial architect of welfare reform. She says:
“I felt that my job was really a non-job and as long as I ticked the boxes, they didn’t really care what I did with them… but they missed the point that these were actually human beings that I was coming into contact with, and going home every night wondering if these people were still alive.”
Shaw’s claims are backed up by a recent report, Fulfilling Potential, compiled by a WP client, Catherine Hale , with support from Mind and the Centre for Welfare Reform.
Of the 500 people on ESA who responded to an online survey, 82% said their WP provider made no effort to adapt jobs on offer or make it easier for them to work. Only 7% said their adviser had a copy of their WCA.
A spokesman for the DWP says Work Programme providers “have the freedom to design any work-related activity so it is appropriate to the person’s condition”, and the DWP “offers more money to providers for helping the hardest-to-help groups into work, such as people on ESA”.
But there is no breakdown of how much of the £1.37bn WP expenditure from June 2011 to 31 March 2014 was spent on helping ESA claimants. He insists that sanctions are “used only as a last resort” and “about 99% of ESA claimants don’t get a sanction”. He adds that the DWP is looking at how to share information about clients’ medical conditions with WP advisers.
Source – The Guardian, 05 Nov 2014
The number of households that North East councils prevented from becoming homeless has rocketed in parts of the region.
In South Tyneside the local authority stepped in on 3,208 occasions in the last 12 months, a 123% rise on the 1,437 figure for the previous year.
This works out at a rate of 47.07 per 1,000 households in the borough, almost five times the national average of 10.11.
Meanwhile, in the same period, Gateshead saw a 65% increase from 2,094 to 3,453, an average of 38.28 per 1,000 households.
Newcastle City Council numbers rose 23% from 3,673 to 4,529, which works at 37.89 per 1,000 households.
There was also a small rise in Northumberland and Durham, but falls in North Tyneside and Sunderland.
Figures released by the Department for Communities and Local Government show preventions and relief in England rose nationally on average 12% from 202,900 to 227,800 between 2012/13 and 2013/14.
Prevention includes things like resolving problems with housing benefit, advice on debt or rent and mortgage arrears, or mediating with families to stop family members being kicked out.
Relief is when a council has been unable to prevent homelessness but helps someone to secure accommodation, even though the local authority is under no statutory obligation to do so.
Coun Allan West, Lead Member for Housing and Transport on South Tyneside Council, said the figure revealed how a policy initiative it took last year was working.
He said: “In 2013, South Tyneside Council’s Place Committee undertook a Commission scrutinising how homelessness in the Borough was tackled and how well the Council was equipped to deal with future demand.
“This led to the development of our new homelessness strategy which made homeless prevention one of our key priorities.
“This is reflected in our updated allocations policy, which gives priority to people at risk of becoming homeless before their case becomes critical.
“We have introduced a Homelessness Forum with representation from key partners including landlords, Public Health and the third sector.
“The forum ensures a collaborative partnership approach to tackling homelessness, sharing good practice and maximising opportunities for early intervention and prevention for homeless households.
“The review established a post of ‘Homelessness Prevention Lead’ within the Council to continue to develop housing and support options for people at risk of homelessness.”
My life on the streets of Tyneside – by homeless man ‘Carl’
Graduate ‘Carl’ has been homeless, on and off, for 16 years now.
He came to the region from Berkshire to study politics and economics at Newcastle University.
By the time he graduated aged 23 with a 2:1, he was in a secure unit at St Nicholas’ Hospital where he was being treated for Bipolar Disorder.
“They let me out for the day for my graduation ceremony and that night when the other students were out having a drink celebrating I was back in the unit pumped up with drugs,” he said.
He describes himself as a ‘hand tapper’, someone who walks the streets asking for money, making anywhere between £25 and £100 a day.
“The beggars are the ones who put signs around their necks and wait for people to come to them,” he said.
Carl said at the moment he sleeps rough in a city centre car park. “It’s best to sleep somewhere with CCTV as it gives you a feeling of security that someone might see if you’re in trouble and help.”
Over the years he has ‘sofa surfed’ with friends, and stayed in hostels, but nowhere permanent for long.
The money he makes he spends on food, tobacco and drink.
“I don’t drink that much,” he says.
He was a heroin user for six to eight years but has been ‘clean’ since June.
Carl is currently taking heroin-substitute buprenorphine, its trade name is Subutex.
“It’s better than methadone, like Peaches Geldof was taking. You can take other drugs as well as Methadone but not with Subutex.
“You’re supposed to crush it and place it under your tongue. I crush it and snort it like snuff.”
However he added: “I’ll probably have a relapse soon.”
His condition means he’s hyperactive.
“I walk the streets all day. Sometimes I don’t sleep.
“It’s OK at the moment with the hot weather. When its cold you keep moving or you die of hypothermia.
“People in the North east are friendlier than down south so I don’t get much grief.”
He says he stays in touch with family down south. His father is the Governor at a primary school, his three sisters and brothers hold down full time jobs.
“Some of us are just different. I’ve had a few jobs but I’m just not reliable.
“Also, my specialism is international politics and economics. I can’t see many employers in that field offering me a job.”
Source – Newcastle Evening Chronicle, 25 July 2014