Tag Archives: payment

Tory DWP is threatening to remove Motability car lifeline from severely disabled man

The DWP: where cruelty is written into the rules.

There’s new devilry afoot from the Department for Work and Pensions, as lawyers Leigh Day report:

A severely disabled man faces losing his lifeline Motability car in the latest blow he has suffered as a result of the enforcement of a benefits rule that he has just received permission to challenge in the courts.

Cameron Mitchell, aged 20, of Carlisle, has to return his Motability car by Thursday, 3 March despite the fact that he is wholly dependent on it for transport between his home, where he lives three days a week, and hospital where he stays for the rest of the week.

Cameron, through his mother and Deputy, Nicola Clulow, is challenging benefits regulations which put on hold Cameron’s Personal Independence Payments (PIP) and Nicola’s Carer’s Allowance after he spent 28 days in hospital, even though he continued to require his parents’ care whilst in hospital.

This week Cameron was granted permission to go ahead with his judicial review of Regulations 29 and 30 of the Social Security (Personal Independence Payment) Regulations 2013 which he argues are discriminatory and irrational. Cameron’s legal arguments will be presented in a High Court hearing later this year after the court agreed that his claim was ‘arguable’.

However, in the months since the legal challenge was launched, Cameron and Nicola have been struggling to deal with the consequences of the enforcement of the rule, the latest of which means the loss of the Motability car.

In December 2021, Cameron’s mum received letters asking her to repay overpayments of PIP and her Carer’s Allowance that the Department of Work and Pensions (DWP) had made while Cameron was in hospital from December 2020.

Leigh Day solicitor Carolin Ott wrote to the DWP asking them not to cut Cameron’s benefit package or claw back any overpayment until a decision had been made by the courts about his legal challenge to the 28-day rule and in response the DWP agreed to stop clawing back overpayments for at least six months.

However, the mobility element of Cameron’s PIP that had been paid to Motability for the car while Cameron was in hospital was still clawed back from Motability in late 2021 (even though the car was needed by his parents to continue caring for him while he was in hospital and later in hospice care). Motability say that without payment, the vehicle needs to now be returned.

Leigh Day has written to the Secretary of State for Work and Pension’s lawyers again asking for the matter to be resolved urgently and has also written to Motability asking for an extension to allow the issue to be resolved by the DWP.

Nicola is deeply distressed by the prospect of losing the vehicle and can’t see how Cameron would be able to spend any time at home if the vehicle is taken away. Cameron has benefited from being able to receive care at home which is an important part of the transition to his full-time home care package. The loss of the Motability car would have a serious, detrimental impact on him and his family.

In his judicial review challenge of the lawfulness of the suspension of PIP and his mum’s Carer’s Allowance during his extended hospital stay, Cameron is arguing that the ‘hospitalisation rule’ breaches his rights because it directly discriminates against him (a person with profound and multiple learning disabilities (PMLD) requiring hospitalisation for a period of more than 28 days) as compared to those with PMLD who are hospitalised for less than 28 days.

He is also arguing that the ‘hospitalisation rule’ indirectly discriminates against those who have PMLD or treats those with PMLD the same as others when it should be treating them differently in recognition of their disability-related needs (which mean that they require care from ‘known carers’, people who know them and their needs whilst they are in hospital). He also argues that the rule is irrational because it cuts across the purpose of PIP.

Nicola Clulow said: “Cameron has been stuck living in intensive care first in Newcastle, then in Carlisle for almost 15 months now. Not because he’s ill but due to problems and delays in providing a home care package that can meet his complex special needs.

“He’s 20 years old and has had to spend days and nights for months watching very sick people who often don’t survive and despite his lack of communication it’s clear to everyone that he was switching off from the world, was depressed and just had no interest in life.

“Contact with the outside world and the ability to go home to be with family are crucial for him. To go out, and especially to go home Cameron requires a great deal of equipment to go with him and this would be impossible without his Motability car.

“Having been called on 21st February 2022 by Motability to say his vehicle must be returned on Thursday 3rd March was one of the most difficult and upsetting situations we have faced because it means that Cameron will once again have to simply stay looking at the four walls of the Intensive Care unit and not get home.”

Leigh Day solicitor Carolin Ott said: “We are very pleased that the court has granted our client permission for a judicial review of the hospitalisation rule which has suspended his PIP and his mother’s Carer’s Allowance, but are deeply concerned by the detrimental impact of the enforcement of the rule whilst Cameron awaits his day in court.

“Cameron is a young man with profound and multiple learning disabilities (PMLD) and like many others with PMLD is dependent on input from his known carers. In circumstances where the NHS alone can’t cover his care needs, his PIP should have never been suspended in the first place. The detrimental impact of that suspension, which on top of causing loss of income and stress is now also causing his family to lose his Motability car, is ongoing and we hope that it will be urgently addressed.”

Source: Cameron Mitchell can judicially review hospital-stay benefits rule but faces losing Motability car | Leigh Day

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Secret DWP benefits survey cherry-picks respondents – so it can lay blame on claimants?

Too much Coffey: the Work and Pensions Secretary (right) seems to have commissioned a survey of benefit claimants in order to say their failure to budget properly has put them into hardship – not her insistence on providing starvation-level payments and using the slightest excuse to cut them off. Meanwhile, she parties.

The Department for Work and Pensions has launched a secret survey – sent only to specially cherry-picked claimants.

The reason seems to be to blame benefit recipients for any hardship they suffer, claiming that poor budgeting skills are the root of the problem rather than the political decision to fix payments at starvation levels – and then to use the flimsiest excuses to stop them.

The survey asks about debts claimants may have, what effect the debts have had on them and what support they need. It is the last question that has raised concerns, as Benefits and Work, which hoisted the red flag on this apparent scam, pointed out:

The full question and list of options is as follows:

What types of help or support, if any, would be most useful in helping you manage your finances?

  • Help with working out what money I have left to spend each/day/week/month.
  • Advice on how to spread my spending so I don’t run out of money
  • Advice on how to reduce my spending
  • Advice on how to reduce my debt
  • Advice on how to increase my income
  • Help with setting up a direct debit/standing order
  • Help with opening a bank account
  • Other (specify)

In this context, advice to increase my income is most likely to relate to those in employment.  In general claimants cannot increase their income unless there is a benefit they could be claiming that they are not aware of.

What is entirely missing from these options are the ones that would actually make a difference to claimants, such as:

  • Pay benefits at a rate that is enough to live on
  • Remove the 5 week waiting time for UC
  • End the long delays for PIP assessments and WCAs

Because there are no such options, this survey will produce results that say that, of claimants who are in debt:

X% say they need advice on working out what money they have left to spend

X% say they need advice on how to reduce their spending

X% say they need advice on how to reduce their debt

Whilst some people may indeed say in the ‘Other’ box that the help they need is a higher rate of benefits, this will not be listed as a percentage in outcomes as everyone’s answers will be worded differently.

In other words, all the support needs will be around claimants not understanding how to manage their money, rather than it being impossible to manage on the money they receive.

See how it works?

Benefits and Work has made Freedom of Information requests to ask how the claimants taking part in this survey are selected, how many are taking part and whether the results of the report are going to be published.

The logical conclusion to be drawn is that the DWP has been stung by having to reveal the findings of its secret report on how people on sickness and disability benefits are struggling with unmet needs.

Work and Pensions Secretary Therese Coffey had repeatedly refused to publish the DWP-commissioned report on disabled people’s experiences of the benefit system – so the Commons Work and Pensions Committee ordered its authors to provide a copy to Parliament. It has now been published.

The report, received by the government in September 2020, stated that many people are using disability benefits such as PIP, which is intended to meet the additional costs of disability, for very basic needs such as food, rent and paying debts:

“The participant had kidney failure, arthritis in his back, legs and arms, depression and bulimia which caused chronic stomach pains. He lived alone in a flat rented from a Housing Association, using Housing Benefit. He was in the ESA Support Group and received PIP. He made monthly repayments for utility bill arrears and had a £5,000 bank loan which he could not afford to repay. His debt repayments meant he could not afford essential day-to-day living needs and used a foodbank. He found it difficult to wash independently due to his arthritis and needed a walk-in shower but could not afford one and seemed unaware that he may be eligible for support through the local authority. He also needed support with cooking and cleaning and received help from a cousin. His cousin would like to claim Carer’s Allowance but neither of them knew how to make an application. He had no other support networks close by.”

It said claimants with invisible disabilities such as mental health conditions often struggle even more than those with physical conditions to meet their basic needs:

“Participants with mental health conditions tended to report a wide variety of basic needs, health and care needs and social needs that were unmet. In comparison, those with profound learning disabilities and severe physical disabilities were typically in the group that identified having fewer unmet needs. While the latter group experienced a high level of need across a range of areas, these were usually being met through a combination of local authority support and informal support networks, usually parents who provided a high level of care.”

And the wellbeing of disabled claimants often depends primarily on being in a household in which another member has a well-paid job:

“The participant has recently moved in with her mother and sister, she had previously lived alone in a council-rented flat but had begun to feel isolated and found paying the rent and bills difficult so decided to move in with her mother. She has a range of health conditions and disabilities including Asperger syndrome, anxiety, ADHD, joint stiffness and IBS. She works 28 hours a week and receives PIP. Before moving to live with her mother she was concerned about how her income would cover essential day-to-day living costs. She also struggled with maintaining her personal hygiene and found it difficult to leave the house as she did not like going out alone. Moving in with her mother has helped her to meet all of her health-related needs.”

The reason Coffey and the DWP kept the report secret seems clear when one notes that last October – more than a year after receiving it – the Work and Pensions Secretary was lying to the public about the system it damns.

As Benefits and Work (again) details:

Coffey was telling the Conservative party conference that:

“PIP has certainly grown in a way that was not anticipated when it was introduced.

“To give you an example, three out of four young people who claim PIP have their primary reason being mental ill health.

“That in itself is 189,000 young people who currently receive benefit focused on that. There may be other benefits they receive as well.

“. . . people can think the benefit system is fair.

“And I think by being able to target that even more so to people who really need that support, may improve that prospect of public perception.”

Having been forced to release a report that shows – even in its watered-down form – that the benefit system is forcing hardship and related physical and psychological torture on claimants, including those who already have significant mental health problems (leading to a threat to life itself?), it seems Coffey has commissioned this new survey in order to manufacture a false justification for herself.

I think I’ll write her a letter. Let’s see how she justifies this web of deceit.

Source: DWP secret survey set to blame claimants for going cold and hungry

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MPs bypass #DWP to publish controversial report on claimants’ experience of #benefits

Boris Johnson isn’t the only Tory minister facing serious consequences for their actions this week. It’s looking bad for Work and Pensions Secretary Therese Coffey too.

Coffey has repeatedly refused to publish a DWP-commissioned report on disabled people’s experiences of the benefit system – so the Commons Work and Pensions Committee has given orders for its authors to provide a copy to Parliament, which will then be published.

The report, The Uses of Health and Disability Benefits was received by the Government in September 2020. The National Centre for Social Research (NatCen) had interviewed disabled people about their experiences of receiving PIP, ESA and Universal Credit.

The committee last month gave the Secretary of State one final chance to publish the report, which she herself admitted fell within the Government’s own protocol for publication.

But Coffey said she would not be reconsidering her decision.

Why not? It seems likely that researchers at NatCen, who wrote the report, found that people on disability and other health-related benefits were overwhelmingly negative about their experience of the system under Tories including Coffey and her forerunners, going right back to Iain Duncan Smith.

NatCen has been ordered to provide a copy of its report by January 27.

“After repeated obstruction from the Secretary of State to keep from public view a piece of work that falls within the Government’s own protocol for publication, we have reached the end of the road,” said Work and Pensions Committee chairman Stephen Timms.

“We would have much rather the DWP had done the right thing and published the report itself, so it is with regret that we must now take the highly unusual step of using our parliamentary powers to obtain a copy from NatCen and publish it ourselves.

“We have been forced to do this to ensure that the reality of disabled people’s experiences of the benefits system can see the light of day.”

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Secret #disability #benefits report WILL be published whether #ThereseCoffey likes it or not

Therese Coffey: it seems she’s been too busy having a good time (in line with many of her Cabinet colleagues, we’ve learned) to publish a report on the quality of her work as it relates to people with disabilities who claim benefits.

Tough luck, Therese!

The Tory Work and Pensions Secretary has been sitting on a report on how claimants are affected by the way she runs disability benefits – presumably because it is damning, even though (allegedly) watered-down.

The benefits concerned are those received by people with long-term illnesses and disabilities: Personal Independence Payment (PIP), Employment and Support Allowance (ESA) and Universal Credit (UC).

Well, she won’t be able to warm her backside on it for very much longer because the Commons Work and Pensions Committee, sick of waiting for her to pull her finger out, has given her an ultimatum.

It is: publish the report by January 11 or we will publish it in spite of you.

The report falls within the government’s protocol for publication so there really is no legitimate reason for any delay.

Committee chairman Stephen Timms (Labour) said:

The Secretary of State has consistently failed to give the Committee a good reason why this piece of research should not be made public. She even admits that it falls within the Government’s own protocol for publication.

The continued refusal to publish the results of the research, as promised to the participants who gave up their time, will do further damage to disabled people’s trust in the Department—which is already in short supply.

The Secretary of State now has a final opportunity to think again and publish the research. If not, the Committee is firmly agreed that we will be left with no choice but to publish the report ourselves.

Source: Coffey ordered to publish secret disability benefits report or MPs will do it for her

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Why IS the #DWP refusing to release report on claimants’ experience of #PIP, #ESA and #UC?

[Image: Black Triangle Campaign].

The Department for Work and Pensions is stalling for time to bury important information on the way its benefit regime treats recipients – again.

It is now six years since I won my battle for the DWP to honour a Freedom of Information request on the number of people who have died after being denied ESA (thousands within two weeks; they hadn’t bothered to collect information beyond that time limit) – and still its officers obstruct requests.

Currently the DWP is refusing website Benefits and Work‘s request to see a report on 120 claimants’ experiences of receiving Personal Independence Payment, Employment and Support Allowance and Universal Credit.

The department is also refusing to allow the Commons Work and Pensions committee to see the report, even in complete confidentiality, raising questions over what ministers are trying to hide.

It seems even the interviewees themselves have not been allowed to see the report, which leads This Writer to question whether its information is accurate. Disability News Service has suggested that it isn’t, after being told by a whistleblower that, after the first draft was produced, ministers told the authors to cut the number of references to “unmet needs” and delete some analysis.

I tend to agree with Charlotte Hughes, who reported on this in her blog The Poor Side of Life:

So even the diluted final version of the report is apparently too scandalous to see the light of day.

From years of past experience we know that the DWP don’t put the needs of disabled people first or even anywhere. Their target is to force people into work regardless of them actually being able to do so.

In the past I’ve seen disabled people forced onto Universal Credit by deception and then forced onto DWP courses with the aim of getting them ‘ready’ for work.

We can’t let the government and the DWP get away with ignoring report requests and also implementing rules that are at best cruel.

We need to remember that the government and the DWP are masters of deception and we must continue to see past their lies. There’s more of us than there are of them and I alongside others will continue to hold them accountable for their actions.

Charlotte’s blog runs entirely on donations and if you want to contribute, follow the link to her site and press the “Donate” button.

With the DWP trying to hide a potential harm to people with long-term illnesses or disabilities, or who are unemployed, all social commentary sites have a responsibility to keep the facts of this matter within the public gaze, which is why I am publishing this information.

Please feel free to pass it on to as many people as possible – either by sharing this article or by referring to the information in conversation, should you get the opportunity.

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Did Tory distraction tactics make you lose track of the DWP’s strange plans for sick and disabled people?

Distractions, distractions: the Tories love them and try to cause as many as possible.

Even while the fuss over the Downing Street Christmas party last year is embarrassing for them, it means you may not have noticed other harms they are inflicting on sections of the population.

For example: the Department for Work and Pensions.

1. It seems the government is quietly pushing through proposals to change the assessment of Personal Independence Payment (PIP) – the main benefit for people with disabilities – even though it only put them out for consultation a short while ago.

The plans to expand the Special Rules for Terminal Illness and to remove the proposed 18-month minimum award period for people receiving PIP were part of a Health and Disability Green Paper and the government ran a consultation on them that ended on October 11, just two weeks before they appeared in Chancellor Rishi Sunak’s Budget statement as schemes that will definitely go ahead.

The Tory government expects to save £70 million over three years by doing this.

Labour has demanded clarification, smelling another Tory stealth cut. And it is true that the plans will have an impact on people with protected characteristics, so Sunak needs to explain why they are not mentioned in the ‘Impacts on Equalities’ section of the Budget.

Of course, it is entirely possible that the impact in this instance will be a good one.

The proposal is to replace the systems that are being cut with “better triaging of cases and testing a new Severe Disability Group”.

While the DWP has a poor history of doing anything “better”, the plan for a “Severe Disability Group” is now quite well-known and would put people with progressive, lifelong conditions into a group where they would never have to face reassessment for the benefit.

It is entirely possible that the whole of the £70 million projected saving would come from this change. This Site – and others – has spent years pointing out that the DWP spends more on constant reassessments that try to find ways to exclude people with disabilities from the payments that make their life worthwhile than it would if it left them alone.

It may be that the government has actually listened for a change and is doing the right thing for once.

I know – it’s a slim chance. But watch this space.

2. Sadly the reliability of any evidence provided by the DWP on proposed savings comes into serious doubt when one learns that the department withheld evidence that the work capability assessment, used to determine whether people are eligible for sickness benefit Employment and Support Allowance (ESA), was linked to 590 suicides:

Dr Paul Litchfield said: “If I had had that evidence available to me, or indeed been told that it was there – you can only ask for stuff if you know that it exists… I would certainly have looked at it and taken it into consideration.”

The information includes secret DWP reviews into benefit-linked deaths and two reports sent to the DWP by coroners aimed at preventing future deaths of claimants.

The revelation suggests that the DWP deliberately tried to prevent its reviewer from suggesting changes that would have saved lives.

3. Dr Litchfield also criticised the DWP as “odd” because, while it accepted his recommendations on policy, the operation side of the department continually and consistently dragged its feet when he proposed changes:

He said he believed the government department was stalling – waiting for the next review, with a different set of proposals, to come along so it wouldn’t have to change anything.

But how far can we trust him on this?

He said the government should develop a new assessment, based on the discredited biopsychosocial (BPS) model of disability. It already is.

This is the idea that the illnesses that prevent people from being able to work are all in the sufferers’ minds, and that they were perfectly capable of having jobs. This in turn led to the “scrounger” and “skiver” lies put about by the Tory and Liberal Democrat coalition government of 2010-2015.

It is important to remember that these beliefs informed New Labour policy on benefits when that party was in charge of the DWP. Current shadow Home Secretary Yvette Cooper, as Work and Pensions Secretary under Gordon Brown, enforced rules that docked assessment points from amputees if they could lift objects with their stumps, while she said claimants with speech problems who could write a sign would receive no points and deaf claimants who could read such signs would have no points for hearing loss. Anybody with mobility issues would be assessed using “imaginary wheelchairs”. She also removed half the mental health descriptors from the assessment, hugely increasing the possibility of suicides if the benefit was withheld.

Dr Litchfield said a new, independent reassessment of the benefit was long overdue. This Writer agrees – but this gentleman and his ideas should be kept very far away from it.

4. Underlying all of this is the question of whether the DWP has a duty of care to benefit claimants.

The department has denied this for many years, so it was welcome to learn that PIP review Paul Gray believes this duty is implicit in all of its work:

But This Writer strongly disagrees that it is a “learning process”. The UK government has been providing benefits to people for many decades now and should be entirely capable of showing proper care for their well-being.

The fact that thousands – possible tens of thousands or indeed hundreds of thousands – of people have died after being denied DWP benefits suggests that there was a failure of care, and that this was a political decision.

5. What are we to conclude from all of the above?

It can only be that the Department for Work and Pensions is a chaotic dis-organisation that fails to uphold its duties properly, with the result that many thousands of people have died who should have been receiving the benefits, and the respect, that is due to them.

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Benefit system for injured war veterans is worse than the DWP

It’s no surprise: the UK has a prime minister who showed his contempt for the armed forces by laying a wreath face down one year. The Ministry of Defence spitting on injured veterans is par for the course.

After a weekend in which Conservative politicians across the UK stood in all their hypocrisy and mouthed empty words of thanks to soldiers they despise… this:

Former members of the forces say they have been left ‘suicidal, homeless and let down’ by a system of payouts that is tough to navigate and appeal, leaving many feeling betrayed by the government they once served.

Thousands of veterans are struggling to get government payouts for injuries caused in service, with some facing poverty and suicide over the issue.

These veterans overwhelmingly report the same things – not getting the level of payment they need and then facing lengthy and complex battles to get an increase.

Does that seem familiar to you?

Payments to injured veterans come in war pensions and the Armed Forces Compensation Scheme (AFCS) – both administered by the Ministry of Defence which, it seems, couldn’t care less.

Anyone physically or mentally harmed during service before April 6, 2005, should receive war pension payments. Those injured after that date must apply to the AFCS.

But in practice, getting what they are owed seems impossible.

According to The Mirror,

Many former soldiers … report that vital medical evidence proving their claims is removed by the time their appeals are heard.

If veterans are unhappy with their war pension or AFCS payment, they can appeal. But for many the appeal process is complicated and long.

Veterans will often give up on the system or – tragically – die before they get any payment increase.

The Mirror‘s article features accounts by, and about, a large number of veterans who have been struggling to receive benefits they deserve after suffering injuries in the name of their country.

It seems to be unspoken Conservative government policy – consider the policy of the Department for Work and Pensions to deprive sick and disabled civilians of the payments they need if they’re to live lives that are close to normal.

This Writer has to ask what the legions of flag-waving patriots who observe Remembrance Day in good faith think of this betrayal.

Source: Thousands of injured war veterans denied full disability benefits in ‘cruel’ move – Mirror Online

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Are you one of the 340,000 PIP claimants who could be owed £16,000 in back pay?

The Department for Work and Pensions has announced that it will be checking 340,000 Personal Independence Payment claims to see if back-payments of £16,000 or more are owed – mostly to claimants with a mental health condition.

The initiative follows – extremely belatedly – a court decision from July 2019, finding that the DWP had not been awarding the correct number of points to some claimants who need prompting or social support to engage with other people face-to-face.

According to Benefits and Work,

Amongst PIP claimants who may have missed out are:

People who have regular meetings with a mental health professional, without which they would not be able to manage face to face encounters;

People who need the input of particular friends or relatives with experience of supporting them in social situations – rather than just any well-meaning friend or relative – to help them manage face to face encounters.

The DWP is not planning to invite claimants for an assessment but may contact them for more information.

This means a brown envelope from the DWP will arrive, out of the blue, through the letterboxes of people who are likely to have a phobia about brown envelopes from government departments.

The most likely outcome from people who are contacted in this way is that the letters will be ignored.

So This Writer is happy to endorse the suggestion, by Benefits and Work, that anyone who believes they may be affected should contact the DWP proactively – get in touch with them without giving them time to get in touch with you.

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Jodey Whiting had an incurable condition. Why did the DWP try to force her into a benefit reassessment?

Death by DWP: Jodey Whiting.

This is a good question – triggered in This Writer’s mind by a reference to a different case.

Please read the following Twitter thread, which was prompted by a tweet referring to the death of DWP benefit claimant Philippa Day:

Yes, why does the DWP force people with incurable or terminal conditions to prove that they still have a lifelong disability or are still dying?

Reading those words, I thought about Jodey Whiting. She had a number of disabilities, including scoliosis which – as far as I can tell – is an incurable condition that requires constant treatment for the length of the sufferer’s life. If untreated, it could be life-threatening.

So it was pointless to demand that she attend a work capability assessment, because it was impossible for her condition to have improved. It could only worsen.

There is an argument that a WCA could take place to ascertain whether a claimant’s payments should increase – but that cannot be used as justification in Ms Whiting’s case because her benefits were stopped.

The DWP’s Green Paper on Disability, released in July this year (2021), acknowledges that it is pointless to keep reassessing people with lifelong and/or terminal conditions and proposes the creation of a Severe Disability Group (SDG). People put in this group would not have to face reassessment.

If the DWP is admitting that it is unreasonable for people with lifelong conditions to face constant reassessment now, then it would also be unreasonable to suggest that they should have faced constant reassessment in February 2017, when Ms Whiting took her own life.

Strangely, this does not seem to have been considered by the High Court when it rejected an appeal for a second inquest into Ms Whiting’s death, last month (October).

I wonder why the court did not consider that the absence of necessity for the assessment that led to Ms Whiting’s benefits being cut was a material consideration in her case.

There’s now a second appeal for another inquest. Perhaps the point could be made this time around?

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A wrong disability benefit decision is overturned every minute of every working day

Philippa Day: Capita paid her family an out-of-court settlement after a court heard her mental illness had been “exacerbated” by the way her benefits were processed.

The Department for Work and Pensions is riddled with incompetence with a wrong benefits decision being overturned every single minute of every working day, according to new analysis.

Readers of This Site may find nothing surprising in the revelation from disability charity Scope about assessment results for Personal Independent Payment.

It’s doubtful that it is incompetence, of course. There is a wealth of information that the DWP deliberately approves wrong decisions by benefits assessors from outsourcing firms like Capita.

Capita, of course, has just agreed to pay off the family of a disabled, mentally-ill woman who died of a drugs overdose after being messed about by the company and the DWP over a period of months.

So why does the DWP – and its outsourced assessment firms – get away with it? Simple: they have cleverly managed to avoid a court making a decision that they are guilty of an offence due to their activities.

Most recently, Capita made an out-of-court settlement to avoid a judgement on the death of Philippa Day.

According to Disability Rights UK,

Thousands have to fight every month to get the main disability benefit Personal Independence Payment.

Scope has demanded urgent action from Government after publishing the analysis which shows that on average, more than 12,000 Disabled people are successfully overturning wrong Personal Independence Payment (PIP) decisions every month.

Disabled people can appeal if their PIP claim has been turned down or if they are awarded less financial support than they had expected.

Scope found that between July 2019 and June 2021, on average there have been 12,579 successful appeals (including mandatory reconsiderations and tribunals) every month – equivalent to 600 every day. Since July 2019 and June 2021, there have been a total of 301,899 successful appeals. 70% of PIP tribunals are successful.

Figures also show the Government spent £120 million fighting disability benefit claims for PIP and Employment Support Allowance (ESA) between 2017 and 2019.

Scope has launched a new petition calling on the government to make sure disabled people get the right benefit decision, first time.

The petition calls for disabled people to have the right to request an appropriate assessor who properly understands a claimant’s condition.

Will it get anywhere? Doubtful.

Therese Coffey – and all the Tory ministers before her, going back to 2010 and Iain Duncan Smith – enjoy killing off vulnerable people too much.

Source: Disability benefits: one wrong decision overturned every minute of every working day | Disability Rights UK

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