Tag Archives: work

#DWP bungled #Waspi women’s #pension-age rise. How long must they wait for #compensation?

WASPI protesters: this image is from 2016 and women born in the 1950s had already spent years protesting against the way the Department for Work and Pensions mistreated them.

The so-called Waspi women have finally won recognition that they were mistreated by the government, after an ombudsman found maladministration by the Department for Work and Pensions.

But they won’t get any compensation for it – at least, not yet – because the Parliamentary and Health Service Ombudsman (PHSO) has no power to order it.

The PHSO found that the DWP failed to act quickly enough, once it knew a significant proportion of women were not aware that the age at which they would qualify for the state pension was going up.

It should have written to the women affected by the change, at least 28 months – more than two years – earlier than it did.

The ombudsman’s report said

Between 1995 and 2004, accurate information about changes to State Pension age was publicly available in leaflets, through DWP’s pensions education campaigns, through DWP’s agencies and on its website.

[But the DWP} failed to give due weight to relevant considerations, including what research showed about the need for ‘appropriately targeted’ information, what was known about the need for individually tailored information, or how likely it was doing the same thing would achieve different results. Despite having identified more it could do, DWP failed to provide the public with as full information as possible. DWP failed to make a reasonable decision about next steps in August 2005.

It did not ‘get it right’. And its failure to use feedback to improve service delivery meant it did not ‘seek continuous improvement’. That was maladministration.

DWP then failed to act promptly on its 2006 proposal to write directly to affected women, or to give due weight to how much time had already been lost since the 1995 Pensions Act.

It did not ‘get it right’ because it did not meet the requirements of the Civil Service Code, and it did not take all relevant considerations into account. And it failed again to use feedback to improve service delivery and ‘seek continuous improvement’. That was also maladministration.

The maladministration led to a delay in DWP writing directly to women
about changes in State Pension age. If the maladministration had not happened, DWP would have begun writing to affected women by December 2006 at the latest, 28 months earlier than it did (in April 2009).

It follows that affected women should have had at least 28 months’ more individual notice of the changes. For women who were not aware of the changes, the opportunity that additional notice would have given them to adjust their retirement plans was lost.

The investigation is not over; its next stage will consider the impact that the injustice had on the women it affected.

The co-chairs of the All-party parliamentary group on State Pension Inequality for Women, Andrew Gwynne (Labour) and Peter Aldous (Conservative) have both welcomed the findings.

“The DWP must urgently address these findings, and advise 1950s women what actions they will take to right the wrongs committed by successive Governments. For too long 1950s women have been ignored, and this must change,” said Mr Gwynne.

And Mr Aldous added: “We now must see a cross-party effort to sort this problem out. This issue is bigger than any administration and has been raised repeatedly over the last 25 years. The PHSO findings must now be scrutinised by the DWP and parliament, and then we must set out about compensating women for this injustice.”

It seems the DWP itself isn’t ready to comment yet:

Waspi women have already waited many years for an admission that they were mistreated by the government, and that they have suffered loss as a result.

It seems they may not have to wait even longer before getting any compensation for the loss they have suffered and the huge amount of distress it has caused.

Source: Women’s state pension: Compensation closer for Waspi campaigners – BBC News

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DWP confirms ESA £5,000 underpayment update next month

The Department for Work and Pensions office in London.

This is fairly straightforward – although when the DWP announced it was doing this, I was among many who thought it was a cover for yet another purge of benefit claimants.

I wonder… When the report is published on July 8, will it include a section on the number of people the Department found to have been overpaid or wrongly paid, and from whom it is now clawing money back?

That might be interesting.

The DWP confirmed it will release a final update on progress of checking 600,000 Employment and Support Allowance (ESA) cases for underpayments next month.

In a brief statement on the GOV.UK website, the DWP announced the statistics will be available from 9.30am on Thursday, July 8 as part of the completion of the exercise – reports the Daily Record.

In the last update, DWP reported that 600,000 ESA claims started the reassessment journey, with 112,000 claimants receiving arrears payments.

The UK Government has already paid out a total of £589million in backdated payments, with claimants receiving an average of £5,000 in January 2020.

Source: DWP confirms ESA £5,000 underpayment update next month – Liverpool Echo

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The DWP carried out dozens of secret reviews into benefit claimant deaths – and deleted them. Why? What did they show?

[Image: Black Triangle Campaign].

If you’ve got nothing to hide, you have nothing to fear, right?

In that case, what is the Department of Work and Pensions afraid of?

Since February 2012 (as far as we can be sure), it has been carrying out secret reviews into the reasons benefit claimants died – but has destroyed records of all such reviews carried out before 2016.

Why? What did they find that the DWP needed to hide?

Freedom of Information requests show that 49 reviews took place between February 2012 and autumn 2014 (all records of them have been destroyed) – and nine reviews took place between August 2014 and April 2016 (but these overlap with other periods where we know the numbers).

The reason this is cause for serious concern is that the DWP’s policies and practices have been linked to the deaths of benefit claimants – particularly those claiming Employment and Support Allowance (ESA) and Personal Independence Payment (PIP) who suffered mental distress – ever since the Tories took over control of that department in 2010 (if not before).

At the time of writing it is only a day since This Site published an article highlighting the fact that more than 300 terminally-ill people have been dying every month after being denied fast-track access to benefits by the DWP.

The department has been rejecting around 100 claims per month.

The concern – as I pointed out yesterday – is that the Department for Work and Pensions intentionally harms people claiming benefits by depriving them of their payments in order to hasten their deaths.

Is that what was revealed in the now-destroyed reviews of the reasons claimants died?

Is that why the DWP shredded them?

If so, then it seems this department’s bosses – and their political leaders from 2010 onwards – have good reason to be afraid. But when will they be brought to justice?

Source: DWP admits carrying out more than 175 secret reviews into benefit deaths in nine years – Disability News Service

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More than 300 terminally ill people died PER MONTH after DWP denied them state benefits

[Image: www.disabledgo.com]

Once again the Department for Work and Pensions has been caught lying about the support it provides to people who are terminally ill.

This Site reported, many years ago, on the scandal when it was discovered that – despite having a policy to put people likely to die within six months on a fast track for benefits – many benefit claims were refused, leaving these people to die in appalling conditions.

So then-Work and Pensions Secretary Amber Rudd announced in 2019 that there would be a “fresh and honest” re-evaluation of the way these benefits were awarded.

It is now two years later, and two charities – the Marie Curie Trust and the Motor Neurone Disease Association – have drawn public attention to official data showing that the DWP is rejecting benefit claims by more than 100 terminally-ill people, every month.

Worse still, the official figures also show that an average of 315 people are dying every month*, never having been able to secure the fast-track benefits that are supposed to help them pass away with dignity.

This is damning:

They say there are “serious concerns” over the government’s “six-month rule” – under which people must prove they have six months or less to live to access fast-track benefits support.

They said there were red flags in the DWP’s ability to recognise when a claimant was approaching the end of life.

I think that is very… charitable.. of them.

It is far more likely that the DWP is simply ignoring the facts in order to avoid paying out the benefit money – knowing that these people will soon be dead; they can’t complain or appeal and expect justice before their condition kills them.

This in turn suggests that nothing at all has changed and that Amber Rudd’s “fresh and honest” review was nothing of the sort.

Here’s some evidence in support of that conclusion:

The charities say that the findings of the review are “being withheld”.

So, after 11 years of Tory control (and it wasn’t much better under neoliberal New Labour) we can say with confidence:

The Department for Work and Pensions intentionally harms people claiming benefits by depriving them of their payments in order to hasten their deaths.

No wonder we all hate having anything to do with that vicious, poisonous arm of the Tory government.

No wonder millions of people suffer anxiety attacks whenever they see an envelop marked “DWP” in their letterbox.

No wonder I said, years ago, that the DWP is not fit for purpose and should be scrapped.

But I’ll tell you why it wasn’t:

In killing thousands of people every year, the DWP is doing exactly what Boris Johnson and his Tories want.

*1,860 people over six months.

Source: Over 1,000 terminally ill people rejected for benefits and Universal Credit each year – Mirror Online

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Deaths and other harms to benefit claimants prompt renewed lawsuits – and calls to investigate DWP

Death by DWP: Philippa Day.

The chickens are coming home to roost at the Department for Work and Pensions.

The families of three benefit claimants – who are said to have died because the DWP deliberately mishandled their claims – are continuing to take the department through the court system in their search for justice.

Publicity around the cases has led to a BBC investigation in which it was found that they are just three out of 150 cases in which the DWP has conducted internal investigations into its own behaviour.

Now the department is facing demands for an independent investigation into its conduct. Long overdue demands, in This Writer’s experienced opinion.

Here‘s the BBC:

Cases where people claiming benefits died or came to serious harm have led to more than 150 government reviews since 2012, a BBC investigation found.

Internal reviews are held by the DWP when it is alleged its actions had a negative impact, or when it is named at an inquest.

Calling for an inquiry, Labour MP Debbie Abrahams said: “It needs to be taken out of the hands of the DWP.”

Ms Abrahams, who previously read out in the Commons the names of 29 people who have died, said: “There needs to be an independent inquiry investigating why these deaths are happening and the scale of the deaths needs to be properly understood.”

The DWP said it had established a new Serious Case Panel in 2019 to consider themes identified from serious cases, which included independent members.

Yeah, right. I opened Gibbons’ Decline and Fall of the Roman Empire the other day. That doesn’t mean I read any of it.

Now let’s hear from Leigh Day solicitors, who represent the three families who are pushing their cases through the courts:

The families spoke to the BBC to share their stories and the legal stages of their cases.

Philippa Day who lived with a long standing mental health illness, and was diabetic, died aged 27 in October 2019, two months after she was found collapsed at home in Nottingham.

On 27 January 2021, HM Assistant Coroner for Nottinghamshire, Gordon Clow concluded that the problems Philippa had with her application for disability benefits were “the predominant… and the only acute factor” which led her to take action on 8 August 2019 that ultimately proved fatal.

Following the inquest, a letter of claim has been sent to DWP and Capita which alleges breach of human rights and negligence by the DWP and Capita arising out of the events which led to Philippa’s death and seeks compensation for the wrongs Philippa and her family suffered. DWP and Capita have three months to respond before claims may be pursued in the High Court.

Death by DWP: Jodey Whiting.

Jodey Whiting, aged 42, took her own life on 21 February 2017. She suffered severe mental health problems and had her benefits terminated a fortnight earlier for not attending a Work Capability Assessment, leaving her with no source of income.

The Attorney General granted their consent last year for an application to the High Court for a fresh inquest into her death, which the High Court will hear on 22 June 2021. Jodey’s mother seeks a fresh inquest to ensure the role played by the DWP in her daughter’s death are publicly and fully investigated.

Death by DWP: Errol Graham.

Errol Graham, was found dead aged 57 in June 2018, eight months after his benefits were stopped because of his failure to attend a fit for work assessment. When his body was found, Mr Graham weighed four-and-a-half stone.

An inquest in 2019 found that DWP and NHS staff had missed opportunities to save Graham, and the coroner concluded that “the safety net that should surround vulnerable people like Errol in our society had holes within it”.

Mr Graham’s family have submitted an application to the Court of Appeal after their judicial review challenging the lawfulness of the DWP’s safeguarding policies was unsuccessful. The family argue that the decision in 2017 to terminate his benefits was unlawful and that the DWP’s safeguarding policies and systems need to be overhauled to provide greater protection to vulnerable benefit claimants who, like Errol, suffer from mental health conditions.

The allegations against the DWP are extremely serious.

They indicate that it has been DWP policy to endanger the lives of benefit claimants.

For that reason, it seems clear to This Writer – and I expect to anybody with the slightest common sense – that the DWP should not be judging its own work with regard to these cases.

I say that for the same reason I say Boris Johnson’s Conservatives should not be conducting inquiries into whether contracts were corruptly handed to Tory cronies – or into whether Johnson himself breached the ministerial code by getting donors to pay for his Downing Street flat’s redecoration.

They are liars; they will always whitewash themselves.

We have seen evidence of such behaviour many times over the last 10 years – reported on This Site, among others.

The work of Debbie Abrahams has been exemplary in trying to get an investigation into this scandal by an organisation we can trust.

It’s true that such efforts have achieved very little, so far.

But attitudes are changing.

As more evidence has come to light, public tolerance of the DWP’s entitled attitude has eroded.

Maybe we are finally about to get some factual answers to questions we have been asking for more than a decade.

Source: Investigation reveals 150 DWP reviews into deaths or harm to benefits claimants | Leigh Day

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Every new MP receives briefing on how Tory social security reforms have harmed us – so they can’t say they don’t know

Long-term readers of This Site will remember Mo Stewart, the researcher into the harm being caused to claimants of sickness and disability benefits by successive Conservative governments’ determination to convert the social security system to a for-profit insurance scheme.

Mo spent 10 years researching and writing a book on this subject: Cash Not Care – The Planned Demolition of the UK Welfare State.

After the 2019 general election, she became concerned that the huge new influx of Conservative MPs – along with those from other political parties – were ignorant of the harm that government policies had caused.

So she wrote a briefing paper specifically addressing the issue and sent it to all of them.

Labour’s John McDonnell has apparently offered to arrange a debate on the subject, if possible.

Whether or not that happens, Mo has provided me with a copy of the document so we all have a record of what these MPs should know – and so they won’t be able to plead ignorance.

And here it is:

Social Policy Abused:
The Creation Of Preventable Harm

Executive Summary

The Preventable Harm Project (the Project) ran for ten years and closed in November 2019, with the evidence identified within the Project findings widely promoted during 2019/20. The Project identified the bipartisan political ambition to eventually remove the UK welfare state, to be replaced by private income replacement health insurance. In order to remove the welfare state, it was first necessary to remove the psychological security provided by the welfare state. This was achieved by the adoption of a flawed disability assessment model, and the manipulation of the general public aided by the tabloid press, that successfully demonised claimants of disability benefit(s). Large numbers of suicides linked to the adoption of the Work Capability Assessment are overlooked by the Department for Work and Pensions, and successive Rule 43 ‘prevention of future deaths’ Coroners’ reports, highlighting the link between the Work Capability Assessment and suicides, have also been disregarded. The Work Capability Assessment was fatally flawed by design and should be abolished, and the departmental intimidation of disability benefit claimants should be outlawed.

Introduction: The Creation of Preventable Harm

1. Introduced in 2008 to restrict access to the new Employment and Support Allowance long-term out-of-work disability benefit, the Work Capability Assessment (WCA) is a ‘non-medical functional assessment’ that disregards all clinical opinion. Since 2010, the WCA has been linked to the deaths of thousands of chronically ill and disabled benefit claimants who applied for state financial support when unable to work, yet were deemed to be ‘fit for work’ by the fatally flawed WCA.

2. Twelve years since the adoption of the WCA there is an identified and growing mental health crisis within the UK linked to claimants of disability benefit(s), and a disturbing increase in suicides directly linked to the WCA, as identified by published academic research but dismissed by the Department for Work and Pensions (DWP).

“The worst thing, I find, is realising that I am forced into looking for a life that I want but have no chance of having. I seriously feel I may kill myself because being sick, having next to no money, no life, no future, no cure, constant pain and constant disapproval defeats me.”

An extract from the ‘Fulfilling Potential? ESA and the fate of the Work-Related Activity Group’ project, conducted by Catherine Hale and published by MIND and the Centre for Welfare Reform.

3. In both 2006 and 2007 the government’s own expert medical panel warned the administration not to adopt the WCA, advising that it was ‘not fit for purpose’ due to the predictable negative impact on public mental health. The expert panel’s clinical opinion was disregarded by the DWP. The removal of clinical opinion from disability assessment using the WCA guaranteed that many of those in greatest need were destined to die, as the state removed the financial and the psychological security of a guaranteed income when unfit to work.

4. There have been two official Rule 43 ‘prevention of future deaths’ Coroners’ reports linking the WCA to suicides, with other Coroners expressing concern at inquests due to the identified enforced suffering of the deceased by the DWP. Coroners’ official Rule 43 reports and identified concerns are disregarded by the DWP, whose social policy reforms since 2010 created preventable harm to those in greatest need linked to intimidation. The constant threat of sanctions, which removes all disability benefit income, leaves the chronically ill and disabled community in need of state financial support living in fear of the DWP.

5. Regardless of the Jobcentre being advised that a claimant is unable to attend an interview due to ill health, disabled claimants are routinely met with an ‘institutional reluctance’ to meet their needs, as identified in Coroner’s reports. Jobcentre staff’s decisions to sanction a claimant can cause death by starvation, in C21st UK, when all income is removed for a period of weeks or months. No-one is held to account when some of those in greatest need are starved to death by the state.

6. The WCA is used to limit access to all state disability funding including the Employment and Support Allowance (ESA), Personal Independence Payment (PIP), Universal Credit and the War Pensions for older working-age disabled veterans, which is a military medical pension not an out-of-work benefit.

7. The WCA is regularly and inappropriately referred to as a ‘medical assessment’ by the DWP, MPs, academics, policy advisers and journalists. The WCA is not a medical assessment and is totally unrelated to clinical opinion. The adoption of the WCA is identified as being attributed to psychocoercion by successive administrations, to remove what once was the psychological security of the welfare state for anyone who is unfit to work.

8. Identified in 2008 by the American Association of Justice as being the second worst insurance company in America, the corporate insurance giant Unum (Provident) Insurance have been advisers to the UK government since 1992, and were appointed as the official UK government consultants for ‘welfare claims management’ from 1994. Concerned by the increase in various conditions that could not be confirmed by blood tests or x-rays, such as chronic fatigue syndrome, Unum Insurance adopted a biopsychosocial (BPS) model of disability assessment, which disregards all clinical opinion.

9. Unum advised the UK government as to how to adopt a similar BPS assessment model in the UK, and funded an assessment centre at Cardiff University for this purpose. The DWP adopted the discredited Waddell-Aylward BPS model of assessment for the WCA, which disregards diagnosis, prognosis, past medical history and prescribed medicines. The human consequences of using the WCA is that many of those in greatest need would die, with many driven to suicide with a common perception that anyone claiming to be unfit to work, and in need of state financial support, will be persecuted by the DWP. The Waddell-Aylward BPS model of assessment failed all academic scrutiny.

Policy recommendations

• Since 2009 every clinical authority in the UK have demanded that the WCA should be abolished. This includes the British Medical Association, the Royal College of General Practitioners, the Royal College of Psychiatrists, the Royal College of Nurses and the British Psychological Society. Introduced by the private health insurance industry, disregarding clinical opinion was always dangerous. The WCA is fatally flawed and should be abolished without further delay, to be replaced with a disability assessment that considers clinical opinion, with many assessments being paper-based, so that the chronically ill and disabled community are no longer intimidated by the DWP.

Research findings
• In order to remove the past psychological security provided by the welfare state it was necessary to discredit vast numbers of disability benefit claimants, aided by the tabloid press, which helped to manipulate the British public.
• Social policies were adopted with a fiscal priority whilst disregarding health and wellbeing, which policymakers failed to take into account when recommending policies which were harmful.
• Since 2010 the social policy reforms, and the additional austerity measures, were destined to have a catastrophic and often fatal consequence for many of those in greatest need. Thousands of chronically ill and disabled benefit claimants have died when ‘killed by the state,’ with a 2014 NHS Digital Adult Psychiatry Morbidity Survey report that identified that almost 50 percent of ESA disability benefit claimants had attempted suicide at some point.
• Prosecuted disability hate crimes, including murder, increased by 213 percent between 2010-2016, during the coalition government’s term in office.
• The relationship between physical health and mental health is well documented. The numbers of benefit claimants who have perished due to social policies since 2010 will never be known.
• Published in September 2016 ‘Cash Not Care: the planned demolition of the UK welfare state’ provides the results of the first six years of independent disability studies research for the Preventable Harm Project. The book is now recommended reading for various social policy, health and legal courses at universities in the UK, Australia, Canada and New Zealand.

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Disabled benefit claimant sends in the bailiffs after suing Atos for negligence

More people need to do this.

A benefit claimant whose partner recorded her Personal Independence Payment assessment interview successfully sued Atos for negligence and failure of its duty of care after her payments were stopped.

She then sent in the bailiffs to enforce the country court’s ruling after the outsourcing giant refused to pay up.

The claimant, known as Rebecca, had to spend two years fighting to get her PIP reinstated after it was wrongly stopped on the basis of false information provided by the assessor.

Rebecca has epilepsy and a resulting heart condition, anxiety, depression and memory problems but her entitlement to the enhanced daily living component of PIP, along with her claim to the benefit itself, was removed by the Department for Work and Pensions on the basis of the assessment.

Eventually she was able to put her case before an appeal panel who listened to the recording of the assessment, compared it with the assessor’s account of the interview, and promptly restored her entitlement to PIP – and to the enhanced rate of the daily living component – until 2023.

Rebecca was so angry at the way she had been treated by Atos and the DWP that she decided to take the assessment firm to court, suing for “mental distress, anxiety and hardship”.

Atos did not bother to defend the claim, which resulted in an award of £2,500 for Rebecca, in compensation and damages.

Perhaps the firm simply thought it could shrug away her attempts to claim the money?

Not so. When Atos failed to pay, she sent the bailiffs in to its London offices, creating a further cost of £2,000.

This is a huge victory – not just financially but morally – for benefit claimants whose claims have been cancelled under false pretences, based on inaccurate assessment reports.

It happened because the assessment was recorded – something that the DWP has resisted for years. Now we know why: it stops that government department from wrongly knocking people off its books. This is a strong indication that every benefit claimant should record their interview.

Atos may wish to consider that the award against it was enlarged because of the length of time it took Rebecca to win her case.

I don’t have the full details but I’m willing to bet this was due to the “mandatory reassessment” malarkey imposed by the DWP, which means claimants have to wait – with no cash to live on – while officers of the department consider whether the decision to cut their benefit was right.

Usually they decide it was, and it is only then that claimants can appeal to a tribunal. Most appeals are won by the claimant.

This Writer would therefore urge anybody who has recorded their assessment, lost benefits, and had to appeal to get them back, to follow Rebecca’s example: don’t just take the money – take legal action!

Once Atos and the DWP have lost a few more cases, they might actually give up and agree that their system is unfair and has to change.

Source: Claimant Successfully Sues Atos And Sends In The Bailiffs When They Don’t Pay Up | Same Difference

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Sick & disabled people to be subjected to same harm as Universal Credit claimants from April

The Department for Work and Pensions is to run trials on a new “integrated” assessment service, putting sick and disabled benefit claimants under the same conditions as Universal Credit claimants.

What a disaster for people with long-term illnesses and disabilities.

Universal Credit is known to be harmful to its claimants. The five-week wait before anything is paid puts most people into debt and forces them to take out advance loans, meaning that the amount they receive – when they do get it – is much less than their government-assessed need, and continues to be so for many months.

This creates serious mental and emotional stress and otherwise fit and healthy UC claimants have done horrifying damage to their own health as a result.

People with illnesses and disabilities are already suffering damage to their own health. The current system already piles mental and emotional stress on them –

Only yesterday I wrote about “brown envelope anxiety”, that pushes sick and disabled people (especially) to avoid opening communications from the government, in the expectation that the message inside will inflict harm upon them.

– and putting them under Universal Credit conditions can only make matters worse.

I notice that the new trial is set to start in April, when the effects of Covid-19 are expected to be dying down.

Is it the Tory aim to immediately replace one fatal attack on sickness and disability with another?

Source: Justin Tomlinson confirms that the new DWP intergrated assessment service to be trialed in April. – The poor side of life

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It’s not the DWP’s envelopes that need changing, but the attitude behind them

Kiss of death: for benefit claimants, letters from the Department for Work and Pensions – no matter what colour the envelope in which they arrive, cause more problems than they solve. It isn’t the packaging of the letters that is the problem, it is the content – and the malice of the people writing it. [Image: www.disabledgo.com]

Can you believe the Department for Work and Pensions is planning to change the colour of its envelopes from brown to white, to encourage disabled people to open its letters?

Officials have apparently discovered the existence of “brown envelope anxiety”, which is a nervous condition triggered in some people whenever they receive an envelope of that colour – denoting a communication from an official source – through the letterbox.

They have wrongly deduced – probably from the name of the condition – that merely changing the colour of the envelope will magic away the anxiety.

How stupid can they be?

As a friend posted on Facebook,

It’s not the envelopes that need changing, DWP and Tory government, it’s your inhumane assessments processes that cause untold harm and distress to many.

I have a total fear of the postie coming to my house; that’s a huge trigger for me, let alone what’s put through the door.

[It’s about] living with never knowing when the review will come up and living with constant financial insecurity and the amount being taken away and leaving you destitute and probably homeless.

To add insult to injury, DWP officials think people with brown envelope anxiety will be more likely to read their white-envelope missives immediately if they print on the front: “IMPORTANT INFORMATION INSIDE. PLEASE OPEN.”

In fact – as they would know if they had asked any experts instead of listening to the tweeting birds inside their empty heads – this is more likely to trigger an anxiety (if not a heart) attack.

Rather than reading the contents of these white envelopes and responding to the Job Centres, it is more likely that overworked doctors will be examining the recipients’ vital signs – if they manage to get to a hospital in time.

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The Tories promised to reform benefits long ago so why do 10 terminally ill people die every day, waiting for their first payment?

Christine McCluskey: when she died, after your Tory government cut her benefits, she weighed just three stone.

The life expectancy of people with terminal illnesses has plummeted because they are being denied end-of-life state benefits.

The system is supposed to support people who are expected to live less than six months – but doesn’t.

The Tories demand that doctors provide a note predicting when their patient is likely to die.

But many physicians have been reluctant to make such predictions, or feared their patients’ health could deteriorate more rapidly if they learned they were not expected to survive very long.

The Tory government of the day promised to change the system in 2019, saying it would bring in modifications that would make it easier for people with terminal illnesses to claim their due.

And nothing has happened.

DWP minister Justin Tomlinson has apologised for the delay – which is a fat lot of good for people who could starve to death before their health condition kills them.

He blamed the delay on the Covid-19 crisis – and warned that it is likely to run on for many more months yet.

Let’s just remember what this means:

The image at the top of this article depicts Christine McCluskey, who died in a humiliating way, weighing just three stone, after Tomlinson’s department wrongly ended her benefit claim.

The 61-year-old grandmother had suffered long-term health problems most of her adult life including Crohn’s disease – which left her with a colostomy bag – osteoporosis, arthritis, a stroke and chronic obstructive pulmonary disease (COPD).

This housebound lady had a feeding tube and a painful fistula that leaked through her abdominal wall, she was severely malnourished and was being investigated for a worrying cough at the time the Department for Work and Pensions assessed her for Personal Independence Payment.

The decision: her payments of £117.85 per week were removed and her mobility car was taken away from her.

Weeks later she was diagnosed with terminal cancer but her payments were not restored. She died four months after her benefits were stopped, weighing just three stone.

She was unable to receive fast-track access to PIP that is available for people with terminal illnesses who have less than six months to live, because she was unable to show when she was likely to die.

Recent estimates obtained by Labour MP Jessica Morden have revealed that 7,260 people died as they were waiting for a verdict on their claim for Personal Independence Payment (PIP), or 10 people per day.

Yes, these people were going to die soon anyway.

But the manner of their death tells us whether the United Kingdom under the Conservatives is a civilised country or primitive and barbaric.

And the UK under the Conservatives clearly falls into the latter category: primitive and barbaric.

Source: DWP shamed as 10 terminally ill people die every day waiting on a benefits decision | Welfare Journal

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