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

 

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Switch from DLA to PIP so disastrous that even PM’s own team is troubled

THERESA MAY was facing a back-bench rebellion over disability benefit cuts yesterday as charities warned that thousands of people are being wrongly assessed.

Tory MP Heidi Allen led the charge after Labour demanded an urgent review of the assessment process.

The MP for South Cambridgeshire, who famously used her maiden Commons speech to launch a searing attack on George Osborne’s benefits cuts, said: “People with disabilities and health conditions already face challenges in life, so we must not add to them.”

She called for a review of the way personal independence payments (PIP), which replace disability living allowances (DLA), are assessed.

Labour had warned that disabled people are being forced to use foodbanks as benefit payments are being stopped incorrectly. Work and pensions select committee chairman Frank Field has written to ministers demanding an overhaul of the current system, which he says fails to consider the impact of people’s disabilities and health conditions. And Labour MP Neil Coyle has demanded answers, saying the assessment process for PIP has “failed on every measure.”

The calls come as the government moves people over from DLA to PIP with thousands of people having their claims rejected only to have the decision reversed on appeal.

Disabled People Against Cuts’s Linda Burnip told the Morning Star that assessors working for private-sector firms Atos and Capita appeared to be “totally ignoring medical evidence.”

She accused the Department for Work and Pensions of simply rubber-stamping fl awed rulings which were then overturned on appeal. “It’s past time something was done about it,” she said, calling for the government to “get rid of the companies, hold them to account, fine them for their negligence.”

An Oxford University study earlier this year revealed that more than 50 per cent of households which use foodbanks include a disabled person.

In the letter to Pensions Secretary David Gauke, Mr Field said that the PIP process used a “rigid” set of questions which saw may people having benefits wrongly withdrawn or drastically reduced.

Mr Field said: “Might you therefore review as a matter of urgency please the quality, accuracy and reliability of the assessment process, and report back on the steps that are being taken to ensure it more accurately reflects applicants’ health conditions?”

The assessments are carried out by privateers Atos and Capita, which are being paid an astonishing £600 million for their PIP contracts — the original contract was for £512m.

Mr Coyle said: “Millions of pounds of public money was being poured down the drain” with DWP officials reviewing many of their decisions and backdating benefits to those who have their PIP reinstated.

To qualify for PIP, claimants must be awarded eight points for the standard rate, or at least 12 for the higher rate. But 13,130 people who were initially awarded no points at all after being assessed went on to receive PIP after an appeal.

The work and pensions select committee will decide whether to continue with its PIP inquiry when Parliament’s summer recess ends on September 5.

https://www.morningstaronline.co.uk/a-55bb-Tory-MPs-Lash-out-at-Mays-Disability-Rights-Cuts-Crisis#.

Blind, severely autistic teenager ordered to be reassessed for benefit he was promised for life

A TEENAGER who is blind, severely autistic and barely able to speak has been ordered to attend a meeting – to check if he should continue to receive benefits.

Private firms pocket more than £500m from hated disability benefit assessments

Two private firms responsible for carrying out disability benefit assessments on behalf of the Department for Work and Pensions (DWP) have pocketed more than half a BILLION pounds of taxpayers cash, despite thousands of “inaccurate assessments” being later overturned in favour of claimants.

Data collected by The Mirror reveals Atos and Capita have made more than £500m from Personal Independence Payment assessments, since the new disability benefit was introduced to replace Disability Living Allowance in 2013.

read more here: http://www.welfareweekly.com/private-firms-pocket-more-than-500m-from-hated-disability-benefit-assessments/

Rhiannon, 14, cares for her dad. Now cuts have made life even harder

Disabled Andy relies on his daughter to cook and shop, but his benefits have been slashed, and it’s pushing the two of them closer to the edge

Fourteen-year-old Rhiannon Doolan’s favourite lesson is PE, and she wants to work in sport when she’s older. But, unlike most children going back to school this week, she is already doing a full-time job: caring for her disabled dad, Andy.

In their two-bed council flat in Liverpool, Rhiannon keeps things as clean as she can: she hoovers, mops, does the dishes, and polishes. It’s been just the two of them for years – “since Rhiannon was in nappies”, Andy says – and she’s got used to doing whatever they need. Or, as Rhiannon puts it quietly to me, “things my dad would like to do but can’t.”

For Andy, 48, that’s a lot. Twenty years ago, he had a double hip replacement and caught MRSA in both legs. He’s had almost 25 operations since, and he can barely walk, then only with crutches. The crutches have brought their own problems – arthritis in his joints – and he can’t straighten his arms; he can barely move his wrists. “I’m useless without her,” he says.

Rhiannon was three years old when she started caring for her dad. “I’d help put his socks and shoes on when I was a toddler. Put cream on his legs [as medicine],” she says. By four, she was helping with shopping, pushing the trolley in the supermarket while her dad stood behind with his crutches. Outside help never came – the council went as far as putting grab-rails near the toilet, but no further. As she got bigger, and her dad’s health got worse, Rhiannon took on more.

“I do breakfasts,” she tells me. Cereal in the week and egg, sausage and bacon on toast at the weekend. For “a big meal” – Rhiannon likes mince and chips best – they cook together. “He struggles but he tries,” she says.

To help him with his medication, Rhiannon puts her dad’s prescription together and then collects it from the pharmacy down the road from the estate. Each day, she helps him get dressed and reach his feet when he washes. There’s no shower in the flat – just a bath with a shower head – and Andy stands in the bath with Rhiannon leaning over the side. “I’m proud of her,” Andy says, pausing. “But she should be out playing. She shouldn’t have to be doing any of this.”

It’s a tough way of life, and one that has just been made even harder. Since before Rhiannon was born, it’s been Andy’s two disability benefits that have paid the bills: disability living allowance (DLA), and because he’s too disabled to work, incapacity benefit (IB). But now – as both benefits are abolished nationally and tougher tests put in their place – Rhiannon has had to watch as her dad’s only support is being taken away.

The first hit came last June, when Andy – put through the “fit for work” test – was, in Rhiannon’s words, given “no points whatsoever”. He promptly had his benefit cut to £46 a week. By the time he could appeal against the decision six months later, he and Rhiannon were living off food hampers they had been given by a charity.

read more here: https://www.theguardian.com/commentisfree/2016/sep/08/rhiannon-carer-disabled-dad-benefits-slashed?

‘I’ve had a heart attack, two strokes and my kidneys are failing…but I’ve still been told I’m fit to work’

Former scientist Phil Williams from Caernarfon said he was devastated to find out he’ll be stripped of his disability benefits after a recent Government assessment

A former scientist who has to undergo 12 hours of dialysis treatment a week because his kidneys are failing has been told he is fit to work.

Philip Williams, 56, from Caernarfon has been plagued by health problems in recent years including kidney failure, loss of hearing and ulcerative colitis – which brings on bouts of extreme diarrhoea and vomiting.

He received a letter from the Department of Work and Pensions (DWP) on Monday saying that his Disability Living Allowance will be stopped next month after a recent medical assessment deemed him ineligible for benefits.

A nurse visited Mr Williams around six weeks ago to carry out an assessment using a points system to determine whether or not he is able to cope around the house alone.

But Mr Williams now feels that the nurse was “unqualified to carry out the assessment” due to her lack of experience in his particular illness.

Mr Williams said that he feels “disgusted” by their decision and claims that DWP made no attempt to contact his GP or renal consultant about his illnesses.

see the video and read more here: http://www.dailypost.co.uk/news/north-wales-news/ive-heart-attack-two-strokes-11805344

Aaron Lane: Talented musician with mental health problems took his own life after DWP ruled him fit to work

Aaron took his own life after he lost his Disability Living Allowance – his parents believe he was worried his benefits would be stopped entirely

A talented musician battling mental health problems took his own life after he was ruled fit to work.

Aaron Lane, who won a place at the prestigious Royal Academy of Music in London in his 20s, suffered psychosis and had been receiving Disability Living Allowance.

But he was recently ruled fit to work under the Tory Government’s crippling benefits changes.

Instead Aaron, who lived alone in a flat, was surviving on Jobseeker’s Allowance.

His parents say he feared he would lose all of his benefits and be left penniless.

After they raised concerns, police forced entry to his home in Newark, Lincs, and found him dead aged 31.

It is understood he had taken his own life.

Aaron’s dad Steve and mum Carol are calling for more detailed checks to be carried out on people with mental health problems before benefits are stopped or changed.

“He used to say every single day that no one would employ him,” said Carol. “He was in his own world yet there was a whole world out there waiting for him. He never gave us any indication of what he was about to do. We will remember Aaron as a happy child. We never had any trouble with him growing up. He never asked for anything. He took what life gave him.”

Steve added: “We believe he took his own life because things were getting on top of him.

“That little bit of extra money allowed him to have the internet at home which brought the world to him. His world was getting smaller and smaller. He was worried that all of his money would be stopped. We don’t blame anyone but Aaron was let down across the system. He was too often a box to tick.

read the rest of this story here: http://www.mirror.co.uk/news/uk-news/aaron-lane-talented-musician-mental-6031644?ICID