800, 000 claimants face losing their incapacity benefit - The Times, Fri 10 Sept 2010

800,000 claimants face losing their incapacity benefit – The Times, Firday 10 September 2010*

George Osborne: said to be demanding up to £10 billion more from the £170 billion social security budget

Jill Sherman Whitehall Editor

Hundreds of thousands of people are likely to lose sickness benefits under a new assault on the welfare state, The Times has learnt.

The Treasury is considering means-testing incapacity benefit — given to those considered too sick to work — a change under which 800,000 people on modest to high incomes would lose it altogether. The entitlement, which is available to those who have paid national insurance contributions, costs the taxpayer more than £6.5 billion a year and goes to more than 2.5 million people.

Millions of disabled and sick people have been on the benefit — which is between £68 and £96 a week — for years and are able to stay on it until they retire, irrespective of their income or that of their partner.

Disability and poverty groups warned yesterday that means-testing would fly in the face of the principle of paying national insurance to fund benefits. They argued that the disabled and mentally ill were becoming the main victims of the Treasury’s spending cuts.

“It would be grossly unfair if someone who had worked for over 30 years and had paid [national insurance] throughout suddenly found the benefit taken away at the moment they needed it,” said Sue Royston, social policy officer for Citizens Advice.

Iain Duncan Smith, the Work and Pensions Secretary, has agreed to £11 billion savings a year. But George Osborne, the Chancellor, is said to be demanding up to £10 billion more from the £170 billion social security budget. Mr Osborne indicated yesterday that he had already identified £4 billion affecting those on “out-of-work benefits”.

“People who think it’s a lifestyle choice to just sit on out-of-work benefits — that lifestyle choice is going to come to an end. The money won’t be there,” he said.

One Whitehall official told The Times that means-testing incapacity benefit, which could save up to £2 billion a year, was being considered. “We are seeking more on incapacity benefit,” he conceded. “If more cuts are made to the welfare budget we should be able to reduce the bigger cutbacks to other Whitehall departments.”

Other benefits under threat include those going to pensioners, such as winter fuel payments and TV allowances, which could save £2.7 billion if scrapped.

Under the latest plans being considered, those on incapacity benefit — or employment and support allowance, which is replacing it — would receive it for a time-limited period of six months to a year. After this, those on higher incomes — generally those with working partners — would lose the benefit, and those on lower incomes would lose part of it. Those on the lowest incomes would still receive income support.

Mrs Royston argued that people would lose all entitlement to incapacity benefit if their partner had an income of about £8,000 a year or had savings of more than £16,000, if the present rules for other means-tested benefits were applied.

“This is causing enormous concern,” she said. “If someone who has worked for years became seriously ill and his partner earned over £150 a week, he would get nothing, despite his contributions.”

Treasury officials believe that many people remain on sickness benefits until they retire even if they could do some type of work.

Figures from the Office for National Statistics, published this week, show that in more than 840,000 households all members of the household over 16 are too sick to work. In a further 612,000 households, at least one member is too sick to work.

The Government is already clamping down on payments to the disabled and has pledged to introduce more rigorous medical tests for all incapacity benefit claimants by next March, but the Department for Work and Pensions (DWP) is already having trouble finding enough doctors to carry out the checks.

The severely disabled, who receive disability living allowance to help to pay for carers, are also facing medical tests for the first time.

Sources at the DWP yesterday made it clear that negotiations were still going on but did not rule out reducing or scrapping benefits for those on higher incomes. “We are presently looking at a range of options for welfare reform and any decisions will be made in the context of the spending review,” a spokesman said. “Our reforms will ensure that the most vulnerable in our society are protected.”

Richard Hawkes, the chief executive of Scope, the disability charity, condemned the plans to means-test incapacity benefit, claiming that people would be denied the support they had paid for.

“People will effectively be penalised for working hard, saving and contributing to society,” Mr Hawkes said. “The Government has made much of its commitment to ensuring that the impact of cost savings is spread fairly, but this feels like another example of disabled people bearing the brunt of cuts.”


*No link provided as The Times is now behind a paywall. 

Bog Off - Exhibit 28 Student Style!

This Bog Off was sent in by @Trufflepotamus, a student at The University Of East Anglia.

My source tells me that the disabled toilets in the accessible student bedrooms are huge wet rooms which are rather good, but this particular toilet seems to have been nothing more than an exercise in ticking boxes. So much so that not only is it not labelled as a disabled toilet, it hasn't even merited a toilet label of it's own. Poor loo, it must be very lonely all on it's own in a corridor facing a glass door without a sign to let anyone know it can be visisted! 

The photos are all taken from standing in the doorway as the door didn't actually open fully and got in the way. 

As I haven't seen this Bog Off in person, it's tricky to comment on the dimensions, but from the photos and impossible to open fully door, it certainly appears as though it would be very difficult to get a wheelchair in there, even a wheelchair as small as my child sized one probably wouldn't fit. The grab rails are a different colour from the walls, which makes them easier to see but there don't appear to be enough rails in the right places to enable transfer, even if a wheelchair could be slotted somewhere between the toilet, the wall, the sanitary disposal bin and the normal bin.


There's also no mirror...so don't bother to bring your lip gloss!

Benefits and Work - September Newsletter

The truth about benefits bounty hunters 
 
MPs returned to the commons today and, as a result, many of us will be bracing ourselves for the next round of misleading and vicious attacks on disabled claimants.
But, in reality, the hate campaign never really let up over the summer recess.  The most distressing example was undoubtedly the threat to unleash private sector bounty hunters on incapacity benefit claimants.

So, to mark the return of the disablist parliament , Benefits and Work looks at what actually happens when government agencies work with the private sector to uncover benefits fraud. 


We reveal:


  • whether incapacity benefit claimants really will be investigated if they spend too much money on flat screen TVs, gardening or DIY equipment;
  • whether disability living allowance claimants will be on the bounty hunters ‘most-wanted’ list;
  • what the only type of fraud likely to be detected by bounty hunters actually is.
Find out what’s really going to happen if the private sector goes claimant hunting in ‘The truth about bounty hunters’.  (This article is members only)

THE RIGHT TO RECORD YOUR MEDICAL

Professor Malcolm Harrington, meanwhile, is carrying out the independent review which is supposed to find out the truth about whether the work capability assessment for employment and support allowance is working.  In our last newsletter we asked you to contact  the professor with your views and experiences. 

We now understand that the professor would also like to know what changes you would make to improve the assessment process.  Very high on our list would be the right to record your medical without the nonsense of having to provide a sound engineer and professional recording equipment. 


So, even if you’ve already made a submission to the review, if you have practical suggestions for improvements, such as being able to record your medical, please email them to


wca.evidence@dwp.gsi.gov.uk


not later than 10 September.


WHERE’S THE BENEFIT?

For further reading about disability benefits issues in general, we can recommend the Where’s the Benefit blog, which was set up in August for the purpose of ‘Campaigning against the government's distressing war on disabled benefit claimants’.  There’s lots of well-informed comment and news, some of it from people you will be familiar with if you are a BBC Ouch regular.

CUTS CAMPAIGN

Meanwhile, CarerWatch are beginning a campaign to ask the Coalition to protect disability benefits before the October cuts. In preparation, they are asking disabled people and their carers to post short accounts of their own fears about benefit cuts and how it will affect them on the CarerWatch site.

MORTGAGE PAYMENT MISERY

One of the cuts planed for October will result in almost half of all claimants who receive mortgage interest payments facing a shortfall.  The majority of those who will fall into arrears will be pensioners and disabled claimants.   The coalition blithely claims that ‘based on conversations with the Council of Mortgage lenders we would expect lenders to demonstrate forbearance in the vast majority of these cases’  You can read more details in the DWP equality impact assessment.

FORUMS RETURN

The forums were closed for a few weeks in August due to a shortage of moderators.  We reopened on 1 September with two new mods – welcome Survivor and DepressedDerek – and below are a few of the good news posts we’ve received since reopening.

DLA Tribunal Result


ESA Success- thankyou!


Don’t give up!


Relief - ESA into Work Related Group


ESA Appeal Success - Harrumble!


ESA Success YIPPPEEEE


IB tribunal


MPs are only back for two weeks before going off on another break for their annual conference jamborees.  We have no doubt that all the major parties will be using the occasion to try to outdo each other in demonstrating how tough they can be on sick and disabled claimants.  Meanwhile, we’ll carry on doing our best to reveal the truth behind the disablist propaganda.


This newsletter can also be read online at:
 
 
Good luck,

Steve Donnison


(c) 2010 Steve Donnison. Benefits and Work Publishing Ltd.  Company registration No.  5962666


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Q.61 Please tell us anything else you think we should know about your claim

This is the actual answer provided on my current application for Disability Living Allowance for Q.61 Please tell us anything else you think we should know about your claim. This post should be read in conjunction with the part answer to Q.31 Do you need someone with you to guide or supervise you when walking outdoors in unfamiliar places in the blog Helping Hands, and the blog Page 18, Other Information IB50 form.

I was diagnosed with Ehlers Danlos Syndrome in 2004 after many years of being fobbed off and dismissed by medical professionals. After so long living with increased disability without knowing the reasons why I was relieved just to get an answer. Perhaps naively I hoped that diagnosis would be the first step towards getting better and regaining the many things I'd lost, friends, relationships, career and family. 

Day to day my life just is what it is, constant pain, dislocating joints, medications, falls, choking, incontinence, mobility equipment and many other indignities are always there but things I deliberately choose not to consider. I make jokes out of difficult situations, give mumbled half answers when people ask how I am, or just insist I'm fine even when it is patently obvious to everyone that I am anything but. I do this because to focus on the difficult things would make me incredibly depressed and to be blunt, I have enough problems already. Depression would just tip me over the edge. So instead I slap a smile on my face, no matter how hard or horrible the day. I smile because otherwise I'd cry and that just gives me a headache. I choose to be happy by focusing on how fortunate I am to have a roof over my head, to be able to see the sun shine, and to live in a country which still, just about, believes that looking after those who are more vulnerable is a collective responsibility. 

Filling out these forms has been a depressing and traumatic process for me. What I expected to be a straightforward task of explaining my disability has actually been a complex and difficult confrontation of the issues I face but choose not to think about on a day to day basis. Not only does it hurt my hands, but it breaks my heart to type the words I avoid saying out loud. That for the past six years I have fought every day; to gain an understanding of my condition, to take the correct medications, to eat the right food, to do the endless, painful, frustrating and incredibly boring physiotherapy exercises, to accept having to use a wheelchair, to learn to accept that the physical pain which is my constant companion will never go away, and will instead be joined by the emotional pain of a million tiny losses. 

It has taken me weeks to fill out this form as every time I try to answer a question I give up. How can I explain what it's like to have forgotten how not being in pain feels? That even the smallest movement can cause one or more joints to dislocate. What it's like to try and do even the simplest tasks with joints that won't hold themselves together, let alone do anything of practical value. When I dislocate my knee just rolling over in bed it's easy to swear a bit and refuse to think about the white hot pain, or subsequent tears, or the shoulder that's dislocated trying to relocate the knee, but that filling that information out on a form defeats me. All those individual dislocations and consequent lost opportunities I ignore in favour of those created, but to see them in glaring detail, not just once but the 53 different ways required by an official form is too much for me to bear. 


Disability Now's Pick Of The Blogs

Big thanks to fellow disability blogger Sarah Ismail for listing me as one of her favourite blogs in her 'Pick Of The Blogs' article for Disability Now

You can see the other blogs Sarah picked as her favourites in the full article at Disability Now.