DLA Medical Assessment Criticised

Budget DLA Medical Assessment CriticisedThe Government’s decision to introduce medical assessments for those in receipt of the Disabled Living Allowance (DLA) has brought a wave of criticism on Chancellor George Osborne’s first Budget.

Describing the ‘unavoidable’ tough Budget on 22 June as one which ‘rewards work’ yet ‘protects the most vulnerable in our society,” the Chancellor pointed to the last decade’s 45% increase in the size of the UK’s Welfare bill, and the need to undertake ‘lasting reform’ in order to reduce the nation’s debts.

“It is right that people who are disabled are helped to lead a life of dignity,” George Osborne insisted in the House of Commons. “We will continue to support them, and we will not reduce the rate at which [DLA] is paid. But three times as many people claim it today than when it was introduced 18 years ago, and the costs have quadrupled in real terms to more than £11 billion, making it one of the largest items of government spending.”

‘DLA IS NOT A BENEFIT’

According to the Chancellor, the new medical assessment, to be introduced for both new and existing claimants from 2013, will be a ‘simpler process’ than the current complex forms. “We can continue to afford paying this important benefit to those with the greatest needs, while significantly improving incentives to work for others,” he said.

However, the Chief Executive of disability charity Scope, Richard Hawkes, insisted there was one simple goal behind the announcement. He said: “The proposal to introduce a new medical assessment for DLA appears designed purely to reduce the number of people eligible for this support.

“DLA is not a benefit, but a basic recognition that it is more expensive to live as a disabled person in our society,” he insisted.

ABSOLUTE LIFELINE

The chief executive of the National Autistic Society, Mark Lever, also suggested that medical assessments could exclude many people affected by autism from receiving the support they and their families need.

“Thousands of individuals and families affected by autism struggle to meet the extra costs of living with a disability,” he said. “All too often they are denied essential benefits and face poverty due to a lack of understanding, support and services. For many, DLA is an absolute lifeline.

“Autism is a serious, lifelong and disabling condition and, without the right support, it can have a profound and sometimes devastating effect,” he added. “It is vital that this is acknowledged in any proposed changes to the way DLA is assessed.

SAFEGUARDS NEEDED

Another organisation with concerns about the announcement was learning difficulties charity Mencap. Their campaigns and policy manager, Esther Foreman, told us: “Strong safeguards must be put in place to ensure that people with a learning disability, who desperately need the support, do not miss out because of these assessments.

“We recognise that cuts have to be made but it is vital that we protect frontline public services enabling people with a learning disability to live independently,” she added. “Rising inflation and continuing growth in numbers of people with a learning disability means that, even if budgets standstill, people with a learning disability are going to be seriously affected.

“We fear that short term cost savings could have long term implications for people with a learning disability and their families and carers.”

MORE: www.scope.org.uk, www.autism.org.uk, www.mencap.org.uk

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4 Comments to “ DLA Medical Assessment Criticised ”

  1. Paul says: Reply

    The Able team are interested in finding out what you think about the Budget. Do please add any comments here!

  2. Barry Culley says: Reply

    I am not being cynical when I say that the move to carry out medical assessments on people applying for or in receipt of DLA is purely intended to have the benefit withdrawn from those receiving it and put out of reach of those applying for it.

    I speak with conviction because I was a victim of just such a scheme when the Tories decided to get people off Invalidity Benefit. I was examined by a doctor on behalf of what was then the Department of Social Security (DSS). He knew nothing at all about my medical history and the examination took only a few minutes. In fact he spent about three times as long calculating the mileage from my home to the hospital and back, paying me for travelling and obtaining my signature for the money. A week or so later I received a phone call from my doctor to come and see him. He had heard from the DSS that their doctor disagreed with his view that I was unfit for work and decided I was fit for limited work. I told him what happened at the ‘examination’ and he said he would write to the DSS and complain strongly. He would also request another ‘examination’ and this time he would insist that the doctor had a copy of my medical notes. In due course I was asked to attend again for the ‘examination’ and this time the doctor had my notes and carried out a proper examination. A week or so later my doctor rang to say that the results of the second examination had overturned the decision arrived at after the first examination and I had been declared unfit for work. My doctor commented that the doctors working for the DSS were simply carrying out a process of cutting back on payment of Invalidity Benefit. Some years earlier the Tories had manipulated people off the Unemployment Benefit list and on to the Sickness Benefit list (for political reasons). In due course the Sickness Benefit claimants had migrated on to the Invalidity Benefit list!

    When my DLA was awarded in 1993 it was awarded “for life”. Subsequently the wording was changed to “indefinitely”. I strongly object to becoming a pawn in yet another Tory chess game. Disabled people have more than enough to put up with in life, without being made to suffer repeated so called ‘medical assessments’. Many of us went through all this when we first applied for DLA and in a lot of cases, such as my own, we only get worse with time not better. I get Care at the lower rate and Mobility at the higher rate and I have more ailments now than I had when DLA was awarded, which is perhaps hardly surprising taking into account the fact that I will be 70 next year. I want nothing to do with Atos or any of the other people the government use to do their dirty work.

    Several friends of mine have been put through very considerable pain during various medical examinations being carried out by order of what is now known as the DWP. Two were arthritis sufferers who had substantial evidence of their conditions from GP’s, Consultants and other. Another friend told the RMO (as they called them then) that he was not going to co-operate with some of the tests he had intended to carry out. Perhaps I was fortunate in that the third RMO Medical I had was the only one in which I suffered pain!

    I have read elsewhere a piece by a well qualified authority on the subject. He says that the Law will require amendment if the government want to change it. The Social Security Contributions and Benefits Act 1992 Part lll, sections 72 & 73 and the Social Security (Disability Living Allowance) Regulations 1991 Parts lll and lV are the legislation in question. If the government want to change that it would require new primary legislation approved by both Houses of Parliament.

  3. reggie says: Reply

    SO Why are disabled “charities” NOT stopping the degridation, humiliation and discrimination and pursecution of vunerable disabled people. DLA ESA Appeals 20 minuite examination to say yey or nay WHEN OUR SPECIALISTS AND DOCTORS say we are ill They are WRITTEN TO BY THE ESA DLA to say WE ARE NOT Disabled or ill? This is a Human Rights issue that ONE OR ALL charites and support agencies should be FIGHTING FOR OUR RIGHTS FOR RESPECT AND DIGNITY. They give criminals and peadophiles in secure units HEATING ALLOWANCE ESA contribution based People who have WORKED 0 !

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