Anger at government reforms to Disability Living Allowance


On Wednesday, disability rights campaigners urged the Lords that the government’s proposed introduction of Personal Independence Payment, to replace the Disability Living Allowance, had serious flaws and requires significant changes.

We-Are-Spartacus-Are-Protesting-Against-Government-ReformsThe website We Are Spartacus, which features the opinions of disabled people on the issue of welfare reform, has submitted an analysis of the PIP regulations to the House of Lords Secondary Legislation Scrutiny Committee.

According to We Are Spartacus:

“In some respects the draft regulations represent an improvement on the consultation draft. However, there are two specific and important areas where the draft regulations differ significantly from the views represented by almost all the organisations that responded to the consultation.

The areas of greatest concern are:

“1. The omission from regulation of the ‘safely, reliably, repeatedly, and in a timely manner’ requirement.

“2. The reduction of the qualifying distance for the enhanced mobility component for getting around from 50 metres to 20 metres.”

In the initial consultation draft, the assessment criteria included the requirement that people be viewed as being able to do an activity only if they could do so ‘safely, reliably, repeatedly, and in a timely manner.’ In the new regulations this has been changed. Now this requirement reads that the consideration is if the activity can be done ‘reliably’.

This has sparked worries. We Are Spartacus insist that it is incredibly important that the requirement specifically mentions safety, reliability and timeliness:

“This qualification is vital because it should ensure the assessor always takes account of issues such as pain, fatigue, breathlessness, nausea etc by building that consideration into the legal framework of the assessment itself.”

It is important that such a qualification has legal force. They point out that:

“The government may intend that healthcare professionals (employed by a mix of contractors and sub-contractors, run by Atos and Capita and thus potentially even more difficult to properly scrutinise than the direct contracting system used in ESA) and decision makers give due regard to the definitions of ‘safely, reliably, repeatedly and in a timely manner’, but if they do not have legal force this cannot be guaranteed.”

The other major area of concern is the reduction in the distance that someone is unable to travel; to make them qualified to receive the enhanced mobility component of the Personal Independence Payment. In earlier drafts people who were unable to walk more than 50 metres qualified, but this has been changed to 20 metres.

We Are Spartacus argue that this will have a significant effect on the lives of the disabled:

The reality is that most wheelchair users are able to walk a little; many can walk 20 metres but not much further. Since 20 metres is too short a distance to accomplish much at all (for example, many people have to walk more than 20 metres to get from their car to their house), many people who can walk a little over this distance will in fact be wheelchair users, at least when they’re not at home.

“Setting the bar so high for the enhanced mobility component of PIP for getting around undermines the objective in paragraph 73 of the Explanatory Memorandum, that PIP should ‘provide a cash contribution to individuals to help them meet the additional costs they face as a result of a long-term health condition or disability’.

“Since powered wheelchairs, scooters, cars, wheelchair accessible vehicles and accessible taxis are all high cost items, the mobility component is extremely important to people with significant difficulty getting around.”

Other disability campaigning groups are also very concerned by such a change and are urging people to write to their MPs to stop it.

 

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  • Janeyoung

    Thanks for that, Ben!

  • http://www.facebook.com/chantal.chaervey Chantal Chaervey

    its high time that all campaiging organisations united to get the message across to adolph cameron and his counterparts what exactly is happening and the impact it is having,, unless the ful;l force is measured, isolated pockets of resistance cannot be heard,, we are being forced into a situation where we are worse than poor, where dickensian standards are being imposed which has to be a breach of human rights on the disabled and those that care for them, and yet ministers have the cheek to demand a 20k pay rise while we suffer and lives are being severly affected and in some case being put at risk, this cannot continue,, there must be someone who can unite everyone

  • Roseanna Donohoe

    I have been diagnosed with Rheumatoid/and Osteoarthritis..have Fibromyalgia and more recently have been definitively assessed to have Bronchiectasis..I can’t walk ONE metre without pain and most of the tasks i want to do daily are too dangerous/too high/too low/too heavy /but mainly too painful to accomplish.I get totally depressed on many occasi0ns and these reforms are frightening and difficult to consider..I pray that someone with understanding and a touch of Humanity tries to deal with these concerns which are valid for us all..Bless…Rose

  • Roseanna Donohoe

    I have been diagnosed with Rheumatoid/and Osteoarthritis..have Fibromyalgia and more recently have been definitively assessed to have Bronchiectasis..I can’t walk ONE metre without pain and most of the tasks i want to do daily are too dangerous/too high/too low/too heavy /but mainly too painful to accomplish.I get totally depressed on many occasi0ns and these reforms are frightening and difficult to consider..I pray that someone with understanding and a touch of Humanity tries to deal with these concerns which are valid for us all..Bless…Rose

  • Debby

    I haven’t been diagnosed. I have seen over 35 doctors .They say the only way for a definite diagnose is to remove my brain. Ouch not a good idea put me off sliced meat.

    Walk 20 meters on a perfect flat surface? In real life pavements and roads are not level. I can’t cope with all the people moving about.

    My sister had just lost her mobility car for her Down’s syndrome little girl…… Liz

  • Debby

    I haven’t been diagnosed. I have seen over 35 doctors .They say the only way for a definite diagnose is to remove my brain. Ouch not a good idea put me off sliced meat.

    Walk 20 meters on a perfect flat surface? In real life pavements and roads are not level. I can’t cope with all the people moving about.

    My sister had just lost her mobility car for her Down’s syndrome little girl…… Liz

  • http://www.facebook.com/paul.sheppard.1238 Paul Sheppard

    Unbelievable. Well actually not. We have come to believe anything possible from this most cruel and unsympathetic of regimes.

    I was feeling actually ok this morning until reading this and the comments. Now I feel crap again.
    Take care Debby and Rose.

  • Preachy

    That safety one covers the vast majority of people with autism, I doubt my son will ever get the ability to go anywhere safely, but if he does not get PIP I will lose Carer’s, as he cannot be left home alone either I will therefore need a job that lets me take at least one, possibly three, autistic young men (other two have asd also but not sure how will progress) with me. Any offers there, employers? Nope thought not!

  • http://www.facebook.com/catalinaholloway Catalina Christina Holloway

    It could be me writing this post. I too have all your conditions & im terrified of losing my mobility car & returning to having ‘no life’. Really feel for all of us its just awfull & the stress & worry makes you feel ill eh?

  • Eddy Boyband

    Labours legacy…………

  • Newsbot9

    Keep blaming everyone else. Your Tories have gone further, and changed the definitions against the poor repeatedly. Trying to deny what you’re doing is downright pathetic.

  • Eddy Boyband

    Keep denying all you like but you can not escape the fact that at a time when the economy was booming and millionaires like the Milibands were only paying a top rate of tax of 40p labour thought that the sick and disabled had it to easy, so they gave the lovely atos a contract to retest every single disabled person who receives benefits.

    Now at the time I don’t remember left wing websites popping up informing their readers about the evil atos and the evil attack by the labour government.

  • Newsbot9

    You’re forgetful, then. Because there has been a strong movement against both parties ongoing moral panic well before the election.

    The only denial is yours of how much worse than Labour the Tories keep making things.

  • michael ward

    i have ostreporisis on my spine and struggle to walk even at a slow pace . just getting up iam in pain . whilst walking i am in pain but dont show it ,

  • hampshirehog

    With all the will in the world, sympathy does not produce funding. The pot is not infinite and the more an individual gets then the tighter the qualification and the fewer receive it. I know several recipients who are not really in need of DLA but who accept it as a right and, quite wrongly, as a compensationfor their disability.

  • Ann from Windy Corner

    Having had Rheumatoid Arthritis for 40 years and also suffering from various agonisingly painful back problems – Spondylolisthesis, Degenerative Scoliosis and Spinal Stenosis I am dreading the thought of losing my Motability Car and being housebound. I am not a scrounger and did work before I retired despite the never ending pain and chronic fatigue. The problem with working is being unable to earn a decent salary. This Government is trying to demonise the disabled and make out we are all scroungers. In my opinion the scroungers are in the minority and it’s a pity they spoil it for the genuinely disabled. This nightmare government don’t have a majority mandate and will really go to town if they get in for a second term.

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