Welfare Reform (Disabled People and Carers)

Debate between Ian Mearns and Caroline Lucas

Tuesday 18th December 2012 Westminster Hall

[Ian Mearns]

My hon. Friend makes a very important point. That is why we are asking for a cumulative impact assessment of all the welfare reforms, including the housing benefit reforms.

Some 65% of respondents in work stated that without DLA they would not be able to work; 30% of disabled people stated that without DLA their carer would not be able to work; and 75% of disabled people said that losing DLA would mean that they needed more social care support from their local authority. Cumulatively, we can see a great deal of worry and concern emanating from the households of disabled people.

The Government say that they have to cut spending, but cutting DLA will simply mean that they have to spend more money on other things. It is clearly a false economy. We need to take into account the knock-on and implementation costs of replacing DLA with PIP. The Hardest Hit coalition concludes that the Government have over-estimated the total amount of savings that that will generate by, potentially, £1.6 billion.

Let us consider what is happening with contribution-based employment and support allowance. This is affecting many of my constituents at the moment. The Government’s decision to place a time limit of 365 days on those in the work-related activity group for ESA and to implement that retrospectively is forcing many disabled people on to jobseeker’s allowance. We should bear it in mind that there is no magic tree sprouting jobs at the moment, particularly not in places such as the north-east of England and particularly not with the Government’s economic plan. We talk an awful lot in the House about welfare to work, but it is a two-part equation—welfare and work—and I am sorry to say that, in my constituency, work is hard to come by, and in the north-east of England as a whole it is particularly hard to come by at the moment.

One of my constituents suffers from bronchial pulmonary dysplasia, is too ill for a heart and lung transplant, has been on steroids for 37 years, has osteoporosis, has kidney failure, cannot walk a single step unaided, has a fracture in her right arm, has left arm damage, has osteoarthritis and is diabetic. She was initially placed in the work-related activity group and told that she would need to find work. It should be borne in mind, as I am sure hon. Members have already fathomed, that she is housebound. Only after my intervention did the Department for Work and Pensions realise that a mistake had been made.

I do not want to talk extensively on the topic of Atos or its assessments, because frankly I would need all day. I have been sent a huge amount of information from concerned constituents and lobby groups for this debate, and I could quite easily speak for 10 hours. Unfortunately, I will not have that privilege, but it is a common occurrence in my constituency that people are concerned and genuinely feel harassed by the assessment process.

[Caroline Lucas (Brighton, Pavilion) (Green)]

This is a very important debate. Does the hon. Gentleman agree that one of the perverse outcomes of the reforms is that the constant reassessment is making sick people even more ill? The financial implications, as well as the health implications, are completely negative. This system simply is not working.