Welfare Reform Bill

Jim Shannon Excerpts

Wednesday 9th March 2011 Commons Chamber

[Mr Duncan Smith]

We are consulting on that. However, this is going to be done later on, so we will have plenty of time to hear many more representations concerning children before we make any decisions. My hon. Friend the Under-Secretary is already talking to various groups about this particular issue.

[Jim Shannon (Strangford) (DUP)]

In relation to the indefinite awards, there is already a system in Northern Ireland whereby people have periodic checks, and I am sure that Northern Ireland is no different from the rest of the United Kingdom. If there is already a system of regular checks in place, why change that?

[Mr Duncan Smith]

Because it does not apply to everybody; it is very patchy. The honest truth is that no award we make should say to people, as has happened too often in the past: “You are in receipt of a particular benefit and we don’t want ever to see you again.” If the hon. Gentleman is arguing, as I think he is, that it is right to see people, surely we should be arguing that it is right to see them all to ensure that when their condition changes, that is met. That is surely fair both to them and to the taxpayer.

--- Later in debate ---

[Mr Byrne]

I am sure that the hon. Lady will have set out, with equal eloquence, the view of the Mayor of London that the measures might actually cost more taxpayers’ money than they will save.

[Jim Shannon]

Will the right hon. Gentleman give way?

[Mr Byrne]

I will take a couple more interventions in a moment.

I want to put on record my thanks to the scores of charities and campaign groups that have helped to brief us and offered to work with us to draw up amendments to improve the Bill in Committee. I am even more grateful to them for their commitment to mobilise their millions of members to help the Government understand why the Bill needs urgent reform. If the Government persist with the illusion that the Bill is immaculate, perfect and beyond improvement, and if they decline to hear the voices of those millions of members of charities and campaign groups that have worked with us, we will have no alternative but to vote against it on Third Reading.

In today’s debate, we will hear a lot of statistics; we will also hear about this record and that proposal. I just hope that the House will remember that behind every statistic is a person—one of our constituents. They are people like my constituent, Colin Hulme, who wrote to me at the end of last week. Mr Hulme suffers from Chiari malformation, a condition that affects about one in 1,000 people. It hit him in 2007, and he had to give up his job as an IT consultant and move home. He is a very brave man. He told me that his disability living allowance means that

“at least I can pay my household bills, my kids will have food on the table and clothes for school. More importantly, it means my wife can provide the care that I need.”

His view is that the Bill is about

“cutting costs and shifting responsibilities rather than improving the lives of sick and disabled people.”

It is a worry for him, and I think that the whole House will acknowledge that that worry is shared by millions of people up and down the country today.

My real point to the Secretary of State in this debate about principles is this: in the debate ahead, let us together put aside the politics of fear and division, and let us have the politics of hope—people’s hope for a job, the hope that they can get the help that they need, and the hope that they can get on and move up in work. That is what welfare reform should be about. That is the instinct expressed in our amendment, and I hope that the House will back it this afternoon.

--- Later in debate ---

[Julie Elliott]

No, not at the moment, although I might in a minute.

As I said earlier, I want to focus my remarks on the most vulnerable. Many of the extremely vulnerable people who have contacted me are suffering from mental health issues and autistic spectrum disorders. Autism is a spectrum condition, which means that, despite some common characteristics, it affects sufferers in different ways and to differing extents. ASDs, as they are commonly known, are largely “hidden” disorders that affect a sufferer’s ability to communicate with others, which means that the annual review will be a real problem. ASD sufferers span the whole disability spectrum. Some are able to live relatively independent lives; others need a lifetime of care or receipt of specialist support.

Approximately one in 100 children and 350,000 adults of working age suffer from ASDs. Of the latter group, only 15% are in full-time employment in the UK. The disability living allowance has been a key benefit, providing for these people the help and support that the additional costs of their disability require. The £1 billion cut over the next three years, when the DLA is replaced by the personal independence payment—

[Jim Shannon]

At the beginning of her remarks the hon. Lady said that reform is necessary, which we all accept. However, does she share my concern that a target to reduce by 20% the number of people in receipt of DLA is the wrong approach, and that the issue should be dealt with through reform alone?

[Julie Elliott]

I totally agree with the hon. Gentleman. Reform is about making the benefit fit the individual need. If the benefit needs to be paid and if it fits the need, it would not be wrong if it went up by 20%.

It is vital that the Bill does not disproportionately hit those with autism and other disabilities, who are all too often overlooked despite being among the most vulnerable in our society. The goal surely must be to support people with autism who cannot work, so that they can live a full and happy life. However, for those who are able to work, DLA has been crucial in helping them into the workplace. Without the DLA, people with autism would be socially isolated and more likely to suffer from poor mental health. The reform of DLA may lead to people with mental health problems missing out, which could have huge knock-on cost impacts on health and social care services. Surely this cannot be this Bill’s motivation—to give less support to people with autism and to increase the knock-on costs to other Government Departments. As it stands, that is what the Bill is in danger of doing. Its implications for people with autism could lead to confusion and frustration, which in turn could lead to more serious health problems. The Government must ensure that the needs of those with ASDs are taken into account.

The proposals for face-to-face assessments are in themselves creating great anxiety among people with autism and with mental health issues. ASDs are a very specialist area of medicine, and the doctors who deal with such disorders are the people who understand them and their implications. Many of the doctors undertaking the assessments will not have a full understanding of ASDs and the specific needs of the people who suffer from them. When a detailed assessment by a specialist has already been undertaken, what is the need for a further assessment, for benefit purposes, to be carried out by someone without that expertise?

As I said at the beginning of my speech, for a welfare reform Bill to work, it must be, as it says, a “reform” Bill that makes benefits easier to access and to understand.