Disabled People

Baroness Browning Excerpts

Thursday 5th May 2011 Lords Chamber

[Baroness Browning]

My Lords, it is a great pleasure to follow my noble friend Lord Rix who has, for many years, been such an inspiration to us all in the field of disability. I also congratulate my noble friend Lord Fellowes of West Stafford on such a memorable maiden speech. Congratulations are due, too, to the noble Lord, Lord Low of Dalston, who has brought this important debate to your Lordships’ House today. I begin by declaring my interests: I am the named carer for an autistic adult who is in receipt of state disability benefits, a vice-president of the National Autistic Society and patron of Research Autism. I hope that your Lordships will indulge me if I confine my remarks to that group of people who would come within the autistic spectrum, people with learning disabilities and those with chronic long-term mental health problems, because I believe there is such an overlap affecting all three of those groupings.

In his opening remarks to the debate, the noble Lord, Lord Low, used the word fearful—a word which other Members of your Lordships’ House have picked up. It is not just people with disabilities who are fearful at present. I hope that your Lordships will not mind if my opening remarks are extremely personal, not just to me but to many other people, as I am sure that many of your Lordships will recognise what I am about to say. I am a parent and I, too, am fearful. If you have a child who is born with a lifelong disability, you know that that child—however long its lifespan and whatever difficulties it will encounter—was not only born with that disability but will die with it. You also know that while you are on this earth, you have the opportunity to try not only to allow that child to fulfil its own potential but to do what you can as a parent to make provision for what will happen to that child when you are no longer around to support it.

It is perhaps in the whole context of things when, as parents, we concern ourselves with all our children’s education, particularly with disabled children's ability to take on what are euphemistically now called life skills, which are so important—perhaps more than we realise at the time—that your waking thought almost every day is: “Have I done enough and what will happen?”. My concern about the Government's reforms, many of which I support, is that, with the grouping which I have mentioned in mind, the reform of DLA is, for example, to reduce by 20 per cent over the next three years the amount of money spent. The focus will be on those most in need, which sounds quite laudable when you listen to it. “For those most in need” sounds a fair way to spend resources which we know are restricted but for the autistic community, for the learning- disabled community and for those with ongoing mental health problems—some have two or three of those conditions—there is a real fear.

I pick up on the excellent speech made by the noble Baroness, Lady Campbell of Surbiton, about independent living. It is probably only in the last 20-plus years that we have really taken on and embraced the opportunity for people with a range of disabilities to be included in society and to exercise their right—and it is their right—for independent living. That will vary from disability to disability and from individual to individual but I know that however severe that disability, each step of the way is hard fought for and won. It is not something which is handed out; very often, people end up having to go to court to exercise their right to get the sort of support they need to sustain independent living.

It is a long process. For many in that group it takes years to bring about, step by step, an ability to look after themselves and to make sure that their personal care can be coped with, that they eat properly and have the right nutrition, and that they maximise their own desire to take part—often in work but more particularly in social activities, too. For example, part of that package of care which is paid for by the state could well be for somebody to be a friend to that person two or three times a week in a befriending package, since they cannot access or make friends as the rest of us would because of the nature of their disability. I cannot emphasise how important what might seem very small, individual parts of a care package are to making the quality of life worth living and to enabling that person to live independently and to take their part in society, as the rest of us do without really thinking about it.

However, when I look at what the Government intend to do, I am concerned that those who have achieved independent living, which has taken many years to construct, will find that because they are no longer regarded as the most in need, those valuable building blocks that have been put in place over many years to allow them to achieve that level of independence will no longer be regarded as important enough to be supported. I say to my noble friend with all due respect, but with absolute certainty, that if what has taken years to put together is removed, it will fall apart in a matter of months. With many disabilities, it is not the case that once you have solved a problem, you have solved it for the rest of that person’s life. It is a bit like a mosaic. This is not a broad-brush painting where you can identify the picture. It is a mosaic made up of many small pieces, all of which are interdependent and important in their own right, but when you have achieved the mosaic, it is a picture that has allowed somebody to take their place in society and fulfil their potential and those important dreams that we heard about just now.

This is not special pleading or the bleeding hearts brigade, but the words of a mother who for 40 years has been on that journey with a child. I am, of course, not the only one. I know that there are thousands of mums like me up and down the country who say to my noble friend in all sincerity: realise where we have come from in the past 20 years and where we are now. The reason why there are so many more payments for DLA and other disability benefits is because 20 years ago people would have been in institutions or, more often than not in the case of people with learning disabilities or autistic spectrum disorders, would be sitting at home, unoccupied, living out an existence with well meaning but very worried elderly parents. The crisis would come only when something happened to those parents, and then the state would know the full cost and consequences of dealing with disabled people in crisis. The cost of dealing with people in crisis is always far more. In fact, it is off the Richter scale compared with the minuscule cost of the basic building blocks that will allow so many disabled people to continue to live independently. I say to my noble friend: do not take those blocks away. It would set this country back years and cause mayhem and disadvantage to the most vulnerable people.