Equality and Human Rights Commission: Disability Commissioner

Lord Addington Excerpts

Thursday 10th May 2018 Grand Committee

[Lord Addington (LD)]

My Lords, this is an interesting debate and, as many people have already stated, it comes down to this question: is disability something that easily fits with the rest of the commission? Personally, I think it should be there but that it needs to be treated slightly differently.

I and my noble friend Lady Thomas are both disabled people under every term of the Act, but our problems in day-to-day life could not be more different. As the noble Baroness, Lady Flather, said, if you have a disability—in my case, dyslexia—you often have to plan to do the normal differently. I am in a total mess if the voice-operated system on my computer breaks down. I cannot function as a normal Member of this House because I do not have access to email. It does not happen very often, but it does happen. Suddenly everything changes.

The perceptions of disabilities always exist in certain contexts. For example: “everyone in a wheelchair is only affected by transport”. That is something I went through many a time on many a Bill. “Dyslexia”, my own disability, “affects you only in the education system”. Both perceptions are patently absurd under any examination.

I recently took part, in the company of Barry Sheerman MP, in a commission on the neuro-diverse community and recruitment. We discovered—I throw this in merely to explain the great diversity—that the neuro-diverse community has tremendous difficulty with big-firm recruitment. It uses a series of online tests that we are bad at. I suspect that nobody else in this Room knew that, although you should have read our commission’s report. The difference is there and although all the other sectors here will have a great degree of difference, it is greater still. Many of the disabilities in the two groups which are to be discussed in the next debate have a great diversity of influence.

I have given the Minister warning of this question, although not much because I probably sent it to the wrong email account. I ask her: is there any evidence that the new approach is working better? I ask because that approach is not one that is reassuring to the huge and diverse disability communities—not “community”. We need to know that there is something working better and that information is getting out there. That is the important bit. Unless the Government can give us that assurance, we are going to have problems because we do not know what is happening.

Also, if your Lordships are looking at this huge, diverse and multifaceted group of things, yes, every disabled person happens to belong to at least one of the other groups in the commission but they will have little turns and changes in emphasis as things are gone through. Everything will be that little bit more complicated and, as my noble friend already said, we need to take some positive action to adopt this. Most bits of that action are actually much easier than people think, certainly with modern technology, but it still has to be taken. Somebody still has to be told that it is their duty to take it and, most of the time, it is my experience that people have to be shown that they can deal with the problem fairly easily.

In my professional life—I have to declare an interest here as chairman of Microlink, which deals with disability adaptation—often merely the structural changes in how something is paid for make life easier. For instance, it is often cheaper to do it without referring to somebody else’s budget and putting a central core down, but that is for another day. We need that reassurance that the information is getting through and that there is a central point, which is going down. If we do not have this, we will come back to this subject. We need the reassurance that it works, so is it being tested and, if so, how? What are the results? Make those public and we can move on.