Mental Health Services: Sign Language Users

Lord Hunt of Kings Heath Excerpts

Monday 2nd February 2015 Lords Chamber

[Lord Hunt of Kings Heath (Lab)]

My Lords, I, too, thank my noble friend for instituting this debate and Sign Health for its valuable briefing. I welcome the input of the noble Lord, Lord Borwick, but my noble friend’s Question was quite specific. I fully accept that however widely you define deafness, the scale of mental health problems is serious and deserving of attention. I thought that the noble Lord, Lord Addington, put it well. The focus on British Sign Language users is valuable in itself, but it is also a signal of more general problems.

Interesting work published recently in the British Medical Journal has shown, first, as is well known, that deaf adults in the UK occupy poorer socioeconomic positions, have poor literacy and have limited access to communicate through speech. Their health is generally poorer than that of the general population, with probable underdiagnosis and undertreatment of chronic conditions. As for mental health, other research shows that 40% of deaf people are likely to experience a mental health problem. Although the incidence rate of schizophrenia is probably similar to that of the hearing population, the rate of common mental health problems is much higher. Going back to the BMJ research published only a week ago, the rates of depression self-reported by deaf participants was 24% overall—32% for women and 14% for men.

In any response to the mental health issues facing many deaf people, it is abundantly clear, as the noble Baroness, Lady Tyler, said, that there is no national strategy to which one can turn to describe what services deaf people could expect from the NHS. That is related to confusion about what should be commissioned at national and local level. We see lots of indications that clinical commissioning groups find it very difficult to commission services for what inevitably will be a small population in their area.

Equally, I fully accept that not all of that can be commissioned at the national level. We need to find a way that will help clinical commissioning groups to commission services locally for these smaller population groups so that there is much more of a cohesive approach. I do not think that CCGs will do it if left to themselves. That is the real problem that we face, alongside the funding issues around commissioning at a national level for speciality services. This is not an easy issue, but we have to do better than at the moment.

A number of noble Lords referred to the position facing speciality services, and I want to add to the points that my noble friend made about this. I want in particular to raise the question of the Deafness Cognition and Language Research Centre at University College London, which I understand is putting together a costed business case for a national neurological service for British Sign Language deaf users. I understand that it has met Norman Lamb; it has also met my colleague Andrew Gwynne. This has clear cross-party support. The centre is putting a business case forward to secure the presence of a clinic beyond 2015; I do not know if the Minister will be able to update me on progress in that area.

My noble friend and other noble Lords have mentioned the Improving Access to Psychological Therapies service, which showed very promising results from the date of its introduction. Other noble Lords referred to the outcome measures. This has clearly fallen foul of the problem of being delegated to CCGs to commission; they are clearly not going to do so. I had the privilege of meeting SignHealth with Mr Norman Lamb. We had a very good hearing and I was left with considerable optimism that some way would be found to fund this. Again, if the Minister were able to give us some updates on the progress of that, I would be very grateful.

We come back to the point that, if this is left to local CCGs, there is no hope for services that need a contribution from each CCG to make it viable. One way or another, we have to find a way for there to be some kind of national leadership. Indeed, if I were to ask for one thing above all else, it is that the Minister would see if his department was prepared to produce some kind of cohesive strategy around deaf issues and mental health issues for deaf people. That would then give us some encouragement that we would be able to tackle these issues in a coherent way. I always thought that national service frameworks were a very good idea; I am not sure that the current Government think so but, if we are not to have them, we need something in their place.

I want to ask the Minister about the equality duty in relation to deaf people. Is he satisfied that the NHS understands its responsibilities under the equality duty? The noble Baroness, Lady Hollins, suggested that many staff in the health service are very much unaware of the issues for deaf people and the barriers that they face. The issue here is that we lack national standards against which local NHS bodies could judge their performance. The noble Baroness raised the question of reception and waiting room experience. The fact is that work has been done showing that 90% of deaf people have missed many GP appointments through not hearing their name called out in the surgery. That is just one example of the kind of communication problems that they face. At this point it would probably be better if I sat down and gave the Minister even more time to answer the questions.