That just reminded me of an event. Twenty years ago, I volunteered to go to a residential home to do some carolling. We were singing all of the well-known carols, and at one point we asked the residents if they had any requests, and a lady put up her hand and said, ‘Yes, stop singing.’ Now, the reason why I mentioned that was because, afterwards, a member of staff informed us that she hadn’t spoken for a couple of years, and my point was, regardless of whether you’re a good singer or a bad singer, you can actually have quite an effect on people. But you don’t necessarily need Government to organise this for you. You can go yourself into your local community and do these things.

One of my staff attended the recent cross-party group on dementia, where those living with dementia were represented and, indeed, present. What was clear is that those living with dementia wish to remain a part of our society. They wish to help others as buddies, and they certainly wish to be heard. I note that this consultation that you’ve started appears to be along the usual Welsh Government format. So, what I wanted to know was: how can you ensure that those who need to be consulted—those who are actually using the services—are reached by this consultation, and are able to respond and are able to have their needs met? Can you highlight how this consultation has been made bespoke for that?

Regarding support services, I just wondered what your thoughts were on the merging of social services departments that are providing some of the treatments and care of dementia patients, usually in their own homes, with the NHS, in order to ensure that the left hand knows exactly what the right hand is doing, and to provide a better delivery of services for dementia patients?