Yes, I'm getting there, because there are limitations that the clinic can't offer because of the number of patients. We have been lucky to access hospice services. It's only to talk about hospices as such, but I think “hospice” nowadays, as Nigel was saying, actually talks about palliative care, about issues that are coming up much earlier than before. We have in fact put our daughters in touch with a special family support person who is a psychologist and specialized in children and teenagers in this kind of situation. This is voluntary support. It's May Court. It's funded by us, citizens. We are seeing it as an important part of our team, because the girls will eventually start protecting their parents and not talking to us about the important difficult issues. They need those services outside. We are lucky because this is in our community, but I don't know how well such services are available elsewhere, for example, in areas where populations are more scattered.
It is difficult, and the one big piece is that ALS is changing all the time. Just now, when we have got used to this normal, a new normal, there will be a change and we have to readjust. And it means a readjustment for all of us in the family, and that is difficult.