You constantly say this about stuff and it's never true.
Ooh, but it is true.
As it's physiological in origin I would call it a medical condition. Whether it's a disability depends on its severity I suppose.
One type, but not all types. But all are disabilities. But you avoid answering again.
@First Aspect, it was myself that sort of introduced it in the first post of this thread. It's something I'm living with, and having to decline treatment because of. Deciding which should get priority. Because of the impact of other treatments on it, I've had things go wrong.
This "conflict of interests" has led to the DNR being questioned by some. There's a very real chance of being left in a PVS, which is something I don't want. I've based this on the short term periods where I've been admitted to hospital due to the epilepsy, where machines have been there keeping me "alive". To be in that state day in day out isn't something I want. Nor do I want anyone being blamed for not "helping me live" like that.
@All uphill seems to have picked up on what I meant, in that there's worse than dying. Not just for myself.
And if I'd checked before starting this thread, to try and keep another on track, I'd have seen
@Beebo's thread on the same subject from late last year.