I totally agree, this is just our personal experience but im sure many will have had more positive experiences. The nhs has been falling apart since i can remember. I recall our newly diagnosed MS group meeting 15 years ago. Her consultant at the time stressed the fact that they cant predict when a relapse will happen, why it will happen, how long it will last, if one will happen etc. Then went on to promote a new 'wonder drug' that cuts relapses down by over %40 in the study they did. Any questions? Erm yes i said, whats to say those people you trialled on were even going to have a relapse over that period anyway, as youve just stated you dont know why or when sufferers get them. He stormed out of the room to be replaced by an MS nurse. From that day on its just been a farce after a farce.
Sadly, MS is widespread. Like Beth, I had a parent who had it for almost all my childhood. My father was 31 when he was diagnosed with it. They didn't have the drugs to control it in those days, and he went downhill fast. I was two when it was diagnosed and I barely remember him walking. He died when he was 45 and I was 16. The brighter news is that MS treatment seems to be going forward in leaps and bounds. All the best to you and your wife, Bob. If treatment can keep the conditions mild, then that is worth a lot in difficult circumstances.
