Just wondered if any other PPMS sufferers had been offered this by their neurologist if so what were the results?
My consultant has never told me what type I have although I know its PPMS as I dont have relapses and my symptoms are slowly getting worse and nothing ever improves. Although I queried why he wants me to try this as I dont have relapses etc he said it has the possibility to slow progression.
Anyone else ever been told this or am I right to be going in there next week to ask to be referred to another consultant who I have more faith in and one who knows what the heck he is actually doing?
Its been a while but I hope you all had a fab xmas and an even better new year…