I’m newly diagnosed, symptoms began a few month ago. Was on solu- medrol for 3 days last month with no response. I’m now beginning plasma exchange, anyone else have this procedure? Did it help?
I'm sure other will chime in soon, but in the meantime, here's our information about plasmapheresis:
MS Navigator Jess
I'm hoping but I believe so because since being on it I have not been in the hospital as much but with the heat it's probably making it worse and I know from experience try and stay inside in the day and out early morning or evening. Try and keep your chin up and keep trying when you are able to.