Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
i have been on betaseron now for about a month, and having the worse relapse i can recall. when i was a copaxone i don't recall having one so severe. i was only on copaxone for 8 months when my neuro decided to switch me. i don't think this was best for me. and now i am at a complete loss. is my MS progressing? i go back to state this is the worst f*****g disease ever. thanks, kelly
I'm on Copaxone now but have had a very had time taking it daily - mostly mentally denying that I have a problem. I need to get better about it, especially since I think I've been having an ongoing relapse for some time now.
I wish I could get a clear answer about whether the pain in my legs and feet are a relapse or just regular every day symptoms. Even my Dr. doesn't know for sure and says that my diabetes makes it even harder to tell what, exactly is happening.
This disease does suck, yes, but any disease at all is the worst. I'm thankful I don't have some of the other autoimmune viruses - Chron's (which my dad eventually died from), lupus, etc. or cancer, Alzheimer's, etc.
May the new year bring new hope for all of us!