I too would suggest your local Ms society. They offer a lot of assistance for care givers (family mbrs) even if it's just an ear you want right now. A year or two ago I was really having some...
I've taken copaxone since I was diagnosed (actually I think 8 yrs ago... I think I've been saying 7) and other then a few lumps where I take the shots no side effects. I've been doing good. I've only...
I had to go to probably 30 different docotors maybe more over 3+ years before I got my ms diagnosis. My aunt had ms and my uncle has lupus so I certainly have a family history. I believe I probably...
It's nice to get the brochure that compares the meds side-by-side. There might even be one online otherwise I bet your neurologist has the info that you can compare them. I live in one of the few...
I was diagnosed at 28. I was lucky I was already with my bf for 5 years at that point and continued to be with him for 5 more. It was a huge choice for me when I broke that relationship off because I...