How do others cope with the flare/exacerbations of ms? I seem to no sooner get over one than the next hits.?
I have rrmm since Oct 05 though had it before that & have had several flare ups while I was on betaferon & then avonex. Couldnt tolerate either so now on a trial drug which is oral, only 1 month in & another flare up. Have lost use of both legs & stumbling around with the walker. Very frustrating for sure.
Yes, it sounds like the regular inteferons are not strong enough/not good for you.
I would talk it over with your neurologist. He/she seems to be doing the right thing in changing the medicines. Did you consider Tysabri? I don’t know where you are located, but here in Denmark, it is used for patients like you with aggressive and multiple attacks.