Quick Links
Resources
About MyMSTeam
Powered By
What Works/doesn't Work?
Hello! I've been researching endlessly the numerous medications for MS. My Neuro prescribed Copaxone, although waiting to receive the prescription has allotted myself time to do research on other medications. I am just wondering what others have tried and what has worked vs what hasn't?
Ten years on Copaxone, MS under control, no side effects other than some skin issues. That I can live with.
I've been on Copaxone since 2008 with no relapses. I take Ampyra for walking, Baclofen for tight muscles, vitamin D3 / 50000 week and Cymbalta. But we are all different. Tell the neuro what's wrong and use what you get. If it doesn't help after 3 months tell the doc and try something else
I have been on Betaseron for 8 yrs and I have had very few problems. Took me about 1 month to get used to it but otherwise it has been okay. I do have injection site bruises .
I've been taking Rebif since diagnosed. Some injection site irritation, but that's it. No new lesions or new issues. Since 2008
Thi Thing I Find Most Frustrating Is Thr Dr's And Federal Government Rules. If They Had To Deal With All The Symptoms Of A Flare Up.
Can Anyone Give Me Pros Or Cons On "AMANTADINE 100 MG CAP" For The Relentless Fatigue?
Sign up for free!
Join
Your privacy is our priority.