Hello. My name is Lori and happy I found this group. I have been on 2 different meds since my diagnosis in December, 2013. The first being Tecfidera. After finding a new lesion it was decided that Tecfidera was not working. Changed to Aubagio this past February. Side affects not agreeing with me. Does anyone in this group have any experience with or info on the new infusion drug Ocrevus? This is the route my Dr would like for me to try.
Medicine info needed: Hello. My name is... - My MSAA Community
Medicine info needed

Written by

lcrosby3
To view profiles and participate in discussions please or .
Read more about...
6 Replies
•
I have done the 2 1/2 doses, no issues feel great. Did 3 rounds of it's counterpart Rituxan no issues there either.
lcrosby3 I just started Ocrevus last week. The one side effect I have had is the fatigue (over and above regular MS lack of energy). The first 4-5 days were the worst and since then I am slowly coming back to a more productive energy level. Otherwise, no sickness, rashes, no other reactions. Good luck to you!
Not what you're looking for?
You may also like...
Help needed with questions and advice
Just had the worst relapse ever. Ended up in hospital for 3 days. Terrible nausea and couldn't...
Needing to decide between copaxone and tecfidera
Hi everyone! I have to decide between copaxone and tecfidera. I’m Jc positive at 3.19. Does anyone...
Diagnosed over 20 years ago.
Hi everyone, my name is Julie. I was diagnosed over twenty years ago. I am on Tecfidera and find...
Tecfidera dosing times
Hi. New to Tecfidera and trying to figure out a dosing time schedule that works for me. Trying to...
Thoughts on Tecfidera
My nuero is switching me to tecfidera. Does anyone have experience with this or knowledge on it?...