I was diagnosed with RRMS in 2007 and this is my 6th therapy. I was hoping to make the Mavenclad conference but we had a snow storm and I was going through a relapse as well. Anyone out there on Mavenclad?
Possibly another MS therapy: I was... - My MSAA Community
Possibly another MS therapy
Hi sweethunnie I'm really sorry that you have been on so many DMTS. Mavenclad is one of the newer ones out there now. 😊 I know that Fancy1959 wanted to go on it, but her Dr said no, because of the risks involved. (Fine print)
I hope your over your relaspes?
What are you taking now? 🤗💕🎄
Thank you for that information. I have been on Aubagio since April of this year. Before that I was on Ocrevus. I had 3 infusions with Ocrevus. It wasnt until the 3rd full strength infusion that really got me sick .It was scary and a horrible experience. I have been on Copaxone, Rebif, Tysabri, Tecfidera, Ocrevus and Aubagio. My neurologist suggested Mavaclad since the others are not a good choice for me since I am on other medications. I may have to stick with Aubagio and deal with the side effects until I can get another therapy that is right for me.Thank you for your response.
I hope ur doing well and hope ur over the relapse. Sorry u have been on so many dmts. I not on mavenclad but I hope someone can answer ur question
sweethunnie I know this is an old post. In a couple days I'll discuss DMT options with my neuro and found this after searching for Mavenclad. I took Aubagio for about 4 months earlier this year but have paused it for about another 4. We thought it might have caused neuropathy but that seems to have been ruled out.
Did you ever go on Mavenclad after all, or continue with Aubagio?