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something specific?

Editing to add- I completed my second round of treatment in 2020, and had some mild side effects but now it is out of my system, my lymphocytes are at a ”normal” level, and I’m being considered stable! Hi all! I’m looking into changing from Gilenya to Mavenclad, and I’m just a bit confused! I’m se...

Trying to talk myself into being on something after 17 years with MS or be more focused on the natural route. Anyone take mavenclad?

Hi i was diagnosed with RRMS in 2012 when i was 26. Now 33 I've tried Copaxone, Gylenya and am on my second year of Mavenclad. With Copaxone i had a relapse and never felt any relief. Also i have permanent divots in my legs and arm because of it. Gylenya I was happy with but still finding symptoms w...

Who else is on Mavenclad or will be starting Mavenclad soon ?

Hey all I'm Sam. I have just joined this group. I was diagnosed in March this year with RRMS. I have chosen mavenclad as a treatment,does anyone have any experience with this ?

Anyone taking Mavenclad??? It was just approved in Canada and my neurologist suggested I start this treatment. Just looking for some info on side effects ??

Is there anyone on this medication that I could talk to start mavenclad tomorrow thanks

I just completed my first dose of Mavenclad. Has anyone used this DMT? If so, let me know your thoughts about it! I just got off Ocrevus.

Hi guys, I haven't been here on for a while now because my health is getting a little bad but I had a very important question. They put me on a new medication and I've had some very serious side effects but one of the ones that is sticking out to me the most is nausea and vomiting. I have had vomiti...

Hi all. Just wondering if anyone has experienced feeling really cold since taking mavenclad? I mean heating on full blast and wearing 3 fleece layers buts hands still ice to touch? It's near the end of May so think this is not too normal..........