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 were there. Then I was told about Mavenclad. Year 1 was un-freaking-believable! Quality of life went from 40 to 110! However 3 days before starting my second year dose (started today), the left side of my tongue became numb. Not concerned really because knowing my body, it’s a flare up not a relapse. But I am loving Mavenclad! Anyone else liking this?
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