I have taken Copaxone, Aubagio, Avonex and Tecfidera. All gave me bad side effects. Anyone using Rituximab?
@motha. Yes. I have only started this past June but so far my blood work is good. Although it's a 2 infusion treatment between 15 days, here it is January and with latest blood work is still good! I'll keep you posted.. .
I was on tecfidera n they just changed it to Vulmerity. Anybody else heard of this?
Are there any other people that are so sensitive to ms meds that they can't take them?