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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?
Is Anybody Able To Share Their Experience Of Aubagio, Telfidera Or Mayzent?
I've Been Successfully On Tecfidera Since Diagnosis 3 Yrs Ago. Now Have To Switch... To Aubagio. A Good Choice? Suggestions? Thank You!
Are There Any Other People That Are So Sensitive To Ms Meds That They Can't Take Them?
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