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Old 01-04-2015, 06:38 AM #1
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I took copaxone for several years and still had two to three relapses, often in the hospital. I do not have any side effects so far from the Rebif other than inj sites...I hope it works and I seem to tolerate it rather well.
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Old 01-04-2015, 02:38 PM #2
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I've been on the interferon's, copaxone, tecfidera, I'm done. I can't take the shots due to allergic reactions to the meds. Same with the oral meds. I'm JC+ so i can't take tysabri and too scared to try gilenya. I'm DMD free and I only symptom management and feel better for it. I do wish you luck on rebif. If anything, I'm no longer afraid of needles
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Dx RRMS April 1992
Yearly flares from 92 to 11
MS induced seizures 2002
Flare Oct 2011
Flare Dec 2011
Left disabled after 2 previous flares
Betaseron '02, Copaxone '12, Tecfidera '13
(allergic reaction to all)
No longer taking any MS therapy meds
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Old 01-04-2015, 08:44 PM #3
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I would have stayed on C...but I now have craters in my tummy and arms, and a hard lump in my thigh from it. Neuro decided to take me off for now. We will see what he says next visit...
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