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After almost 6 years on copaxone i just cant do the daily injections anymore but i dont think im ready to switch to the new pills until there is more information out there on them. Im thinking of switching to rebif and am looking for any thoughts or experiences you might have to help me with my decision. I see my neurologist in October and will switch at that point. Thanks!!
@A MyMSTeam Member.. Hi! when I lost my insurance the MS Society paid for my injections until I got my medicare....
you may want to switch to the 40mg three times a week copaxone - i found the flu like symptoms with rebif hard to take. i switched from Rebif to Copaxone and did much better. it is the daily injection but as soon as the 3 times a week is available in Canada - I'm on it. Good luck.
i have had no side effects with Rebif. I take Aleve before as well
check on tysabri,its an i.v. every 28 days.i have been on it 5 years and have done really good.We are really close to a cure for m.s. "I BELIEVE THAT WITH ALL MY HEART"good luck and God Bless.
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