Quote:
Originally Posted by SallyC
I'd probably give it 6 months (If you can) and if it is not helping you
to feel better or to stop new lesions, then I would chuck it and try
something else. Not all DMDs are for all peeps with MS.
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Quote:
Originally Posted by skywalker1988
I've been on Ribif since the early part of April and I was wondering if this has made anyones MS worse than it was. It seems so to me, but maybe Rebif needs more time to work in my body. Ever since I've been on Rebif, I've had MS Hugs and alot of pain to go with it. Plus the places where I put the shots at are all red and sore
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I didn't take Rebif, I was placed on Avonex. That lasted a couple of months. Then I have an optic neuritis flare up. And had blood work, discovering that I had developed anti-bodies to interfurons. That was my one and only interferon and it didn't last much longer than a couple of months. I'd been on Copaxone prior to Avonex. Has your neuro considered Copaxone? Have you considered Copaxone?
Along with the upcoming MRI, will you neuro also have bloodwork done, to test your blood levels, too?