Thanks everyone for your welcome. I've heard of LDN, but I don't have any symptoms, so I am not sure if it would be of any help to me.

As far as the Rebif, I really don't think that it is worth risking damaging my bone marrow permanently for the small possibility that it may help me 30%.

It's confusing. I am only on 1/2 dose and personally I feel as though it's working more as a placebo. My doctors scared me so much in the beginning that now I am afraid to stop it.