I am DizzyDean, new to this group.

I have RRMS, Sx started perhaps 17 years ago, but no Dx until a few years ago. Its been mild, more nuisance than disability really, my episodes/relapses seem to be spaced a few years apart so far. Over the years Sx have included ON, Lhermite's, numbness, tingling, tinnitus, but nothing that hasn't resolved after a bit.

Today I take LDN and a ton of vitamins., but I am "toying with tysabri" and "considering copaxone". I know that sounds like a weird dichotomy, to choose either the mildest and arguably least effective drug, or instead choose the most effective and potentially most dangerous one. I'm still negotiating all of this with my Dr, who doesn't seem keen on my doing tysabri as a firstline therapy but would probably go for it if I absolutely told him no way to ABCR.