Hi, I'm 27 and I have MS for ~3 years now.
I was on Rebif first, but it was not good for me (had attacks 2 times) and 1,5 year ago I've started to take Tysabri.
And it was really great.No side effects, no allergy - nothing.
But in October I was diagnosed with an anemia (Hb62) I had blood transfusions already 2 times but it keeps falling.
We stopped treatment with Tysabri of course (but it still in my body, like for 2 months) and hope it'll be better soon.
Did anyone have smth like this? Because my doctors are really confused as I see...