Tysabri didn't work for me and my MS seems to be progressing. And my veins in my arms are basically gone. I’m confused. I hardly decided to try with Tysabri and now it can not help me. Does anybody else have same experience? It would be nice to know that I’m not alone.
Definitely, you are not alone. Tysabri also didn't work for me at all. The only thing it helped with was to relieve some pain. First I was desperate but when I heard that many people react on Tysabri like me, I stopped to worry about it. I’m taking Copaxone again. Hope you feel better soon.
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