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.
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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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