Hello! I was just wondering if there’s anyone on here that’s started the treatment Tysabri? I’m currently on Copaxone and the neurologist wants me to move over to Tysabri soon. The reason I’m asking is because I’d planned on going travelling next year and am really hoping this new treatment isn’t going to change that. Has anyone been travelling whilst on this treatment? I know it’s monthly infusions so just wondering if anyone knew of a way that could be worked around it eg having it done in different hospitals around the world? Any advice would be great! Thanks!
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