my MS nurse and neurologist have told me to take Tecfidera, after my last relapse before Xmas. Have read the information given and recent posts from some who are on it. To tell you the truth the more I read, the less I want to take it. Am I the only one with the attitude that I am well so why would I want to take a drug that will give me more symptoms. I go bright red in the face already when I get stressed/wound up.
Argh! !!!!! Damned if I do and damned if I don’t. So much easier if on diagnosis they gave us a crystal ball and then we would know for sure if we were doing the right thing.
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