As a person who has an "intolerance" to all other MS disease modifying drugs, I am very satisfied with Tysabri. I haven't had any bad reactions to it, and more importantly I haven't had any relapses since I've been on it. I hear lots of people complaining about having to inject themselves every day, every other day, or once a week with one of the 6 MS drugs. I didn't have a problem with the method of administering the drug, just the violent illness that came after.
Aren't we all lucky that we have so many options to treat MS now!? It used to be your only choice was Prednisone. Don't even get me started on how awful that is.
Ten years from now there's no telling how much medicine will have advanced, for MS and other diseases that are currently incurable. I am prone to fantasize about living in another time in history, but who am I kidding? This is a good time to be alive!
I agree with the 1950s saying, "Living better through Chemistry"!
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