The Avonex that I have been on for @ 8 years does not seem to be working - new lesions even with IV steroids added to the mix. Now my DR. is suggesting Tysabri but I'm not sure. I have no outword signs (no one can even tell unless I tell them). Should I wait until I get worse or take it to prevent getting worse? I'm not sure if the risk is worth it yet. Does anyone have any experience with Tysabri?
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Just read this article and so can relate. MS is a robber grabber! If I go out I have to deal with getting tired or if it's hot - forget it! It's just easier to stay home, turn on the AC, and lie down in bed - REPEAT... Such is the story of my life!