I was just recently diagnosed with MS. The MRI of the brain showed 50-60 lesions. I don't have too many symptoms other than lightheaded spells that last 15-20 seconds and occur once every 5 mins to 5 hours apart (depending on whether I am seated or moving around). Sometimes I experience clumsy movement in the right leg or right arm during such a spell & then everything is back to normal after the 15 seconds.
My first neurologist didn't explain all my choices very well & just prescribed Avonex for me. A second neurologist recommended I go on something more aggressive considering the number of lesions I already have. He suggested, Tysabri.
I am concerned about PML, of course. Can you guys share your experiences with the drugs you are on or have used. Any thoughts on Copaxone, Avonex, etc?
Secondly, I read that patients with a weakened immune system have a greater chance of PML. That would mean I would be better off going straight to Tysabri than weakening the immune system with another drug like Avonex & then moving to Tysabri.
This website is a great resource.
My first neurologist didn't explain all my choices very well & just prescribed Avonex for me. A second neurologist recommended I go on something more aggressive considering the number of lesions I already have. He suggested, Tysabri.
I am concerned about PML, of course. Can you guys share your experiences with the drugs you are on or have used. Any thoughts on Copaxone, Avonex, etc?
Secondly, I read that patients with a weakened immune system have a greater chance of PML. That would mean I would be better off going straight to Tysabri than weakening the immune system with another drug like Avonex & then moving to Tysabri.
This website is a great resource.
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