Diagnosed in 2008. Copaxone for awhile, could not tolerate shots everyday, site reactions were horrible. On Avonex now, just did a follow up with the Doc, I thought I wasn't doing to bad,, we did the motor skills test, I failed. My balance has been getting worse but, I have been adjusting. He said, 'Sometimes there are issues with out having a noticed exacerbation'
So are they silent?
Going for MRI tomorrow, and JC virus test. He is considering Tysabri. I am REALLY uncomfortable with that.. I have looked at some of the blogs here, but have not seen any posts from someone who has gotten PML from it..
Any opinions, or additional resources is greatly appreciated.