is anyone currently using or have recently tried Tysabri?? i am going to have my first IV this month and am a little anxious about it. hopefully it will be all its cracked up to be. if anyone has experience with this new drug please let me know.
thanks,
di
I asked my neurologist about it today, and sadly, it's not available in my country yet. It sounds really good. Same efficiency as Betaseron and Rebif, but with only one IV injection a month.
Just wondering is Tysabri available in Ireland. Only on Rebif a year or so but no one has mentioned Tysabri to me or anyone I know with MS. Any info on the drug much appreciated.