Hi all (Ciao!) I i just joined the community and I am really glad to share my experience with you. First of all, please accept my apologies for my poor english, I am from Italy and I will try my best. I am here because my wife has been diagnosed ten years ago and after some years with Betaferon she's facing a bad period (so many relapses in 18 months) and has been just shifted to endoxan (cyclophosphamide). Indeed she could not get tysabri being positive to JCV and fingolimod is not yet available in her ms department here. I am trying to figure out what I can do to to help her. Thank you very much for reading, you are all very nice people.