My Dr. would like me to change my MS drug, I am currently on Copaxone. No new lesions on MRI but am having difficultly walking. He gave me two choices Tysabri or CellCept. I haven't been able to find out much about CellCept, its primary use is to prevent rejection of transplanted organs, but it is used in MS and lupus. My BIG question is to those that are taking Tysabri- DO YOU FEEL BETTER?
My Dr. also would like me to have a bone marrow test prior to starting Tysabri. As anyone had one? Any help would be appreciated.