On Cellcept for about a year

It took 6-7 months for the Cellcept to take affect. I was wheelchair bound and even though I am still in a power chair, I can use a walker now short distances, I am much more independent. If I could get rid of the hand problems, I would be even happier. I did not have any problems w/ side affects. I was percribed this at the Mayo Clinic in Rochester, MN. I switched to Wayne State University in Detroit, MI as that is only three hours from me. Dr. Lewis has opted to keep me on it. Due to disasterous events in getting a dx, I am having severe trust issues w/ any doctor. I went to five Neuro’s before I decided on Dr. Lewis; however, I still do not feel completely secure. I really wonder if they “just don’t know enough”.