Had a pretty informative visit with my Neuro yesterday. It was my follow up after the 2nd Opinion that confirmed I do have MS. She had recommended 2 treatment options, Copaxone or Aubagio. I had done my research on both, and had pretty much decided I wanted to try Copaxone. My Neurologist said Copaxone would be fine, but he thought it wasnt strong enough for me. He said my MRI and to see me in person were like 2 different people, that by the looks of my MRI he wouldn’t expect to see me walking, and while my walking was a little off ( which surprised me, I thought I was walking well!), he said I actually looked great! I also have severe spinal stenosis in my neck, but I cant even tell. So after much thought I decided to go with Aubagio.
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