Everyday and every movement is a challenge, but I won't give up.
I did just see my neurologist today.  He did say that there is talk and Shared Solutions is thinking about reducing the medication for Copaxone.  He also did say something about a new experamental drug that I might qualify to be in, but I don't know about being a guniea pig.  I have heared about bad side effects from experemental drugs.  For that, I would have to move to Denver which is something I've considered anyway.  This new drug repaires the damage that has been done.  I do not know the name or anything about it, but I bet I could find out.