I stopped taking the Copaxone in June of 2010. They warned me I would be in a wheel chair in six months and drastic changes would happen to my MRI. Well, last MRI showed NO changes. not better, not worse. I feel dramatically better WITHOUT the Copaxone. I felt simply awful on it. I couldnt think, function, and didnt have the energy to get out of my own way. I feel like my old self again. I still have MS, but at least I can deal with that.