Thank you, Barb and Frank, for your input. I am doing pretty good, haven't started the Copaxone yet, I assume by monday it will be here. Only time will tell I guess. It is good to know that there are other options if it doesn't work though. Has anyone taken Ampyra, the neuro ordered that for me too. I googled it, and it said it is for difficulty walking, and the side effects included making MS worse and causing relapses, among other things. I don't have difficulty walking (knock on wood) so I will definitely ask her about it.