Two ideas. First, if you know the reactions to Copaxone are temporary and not
serious can you put up with them? I've had a few of these and have learned not
to panic and hold a hand until it goes away. Of course mine may not be as bad
as yours. The other idea is Novantrone. It's scary, because it's a chemo drug
but MS people get smaller doses and only every three months. I've just started
on it and my Neuro says all of his patients on it are doing well, some have had
no further exacerbations.
Kai