I have just started this for muscle spasms in my back…has anyone feedback?
I’ve got on great with it - no side-effects at all. But I’m just beginning to think it’s no longer doing the trick, as my neuro already thinks I take too much, and now even that’s not working properly. I’m going to have to ask about switching, or supplementing it with something else.
Was on it for a couple of years worked well, but side effects were muscle weakness - changed to tizanidine.
Just increase dose gradually as directed by neuro or MS nurse.
good luck, Jen x
Tizanadine is a good alternative. It didn’t agree with me unfortunately but I’m on sativex now and it’s fantastic!