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.
Tina
Hi Rosie,
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!