Been on Copaxone for a couple of weeks now and all is well BUT I woke this morning with a bit of an echo in my ears, like I had water in there. It's still bothering me 12 hours later, still a bit noisy in my head but hearing is ok I think.

Had a quick search and deafness has been known with Copaxone, as it has been of course with a relapse. I'll call me doctor if it continues, but thought I'd ask my private consultants first.

I'm behind with my replies I know. Been busy, will try to catch up tomorrow. Regards to all.

what did you say? eh?

Nope, no hearing issues with me and C. I hope you feel better.

Nice to see you back, we missed you!

C was my first DMD to try. It didn't help my MS so I discontinued using it. I have had los of hearing in my left ear but I don't know if it's because of the C, because of the MS or if it's just something that was going to happen anyway.

My Dad had profound hearing loss in his left ear. He was never dx with MS but looking back and piecing all his sx together makes me think he just might have had it.....along with all his other medical issues.

I'm so tired of saying "huh?". I refuse to say "talk into my good ear". Just not ready for that yet!