Has anyone used Botox to confirm a diagnosis of middle ear myoclonus?
My MEM is not consistent enough (although it happens everyday with some days being very difficult) to get a confirmed diagnosis. My neurotologist is willing to perform surgery where he cuts a small muscle that covers my eardrum in "the hopes" of giving me relief. The surgery is out of pocket and expensive and permanent with no guarantee of relief.
I just wonder if anyone has used Botox and got the clicking to stop even if only for a short time? If Botox stopped the clicking it would be pretty certain that it is in fact middle ear myoclonus.
Thanks for any replies.
My MEM is not consistent enough (although it happens everyday with some days being very difficult) to get a confirmed diagnosis. My neurotologist is willing to perform surgery where he cuts a small muscle that covers my eardrum in "the hopes" of giving me relief. The surgery is out of pocket and expensive and permanent with no guarantee of relief.
I just wonder if anyone has used Botox and got the clicking to stop even if only for a short time? If Botox stopped the clicking it would be pretty certain that it is in fact middle ear myoclonus.
Thanks for any replies.