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Originally Posted by Topsie
Hi I have both Palatal Myoclonus (only 1 in 2 million people have this) and Spinal Myoclonus (only 1 in 3 million people have this). I am searching and really hoping that there is someone else out there with these conditions with whom I can get some support and relate to about these difficult conditions. Please write! Thanks so much.  Topsie |
I was diagnosed with it last year. Basically, I get the crunching noises (rice krispies) in my middle ear and the plugged feeling that won't go away. Its extremely hard to treat. It started after my concussion in the Summer of 2005. I had a bit of luck with Effexor. My ear starting to unplug and stayed unplugged for a couple of hours after taking the medication, then it plugged up again. The medication hasn't worked since. I am hoping that it has something to do with migraines.