Myoclonus anonymous support group with information on diagnosis, treatment, symptoms, along with personal stories and experiences with Myoclonus. You're not alone.
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These snippets show some of the most common themes mentioned in this experience's stories:
- "After 2 days of constant tremors and stuttering, I went to my GP and was told it was a reaction to the Prozac I was taking for manic depression..."
- "Now 12 years later I am seeing a new neurologist who listened to me and said straight away that I have Myoclonus..."
- "Julie When I was seventeen I was hospitalized for extreme manic depression and schizo - affective disorder..."
46% of people who have this experience are in their twenties, 46% are in their thirties, and 23% are in their teens. 100% of people who have this experience are women.
Here are a few tips...
- My symptoms started slowly at night while trying to fall asleep. Occasional unvoluntary body movements would occur causing sleep impossible. At first I didnt think symtoms were such a big deal, until they progressively got more intense.
- Hi, I have suffered Myoclonus since December 2003. I am asthmatic and i took a bad attack and had to go to hospital. My brother called a taxi but when he seen i was getting worse he called an ambulance. He was told to get in whatever came first which was
Other experience groups that have been combined into this group include: None yet.
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