I Have Myoclonus


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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7 Stories

Me And Myoclonus

Well I was diagnosed last summer after being seen by a Neurologist.  Was sent there by my family doctor who thought I might have M.S. My...

My Myoclonus...

I am not sure how to begin my story... First I am 33 years old and have been battling Myoclonus since I was 24. In the spring of 1998...

I Have Myoclonus

Hello! I got sick about 9 years ago, I'm 27 now, and I was in my first year of college. I have had myoclonus for a few years now. I became...

Myoclonus At 17

When I was seventeen I was hospitalized for extreme manic depression and schizo-affective disorder. The morning of the hospitalization I...

Myoclonus Nightmare

i started with problems in 1998 at the age of 19 I am now 31 from England.  I started with flu like symptoms and then wham I started...

I Have Myoclonus!

The ******* started over a year ago.  First a few times when I went to sleep.  It has gradually gotten worse.  In the course of finding...

Me And My Myoclonus

Hi,my name is Julie and i am 35 years old. I have suffered Myoclonus since December 2003 when i was 29. I am asthmatic and i took a bad...
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Members Sharing the Experience "I Have Myoclonus"
12 Members
This Experience at a Glance
Story highlights
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..."
And the Story Awards Go to...
Most Popular: My Myoclonus...
Most Recent: I Have Myoclonus!
Statistics:

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.

You may cite any I Have Myoclonus statistics, provided you link back to this page
Check out this group's What Is It Like To Have Myoclonus guide, where people with this experience share their tips and hints.

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
Members said this page is also related to: Do You Have Myoclonus? , What is it like to Have Myoclonus? ,Have Myoclonus personal stories, Have Myoclonus personal experiences

Other experience groups that have been combined into this group include: None yet.
This is an experience group where everyone says: I Have Myoclonus. It features support, personal stories and experiences, advice, chat, talk, forums, videos, pictures and resources from real people, just like you. It's free to join, and the people in this group would love to meet you! If you've had this experience, or plan on having it in the future, simply click 'Me Too' or 'Plan To' and add it to your experiences. As you add more experiences, we're better able to recommend interesting people to you that share many of your personal experiences.

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