I Have Tardive Dyskinesia


A Tardive Dyskinesia anonymous support group with information on diagnosis, treatment, symptoms, along with personal stories and experiences with Tardive Dyskinesia. You're not alone.

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8 Stories

Cant Stand The Painandthey

 hi i have tardive dyskinesia, my dr gave me gedon for depression i was taking it for almost a year when the symptoms began happening...

Scared

i have been worried since the doc said Tardive Dyskinesia. my issues are uncontrollable eye movement (raising of the eyebrows or lowering...

Public Awareness Campaign On Drugs That Cause Td

Hello I am doing research for a consumer awareness campaign whose mission is to show the reality of Tardive Dyskinesia and other...

I'm Looking For Answers

I currently went off of Geodon and I'm experiencing muscle spasms all over my body, eye spasms, etc. Will these symptoms get worse? I'd...

Cant Stand The Painandthey

 hi i have tardive dyskinesia, my dr gave me gedon for depression i was taking it for almost a year when the symptoms began happening...

Worried

I am an artist that is worried that my days of painting could be over if the tremors and pain continue. No one seems to know if it is TD or...

Mistaken Beginning

on aug 24/12, i fell down a flight of stairs at a subway station.in rehab for 10 weeks, they noticed my shaky legs, burning crotch and total...
Members Sharing the Experience "I Have Tardive Dyskinesia"
15 Members
This Experience at a Glance
Story highlights
These snippets show some of the most common themes mentioned in this experience's stories:
  • "hi i have tardive dyskinesia, my dr gave me gedon for depression i was taking it for almost a year when the symptoms began happening, i ve stopped the drug but the symptoms are still here i am having a really hard time with it sometimes i cant even get out of bed, i feel like no one understands..."
And the Story Awards Go to...
Most Popular: Worried
Most Recent: Mistaken Beginning
Statistics:

25% of people who have this experience are in their thirties, 19% are in their forties, and 13% are in their sixties. 50% of people who have this experience are men.

You may cite any I Have Tardive Dyskinesia statistics, provided you link back to this page
Check out this group's What Is It Like To Have Tardive Dyskinesia guide, where people with this experience share their tips and hints.
Members said this page is also related to: Do You Have Tardive Dyskinesia? , What is it like to Have Tardive Dyskinesia? ,Have Tardive Dyskinesia personal stories, Have Tardive Dyskinesia 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 Tardive Dyskinesia. 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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