Kathie, a real patient living with TD
Real people,
real TD experiences
If you're experiencing uncontrollable body movements, you're not alone.
Hear from people affected by TD. Get inspired to take the first step toward managing your TD.
Shelly & Matt’s Story
Living With Bipolar Disorder and tardive dyskinesia
“Looking back, I think I kind of tried to ignore the symptoms at first because I didn’t even want to acknowledge them.”
Shelly and Matt were compensated by Neurocrine Biosciences, Inc. to share their story
Jeff’s Story
Living With Schizophrenia and tardive dyskinesia
“I woke up one morning and I noticed that my cheeks were puffing in and out uncontrollably.”
Jeff was compensated by Neurocrine Biosciences, Inc. to share his story
A Conversation worth having
“That’s really the most important thing, is to have a good rapport with your doctors.”
Kathie
Living With depression and tardive dyskinesia
Jeff and Kathie were compensated by Neurocrine Biosciences, Inc. to share their stories
Finding Your Community
“People judge you by your movements—that’s not who you are. And don’t let that defeat you from living your life.”
Jeff
Living With Schizophrenia and tardive dyskinesia
Jeff and Kathie were compensated by Neurocrine Biosciences, Inc. to share their stories
Are you or a loved one living with tardive dyskinesia (TD)?
By sharing your story, you may be able to educate others living with this condition. If you're a US resident and 18 years or older, please call 1-844-706-5724 to find out if you qualify for the Neurocrine Biosciences, Inc. Patient Ambassador Program.*
*Qualified candidates who are selected will be compensated for their involvement and time. Please note that not all candidates will be selected to participate in the program.
TD Treatment options are available.
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You can use the Doctor Discussion Guide to get helpful info on how to have a productive in-person or telemedicine appointment.
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Find out how TD can be treated and what to discuss with your healthcare provider
Learn more about treating TD
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