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.
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SIGN UP TO LEARN MORE ABOUT THE AMBASSADOR PROGRAMJeff’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 1-800-256-5290 or click the link below 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.
LEARN ABOUT THE AMBASSADOR PROGRAM
Within the last year, the Doctor Discussion Guide has been downloaded over 115,000 times,‡ helping many have meaningful discussions with their doctor.
‡Source: Google Analytics 4, January 1, 2025–August 31, 2025.
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