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As many as 1 in 100 kids show signs of Tourette Syndrome – most of them undiagnosed, misdiagnosed and/or misunderstood.
NJCTS provides answers for these kids and their families through referrals to programs and services, education and training so that families, peers and professionals will be better qualified to help those with TS, and support of research programs so that we can find better treatments and a cure.
In the news
- 12 MarRead more
The goal of the presentation was to spread awareness about TS and its symptoms. For someone with TS, an encounter with law enforcement can be
- 06 MarRead more
NJ Center for Tourette Syndrome and Associated Disorders (NJCTS) are excited to announce that both Dietz & Watson and Black Bear Deli Brand have pledged
- 24 FebRead more
NJCTS Youth Advocate Jatin Nayyar, 17, of Morganville presented an introduction to Tourette Syndrome to a group of elementary school kids during an afterschool program
- 19 FebRead more
The Rutgers Tourette Clinic at the Graduate School of Applied and Professional Psychology “It took seven years to get a diagnosis for my son,” said
- 29 JanRead more
“Research into better treatments for TS cannot be done without the participation of individuals and families.” Dr. Jay A. Tischfield The NJCTS mission did not
- 27 JanRead more
Applications are currently being accepted for the annual NJCTS Tim Howard Leadership Academy, an intensive four-day program promoting self-empowerment, self-leadership, and resilience for teens living
- 07 JanRead more
For the past 15 years, NJ Center for Tourette Syndrome (NJCTS), has been providing support and services to families and individuals living with Tourette Syndrome