About Us
As many as 1 in 100 individuals show signs of Tourette Syndrome – most of them undiagnosed, misdiagnosed and/or misunderstood. NJCTS provides answers for these individuals 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.
Services:
- Education Outreach to medical and educational professionals
- Advocacy and Support for Families and Individuals
- Support of Ongoing Research
FAQ’S ABOUT TOURETTE SYNDROME
The answered have been provided with help from the National Institutes of Health. If you have unanswered questions, please call us at 908.575.7350.
- Camp FantasTIC – NJCTS Family Retreat
JUNE 12, 2021
- Family Support Group: Understanding and Treating Selective Mutism as a Social Communication Anxiety Disorder
JUNE 17, 2021
- Family Support Group: The Genetics of TS & Saying I Do
JULY 22, 2021
- NJCTS Virtual Tim Howard Leadership Academy
August 6, 2021