Current Tourette Syndrome treatments and genetics research will be discussed March 9 at Overlook Medical Center’s Atlantic Neuroscience Institute. SUMMIT – Everyone in the New Jersey Tourette Syndrome community is invited to attend an afternoon of presentations on TS treatments and genetics research from 1 to 5 p.m. Saturday, March

Yale University’s Dr. Robert King will interview individuals and families interested in participating in the genetics sharing program February 14-16 at Rutgers University. PISCATAWAY – Would you like to see more people working on a cure for Tourette Syndrome? How about research on medications specifically for TS? Now is your

Registration is now open for this walk, which will support NJCTS’ statewide education outreach and peer advocacy efforts MAHWAH – The New Jersey Center for Tourette Syndrome & Associated Disorders (NJCTS) is going to college! The New Jersey Walks for TS program has expanded beyond Mendham to the beautiful campus

WASHINGTON, D.C. – The New Jersey Center for Tourette Syndrome & Associated Disorders (NJCTS) is proud to announce that the Collaborative Academic Research Efforts (CARE) for Tourette Syndrome Act of 2013 has been reintroduced as bill H.R. 146 to the United States House of Representatives by Congressman Albio Sires (D-NJ8).

Teenagers Michael Cannizzaro and Tess Kowalski detail their experiences in how a diagnoses, or lack thereof, has affected their life at home, in school and in their communities. FREEHOLD – Many children and families affected by Tourette Syndrome struggle with the process of getting an initial diagnosis. Some diagnoses take

Thirteen-year-old Tess Kowalski educates the students and teachers at Millstone River School about the neurological disorder on behalf of her 9-year-old sister Paige PLAINSBORO – Tess Kowalski is a pro at delivering in-service presentations on behalf of the New Jersey Center for Tourette Syndrome & Associated Disorders (NJCTS) to schools