Our Mission
Providing Support to Those With Tourette Syndrome Throughout the Carolinas
The Tourette Association of America Greater Carolinas Group provides support and resources for children & adults with Tourette Syndrome, living in North and South Carolina. We are an Affiliate Support Group under the Tourette Association of America.
What We Offer
Training
We offer presentations and in-service training for schools, law enforcement, healthcare providers, and community groups across the Carolinas – helping educators, professionals, and families understand Tourette Syndrome and respond with confidence and compassion.
Bring a training to your school or organization!
Resources
From school accommodation guides to CBIT treatment information, our resource library brings together trusted, practical tools for individuals, parents, and educators living and working with Tourette Syndrome and tic disorders – all in one place.
Events
Connect with people who understand. We host support meetings and community events across North and South Carolina – both in person and online – for individuals with TS, parents, and caregivers.
See what’s coming up and join us!
Understanding Tourette Syndrome
Tourette Syndrome is a neurodevelopmental disorder that affects children, adolescents and adults. The condition is characterized by sudden, involuntary movements and/or sounds called tics. Tics can range from mild/inconsequential to moderate and severe, and are disabling in some cases.
Tourette Syndrome is one type of Tic Disorder. Tics are the primary symptoms of a group of childhood-onset neurological conditions known collectively as Tic Disorders and individually as Tourette Syndrome (TS), Persistent (Chronic) Motor or Vocal Tic Disorder, and Provisional Tic Disorder. These three Tic Disorders are named based on the types of tics present (motor, vocal/phonic, or both) and by the length of time that the tics have been present.
Ways To Get Involved
Become a Volunteer
Contact us to learn more about our mission and how you can be involved.
Advocate for Tourette Syndrome
Take action to advocate for stronger support for people living with TS and other Tic Disorders.
By completing this form, you will send a letter to your Senators and Representative on behalf of the 1.4 million Americans who live with TS and other Persistent Tic Disorders. These letters are key to gaining support and ensuring federal funding for Tourette Syndrome research and public health education. For a personal touch, please consider adding a story to your letter
If you’d like to help us out and support our cause, please consider donating!
