Tourette Association of America

Founded in 1972, the Tourette Association of America is the only national organization serving the community, and works to raise awareness, advance research, and provide ongoing support to patients and families impacted by Tourette Syndrome and other Tic Disorders. To this end, the TAA directs a network of Chapters, support groups, and Centers of Excellence across the country. The TAA is a nonprofit 501(c)(3) organization.

In cooperation with the US Centers for Disease Control and Prevention, the TAA has created a library of comprehensive materials in a variety of languages about TS and Tic Disorders. These guides are free for the community and will be provided at our exhibit booth.  

In addition to these resources, the TAA provides no-cost medical education presentations on the diagnosis and treatment of TS and other Tic Disorders for medical providers across the country. Please contact Programs@tourette.org for more information on how to set one up at your institution! 

For more information on TS and other Tic Disorders, call 1-888-4TOURET, visit www.tourette.org, and follow Tourette Association on Facebook, X, Instagram, LinkedIn, TikTok and YouTube.