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Join us on March 4, 2026, in Washington, D.C., for Tourette National Advocacy Day, where we’ll meet with legislators to champion critical funding for TS research and education and push for vital legislation to advance and improve treatment.
Early Bird pricing ends January 21 – register now to save $50 per ticket!
Founded in 1972, the Tourette Association of America (TAA) 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 (TS) and Tic Disorders.
From free monthly educational webinars, to national in-person events and conferences, to online support groups, fun fundraisers, and more, there is no shortage of ways to learn, get involved, and be part of the TS and Tic Disorder community!
A diagnosis of Tourette Syndrome or another Tic Disorder can seem overwhelming.
Local support for children, families and adults with Tourette Syndrome and other Tic Disorders.
Find information about Comprehensive Behavioral Intervention for Tics treatment.
Our 50th Anniversary marked the launch of the TAA’s inaugural 5-year Strategic Plan.
Support the TS & Tic Disorder community by checking out our merch store!