The Tourette Association of America is the leading U.S. nonprofit organization serving people affected by Tourette syndrome and tic disorders. Founded in 1972, it focuses on awareness, education, research, support, and advocacy for patients, families, and professionals.
Healthcare and disability policy, education and school accommodations, research funding, public awareness and anti-stigma efforts, access to treatment and support services, and advocacy for federal support for Tourette syndrome programs.
Primarily supported by donations, grants, fundraising events, and contributions from individuals, foundations, and corporate supporters.
Network of local chapters, support groups, and Centers of Excellence; Youth Ambassador program; partnerships with the CDC and research/medical professionals; associated with Tourette syndrome advocacy leaders and community volunteers.
non-profit 501(c)(3)
