Our 50th year marked the launch of our 5-year Strategic Plan to increase awareness, provide support, and fund research for those affected by Tourette Syndrome, Tic Disorders, and co-occurring conditions. We made significant progress in the first year of our plan and are looking forward to building on that momentum in the year to come. By identifying five priorities in our plan: Support & Education, Research & Clinical Application, Revenue Development & Partnerships, Organization & Culture, and Awareness & Advocacy, we will reach our ultimate goal of making an impact in the lives of those affected by TS and Tic Disorders, reaching more people, addressing new challenges, and providing the much-needed support and resources to positively impact our community.
The TAA invites everyone to join in the journey, because together we are #UncontrollableUnstoppable.
A diagnosis of Tourette or Tic Disorder can seem overwhelming.
Local support for children, families and adult with Tourette Syndrome and Tic Disorders across the nation.
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Our 50th Anniversary marks the launch of the TAA’s inaugural 5-year Strategic Plan.
