Tourette syndrome resources. the tourette association of america, in cooperation with the centers for disease control and prevention, created a library of comprehensive materials in a variety of languages about tourette syndrome and tic disorders. these guides are free for the community and support children, young adults, educators, law. Summer is the perfect time to get involved! there are so many ways to get involved and support our shared mission. find in person and virtual events, opportunities to volunteer, and more, via the link below. get involved with us icon find a providercreated with sketch. find a provider group 18created with sketch. tools & info group 16created with sketch. attend an event group 10created with.
The tourette association of america has designed a virtual quilt to showcase the tourette syndrome and tic disorder community, entwined with stories of inspiration, hope and community. this virtual quilt is a narrative of our unique experiences and stories to embrace and comfort one another. ts may impact everyone differently, but we are all. The tourette health and education program has conducted more than 1,350 educational events for professionals and community members in all 50 states in the united states, as well as in washington, dc, the us virgin islands, puerto rico, st. maarten, and canada. additionally, more than 50 webinars have been held virtually, with no state affiliation. Tourette association of america. the tourette association of america ( taa ), based in bayside, new york, united states, is a non profit voluntary organization and the only us health related organization serving people with tourette syndrome. it was founded in 1972 as the tourette syndrome association (tsa), later changing its name. The tourette association of america is a non profit organization working to make life better for all people affected by tourette and tic disorders, offering resources and referrals to help individuals and families cope with the challenges related to these disorders.
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