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.

History

It was founded in 1972 as the Tourette Syndrome Association (TSA) by five couples, parents of children with Tourette syndrome including Bill and Eleanor Pearl,[1][2] along with psychiatrist Arthur K. Shapiro and his wife, Elaine.[3][4] In 2015, the organization's name was changed from TSA to TAA.[5]

Mission and structure

The TAA's mission is to identify the cause of, find the cure for and control the effects of Tourette syndrome. As of 2008, it had 35 US chapters, 300 support groups, and international contacts around the world.[6]

Activities

The TAA "has been the major driving force in scientific and clinical progress relevant to TS", using its resources to encourage research and scientific initiatives,[7] and working tirelessly to promote information about TS.[1] It has worked for recognition of Tourette syndrome as an organic disorder, lobbying the public, the government, and physicians. It is adept at winning grants and shaping media treatment of the condition.[3] Since its inception, research spurred by the TAA has grown in volume and sophistication, including controlled treatment studies and studies of pathophysiology and etiology.[8] Many new research findings are the direct result of the TSA's "active facilitation of large collaborative research consortia in genetics, neuro-imaging, clinical trials, and the behavioral sciences", and their "concerted effort to identify current research advances, disseminate them among the scientific and clinical communities, and establish networks of basic and clinical scientists from all over the world".[7]

Advocacy

Notable Tourette Syndrome Youth Ambassadors include Logan T. Kurtz,[9][10] an advocate for youths with Tourette Syndrome from Calabasas, California.[11][12]

Media

In 2005 HBO produced in conjunction with the TAA an Emmy Award-winning documentary film, I Have Tourette's but Tourette's Doesn't Have Me.

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References
  1. Cohen DJ, Jankovic J, Goetz CG, (eds). Advances in Neurology, Vol. 85, Tourette Syndrome. Lippincott, Williams & Wilkins, Philadelphia, PA, 2001, pp. xvii–xviii.
  2. Paid Notice: Deaths, Pearl, Eleanor. New York Times, April 13, 1999. Retrieved on February 28, 2008.
  3. Pagewise, Inc. Tourette syndrome. Archived 2005-02-08 at the Wayback Machine Retrieved on June 29, 2006.
  4. Kushner, HI. A Cursing Brain?: The Histories of Tourette Syndrome. Harvard University Press, 2000. pp. 176–186. ISBN 0-674-00386-1.
  5. A new name. Tourette Association America. Retrieved on February 15, 2015.
  6. Tourette Syndrome Association. About TSA. Retrieved on February 28, 2008.
  7. Walkup, JT, Mink, JW, Hollenback, PJ, (eds). Advances in Neurology, Vol. 99, Tourette Syndrome. Lippincott, Williams & Wilkins, Philadelphia, PA, 2006. p. xv.
  8. Black, KJ. Tourette Syndrome and Other Tic Disorders. eMedicine (March 22, 2006). Retrieved on June 27, 2006.
  9. "Teenager strives to educate peers about Tourette's Syndrome". theacorn.com.
  10. "Logan Kurtz Tourette Syndrome Youth Ambassador With Definite Possibilities". patch.com.
  11. "Logan Kurtz: Speaking Out About Tourette Syndrome". patch.com.
  12. "Redefining normal". jewishjournal.com.
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