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Knowledge, education and understanding are uppermost in management plans for tic disorders, [6] and psychoeducation is the first step. [14] [15] A child's parents are typically the first to notice their tics; [16] they may feel worried, imagine that they are somehow responsible, or feel burdened by misinformation about Tourette's. [14]
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.
Tourette syndrome is defined only slightly differently by the WHO; [4] [8] in its ICD-11, the International Statistical Classification of Diseases and Related Health Problems, Tourette syndrome is classified as a disease of the nervous system and a neurodevelopmental disorder, [18] [19] and only one motor tic and one or more vocal tics are ...
John Davidson MBE (born 1 June 1971) is a Scottish campaigner for Tourette syndrome, who lives in Galashiels. [2] At age 16, Davidson was the subject of the BBC TV documentary John's Not Mad (1989) about the manifestations of Tourette syndrome with which he lived, and a number of follow-up BBC documentaries throughout his life.
Jessica Thom (born 14 July 1980) is a British theatre-maker and comedian who established Touretteshero, an alter-ego and project aimed at increasing awareness of Tourette syndrome, the neurological condition which she was diagnosed with in her early twenties. [1]
Landon Barker, Travis Barker‘s son, discussed his experience living with Tourette syndrome. Landon, 20, took to TikTok on Monday, March 4, to respond to a comment asking whether he was diagnosed ...
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