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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]
Although I haven’t exhibited obvious symptoms of Tourette’s in over 17 years, vivid memories of others’ responses to my having Tourette’s have stuck with me. Let’s face it.
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 ...
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.
Tourettism refers to the presence of Tourette-like symptoms in the absence of Tourette syndrome, as the result of other diseases or conditions, known as "secondary causes". Tourette syndrome (TS) is an inherited neurological condition of multiple motor and at least one vocal tic .
Tic disorders occur along a spectrum, ranging from mild (transient or chronic tics) to more severe; Tourette syndrome is the more severe expression of a spectrum of tic disorders, which are thought to be due to the same genetic vulnerability. [23] Nevertheless, most cases of Tourette syndrome are not severe. [23]
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