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The information provided in materials on Living With TS was supported by Grant/Cooperative Agreement Number 04211 from the Centers for Disease Control and Prevention (CDC).  The contents are solely the responsibility of the authors and do not necessarily represent the official views of CDC.  The information contained herein is intended for the reference of and use by adults with Tourette Syndrome, educators, allied professionals and clinicians.  The material is displayed with the permission of the authors.

You should not rely on the information posted on this Web Site as a substitute for consultations with qualified health care professionals who are familiar with individual medical conditions and needs. The Tourette Association strongly recommends that care and treatment decisions related to Tourette Syndrome and any other medical condition be made in consultation with a patient's physician or other qualified health care professionals who are familiar with the specific individual's health situation.


Sharing information and support is at the heart of the Tourette Association's mission. This section of our site is the place to access informative articles discussing the everyday challenges of living with adult TS.  One of these days, TS will be "irrelevant".  Until then, the Tourette Association offers these articles to shed light, break down issues into manageable components, stimulate your creative problem solving, and support self advocacy.  Please send any thoughts or comments to

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