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Gilles de la Tourette
in both Dutch/EnglishNederland telt ongeveer 10.000 mensen die in lichte of ernstigere mate lijden aan het syndroom van Gilles de la Tourette. De aandoening is genoemd naar de Franse arts George Gilles de la Tourette.
Holland has roughly 10.000 people who are suffering from the Tourette syndrome.
Varying from light to more heavy symptoms.
The illness is named after the French doctor, George Gilles de la Tourette.
Life's A Twitch!
"Life's A Twitch!" ™ is a website based on the work of B. Duncan McKinlay, Ph.D. in the area of Tourette Syndrome (TS) and associated disorders.
Parent Patch
Where Parents & Educators Can Find Everything
They Need in One Place!
The Pennsylvania Tourette Syndrome Association
The Pennsylvania Tourette Syndrome Association, Inc. is a non-profit agency, affiliated with the National Tourette Syndrome Association, created to serve the needs of PA citizens with Tourette Syndrome. They provide information, referral and advocacy services without regard to race, creed, national origin, or sex. The PA TSA is not a substitute for adequate medical diagnosis or treatment. The agency provides no direct services, so it does not intrude upon the patient-physician relationship.
The Tourette Syndrome Association of New Jersey
The Tourette Syndrome Association of New Jersey is a non-profit organization whose membership includes individuals with Tourette Syndrome,. their families, friends, and interested professionals. All of our funding comes from contributions and all of our workers are volunteers.
Tourette Page by Leslie Packer
Represents a culmination of her experiences as a parent, family member, advocate, and psychologist.
Tourette Spectrum Disorder Association Inc
The Tourette Spectrum Disorder Association is a non-profit organization dedicated to providing up-to-date, accurate information about Tourette syndrome. Combined with the information accessible by following our links, we think you will find helpful, comprehensive information on this often puzzling disorder.
Tourette Syndrome Association, Inc.
Founded in 1972 in Bayside, New York, the Tourette Syndrome Association, Inc., or TSA, is the only national voluntary non-profit membership organization in this field. Its mission is to identify the cause of, find the cure for and control the effects of this disorder. Today, TSA has grown into a major national health-related organization with approximately 50 U. S. Chapters and 300 support groups, and International Contacts around the world
Tourette Syndrome Foundation of Canada
In both French/EnglishThe Tourette Syndrome Foundation of Canada is a national voluntary organization dedicated to helping individuals with Tourette Syndrome and their families by: gathering and distributing information, promoting local self-help
and professional services and promoting research.
Tourette Syndrome News
Would you like to stay informed of the latest news on Tourette Syndrome? Would you like to be made aware of medical advances in TS, read personal life stories of other TS patients and/or their loved ones, see special articles written by members of our Tourette Syndrome.com Community and get special free offers and discounts to shop in our online mall? I hope the answer is "Yes!"
tourette.net
Excellent Resource Website
Welcome to my Tourettes Syndrome Page
This summer I worked at The Empire State Speech and Hearing Clinic which is a special education camp located in Spencer, New York. While working at the camp, I gained experience in working with children who possessed various disabilities such as Autism, MR, Deaf and Hearing Impaired, Emotionally Disturbed, Learning Disabled, and Tourettes.
