A good quick resource, this website offers “fast facts” and information on famous people who have Tourette Syndrome. A site to visit if you want more information but don’t want to wade through a bigger website.

A woman started this site after her own sons were diagnosed with Tourette Syndrome. It is a site unlike many others, as it focuses on the majority of TS sufferers who have mild symptoms. Many websites focus on the “worst case scenario” and ignore that most sufferers will never have such severe symptoms. This would be a good site to visit if your child has just been diagnosed with TS and you want to keep things in perspective. There are many personal stories here, as well as recommended books and sites.

This site is a great place to get reliable information about Tourette Syndrome and its treatments. The association is committed to educating people about TS, and has publications and videos available. You can also find out more about how to get involved – either by helping TSA or by learning more about legislative action and public policy concerning Tourette Syndrome.

A great resource for a variety of disorders, the name stands for “Worldwide Education and Awareness for Movement Disorders.” This site has an incredibly complete glossary, plus information on all the movement disorders. You can even chat or post to the message boards.