Find all needed information about Tourette Syndrome Support Services. Below you can see links where you can find everything you want to know about Tourette Syndrome Support Services.
https://tourette.org.au/services/
Services. Who we are. TSAA is a volunteer run, membership based organisation, established in 1989 by families and medical professionals who recognised the need for support and awareness in the community for those who have Tourette Syndrome. Today we have hundreds of members throughout Australia. ... Support to people with Tourette Syndrome and ...
Local support for children, families and adult with Tourette Syndrome and Tic Disorders across the nation. Learn More. Our Strategic Priorities. TAA identifies steps toward mission fulfillment with respect to organizational unity, efficiency and impact. Learn More.
https://tourette.org/resources/local-support/
Chapters and Support Groups. Our Chapters and Support Groups provide local support across the nation for families, individuals, and adults with Tourette Syndrome and Tic Disorders and the professionals who serve them.
https://www.cdc.gov/ncbddd/tourette/families.html
Your local Tourette Association chapter external icon can help you connect with other families through conferences, support groups and other events. Parent-to-Parent Programs external icon provide information and emotional support to families of children who have special needs.
http://fsp.unc.edu/node/84
Understanding Tourette Syndrome Tourette Syndrome is a condition of the nervous system that causes people to have tics, or rapid, sudden movements and vocal outbursts over which they have little or …
https://www.cdc.gov/ncbddd/tourette/links.html
Links to other websites about Tourette Syndrome. Links with this icon indicate that you are leaving the CDC website.. The Centers for Disease Control and Prevention (CDC) cannot attest to the accuracy of a non-federal website.
https://tourette.ca/support/
Support. Tourette Canada offers many kinds of support to a wide range of Canadians, and we’re always trying to reach even more. Choose a support option on the left depending on who you are (e.g. a parent or educator), or look at at a complete list of programs and services or resources instead.
https://tourette.org.au/services/information-support/
Dr George Gilles de la Tourette (1857 - 1904) was a neurologist living in France. He was the first to identify the syndrome by giving a description of the Marquise de la Dampierre, a noble woman whose symptoms included copralalia. She lived to the age of 86.
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