TSAA is a voluntary and non-profit organisation consisting of people with TS, their families, health and education professionals and other interested and concerned people.
The association disseminates educational materials in the fields of health care, education and welfare service, provides telephone counselling and operates support groups.
We support parent advocacy and other services to help families and individuals cope with problems that may occur with TS. The association publishes a quarterly newsletter, holds annual conferecnes and a national camp program. We continue to work towards seeking better treatments and improving the overall quality of life for people with TS.