Tourette Syndrome Association of Australia 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 counseling and operates support groups. We support parent advocacy and other services to help families cope with problems that may occur with TS. The association regularly publishes a newsletter and organises workshops. The Association keeps a register of doctors who are experienced in diagnosing and treating TS. We continue to work towards better treatments and improving the overall quality of life for people with TS.

Source: Tourette Syndrome Association of Australia