Our mission is to identify the cause of, find the cure for and control the effects of Tourette Syndrome.

Founded in 1972 in Bayside New York, the national Tourette Syndrome Association is the only national voluntary non-profit membership organization in this field. We offer resources and referrals to help people and their families cope with the problems that occur with TS. We raise public awareness and counter media stereotypes about TS. Our membership includes individuals, families, relatives, and medical and allied professionals working in the field.

Program development
Education and medical programs
Research
Public Policy
Events