P.O. Box 50030 London, ON N6A 6H8 info@rett.ca (519) 474-6877

Who is O.R.S.A.?

The Ontario Rett Syndrome Association (O.R.S.A.) is a volunteer, not-for-profit charity for parents, caregivers, researchers, medical professionals and other interested support agencies and individuals. O.R.S.A. became incorporated in 1991. Its Board of Directors is comprised of parents and caring citizens. O.R.S.A. provides information through a website, a newsletter and conferences. Support is provided to families regionally. The association funds Canadian research projects, three Rett Syndrome Clinics, a resource centre and developed the Canadian Rett Syndrome Registry. O.R.S.A. advocates to the needs of individuals with Rett syndrome and their families provincially and nationally.  Click here to view in French.

Our Mission

The Ontario Rett Syndrome Association (O.R.S.A.) exists to ensure that children and adults with Rett Syndrome are enabled to achieve their full potential and enjoy the highest quality of life within their community.  Click here to view in French.

Board of Directors

President-Kevin Morton
President Elect-Bryan Higgins
Treasurer-Jodi Dwyer
Secretary-Scott Campbell

Stephanie Almeida
Brandon Hall
Sherry Lawrence
Jordan Lepkan
Keri-Ann Richard
Jennifer Young

O.R.S.A. Rett Syndrome Brochure

 Registration #  890178999RR0001