RSAA aims to: Support families and others in coping with Rett syndrome, Collect and distribute accurate information on the disorder, Promote community awareness of the condition, Assist, where possible, research into the syndrome, and Liaise with other groups interested in Rett syndrome.
Who can Join
Anyone interested in Rett syndrome
phone for details
Where we meet
PO Box 3497
Phone and email support Gatherings Newsletter Brochure/Flier Fact sheets Library Conferences
Over the years, gatherings have been held in all mainland capital cities including Sunshine Coast (Qld).
Enhance the quality of life of persons with Rett syndrome.