Formed in Melbourne in July 1989, the Rett Syndrome Association of Australia Inc. (RSAA) is a not-for-profit organisation which is managed by a Committee of volunteers, most of whom are parents of children with Rett syndrome.
The Association seeks to enrich the quality of life for persons with the syndrome and their families, and be of assistance to anyone interested in the disorder. July 2014 marked the 25th anniversary of the Association’s formation.
Members of the present RSAA Committee are as follows:
President Claude Buda (NSW)
Vice-President Bill Callaghan (VIC)
Secretary Caroline Dempster (WA)
Treasurer Tony Cagliuso (SA)
Assist. Treasurer Karen Rodda (SA)
Family Support Co-ordinator Sue Hallenstein (VIC)
Jayne Bowden (TAS)
Elizabeth Davies (VIC)
Michelle Denniss (QLD)
Eric Gowans (SA)
Kristy Klingner (SA)
Dagmar Lockwood (SA)
Mary-Anne Rome (VIC)
Kirsty Sale (SA)
Madeleine Saric (VIC)
Georgia White (NSW) .
Recent RSAA annual general meetings
Content of the 2017/18 RSAA annual general meeting which took place in Melbourne on 17 November 2018, can be viewed by clicking on the following link
Content of the 2016/17 RSAA annual general meeting which was held in Melbourne on 23 September 2017, can be viewed by clicking on the following link