First Point of Contact


If your child has been recently diagnosed with Angelman syndrome or you would like to make immediate contact with our association or have questions about Angelman syndrome, we welcome you to call your State Representative listed below. If for some reason you are unable to get through, please call our National President or National Vice President also listed below.

Contact Us

By snail mail: If you have any questions or comments, write to: Angelman Syndrome Association Australia PO Box 554 Sutherland NSW Australia 1499.

National President & National Vice President:

National President (QLD)

Fiona Lawton
0488 996 181

Vice President  (WA)

Kane Blackman
0418 255 549

State Representatives & Committee Members:

New South Wales
Sue Hones
0414 648 628


Chloe Simons

0400 048 348

South Australia
Peta Perrie
0409 386 300

Western Australia




Laura Greene

0434 435 097

Lysandra Callahan

National Secretary & National Treasurer

National Treasurer
Kevin Kennedy 
5 Birok Ave Engadine NSW 2233
02 9520 5857


National Secretary

Committee Members:

Sally Hartmanis (VIC)

Chrissy Cimino (VIC)

Anne Funke

0457 616 168

First Point of Contact​

Contact your State Representative here

If for some reason you are unable to get through, contact our National President or National Vice President here

Visit the GiveNow Website

Our Mission

The ASAA was established to support, inform, educate, network, promote research and to advocate for families affected by Angelman syndrome - read more

© 2005 - 2018 Angelman Syndrome Association Australia. All Rights Reserved.

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FAST Australia
The Foundation for Angelman Syndrome Therapeutics Australia (FAST Australia) is an organisation of families and professionals dedicated to funding research to provide treatments that will improve the symptoms of Angelman syndrome and ultimately that will provide a cure (see website).