About VAA

The VAA is a not-for-profit patient support organisation, promoting greater awareness, friendly interaction, patient education and research.

Anyone with an interest in this condition, be they a person with vitiligo, a family member, a friend, a clinician, a scientist, an allied medical professional or a philanthropist can join this not-for-profit association and its affiliated Patient Support Groups.

Our aim is to minimise and eliminate the social stigma of vitiligo, by increasing public awareness and assisting in the development of vitiligo education, research and international collaboration.

Office Bearers

Adrian Mar
President, VIC
Jennifer Nguyen
Secretary, VIC
Stephen Niederberger
Treasurer, WA

Committee Members

Nada Karadzic
QLD
Shobhan Manoharan
QLD
Sachin Vaidya 
SA
Perette Minciullo
WA
Prasad Kumarasinghe
WA
Aaron Frederiks
WA
Richard Wittal
NSW
Michelle Rodrigues
VIC
Tanya Tyler
NSW
Monisha Gupta
NSW

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