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.