• Working together

    to assist patients

    with vitiligo

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

  • Reaching Out

    Supporting members through

    • Online networking
    • Support Groups
    • Professional links
    • Treatment advice
  • Education

    Reliable information for

    • patients
    • carers
    • health professionals
    • the general community
  • Confronting the Stigma

    Together we must

    • dispel myths & misunderstandings
    • acknowledge the psychological impact
    • raise government & community awareness
    • promote acceptance and tolerance
  • Promoting Research

    We encourage support for

    • clinical trials
    • laboratory research
    • international collaborations



A Message from the Foundation President:
I am delighted to welcome all visitors to the website of the Vitiligo Association of Australia. Vitiligo is a disease affecting 1% of the world's population but the attention it receives from medical circles, healthcare policy planners, and research organisations is totally inadequate.
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Support Groups

Does your state have a support group? If so, why not join up and meet with others to share your experience and help others. If there is no group in your area why not think about starting one up? The VAA can help you do so!
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Camouflage Road Tests


Skin camouflage is an important part of the care of vitiligo, regardless of gender and age. There are a number of products available which can be recommended to people with vitiligo, and we have tested them out for you to decide which may be best suited to your needs.
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Vitiligo Association of Australia

Vitiligo Association of Australia is a not-for-profit patient support group promoting greater awareness, friendly interaction, patient education and research. Our site is currently undergoing maintenance.

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