About Association Of Australia

Founded in September 2010, the Vitiligo Association of Australia (VAA) is a national non-profit organization dedicated to supporting individuals affected by vitiligo, raising public awareness, and promoting scientific research across Australia. With approximately 650 members including patients, carers, health professionals, and researchers, the VAA serves as a vital hub for information, advocacy, and community connection.

The Association’s mission is fourfold: to provide direct support to those living with vitiligo, educate the wider public to reduce stigma, connect members to expert medical advice, and encourage research that can improve treatment and, ultimately, lead to a cure. Through its website, the VAA offers access to dermatology specialists, patient resources, and credible online information tailored to the Australian context.

Current and upcoming projects reflect the VAA’s commitment to practical solutions. The Camouflage Project will provide online guidance about cosmetic camouflage products to help individuals manage the visible aspects of vitiligo with confidence. The organization is also developing dedicated resources and support services for young adults and children, ensuring that the next generation has the tools and encouragement to thrive.

Beyond patient support, the VAA actively contributes to the advancement of vitiligo research. It awards an annual research grant to local scientists, fostering innovation and collaboration within Australia’s medical community. Fundraising events help sustain these initiatives while also building public awareness of the condition.

Through its combination of emotional support, educational outreach, and research investment, the Vitiligo Association of Australia continues to strengthen the voice of the vitiligo community nationwide, empowering individuals to live fully, without limitations, and inspiring hope for future breakthroughs.