Vitiligo Association of Australia

The VAA is a not-for-profit. Promoting greater awareness,. Dispel myths and misunderstandings. Acknowledge the psychological impact. Raise government and community awareness. Promote acceptance and tolerance. We encourage support for. A Message from the Foundation President. 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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PAGE TITLE

Vitiligo Association of Australia

DESCRIPTION

The VAA is a not-for-profit. Promoting greater awareness,. Dispel myths and misunderstandings. Acknowledge the psychological impact. Raise government and community awareness. Promote acceptance and tolerance. We encourage support for. A Message from the Foundation President. 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!

CONTENT

This web site vitiligo.org.au states the following, "Raise government and community awareness." We noticed that the webpage stated " A Message from the Foundation President." It also said " 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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Vitiligo - Home

This website will explain the disease Vitiligo and the Integumentary System. It will talk about the symptoms, causes, and treatments of the disease. It will also share the functions and parts of the Integumentary System. Start your own free website. A surprisingly easy drag and drop site creator.

Associação de Portadores de VitiligoPsoaríse Mãos Amigas

Sábado, 23 de abril de 2011. Sexta-feira, 8 de abril de 2011. Associação de portadores de vitiligo e de psoríase promovem palestra a estudantes. Alunos apoio o movimento mãos amigas. Jannecy Mascarenhas, fala da Psoríase. Sábado, 19 de março de 2011. Ajudar para Portadores de Psoaríase. Entrevista publicada na Revista veja.