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The Australian Alopecia Areata Foundation (AAAF)

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The Australian Alopecia Areata Foundation (AAAF), a beacon of support for those navigating the challenges of alopecia areata. Founded by Chel Campbell, the AAAF serves as a vital resource offering guidance, education, and a sense of community for individuals and families grappling with alopecia areata.

A Source of Comfort and Knowledge

Kay highlights the AAAF as an invaluable source of support, especially for families dealing with the emotional complexities of hair loss, particularly in children. Acknowledging the profound impact on parents, the AAAF extends a helping hand with information on the latest treatments and a robust support system.

Navigating the Journey in Schools

When a child faces hair loss, the AAAF steps in to provide essential tools, including support packs and educational resources tailored for schools. Parents can print off these packs, offering valuable insights to teachers and classmates on how to navigate the challenges associated with alopecia areata.

Comprehensive Support Packs

For parents, the AAAF has comprehensive support packs designed to address common concerns, offering information and guidance. These packs become a lifeline for parents who may grapple with feelings of self-blame, despite understanding that hair loss is not their fault.

Teenage and Support and Creative Outlets

Recognizing the unique challenges faced by teenagers dealing with alopecia areata, the AAAF provides specialized support packs.

Dolls Just Like Me: A Special Touch

Kay brings attention to Mattel's Barbie dolls designed for children experiencing alopecia areata. If the AAAF doesn't have these dolls available, Kay encourages individuals to explore Mattel's offerings, providing a meaningful and relatable gift for young girls facing hair loss.

A Warm Invitation for Connection

In closing, Kay extends a warm invitation to anyone feeling isolated or in need of support to reach out to the AAAF. The foundation's compassionate staff, including Vesna, Chel, and Georgia, are ready to offer understanding and assistance, drawing from their own experiences with alopecia areata.

The AAAF stands as a pillar of strength, ensuring that no one faces the journey of alopecia areata alone. If you find yourself in need, Kay encourages reaching out to this dedicated foundation, where compassion and support are just a call away.

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Think you may have hair loss? Consider booking in an online or in person consultation with us.


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