It’s time to register your interest in our yearly camp!!

What is the AAAdventure camp? It’s super fun, filled with memorable experiences, and a fantastic opportunity to meet other kids with Alopecia Areata. Plus, it’s a chance to have an Continue reading →

Chel (our President) and Vesna (our Vice President) donated their long locks at our Victoria Open Day. Thank you for being such amazing role models and supports to our community!

Congratulations to Amy M, our AAAF 2023 Supporter of the Year! 🌟 Your dedication to raising awareness for Alopecia Areata and engaging your community is truly inspiring. As a token of our appreciation, we’re gifting Amy a $100 gift voucher. Continue reading →

In a world where individuality is celebrated, Neva, an 8-year-old with a heart full of courage and a radiant smile, is taking her message of self-love and resilience to the world. Diagnosed with alopecia at the tender age of four, Continue reading →