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!
This is Arthur, who will be undertaking a 100km run (wow!!!) in support of AAAF this coming February 2024. He has already raised almost $2000 in donations, the momentum is building and it’s time to get more people involved!
Dive into the empowering stories and latest updates in the November 2023 issue of Raise Magazine! Meet our amazing committee, explore job opportunities, stay informed on research updates, and more. View the latest issue through this link: https://aaaf.org.au/wp-content/uploads/2023/11/Raise-November-2023-1.pdf
The study is investigating the socio-economic burden of Alopecia Areata (AA) on adolescents, adults, and their caregivers/partners. This analysis will be used to generate Quality-Adjusted Life Years, a quantitative measure for how patient’s lives are impacted, which may facilitate assessments Continue reading →
As Alopecia Awareness Week approaches, the highly anticipated AAAdventure Camp stands out as a beacon of support and connection for children grappling with alopecia.
Scheduled to take place on November 11th and 12th, this year’s camp promises an unforgettable experience for Continue reading →
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 →