We are gearing up for November’s camp! Getting so excited! If your kid has alopecia and you would like to be involved, please here to express your interest so that we can save your spot!

What do you think of our Wigs For Kids logo?

The Wigs For Kids grant program has been operating since 2012 (can you believe it?!) and we figured it was time for a logo!

Click here to learn more about Continue reading →

Mairead was diagnosed with AA at 13 years old in primary school, which progressed to AU by high school, where Mairead ended up shaving the last of her hair off at 17 years old.

Mairead is joining the AAAF committee Continue reading →

Wishing a very Merry Christmas to all who are celebrating! We hope you have a wonderful, safe and happy time with your families and friends.

Please be aware that there may be small delays with emails and inquiries via social Continue reading →

Thank you to everyone who joined us at the AAAdventure Camps over November throughout the country! We were so excited to have 85 attendees and reconnect after so many months either in lockdown or with limited in-person events. 

Activities included Continue reading →

November has been a big month for us! Not only have we celebrated Alopecia Areata Awareness Week but we have also welcomed two new team members: 

Say a big HELLO to our new NSW Branch Manager – Carlo! 👋🏼

Carlo Continue reading →

AAAF is very excited to announce our new QLD Branch Manager – Greg T! 

Greg shared with us some insight from his experience with alopecia areata – “With Alopecia it starts from day one. A journey through life that brings Continue reading →