Who we are


Alopecia Areata: The shame and embarrassment of this disease devastates the lives of too many women and girls when treatments do not work. Since 2007 Bald Girls Do Lunch has connected with over 3,000 to restore self-confidence and conquer isolation. With requests for meet-ups in every state and beyond the USA, Bald Girls is answering the plea for women to find others for community and support. From intimate groups to style workshops to restoring her looks, BGDL puts women on the track to normalcy and living well with this disease. Learn more...





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Take Action TODAY

January 22nd, 2020 by Chassin

Please take action TODAY to make the most of this inspiring moment for all of us living with AA.

Photo Credit: MSNBC

THANK YOU for joining Bald Girls Do Lunch in celebrating Massachusetts Representative Ayanna Pressley. And, expanding our work to support more girls and women living with AA.

It’s a beautiful step forward for awareness, acceptance, and the Bald Girls community.

MAKE MY SPECIAL GIFT NOW

Posted in 2020, AA Support Network Blog, About BGDL, Action Alert, alopecia areata, diagnosis, Donate, Friends of BGDL, fundraising, How to: talk about alopecia, Massachusetts, media coverage, support, supporters, Talking about alopecia