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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Make an impact this Mother’s Day

May 6th, 2019 by Chassin

AmazonSmile Bald Girls Do Lunch

Find the perfect gift for Mother’s Day and automatically donate to Bald Girls Do Lunch Inc when you shop at smile.amazon.com/ch/20-8649864. #AmazonSmile

Shop Now


Alopecia support is here.

March 2nd, 2019 by Chassin

Shannon’s Story from Concert Pharmaceuticals, Inc on Vimeo.

You’re not alone if you’re wondering how do I cope with alopecia areata knowing there’s no alopecia cure? One way to feel supported is right here: watching and reading personal stories  — people like yourself living with alopecia.

Watch Shannon’s heartfelt story: how she talks to herself and to others.

We thank Concert Pharmaceuticals for including our Bald Girls ambassador, Shannon, in their patient web portal for alopecia areata at ConcertPharma.com/patients/

Read Shannon’s Interview