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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 a New Alopecia Areata Patient Survey: Improving Quality of Life Outcomes

June 26th, 2018 by Chassin

Alopecia Areata Survey

Alopecia Survey now open! Professor Garrett Huck at Penn State is researching the attitudes and feelings of people over 18 living with any form or duration of alopecia areata (AA, AT, AU). This survey is open to all qualifying individuals in the USA, Canada, UK, Australia, New Zealand and beyond … well, anywhere because people with AA are everywhere.

It takes only 20 minutes to complete.

To thank you for taking part in this comprehensive online survey, you’ll be entered to win an Amazon gift card. Sweet! Surveys can be fun and enlightening. Enjoy!

Start the Survey Now!