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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Posts


Now recruiting Alopecia Areata Clinical Trial: THRIVE-AA1

March 24th, 2021 by Chassin

THRIVE-AA1

A clinical research study is currently recruiting adults in the US and Canada.

The preliminary requirements to participate in this study of an oral investigational drug are:

  • • Adults ages 18-65
  • • A diagnosis of alopecia areata
  • • 50% or greater scalp hair loss

For more detailed clinical information visit https://bgdl.org/THRIVE-AA1.

Bald Girls Do Lunch is providing this announcement for informational purposes only. Bald Girls Do Lunch does not imply endorsement.  The decision to participate is voluntary and wholly the responsibility of the individual person.

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Pro Athlete Partners with Bald Girls Do Lunch!

March 10th, 2021 by Chassin

We’re so excited!

American professional volleyball player Deja McClendon, is joining Bald Girls Do Lunch® to promote awareness about alopecia areata and Bald Girls Do Lunch as part of the Athletes Unlimited’s Pro Causes initiative.

“I really love the Bald Girls cause and how they bring back confidence in women by giving them an outlet to express themselves and talk through the stigma of being a bald woman,” says Deja who was diagnosed with alopecia when she was 12.

Yes! I’ll Give to Honor Deja’s Awareness Work

Deja