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


Living with Alopecia Areata

October 22nd, 2018 by Chassin

Alopecia Sleep Hat

You’ve heard first hand how disruptive an alopecia areata diagnosis can be. The shock, anxiety and shame can send women into hiding from social activities, even some types of work. Like Shirley…

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Bald Girls Loves the Alopecia Areata style of Jada Pinkett Smith

June 4th, 2018 by Chassin

Bald Girls Loves the Alopecia Areata style of Jada Pinkett Smith

Handfuls of hair coming out in your hands? Jada Pinkett Smith gives her own first-hand account of this shocking experience. We’re inspired by Jada’s colorful choices to rock the headwrap.

Read Her Story

This is how we do it at Bald Girls Do Lunch events.

Bald Girls Alopecia Areata Style


Alopecia Support with Bald Girls Do Lunch Changed My Life!

April 27th, 2017 by Chassin

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