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


We Believe: love has no boundaries.

December 12th, 2018 by Chassin


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…

Read More


Concert Pharma Tweet Keen on Importance of Our Alopecia Support

September 18th, 2018 by Chassin

I Want to Give Women Support and Smiles


A Brand New Alopecia Survey Needs You!

August 2nd, 2018 by Chassin

Take the survey before August 2nd and you’ll be be entered into random daily drawing for one of five $25 Amazon gift cards.

Privacy: Providing your email is optional. No answers will be saved or associated with your email by the survey creator, Foresite Capital. No individually identifiable responses will be saved.

Eligibility: take the survey if you have alopecia areata yourself or on behalf of any other person who has AA.
Ages: open to all ages, gender and orientations

Start the Survey Now!


Little Rock Alopecia Events: RSVP by 3/27

March 18th, 2018 by Chassin

Bald is Beautiful in Arkansas

We’ve got a seat for you! Friendship, research news, beauty and more with Thea Chassin: Live Well with Alopecia™ tips for Spring 2018.

  • • Who understands alopecia? Women like you!
  • • Learn fashion tips and tricks for your wigs, hairstyles and head wraps
  • • We’ve got you covered: best brow shapes, faking a lash line and makeup demo
  • • Be comfy. Be yourself. We love all options: wear your wigs, hair, hats or bald look

RSVP Here for Breakfast

RSVP Here for Dinner


Bald Girls’ Alopecia Areata Voices for the FDA

March 11th, 2018 by Chassin

FDA

As part of our Bald Girls community, you know firsthand the impacts of alopecia areata. That’s also what the FDA wants to learn. They held an AA patient-focused meeting in September 2017 attended by Bald Girls Do Lunch CEO, Thea Chassin.

Join the Conversation


Alopecia Support with Bald Girls Do Lunch Changed My Life!

April 27th, 2017 by Chassin

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