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


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


Little Rock, Arkansas Event: April 29

March 17th, 2018 by Chassin

Bald is Beautiful in Arkansas

Got alopecia? Join Bald Girls Do Lunch CEO, Thea Chassin, for friendship, camaraderie and her Live Well with Alopecia™ Spring 2018 tips.

  • • Meet locals like yourself who understand the challenges of alopecia.
  • • Get answers to questions about living with alopecia and treatment regimens.
  • • Need eyebrow help? We’ve got you covered with our BGBrows demo.
  • • Be comfy. Be yourself. We love all options: wear your wigs, hair, hats or bald look.

Register Here


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


Talk to the FDA! Alopecia Areata Patient Views Needed

November 12th, 2017 by Chassin

FDA

Our submissions page to Talk to the FDA via the Bald Girls Do Lunch impact statement is now closed.

You may enter your comments through 11:59 pm eastern, November 13, 2017 directly to the FDA here.


Alopecia Support with Bald Girls Do Lunch Changed My Life!

April 27th, 2017 by Chassin

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Alopecia Beauty in North Carolina

March 29th, 2017 by Chassin


Sandra met us in Raleigh, NC a few years ago. This inspiring motivational speaker and singer continues to spread her message of self-acceptance to boost more women with alopecia.

“Bald Girls Do Lunch in Raleigh was a blessed event. Thea has a wealth of knowledge and a heart of gold. It takes great strength and courage to walk boldly and confidently as a bald women in this society. Not only does Thea live her song, but she inspires women all over the world to do the same.”


Beauty Blogger Raves about Brow Pen

September 22nd, 2016 by Chassin


Read the Review by Carly Severn.

Buy Here


How to help a friend with alopecia areata find her true beauty

August 8th, 2016 by Chassin

alopecia areata friendship

Heidi showed us the power of her friendship in helping a close friend to live well with alopecia areata. In this follow-up we find out how Heidi does it. In fact, she told us how alopecia areata resonates with her own life, even though she herself has normal hair.

Her insights are very cool. Enjoy! Guest commentary from interview with Heidi S. of New Jersey. Read More

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Friendship Makes the Difference in Alopecia Areata Support

July 12th, 2016 by Chassin

Heidi and Allison

When friendship involves alopecia, it can be an opportunity for strength and support.

That’s what Heidi from New Jersey told us when her best friend, Allison, opened up about having alopecia areata, not something she did often. Read More

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