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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BGDL Facebook Page




Posts


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

Posted in 2018, alopecia areata, Alopecia Lifestyle, Awareness, beauty, diagnosis, Friends of BGDL, How to: talk about alopecia, inspiration, support, supporters, Talking about alopecia, What Women Say


Buy One. We Gift One!

October 13th, 2018 by Chassin

Alopecia Sleep Hat

Purchase one Alopecia Sleep Hat in the month of October for yourself or someone you love with alopecia or going through chemo. We will include your words of encouragement when we gift a sleep hat in our Alopecia Care Kit.

Buy One. We Gift One With Your Wishes.

Posted in 2018, accessories, alopecia areata, Alopecia Lifestyle, fashion, Friends of BGDL, Hats, headwear, support, supporters


Join Us! Brunch in Dallas, TX October 13. RSVP today.

October 7th, 2018 by Chassin

Dallas Event

Join Us

Posted in 2018, Awareness, beauty, beauty event, event, support, Texas


Concert Pharma Tweet Keen on Importance of Our Alopecia Support

September 18th, 2018 by Chassin

I Want to Give Women Support and Smiles

Posted in 2018, alopecia areata, Awareness, support, supporters, Talking about alopecia


Seattle, Washington Event: May 12

April 30th, 2018 by Chassin

Bald is Beautiful in Seattle

Got alopecia? Join Bald Girls Do Lunch CEO, Thea Chassin, for friendship, camaraderie and her Live Well with Alopeciaâ„¢ 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

Posted in 2018, alopecia areata, Alopecia Lifestyle, brows, event, How to: talk about alopecia, Make-up, Seattle, support, Treatments, wigs, workshops


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 Alopeciaâ„¢ 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

Posted in 2018, alopecia areata, Alopecia Lifestyle, brows, event, How to: talk about alopecia, Make-up, support, Treatments, wigs, workshops


Alopecia Support with Bald Girls Do Lunch Changed My Life!

April 27th, 2017 by Chassin

DONATE

Posted in 2017, AA Support Network Blog, alopecia areata, diagnosis, New York, support, supporters, Talking about alopecia, Thea Chassin


Your Gifts Help More than Ever

April 6th, 2017 by Chassin

DONATE

Posted in 2017, Awareness, Donate, support


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.”

Posted in 2017, alopecia areata, Awareness, support, Talking about alopecia, Videos

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