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...





Global Skin Logo - International Alliance of Dermatology Patient Organizations

BGDL Facebook Page




Posts


Lights on! Every night in September!

September 14th, 2020 by Chassin

Every Night in September! Easy trip close to the NY State Thruway in New York's Albany Capital Region. A very special…

Posted by Bald Girls Do Lunch on Thursday, September 10, 2020

Posted in 2020, alopecia areata, Awareness, New York, support, supporters, Women with Alopecia Month


Alopecia Awareness Campaign

September 8th, 2020 by Chassin
King Queen Towers

Atlanta’s King and Queen Towers shine blue in the alopecia areata awareness campaign of CoNCERT Pharmaceuticals. #LightItUpBlue

Posted in 2020, AA Support Network Blog, event, support, supporters


#LightItUpBlue for Alopecia Awareness Month

September 7th, 2020 by Chassin

Posted in 2020, AA Support Network Blog, beauty event, event, support, supporters


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

Posted in 2020, AA Support Network Blog, About BGDL, Action Alert, alopecia areata, diagnosis, Donate, Friends of BGDL, fundraising, How to: talk about alopecia, Massachusetts, media coverage, support, supporters, Talking about alopecia


Shop Cyber Monday Deals and Donate!

November 26th, 2018 by Chassin

AmazonSmile Bald Girls Do Lunch

Shop for Cyber Monday and automatically donate to Bald Girls Do Lunch Inc when you shop at smile.amazon.com/ch/20-8649864. #AmazonSmile #StartWithaSmile

Shop Now

Posted in 2018, accessories, Action Alert, alopecia areata, discounts, Donate, Group discount, support, supporters


Act Now: AmazonSmile donation rate now 10x from Oct 29 – Nov 2

October 30th, 2018 by Chassin

AmazonSmile Bald Girls Do Lunch

Through Nov 2, AmazonSmile is donating 5% (ten times the usual amount) to Bald Girls Do Lunch Inc when you shop at smile.amazon.com/ch/20-8649864. #AmazonSmile #StartWithaSmile

Shop Now

Posted in 2018, accessories, alopecia areata, beauty, discounts, Donate, event, fashion, Group discount, support, supporters


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


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

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