September 17th, 2020 by Chassin

Free and Downloadable Infographic about Alopecia Areata
Everything you’ve always wanted to tell other people is right here. We are so delighted with this beautiful and practical infographic created and made available for download by Concert Pharmaceuticals. Thank you Concert!
Posted in 2020, alopecia areata, Friends of BGDL, How to: talk about alopecia, Talking about alopecia
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
September 8th, 2020 by Chassin
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
June 1st, 2020 by Chassin

Ms. Paige Clarke-Jeffers announces the enrollment of Black women with all forms of alopecia areata in her research project: “Black Women’s Experiences of Living with Alopecia” at Birmingham City University, United Kingdom. The study is for her Masters of Health Psychology dissertation.

Posted in 2020, AA Support Network Blog, Action Alert, alopecia areata, Friends of BGDL, psychology, research, support, UK, What Women Say
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.
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
December 6th, 2019 by Christie Elizondo

Thea Chassin (middle) with two European researchers for GRIDD: Global Research on the Impact of Dermatological Disease. Ms Chassin is the founder and CEO of Bald Girls Do Lunch.
Memo to: Awesome Bald Girls Do Lunch community
Your voices about life with alopecia areata, the ‘voice of the patient’, gains influence in today’s dermatology research. Your participation is the backbone of Bald Girls Do Lunch. You tell us what impacts you most.
“The candor and sheer guts of the BGDL community was top of my mind,” reports Thea Chassin.
Posted in 2019, AA Support Network Blog, Action Alert, dermatology, Friends of BGDL, How to: talk about alopecia, Medical, Testimonials, Thea Chassin
November 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/
Posted in 2019, AA Support Network Blog, alopecia areata, Alopecia Lifestyle, Awareness, Friends of BGDL, How to: talk about alopecia, research, Talking about alopecia, video, Videos