Lights on! Every night in September!
September 14th, 2020 by ChassinEvery 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
Posts
Alopecia Awareness Campaign
September 8th, 2020 by Chassin
Atlanta’s King and Queen Towers shine blue in the alopecia areata awareness campaign of CoNCERT Pharmaceuticals. #LightItUpBlue
#LightItUpBlue for Alopecia Awareness Month
September 7th, 2020 by Chassin@ConcertPharma #LightItUpBlue for #AlopeciaAreata awareness in #Atlanta Sept 2-3 and 5-8. #concertcares about patients with autoimmune hair loss disease.Thank you CoNCERT! pic.twitter.com/IGWV8gnzAt
— Bald Girls Do Lunch, alopecia areata nonprofit (@alopecia) September 2, 2020
New Alopecia Research Opportunity. Thank you, participants! Recruitment is now closed.
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.
Take Action TODAY
January 22nd, 2020 by ChassinPlease 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.
Alopecia Areata Patient Voices in Research
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.
Alopecia support is here.
November 2nd, 2019 by ChassinShannon’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/
