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December 1st, 2022 by admin
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Mario M. Cuomo Bridge Turns Blue for NY Alopecia Areata Awareness September 16, 2021
September 10th, 2021 by Chassin
DETAILS:
6:30 pm, Tarrytown Riverwalk, Tarrytown NY
Meetup location: On the Riverwalk just west of 240 West Main St. Park in Lot E
- Meet Thea Chassin, Founder of Bald Girls Do Lunch
- Watch the bridge turn from daylight to blue
- Photo-ops fun: bring a blue LED or wear something blue
- Creative? Make a sign: #LightitUpBlue4AlopeciaAreata
Alopecia Areata Month, Bald Is In!®
March 20th, 2021 by Chassin
Take a selfie. Save the date. Celebrate 2021 Alopecia Awareness Month. BALD IS IN! for the month of September.
Your photo will appear in our first annual Bald Is In selfie collage.
Send your selfie to thea@BaldGirlsDoLunch.org
Together we get closer to the day when bald women are as easily accepted as bald men.
Free and Downloadable Infographic about Alopecia Areata
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!
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/
Living with Alopecia Areata
October 22nd, 2018 by Chassin
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…
