Bald Girls Do Lunch, Inc., P O Box 9122, Scarborough, NY 10510
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...
BGDL Fact Sheet
Posts
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!
Please take action TODAY to make the most of this inspiring moment for all of us living with AA.
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.
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/
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…
Alopecia Areata Awareness Month 2018 #AlopeciaAreataAwareness pic.twitter.com/UA77aPjM93
— CoNCERT (@ConcertPharma) September 17, 2018
Take the survey before August 2nd and you’ll be be entered into random daily drawing for one of five $25 Amazon gift cards.
Privacy: Providing your email is optional. No answers will be saved or associated with your email by the survey creator, Foresite Capital. No individually identifiable responses will be saved.
Eligibility: take the survey if you have alopecia areata yourself or on behalf of any other person who has AA.
Ages: open to all ages, gender and orientations
We’ve got a seat for you! Friendship, research news, beauty and more with Thea Chassin: Live Well with Alopecia™ tips for Spring 2018.
As part of our Bald Girls community, you know firsthand the impacts of alopecia areata. That’s also what the FDA wants to learn. They held an AA patient-focused meeting in September 2017 attended by Bald Girls Do Lunch CEO, Thea Chassin.
