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...
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DETAILS:
6:30 pm, Tarrytown Riverwalk, Tarrytown NY
Meetup location: On the Riverwalk just west of 240 West Main St. Park in Lot E
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.
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hyperlinks to email thea@BaldGirlsDoLunch.org
Together we get closer to the day when bald women are as easily accepted as bald men.
We’re so excited!
American professional volleyball player Deja McClendon, is joining Bald Girls Do Lunch® to promote awareness about alopecia areata and Bald Girls Do Lunch as part of the Athletes Unlimited’s Pro Causes initiative.
“I really love the Bald Girls cause and how they bring back confidence in women by giving them an outlet to express themselves and talk through the stigma of being a bald woman,” says Deja who was diagnosed with alopecia when she was 12.
Yes! I’ll Give to Honor Deja’s Awareness Work
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
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
