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
Elizabeth K: Alopecia onset age 23
Occupation: Dental Hygienist
What BGDL means to Elizabeth: “A fun, informative and special organization”
DONATE to Bald Girls Do Lunch. We help women like Elizabeth.
Super cute video from the Australia Alopecia Areata Foundation. With puppets and children, any child you know will understand your alopecia much better from this video: Watch HERE Ages 4-12.
Visit HERE and see why BGDL is a top-rated alopecia nonprofit for the fourth straight year.
Thanks to our donors, volunteers and people like you, we are one of the first winners of a 2015 Top-Rated Award from GreatNonprofits. Read our great reviews and add your story.
Documentary Pinkham: Finding Lifelong Passion After Alopecia
Film “Pinkham” by Cineastas features woman with alopecia in Portland, Oregon.
Tackling the first year with ‪#‎alopecia‬ areata head on. How Christine nailed it and told her boss! http://bgdl.org/1LRZA8U
6 Questions for Alopecia Patient on Xeljanz http://bgdl.org/1Jqgj0J
Alopecia areata patient on Xeljanz talks to Bald Girls Do Lunch alopecia support founder Thea Chassin.
Meet Thea Chassin and women with alopecia areata in Rhode Island on August 4, 2015 (or Northern CT August 6)
Not only does our Empowering Alopecia Network  uplift and inspire,  every attendee goes home with a goody bag filled with scarves, beanies and a synthetic wig.
