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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We’ve got a seat for you! Friendship, research news, beauty and more with Thea Chassin: Live Well with Alopecia™ tips for Spring 2018.
Got alopecia? Join Bald Girls Do Lunch CEO, Thea Chassin, for friendship, camaraderie and her Live Well with Alopecia™ Spring 2018 tips.
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.
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
For a personal look at how two women are living (and thriving) with Alopecia, check out these stories on the blog:
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Could super-superficial jabber about celeb hairstyle changes be just the right opening to get your conversation started?
Changing a wig-wardrobe is not a one-size-fits-all situation for every woman with AA. At one end of the spectrum are those terrified of changing their look, simply due to fear of change and drawing attention to themselves. At the other end are people who justifiably require a consistent look for professional reasons. Yet, there’s a vast territory in between. Where are you on this spectrum? Are you doing what you want on your own terms?
