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...
Upcoming Events BGDL Fact Sheet
Posts
Purchase one Alopecia Sleep Hat in the month of October for yourself or someone you love with alopecia or going through chemo. We will include your words of encouragement when we gift a sleep hat in our Alopecia Care Kit.
Spring In The City from Bald Girls Do Lunch on Vimeo.
Video: “It’s Only Hair”
From the Department of Anthropology at Goldsmith’s College in London – Life experiences with alopecia areata.
Got alopecia? Join Bald Girls Do Lunch CEO, Thea Chassin, for friendship, camaraderie and her Live Well with Alopecia™ tips.
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.
