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
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…
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.
Alopecia Areata Awareness Month 2018 #AlopeciaAreataAwareness pic.twitter.com/UA77aPjM93
— CoNCERT (@ConcertPharma) September 17, 2018
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.
Handfuls of hair coming out in your hands? Jada Pinkett Smith gives her own first-hand account of this shocking experience. We’re inspired by Jada’s colorful choices to rock the headwrap.
Got alopecia? Join Bald Girls Do Lunch CEO, Thea Chassin, for friendship, camaraderie and her Live Well with Alopecia™ tips.
