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...
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/
Sandra met us in Raleigh, NC a few years ago. This inspiring motivational speaker and singer continues to spread her message of self-acceptance to boost more women with alopecia.
“Bald Girls Do Lunch in Raleigh was a blessed event. Thea has a wealth of knowledge and a heart of gold. It takes great strength and courage to walk boldly and confidently as a bald women in this society. Not only does Thea live her song, but she inspires women all over the world to do the same.”
