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/
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.
Holiday time for many means friends and family gathering round. This season, you might be new to alopecia. Or, maybe it’s resurfaced. Or, maybe you’ve decided to take a new approach and let others in a bit more about what this condition is and isn’t.
Our BGDL appearance on the TODAY show can help. Just send the link around or click, sit back and enjoy yourself. There are millions of us. Often hiding in plain sight. All around the world.
