November 2nd, 2019 by Chassin
Shannon’s Story from Concert Pharmaceuticals, Inc on Vimeo.
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/
Posted in 2019, AA Support Network Blog, alopecia areata, Alopecia Lifestyle, Awareness, Friends of BGDL, How to: talk about alopecia, research, Talking about alopecia, video, Videos
October 22nd, 2018 by Chassin
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…
Posted in 2018, alopecia areata, Alopecia Lifestyle, Awareness, beauty, diagnosis, Friends of BGDL, How to: talk about alopecia, inspiration, support, supporters, Talking about alopecia, What Women Say
October 7th, 2018 by Chassin
Posted in 2018, Awareness, beauty, beauty event, event, support, Texas
October 6th, 2018 by Chassin
Posted in 2018, About BGDL, alopecia areata, Awareness
November 27th, 2017 by Chassin
Bald Girls Do Lunch is donor-supported. You can be a Bald Girls donation hero today. Your friendship and support works to stop alopecia areata anxiety and shame.
Posted in 2017, About BGDL, Awareness, Friends of BGDL, fundraising
April 6th, 2017 by Chassin
Posted in 2017, Awareness, Donate, support
March 29th, 2017 by Chassin
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.”
Posted in 2017, alopecia areata, Awareness, support, Talking about alopecia, Videos
