<img height="1" width="1" style="display:none" src="https://www.facebook.com/tr?id=267266150391144&amp;ev=PageView&amp;noscript=1">
Bald Girls Do Lunch

Blog

Alopecia Areata Support Network

Giving Assistant

Women With Alopecia Areata Support Network Blog

Alopecia support is here.

Posted by Thea Chassin

March 8, 2019 at 9:00 AM

Shannon, living with Alopecia Areata

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.


Shannon's Story from Concert Pharmaceuticals, Inc on Vimeo.

Watch Shannon’s heartfelt story: how she talks to herself and to others.

We thank Concert Pharmaceuticals for including our Bald Girls Do Lunch ambassador, Shannon, in their patient portal for alopecia areata at ConcertPharma.com/patients/

Meet Shannon

Topics: coping with alopecia, women living with alopecia, stories of women with alopecia, talking about alopecia, alopecia awareness