Ms. Paige Clarke-Jeffers announces the enrollment of Black women with all forms of alopecia areata in her research project: “Black Women’s Experiences of Living with Alopecia” at Birmingham City University, United Kingdom. The study is for her Masters of Health Psychology dissertation.
Please take action TODAY to make the most of this inspiring moment for all of us living with AA.
THANK YOU for joining Bald Girls Do Lunch in celebrating Massachusetts Representative Ayanna Pressley. And, expanding our work to support more girls and women living with AA.
It’s a beautiful step forward for awareness, acceptance, and the Bald Girls community.
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 storiesÂ Â â€” people like yourself living with alopecia.
WatchÂ Shannon’s heartfelt story: how she talks to herself and to others.
We thank Concert Pharmaceuticals for including our Bald GirlsÂ ambassador, Shannon, in their patient web portal for alopecia areata at ConcertPharma.com/patients/
Your gift gives custom alopecia hats designed by Bald Girls Do Lunch to women in need.
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.