Alopecia areata is no joke. The controversy at the 2022 Academy Awards ceremonies helped raise important awareness of alopecia areata,…

Spotlight on Community Member Keya Trammell In honor of Black History Month, we wish to spotlight community member, Keya Trammell….

An open letter to the Academy of Motion Picture Arts and Sciences from the National Alopecia Areata Foundation (NAAF), our…

Alopecia Areata Language in Omnibus Bill The recently passed congressional Omnibus FY 2023 Appropriations bill includes the following language created…

Shamsha Damani is a seasoned healthcare professional with a strong track record of driving business growth. With over 20 years…

As we come to the close of 2022, we look upon these past 12 months as among the most pivotal…

2023 Conference – Save the Date! Join us for the National Alopecia Areata Foundation’s 38th Annual Conference in Denver, Colorado, …

Abigail Martinez joined the team as NAAF’s inaugural Medical Student Fellow in June. Abby attends medical school at Albany Medical…

When you participate in a survey that comes to you in a NAAF email, what happens to your responses? For…

Eight-year-old Caroline was diagnosed with alopecia areata in October 2020. By December of that same year, she had received her…

Volunteer at our Patient Conference NAAF is always looking for enthusiastic volunteers for our annual alopecia areata patient conference. We…

Join A Support Group After an alopecia areata diagnosis, it is important to realize that you are not alone. NAAF…

There are several things you can do to cope with the emotional effects caused by alopecia areata, but one of…

NAAF’s Youth Mentor Program  Do you have a child/teen with alopecia areata between the ages of 5 and 18 who…