Register Now for NAAF's 39th Annual Patient Conference June 27-30, 2024 in Washington, D.C.!
There’s no need to go it alone. NAAF support systems can help. At any given time, about 700,000 people in…
An open letter to the Academy of Motion Picture Arts and Sciences from the National Alopecia Areata Foundation (NAAF), our…
Abigail Martinez joined the team as NAAF’s inaugural Medical Student Fellow in June. Abby attends medical school at Albany Medical…
Eight-year-old Caroline was diagnosed with alopecia areata in October 2020. By December of that same year, she had received her…
Just because you’re not yet voting age doesn’t mean you can’t make a difference! Read about Joshua’s experience and reach…
Alopecia areata community member Dylan Huang generously shares his story and what he’s taken from the experience of having alopecia…
