News - National Alopecia Areata Foundation

September is all about the alopecia areata community. We are strong individually but when we work together, we have super-powers! It’s…

There’s no need to go it alone. NAAF support systems can help. At any given time, about 700,000 people in…

Help Make Wigs More Affordable with New Legislation You can help make cranial prosthetics, or wigs, more affordable by asking…

Today, the U.S. Food and Drug Administration (FDA) approved LITFULO™ for severe alopecia areata, marking the second FDA-approved treatment for…

Isoken Igbinedion, Ifueko Igbinedion and Simone Kendle, the founders of Parfait Wigs – a NAAF Conference vendor – appeared on…

Ask your congressional representative and senators to co-sponsor H.R. 4034 and S. 1922, new legislation in the House and Senate…

Does alopecia areata (AA) affect all races and ethnic groups equally? If yes, why is this important? Knowing AA prevalence…

Let’s do something about alopecia areata! Let’s WALK FOR ALOPECIA™! The National Alopecia Areata Foundation (NAAF) is excited to…

The last week of April saw NAAF’s Communications Director, Gary Sherwood, and Legislative Liaison, Brittany Foxworth, take an active role…

Portrait of a Teen Fundraiser Spring has sprung and with it are opportunities to support the alopecia areata community! John…