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Your participation in the Alopecia Areata Registry, Biobank & Clinical Trials Network helps advance our research to better understand alopecia areata and develop safe and effective treatments.Learn More
Learn more about common reactions your child may have to alopecia areata and get resources to help him or her have positive experiences at school and with friends.Find Resources
There’s strength in numbers. NAAF’s national network of support groups and phone contacts offer another way to create a sense of community — no matter where you live.FIND A GROUP
Alopecia Marketplace Homepage Section
Shop for products and accessories
Find eyelashes, eyebrows, hairpieces, scarves and hats to help cover bare patches or address total hair loss. You can also find supportive books written by others with alopecia areata here. When you shop the vendors in our Alopecia Areata Marketplace, just mention "NAAF" each time at checkout and they’ll donate 10% of your purchase to NAAF.
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What’s happening in your community
The FDA wants to hear your story!
The Food & Drug Administration (FDA) is holding a public meeting on September 11, 2017 at their Campus in Silver Spring, Maryland to hear directly from you about what it's like to live with alopecia areata. This is a rare opportunity to talk about how the disease symptoms and current management options impact our community. There is no overstating the importance of this meeting, as the testimony you provide could directly affect treatment development for years to come. NAAF will be there and we hope to see you there as well!LEARN MORE