Register Now for NAAF's 39th Annual Patient Conference June 27-30, 2024 in Washington, D.C.!


Our calendar of events keeps our supporters informed of virtual and in-person support group meetings, webinars, fundraisers, walk-a-thons and more! We are happy to list your meeting, walk-a-thon, fundraiser, etc. The possibilities are endless. If you can think of it, you can do it. We are here to help you make your specific event a success. Let us know what we can do for you, be it providing you with materials to disperse, targeting a specific demographic for a mailing, or notifying the NAAF community on your upcoming event.

Send your event details to us at to be included on the calendar. If you know of other events that would be of direct interest to NAAF supporters, please let us know about them as well.

NOTE: The National Alopecia Areata Foundation’s Support Group and Telephone Support Contact information on this and any other NAAF page, is intended for people with alopecia areata and their loved ones to easily find services in their area. Contacting individuals on this list directly to engage in commercial activities of any kind is strictly prohibited.

Novel developments in treating alopecia areata: What is Type 2 inflammation and why is it important?

Virtual Event

Wednesday, July 17, 2024 | 4:00 PM, PDT

Have you ever wondered how eczema, allergies, and inflammation might be linked to alopecia areata? Join us for an insightful webinar with Drs. Emma Guttman and Benjamin Ungar as they discuss their significant research on alopecia areata and Type 2 inflammation, an inflammatory response linked to allergic conditions. They will explain how this research has paved the way for a new clinical trial in children to investigate a potential treatment for alopecia areata. This new study is backed by a recent $6 million grant from the National Institutes of Health to Mount Sinai. Don’t miss this chance to learn about the latest advancements and their implications for the future of alopecia areata treatment.