Events

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 info@naaf.org 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.

#Webinars

Upcoming Webinar

Virtual Event

Wednesday, July 30, 2025 | 4:00 PM, PDT

Alopecia Areata Research Powered by You: How Patient Perspectives Drive Progress

Wednesday, July 30, 2025 4PM PST/ 6PM CST/ 7PM EST

Have you ever been asked to fill out a survey about what it’s like to live with alopecia areata — for you or your child? When you share how this disease affects your daily life and how it makes you feel, your answers do more than just sit in a file — they become part of important research. Every story and every survey helps researchers better understand the real impact of alopecia areata.

Join Dr. Arash Mostaghimi and Samantha Gregoire as they talk about their research, inspired by the alopecia areata community. They’ll explain how your experiences and voices are driving progress toward better care and a better understanding of this autoimmune disease.