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.

Upcoming Webinar

Virtual Event

Wednesday, April 22, 2026 | 4:00 PM, PDT

The Power of Peer Support: Teens with Alopecia Areata Supporting Each Other

WEDNESDAY, APRIL 22, 2026 4PM PDT/ 6PM CDT/ 7PM EDT

As we approach Mental Health Awareness Month in May, join us for a conversation about the role of connection and peer support in the lives of teens with alopecia areata. Led by behavioral health therapist, Mary Wills, MSW, LISW-S, this webinar will explore how friendships and shared experiences can support emotional well-being during adolescence. We’ll discuss how teens and young adults can support one another, build meaningful connections, and create spaces where they feel understood. Participants will also learn how peer support can strengthen resilience, the importance of healthy boundaries, and when it may be helpful to seek additional support. This webinar is intended for teens, young adults, and the adults who support them.