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.

All Dates

#Webinars

Patient Voices: Alopecia areata clinical trial experiences

Virtual Event

Wednesday, May 22, 2024 | 4:00 PM, PDT

WEDNESDAY, MAY 22, 2024 – 7PM ET/ 6PM CT/ 4PM PT

Have you wondered what it’s like to participate in a clinical trial? This webinar will feature a panel of alopecia areata community members talking about their clinical trial experiences. What factors influenced their decision to join a trial? What was participation like? How do they feel about contributing to alopecia areata treatment development?

Panelists Brandi Meyer, April Noel, and Sandra Kelberlau will discuss their paths to joining a clinical trial and how that decision has impacted living with alopecia areata for them. Dermatologist Dr. Tiffany Mayo will join the panel to answer medical questions.

Join the webinar to learn more and get answers to your questions.