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

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.

San Francisco, CA Virtual Support Meeting

Virtual Event

Thursday, May 16, 2024 | 7:30 PM, PDT

This support group is an ideal place to come and talk with others about living with alopecia areata. It is the place to gain knowledge from those who have had years of experience. With time comes the ability to deal and cope with your own hair loss or that of a loved one. We are very fortunate that so many are willing to bring to the meetings their wisdom and advice to share in a direct but compassionate manner that reflects understanding and concern. The support group experience has its rewards for all who attend.

Minneapolis, MN In-Person Support Meeting

Richfield, Minnesota

Sunday, May 19, 2024 | 2:30 PM, CDT

This support group is an ideal place to come and talk with others about living with alopecia areata. It is the place to gain knowledge from those who have had years of experience. With time comes the ability to deal and cope with your own hair loss or that of a loved one. We are very fortunate that so many are willing to bring to the meetings their wisdom and advice to share in a direct but compassionate manner that reflects understanding and concern. The support group experience has its rewards for all who attend.

Sterling Heights, MI In-Person Support Meeting

Sterling Heights, Michigan

Tuesday, May 21, 2024 | 7:00 PM, EDT

This support group is an ideal place to come and talk with others about living with alopecia areata. It is the place to gain knowledge from those who have had years of experience. With time comes the ability to deal and cope with your own hair loss or that of a loved one. We are very fortunate that so many are willing to bring to the meetings their wisdom and advice to share in a direct but compassionate manner that reflects understanding and concern. The support group experience has its rewards for all who attend.

Additional Dates:  July 16  |  September 24 |  November 7

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, Katie Robberson, 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.

Philadelphia, PA Virtual Support Meeting

Virtual Event

Tuesday, May 28, 2024 | 7:00 PM, EDT

This support group is an ideal place to come and talk with others about living with alopecia areata. It is the place to gain knowledge from those who have had years of experience. With time comes the ability to deal and cope with your own hair loss or that of a loved one. We are very fortunate that so many are willing to bring to the meetings their wisdom and advice to share in a direct but compassionate manner that reflects understanding and concern. The support group experience has its rewards for all who attend.

NAAF Patient Conference 2024

Washington, D.C.

Thursday, June 27, 2024 | 12:00 PM, EDT

  • Special guests and knowledgeable speakers will offer inspiration.
  • Medical professionals will share valuable information and advice to better understand and manage alopecia areata.
  • Expert researchers will detail the latest findings of recent clinical trials and soon to be approved drugs coming to market!
  • Kids (5-17) will make new friends and wonderful memories at the Children’s Conference Camp.
REGISTER HERE

2024 Conference Sponsors

     SANOFI  MATTEL  NEKTAR    AbbVie