The Annual NAAF Conference is the largest gathering of the alopecia areata community in the world! Whether you were newly diagnosed, have lived with alopecia areata for some time, are seeking support, or want to learn more for a loved one, this conference is for you. 41st Annual NAAF Conference June 25-28, 2026 • Orlando, FL Complete an Interest Form to be the first to know when registration opens for the 41st Annual NAAF Conference to take advantage of our Early Bird rate! Complete an Interest Form Sessions This life-changing event brings together scientific and medical professionals to discuss advancements in research and treatments, as well as inspirational speakers and subject matter experts to share their knowledge to empower community members on how to live their best life with alopecia areata. Session themes include: Treatment & Research Support Groups Parents & Family Social Activities Wigs & Camouflage Education & Empowerment New in 2026! The 41st Annual NAAF Conference will feature new and enhanced programming based on feedback from our community, including sessions for: Individuals with skin of color living with alopecia areata Young adults with alopecia areata aged 18-30 years old Parents of children with alopecia areata Community members living with mild to moderate alopecia areata An example Conference at a Glance Schedule can be found here. Sessions, speakers, panelists, and social activities vary from year to year. If you would like to recommend a session topic and abstract for a session you will present, please complete this Annual NAAF Conference Call for Presentations form. Youth Camp NAAF’s Youth Camp is designed for children and adolescents ages 5-17 who are living with alopecia areata or have a loved one with the condition. Camp participants are divided into three age groups: 5–10-year-olds, 11–13-year-olds, and 14–17-year-olds. Age-appropriate programming, including activities, games, and field trips are thoughtfully planned and executed by NAAF staff and Corporate Kids Events (CKE) with your children’s fun, safety, and self-esteem in mind. An example Youth Camp schedule can be found here. Activities, times, and special guests vary from year to year. First Time Attendees To make the conference experience possible for the alopecia areata community, first-time attendees are eligible for financial assistance to help cover expenses such as registration and lodging. In addition, first-time attendees will be connected with a Conference Ambassador. For more information, contact us at conference@naaf.org. Walk For Alopecia™ Kickoff Lunch Each year at the Annual NAAF Conference, we kick off the Walk For Alopecia, the world’s largest fundraising and awareness campaign for alopecia areata. All attendees are encouraged to attend this high-energy session, which includes a complimentary lunch, inspirational speakers, and exciting surprises. Learn more about the Walk For Alopecia here. Exhibitors We welcome exhibits from pharmaceutical companies and other businesses with FDA-approved treatments for alopecia areata, as well as companies and individuals promoting books and materials to empower individuals living with alopecia areata, wigs and headscarves, and cosmetic solutions to manage living with alopecia areata. Pharmaceutical, biotechnology companies and research institutes should contact Robbie Baker, Chief Growth Officer, at robbie@naaf.org. All other commercial businesses (e.g., wigs, headscarves, and makeup/camouflage) and individuals interested in exhibiting at the NAAF Annual Conference should complete a 2026 Conference Interest Form. Space is available on a first-come basis. Complete an Interest Form Sponsorship Opportunities Please contact Robbie Baker, Chief Growth Officer, at robbie@naaf.org if you are interested in sponsorship opportunities for the Annual NAAF Conference. Change a Life Today Want to share the powerful experience of the patient conference with a member of the alopecia areata community for whom cost is an obstacle? Generous donations from friends like you have made it possible for more than 2,000 individuals with alopecia areata to attend this conference over the past 30 years. You can change a life today by making a gift to our financial assistance fund that will provide the help, hope, and sense of belonging that comes from attending the conference. No matter what amount you are able to give, we are grateful!. Make a Donation
