At NAAF, we know that the lived experiences of people with alopecia areata are essential to advancing research, improving care, and shaping meaningful support, resources, and treatments. We are inviting members of our community to join NAAF’s Lived Experience Network. By sharing your information, you may be considered for opportunities such as focus groups, interviews, patient advisory panels, content review, media opportunities, and other engagements that help inform our work and that of our partners. Please note we are only accepting participants in the U.S. at this time. Some opportunities are compensated, while others are volunteer. Participation is always optional, and you can decide which opportunities are right for you. If you would like to be considered, please take a few minutes to complete this form. Your insights can help researchers, healthcare providers, industry partners, and advocates better understand the real-world impact of alopecia areata and identify ways to improve the lives of those affected by the disease.
