Upcoming Webinar

Have you ever been asked to fill out a survey about what it’s like to live with alopecia areata — for you or your child? When you share how this disease affects your daily life and how it makes you feel, your answers do more than just sit in a file — they become part of important research. Every story and every survey helps researchers better understand the real impact of alopecia areata.

Join Dr. Arash Mostaghimi and Samantha Gregoire as they talk about their research, inspired by the alopecia areata community. They’ll explain how your experiences and voices are driving progress toward better care and a better understanding of this autoimmune disease.