Equity in AA Care: Stories and Insights in Alopecia Areata is a multi-part video series that explores the experience of alopecia areata from diagnosis to treatment access, and the policy environment. We brought together patients and physicians to discuss how delays in diagnosis, often due to misconceptions or dismissal, can have lasting emotional and clinical consequences. Join Nicole Friedland, Head of NAAF, Dr Brittany Craiglow, Alopecia Areata advocate Georgia Van Cuylenburg and mother and son Joanna and Elliot Rosen to hear their stories of why early diagnosis of alopecia areata is essential and how timely, compassionate care can transform lives.

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