Watch & Learn

NAAF has a wide variety of resources to increase awareness and understanding of alopecia areata, including educational webinars, patient videos and inspiring community voices. We hope these videos, webinars and stories not only leave you better informed but empowered as well.

Alopecia Areata Patient Videos

We can always learn and gain confidence from those who have shared similar experiences to our own. These videos feature a diverse group of alopecia areata community members sharing their life’s highs and lows, and their advice to others who are also going through journeys not unlike their own.

Community Voices

If there was one thing you could tell your friends about alopecia areata, what would it be?  What’s one thing you would like to tell your dermatologist, parents, co-workers, or classmates? NAAF asked our community these very questions and we hope you’ll find these patient perspectives both candid and informative. And if you’re an alopecia areata patient, you may find your experience is similar to that of the patients featured here. Learn how you can share your voice.

Webinars

NAAF is pleased to offer free webinars in the You Are Not Alone: Education and Empowerment Webinar Series. We recognize the crucial need for the patient community to interact with medical professionals and experts with experience on topics specific to alopecia areata. These webinars cover a variety of relevant topics presented by a diverse set of speakers that will empower and educate community members wherever they are on their journey with alopecia areata.

NAAF gratefully acknowledges the support provided for the You Are Not Alone: Education and Empowerment Webinar Series from our partners.

Upcoming Webinar

Novel developments in treating alopecia areata: What is Type 2 inflammation and why is it important? WEDNESDAY, JULY 17, 2024 – 7PM ET/ 6PM CT/ 4PM PT Have you ever wondered how eczema, allergies, and inflammation might be linked to…

Patient Voices: Alopecia areata clinical trial experiences

Have you wondered what it’s like to participate in a clinical trial? This webinar features 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…

Making Alopecia Areata Work at Work: My Personal Journey

Award winning career coach, best-selling author and 2023 NAAF Conference Opening Session Speaker- Joyel Crawford shares her personal journey of navigating alopecia areata in the workplace. Despite the challenges, she turned her diagnosis into an opportunity for growth and empowerment. Through…

Dating with Alopecia

Dating can be challenging for anyone. After an alopecia areata diagnosis, it is often scary and overwhelming. In this webinar, licensed psychotherapists, Alison Mann and Donna Astor-Lazarus, will discuss how to overcome common obstacles such as anxiety and negative body…

What’s New In Pediatric Alopecia Areata Treatment?

In 2023, the FDA approved the first treatment for alopecia areata in adolescents. Pediatric dermatologist Brittany Craiglow, MD, will bring us up to date on alopecia areata in children and the current treatment landscape.  Note on clinical trials: Dr. Craiglow…

Men & Alopecia Areata: Our unique experiences

It’s time to talk about how alopecia areata affects men. Hear from a group of men to learn about some of the challenges they have faced living with this disease. This webinar was moderated by NAAF Board member, Tyrone Folliard-Olson,…