Patient Conference

This unforgettable experience will connect you with a network of people who share similar challenges to those you may face. Special guests and speakers will offer inspiration, professional caregivers will share medical information and advice to better understand and manage alopecia areata, and expert researchers will detail the latest findings of NAAF’s Treatment Development Program. A panel of researchers and representatives of companies pursuing or producing treatments will provide the extraordinary opportunity to directly address questions to the very people most intimately involved in the search for treatments and a cure for alopecia areata.

The Children’s Conference Camp supports children with alopecia areata by nurturing their self-esteem through carefully planned activities by the Corporate Kids Events (CKE) team. Support arises spontaneously as the kids interact with others who have alopecia areata, as well as their siblings and friends, in a fun, creative, and active environment. Kids, Tweens and Teens are sure to adapt quickly and make new friends and wonderful memories. Creative arts and activities are interspersed throughout the weekend.

We hope you can join us for this uniquely wonderful experience!

You will: 

• Learn you are not alone.
• Hear about the latest research progress and opportunities for your involvement.
• Share personal connections with people who understand and care.
• Learn about useful products for people with alopecia areata.
• Exchange ideas, support, and advice.
• Enjoy inspiring sights, stories, and experiences.
• Develop personal memories that will last a lifetime.
• Become empowered to go home and make a difference.

SAVE THE DATE for our 2023 Conference in Denver, Colorado – June 30 – July 2, 2023!

View the slideshow below from our 2022 Conference in Washington, D.C.