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Walk For Alopecia Exceeds $1.2M Fundraising Goal

Thank you and congratulations to the alopecia areata community for helping us reach this incredible milestone and bringing greater awareness to this autoimmune disease. There is still time to donate to the Walk For Alopecia Presented by Pfizer to make an even greater impact and help drive the NAAF mission forward.

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September is Alopecia Areata Awareness Month

Learn how you can increase awareness, reduce stigma, and empower those living with alopecia areata locally and nationally.

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Brave Barbie & Brave Ken Bring Joy to Children with Alopecia Areata

NAAF distributes Brave Barbie and Brave Ken through multiple in-person activities including the Walk For Alopecia, Annual NAAF Conference, and local NAAF support groups.

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Accepting Applications: Teen Advocacy Fellowship

NAAF's Teen Advocacy Fellows program empowers our young adult community members to share their stories with policymakers to create change for the nearly 7 million Americans affected by alopecia areata. Sign up by October 31 to join the inaugural class of Fellows led by Volunteer Coordinator Abby TerHaar.

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2026 Conference Registration Opens Soon

Registration will open in October for the 41st Annual NAAF Conference and Youth Camp in Orlando, FL, on June 25-28. Complete an interest form today to be the first to know when the registration opens to take advantage of the Early Bird rate — our lowest price!

Join Us in 2026

NEW! Treatment & Insurance Navigation Toolkit

Designed to empower individuals and families to navigate their treatment journey, this toolkit includes current information, practical strategies, and helpful resources about treatments, commercial insurance, and more.

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A woman is indoors in a hospital room. Her head is shaved due to chemotherapy. She is listening to her doctor give a prognosis.

Keira's family found hope, resources, and community with NAAF.

Your gift will help continue providing support to families when they need it most, as well as fund research to advance more treatments for alopecia areata.

DONATE TODAY

Youth Apparel is Now Available in the NAAF Swag Store

Your entire family can show their love for NAAF and raise awareness! Youth apparel in sizes YXS-YXL is now available in the NAAF Swag Store, including T-shirts, baseball tees, long-sleeved shirts, sweatshirts, and sweatpants. Proceeds from every sale support the NAAF mission.

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Help the Alopecia Community for Years To Come

Secure your future and build a lasting legacy for NAAF. Create a plan to protect the people and causes you love with this free estate planning tool.

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What is Alopecia Areata?

Alopecia areata is a common autoimmune disease, causing sudden hair loss on the scalp, face, and sometimes other areas of the body. There are different levels of alopecia areata severity. The three main types of alopecia areata are patchy, alopecia totalis (total hair loss on the scalp), and alopecia universalis (total hair loss on the body).

Learn the facts.

Latest News

#News

Board of Directors Announces Retirement of NAAF President & CEO Nicole Friedland, Leaving a Lasting Legacy of Positive Mission Impact

The Board of Directors of the National Alopecia Areata Foundation (NAAF) announced today that Nicole Friedland will retire as President…

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#Research

NAAF Student Internship Awardees Publish Research on Alopecia Areata

The National Alopecia Areata Foundation (NAAF) is thrilled to report that two recent Student Internship Awardees have had their NAAF-supported…

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#Research

LEQSELVI (Deuruxolitinib) Now Available in U.S. for Adults with Severe Alopecia Areata

Sun Pharmaceutical Industries Limited (Sun Pharma) today announced LEQSELVI™ (deuruxolitinib) is now commercially available for the treatment of severe alopecia…

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#News

Armani Latimer Inspires the Alopecia Areata Community

Where Is DCC’s Armani Latimer Now? All About the Cheerleader’s Life After Hanging Up Her Uniform Armani Latimer, a retired…

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#Advocacy

NAAF President & CEO Nicole Friedland and NAAF Board of Directors Member Brett King, MD, PhD, Spotlighted by the University of California, Santa Cruz

UC Santa Cruz alumni at the forefront of alopecia research and advocacy NAAF President & CEO Nicole Friedland and NAAF…

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#News

NAAF Speaker and Advocate Abby Andrew Shares About Her Alopecia Journey with Health

Alopecia Gave Me the Freedom to Be Whoever I Want Abby Andrew, a NAAF speaker and advocate, shares her alopecia…

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#News

NAAF Board of Directors Member Shamsha Damani Writes About Her Alopecia Journey for Health

What I Wish I Knew About the Importance of Meeting Others With Alopecia Areata Shamsha Damani, a NAAF Board of…

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Researcher and patient #News

Q32 Bio Receives Fast Track Designation for Investigational Treatment for Alopecia Areata

Q32 Bio announced that it has received a Fast Track designation for bempikibart, its investigational treatment for alopecia areata (AA),…

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Gavel #News

Sun Pharma’s LEQSELVI Released From Patent Litigation Hold

There was good news for Sun Pharmaceutical Industries, Ltd. (Sun Pharma) and the alopecia areata community in the form of…

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Headshots of Award Recipients #Research

Announcing NAAF’s Newest Grant Recipients

NAAF is thrilled to announce the recipients of the 2024 Early Career Awards and Research Grants! Three investigators have been…

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#Webinars

Upcoming Webinar

Through Our Eyes: The Sibling Experience of Alopecia Areata WEDNESDAY, OCTOBER 22,…

Register Now!

Get Involved

volunteers at NAAF alopecia areata conference

Be a NAAF Conference Volunteer

Become a NAAF Conference Volunteer NAAF is always looking for enthusiastic volunteers for our annual alopecia areata patient conference. We…

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Support Groups

Join A Support Group After an alopecia areata diagnosis, it is important to realize that you are not alone. NAAF…

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One-on-One Phone Support

Would you like some one-on-one phone support? NAAF can help you with that. There are several things you can do…

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NAAF Youth Mentor Program

Have you heard of the NAAF Youth Mentor Program? Do you have a child or teen with alopecia areata between…

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Impact

7M

Americans affected by alopecia areata

Research

Largest non-profit funder of alopecia areata research in the world

40+

Years as the VOICE of the alopecia areata community

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