Our Movement Needs You Make a generous gift in support of the alopecia areata movement before December 31 and it will be matched up to $25,000! GIVE NOW Our Thanks to You! You can still help by making a contribution to the Walk For Alopecia today in support of research and services! LEARN MORE New Wig Reimbursement Resource Tips and tools to help you advocate for insurance coverage, including filing claims and appealing denials. LEARN MORE Help for Today, Hope for Tomorrow Help the alopecia areata community now and for years to come. We are excited to announce our partnership with FreeWill, a complimentary online tool designed to help with your estate planning. You can help support alopecia research, support, and awareness by directing a gift to NAAF through your will or estate plan.. LEARN MORE Find a Youth Mentor NAAF’s Youth Mentor Program connects children living with alopecia areata to dedicated young adult mentors to formulate lasting bonds while providing support and guidance on dealing with the day-to-day challenges stemming from alopecia areata. LEARN MORE New Wig Resource Buy 1/Give 1 opportunity thanks to C&S Fashions LEARN MORE I am... Choose one Newly Diagnosed Looking For Help Working on Research Raising Awareness Making a Donation Interested in Advocacy Looking for Ways to get Involved 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. Get Support How can we help? Choose one I need help I'm newly diagnosed I’m not sure where to start Latest News #News LEQSELVI™ Commercial Launch Indefinitely Delayed Due to Patent Ruling This past July, the U.S. Food and Drug Administration (FDA) approved LEQSELVI™ (deuruxolitinib) for alopecia areata, making it the third… Learn More #Advocacy 2nd Annual Walk For Alopecia Exceeds $900,000 Goal The National Alopecia Areata Foundation (NAAF) is proud to announce its 2nd Annual Walk For Alopecia™ has exceeded its $900,000… Learn More #News Challenges in Alopecia Areata and Opportunity to Drive Change Last year, Nicole Friedland, NAAF President and CEO, participated in an expert steering committee, the Alopecia Areata Consensus Task Force,… Learn More #News FDA Approves LEQSELVI™ for Adults with Severe Alopecia Areata Today, the U.S. Food and Drug Administration (FDA) approved LEQSELVI™ (deuruxolitinib) for alopecia areata, marking the third FDA-approved treatment for… Learn More #News NAAF Awards New Research Grants NAAF awards research grants to researchers with promising proposals to learn more about alopecia areata – what is happening in… Learn More #Enews Exciting New Wig Resource for the Alopecia Areata Community NAAF is thrilled to announce a new collaboration with C&S Fashions Inc., a company that has been at the forefront… Learn More #News Wig Bills Make Progress in California and New York This past February, California Assembly Member Marc Berman (D-Menlo Park) introduced AB 2668 – Health Insurance Coverage for Wigs. This… Learn More #News NAAF Applauds NIH Award to Mount Sinai for Alopecia Areata Research The National Alopecia Areata Foundation applauds the announcement that the National Institutes of Health (NIH) has awarded a $6.6 million… Learn More #News NAAF Team Attends American Academy of Dermatology Meeting in San Diego Members of the NAAF team represented the organization and the alopecia areata patient community at the 2024 Annual Meeting of… Learn More #News Dr. Brett King to Speak at NAAF Conference It was June 2014 when the electrifying news came out of Yale University that a dermatologist named Brett King saw… Learn More #Webinars Upcoming Webinar Identity and self-acceptance with alopecia areata: A community panel discussion THURSDAY, JANUARY… Register Now! Get Involved 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… Learn More Support Groups Join A Support Group After an alopecia areata diagnosis, it is important to realize that you are not alone. NAAF… Learn More 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… Learn More NAAF Youth Mentor Program Have you heard of the NAAF Youth Mentor Program? Do you have a child or teen with alopecia areata between… Learn More Research I am interested in... Clinical Trials Webinars Research Grants Health and Research Ambassadors Resources I am interested in... Patient Videos Webinars Alopecia Areata School Guide Emotional Wellness Support Groups NAAF's Annual Conference Doctor Finder 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 Sign up to be an Advocate! Sign up Welcome to the NAAF Website
