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Effective URL: https://www.naaf.org/
Submission: On May 21 via api from DK — Scanned from DK
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Skip to content Register Now for NAAF's 39th Annual Patient Conference June 27-30, 2024 in Washington, D.C.! * Alopecia Areata * Be An Advocate * News * Patient Conference * Medical Professionals * Doctor Finder * * Alopecia Areata ALOPECIA AREATA * Alopecia Areata * Symptoms and Diagnosis * Alopecia Areata Types * Alopecia Areata Treatments * Related Conditions * Living with Alopecia Areata * Alopecia Areata in Children * FAQs * Glossary * Resources For… * Newly Diagnosed * Parents & Children * Youth & Teens * Adults * School Staff * Medical Professionals * Watch & Learn * Videos * Community Voices * Webinars * Our Community * Events * Be An Advocate * Get Involved * Support SUPPORT * Get Support * Join A Support Group * NAAF Youth Mentor Program * Patient Conference * One-on-One Phone Support * Support for Parents * Resources For… * Doctor Finder * Insurance Reimbursement * NAAF Patient Brochures * Brave Barbie * Wig Resources * Watch & Learn * Videos * Community Voices * Webinars * Our Community OUR COMMUNITY * Events List * Conference * Support Groups * Fundraiser * Awareness * TeamUp * Webinars * Watch & Learn * Videos * Community Voices * Webinars * Get Involved GET INVOLVED * Donate * Donate Online * Donate by Mail * Send a Wire Transfer * Donate Stock * Legacy Giving * Employer Matching * Workplace Giving * Donate a Vehicle * Take Action * Make Your Voice Heard! * Be An Advocate * Contact Your Representatives * NAAF Legislative Liaison Program * NAAF Legislative Mentor Program * NAAF Legislative Agenda * Alopecia Areata Awareness as Advocacy * Advocacy in Schools * Alopecia Areata Awareness Month * Volunteer * Be a NAAF Conference Volunteer * Be a NAAF Support Group Leader * Be a NAAF Youth Mentor * Be a NAAF Telephone Support Contact * Health and Research Ambassador Program * Fundraising & Awareness * Walk For Alopecia™ * Find a Fundraiser * Start a Fundraiser * Facebook Fundraisers * TeamUp * Third Party Events * Treatments TREATMENTS * Treatments Overview * Available Treatments * Approved Treatment FAQs * Insurance Reimbursement * Resources * Doctor Finder * Living with Alopecia Areata * Insurance Reimbursement * FAQs * Watch & Learn * Videos * Community Voices * Webinars * Research RESEARCH * Our Research * Funded Research * Research Summits * For Researchers * Research Grants & Awards * Clinical Study Recruitment * Participate in Research * Clinical Trials & Research Studies * Health and Research Ambassador Program * Watch & Learn * Webinars * Community Voices * Videos * Donate WE ARE STRONGER TOGETHER! The annual National Alopecia Areata Foundation Conference is the largest gathering of the alopecia areata community in the world…and you are invited! READ MORE SUPPORT THE FUTURE OF ALOPECIA AREATA RESEARCH AND SERVICES 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 FDA APPROVES LITFULO™ (RITLECITINIB) FOR ADULTS AND CHILDREN AGES 12+ WITH SEVERE ALOPECIA AREATA Learn about the second U.S. Food and Drug Administration (FDA) approved treatment for alopecia areata. 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 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 #Enews NAAF GRANTS: STUDENT INTERNSHIP AWARDS AND TRAVEL GRANT APPLICATIONS NOW OPEN Applications for Student Internship Awards for 2024 are now open. These awards support students (undergraduate, graduate, or medical), residents, or… Learn More #Enews WE ARE STRONGER TOGETHER! Wherever you or your loved one is on their journey with alopecia, we are strongest when we come together as… Learn More #News ALOPECIA AREATA RESEARCH DEPENDS ON CLINICAL TRIAL VOLUNTEERS Media reports of two newly approved drugs for treating alopecia areata brought good news to many people living with the… Learn More #News NAAF APPLAUDS NIH AWARD TO MOUNT SINAI FOR ALOPECIA AREATA RESEARCH Emma Guttman-Yassky, MD, PhD The National Alopecia Areata Foundation applauds the announcement that the National Institutes of Health (NIH) has… 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 #Advocacy NAAF’S YOUNGEST LEGISLATIVE MENTOR SCORES SUCCESS Stephanie Milewski, age 12, signed up to be a Legislative Mentor (a legislative advocate under voting age) this past November…. Learn More #News AZIZA SHULER TO SPEAK AT NAAF PATIENT CONFERENCE THIS JUNE Emmy Award-winning CBS Philadelphia and Reporter Aziza Shuler will be the closing speaker at NAAF’s Patient Conference in Washington, DC,… Learn More #News NAAF ADDS TWO NEW BOARD MEMBERS NAAF is proud to announce that David Granson and Lisa Bard Levine, MD, MBA,… Learn More #Advocacy NIAMS LEADERSHIP MEETS WITH NAAF Key leaders of the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) met with NAAF President & CEO,… Learn More More News #Webinars PATIENT VOICES: ALOPECIA AREATA CLINICAL TRIAL EXPERIENCES WEDNESDAY, MAY 22, 2024 – 7PM ET/ 6PM CT/ 4PM PT Have… Register Now! More webinars GET INVOLVED 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 AWARENESS MONTH PARTNERS This Alopecia Areata Awareness Month, NAAF wishes to thank the following vendors, businesses and individuals who are Awareness Month Partners… Learn More 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 More ways to get involved. 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 OUR IMPACT 116K Community members across the United States $5.7M Spent by NAAF for funding research 921 Meetings with State Legislators SIGN UP TO BE AN ADVOCATE! Sign up WELCOME TO THE NAAF WEBSITE Video Player is loading. Play Video PlaySkip Backward Mute Current Time 0:00 / Duration 0:52 Loaded: 0.00% 0:00 Stream Type LIVE Seek to live, currently behind liveLIVE Remaining Time -0:52 1x Playback Rate Chapters * Chapters Descriptions * descriptions off, selected Captions * captions settings, opens captions settings dialog * captions off, selected Audio Track Picture-in-PictureFullscreen This is a modal window. Beginning of dialog window. Escape will cancel and close the window. TextColorWhiteBlackRedGreenBlueYellowMagentaCyanOpacityOpaqueSemi-TransparentText BackgroundColorBlackWhiteRedGreenBlueYellowMagentaCyanOpacityOpaqueSemi-TransparentTransparentCaption Area BackgroundColorBlackWhiteRedGreenBlueYellowMagentaCyanOpacityTransparentSemi-TransparentOpaque Font Size50%75%100%125%150%175%200%300%400%Text Edge StyleNoneRaisedDepressedUniformDrop shadowFont FamilyProportional Sans-SerifMonospace Sans-SerifProportional SerifMonospace SerifCasualScriptSmall Caps Reset restore all settings to the default valuesDone Close Modal Dialog End of dialog window. NAAF supports research to find a cure or acceptable treatment for alopecia areata, supports those with the disease, and educates the public about alopecia areata. NAAF 65 Mitchell Blvd., Suite 200-B San Rafael, CA 94903 For donations and payments: NAAF PO Box 1270 Suisun City, CA 94585 Phone: 415-472-3780 Email: info@naaf.org NAAF * About NAAF * Strategic Plan * Our Partners * Our Staff * Board of Directors * Research Advisory Council * Scientific & Medical Advisory Task Force * Financial Information * Policies RESOURCES * Support * Newly Diagnosed * Parents & Children * Youth & Teens * Adults * School Staff * Medical Professionals * Doctor Finder Candid Seal BBB NHS Charity Navigator YouTube Twitter Facebook Instagram NAAF ©2024 | Privacy Policy | Terms & Conditions Donate! Stay Connected! GET THE LATEST NEWS! Stay informed about treatments, upcoming events, advocacy and more. "*" indicates required fields Email* Address* ZIP / Postal Code Name This field is for validation purposes and should be left unchanged. Notifications