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Joyel Crawford

Legislative Advocate at National Alopecia Areata Foundation

Joyel Crawford, MBA, CPCC, PHR, is a seasoned keynote speaker, certified professional career coach, and HR learning and development expert, with over 20 years of experience. As the CEO and Founder of Crawford Leadership Strategies, LLC, Joyel motivates and inspires individuals to achieve their career and business goals, and is also a bestselling author of "Show Your Ask." Joyel serves as the inaugural member of the contributor's network for Black Enterprise Magazine, providing career advice through the "Ask Your Fairygodmentor®️" column. Additionally, Joyel is an active member of ForbesBLK, a legislative advocate for the National Alopecia Areata Foundation, and has held various guest speaking roles at notable organizations, including The New York Times and The Philadelphia Inquirer, focusing on professional development and leadership. Joyel holds an MBA from Fairleigh Dickinson University and a Bachelor of Arts in Psychology from Elon University.

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Philadelphia, United States

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National Alopecia Areata Foundation

The National Alopecia Areata Foundation (NAAF) serves the community of people affected by an autoimmune skin disease called alopecia areata that results in hair loss and emotional pain. NAAF is a 501(c)(3) nonprofit organization founded in 1981 and headquartered in San Rafael, CA. Our Federal Tax ID# is 94-2780249. Mission NAAF drives research to find a cure and accessible treatments for alopecia areata, supports those impacted, and educates the public about the disease. Governance NAAF is governed by a volunteer Board of Directors with advice from two Research Advisory Councils--the Basic Research Advisory Council and the Clinical Research Advisory Council. NAAF consistently meets or exceeds the rigorous standards of excellence for good governance and transparency set forth by the National Health Council and the Better Business Bureau Wise Giving Alliance. Programs To carry out our mission NAAF staff members serve our constituents in three primary program areas: support, awareness & advocacy, and research to find a treatment or cure. Highlights from each program area are presented in our award-winning Annual Reports and Newsletters. Vision And Values Our work with and for the community of people affected by alopecia areata -- including the family, friends, medical professionals, research scientists, biopharmaceutical developers and government representatives who care about them -- is informed by a Vision for each of our program areas that articulates what we aspire to as a result of our work together and ten Core Values that guide how we work together as a team to carry out our mission and move toward our vision.


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