African American Wigs partners with National Alopecia Areata Foundation

HUMBLE, Texas - EntSun -- NAAF Ascot Fund

NAAF's Ascot Fund puts hair prostheses within reach! This special program was established thanks to an anonymous donor who wished to help adults and children with alopecia areata purchase a hairpiece. A small number of organizations offer assistance for hairpieces and wigs to children but not to adults, making this program the first we know of its kind. Over one hundred individuals have benefited from the fund since the start of the program in January 2004.

You are eligible for the Ascot Fund if you meet the following requirements:

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• have been diagnosed with alopecia areata by a dermatologist or doctor,
• are unable to purchase a hairpiece due to financial challenges,
• are not already in possession of the hairpiece shown on the application,
• have not already paid for the full balance of the cost of the hairpiece.
  
  (The Ascot Fund is a pre-purchase program; reimbursements are not provided for any purchases paid in full either by credit card or other financial means).

The maximum amount awarded is $500. The applicant needs to be able to pay any balance beyond the award amount.

Please call NAAF at 415-472-3780 and ask them about the ASCOT Scholarship.

To receive assistance in ordering your wig, please contact us at African American Wigs, 800-277-3710

About African American Wigs

African American Wigs is a black owned & USA based wig store. Shop the highest density human hair wigs and quality hair wigs for black women, hair extensions, closures, frontals and braiding hair.

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About NAAF

The National Alopecia Areata Foundation (https://www.naaf.org) (NAAF) serves the community of people affected by an autoimmune skin disease called alopecia areata that results in hair loss and emotional pain. (https://www.youtube-nocookie.com/embed/EP9o26gs...) 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 supports research to find a cure or acceptable treatment for alopecia areata, supports those with the disease, and educates the public about alopecia areata.