Wigs For Kids Equals Family

November 16, 2017

No matter the why, life with hair loss can be difficult. From bullying to losing your confidence, these four girls have continued their journey of looking themselves and living their lives through the help of Wigs for Kids. From the very beginning, each recipient is taken in as family and provided with the love and support to help boost their confidence again.

If you or a loved one is experiencing hair thinning or hair loss, learn more about solutions available to you on the Jeffrey Paul Blog.

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Minka Finds Joy on the Ice

Minka is 8 years old and in the second grade. She begin to experience hair loss at the age of 7 months old. Minka’s hair loss is caused by an auto-immune disease called alopecia. Minka can often be found gliding on the ice — this young girl is an accomplished figure skater, winning first place […]

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Cara Is An Inspiration to Her Classmates, Friends & Family

Cara was diagnosed with Alopecia Universalis when she was four years old. At the beginning she wore a hat to conceal her hair loss. Years later Cara’s mom learned about Wigs for Kids through a support group, and Cara received her first wig at the age of eight. Cara is now ten years old and […]

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Emily & Wiggala — BFFs

Emily first became part of the Wigs for Kids family when she was nine years old. She was diagnosed with alopecia. Initially Emily had bald spots the size of a quarter and by the age of 12 and in the sixth grade, she had lost all of her hair. Emily was fitted with a hairpiece […]

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About Wigs For Kids

Wigs For Kids is a nonprofit organization that helps children experiencing hair loss stemming from chemotherapy, radiation therapy, alopecia, trichotillomania, burns, and other medical causes. Stylists and regular people just like you work together to give recipients the self-esteem and self-image they deserve.

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