Devoted to kids living with Alopecia

We are the only non-profit devoted specifically to helping children living with the hair-loss disease, alopecia areata. We do so by raising awareness about alopecia, providing support for children and their families, and building self esteem in children living alopecia.

The Kid's wig tour started when their daughter Maddie (then 5) was diagnosed with alopecia. They could not find a support group specifically for kids with alopecia. They were interviewed about this in the local newspaper and based on the overwhelming response and with the help of family and friends started the kid’s wig tour project.

“Every dollar I raise is going to the Kid's wig tour, a non-profit organization dedicated to localized support, events, and resources to help ...”

Khoda Ivy Carter

Diagnosis: Alopecia
Location: Birmingham, Arkansas

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Camilla

Diagnostic: Leukemia
Location: Jacksonville, FL

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Kennedy

Diagnosis: Alopecia
Location: Flint, Michigan

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Kelsi

Diagnosis: Alopecia
Location: Helena, Arkansas

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Skye

Diagnosis: Alopecia
Location: Bowling Green, Kentucky

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Mayah

Diagnosis: Alopecia
Location: North Carolina

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Monae

Diagnosis: Alopecia
Location: Philadelphia, PA

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Maleiya

Diagnosis- Alopecia
Location: Pensacola, FL

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Riley

Diagnosis: Alopecia
Location: Baltimore, MD

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Aniyah

Diagnosis: Alopecia
Location: Memphis, TN

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Mila

Diagnostic- Alopecia Location: Sacramento, CA

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Akairah

Diagnosis: Alopecia
Location: Baton Rouge

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Children's Alopecia Project 

FAQ

Devoted to kids living with Alopecia

U.S. | Texas

10Midway Rd, Suite 220, Carrollton, TX 75007

Germany

Torstr. 111, Vorderhaus, 1. OG, 10222 Berlin

India

Corporate Edge, Suite #3020, DLF Epitome, Cyber City

Israel

Yigal Alon 11a, Alon Tower 1, 4rd Floor – Be All Offices

U.S. | Texas

10Midway Rd, Suite 220, Carrollton, TX 75007

Germany

Torstr. 111, Vorderhaus, 1. OG, 10222 Berlin

India

Corporate Edge, Suite #3020, DLF Epitome, Cyber City

Israel

Yigal Alon 11a, Alon Tower 1, 4rd Floor – Be All Offices