Children's Alopecia Project

The Children’s Alopecia Project (CAP) is a nonprofit organization dedicated to supporting children with alopecia by building self-esteem, confidence, and community. CAP provides programs, resources, and events designed to help kids with alopecia feel connected, empowered, and understood.

Through national camps like Alopeciapalooza and local support groups, CAP creates opportunities for children and families to connect with others living with alopecia. CAP also promotes alopecia awareness and education through initiatives like the CAP2U Speaking Tour, helping schools and communities better understand alopecia and support inclusivity.

The Children’s Alopecia Project is committed to helping kids with alopecia feel seen, supported, and confident just as they are.

Support CAP Kids

WE BRING CAP2U

THE CAP2U SPEAKING TOUR

To have Jeff Woytovich speak at your child’s school during a CAP2U Speaking Tour or to make a house visit with a Bag of Books for your CAP Kid to donate to their school library, click a link below.

CAP2U TOUR

Donate Today

THE CAP MISSION

To help any child in need who is living with hair loss due to all forms of Alopecia. We change the emphasis from growing hair to growing confidence. building self-esteem, providing support, and raising awareness.

– Jeff Woytovich, Founder

Our Mission

What a Wonderful Camp!

Another Successful Alopeciapalooza camp in Indiana!!

Join Us Next Year!

OUR GOALS

You are more, even if your hair is less.

Confidence
Know that you are perfect the way you are. You are an original, not a copy.
Self-Esteem
It is normal to be different because everyone is different, and that makes you normal.
Support
If one person has alopecia in your family, you all have alopecia.

CONNECT WITH US

We have more than 50 Local CAP Groups throughout the Country and World.

Find a place for you to get connected and get the support you or your CAP kid needs.

FIND YOUR SUPPORT

Donations are always needed!

#CapKidAppeal

Donate and change a life! The mission of CAP is to help all children with alopecia, and we will continue do everything in our power to keep CAP Kids free at all Alopeciapalooza, programs, and events. The best part about what we do is that it’s not just for the child/teen with alopecia. The best thing is that what we do is help the entire family because when one person has alopecia in a family, the whole family has to deal with it and at CAP, we deal with the whole, wonderful family!