CAP Kid Group Socalla

CAP Kid Group Socalla We want to build self-esteem, provide support and raise awareness. It's that simple! Build Self-Esteem
2. Provide Support
3. It is not contagious.

What we want to do is simple when compared to finding a cure or the first FDA-approved treatment that works!

1. Raise Awareness

These are the most important things CAP does on a daily basis. We will continue and with your support, we will move forward making a difference in the life of a child and their family. We can't fix everything but we try every time!
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Welcome! Alopecia is an autoimmune disease that is not life-threatening but is life-altering. You can't catch it and it does not hurt. It is almost like your body is allergic to hair, which causes it to fall out. If you are in need of Alopecia advice and coaching, contact our CAP Kid Family Advocate, Deeann Graham at [email protected]

The main page is at Facebook.com/ChildrensAlopeciaProject so don't forget to like us! The Mission of the Children's Alopecia Project is to help any child in need living with hair loss due to all forms of alopecia. Jeff Woytovich, Founder
www.ChildrensAlopeciaProject.org


We want to build self-esteem, provide support and raise awareness.

06/16/2026

No matter where you live, if you have a child living with any type of Alopecia, you have a CAP Kid!! We change the emphasis from growing hair, to growing confidence, building self-esteem, providing support and raising awareness! Help us by visiting ChildrensAlopeciaProject.org and share Children's Alopecia Project with everyone on Facebook!

06/12/2026

Don’t miss out. Three camps left in 2026. Alopeciapalooza.org (8/7/26- 8/10/26), CapKidCampPacificNorthwest.org (10/2/26-10/4/26), and CapKidCampNewYork.org (10/9/26 -10/11/26)

CAP APPROVED: A Paid Online Survey for Parents of 12-17-year-old Children Living with Alopecia. Brox AI, a U.S.-based su...
06/05/2026

CAP APPROVED: A Paid Online Survey for Parents of 12-17-year-old Children Living with Alopecia. Brox AI, a U.S.-based survey company, is seeking parents and caregivers of children (ages 12–17) with alopecia areata living in the U.S. This survey is commissioned by one of the world’s largest pharmaceutical companies, which seeks to understand the real experiences of children with alopecia areata and to improve treatment and care for them. This online survey takes about 1 hour, and upon successful completion, you will receive a $50 online gift card of your choice (VISA, Amazon, Walmart, Starbucks, and more). Go to

General Information

CAP Kid Group Get-Togethers around the country will be announced soon for May through December. We are starting in PA an...
04/25/2026

CAP Kid Group Get-Togethers around the country will be announced soon for May through December. We are starting in PA and ending in CA. The NuGo CAP Van is ready to go! Keep your eyes peeled for more announcements!

04/15/2026

Registration is open and waiting for you to register your CAP Kid and the rest of your family for the best four day weekend of the year for building self-esteem and bonding with families from around the United States and world! Alopeciapalooza.org

Today, April 14, we celebrate Children with AlopeciaDay. Our kids with Alopecia are different and that difference makes ...
04/14/2026

Today, April 14, we celebrate Children with Alopecia
Day.

Our kids with Alopecia are different and that difference makes them normal because we are all different and perfect just as we are. If you can change something you don't like, do it. If you can't, own it! You are a perfect original and not a cheap copy of someone else. Be you, it's you that people love, be strong, stay kind and be the leader moving in any direction you want to go!

Donate at
ChildrenWithAlopeciaDay.org and help CAP with camps, get-togethers, support groups, CAP2U Speaking Tours and everything else we program for CAP Kids and their families. BTW, all kids with Alopecia are CAP Kids! Thank you.


Follow us at Facebook.com/ ChildrensAlopeciaProject and share to everyone.

Today, April 14, we celebrate Children with AlopeciaDay. Our kids are different and it’s that difference that makes them normal because we are all different ...

Daily Children with Alopecia Day posts can be found at Facebook.com/ChildrensAlopeciaProject is on April 14th. Donatio...
04/09/2026

Daily Children with Alopecia Day posts can be found at Facebook.com/ChildrensAlopeciaProject

is on April 14th. Donations make it all possible, so please visit ChildrenWithAlopeciaDay.org and help a child living with hair loss and Alopecia. Thank you.

"We change the emphasis from growing hair to growing confidence, building self-esteem, providing sup

Address

Buena Park, CA

Telephone

+16104681011

Website

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