CAP Kid Group Socalla

10/12/2026

https://childrensalopeciaproject.org/2026/10/12/child-alopecia-help-is-coming/

Alopecia can change a child’s day fast. Find practical support for confidence, school belonging, and family connection when hair loss feels overwhelming.

10/12/2026

https://childrensalopeciaproject.org/2026/10/10/support-teen-body-image-alopecia/

Learn how to support teen body image when alopecia changes appearance, with compassionate words, school support, and peer connection that builds confidence.

09/18/2026

👉 Visit ChildrensAlopeciaProject.org and click CAP Coffee to shop! Great coffee. Confident kids. Now THAT’S good taste. ☕❤️ https://www.facebook.com/share/p/18SqWe7fDZ/

09/04/2026

Look closely at this picture.

You see lots of smiling faces. But what you may not see are the children who once believed they were the only ones—the children who hid beneath hats and wigs, feared being stared at, and wondered whether losing their hair meant losing a part of themselves.

Then they found CAP.

They walked into a community where no explanation was necessary. They met other kids who understood. They watched hats come off, friendships begin, and confidence replace fear. For some children, it was the first time they truly believed: “I am perfect just as I am.”

But CAP cannot do this alone.

To parents of children with alopecia: Please get involved. Bring your child to a CAP event. Join a CAP Kid Group. Volunteer, fundraise, share our posts, and help another family find us. Your participation could give your child—and someone else’s child—a community they will carry for life.

To adults living with alopecia: You understand what these children may face better than almost anyone. Please turn that understanding into action. Your financial support can help give a child today the acceptance, confidence, and belonging you may have needed when you were young.

To everyone else: You do not need to have alopecia or know someone who does to change a child’s life. You simply need to believe that every child deserves to feel accepted, included, and proud of who they are.

A donation to the Children’s Alopecia Project does not grow hair.
It grows confidence.
It grows friendships.
It grows stronger families.
It reminds children that they are never alone.

CAP has been changing lives since 2004. With your help, we can continue reaching children and families for generations to come.
Please don’t just scroll past these faces.

Donate. Volunteer. Share. Get involved

Every child deserves the chance to stand tall, be seen, and know—with absolute certainty—that they are perfect just as they are.
Because everyone is different, everyone is normal.

❤️ Give today at ChildrensAlopeciaProject.org

08/24/2026

Another great Get together! Sorry if you missed the Cap Kid Group Get-Together in Montclair. If you were there, you know why it was great!! It was great meeting you all, thank you!!

08/22/2026

Last night's Get-Together went great. Tomorrow is the next one. Will you be there? In Montclair, CA, check out the video from the Get-Together last night in Vegas and then register at https://form.jotform.com/Knjoz/cap-kid-group-2026-get-togethers

08/19/2026

It’s almost time for the CAP Kid Group Get-Together in Montclair, California!! This Sunday, August 23, from 1pm to 5pm at Main Event, 5201 Montclair Plz Ln, Montclair, CA 91763. We will meet at 1pm sharp, make introductions, chat, take a group photo, and pass out the game cards and wristbands for bowling and laser tag. At 1:30, lunch is served, and then we go have fun!!! Register today at

Please click the link to complete this form.

08/12/2026

Check out the video of Alopeciapalooza 2026 at https://youtu.be/wDlG2JDbCLY?si=hsdfEgdhddXzVd76

Alopeciapalooza may be over, but the friendships, confidence, and sense of belonging we created do not have to end.

To every parent who brought your family to camp: thank you for loving your children exactly as they are and for helping them grow up knowing that their worth has nothing to do with how much hair they have.

At Alopeciapalooza, our kids found something incredibly important:
They found their tribe.

Now we need your help keeping that tribe strong.

Please share the Children’s Alopecia Project on social media. Tell people what CAP and Alopeciapalooza have meant to your family.

Consider hosting a fundraiser and helping organize CAP Kid Group Get-Togethers so our kids can continue building friendships and remember all year long that they are never alone.

CAP depends on awareness, donations, and families like yours spreading the word.

Every share helps.
Every fundraiser helps.
Every donation helps.
Every CAP Kid connection matters.

Together, we can make sure every child with alopecia knows they are loved, accepted, confident, and part of a community that cares. Lucky for us, a nine-year-old CAP Kid gave me the exact words I needed to leave camp on a high note.

"I love camp (Alopeciapalooza) because everyone knows how I feel. And no one stares at me. And that makes me feel good."

Learn more, share CAP, get involved, or donate:
https://linktr.ee/childrensalopeciaproject

“Our kids found their tribe. Now let’s make sure they never lose it.”



https://youtu.be/wDlG2JDbCLY?si=hsdfEgdhddXzVd76

Another great Alopeciapalooza! Help us by donating at ChildrensAlop...

07/28/2026

This Friday, July 31, is the deadline to register for Alopeciapalooza from August 7-10! Go to Alopeciapalooza.org and don’t miss out! Check out the schedule, close your eyes and imagine your child with Alopecia experiencing it all while you and your family look on with a smile on your face and tears in your eyes, the good tears! See you there:-)

07/21/2026

It's hard to believe, but we are only 17 Days away from the start of Alopeciapalooza 2026!! https://youtu.be/qAGOam97bWo?si=wMMf5bFXi1LMk96P - Don't forget to register at Alopeciapalooza.org

Children's Alopecia Project changes the emphasis from growing hair ...