CRANIO ANGEL NETWORK
 
 



Cranio Angel Network (CAN) is a charitable awareness program providing handmade flower headbands and pirate hats for boys and girls born with Craniosynostosis.


Craniosynostosis is a birth defect that usually requires surgery. Oftentimes, the surgery requires an incision from ear-to-ear across the top of their head. This leaves a large scar that is visible until their hair grows in. The Cranio Angel Network provides headbands and hats to these boys and girls to wear after their surgery to help cover their scar and give them some pampering during their time of healing.


If you would like to help CAN purchase supplies for this program, please click HERE. CAN can also always use Forever Postage Stamps. You can purchase them HERE and have them shipped directly to us (click HERE for address).


This program also hopes to promote awareness of Craniosynostosis because early diagnosis is crucial to providing adequate treatment.


If you would like to meet other Cranio families and/or support our program, please consider joining us every October for our Annual Shamu & You Family Walk.


Thank you for your support and please check the website regularly to Meet The Angels and become a fan of our Facebook page to help promote awareness.

We have raised over $45,000

to help families pay for Cranio expenses!

We CAN increase Craniosynostosis Awareness

1459 Angels

in

25 Countries


Craniosynostosis

Occurs

1 in 2,000 births


Early Diagnosis is Crucial