Our Mission: To surprise kids with craniofacial difference (Newborn thru 20) as they face, sometimes numorous, procedures, test, or surgeries that can fill a child's life who has been born with craniosynostosis and/or other abnormality of the face or skull.
Fact is one in 50 children are born with a craniofacial defect that can sometimes require a lifetime of follow-up which can include numorous corrective procedures. As I found with my daughter's skull reconstruction when she was 10 yrs old one little card or a quick note from a stranger can be all it takes to help give a child an extra boost of courage.

Extended C.A.R.E. card request(please check back regularly)

We ask that all our featured CARE kiddos recieve cards before and in a timely manner after their operations and procedures.
However, a few of our families have so much going on that they might need multiple request for outpouring of love, prayers, and cards for countless procedures.
On this page we will Feature our Cranio Family Members that need extended request for continuous cards sent their way. You can click on their pictures to be led to the most recent procedure they are undergoing but we urge you to read about them and send cards and notes for ongoing support.


JAXSON
Jaxson was born on May 27, 2011.
He has multiple congenital issues including metopic craniosynostosis, agenesis of the corpus callosum, tethered spinal cord, cleft palate and pierre robin sequence.
 He has already had three surgeries to correct his airway including mandibular distractors. Dr's are still working on his airway and may eventually lead to a trach.
July 13th, 2011 is his endoscopic metopic cranio surgery.
Please pray for him, his family, the doctors, nurses and staff.
If you would like to follow Jaxson's journey please "like"  FB page (The Hoffman George's).
Please Send cards to Jaxson
CARE
c/o Jaxson G.
PO Box 1396
Bellevue, NE 68005-1396


Have a child you would like signed up for a card launch?
Email Us Care4Cranio@hotmail.com

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