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This fundraiser ended on 10/01/12

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Help support Shelby and Summer in creating care packages for families of Craniosynostosis

I am the mother of 5 month old Jackson. He has Sagittal Synostosis, this is the most common form of craniosynostosis. It was very difficult to even find out that my perfect baby had a birth defect and TO HIS SKULL! Scary business. We had surgery July 13th 2012 and Jackson is in a helmet to help the shaping of his head. He is doing so awesome and boy is he a cutie! During our difficult time I found a support group called CranioCareBears. Shelby and Summer are the founders and fellow cranio moms and were there every step of the way even gifting us a care package for the hospital! Creating this gift packages and mailing them cost a lot of money so I set this page up to help raise money to donate to them to help show my appreciation .
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