I have gotten some requests/suggestions to create a FB page for Mason's surgery updates. I have turned it into a page for prayers, and would GREATLY appreciate your help in sharing his page with everyone you know (share the link in your status, click "Share" on the post that I recently wrote on the page, etc.). The more people we have praying for him on the day of his surgery, the better. Thank you as always for your support, love, and prayers!
Link for his Facebook page: www.facebook.com/prayersformasonrobertson
We created this blog to keep everyone posted on Mason's upcoming major skull surgery on December 10, 2013. Mason was diagnosed with a rare birth defect called Craniosynostosis at his 1 month well visit. We also hope to bring awareness to this condition in hopes of helping out other babies and children with Craniosynostosis. Please continue to keep our sweet baby boy in your prayers!
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