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!
Wednesday, October 16, 2013
December 10, 2013
We found out on Monday that Mason's surgery will be on December 10th at noon. This is the day he turns 4 months old. The scheduler and I are playing phone tag, and I am trying to get more information and details regarding everything... will post more as soon as we catch each other. Thank you all for your continued thoughts and prayers.
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