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!
Monday, December 23, 2013
Updates coming soon...
Hi everyone! I'm so sorry about my lack of posts since surgery! I promise I will post soon. I haven't had a lot of free time since surgery while taking care of Mason and prepping for Christmas. I also know how emotional it will be to re-hash surgery and the days in the hospital. I promise I will though, especially for the cranio parents facing surgery that need to know what happens. Will also post lots of pics. Merry Christmas!!!
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment