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David Ryan's Journey: Sagittal Craniosynostis

This blog serves two main purposes: to concrete the memories we made along this journey, and to help others. I sincerely hope that this blog offers comfort and hope to parents and families whose children are diagnosed with craniosynostosis, or any other disorder.

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David Ryan's Journey: Sagittal Craniosynostis | davidscabesa.blogspot.com Reviews
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This blog serves two main purposes: to concrete the memories we made along this journey, and to help others. I sincerely hope that this blog offers comfort and hope to parents and families whose children are diagnosed with craniosynostosis, or any other disorder.
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1 and this one
2 and so
3 a new hat
4 complete with fancy
5 houdini proof
6 baby proof velcro
7 and 26 holes
8 posted by breanna
9 2 comments
10 yeah
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and this one,and so,a new hat,complete with fancy,houdini proof,baby proof velcro,and 26 holes,posted by breanna,2 comments,yeah,and 6 month olds,ministry,1 comment,school bus,he said again,factor,not wai,just kidding,what a relief,the great divide,easier
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David Ryan's Journey: Sagittal Craniosynostis | davidscabesa.blogspot.com Reviews

https://davidscabesa.blogspot.com

This blog serves two main purposes: to concrete the memories we made along this journey, and to help others. I sincerely hope that this blog offers comfort and hope to parents and families whose children are diagnosed with craniosynostosis, or any other disorder.

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1

David Ryan's Journey: Sagittal Craniosynostis: The Great Divide

http://davidscabesa.blogspot.com/2010/04/great-divide.html

David Ryan's Journey: Sagittal Craniosynostis. This blog serves two main purposes: to concrete the memories we made along this journey, and to help others. I sincerely hope that this blog offers comfort and hope to parents and families whose children are diagnosed with craniosynostosis, or any other disorder. Wednesday, April 28, 2010. Subscribe to: Post Comments (Atom). Beginning of the Story. Little Lydia and David. Visit with the Doc. A decision {Too Large} for us. The Lord is Good: David is born.

2

David Ryan's Journey: Sagittal Craniosynostis: April 2010

http://davidscabesa.blogspot.com/2010_04_01_archive.html

David Ryan's Journey: Sagittal Craniosynostis. This blog serves two main purposes: to concrete the memories we made along this journey, and to help others. I sincerely hope that this blog offers comfort and hope to parents and families whose children are diagnosed with craniosynostosis, or any other disorder. Wednesday, April 28, 2010. Little Lydia and David. David and Lydia will always be bonded in my heart. The US. - they were missionaries. Fast forward to the next day. We made sure Kelli and Lydia kne...

3

David Ryan's Journey: Sagittal Craniosynostis: It's All Old Hat

http://davidscabesa.blogspot.com/2010/05/its-all-old-hat.html

David Ryan's Journey: Sagittal Craniosynostis. This blog serves two main purposes: to concrete the memories we made along this journey, and to help others. I sincerely hope that this blog offers comfort and hope to parents and families whose children are diagnosed with craniosynostosis, or any other disorder. Sunday, May 16, 2010. It's All Old Hat. That's right: We're one hat down! David got his new helmet on Tuesday. Here is David when his helmet was brand new vs. the very end (16 weeks difference):.

4

David Ryan's Journey: Sagittal Craniosynostis: Clarity

http://davidscabesa.blogspot.com/2010/06/as-we-weighed-traditional-surgery-and.html

David Ryan's Journey: Sagittal Craniosynostis. This blog serves two main purposes: to concrete the memories we made along this journey, and to help others. I sincerely hope that this blog offers comfort and hope to parents and families whose children are diagnosed with craniosynostosis, or any other disorder. Wednesday, April 28, 2010. As we weighed the traditional surgery and the endoscopic surgery, we felt no clarity. One day, we felt one way – the next day, the other. What he was supposed to do. I was...

5

David Ryan's Journey: Sagittal Craniosynostis: The Wait

http://davidscabesa.blogspot.com/2010/04/wait.html

David Ryan's Journey: Sagittal Craniosynostis. This blog serves two main purposes: to concrete the memories we made along this journey, and to help others. I sincerely hope that this blog offers comfort and hope to parents and families whose children are diagnosed with craniosynostosis, or any other disorder. Wednesday, April 28, 2010. Oh, the wait. How often I wished that they would have told us "Your son needs surgery. Now. We'll do it right now." In many ways, it would have been so much. Plainly, I wa...

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David Ryan's Journey: Sagittal Craniosynostis

David Ryan's Journey: Sagittal Craniosynostis. This blog serves two main purposes: to concrete the memories we made along this journey, and to help others. I sincerely hope that this blog offers comfort and hope to parents and families whose children are diagnosed with craniosynostosis, or any other disorder. Sunday, May 16, 2010. It's All Old Hat. That's right: We're one hat down! David got his new helmet on Tuesday. Here is David when his helmet was brand new vs. the very end (16 weeks difference):.

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