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Our journey with metopic craniosynostosis

Tuesday, January 3, 2012. I recently learned that this blog is a common hit on search engines for our metopic cranio. I want to serve as support to parents who are in this valley of decision regarding their precious children. However, other than very infrequent updates I will not be monitoring this site any longer. If any one would like more information about our journey I would love to help you. My email is roopert5@hotmail.com. Thursday, September 22, 2011. Monday, March 16, 2009. Our family is going t...

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Our journey with metopic craniosynostosis | ourlittleboneheads.blogspot.com Reviews
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Tuesday, January 3, 2012. I recently learned that this blog is a common hit on search engines for our metopic cranio. I want to serve as support to parents who are in this valley of decision regarding their precious children. However, other than very infrequent updates I will not be monitoring this site any longer. If any one would like more information about our journey I would love to help you. My email is roopert5@hotmail.com. Thursday, September 22, 2011. Monday, March 16, 2009. Our family is going t...
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Our journey with metopic craniosynostosis | ourlittleboneheads.blogspot.com Reviews

https://ourlittleboneheads.blogspot.com

Tuesday, January 3, 2012. I recently learned that this blog is a common hit on search engines for our metopic cranio. I want to serve as support to parents who are in this valley of decision regarding their precious children. However, other than very infrequent updates I will not be monitoring this site any longer. If any one would like more information about our journey I would love to help you. My email is roopert5@hotmail.com. Thursday, September 22, 2011. Monday, March 16, 2009. Our family is going t...

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ourlittleboneheads.blogspot.com ourlittleboneheads.blogspot.com
1

Our journey with metopic craniosynostosis

http://ourlittleboneheads.blogspot.com/2008/12/hey-everyone-just-wanted-to-post-quick.html

Friday, December 5, 2008. Hey everyone - Just wanted to post a quick update on the latest with the girls. Our family is going to participate in a research study completed by Seattle Childrens Hospital inconjunction with two universities to further ID what causes cranio. We are an interesting case because it has affected all three kids with two different mommies. We are probably the only ones with this spread out there. We are SOOOO special. How are the girls after the surgery? December 10, 2009 at 1:07 PM.

2

Our journey with metopic craniosynostosis: HOW???

http://ourlittleboneheads.blogspot.com/2008/11/how.html

Thursday, November 13, 2008. So far we have surgery scheduled for less than two weeks away. The only thing that will change that is one of three things: Illness. Our third opinion next Tuesday comes up with something different that we trust more. Or divine inspiration that would likely come from prayer/ and or the number two option anyway. So it is Dr. Vicari (Chicago)or bust. Subscribe to: Post Comments (Atom). Our journey with metopic craniosynostosis. The verdict is in.NO SURGERY NEXT WEEK!

3

Our journey with metopic craniosynostosis: This just arrived... the science hasn't...

http://ourlittleboneheads.blogspot.com/2009/02/this-just-arrived-science-hasnt.html

Tuesday, February 3, 2009. This just arrived. the science hasn't. We have an appointment for Leah next week with Dr. Havlik at Riley (craniofacial surgeon). Update to follow. Subscribe to: Post Comments (Atom). Our journey with metopic craniosynostosis. This just arrived. the science hasnt.

4

Our journey with metopic craniosynostosis: Leahs visit with Dr. Havlik

http://ourlittleboneheads.blogspot.com/2009/03/leahs-visit-with-dr-havlik.html

Monday, March 16, 2009. Leahs visit with Dr. Havlik. What a great blog! Thanks so much for your detailed posts. Its helped us reconsider our sons surgery! He is also borderline mild with metopic cranio! Its amazing to hear that all your 3 kids have cranio! Its amazing what we go through for our kids! Thanks again for your posts and information. December 12, 2009 at 12:23 PM. Subscribe to: Post Comments (Atom). Our journey with metopic craniosynostosis. Leahs visit with Dr. Havlik.

5

Our journey with metopic craniosynostosis: November 2008

http://ourlittleboneheads.blogspot.com/2008_11_01_archive.html

Tuesday, November 18, 2008. The verdict is in.NO SURGERY NEXT WEEK! Hey everyone. Thank you so much for your calls, emails and prayers. We met with Dr. Vicari in Chicago today and we are cancelling the surgery for next week. Wahhoooo! Thursday, November 13, 2008. She will be in the pediatric intensive care unit for at least 1 day - likely two then hopefully transferred for the next three to five days for continued healing before returning home. They will wake her up as soon as possible after the surg...

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Our journey with metopic craniosynostosis

Tuesday, January 3, 2012. I recently learned that this blog is a common hit on search engines for our metopic cranio. I want to serve as support to parents who are in this valley of decision regarding their precious children. However, other than very infrequent updates I will not be monitoring this site any longer. If any one would like more information about our journey I would love to help you. My email is roopert5@hotmail.com. Thursday, September 22, 2011. Monday, March 16, 2009. Our family is going t...

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