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Congenital Diaphragmatic Hernia Blogs Webring

Webring Community of blogs for families and doctors of children born with Congenital Diaphragmatic Hernia (CDH), a rare and sometimes deadly birth defect that affects 1600 babies a year in the U.S.

Ring ID: CDHblogsring - Ring Master: CHERUBS

Category: ► Health and Wellness

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Members

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► Samuel Kenneth Finzer

Updates on our son which was born with a Diaphragmatic Hernia.

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► Joshua

Joshua's road to recovery....

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► The Jack Ryan Gillham Foundation

The JRG Foundation is a non-profit organization that was formed in memory of our son, Jack, who passed away in August off 2007 due to complications from CDH. The JRG Foundation is dedicated to easing the financial strain for families of critically ill ba

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► Kamryn Hope's Blog

Kamryn Hope was diagnosed at 13 weeks with CDH. This blog is our way of documenting the journey for our friends, family, and others experiencing a similar diagnosis.

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► Zoe Holtz Henry's CDH Story

Zoe Holtz Henry was born with a right side CDH on August 12, 2008. She was on ECMO for 2 weeks at Legacy Emanuel Hospital in Portland. She was in the NICU for 3 months before going home. She is still on oxygen and being treated for pulmonary hypertensi

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► Princess Madelyn

Our journey with CDH.

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► What's New in My World

This website is a way that family and friends can keep up with Josh and the progress he is making each day!

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► Aiden and CDH

I created this blog site to keep our family and friends updated on Aiden's progress with CDH.

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► Hopie Clyde

I'm a mom of a son that was born with CDH and I'm happy to report that he's doing GREAT!!! This is our family's blog. Feel free to read and enjoy the crazy life we live!!!

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