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Congenital Diaphragmatic Hernia

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Site-ring on Congenital Diaphragmatic Hernia

► Congenital Diaphragmatic Hernia Blogs Webring

Congenital Diaphragmatic Hernia Blogs Webring

Ring ID: CDHblogsring

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.

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Web-Sites on Congenital Diaphragmatic Hernia

CHERUBS Congenital Diaphragmatic Hernia Information Blog

CHERUBS Congenital Diaphragmatic Hernia Information Blog

The latest news and research on Congenital Diaphragmatic Hernia, research, support and awareness!

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Congenital Diaphragmatic Hernia Blogs Webring

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.

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CHERUBS Myspace CDH Blog

CHERUBS Myspace CDH Blog

CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support

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Congentital Diaphragmatic Hernia Awareness United

Congentital Diaphragmatic Hernia Awareness United

This ring is not assosiated with any CDH support group it is to Unite the CDH community and to allow families to share their stories and support one another.

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CHERUBS Blog Ring Page

CHERUBS Blog Ring Page

CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support

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Baby Claire

Baby Claire

Claire was diagnosed with a left-sided congenital diaphragmatic hernia (CDH) in February 2007 during her 19-week ultrasound. She was born in June 2007, had repair surgery when she was 6 days old, and came home from the hospital after 3 weeks.

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Liviana's Journey

Liviana's Journey

Liviana was born January 18, 2008 with a Congenital Diaphragmatic Hernia. This blog follows the journey from her diagnosis in utero in October 2007 to present.

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Par

Par

Philip Andrew Rich ("Par") was diagnosed with a congenital diaphragmatic hernia (CDH) in July 2007 at 21 weeks gestation. He was born November 1, 2007. After 57 days in the NICU, he was sent home. Here you can read his amazing story, along with all the pr

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Shane's Street | Life After Losing A Child to CDH

Shane's Street | Life After Losing  A Child to CDH

Finding happiness again after losing my only child to Congenital Diaphragmatic Hernia at age 6 and a half. In memory of Shane Torrence (1/28/93 - 9/11/99) For more information on CDH, visit http://www.cdhsupport.org

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Blog in memory of Shane Torrence

Blog in memory of Shane Torrence

Shane Torrence's blog at CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support

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