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Congenital Diaphragmatic Hernia Blogs Webring

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:(: Ring ID: CDHblogsring - Ring Master: CHERUBS :):

 

 

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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Birthing options for CDH babies.

Birthing options for CDH babies.

It is my goal here to make sure that you know you have choices. This site is not intended to give medical advice, but is a personal goal of persuading you to make the decisions for yourself. Do your research from this website and online, interview Docto

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Freed Family CDH web page

Freed Family CDH web page

Our family now has 3 surviving CDH Repairs and the loss of one at birth The oldest is now 44 (RCDH) My Brother Next 30 (RCDH) Our Daughter Next 25 (LGDH) Our Son last (lost at birth 21 years ago) Nephew Debbie & Gerry Freed & Family

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Our Pregnancy and CDH

Our Pregnancy and CDH

I'm Lori. This blog is about mine and my husband's journey through the pregnancy with our first child who was diagnosed with CDH at 22.5 weeks. He was born on Dec 29, 2009 at the University of Virginia Medical Center via scheduled induction.

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Finley's Blog

Finley's Blog

Started this blog shortly after learning at our 20 week ultrasound that our baby has a left-sided CDH. Using this blog to keep friends and fanily updated, as well as hopefully to help other families in the future.

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A story unfolding...

A story unfolding...

A new mom dealing with the loss of her baby girl of only eight days! Baby Savannah was born unexpectedly with CDH August 23rd, 2010 and was taken off ECMO August 31st, 2010. Her condition was even more rare than typical CDH, and her condition was incompat

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Remembering Evie and Ally

Remembering Evie and Ally

This site is for the remembrance of both my daughters. Both diagnosed with CDH pre birth. My first Evie lived a short 14 hours. My second Allyson we were blessed to have for 15 months. Apparently our case is 99.9% genetic although there is nothing gen

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Freed Famil CDH Web Page

Freed Famil CDH Web Page

Some History, back-ground and Sucesses related to the FREED Family and our Involvement with CDH (4 family members)

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Sandy Spence Babies

Sandy Spence Babies

Madelyn Spence's CDH journey and our life after her death.

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Jayden's CDH and HRHS journey

Jayden's CDH and HRHS journey

Jayden was born with right sided CDH and hypoplastic right heart syndrome. He spent 47 days in the hospital and still needs an additional 2 open heart surgeries.

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Peace Frog ID: Muffin

Peace Frog ID: Muffin

It is about my dog's kidney problems and about Ned Dellinger, a Congenital Diaphragmatic Hernia baby, and my nephew

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