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Cdh

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Site-rings on Cdh

► Congentital Diaphragmatic Hernia Awareness United

Congentital Diaphragmatic Hernia Awareness United

Ring ID: Congenital_Diaphragmatic_Hernia_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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► Congentital Diaphragmatic Hernia Awareness United

Congentital Diaphragmatic Hernia Awareness United

Ring ID: Congenital_Diaphragmatic_Hernia_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.

Home: Congentital Diaphragmatic Hernia Awareness United
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Ring: View Members (1) - Join this Ring
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► 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 Cdh

My child was born with CDH

My child was born with CDH

A blog chroncling my journey with my child who was born with CDH in 1999 at New Delhi, India. Its been a crazy roller-coaster but I remember each moment of it. The highs and lows and the long points stretching in between. Come with me while I share the ri

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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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In God's Sight: Life after CDH

In God's Sight: Life after CDH

A blog about our 2 year old son who was born with a diaphragmatic hernia & now there is no stopping him!

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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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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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Skyla Manawa Temaipi, LCDH 13/10/07-13/06/08

Skyla Manawa Temaipi, LCDH 13/10/07-13/06/08

My little CDH Angel, Skyla Manawa Temaipi. Skyla was born with at 34wks weighing 3pound 6, 1.7kg. Born with CDH, VSD, Coarctation of Aorta, Cleft Palate and No right side clavical. She also had NEC twice, Paraflu, RSV Bronch, Phenmonia, Staph infections,

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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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Princess Madelyn

Princess Madelyn

Our journey with CDH.

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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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Our Little Sunshines CDH journey

Our Little Sunshines CDH journey

following the journey of 'sunshine' who was diagnosed with left sided CDH, he is due in November 09

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