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		<title>CDH Clubhouse - Congenital Diaphragmatic Hernia Support Group hosted by CDH International - Blogs - kimberlydawn</title>
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		<description><![CDATA[CDH International - The World's Oldest, Largest and Leading  Congenital Diaphragmatic Hernia Charity.  Supporting CDH Research, Awareness and Patient Families Since 1995 in 84 Countries.]]></description>
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			<title>CDH Clubhouse - Congenital Diaphragmatic Hernia Support Group hosted by CDH International - Blogs - kimberlydawn</title>
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			<title>A Little Miracle</title>
			<link>https://cdhboards.org/entry.php?520-A-Little-Miracle</link>
			<pubDate>Mon, 10 Oct 2011 20:02:46 GMT</pubDate>
			<description>My son was born with a Left Congenital Diaphragmatic Hernia in January of this year.  He was placed on a vent, then an occilator and then ECMO for 17...</description>
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<blockquote class="blogcontent restore">My son was born with a Left Congenital Diaphragmatic Hernia in January of this year.  He was placed on a vent, then an occilator and then ECMO for 17 days with nitric oxide. He had his repair done on day 2 on ECMO he was very critical they doctors gave him less than a 10% chance to survive.  Now he is 9 months old he is in the hospital now in the PICU before we left her in April to go home the doctors thought that he might have reherniaed on that left side.  We came for a cough on Monday of last week and he had surgery on Thursday.  The doctors went on the right side because they thought he had a bilateral diaphragmatic hernia and he did they repaired it and he''s doin really good.  If any one out there has information on bilateral diaphramatic hernias email me at <a href="mailto:kimberly_adkins2009@yahool.com">kimberly_adkins2009@yahool.com</a> thank you</blockquote>


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