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		<title>CDH Clubhouse - Congenital Diaphragmatic Hernia Support Group hosted by CDH International - Blogs - KimFitzgerald</title>
		<link>https://cdhboards.org/blog.php?3342-KimFitzgerald</link>
		<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 - KimFitzgerald</title>
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			<title>CDH Repair</title>
			<link>https://cdhboards.org/entry.php?651-CDH-Repair</link>
			<pubDate>Thu, 09 Feb 2012 19:00:49 GMT</pubDate>
			<description>---Quote (Originally by KimFitzgerald)--- 
My little boy is a CDH survivor and he is now 2.  We just went to our yearly follow-up appointment with...</description>
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					<img src="images/misc/quote_icon.png" alt="Quote" /> Originally Posted by <strong>KimFitzgerald</strong>
					<a href="showthread.php?p=65545#post65545" rel="nofollow"><img class="inlineimg" src="images/buttons/viewpost-right.png" alt="View Post" /></a>
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				<div class="message">My little boy is a CDH survivor and he is now 2.  We just went to our yearly follow-up appointment with Pediatric Surgery.  According to his x-ray his diaphram is up to high.  The doctor refered to it as being &quot;loose&quot;.  We are now looking at a repair.  Has any other family had this or a similar issue?</div>
			
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			<dc:creator>KimFitzgerald</dc:creator>
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