<?xml version="1.0" encoding="ISO-8859-1"?>

<rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/">
	<channel>
		<title>CDH Clubhouse - Congenital Diaphragmatic Hernia Support Group hosted by CDH International - Blogs - TanyaLynn</title>
		<link>https://cdhboards.org/blog.php?11011-TanyaLynn</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>
		<language>en</language>
		<lastBuildDate>Mon, 25 May 2026 06:41:12 GMT</lastBuildDate>
		<generator>vBulletin</generator>
		<ttl>60</ttl>
		<image>
			<url>https://cdhboards.org/images/misc/rss.jpg</url>
			<title>CDH Clubhouse - Congenital Diaphragmatic Hernia Support Group hosted by CDH International - Blogs - TanyaLynn</title>
			<link>https://cdhboards.org/blog.php?11011-TanyaLynn</link>
		</image>
		<item>
			<title>Looking for ECMO and CDH MOMS TO TEENAGE GIRLS</title>
			<link>https://cdhboards.org/entry.php?1021-Looking-for-ECMO-and-CDH-MOMS-TO-TEENAGE-GIRLS</link>
			<pubDate>Sat, 09 Jan 2016 19:41:54 GMT</pubDate>
			<description>Hi I am Tanya and I had my beautiful princess 14 years ago and she was born with a left side CDH was full term and had pulmonary hypertension among...</description>
			<content:encoded><![CDATA[<!-- BEGIN TEMPLATE: blog_entry_external -->
<blockquote class="blogcontent restore">Hi I am Tanya and I had my beautiful princess 14 years ago and she was born with a left side CDH was full term and had pulmonary hypertension among being on vent from day one and she was placed on EMCO and had her CDH surgery on it and then was removed she was in the hospital for over 6 months and she has had many surgeries and problems she was doing really well and we noticed she wasn't showing signs of becoming a lady and she was still small so now we find out she has Turners and her puberty gland is non active.  They are saying the gland is from the stroke she had when on EMCO so I'm reaching out to others mom's any problems or other things from EMCO just now showing up.  Thanks</blockquote>


<!-- END TEMPLATE: blog_entry_external -->]]></content:encoded>
			<dc:creator>TanyaLynn</dc:creator>
			<guid isPermaLink="true">https://cdhboards.org/entry.php?1021-Looking-for-ECMO-and-CDH-MOMS-TO-TEENAGE-GIRLS</guid>
		</item>
	</channel>
</rss>
