<?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 - asiunia01</title>
		<link>https://cdhboards.org/blog.php?3464-asiunia01</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>Fri, 24 Apr 2026 09:53:56 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 - asiunia01</title>
			<link>https://cdhboards.org/blog.php?3464-asiunia01</link>
		</image>
		<item>
			<title>My Mikalela with CDH:)</title>
			<link>https://cdhboards.org/entry.php?462-My-Mikalela-with-CDH-)</link>
			<pubDate>Thu, 09 Jun 2011 07:26:16 GMT</pubDate>
			<description>Hi!:) 
7 June 2010 my daughter it has been born with CDH. We are spent in hospital four months... 
In Poland is equipment not enough... and does not...</description>
			<content:encoded><![CDATA[<!-- BEGIN TEMPLATE: blog_entry_external -->
<blockquote class="blogcontent restore">Hi!:)<br />
7 June 2010 my daughter it has been born with CDH. We are spent in hospital four months...<br />
In Poland is equipment not enough... and does not have fundation CDH...  My daughter has year..:) Mam nadziej&#281; &#380;e macie t&#322;umacza w wyszukiwarce poniewa&#380; s&#322;abo znam angielski i nie chce robi&#263; b&#322;&#281;dów. Natomiast chc&#281; &#380;eby&#347;cie zrozumieli nasz&#261; histori&#281;... Mikalela po urodzeniu spedzi&#322;a miesi&#261;c i tydzie&#324; na oddziale intensywnej terapi potem jeszcze trzy miesi&#261;ce w szpitalu... Przesz&#322;a dwie powa&#380;ne operacje na Przepukline Przeponow&#261; Wrodzon&#261;.<br />
W Polsce wiedza na temat CDH jest bardzo ma&#322;a... Nie ma specjalistycznego sprz&#281;tu... Szukam pomocy i kontaktów z rodzicami dzieci chorych na CDH.<br />
<br />
[Img] http://cdhsupport.org/members/weblogs/upload/124/17592885714df075190de53.jpg [/ img]<br />
07.06.2010<br />
<br />
[Img] http://cdhsupport.org/members/weblogs/upload/124/13211094564df0752f0e853.jpg [/ img]<br />
07.06.2011</blockquote>


<!-- END TEMPLATE: blog_entry_external -->]]></content:encoded>
			<dc:creator>asiunia01</dc:creator>
			<guid isPermaLink="true">https://cdhboards.org/entry.php?462-My-Mikalela-with-CDH-)</guid>
		</item>
	</channel>
</rss>
