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	<title>Comments on: Avoid Wrong Diagnosis</title>
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	<link>http://www.jpouch.net/2008/04/15/avoid-wrong-diagnosis/</link>
	<description>Stories: Ostomy, Ileostomy, Jpouch, Colitis, Crohn&#039;s, Surgery and Support</description>
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		<title>By: marsupial</title>
		<link>http://www.jpouch.net/2008/04/15/avoid-wrong-diagnosis/#comment-246</link>
		<dc:creator>marsupial</dc:creator>
		<pubDate>Sat, 26 Jul 2008 00:53:56 +0000</pubDate>
		<guid isPermaLink="false">http://ucstory.wordpress.com/?p=327#comment-246</guid>
		<description>This happened to me as well--2 months after I received my ileostomy, my surgeon sprung the news on me--he said my pathology report from the surgery &quot;strongly favored Crohn&#039;s,&quot; and that getting the j-pouch a few months down the road may be tricky.  I immediately burst into tears.  After so many tests during the previous 2 years, never did anything ever indicate I had Crohn&#039;s.  My surgeon said to meet with my GI.

She reviewed the pathology report with a number of people, took some blood...a month later she also gives me the Indeterminate Crohn&#039;s/Colitis diagnosis, yet felt I was still a strong candidate for the j-pouch, and said she would make this argument to my surgeon.  He trusted her opinion, and after he discussed withe me the complications that could arise if I indeed have Crohn&#039;s with a j-pouch, he felt comfortable doing the surgery on me.

He said everything looked great when they did the j-pouch--no signs of Crohn&#039;s, yet even that pathology report came back favoring Crohn&#039;s.  So, who the hell knows?  All I know is that, knock on wood, I&#039;ve had next to no problems in the 9 months since getting my j-pouch.  If Crohn&#039;s does eventually rear its ugly head and I have to get a permanent ileostomy, I think now I&#039;m in a better emotional state of mind to handle it, not to mention my body has returned to full strength.

Thanks for the info about the webcast--I will definitely tune in.</description>
		<content:encoded><![CDATA[<p>This happened to me as well&#8211;2 months after I received my ileostomy, my surgeon sprung the news on me&#8211;he said my pathology report from the surgery &#8220;strongly favored Crohn&#8217;s,&#8221; and that getting the j-pouch a few months down the road may be tricky.  I immediately burst into tears.  After so many tests during the previous 2 years, never did anything ever indicate I had Crohn&#8217;s.  My surgeon said to meet with my GI.</p>
<p>She reviewed the pathology report with a number of people, took some blood&#8230;a month later she also gives me the Indeterminate Crohn&#8217;s/Colitis diagnosis, yet felt I was still a strong candidate for the j-pouch, and said she would make this argument to my surgeon.  He trusted her opinion, and after he discussed withe me the complications that could arise if I indeed have Crohn&#8217;s with a j-pouch, he felt comfortable doing the surgery on me.</p>
<p>He said everything looked great when they did the j-pouch&#8211;no signs of Crohn&#8217;s, yet even that pathology report came back favoring Crohn&#8217;s.  So, who the hell knows?  All I know is that, knock on wood, I&#8217;ve had next to no problems in the 9 months since getting my j-pouch.  If Crohn&#8217;s does eventually rear its ugly head and I have to get a permanent ileostomy, I think now I&#8217;m in a better emotional state of mind to handle it, not to mention my body has returned to full strength.</p>
<p>Thanks for the info about the webcast&#8211;I will definitely tune in.</p>
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