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	<title>Comments on: One year celebration for my J-pouch</title>
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	<description>Support for those with inflammatory bowel diseases.</description>
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		<title>By: Kari</title>
		<link>http://ucvlog.com/2010/02/16/one-year-celebration-for-my-j-pouch/#comment-1366</link>
		<dc:creator><![CDATA[Kari]]></dc:creator>
		<pubDate>Mon, 26 Jul 2010 06:55:21 +0000</pubDate>
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		<description><![CDATA[I am very glad to have found your site and your facebook page. I have Familial adenomatous polyposis (FAP). I was diagnosed at 4 (was youngest ever), had my intestine removed and got a J-Pouch when I was 9. I have now just celebrated 16 years with a J Pouch. I am trying to make my disease more known as it is a genetic disease that does not skip generations. I lived my life like any other person. I never changed activities or foods. I lived every day as it came and never stopped because of having FAP. When I had surgery doctors told me 3 to 6 months of recovery and i was doing everything including swimming a month after my surgery. I have had no complication and I look forward to talking with more people who have J-pouches.

Thank you again and Congrats on 1 year.]]></description>
		<content:encoded><![CDATA[<p>I am very glad to have found your site and your facebook page. I have Familial adenomatous polyposis (FAP). I was diagnosed at 4 (was youngest ever), had my intestine removed and got a J-Pouch when I was 9. I have now just celebrated 16 years with a J Pouch. I am trying to make my disease more known as it is a genetic disease that does not skip generations. I lived my life like any other person. I never changed activities or foods. I lived every day as it came and never stopped because of having FAP. When I had surgery doctors told me 3 to 6 months of recovery and i was doing everything including swimming a month after my surgery. I have had no complication and I look forward to talking with more people who have J-pouches.</p>
<p>Thank you again and Congrats on 1 year.</p>
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