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    <title>CancerCompass Message Board: colonic j pouch</title>
    <description>CancerCompass message board discussion started by stjohn on 3/3/2008</description>
    <link>http://www.cancercompass.com/message-board/message/all,21587,0.htm</link>
    <pubDate>Fri, 05 Dec 2008 00:00:00 GMT</pubDate>
    <lastBuildDate>Fri, 05 Dec 2008 00:00:00 GMT</lastBuildDate>
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      <title>colonic j pouch</title>
      <description>In May I will have my temporary ileostomy &amp;quot;taken down&amp;quot; and begin adapting to my colonic j pouch.&amp;nbsp; I&amp;#39;ve read a few posts related to difficulties with frequency, gas, continence etc. with the j pouch.&amp;nbsp; I&amp;#39;d appreciate any tips that you might share in how you managed these problems.&amp;nbsp; I was hoping to take a trip via plane&amp;nbsp;in the fall -- but after reading some of the literature and posts am wondering if this is a reasonable idea.Thanks, stjohn</description>
      <author>stjohn</author>
      <pubDate>Mon, 03 Mar 2008 00:00:00 GMT</pubDate>
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      <title>RE: colonic j pouch</title>
      <description>Hi stjohn,I had my takedown in March 2004. I had 2 out of state and one out of country weddings to attend that summer (June, July and September) -- all by plane. I wasn&amp;#39;t sure I&amp;#39;d be recovered enough to swing it. Though I may not have been 100%, I was able to do all three with no problem. If you haven&amp;#39;t begun already, I&amp;#39;d recommend taking probiotics daily (something like pb8 or culturelle). Adding a good, organic yogurt to your diet is a good idea, too. I also found that Metamucil wafers were helpful for fiber (and decreasing or slowing output). For a little more help in slowing things down, you can try taking anti-diarrheal (ie. lopermide) tabs, though they tended to give me more gas and stomach aches. I actually found that taking a half pill of vicodin really worked great for slowing things down -- I still do this when I know that I&amp;#39;ll be out a while and not near a convenient toilet. Aside from that, I&amp;#39;d suggest getting flushable wipes (Kleenex Cottonelle or Scott are good) and for the weeks following the takedown, I&amp;#39;d definitely suggest getting Calmoseptine for butt-burn -- I even brought it to the hospital for the days after the takedown, and I&amp;#39;m glad I did.&amp;nbsp;Also, do you know about the j-pouch.org site and its forums? If not, go check it out. There are some great, supportive folks in there. And they&amp;#39;ll be happy to answer all your questions and concerns. There&amp;#39;s even a nurse (Jan Dollar) on there who has had the surgery and is very active on the forum.Anyway, for me, after the first couple of weeks after the surgery I couldn&amp;#39;t imagine the butt-burn and pouch functioning right. The good news is that it things just clicked, and though I&amp;#39;ve had some ups and downs, things haven&amp;#39;t been better than they are now 4 years later.Feel free to ask me any questions.Best,Jon &amp;nbsp;</description>
      <author>scacco</author>
      <pubDate>Tue, 04 Mar 2008 00:00:00 GMT</pubDate>
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      <title>RE: colonic j pouch</title>
      <description>Jon,I can&amp;#39;t thank you enough for taking the time to share your experience and tips with me.&amp;nbsp; I&amp;#39;ve taken notes -- and will try&amp;nbsp;all of your suggestions.&amp;nbsp; You also gave me real hope that I can return to my active lifestyle.&amp;nbsp; Thanks again - your note really brightened my day.Best wishes, stjohn&amp;nbsp;&amp;nbsp;</description>
      <author>stjohn</author>
      <pubDate>Thu, 06 Mar 2008 00:00:00 GMT</pubDate>
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