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		<title><![CDATA[discussion boards — has anyone had met. to other parts of body afer c.c opt.]]></title>
		<link>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?id=331</link>
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		<description><![CDATA[The most recent posts in has anyone had met. to other parts of body afer c.c opt..]]></description>
		<lastBuildDate>Mon, 15 Jan 2007 18:45:36 +0000</lastBuildDate>
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			<title><![CDATA[Re: has anyone had met. to other parts of body afer c.c opt.]]></title>
			<link>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=1475#p1475</link>
			<description><![CDATA[<p>In my case, about a year after the liver resection, tumors metastized back to the remaining half of the liver, and, at that time, I was told no more operations could be done.&nbsp; So in subsequent years I&#039;ve been on 5 clinical trial chemo programs, some which worked for awhile and some which did not work, and 2 surgical procedures -- with the most recent being insertion (in November) through a catheter of radiation beads into the liver -- which stablized tumor growth as seen in a CT scan in December.</p><p>The most encouraging thing is that during the time I&#039;ve had CC new treatments have continually become available.</p><p>Jeff G mentions stress and anxiety -- which is my middle name -- long before I had CC.&nbsp; So I deal with that the best I can, but I guess it&#039;s just my nature.&nbsp; I&#039;m too impatient to sit around a lot, and I am able to get involved in new and exciting projects which are very stressful but frequently in a positive way, and they also keep my mind off my medical concerns.</p><p>Good luck and keep a positive attitude.</p><p>Jerry Daniels<br />Platteville, WI</p>]]></description>
			<author><![CDATA[null@example.com (Jerry D)]]></author>
			<pubDate>Mon, 15 Jan 2007 18:45:36 +0000</pubDate>
			<guid>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=1475#p1475</guid>
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			<title><![CDATA[Re: has anyone had met. to other parts of body afer c.c opt.]]></title>
			<link>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=1473#p1473</link>
			<description><![CDATA[<p>ty you Jeff G &#039;Good luck and bless you</p><p>agnes</p>]]></description>
			<author><![CDATA[null@example.com (mcoliver)]]></author>
			<pubDate>Sun, 14 Jan 2007 00:03:16 +0000</pubDate>
			<guid>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=1473#p1473</guid>
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			<title><![CDATA[Re: has anyone had met. to other parts of body afer c.c opt.]]></title>
			<link>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=1466#p1466</link>
			<description><![CDATA[<p>Agnes:&nbsp; My experience would suggest trying a different type of chemo regimen. Due to the fact it has mets tells me it is systemic.&nbsp; I know you probally have heard this before, but different chemo regimens work differently on individuals with cc.&nbsp; I would discuss the options with your Oncologist.&nbsp; I have had operation, 3 different regimens of chemo and 3 weeks of 3D radiation on my liver.&nbsp; I am about to begin a 4th regimen of chemo (Oxaliplatin and xeloda tablets).&nbsp; One thing I have come to understand when my cancer returned and mets and is still lingering, is it&#039;s not my fault and it&#039;s not because I&#039;m not being positive or trying hard enough.&nbsp; It is the CC and it has to be confused with different treatments; chemo, relaxation, diet.&nbsp; Also , as best as possible keep the anxiety and stress levels low.&nbsp; Consider prescription anxiety and sleep aids.&nbsp; In my opinon cc strives on the adrenaline created from stress and anxiety as well as causing your other body organs to go haywire.&nbsp; <br />Tell your husband to keep his chin up and consider discussing another chemo combination with Oncologist.&nbsp; Many times I have thought about just let nature take it&#039;s course, but I&#039;m just to darn stubborn I guess.&nbsp; </p><p>JeffG.&nbsp; <br />&nbsp; &nbsp; &nbsp; P.S.&nbsp; Agnes, March, 2007 will be 8 years since first diagnosed THERE IS HOPE!</p>]]></description>
			<author><![CDATA[null@example.com (JeffG)]]></author>
			<pubDate>Sat, 13 Jan 2007 00:33:38 +0000</pubDate>
			<guid>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=1466#p1466</guid>
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			<title><![CDATA[has anyone had met. to other parts of body afer c.c opt.]]></title>
			<link>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=1463#p1463</link>
			<description><![CDATA[<p>my husband had cc opt. in feb.2006 had rad&amp;chemo then we found out it met. to the liver and old site. What can we except know <br />thanks &lt; agnes</p>]]></description>
			<author><![CDATA[null@example.com (mcoliver)]]></author>
			<pubDate>Fri, 12 Jan 2007 18:26:54 +0000</pubDate>
			<guid>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=1463#p1463</guid>
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