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		<title><![CDATA[discussion boards — What do I do now???]]></title>
		<link>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?id=8767</link>
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		<description><![CDATA[The most recent posts in What do I do now???.]]></description>
		<lastBuildDate>Tue, 28 Aug 2012 05:49:50 +0000</lastBuildDate>
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			<title><![CDATA[Re: What do I do now???]]></title>
			<link>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=64651#p64651</link>
			<description><![CDATA[<p>Maria...chiming in a bit late, but wanted you to know that I am sending tons of good wishes your way.&nbsp; Fingers are crossed too.<br />Hugs,<br />Marion</p>]]></description>
			<author><![CDATA[null@example.com (marions)]]></author>
			<pubDate>Tue, 28 Aug 2012 05:49:50 +0000</pubDate>
			<guid>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=64651#p64651</guid>
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			<title><![CDATA[Re: What do I do now???]]></title>
			<link>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=64613#p64613</link>
			<description><![CDATA[<p>Thank you Eli and Lainy!!!! Did my MRI this morning, and now the results have to go through a bunch of doctors before it reaches me... That&#039;s how it works here. <br />Again, thank you so much for support!!<br />&lt;3<br />Maria</p>]]></description>
			<author><![CDATA[null@example.com (Maria)]]></author>
			<pubDate>Mon, 27 Aug 2012 09:15:38 +0000</pubDate>
			<guid>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=64613#p64613</guid>
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			<title><![CDATA[Re: What do I do now???]]></title>
			<link>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=64612#p64612</link>
			<description><![CDATA[<p>Maria, I vote with Eli. Chemo does keep on tick&#039;n for a while. Wait (i KNOW IT&#039;S TOUGH) to see the Scan results. We will all be waiting right with you!</p>]]></description>
			<author><![CDATA[null@example.com (Lainy)]]></author>
			<pubDate>Mon, 27 Aug 2012 02:53:48 +0000</pubDate>
			<guid>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=64612#p64612</guid>
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			<title><![CDATA[Re: What do I do now???]]></title>
			<link>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=64601#p64601</link>
			<description><![CDATA[<p>Maria, I think you made the right choice to take a break from GemCis. I know it&#039;s very toxic. It took just a couple of cycles for my wife to become very depressed. She cried after each treatment. She just could not help it. I think GemCis played nasty tricks with her mind. She took an extra week break between 5th and 6th cycles, at the urging of her oncologist. The short break made a big difference to how she felt.</p><p>Maria, don&#039;t feel bad about taking a break. Take time off to heal your mind and body. As you know, chemo keeps working for a while after you stop it.</p><p>Best of luck with your MRI results on Monday. Please let us know what options the doctors present to you.</p>]]></description>
			<author><![CDATA[null@example.com (eli)]]></author>
			<pubDate>Sun, 26 Aug 2012 19:38:03 +0000</pubDate>
			<guid>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=64601#p64601</guid>
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			<title><![CDATA[What do I do now???]]></title>
			<link>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=64579#p64579</link>
			<description><![CDATA[<p>I feel like in a crossroad at the moment..... If anyone has any thougths I would appreciate it.</p><p>This past tuesday I was supposed to have my 38th round of iv chemo, and my 7th GemCis since the 6 month break I had Jan-June.<br />I had to start chemo again since my silent tumors had started growing again after a chemoembolization that didn&#039;t do any good.<br />When I took this break (after 18 months on chemo) it was after listening to my very strong inner voice telling me I needed it. I was doing good really, but having this feeling it was harming me.<br />Looking back this was a good decision, but having the embo wasn&#039;t.</p><p>So now after 6 rounds of chemo I just couldn&#039;t take another one... My white bloodcount hasn&#039;t recovered well lately, I suppose my bonemarrow is getting tired. This is the only objective sign. The rest is a feeling.<br />I couldn&#039;t sleep two nights before going to the hospital for the chemo, didn&#039;t now why. Then the day before I was just crying the whole day, and it came to my mind that I didn&#039;t want the chemo. I just felt NOOOOO.<br />I went there anyway, and my WBC was exactly enough for chemo. But when the nurse was about to connect it, I just couldn&#039;t do it. Started to cry just by seeing it. And I&#039;m NOT someone crying a lot.<br />So I went home. Feeling better and better these last days, happy again, singing.<br />Now on Monday it&#039;s time for MRI, and then doctor&#039;s appointment.<br />But, they always leave it so much up to me to decide. Because they don&#039;t have any good ideas at this point. This is Sweden, so there&#039;s no insurence-problem whith treatments.<br />I just don&#039;t now what to do. There are no other hospitals or doctors I can go to, this country is very small, we only hace 300 cases of CC/year. <br />I know I now have to wait for results and to speak to the doctor, but it is so hard to know what to do at this point. I know you can&#039;t go on with chemo forever, then chemo will kill you in the end, at least GemCis.</p><p>Thanks for listening!</p>]]></description>
			<author><![CDATA[null@example.com (Maria)]]></author>
			<pubDate>Sat, 25 Aug 2012 14:56:37 +0000</pubDate>
			<guid>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=64579#p64579</guid>
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