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	<title>PSC Medical Blog &#187; Mike</title>
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	<description>Primary Sclerosing Cholangitis</description>
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		<title>Finally an update on me</title>
		<link>http://psc.zaloudek.net/2008/06/16/finally-an-update-on-me/</link>
		<comments>http://psc.zaloudek.net/2008/06/16/finally-an-update-on-me/#comments</comments>
		<pubDate>Mon, 16 Jun 2008 17:07:43 +0000</pubDate>
		<dc:creator>Mike</dc:creator>
				<category><![CDATA[PSC]]></category>
		<category><![CDATA[liver]]></category>
		<category><![CDATA[transplant]]></category>

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		<description><![CDATA[Back when I created this page, I was thinking there would be more news to report, but I am glad there hasn&#8217;t been. That being said, I will try to update more &#8211; Famous last words
To recap, in 1999, I was diagnosed with PSC after abnormal liver function tests from a life insurance physical indicated [...]]]></description>
			<content:encoded><![CDATA[<p>Back when I created this page, I was thinking there would be more news to report, but I am glad there hasn&#8217;t been. That being said, I will try to update more &#8211; Famous last words<br />
To recap, in 1999, I was diagnosed with PSC after abnormal liver function tests from a life insurance physical indicated a problem. PSC&#8217;s main symptoms are fatigue and itching which have affected me somewhat over the years. Typically people will need to get a liver transplant 10-15 years from time of diagnosis. The first time I had problems started in 2005 where I became jaundiced and had a lot of pain in the abdomen. I was hospitalized at Johns Hopkins for a week. They did an ERCP procedure (endoscopy) to clear out blockages and stones from the bile ducts. This is called a &#8220;cholangitis attack&#8221; and is common in later stages of PSC.<br />
When I was in Johns Hopkins in then, they said it appeared that things had worsened and that I would need a transplant within 5 years. I was put through the extensive transplant evaluation process and put on the transplant list in 2006. Since 2006 I have had regular checkups and blood work but I have remained stable and generally healthy. They measure how close to a transplant you are by a scoring system known as MELD.  &#8220;Model for End Stage Liver Disease&#8221; The higher the score on a 6-40 scale, the sicker you are and the sooner you will get a transplant. Other than a score of 8 when I was in the hospital, my score has been at 6 for the last few years.<br />
I do take medications, mainly Urso, a bile acid. There were a few studies over the last few years that tried to show a higher dose of Urso was more beneficial to PSC patients, but Unfortunately the study results have not proven that. I was on the higher dosage also, but not participating in the studies. Day to day I feel pretty normal. I avoid alcohol and eat reasonably heathy. I do have pains that come and go in my abdomen. Sometimes they are sharp stabbing pains that alarm people I am with. Other times they are a dull aching or heartburn feeling. So far these have only been short term things, but every time it happens I wonder if it will end in a hospital stay. The day before I went in the hospital in 2005 I felt very normal and did a long bike ride so sometimes there is little warning. </p>
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