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	<title>Comments on: What do you do when you have to keep going?</title>
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	<link>http://workingwithchronicillness.com/2009/05/what-do-you-do-when-you-have-to-keep-going/</link>
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		<title>By: Mary</title>
		<link>http://workingwithchronicillness.com/2009/05/what-do-you-do-when-you-have-to-keep-going/comment-page-1/#comment-18643</link>
		<dc:creator>Mary</dc:creator>
		<pubDate>Thu, 04 Jun 2009 19:38:51 +0000</pubDate>
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		<description>I put an applause ringtone on my cell phone.  When I have really done a great job &amp; it took a lot of my energy I give myself a standing ovation.  Sometimes you just have to throw your own party!</description>
		<content:encoded><![CDATA[<p>I put an applause ringtone on my cell phone.  When I have really done a great job &amp; it took a lot of my energy I give myself a standing ovation.  Sometimes you just have to throw your own party!</p>
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		<title>By: Rosalind</title>
		<link>http://workingwithchronicillness.com/2009/05/what-do-you-do-when-you-have-to-keep-going/comment-page-1/#comment-17779</link>
		<dc:creator>Rosalind</dc:creator>
		<pubDate>Thu, 07 May 2009 19:04:47 +0000</pubDate>
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		<description>Thanks for sharing this, Sue.  It can be lonely some days knowing that you&#039;re alone dealing with this - no matter how many people you&#039;re surrounded by.  You&#039;re right to appreciate what you&#039;ve got and to keep doing it.  The alternative can look better but rarely is!</description>
		<content:encoded><![CDATA[<p>Thanks for sharing this, Sue.  It can be lonely some days knowing that you&#8217;re alone dealing with this &#8211; no matter how many people you&#8217;re surrounded by.  You&#8217;re right to appreciate what you&#8217;ve got and to keep doing it.  The alternative can look better but rarely is!</p>
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		<title>By: Sue Morgan</title>
		<link>http://workingwithchronicillness.com/2009/05/what-do-you-do-when-you-have-to-keep-going/comment-page-1/#comment-17772</link>
		<dc:creator>Sue Morgan</dc:creator>
		<pubDate>Thu, 07 May 2009 16:47:13 +0000</pubDate>
		<guid isPermaLink="false">http://workingwithchronicillness.com/?p=848#comment-17772</guid>
		<description>I really related to this story. I am the Administrator for a 125 bed Skilled and Rehabilitation facility. I was diagnosed with MS 7 years ago and have been on Rebiff therapy almost that long. Many days I look out my window at my car and think &quot;how am I ever going to be able to drive home?&quot; My job is 24/7 and has its rewards but also has its share of down side. You can&#039;t put off a family who needs to see you or staffing problems because you are having a bad day. No one cares how tired you are. They are caught up in their own medical dramas. I virtually vegetate on the wekends trying to store up enough energy to go at it another week. Week day evenings it&#039;s a light supper and in bed with the TV by 8:pm. It really is a matter of survival. I am my sole support. But I have often thought that if I did not have a job that fortunatly I can do from a wheelchair if necessary, just what would I do? I am still far more active than other people I know who had had  MS as long as I have and I think I owe that to my job and the the Rebif. So I will continue on even when I myself don&#039;t know how I am going to do it because to pull out of a 30 year carreer would, I am afraid, leave me hopelessly adrift. You just get through the day the best way you can for as long as you can. It works for me so far.</description>
		<content:encoded><![CDATA[<p>I really related to this story. I am the Administrator for a 125 bed Skilled and Rehabilitation facility. I was diagnosed with MS 7 years ago and have been on Rebiff therapy almost that long. Many days I look out my window at my car and think &#8220;how am I ever going to be able to drive home?&#8221; My job is 24/7 and has its rewards but also has its share of down side. You can&#8217;t put off a family who needs to see you or staffing problems because you are having a bad day. No one cares how tired you are. They are caught up in their own medical dramas. I virtually vegetate on the wekends trying to store up enough energy to go at it another week. Week day evenings it&#8217;s a light supper and in bed with the TV by 8:pm. It really is a matter of survival. I am my sole support. But I have often thought that if I did not have a job that fortunatly I can do from a wheelchair if necessary, just what would I do? I am still far more active than other people I know who had had  MS as long as I have and I think I owe that to my job and the the Rebif. So I will continue on even when I myself don&#8217;t know how I am going to do it because to pull out of a 30 year carreer would, I am afraid, leave me hopelessly adrift. You just get through the day the best way you can for as long as you can. It works for me so far.</p>
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