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	<title>Comments on: I choose PACING</title>
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	<description>Living with NEID (CFIDS)  &#38; FMS</description>
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		<title>By: Dominique</title>
		<link>http://www.4wallsandaview.com/cfids/i-choose-pacing/comment-page-1/#comment-484</link>
		<dc:creator>Dominique</dc:creator>
		<pubDate>Fri, 12 Feb 2010 21:10:18 +0000</pubDate>
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		<description>Johan -  I remember reading you do weights and cardio.  I am just not able to do either.  The weights put me in such horrific pain afterwords.  And cardio was causing me to not just crash but black out as well.  I am so glad you can do it though.  

Yeah, I haven&#039;t heard many people who have our illness being able to do the GET.  I tried and my doctors finally told me no weights and not cardio.  Just walking slowly, 2-3 times a week for up to 20 minutes, that&#039;s it.  I am not consistent because of repeated flareup but I do try to do it as often as I can.  I seem to be more consistent with it in the summer months.

I lived in Phoenix, AZ for a year and the dry heat helped me so much that I could do a little more walking.</description>
		<content:encoded><![CDATA[<p>Johan &#8211;  I remember reading you do weights and cardio.  I am just not able to do either.  The weights put me in such horrific pain afterwords.  And cardio was causing me to not just crash but black out as well.  I am so glad you can do it though.  </p>
<p>Yeah, I haven&#8217;t heard many people who have our illness being able to do the GET.  I tried and my doctors finally told me no weights and not cardio.  Just walking slowly, 2-3 times a week for up to 20 minutes, that&#8217;s it.  I am not consistent because of repeated flareup but I do try to do it as often as I can.  I seem to be more consistent with it in the summer months.</p>
<p>I lived in Phoenix, AZ for a year and the dry heat helped me so much that I could do a little more walking.</p>
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