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	<title>Blisstree &#187; public-awareness-campaign-cfids</title>
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		<title>Public Awareness for Chronic Fatigue Syndrome</title>
		<link>http://www.blisstree.com/articles/public-awareness-for-chronic-fatigue-syndrome-4/</link>
		<comments>http://www.blisstree.com/articles/public-awareness-for-chronic-fatigue-syndrome-4/#comments</comments>
		<pubDate>Thu, 02 Nov 2006 03:55:54 +0000</pubDate>
		<dc:creator>laura</dc:creator>
				<category><![CDATA[Diseases & Conditions]]></category>
		<category><![CDATA[CFIDS]]></category>
		<category><![CDATA[CFS Awareness]]></category>
		<category><![CDATA[Chronic Fatigue Syndrome/Fibromyalgia]]></category>
		<category><![CDATA[FM]]></category>
		<category><![CDATA[Jennie-Spotila]]></category>
		<category><![CDATA[Management of CFS]]></category>
		<category><![CDATA[News & Research]]></category>
		<category><![CDATA[public-awareness-campaign-cfids]]></category>

		<guid isPermaLink="false">http://cfssquared.com/2006/11/01/public-awareness-for-chronic-fatigue-syndrome/</guid>
		<description><![CDATA[Its the first week of November, and that means theme day for the Science and Health Channel of b5 media, is once again happening.  This month&#8217;s theme is to pass along a little link love.  I have been thinking and thinking and thinking about who to link to, and why they should get a special mention.  Here is what I have decided.  I read quite a few blogs about living with CFS and chronic illness in general.  I read sites about medications and alternative treatments&#8230;..so many that I just can&#8217;t decide.  There are quite [...]<p>Post from: <a href="http://www.blisstree.com">Blisstree</a></p>
<p><a href="http://www.blisstree.com/articles/public-awareness-for-chronic-fatigue-syndrome-4/">Public Awareness for Chronic Fatigue Syndrome</a></p>
]]></description>
			<content:encoded><![CDATA[<p>Its the first week of November, and that means theme day for the Science and Health Channel of b5 media, is once again happening.  This month&#8217;s theme is to pass along a little link love.  I have been thinking and thinking and thinking about who to link to, and why they should get a special mention.  Here is what I have decided.  I read quite a few blogs about living with CFS and chronic illness in general.  I read sites about medications and alternative treatments&#8230;..so many that I just can&#8217;t decide.  There are quite a few listed on my blogroll, so once you are done reading today&#8217;s post go click on one of those great links to read someone else&#8217;s point of view.  Because they are all great.  </p>
<p>No indeed, my link will be a little different, because its not really a link at all.  Its a reminder that the CFIDS Association of America is doing a huge campaign right now, for public awareness.  Part of this campaign is that tonight (Nov 2) there will be a spot discussing CFS on NBC Nightly News, and again on Friday (Nov 3) on Fox morning news &#8211; please check your local listings.  Participating in these discussions will be experts on CFS research, physicians specializing in CFS, and patients who live with this illness.  I should mention here specially, that one of my regular readers and frequent commenters Jennie Spotila will be speaking as a PWC for these interviews.</p>
<p>Jennie has been a great help to me, over the last few months, while I struggle to regain control of my health (as have a whole lot of other readers, and bloggers).  I wish her huge amounts of luck while she faces those cameras, and all of those inquiring journalists.  &#8220;Go get &#8216;em, Jennie!!!!&#8221;</p>
<p>Post from: <a href="http://www.blisstree.com">Blisstree</a></p>
<p><a href="http://www.blisstree.com/articles/public-awareness-for-chronic-fatigue-syndrome-4/">Public Awareness for Chronic Fatigue Syndrome</a></p>
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