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	<updated>2026-05-18T14:22:58Z</updated>
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		<id>https://me-pedia.org/w/index.php?title=Talk:Inflammation&amp;diff=82950</id>
		<title>Talk:Inflammation</title>
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		<updated>2020-06-25T15:31:41Z</updated>

		<summary type="html">&lt;p&gt;Yvonne:/* ME/CFS after Coccidioidomycosis (Valley Fever) -- 174.17.99.52 11:09, June 25, 2020 (EDT) -- 174.17.99.52 11:09, June 25, 2020 (EDT) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;ME/CFS after Coccidioidomycosis (Valley Fever) &lt;br /&gt;
&lt;br /&gt;
After a bout with Valley Fever in 2008, I have been experiencing many of the post-symptoms of ME/CFS. &lt;br /&gt;
&lt;br /&gt;
In 2008 I developed a cough that was activated by my attempts to speak, pneumonia, hives the size of a human hand on the inside of my thighs, FINALLY my doctor decided to test me for Coccidioidomycosis. &lt;br /&gt;
&lt;br /&gt;
Upon further examination it was found that the fungus had created several (3] holes in my lungs. &lt;br /&gt;
&lt;br /&gt;
For the next two years, I had CT scans every 6 months to ensure the fungus had not spread.&lt;br /&gt;
&lt;br /&gt;
As the years passed, I continued to experience brain fog, low orthostatic tolerance, poor sleep, inability to focus, low energy levels. &lt;br /&gt;
&lt;br /&gt;
ME/CFS has stolen the life I once knew.&lt;/div&gt;</summary>
		<author><name>Yvonne</name></author>
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