Quixotic: My M.E. Blog
Monday, January 9, 2012

What's In A Name

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I'm not treading any new ground here, but I was reflecting today on what a truly unfortunate label "Chronic Fatigue Syndrome" ...
Thursday, January 5, 2012

New Blood Tests Clarify My Diagnosis/Treatment Plan

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About 2 weeks ago, I received a copy of my most recent blood work.  This was the blood panel that was ordered by my ME specialist and which ...
Wednesday, January 4, 2012

Stomach Medication = Candida Overgrowth

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In my 12/20 post, I discussed my theory that years of acid reducing stomach medications may have contributed to my ME.  It turns out I was r...
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Monday, January 2, 2012

Donating To ME Research

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On the heels of my last post, discussing why ME/CFS research is behind the times, I decided to donate funds to an ME/CFS research laboratory...
Thursday, December 29, 2011

Why is ME/CFS research so far behind the times?

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Why is ME/CFS research and awareness so far behind the times?  The most oft cited answers to this question are (1) it is not life threateni...
Wednesday, December 28, 2011

Things That Make It Better

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This may seem like a strange topic to be posting after a crash, but bear with me.  There's no doubt that, overall , I have improved over...
Tuesday, December 27, 2011

Things That Make It Worse: Altitude and Air Travel

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I'm starting a series of posts tracking what makes my ME symptoms better and worse.  While I've discovered a number of things that h...
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About Me

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Patrick W. Calvin
I came down with ME in June, 2011. I was diagnosed six months later. This blog tracks my progress; my successes and failures along the path to (hopefully) sustained remission. I live with my wife and two young daughters in Southern California.
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