Quixotic: My M.E. Blog
Sunday, February 15, 2015

Re-Ranking My Supplements

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As I wrote about in my last post , I've been planning to rank all of my supplements and prescriptions in order of most effective to leas...
4 comments:
Saturday, February 7, 2015

I changed doctors. My new path....

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For the past several years, I have regularly seen two doctors for ME/CFS.  One of them is a well-respected ME/CFS specialist.  (I call him D...
4 comments:
Monday, January 12, 2015

2014 - My Health in Review

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2014 saw significant improvement for me again.  Based on an average of all 365 days of my daily health chart, my daily health rating went up...
4 comments:
Thursday, January 8, 2015

On Celebrex, Pain, and My ****

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[This post contains some detailed descriptions dealing with male anatomy.  If that bothers you, don't read on.] Just after Christmas...
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Thursday, December 25, 2014

You know you have ME/CFS when...

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The Christmas gift you are most excited about is a pair of battery-heated socks. 
1 comment:
Sunday, December 21, 2014

No More Methylation Experiments

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I started experimenting with Nutrigenomics and Amy Yasko's methylation protocol almost two years ago, in March, 2013.  Prior to that, I ...
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Thursday, November 20, 2014

No Interferon for me

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I wrote in my October 12th post  that Dr. C offered to give me samples of Interferon injections, combined with Prozac, as a short-term (1 - ...
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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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