Tag Archives: GcMAF

…a little better all the time…

Posted on May 29, 2012 by

Memorial Day weekend is my sickiversary. Eight years today. Things are looking up, though – I think I’m doing better now than any point since the end of 2007. Among the indications of improvement: I’ve been playing Words With Friends … Continue reading →

Posted in ME/CFS | Tagged , , , , , | 45 Comments

The Post-Appointment Post, 2012

Posted on April 5, 2012 by

I’ve been away from the blog because of my annual appointment with Dr. Cheney on March 20th. First I was trying to rest up to get ready for it, then I was trying to recover from it. This was the … Continue reading →

Posted in ME/CFS | Tagged , , , , , , , , | 33 Comments

The End of IRIS

Posted on February 26, 2012 by

Well that sucked. Some of you may remember that I’ve been dealing with IRIS caused by my experimental treatment, GcMAF (see my previous posts, “Everybody Gets Through IRIS” and “Further Adventures in IRIS”, and if you want a brief explanation of … Continue reading →

Posted in ME/CFS | Tagged , , , , | 33 Comments

Further Adventures in IRIS

Posted on September 22, 2011 by

My first entry on this subject, “Everybody Gets Through IRIS,” is here, and a third, “The End of IRIS,” is here. My immune system is still freaking out for fun and profit. Yes, it’s true, we’ve reached the six-week mark … Continue reading →

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“Everybody Gets Through IRIS.”

Posted on August 18, 2011 by

There’s a second entry on this topic, “Further Adventures in IRIS,” here, and a third, “The End of IRIS,” here. That’s what Dr. Cheney told me at my appointment in April. IRIS, approximately, is what happens when your immune system … Continue reading →

Posted in ME/CFS | Tagged , , , | 16 Comments

The Post-Appointment Post

Posted on April 16, 2011 by

The information contained in this post is my interpretation of Dr. Cheney’s recommendations for me. This is not medical advice. Please don’t change your treatment plan based on anything in this post. The previous two times we’ve done the drive … Continue reading →

Posted in ME/CFS | Tagged , , , , , , , , , | 18 Comments