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Lessons from ME/CFS: Finding Meaning in the Suffering

Andrew Gladman muses upon what lessons he has taken from two years of ME/CFS. If you’re aware of my previous articles here at Phoenix Rising  then it’s pretty clear that I don’t generally spend my time musing upon the philosophy of the disease. I find it better to spend my time reading research and trying my best to break it

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ME/CFS: In Free Fall Through the Looking Glass

Jody Smith continues to try to put into words the horror of the altered state that hobbles the brains of those with ME/CFS …  If you’re not a fan of hallucinatory drugs you’re gonna hate ME/CFS. When I first became ill in March of 1992, the feeling of altered reality inside my head, the shaking which could not be seen

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No Longer Naive in the Ways of The Beast

After having lived for years with ME/CFS, Jody Smith learned there’s more to this beast of an illness than she realized, and that what might help one person may not help others … When I first got back online five years ago, I was naive in the ways of this beast we call ME/CFS. I guess I thought that whatever it

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The Fable known as The PACE Trial

Graham, Janelle and Bob, have once again excelled themselves with their latest take on the ‘poisoned apple’ that was the PACE Trial… Once upon a time, long, long ago a king and queen ruled over a distant land. The queen was kind and…. Whoops, sorry there! I got confused for a moment. Wrong fantasy tale… Several years ago a team

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The Chronic Fatigue Initiative and Interview with Mady Hornig

In a follow-up article to the recent IACFS/ME conference presentation in San Francisco, and after speaking at length with Dr. Mady Hornig, ‘searcher’ delves deeper into the impressive work being completed by the Chronic Fatigue Initiative, and focuses in on those cytokine results … Members of the Chronic Fatigue Initiative (CFI) and Scott Carlson, the executive director of the Hutchins Family

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Leptin

Andrew Gladman reflects upon the recent IACFS/ME conference and the buzz surrounding a small molecule, leptin. It’s safe to say that the past couple of weeks, following the IACFS/ME 2014 conference, have been something of a whirlwind in terms of new ME/CFS research being unveiled. Now that the dust has had a chance to settle let’s take a step back

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Science to Patients: Talking ME, Exercise and the Mitochondria – with Dr Charles Shepherd

The latest video release from the Dutch group ME/cvs Vereniging, with Dr Charles Shepherd from the UK ME Association, and announcing a live chat session to be held Thursday, April 10, 2014… ME/cvs Vereniging launched a series of broadcasts from expert clinicians and researchers in January 2013, as part of a government subsidized project called, “Science to Patients”. Each expert

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