K De Meirleir: Conference speech August, 6th:"Biomarkers which identify CFS/ME patients"

This is a bit naughty, since there isn't a proven biomarker.

I think there is a difference between “a” biomarker and “the ultimate” biomarker for ME. There are a lot of bloodlevels or other markers “off” in patients, but we just don’t know yet if it specific enough for this one disease.

KDM has presented these findings of a combination of four biomarkers to diagnose ME more often, so it’s not new. I do find it interesting because those four levels are indeed off in my case, so I would be interested if this was replicated.
 
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