Paul Garner on Long Covid and ME/CFS - BMJ articles and other media.

Did he have Covid and long Covid or did he have ME/CFS?
This is the problem with the 'hurry' for people to get an ME/CFS diagnosis. Most descriptions of ME/CFS begin with something like "ME/CFS (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome) is a chronic, debilitating illness characterized by profound fatigue, post-exertional malaise, and multi-system symptoms that significantly impair daily functioning."

Chronic is the key word here. If you 'recover' a couple of months after a diagnosis, then presumably the diagnosis was wrong(?)
 
This is the problem with the 'hurry' for people to get an ME/CFS diagnosis. Most descriptions of ME/CFS begin with something like "ME/CFS (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome) is a chronic, debilitating illness characterized by profound fatigue, post-exertional malaise, and multi-system symptoms that significantly impair daily functioning."

Chronic is the key word here. If you 'recover' a couple of months after a diagnosis, then presumably the diagnosis was wrong(?)
He says that he was told he met the Canadian Consensus Criteia for ME. He wasn’t diagnosed. He really should have got himself referred if he was concerned, but then he recovered so I guess there wasn’t time.
 
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