Evergreen
Senior Member (Voting Rights)
I think defining PEM only as a delayed crash is problematic. This is particularly important when PEM is rightly regarded as the core feature of ME/CFS and is often touted as a feature that contraindicates exercise therapies. If patients and clinicians are unsure early on whether they have ME/CFS or not, then they can endure years of unnecessary confusion, and do things that may be detrimental to their long-term health as @Utsikt described above.
I think @richie put this well:
PEM during mild and moderate severity for me was mostly just feeling more crap following overexertion often for weeks or months. It didn't send me to bed like flu would. I wonder if it had, would I have deteriorated over time as I did? But again, if PEM is defined narrowly as completely incapacitating, then someone like me during that time could be considered as not having PEM.
This is from p.148 of the 2007 NICE guidelines - I thought it was a nice way of seeing how PEM was characterized in the 2000s:

The UK CMO 2002 report heavily emphasizes the delayed nature of PEM, but also acknowledges:
By contrast, the Canadian 2003 criteria, while being very clear that PEM is a core feature separate from fatigue, do not highlight delay nearly as much:
The International Consensus Primer, endorsed by many clinicians, does not emphasize delay either:
The 2021 NICE guidelines use the words "often" and "typically" to qualify delay in PEM, but do not qualify the disproportionate or prolonged nature of it at all:
This is my n=1: I’ve had plenty of instant PEM when I was gaslit into exercising 6-24 months post covid. I fully believed that I did not have PEM because it was not delayed. Nobody told me that I didn’t have PEM, they just told me that exercise would make things better.
In retrospect, it’s obvious that I had PEM, because it looked exactly like the often delayed PEM that I now experience when I’m unable to pace properly, 36 months post covid.
I think @richie put this well:
Differences in the way individual's body works and the demands on them and how they manage their activity will all impact on how PEM manifests. E.g. I had crashes from onset, but when my ME/CFS improved to mild and I was able to work half-days, I did not get severe crashes like others describe, and like I had previously experienced. But I remember very clearly that even though there was variation in how I felt at the beginning of the day, every single day, I would start feeling awful every day at about 11/11.30am. I had to go to bed as soon as I got home from work. The exacerbation of symptoms started during the exertion, and continued for the rest of the day. Not calling that PEM doesn't make sense to me."ME needs PEM and PEM needs to be delayed" goes well beyond cohorting and may leave many patients int the netherworld of MUPS, thrown out of the ME boat into the hands of whom? If PEM is observably delayed in the majority of patients with ME diagnosis then it is reasonable to hypothesise that the delay is related to the overall ME biology but it may be that patients with similar biology simply present PEM in another way. That happens in many conditions.
PEM during mild and moderate severity for me was mostly just feeling more crap following overexertion often for weeks or months. It didn't send me to bed like flu would. I wonder if it had, would I have deteriorated over time as I did? But again, if PEM is defined narrowly as completely incapacitating, then someone like me during that time could be considered as not having PEM.
I'm not sure this is universally true.PEM is a term created by clinicians listening to patients and discussing with other clinicians, and giving a name to a pattern of worsening way out of proportion to exertion their patients described. That pattern including a delay between the patient doing a bit more activity than usual, and getting much sicker a day or two later, and in many cases that lasted for days or weeks, and the amount of worsening would be way out of proportion to the exertion, which would have not caused any symptoms before the illness.
It is this observed pattern those doctors named PEM. And this pattern that more clinicians writing guidelines and definitions named PEM.
This is from p.148 of the 2007 NICE guidelines - I thought it was a nice way of seeing how PEM was characterized in the 2000s:

The UK CMO 2002 report heavily emphasizes the delayed nature of PEM, but also acknowledges:
That alone suggests to me that the primary feature of PEM is not the delay, but the prolonged nature of it.Younger patients do not always experience the delayed onset of symptoms after increased physical or cognitive activity, but they generally do have a prolonged recovery period after activity.
By contrast, the Canadian 2003 criteria, while being very clear that PEM is a core feature separate from fatigue, do not highlight delay nearly as much:
They go into more detail here:Post-Exertional Malaise and/or Fatigue: There is an inappropriate loss of physical and mental stamina, rapid muscular and cognitive fatigability, post exertional malaise and/or fatigue and/or pain and a tendency for other associated symptoms within the patient's cluster of symptoms to worsen. There is a pathologically slow recovery period-usually 24 hours or longer.
The malaise that follows exertion is difficult to describe but is often reported to be similar to the generalized pain, discomfort and fatigue associated with the acute phase of influenza. Delayed malaise and fatigue may be associated with signs of immune activation: sore throat, lymph glandular tenderness and/or swelling, general malaise, increased pain or
cognitive fog. Fatigue immediately following activity may also be associated with these signs of immune activation. Patients who develop ME/CFS often lose the natural antidepressant effect of exercise, feeling worse after exercise rather than better. Patients may have a drop in body temperature with exercise. Thus fatigue is correlated with other symptoms,
often in a sequence that is unique to each patient. After relatively normal physical or intellectual exertion, a patient may take an inordinate amount of time to regain her/his pre-exertion level of function and competence. For example, a patient who has bought a few groceries may be too exhausted to unpack them until the next day. The reactive fatigue of post-exertional malaise or lack of endurance usually lasts 24 hours or more and is often associated with impairment of cognitive functions. There is often delayed reactivity following exertion, with the onset the next day, or even later. However, duration of symptoms also varies with the context. For example, patients who have already modified their activities to better coincide with the activity level they can handle without becoming overly fatigued will be expected to have a shorter recovery period than those who do not pace themselves adequately.
The International Consensus Primer, endorsed by many clinicians, does not emphasize delay either:
PENE: a pathological, low threshold of fatigability
• post-exertional exhaustion & symptom flare
- immediate or delayed, & not relieved by rest
• prolonged recovery period
Post- Exertional Neuroimmune Exhaustion (PENE pen-e)
Normal fatigue is proportional to the intensity and duration of activity, followed by a quick restoration of energy. PENE is characterized by a pathological low threshold of physical and mental fatigability, exhaustion, pain, and an abnormal exacerbation of symptoms in response to exertion. It is followed by a prolonged recovery period.
The 2021 NICE guidelines use the words "often" and "typically" to qualify delay in PEM, but do not qualify the disproportionate or prolonged nature of it at all:
In my view, that's because the disproportionate and prolonged parts are the absolutely essential ones.Post-exertional malaise after activity in which the worsening of symptoms:
-is often delayed in onset by hours or days
-is disproportionate to the activity
-has a prolonged recovery time that may last hours, days, weeks or longer.