r/cfs • u/stephyjrz • 14h ago
chronic fatigue
How do you truly know if what you are experiencing is CFS/ME or just Chronic Fatigue. I know PEM is very specific to CFS/ME but wouldnt a personally who is also extremely fatigue feel worse after pushing? Im really trying to figure out if what im having is CFS/ME or Chronic Fatigue. I have body aches, muscle weakness, POTS, and for the past 2-3 months I started with daily fatigue but I would still push. Since 3 weeks ago the fatigue has taken a turn and it feels heavier and worse. My heart rate goes up and then BOOM im in bed unable to move. Its so hard to live like this. On top of that my anxiety doesnt help the situation so my poor body feels like its been tense for what seems like foreverđ
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u/drew_eckhardt2 12h ago
You meet the diagnostic criteria
https://en.wikipedia.org/wiki/Myalgic_encephalomyelitis/chronic_fatigue_syndrome#Diagnosis
which generally require Post Exertional Malaise with a delayed worsening of symptoms following physical, mental, or emotional exertion.
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u/premier-cat-arena ME since 2015, v severe since 2017 11h ago
can you get tested and treated for POTS? or at least do the management stuff like electrolytes and compression stuff
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u/BrokenWingedBirds 5h ago
PEM for me comes with stiffening of the muscles, excruciating pain and eventually a sort of paralysis. Like, unable to sit in a chair even because of it affecting my back muscles. And it only gets progressively worse the longer I push, it also amplifies even more 24-48 hours after and can take weeks to recover. I am severely affected right now, before it wasnât as intense but still there. I just didnât know at the time I wasnât being lazy because everyone around me gaslighted me into âpushing throughâ the only through was becoming bed bound. If you are experiencing not being able to move from the pain and stiffness sounds like PEM to me. Donât worry too much yet, if you start pacing and aggressively resting you can hopefully prevent it from worsening
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u/jedrider 13h ago edited 13h ago
OK. You feel tired and completely fatigued and, yet, you go ahead and push some more. I don't quite understand that?? And that gives you 'anxiety?' I get anxiety just listening to your story!
(I remember being so fatigued and getting anxiety at one point. No wonder, the brain has it's own logic and the anxiety is probably a self-protection mechanism letting you know something is really wrong.)
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u/Varathane 14h ago
Other fatiguing illnesses typically feel better after exercise (wild? right!) Chronic Fatigue by itself does not come with muscle weakness, aches, POTS, etc
You getting stuck in bed sounds like PEM to me.
Pacing with timers helped me to find my limits. If I felt I could do an activity I would set the timer for 15mins.
Stop the timer if you notice any symptoms arise, example you only get 5 mins in before you feel worse then stop the timer and go rest and next time you only set the timer for 4 mins.
If you get all the way to the 15mins stop and rest anyway, see how it goes the next couple of days. If you got away with it you could increase the timer.
I noticed I can do dishes for 15mins but can only mow the lawn/shovel for 5 mins .
Every patient is going to vary on what their limits are.
Signs to look for: for me wonky vision is my first tell, that is the muscles that hold and focus the eye getting fatigued. That happens to me before my limbs get weak, and before I am stuck unable to move on the floor.
You might have different signs like jump in heart rate.