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it's actually so concerning how many times this has happened. And it's sad because I see people struggling, crying, and upset over their symptoms. Word for word describing PEM, but then when you comment and ask if they've considered ME/CFS, they ignore it🥲 And so I worry for them, because if it is MEC/FS, and they are continuing to trigger PEM, they will likely get worse before they accept what is happening to them. I do not wish that on anyone, because it is what happened to me! I didn't know
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it's actually so concerning how many times this has happened. An…
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