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Systemic bias against people with ME has been helped along for decades.

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And if anyone with ME/CFS could pose a real physical danger to such a conference! Sorry, jokes asides, this simply makes me mad. Yes, I was able to get a little better with Pacing, neurotraining and so on. But I got A LOT better as a more or less side effect after I took Paxlovid due to a COVID-19 infection. And this is not psychosomatic, as I feared to get a lot worse with Covid.

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