Wow, extremely interesting! I remember a big arcticle about this new disease, l think in the New York Times

Yes, Paul! Absolutely!!!

Thanks for sharing this, Paul

Sounds super interesting! Might be an explanation for the fatigue, felt weakness and felt low energy?

I think we should not talk ABOUT patients or doctors, but WITH them.

Years ago l hated the word #psychosomatic, because on my own illness and recovery journey from #mecfs and other illnesses, l felt misunderstood and stigmatized. But at this conference there was no "all in your head", there was cutting-edge #neuroscience!

Very interesting!

Ich finde es gut, dass eine medizinische Fachgesellschaft bei einer so komplexen Erkrankung in verschiedene Richtungen denkt. Ich kann aber auch die Kommentare unter diesem Post verstehen. Ich hatte selbst lange ME/CFS und hatte genauso reagiert. Inzwischen sehe ich es differenzierter

davidarobson.substack.com/p/the-nordic...