[ME/CFS Research Foundation] International ME/CFS Conference 2026 7–8 May

Five hours til this kicks off! If you're there please post something. A selfie with @MelbME or even a pic of the coffee stand in the conference hallway!
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Scheibenbogen, Fluge and Ponting are three of first five people on stage so it starts with a bang. Then Michelle "PET tracer" James is after them.

I believe the whole thing is meant to be broadcast live too. Register: https://cloud.seatable.io/dtable/forms/custom/conference2026en/
 
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What presentations is everyone looking forward to/interested in?
Lots but there is a study on ATP phosphocreatine ratios mid afternoon Thursday that I want to see. Phosphocreatine is an overlooked energy source, used for the very first few seconds of energy. Creatine kinase is supposed to catalyse its use, Wust found less CK than he expected, I reckon there's a clue floating round in that space if we keep looking!
 
Evidently 6500 watching online. Chris gave a great opening talk.

Looking forward to Michelle James shortly on whole-body PET, followed by Qiang Yu talking about their team's advanced MRI diffusion study ("neuroinflammation") that we had questions re the interpretation in this thread, and then another neuroimaging talk. The last is on functional MRI that might complement their previous structural studies eg this one recently.
 
I didn't manage to register for this but local UCL colleagues are attending.

I don't think we expected HLA genes to come up but I wonder why Chris seems to be suggesting that BTN2A1 is not immunological. Maybe it isn't but it seems likely on the face of it.
 
Those of us who block trackers on our computers/phones can't see tweets - we either get blank space or an error message. So it would be really useful and appreciated if the text of tweets could be copied and pasted into posts. Sorry for the extra work!
 
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