Katie reporting on what sounds like a travesty of a training module on ME/CFS from the NHS. David Strain in the saddle on that one was he?
Appeals to reason and compassion having failed, maybe public shaming might work…
Chris Ponting’s paper on identifying ME through blood markers has made it into New Scientist. Still puzzled though - he completely ignores previous claims of blood based biomarkers including Ron Davis’s nanoneedle. I questioned him on Bluesky but got no answer. www.newscientist.com/article/2447...
Levels of certain cells, fatty molecules and proteins in the blood are different in people with chronic fatigue syndrome than in those without it, which could help doctors spot the condition sooner
A big thank you to BBC Breakfast for giving us this platform. Truly humbled by @swastrosarah.bsky.social#There4ME
When I’ve been at my lowest, what’s stopped me ending my life is the possibility that something may turn up. In all the complexity of human nature and the unpredictability of experience, something new may happen. So far it always has, though it’s been a damn close run thing.
I just signed this important petition on Organise, please can you add your name? Introduce a #CleanAirPolicyorganise.network/s/92eb131a260b
Join me and sign the petition:
Hi Linda! Who else we know is on here?
Want to Feel less bad about not being able to exercise? Let Adam Rose show you the down side of the gym youtube.com/shorts/8gDQ7...
YouTube video by Adam Rose
Disappointed and surprised by AMA's poorly-researched article on #LongCOVID. CDC, Mayo, NIH all understand that graded exercise therapy is contraindicated in people with PEM. AMA is giving physicians advice that will cause harm. That isn't good for patients or providers.