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David Davies-Payne

@d2p.bsky.social
1.9K followers 1.5K following 187 posts

Paediatric Radiologist, Aotearoa New Zealand Following more immunologists than radiologists #MECFS #LongCOVID and a bit of #MacDev #iOSDev he/him ddp.nz | dysimmune.nz

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David Davies-Payne @d2p.bsky.social · 22/09/2026
"…18% of patients with coronary function testing-confirmed ANOCA meeting diagnostic criteria for #MECFS. Invasive cardiopulmonary exercise testing (iCPET) in patients with [both] reveals a primary peripheral, not cardiac, limitation to exercise." #Cardiology journals.physiology.org/doi/10.1152/...
journals.physiology.org
Hemodynamic Phenotyping in ME/CFS and ANOCA: Complementary Insights from Coronary Function Testing and Invasive Cardiopulmonary Exercise Testing | American Journal of Physiology-Heart and Circulatory Physiology | American Physiological Society
This single-center cohort study sought to evaluate the association between Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Angina with Non-Obstructive Coronary Arteries (ANOCA), by determining the observed frequency of ME/CFS among patients with ANOCA diagnosed by coronary function testing (CFT). Additionally, we performed an exploratory analysis of the diagnostic utility of invasive cardiopulmonary exercise testing (iCPET) in ME/CFS patients with CFT-confirmed ANOCA, with the aim of identifying the predominant physiological mechanism responsible for exertional limitation in this population. Systematic medical record review of 261 patients with CFT-confirmed ANOCA was performed using standardized diagnostic criteria to identify concurrent ME/CFS diagnosis. ME/CFS was identified in 47 patients, representing an observed frequency of 18%. The only statistically significant difference between ANOCA patients with and without ME/CFS was a higher frequency of connective tissue disease in the ME/CFS group (p = 0.0221). In a separate cohort of 27 patients with ME/CFS who underwent iCPET, 24 patients (89%) had CFT-confirmed ANOCA. The diagnosis of ANOCA by CFT prompted a change in medical management in 81% of patients in this cohort. iCPET revealed a primary peripheral limitation to exercise, characterized by impaired peak systemic oxygen extraction despite normal peak oxygen delivery. This study demonstrates a clinically significant association between ME/CFS and ANOCA. These findings underscore the clinical value of CFT in patients with ME/CFS and exertional chest pain and highlight iCPET as a complementary tool for hemodynamic phenotyping in this population. Prospective studies incorporating simultaneous CFT and iCPET with molecular phenotyping are warranted.
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David Davies-Payne @d2p.bsky.social · 13/08/2026
"While these findings are preliminary and the hypoxic challenge not equivalent to physical exertion, the experimental findings of our study support the concept of impaired neuro-metabolic and vascular adaptive capacity in ME/CFS." #MECFS #MRI #neuroimaging www.medrxiv.org/content/10.6...
medrxiv.org
Experimental hypoxia to probe neuro-metabolic and vascular dysregulation in ME/CFS: a multimodal proof-of-concept MRI study
Background Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a poorly understood, debilitating multisystem condition. Converging evidence implicates impaired cellular bioenergetics, neuro...
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David Davies-Payne @d2p.bsky.social · 28/07/2026
…"long COVID and ME/CFS displayed higher proportions of type IIa/IIx fibers, and signs of intrinsic mitochondrial dysfunction, observations that were not seen following bed rest." #MECFS #LongCovid www.nature.com/articles/s41...
nature.com
Skeletal muscle properties in long COVID and ME/CFS differ from those induced by bed rest - Nature Communications
Low aerobic capacity in patients with long COVID and ME/CFS is often attributed to physical inactivity. The authors show that long COVID and ME/CFS patients have distinct skeletal muscle changes that ...
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David Davies-Payne @d2p.bsky.social · 16/06/2026
📢 The WE&ME Foundation announces a biomedical research call for #MECFS 🔬🙋🏻‍♀️ • Indicative: ~7 projects funded, subject to quality • Budget: EUR 120,000 to EUR 180,000 per project • International applications • Selection by international jury 👉 www.weandmecfs.org/weme-projects/
weandmecfs.org
WE&ME Projects • WE&ME Stiftung
Scope of the Call This call is open to research teams that aim to advance our understanding of the biological mechanisms of Myalgic
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David Davies-Payne @d2p.bsky.social · 12/05/2026
WatchME for iPhone and Apple Watch v2.10 now available To help #pwME with daily pacing for #MECFS iOS 17 | watchOS 10 Free. No data collected. apps.apple.com/app/watchme/... #MEAwarenessDay
apps.apple.com
WatchME App - App Store
Download WatchME by David Davies-Payne on the App Store. See screenshots, ratings and reviews, user tips, and more apps like WatchME.
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David Davies-Payne @d2p.bsky.social · 12/05/2026
This is very welcome news. It will extend the initial findings from DecodeME at the University of Edinburgh, led by Prof Chris Ponting @cgatist.bsky.social #MECFS #LongCovid
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ME/CFS Science @mecfsscience.org · 06/05/2026
1) 1) Interesting interview of Dr. Audrey Ryback by David Tuller. Her recent study showed that there are likely two age peaks for when people get ME/CFS. It helps to characterise ME/CFS as a unique clinical entity.
Screenshot of interview of Audrey Ryback by David Tuller on bimodal onset patterns in ME/CFS.
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David Davies-Payne @d2p.bsky.social · 05/05/2026
WatchME v2.10 public beta - To help with daily pacing: #MECFS #LongCovid #iOS 17+ | #watchOS 10+ | Free | No data collected testflight.apple.com/join/PoR8lKli
testflight.apple.com
Join the WatchME beta
Available on iOS
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Fred Rossi @darthfoo.bsky.social · 04/05/2026
A quote from my new piece, The Inventory of Loss. “The grief is ongoing because the illness is ongoing, and new losses arrive as old ones calcify into something you have learned to carry.” darthfoo.substack.com/p/the-invent... #LongCOVID #MECFS #PwME
darthfoo.substack.com
The Inventory of Loss
What chronic illness takes that no one warns you about
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David Davies-Payne @d2p.bsky.social · 01/05/2026
Request for #LongCovid subjects for a research study 🙋🏻‍♀️💪🏼💉🩸 - Women aged 18+ - In #Melbourne #Victoria - 1️⃣ blood sample & questionnaire Looking for a signature in platelet microRNAs Dr Sarah Annesley Dr @danielmissailidis.bsky.social La Trobe Uni Entry survey redcap.latrobe.edu.au/redcap/surve...
redcap.latrobe.edu.au
CCC screen
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Charlie Hillier @charliehillier.bsky.social · 31/03/2026
My good friend Tom Micklem who I first met back in university is running the London Marathon to raise money for Action for ME! @actionforme.bsky.social You can read about it and donate here, good luck Tom!: 2026tcslondonmarathon.enthuse.com/pf/tom-micklem
2026tcslondonmarathon.enthuse.com
Tom is running the London Marathon
Hello everyone Should all go to plan, I will be running the London marathon in April and I am taking the opportunity to raise some money for Action for M.E. Myalgic encephalomyelitis (M.E.), or chroni
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Fred Rossi @darthfoo.bsky.social · 30/03/2026
A quote from my piece, The Debt Came Due. “There is a version of my life that exists in my memory like a photograph from a trip I’ll never take again. In that version, I wake up and get out of bed without negotiating with my body first.” #LongCOVID #MECFS #PEM #PwME substack.com/home/post/p-...
substack.com
The Debt Came Due
Notes From a Crash
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Prof Christina Pagel @chrischirp.bsky.social · 27/03/2026
I wrote about the findings from the inquiry about the impact of the pandemic on the NHS, and the mistakes of the first year. I hope it makes you angry - it should make us all angry. open.substack.com/pub/christin...
open.substack.com
The UK Covid Inquiry has laid bare the avoidable horror of the second Covid wave
It is becoming ever clearer both how devastating the second wave of winter 2020/21 was, and how much of that devastation could have been avoided.
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David Keegan @drdavidkeegan.bsky.social · 23/03/2026
SARS-CoV-2 (COVID-19) is anything but a common cold. Each infection can cause severe illness and even death in children at rates +++ higher than the common cold. It triggers long-covid (now the most common chronic illness in children) and other cobditions like diabetes. Not the common cold.
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Simon McGrath @simonmcg.bsky.social · 21/03/2026
Patients were central to the team that found ME/CFS is most likely to start in the teens and early middle age. Two age peaks is unusual for any disease and might help unravel ME's causes. academic.oup.com/ooim/advance... 1/ team credits to follow
academic.oup.com
Incidence age is bimodal for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, with higher severity burden for early onset disease
Abstract. Myalgic Encephalomyelitis, or Chronic Fatigue Syndrome (ME/CFS), is a disease of uncertain origin. Studies of Norwegian health records have sugge
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David Davies-Payne @d2p.bsky.social · 17/03/2026
"findings reveal widespread alterations in multiple NII- derived metrics across white matter fibres, suggesting complex inflammatory processes affecting white matter microstructure in ME/CFS patients." #MECFS #MRI #neuroimaging #radiology onlinelibrary.wiley.com/doi/10.1002/...
onlinelibrary.wiley.com
Evidence of White Matter Neuroinflammation in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Diffusion‐Based Neuroinflammation Imaging Study
Diffusion-based neuroinflammation imaging (NII) reveals widespread white matter abnormalities in ME/CFS patients, undetected by conventional DTI. NII metrics associate with mental health, disability ....
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David Davies-Payne @d2p.bsky.social · 16/03/2026
🙋🏻‍♀️💪🏼💉🩸 Request for subjects for a research study - Women aged 18+ - In #Melbourne #Victoria - With #LongCovid & #MECFS Looking for a signature in blood platelet microRNAs One blood sample & questionnaire Study being run by - Dr Sarah Annesley - Dr Daniel Missailidis @danielmissailidis.bsky.social
Flyer from La Trobe University with a prominent red background.

Looking for Long COVID patients

Have you had a COVID-19 infection and are suffering from unexplained fatigue, respiratory issues, brain fog or muscle pain 3+ months post infection? Are your symptoms worse after exertion?

You may be suffering Long COVID.

We would love to hear from you!

If you live in Victoria and would be willing to donate a blood sample, please contact Dr Sarah Annesley at s.annesley@latrobe.edu.au or Prof Stephanie Gras at s.gras@latrobe.edu.au
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Eric Topol @erictopol.bsky.social · 04/03/2026
The proteome (>7,000 circulating proteins) in people with ME/CFS exhibits immune system, vascular and metabolic dysregulation compared with controls (and likely homologous in #LongCovid) www.cell.com/cell-reports...
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Tom Kindlon @tomkindlon.bsky.social · 27/02/2026
Exciting to read about some of the expensive ME/CFS & long Covid research planned in Germany (using some of€500 million budget) including that using long-term samples which allow comparisons of samples before and after developing the conditions www.helmholtz.de/en/newsroom/... #LongCovid #MEcfs
Long COVID, ME/CFS, and other post-infectious diseases pose new questions for medicine and society. With the long-term data from the NAKO Health Study, Germany now aims to systematically clarify why some infections leave lasting effects and how those affected can be better supported.

Post-infectious diseases are on the rise. Infections such as COVID-19 can lead to chronic conditions such as Long COVID or ME/CFS months or even years later, affecting hundreds of thousands of people in Germany.
As part of the National Decade Against Post-Infectious Diseases, the Federal Ministry of Research, Technology, and Space (BMFTR) is investing approximately 500 million euros over the next decade to systematically research causes, disease mechanisms, diagnostics, and therapies and to improve care.
The NAKO Health Study, with 200,000 participants, provides crucial long-term data and enables a rare before-and-after comparison with data and biosamples from before, during, and after infection.
The aim of research is to determine the actual prevalence of post-infectious diseases more accurately, to better understand the underlying biological processes, and to effectively support those affected through targeted interventions in the future.
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David Davies-Payne @d2p.bsky.social · 25/02/2026
"… revealing widespread transcriptional remodeling across both innate and adaptive immune compartments." "Mechanistically, we identify Galectin-9–TIM-3 interaction as a potential pathway driving ɣ𝛿 and MAIT cell depletion in LC." #MECFS #LongCovid #GDTcells www.frontiersin.org/journals/imm...
frontiersin.org
Frontiers | Single-cell analysis reveals immune remodeling of monocytes, NK cells, T cell exhaustion, and Galectin-9–associated depletion of gamma delta and mucosal-associated invariant T cells in Lon...
IntroductionThe cellular mechanisms underlying Long COVID (LC) associated with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) remain poorly unde...
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Paul Krugman @pkrugman.bsky.social · 17/02/2026
To understand the catastrophic turn in U.S. health policy, follow the money paulkrugman.substack.com/p/how-the-ka...
paulkrugman.substack.com
How the Kakistocracy Became a Quackistocracy
Corruption is a germ’s best friend
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Mark Ungrin @mark-ungrin.bsky.social · 11/02/2026
Huh. It's almost as if betting the world on a game of "let's pretend" between a bunch of pseudoscientific cosplayers wasn't a great public health strategy for dealing with COVID after all. 🤔 It must be nothing though. I'm sure we could trust management-class MDs to tell us if they got it wrong...
fred.stlouisfed.org
Population - With a Disability, 16 Years and over
Population - With a Disability, 16 Years and over
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David Davies-Payne @d2p.bsky.social · 26/01/2026
"We found that plasma concentrations of MASP-2/C1Inh were significantly higher in patients with long COVID relative to healthy convalescent individuals, indicating sustained activation of the lectin complement pathway." #LongCovid onlinelibrary.wiley.com/doi/10.1111/...
onlinelibrary.wiley.com
Activation of the Lectin Pathway Drives Persistent Complement Dysregulation in Long COVID
The complement cascade, a series of blood proteins that assists in the recognition and neutralisation of pathogens, either independently or in conjunction with antibodies, is persistently activated i...
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Eric Topol @erictopol.bsky.social · 19/01/2026
Eminence-based medicine ;-)
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David Davies-Payne @d2p.bsky.social · 09/01/2026
Multi-omics identifies lipid accumulation in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome cell lines: a case-control study @danielmissailidis.bsky.social et al. #MECFS link.springer.com/article/10.1...
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Kai Kupferschmidt @kakape.bsky.social · 18/12/2025
“This year, renewables surpassed coal as a source of electricity worldwide, and solar and wind energy grew fast enough to cover the entire increase in global electricity use from January to June according to energy think tank Ember“ @science.org’s Breakthrough of the Year is the growth of renewables
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Johan Van Weyenbergh @johanvawe.bsky.social · 16/12/2025
More evidence-based disease mechanisms = less #stigma for Long COVID patients! 👇👇👇👇 Human #genetics implicate thromboembolism in the pathogenesis of #LongCOVID in individuals of European ancestry. www.nature.com/articles/s44...
nature.com
Human genetics implicate thromboembolism in the pathogenesis of long COVID in individuals of European ancestry - Nature Cardiovascular Research
Schuermans et al. discovered that genetic predisposition to thromboembolism is associated with a greater risk of post-acute sequelae after SARS-CoV-2 infection, including long COVID, and downstream an...
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Valentin Riedl @vavatin.bsky.social · 16/12/2025
fMRI signals “up,” but neural metabolism might be going “down.” In our @natneuro.nature.com paper, we demonstrate that about 40% of voxels with robust BOLD responses exhibit opposite oxygen metabolism, revealing two distinct hemodynamic modes. rdcu.be/eUPO8 funds @erc.europa.eu #neuroskyence 🧵:
BOLD signal changes can oppose oxygen metabolism across the human cortex, Nature Neuroscience
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Tom Kindlon @tomkindlon.bsky.social · 09/12/2025
Well done & thanks to these healthcare professionals (PTs)/similar ( @sunsopeningband.bsky.social @profmarkfaghy.bsky.social et al) for this new e-letter 👏 "In the Long Run, Misleading Participants Will Harm More Than Help in Long COVID Research" bmjopen.bmj.com/content/15/1... #LongCOVID #PEM
Published on: 9 December 2025
In the Long Run, Misleading Participants Will Harm More Than Help in Long COVID Research
Todd E. Davenport, Professor & Chair University of the Pacific, Workwell Foundation
Other Contributors:
Staci R. Stevens, Exercise Physiologist
Mark A. Faghy, Professor
Jessica DeMars, Respiratory Physiotherapist
J. Mark Van Ness, Professor & Chair
Respect for persons, beneficence, and justice are bedrock ethical principles in science. They are especially important when studying vulnerable populations. Billias et al. argue that deception is necessary to assure the internal validity of their exercise study involving people living with long COVID.[1] Here, we assert the use of deception is ethically indefensible and scientifically unnecessary in this population. It undermines informed consent, increases risks for harms, exploits the vulnerability of participants, and erodes trust in science and health care, all while exploring a question that already has been asked and answered satisfactorily enough to inform clinical recommendations.

Physical activity is a common trigger for post-exertional malaise (PEM),[2 3] which is common in people living with long COVID.[4] PEM involves an impaired recovery response from exertion that is distinct from deconditioning.[5 6] The hallmark of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is PEM. Exercise is no longer recommended in contemporary clinical guidance for ME/CFS, because an accumulation of evidence from research and lived experience suggests it is likely to cause avoidable harms.[7] Exercise prescription without adequate safeguards for PEM even may be considered negligent practice. The protocol acknowledges people living with PEM often worsen with exercise dosages that may be appropriate for other conditions.[1] Several of the authors of this protocol also previously published a systematic review acknowledging risks of exercise in people with long COVID related to PEM.[8] However, the author…
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Fred Rossi @darthfoo.bsky.social · 01/12/2025
I’m excited to share my latest work, “The Small Life.” It explores the little things that still bring me joy as I navigate #LongCovid and #MECFS. #ChronicIllness substack.com/home/post/p-...
substack.com
The Small Life
Calculating Worth with Diminished Returns
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David Davies-Payne @d2p.bsky.social · 24/11/2025
This blog post is a very accurate characterisation of the experience of living with #PostExertionalMalaise #PEM. Recommended reading for healthcare professionals who want to understand #MECFS and #LongCovid. You generally only see these patients when they're at their best — not in the aftermath.
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Ali Christy, MD, PhD @oligoclonalband.medsky.social · 15/11/2025
I never met Alice Wong in person, but like so many great writers I felt like I knew her - and unlike many, when I emailed she emailed right back. ❤️ Peds neurologist @dianacejasmd.bsky.social has a beautiful essay in Wong's Disability Visibility collection - I recommend it to physicians. #neurosky
The cover of Disability Visibility edited by Alice Wong, black text on a white background with colorful triangles
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Anil van der Zee @anilvanderzee.bsky.social · 13/11/2025
After some hardcore protesting in Germany!! Well done‼️‼️🇩🇪🇩🇪 "The coalition plans to invest 500 million euros by 2036 in the fight against #LongCovid and chronic fatigue syndrome (#MECFS)." www.spiegel.de/politik/karl...
spiegel.de
(S+) Ex-Gesundheitsminister Lauterbach: Forschung gegen ME/CFS wird ausgeweitet
Union und SPD wollen mehr Geld in die Erforschung postinfektiöser Erkrankungen wie Long Covid stecken. Deutschland könne damit zum weltweiten Vorreiter werden, sagt Ex-Gesundheitsminister Lauterbach.
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Tom Kindlon @tomkindlon.bsky.social · 13/11/2025
From Daniel Missailidis, PhD @danielmissailidis.bsky.social (Victoria, Australia) People with ME/CFS, Long Covid, and healthy volunteers sought drive.google.com/drive/folder... #MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME #LongCovid
I am recruiting for a couple of studies but chiefly doing this via one study recently funded by ME Research UK (grant held by Dr. Sarah Annesley).

Looking for females only, residing in VIC, Australia only due to short sample lifespan (part of this work is various experiments being done on platelets). Information doc provided below.

We only require a few short-form survey items and one combined blood draw to get what we need for these studies.

If anybody has questions or needs help parsing the info or accessing the documents, filling out anything, etc, email me at D.Missailidis@latrobe.edu.au and we'll see what we can do to accommodate your requirements to allow to you participate. (I will not reliably see or respond to replies on s4me)

Link to initial onboarding materials, it should all be self-contained and explanatory from the "START HERE (instructions)" document.: https://drive.google.com/drive/folders/1y_mZjdQMUlCOJobve2adryxbkkNaNQtS
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Dr Victoria Austen @vickyausten.bsky.social · 03/11/2025
WTAF. This is an absolute travesty. Teen Vogue has consistently been a light in the dark and once again the corporate overlords just end it all.
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Rolling Stone @rollingstone.com · 16/10/2025
Long Covid Is Real — And It’s Changing an Entire Generation Hundreds of thousands of kids in America are struggling with an illness that many doctors and schools refuse to recognize.e Feature: www.rollingstone.com/culture/cult...
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David Davies-Payne @d2p.bsky.social · 23/09/2025
"described for the first time widespread abnormalities in the function of unmyelinated C fibers, both somatosensory and sympathetic, that could represent a common pathophysiological mechanism explaining the multiplicity of symptoms in #longCOVID" #MECFS onlinelibrary.wiley.com/doi/10.1002/...
onlinelibrary.wiley.com
Microneurography Reveals Unmyelinated Small Nerve Fiber Dysfunction in Long COVID
Objective To review the microneurography findings of long coronavirus disease 2019 (COVID) patients who presented to the clinic with multisystem involvement affecting neurological, cardiovascular, g.....
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David Davies-Payne @d2p.bsky.social · 21/09/2025
WatchME for iPhone and Apple Watch v2.8 now available To help #pwME with daily pacing iOS 17 | watchOS 10 Free. No data collected. apps.apple.com/app/watchme/...
apps.apple.com
‎WatchME
‎For people with ME/CFS. This app helps you to pace and stay within your capacity envelope. Use your watch and phone to monitor your daily heart rate, steps and distance. Integrated with HealthKit....
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Brian Hughes @bmhughes.bsky.social · 09/09/2025
The Irish health service has initiated a process to develop a clinical guideline for ME (#MyalgicEncephalomyelitis). I am honoured to be part of its Steering Group The process so far has been extremely progressive I am hugely optimistic that a world-leading guideline will be produced #pwME #MECFS
hse.ie
Myalgic Encephalomyelitis (ME) - HSE.ie
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DecodeME @decodemestudy.bsky.social · 15/08/2025
“DecodeME shows the incredible level of support that the ME/CFS patient community can give to research that involves them on a deep and meaningful level. Without the community, we could not have achieved all that we have.” Andy Devereux-Cooke (PPI Member and Co-Investigator)
Photo of Andy Devereux-Cooke, PPI member and Co-investigator, next to his quote: "DecodeME shows the incredible level of support that the ME/CFS patient community can give to research that involves them on a deep and meaningful level. Without the community, we could not have achieved all that we have"
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DecodeME @decodemestudy.bsky.social · 12/08/2025
"DecodeME is now calling on researchers worldwide to join us in accelerating ME/CFS research.” - Prof Chris Ponting (DecodeME Investigator). We encourage researchers to explore and build on our findings. Apply for access to our rich dataset now shorturl.at/F8aOM
Image of Chris Ponting next to quote "This is a wakeup call. These extraordinary results speak the language of people with ME/CFS, often recounting people's ME/CFS symptoms. DecodeME is now calling on researchers worldwide to join us in accelerating ME/CFS research"
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Binita Kane @binitakane.bsky.social · 11/08/2025
My piece for The RCP Commentary Magazine for #SouthAsianHeritageMonth. This is my lovely Mum and Dad in 1969. Immigrants helped build the NHS www.rcp.ac.uk/78702?utm_so...
rcp.ac.uk
Roots to Routes: why South Asian Heritage Month matters to the NHS
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David Davies-Payne @d2p.bsky.social · 12/08/2025
"we identified significant differences in cfRNA contributions from multiple immune cell types. Notably, we observed a decrease in platelet-derived cfRNA and an increase in pDCs, monocytes, and certain T cell subset-derived cfRNA" #MECFS www.pnas.org/doi/10.1073/...
pnas.org
Circulating cell-free RNA signatures for the characterization and diagnosis of myalgic encephalomyelitis/chronic fatigue syndrome | PNAS
People living with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) experience heterogeneous and debilitating symptoms that lack suffici...
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David Davies-Payne @d2p.bsky.social · 07/08/2025
"includes seven Tier 1 genes, with BTN2A2 and TRIM38 eQTLs colocalised with ME/CFS risk […] Complexes involving butyrophilin3 and -2 homologues […] allow innate-like Vγ9Vδ2 T cells to distinguish self-derived from non-self-derived pyrophosphate antigens" #gdTcells #MECFS @forum-gd.bsky.social
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David Davies-Payne @d2p.bsky.social · 06/08/2025
"The project is part of a “notable increase” in ME/CFS research in recent years, Bosch says—a trend he attributes to a mix of patient advocacy, the failure of psychological and behavioral explanations for the condition, and increasing awareness of #MECFS thanks to its similarities to #LongCovid."
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Brian Hughes @bmhughes.bsky.social · 06/08/2025
Proud to be on the Science Advisory Board for DecodeME, a peripheral role but a fantastic vantage point from which to witness such outstanding work by Chris Ponting @cgatist.bsky.social and colleagues #MECFS #pwME www.theguardian.com/society/2025...
theguardian.com
Scientists find link between genes and ME/chronic fatigue syndrome
Large study suggests people’s genetics could ‘tip the balance’ on whether they would develop the illness
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David Davies-Payne @d2p.bsky.social · 06/08/2025
With clear evidence of a genetic predisposition linked to relevant biological pathways, these findings need to mark a turning point away from medicine's historic failure to correctly research this disease and meet its duty of patient care. #MECFS #DecodeME
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Binita Kane @binitakane.bsky.social · 06/08/2025
DECODE ME has published its results. Massive congratulations to @cgatist.bsky.social and team in Edinburgh. Let’s hope this is the start of a paradigm shift in how we view, research and treat this dreadful illness. www.decodeme.org.uk/initial-dna-...
decodeme.org.uk
Initial DecodeME DNA Results - DecodeME
06 August 2025 The DecodeME team is delighted to announce that the initial analysis of 15,579 DNA samples is complete, and we have important news to share. Main findings from our analysis  Your genes ...
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David Davies-Payne @d2p.bsky.social · 06/08/2025
Thank you Professor Chris Ponting @cgatist.bsky.social and the team at @decodemestudy.bsky.social #MECFS #genomics
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