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https://www.sciencedirect.com/science/article/abs/pii/S0738399125007487 Stigmatisation in medical encounters for patients with fibromyalgia: A focus group study Hõbe Treufeldt, Christopher Burton Division of Population Health, School of Medicine and Population Health University of Sheffield...

Welsh Senedd Debate on Severe and Very Severe ME – 15th October - POSTPONED to 26th Nov. Adam Price, MS, was due to lead the Members Debate on Severe and Very Severe ME tomorrow in the Welsh Senedd (Parliament), but on Sunday he suffered a close family bereavement. 1/4

https://record.assembly.wales/Motion/8884 NDM8884 - Member Debates Tabled on 24/04/2025 | For debate on 15/10/2025 To propose that the Senedd: 1. Notes that myalgic encephalomyelitis (ME) is a chronic and disabling illness at all levels of severity. 2. Notes that of those suffering from ME...

I'm guessing this is the same dataset. https://ourarchive.otago.ac.nz/esploro/outputs/conferencePaper/DNA-methylation-changes-in-peripheral-blood/9926778205401891 Conference paper Open access DNA methylation changes in peripheral blood from Myalgic Encephalomyelitis/Chronic Fatigue Syndrome...

https://www.eurekalert.org/news-releases/1101257 News Release 10-Oct-2025 Enduring outcomes of COVID-19 work absences on the US labor market JAMA Network Open Peer-Reviewed Publication JAMA Network About The Study: In this cohort study of employed workers in the U.S., the new year-round...

https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2839932 Original Investigation Public Health Enduring Outcomes of COVID-19 Work Absences on the US Labor Market Julia M. Dennett, PhD1,2; Evan J. Soltas, PhD3,4; Gopi Shah Goda, PhD5 et al JAMA Netw Open Published Online: October...

She has a website here https://www.j-philbrickartist.com/bio Her thesis was funded by ANZMES

https://www.j-philbrickartist.com/_files/ugd/3b902b_819864a3d0474c168746adcaf0792a02.pdf ABSTRACT People living with ME/CFS often spend most of their time at home, either as a preventative measure to protect their limited energy levels, or due to symptom severity where they cannot leave the...

Adam D. First proposed blood test for chronic fatigue syndrome: what scientists think. Nature. 2025 Oct 9. https://www.nature.com/articles/d41586-025-03299-8

https://www.nature.com/articles/s41746-025-01939-x Article Open access Published: 08 October 2025 Systematic review: digital biomarkers of fatigue in chronic diseases Nana Yaw Aboagye, Chloe Hinchliffe, Silvia Del Din, Wan-Fai Ng, Kenneth F. Baker & Mark R. Baker npj Digital Medicine...

Some media links on this paper, for what they are worth: Go to, https://www.geneonline.com/blood-test-developed-by-university-of-east-anglia-and-oxford-biodynamics-diagnoses-chronic-fatigue-syndrome-with-96-accuracy/ https://medicalxpress.com/news/2025-10-blood-chronic-fatigue-accuracy.html...

Press release from UEA: https://www.uea.ac.uk/about/news/article/revolutionary-blood-test-for-me-chronic-fatigue-unveiled-1 Revolutionary blood test for ME / Chronic Fatigue unveiled By: Communications Wednesday 8 October 2025 SHARE X (formerly known as Twitter) ShareFacebook ShareLinkedIn...

[The full poster may or may not be longer] https://www.sciencedirect.com/science/article/abs/pii/S0960896625002196 Neuromuscular Disorders Volume 53, Supplement, September 2025, 105492 29PMyological evaluation of patients with post-acute COVID-19 syndrome F. Authier 1 2, M. Aoun Sebaiti 1, S...

https://crowdfund.berkeley.edu/project/47768 Trial By Error: Reporting on ME, ME/CFS, Long COVID, & so on... Ten years ago this month, I launched Trial By Error with a 15,000-word investigation of the fraudulent PACE trial, which tested cognitive behavior therapy and graded exercise therapy...

https://anzmes.org.nz/press-release-anzmes-publishes-critical-guide-to-help-doctors-navigate-me-cfs-research-and-avoid-harmful-treatments/ Press release – ANZMES publishes critical guide to help doctors navigate ME/CFS research and avoid harmful treatments October 7, 2025 by anzmes01 7th...

Tomorrow, Tue 7 Oct, the Welsh Senedd Business Committee will consider allocating 15 Oct to a Severe/Very Severe ME debate. It has a good chance of being selected. #pwME in Wales please help, email your MS and ask them to back MS Adam Price’s Motion. Find your 1/2...

A difference between the MEA and ME Research UK is the latter has supported lots of research outside the UK. While the only study I can recall the MEA funding outside the UK is the LDN one in Canada. That is an unusual one as the researchers got money from the Canadian authorities for the...

Many may be unaware but around 20 years ago, Action for ME got very close to the NHS and the setting up of the clinics. They even had a person on staff, I think her name was Maria Shortis, who was seconded from the NHS and whose full salary was paid for by the NHS as I recall. Might have been...

Paywall: https://www.journals.uchicago.edu/doi/abs/10.1086/736031 Signs: Journal of Women in Culture and SocietyVolume 51, Number 1 Lesbian AIDS: An Illness of One’s Own? Emily Lim Rogers Abstract This article examines the term “lesbian AIDS” as a lens to explore contested definitions of...

https://www.eurekalert.org/news-releases/1100722 NEWS RELEASE 3-OCT-2025 POTS common in patients with long COVID Peer-Reviewed Publication KAROLINSKA INSTITUTET A new study from Karolinska Institutet in Sweden shows that an unusual heart rhythm disorder, POTS, is particularly common in...