UK Government Publishes Final Delivery Plan to Transform ME/CFS Care and Research
On 22 July 2025, the UK Government released its Final Delivery Plan for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS),…
Third delay to ME care plan prompts backlash from patients
The health department failed to explain the postponement to its long-awaited strategy for treating chronic fatigue syndrome which…
Labour MPs Rebel Against Welfare Cuts: Disabled People Urged to Act Now
Over 100 Labour MPs are rebelling against the UK government’s proposed Welfare Reform Bill, which could strip support…
Hope is the biomedical not biopsychosocial approach for ME/CFS
The published article Patients with severe ME/CFS need hope and expert multidisciplinary care by Miller et al. (14…
Suffolk and North East Essex Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and Long Covid Service Contract Award
Suffolk and North East Essex Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and Long Covid Service Contract Award The NHS…
ME Voices Wales / Lleisiau ME Cymru
WAMES is co-coordinating a series of on-line consultation events for people with ME in Wales called ME Voices…
SAD LOSS OF Byron M. Hyde, MD
Dr. Byron M. Hyde, a distinguished pioneer in Myalgic Encephalomyelitis (ME) research, passed away on November 17, 2024….
Trial By Error: PACE Authors Respond to Monbiot Column with Tired Arguments
David Tuller critiques the PACE trial authors for their response to George Monbiot’s column on ME/CFS, accusing them…
Personen met ME/CVS ondersteunen in het ziekenhuis
The hospital support pack translated into Dutch Ondersteuning ME-patiënten in het ziekenhuis.ME Centraal
PrecisionLife and Metrodora Institute share first insights with ME/CFS, Long COVID participants in MetX research study
MetX Study Shares First Results with Participants