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…
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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…
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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…
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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….
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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…
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Personen met ME/CVS ondersteunen in het ziekenhuis
The hospital support pack translated into Dutch Ondersteuning ME-patiënten in het ziekenhuis.ME Centraal
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PrecisionLife and Metrodora Institute share first insights with ME/CFS, Long COVID participants in MetX research study
MetX Study Shares First Results with Participants
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Maeve Boothby O’Neill: the Chronic Collaboration speaks to Dr William Weir
https://www.youtube.com/watch?v=JME4iroEIF8
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Trial By Error: Guardian Publishes Response to Boothby O’Neill Inquest
By David Tuller, DrPH My heart sinks every time I see another ridiculous article from a member of…
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Open letter from Parents and Carers
An open response from parents and carers of people with Severe Myalgic Encephalomyelitis to ‘Management of Nutritional Failure…