Category Archives: News
Prof Brian Hughes: 2021 NICE guideline myths
Getting it Right: Addressing myths about the 2021 NICE guideline for ME/CFS Brian Hughes is an academic psychologist and university professor in Galway, Ireland with a blog called the Science bit. On World ME Day 2023 he spoke to … Continue reading
Research review: Biomarkers for ME/CFS
Biomarkers for ME/CFS: a systematic review Australian researchers found 101 key studies in ME/CFS that varied in efficacy, quality, and potential to be developed into a diagnostic biomarker. Most were blood-based and measured a range of dysfunction. “Many of … Continue reading
Review: Exercise intolerance in ME/CFS & PASC: more in common than not?
Exercise Pathophysiology in ME/CFS and PASC This review finds the mechanisms of systemic blood flow, ventilatory control, hemodynamic and gas exchange derangements to be involved in exercise intolerance in both conditions. Exercise Pathophysiology in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome and … Continue reading
Pacing my way through Pain Clinic
Avoiding PEM by pacing my way through Pain Clinic PF gives her experience of an ME/CFS friendly way of attending a Pain Clinic in south Wales. As my referral to the Pain Clinic was made during Covid lockdown I … Continue reading
Poem: PEM at 2am
PEM at 2 am by Ffion For World ME Day, 12th May 2023 “M.E. – the disease where pushing harder can make you sicker” Shattered… Battered… Shell-shocked… Dazzled… Detonated from sleep… By explosion in my brain. Perspiration… Prostration… Nausea… … Continue reading
Poem about PEM: The Cost of Living
The Cost of Living: from and to, or… Thoughts from my bed by Rachel Hazlewood I try to live my life – and then I find I’m back in bed again: Exhausted, drained, wrung out and weak; Too tired … Continue reading
Top Tips handout for GPs
Top tips handout for GPs from Doctors with ME A new handout for GPs from Doctors with ME: outlines what ME/CFS is and is not gives the key symptoms of ME highlights Post-Exertional Malaise (PEM) or Post Exertional Symptom … Continue reading
Diagnosing ME/CFS in people with Long COVID: US CCC statement
Diagnosing ME/CFS in People with Long COVID The US ME/CFS Clinician Coalition have produced a Consensus Statement about Long COVID. Since 2020, we’ve been seeing people with Long COVID whose symptoms overlap with ME/CFS. We recommend you consider ME/CFS … Continue reading
Safe Long COVID & ME/CFS rehabilitation
Safe Long COVID Rehabilitation a video from Long COVID Physio Physiotherapists living with Long COVID have produced a short video [5 mins 15] for fellow physios explaining the importance of providing safe rehabilitation for people with LC and ME/CFS. … Continue reading
PEM: Running out of battery & feeling intensely unwell: a carer’s perspective
PEM: Running out of battery & feeling intensely unwell: a carer’s perspective I guess you’ve probably heard of Myalgic Encephalomyelitis – by its abbreviation ‘ME’. Maybe you’ve got an idea that it’s about being tired all the time. That … Continue reading
