Tag Archives: ME Research UK

European Commission funding opportunities for ME/CFS

EC invites ME/CFS researchers to compete for grants   The European ME Coalition reports: “More than 2 years after the adoption of the ME/CFS resolution, the European Commission has finally taken an initiative to support research on ME/CFS. The Horizon … Continue reading

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Ensuring the voice of the very severely affected ME/CFS patient is heard in research

Ensuring the voice of the very severely affected Myalgic Encephalomyelitis/Chronic Fatigue Syndrome patient is heard in research-a research model, by  Helen Baxter   Research article abstract: Most of the research about Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has focused on ambulant … Continue reading

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All in your head? Brain research in ME/CFS

ME Research UK blog post: All in your head? Brain research in ME/CFS,  8 February 2021   Following last week’s introduction to the brain, here is an overview of some of the brain research conducted in ME/CFS in recent years, … Continue reading

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Protective effect of hemin against experimental CFS in mice: possible role of neurotransmitters

Protective effect of hemin against experimental Chronic Fatigue Syndrome in mice: possible role of neurotransmitters, by Vandana Thakur, Sumit Jamwal, Mandeep Kumar, Vikrant Rahi & Puneet Kumar  in Neurotoxicity Research (2020) [doi.org/10.1007/s12640-020-00231-y]   Research abstract: Chronic fatigue syndrome (CFS) is … Continue reading

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Symptoms of ME/CFS

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Cerebral blood flow and heart rate variability in CFS

Cerebral blood flow and heart rate variability in Chronic Fatigue Syndrome: a randomized cross-over study, by Anneleen Malfliet, Roselien Pas, Raf Brouns, Joris De Win, Samar M Hatem, Mira Meeus, Kelly Ickmans, Robbert-Jan van Hooff, and Jo Nijs in heart 2018; 21:E13-E24 BACKGROUND: Pain, fatigue, and concentration difficulties … Continue reading

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Could we finally have a definitive biomarker for ME/CFS?

ME Research UK blog post, 9 June 2017: Could we finally have a definitive biomarker for ME/CFS? It’s a recurring theme, but the diagnosis of ME/CFS is severely hampered by the lack of a test that can distinguish people with … Continue reading

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Overview of vision problems in ME/CFS

ME Research UK article, 13 Feb 2017: Shifting focus Problems with vision are relatively common among people with ME/CFS, the majority of whom report symptoms such as hypersensitivity to light, difficulties focusing, and dry eyes. But despite their significant impact … Continue reading

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New Australian genetic marker detection study

ME Research UK blog post, 6 November 2016: New study – Genetic marker detection Prof Brett Lidbury and colleagues at the John Curtin School of Medical Research, Australian National University in Canberra are conducting an ongoing programme, funded by charities in … Continue reading

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Nose & throat inflammation & HPV vaccinations in ME

ME Research UK article, 19 October 2016: Nose and throat inflammation There are many different triggers for ME/CFS. In most people, the illness starts with an infection, often viral, but others report a vaccination or immunisation as the initial event. … Continue reading

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