Category Archives: News

The psychological impact of dependency in adults with CFS

Research abstract: Chronic fatigue syndrome/myalgic encephalomyelitis can limit functional capacity, producing various degrees of disability and psychological distress. Semi-structured interviews explored the experiences of adults with chronic fatigue syndrome/myalgic encephalomyelitis being physically dependent on other people for help in daily … Continue reading

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Immune system dysfunction in ME/CFS as a potential biomarker

Bateman Horne Center blog, by Dr Suzanne Vernon, 15 April 2016: Uncovering Biomarkers – Fcg receptors in ME/CFS Uncovering Biomarkers – Is protein dysfunction a risk factor for the development of ME/CFS? The Bateman Horne Center (BHC) is determined to bring ME/CFS and … Continue reading

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Methods of evaluating ME interventions

Research abstract: INTRODUCTION The current study provides data from two patients with myalgic encephalomyelitis, who charted several of their symptoms over time. CASE PRESENTATION Each patient charted domains that were relevant to them, and they were attempting to assess the … Continue reading

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Women assess quality of healthcare services in Norway

Research abstract: Objective: To test the association between self-rated health and self-rated degree of chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME), and CFS/ME patients’ assessment of quality of primary care, specialist care and coordination of care. Design: Cross-sectional study. Setting: Self-reported questionnaire … Continue reading

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ME and rituximab in Notodden Norway

ME-foreldrene blog: Lecture by Hanne Thürmer, Notodden. RituxME and current development, 13 April 2016 Lecture by dr Hanne Thürmer, Notodden Hospital Original in Norwegian/Norsk original From a lecture given at the local department of the Norwegian ME-association in Notodden, avd … Continue reading

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Are people with ME disabled?

TIPSFORME blog: Are you Disabled?, by Jenny, 15 April 2016 On Twitter there have been some interesting discussions this week about disability identity and ME. I think this is worth everyone with ME thinking about. For most of us ME is … Continue reading

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Video interview with parent Mary Dimmock about her son and rituximab

Episode 78 of Llewellyn King’s ME/CFS Alert videos interviews Mary Dimmock, whose son has ME and who is receiving RITUXAN (rituximab) treatment privately. (24 mins)    

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An examination of an ME online community discussion

Research abstract: Online communities, created and sustained by people sharing and discussing texts on the internet, play an increasingly important role in social health movements. In this essay, we explore a collective mobilization in miniature through an in-depth analysis of … Continue reading

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