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ME/CFS: major impact on lives of both patients & family members
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): Major impact on lives of both patients and family members, by Esme Brittain, Nina Muirhead, Andrew Y Finlay and Jui Vyas in Medicina 2021, 57(1), 43; [doi.org/10.3390/medicina57010043] (This article belongs to the Special Issue ME/CFS: Causes, … Continue reading
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Tagged Andrew Y Finlay, Cardiff University, Dr Nina Muirhead, Esme Brittain, family impact study, FROM-16, Jui Vyas, QoL, Quality of life, WHOQoL-Bref26
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ME/CFS: significant negative impact of quality of life of both patients & family members
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): significant negative impact of Quality of Life of both patients and family members, by Esme Brittain During my 3rd year at Cardiff medical school, I conducted a 6-week research project looking at the impact … Continue reading
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Tagged Cardiff University, Esme Brittain, Family Reported Outcome Measures, FROM-16, QoL, Quality of life, WHOQoL-Bref26
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CFS & Quality of Life
Chronic fatigue syndrome and quality of life, by Deb Roberts in Patient Related Outcome Measures Vol 2018, #9, pp 253-262 [Published August 1, 2018] Article abstract: Chronic fatigue syndrome (CFS), also known as myalgic encephalomyelitis (ME), is a challenging long-term condition (LTC) with complex … Continue reading
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Tagged Deb Roberts, Patient-Reported Outcome Measures, PROMS, QoL, Quality of life, WHOQoL-Bref26
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