Tag Archives: WHOQoL-Bref26

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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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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