Tag Archives: Family Reported Outcome Measures
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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