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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