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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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The presence of overlapping quality of life symptoms in primary antibody deficiency (PAD) & CFS
The presence of overlapping quality of life symptoms in primary antibody deficiency (PAD) and chronic fatigue syndrome (CFS), by Rhea A Bansal, Susan Tadros, Amolak S Bansal in Allergy, Asthma & Clinical Immunology Vol 16, no: 21 (2020), March 30, … Continue reading
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Tagged Amolak S Bansal, immunoglobulin replacement therapy, PADS, primary antibody deficiency, QoL, Quality of life, Rhea A Bansal, Susan Tadros
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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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Interdisciplinary group treatment may improve quality of life in CFS/ME
Research highlights: Interdisciplinary group treatment may improve quality of life in CFS/ME. Psychological Flexibility (PF) has applied utility in the treatment of CFS/ME. Changes in PF activity/occupational engagement suggest greatest benefit in CFS/ME. Research abstract: Objective: Psychological Flexibility (PF) is a … Continue reading
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Tagged acceptance, Interdisciplinary group treatment, psychological flexibility, QoL, Quality of life
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The role of illness acceptance and neuroticism in CFS on quality of life
Abstract OBJECTIVE Increasing the quality of life (QoL) of patients with chronic fatigue is challenging because recovery is seldom achieved. Therefore, it is important to identify processes that improve QoL. This study examined the extent of improvement related to cognitive … Continue reading
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Tagged cognitive behavioural therapy, neuroticism, QoL, Quality of life
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