Tag Archives: HRQOL
Research: Effect of dietary Coenzyme Q10 plus NADH supplementation on fatigue perception & health-related quality of life in ME/CFS
Effect of dietary Coenzyme Q10 plus NADH supplementation on fatigue perception and health-related quality of life in individuals with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: a prospective, randomized, double-blind, placebo-controlled trial, by Jesús Castro-Marrero, Maria Jose Segundo, Marcos Lacasa, Alba Martinez-Martinez, Ramon … Continue reading →
Health-related quality of life in Norwegian adolescents living with CFS
Health-related quality of life in Norwegian adolescents living with Chronic Fatigue Syndrome, by Wenche Ann Similä, Vidar Halsteinli, Ingrid B Helland, Christer Suvatne, Hanna Elmi, Torstein Baade Rø in Health Qual Life Outcomes. 2020 Jun 5;18(1):170 [doi: 10.1186/s12955-020-01430-z] Research … Continue reading →
Health-related quality of life in patients with ME/CFS: an Australian cross-sectional study
Health-related quality of life in patients with myalgic encephalomyelitis/chronic fatigue syndrome: an Australian cross-sectional study, by N Eaton-Fitch, SC Johnston, P Zalewski, D Staines & S Marshall-Gradisnik in Quality of Life Research, 22 January 2020 Research abstract: Background: Myalgic … Continue reading →
Development of a conceptual framework to underpin a health-related quality of life outcome measure in paediatric CFS/ME: prioritisation through card ranking
Development of a conceptual framework to underpin a health-related quality of life outcome measure in paediatric chronic fatigue syndrome/myalgic encephalopathy (CFS/ME): prioritisation through card ranking, by Roxanne M. Parslow, Nina Anderson, Danielle Byrne, Kirstie L Haywood, Alison Shaw & Esther … Continue reading →
Poor quality of life in young people with ME/CFS
An ME Research UK article comments on the recent research in Norway into adolescents with CFS: For such a devastating illness, there is surprisingly little information in the scientific literature about patients’ experiences of living with ME/CFS day-to-day. The few … Continue reading →
