Author Archives: wames

Impact of Coronavirus: people with chronic illness say “I feel forgotten”

Chronic Illness Inclusion Project blog post: “I feel forgotten”, by Anna Ruddock, June 1 2020   A submission to the Women and Equalities Committee about the impact of coronavirus on people with chronic illness. In April, the Women and Equalities … Continue reading

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Scientists call for more European research on ME/CFS

European ME Coalition Press Release: Scientists call for more European research on ME/CFS, 10 June 2020   More than one hundred scientists have signed an open letter calling for more European research into the illness Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). … Continue reading

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Physical activity measures in patients with ME/CFS: correlations between peak oxygen consumption, the physical functioning scale of the SF-36 questionnaire, & the number of steps from an activity meter

Physical activity measures in patients with myalgic encephalomyelitis/chronic fatigue syndrome: correlations between peak oxygen consumption, the physical functioning scale of the SF-36 questionnaire, and the number of steps from an activity meter, by CMC van Campen, Peter C Rowe, Freek … Continue reading

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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

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The Health Minister, Covid-19, ME, rehabilitation & NICE

The Health Minister comments on Covid-19, ME, rehabilitation & NICE   The Health Minister Vaughan Gething has replied to the letter WAMES sent to him on International ME Awareness Day highlighting the links between Covid-19, PVFS and ME, and requesting … Continue reading

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The concept of ‘illness without disease’ impedes understanding of CFS: a response to Sharpe & Greco

The concept of ‘illness without disease’ impedes understanding of chronic fatigue syndrome: a response to Sharpe and Greco, by Steven Lubet, David Tuller in BMJ Medical Humanities. Published Online First: 01 June 2020. [doi: 10.1136/medhum-2019-011807]   Article abstract: In a … Continue reading

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Metabolic dysfunction in ME/CFS not due to anti-mitochondrial antibodies

Metabolic dysfunction in myalgic encephalomyelitis/chronic fatigue syndrome not due to anti-mitochondrial antibodies, by Isabell Nilsson, Jeremy Palmer, Eirini Apostolou, Carl-Gerhard Gottfries, Muhammad Rizwan, Charlotte Dahle and Anders Rosén in Front. Med., 31 March 2020 [doi.org/10.3389/fmed.2020.00108 ]   Research abstract: Metabolic profiling … Continue reading

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Modeling disability: softly making the invisible visible

Modeling disability: softly making the invisible visible, by Libby Evan (2020) Bachelor of Fine Arts Senior Papers 74   Research abstract: “I am not asking for pity. I am telling you about my disability.” – Eli Clare1 In the following … Continue reading

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Sleep problems in adolescents with CFS: a case-control study nested within a prospective clinical cohort

Sleep problems in adolescents with CFS: A case-control study nested within a prospective clinical cohort, by Maria Elizabeth Loades, Katharine A Rimes, Trudie Chalder in Clinical Child Psychology and Psychiatry, May 22 2020 [doi.org/10.1177/1359104520918364]   Research abstract: Sleep problems have … Continue reading

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Review of the quality control checks performed by current genome-wide & targeted-genome association studies on ME/CFS

Review of the quality control checks performed by current genome-wide and targeted-genome association studies on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, by Nuno Sepulveda, Anna D Grabowska, Eliana M Lacerda, Luis C Nacul in Frontiers in Pediatrics. May 7, 2020 [doi: 10.3389/fped.2020.00293 … Continue reading

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