Tag Archives: housebound

Experiences of living with severe CFS/ME

Experiences of living with severe Chronic Fatigue Syndrome/Myalgic Encephalomyelitis, by  Victoria Strassheim, Julia L Newton and Tracy Collins in Healthcare 2021, 9(2), 168 [doi.org/10.3390/healthcare9020168] (This article belongs to the Special Issue ME/CFS – the Severely and Very Severely Affected)   Research … Continue reading

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Homebound versus bedridden status among those with ME/CFS

Homebound versus bedridden status among those with Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome, by  Karl Conroy, Shaun Bhatia, Mohammed Islam and Leonard A Jason in Healthcare 2021, 9(2), 106 [doi.org/10.3390/healthcare9020106] (This article belongs to the Special Issue ME/CFS – the Severely and … Continue reading

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Health Care responsibility & compassion-visiting the housebound patient severely affected by ME/CFS

Health Care responsibility and compassion-visiting the housebound patient severely affected by ME/CFS, by  Caroline Kingdon, Dionysius Giotas, Luis Nacul and Eliana Lacerda in Healthcare 2020, 8(3), 197 [doi.org/10.3390/healthcare8030197] [This article belongs to the Special Issue ME/CFS – the Severely and … Continue reading

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Being a housebound digital academic

The Sociological review blog post, by Anna Wood, 17 November 2017:  Being a Housebound Digital Academic I have been housebound with a chronic health condition (Myalgic Encephalomyelitis, ME) since 2008. Yet over the last few years I’ve published three papers and … Continue reading

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Housebound people with ME have greater physical impairment

Research abstract: Objectives: The objective of this study was to examine individuals with myalgic encephalomyelitis and chronic fatigue syndrome who are confined to their homes due to severe symptomatology. The existing literature fails to address differences between this group, and less severe, nonhousebound patient … Continue reading

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