Guest guest Posted August 26, 2012 Report Share Posted August 26, 2012 A qualitative natural history study of ME/CFS in the community. Authors: , V.R., , L.A., & Hlavaty, L.E. (2012). Journal: Health Care for Women International. Abstract: In previous qualitative research on Myalgic Encephalomyelitis/chronic fatigue syndrome (ME/CFS), researchers have focused on the experiences of patients with ME/CFS in tertiary care samples. This qualitative study examined the natural history of people with ME/CFS (n = 19) from community-based sample. Findings highlighted multilayered themes involving the illness experience and the physical construction of ME/CFS. In addition, this study further illuminated unique subthemes regarding community response and treatment, which have implications for understanding the progression of ME/CFS as well as experiences of those within patient networks. There is a need for more longitudinal qualitative research on epidemiological samples of patients with ME/CFS. DOI:10.1080/07399332.2012.684816 Posted online at: http://www.tandfonline.com/doi/full/10.1080/07399332.2012.684816 Quote Link to comment Share on other sites More sharing options...
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