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Disability and Rehabilitation Volume 36, 2014 - Issue 5
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Research Article

Use of an online survey to explore positive and negative outcomes of rehabilitation for people with CFS/ME

Peter William GladwellNorth Bristol NHS Trust BristolUKCorrespondence[email protected]
,
Derek PhebyBuckinghamshire New University, Society and Health UxbridgeUK
,
Tristana RodriguezAction for ME BristolUK
&
Fiona PolandHealth and Society, University of East Anglia NorwichUK
Pages 387-394 | Received 21 May 2012, Accepted 16 Apr 2013, Published online: 04 Jun 2013

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Read on this site (5)

Suzanne Broadbent, Sonja Coetzee, Rosalind Beavers & Louise Horstmanshof. (2020) Patient experiences and the psychosocial benefits of group aquatic exercise to reduce symptoms of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: a pilot study. Fatigue: Biomedicine, Health & Behavior 8:2, pages 84-96.
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Anna Cheshire, Damien Ridge, Lucy Clark & Peter White. (2020) Guided graded Exercise Self-help for chronic fatigue syndrome: patient experiences and perceptions. Disability and Rehabilitation 42:3, pages 368-377.
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Anna Sheridan. (2015) Response to Gladwell et al.: concerns about safety for GET. Disability and Rehabilitation 37:5, pages 464-464.
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Robert Courtney. (2015) Harms and benefits associated with exercise therapy for CFS/ME. Disability and Rehabilitation 37:5, pages 465-465.
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Peter William Gladwell. (2015) Author’s comments in response to letters by Tom Kindlon, Anna Sheridan and Robert Courtney. Disability and Rehabilitation 37:5, pages 468-469.
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Articles from other publishers (9)

Marjon E. A. Wormgoor & Sanne C. Rodenburg. (2023) Focus on post-exertional malaise when approaching ME/CFS in specialist healthcare improves satisfaction and reduces deterioration. Frontiers in Neurology 14.
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Michael Sharpe, Trudie Chalder & Peter D White. (2021) Evidence-Based Care for People with Chronic Fatigue Syndrome and Myalgic Encephalomyelitis. Journal of General Internal Medicine 37:2, pages 449-452.
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P.D. White & J. Etherington. (2021) Adverse outcomes in trials of graded exercise therapy for adult patients with chronic fatigue syndrome. Journal of Psychosomatic Research 147, pages 110533.
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Karen Pilkington, Damien T. Ridge, Chinonso N. Igwesi-Chidobe, Carolyn A. Chew-Graham, Paul Little, Opeyemi Babatunde, Nadia Corp, Clare McDermott & Anna Cheshire. (2020) A relational analysis of an invisible illness: A meta-ethnography of people with chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) and their support needs. Social Science & Medicine 265, pages 113369.
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Eva Stormorken, Leonard A. Jason & Marit Kirkevold. (2017) Factors impacting the illness trajectory of post-infectious fatigue syndrome: a qualitative study of adults’ experiences. BMC Public Health 17:1.
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Anne Helen Hansen & Olaug S. Lian. (2016) Experiences of general practitioner continuity among women with chronic fatigue syndrome/myalgic encephalomyelitis: a cross-sectional study. BMC Health Services Research 16:1.
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Miriam Mallet, Eleanor King & Peter D. White. (2016) A UK based review of recommendations regarding the management of chronic fatigue syndrome. Journal of Psychosomatic Research 88, pages 33-35.
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Anne Helen Hansen & Olaug S Lian. (2016) How do women with chronic fatigue syndrome/myalgic encephalomyelitis rate quality and coordination of healthcare services? A cross-sectional study. BMJ Open 6:4, pages e010277.
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Michael Sharpe, Kimberly A Goldsmith, Anthony L Johnson, Trudie Chalder, Jane Walker & Peter D White. (2016) Patient reaction to the PACE trial ? Authors' reply. The Lancet Psychiatry 3:2, pages e8-e9.
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