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Anna M. Carapellotti, Hannie (J.E.M.) Meijerink, Christine Gravemaker-Scott, Lucia Thielman, Renée Kool, Natalie Lewin & Tineke A. Abma. (2023) Escape, expand, embrace: the transformational lived experience of rediscovering the self and the other while dancing with Parkinson’s or Multiple Sclerosis. International Journal of Qualitative Studies on Health and Well-being 18:1.
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Fiona J. R. Eccles, Natalie Sowter, Terry Spokes, Nicolò Zarotti & Jane Simpson. (2023) Stigma, self-compassion, and psychological distress among people with Parkinson’s. Disability and Rehabilitation 45:3, pages 425-433.
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Luke Murray, Pirjo Vuoskoski, Josh Wellman & Clair Hebron. (2022) ‘’It was the end of the world” – The lifeworld of elite male rugby union players living with injury. An interpretative phenomenological analysis. Physiotherapy Theory and Practice 38:9, pages 1219-1232.
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Ross Parry, Olivier Buttelli, Narjis Sellam, Jacques Riff, Marie Vidailhet, Marie-Laure Welter & Elodie Lalo. (2022) ‘Le regard des autres’: the experience of walking in social environments as a person with Parkinson’s disease. Psychology & Health 0:0, pages 1-24.
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Alison Rowsell, Ann Ashburn, Carolyn Fitton, Victoria A. Goodwin, Sophia Hulbert, Sarah E. Lamb, Emma McIntosh, Alice Nieuwboer, Ruth Pickering, Lynn Rochester, Kim Chivers-Seymour & Claire Ballinger. (2022) Participant expectations and experiences of a tailored physiotherapy intervention for people with Parkinson’s and a history of falls. Disability and Rehabilitation 44:5, pages 727-735.
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Catherine Mariam George, Elizabeth Mary Thomas, Nicy Kuriakose, Saloni Kshirsagar & Reema Samuel. (2021) Psychosocial Difficulties (PSD) Experienced by People across Brain Disorders and the Implications for Occupational Therapy: A Cross-Sectional Study. Occupational Therapy In Health Care 35:3, pages 268-285.
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Andrew Morgan, Fiona J. R. Eccles & Pete Greasley. (2021) Experiences of living with dystonia. Disability and Rehabilitation 43:7, pages 944-952.
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Tom Staunton. (2020) Icarus, Grannies, Black Holes and the death of privacy: exploring the use of digital networks for career enactment. British Journal of Guidance & Counselling 48:5, pages 611-622.
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Ross Parry, Olivier Buttelli, Jacques Riff, Narjis Sellam, Marie Vidailhet, Marie-Laure Welter & Elodie Lalo. (2019) “The whole perimeter is difficult”: Parkinson’s disease and the conscious experience of walking in everyday environments. Disability and Rehabilitation 41:23, pages 2784-2791.
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Clorinda Panebianco & Carol Lotter. (2019) Shifting ‘stuckness’ in Parkinson’s disease: a music therapy case study. Journal of the Musical Arts in Africa 16:1-2, pages 77-97.
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Christie L. Stilwell, Susan L. Hutchinson & Brad A. Meisner. (2019) ‘I’ve got Parkinson’s and that makes a difference’: Understanding health and leisure through a Parkinson’s disease diagnosis. Loisir et Société / Society and Leisure 42:1, pages 43-55.
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Aleksandra Kudlicka, John V. Hindle, Laura E. Spencer & Linda Clare. (2018) Everyday functioning of people with Parkinson’s disease and impairments in executive function: a qualitative investigation. Disability and Rehabilitation 40:20, pages 2351-2363.
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Marna de Bruyn & Josh Cameron. (2017) The occupation of looking for work: An interpretative phenomenological analysis of an individual job-seeking experience. Journal of Occupational Science 24:3, pages 365-376.
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Tammy L. Sheehy, Meghan H. McDonough & S. Elizabeth Zauber. (2017) Social Comparisons, Social Support, and Self-Perceptions in Group Exercise for People With Parkinson's Disease. Journal of Applied Sport Psychology 29:3, pages 285-303.
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Mohammad S. Nazzal & Hanan Khalil. (2017) Living with Parkinson’s disease: A Jordanian perspective. Scandinavian Journal of Occupational Therapy 24:1, pages 74-82.
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Jack K. Garlovsky, Jane Simpson, Richard A. Grünewald & Paul G. Overton. (2016) Impulse control disorders in Parkinson’s disease: Predominant role of psychological determinants. Psychology & Health 31:12, pages 1391-1414.
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Summer C. Martin. (2016) The experience and communicative management of identity threats among people with Parkinson's disease: Implications for health communication theory and practice. Communication Monographs 83:3, pages 303-325.
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Fung Kei Cheng. (2015) Recovery from Depression Through Buddhist Wisdom: An Idiographic Case Study. Social Work in Mental Health 13:3, pages 272-297.
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Jane Simpson, Helen McMillan, Ira Leroi & Craig D. Murray. (2015) Experiences of apathy in people with Parkinson’s disease: a qualitative exploration. Disability and Rehabilitation 37:7, pages 611-619.
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Björg Thordardottir, Maria H. Nilsson, Susanne Iwarsson & Maria Haak. (2014) “You plan, but you never know” – participation among people with different levels of severity of Parkinson’s disease. Disability and Rehabilitation 36:26, pages 2216-2224.
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Linda Dauwerse, Annette Hendrikx, Karen Schipper, Chris Struiksma & Tineke A. Abma. (2014) Quality-of-life of patients with Parkinson’s disease. Brain Injury 28:10, pages 1342-1352.
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David
J. Ward. (2011) The lived experience of spiritual abuse. Mental Health, Religion & Culture 14:9, pages 899-915.
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Elizabeth Cassidy, Frances Reynolds, Sandra Naylor & Lorraine De Souza. (2011) Using interpretative phenomenological analysis to inform physiotherapy practice: An introduction with reference to the lived experience of cerebellar ataxia. Physiotherapy Theory and Practice 27:4, pages 263-277.
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JonathanA. Smith. (2011) Evaluating the contribution of interpretative phenomenological analysis. Health Psychology Review 5:1, pages 9-27.
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Fiona J. R. Eccles, Craig Murray & Jane Simpson. (2011) Perceptions of cause and control in people with Parkinson's disease. Disability and Rehabilitation 33:15-16, pages 1409-1420.
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Fiona J. R. Eccles & Jane Simpson. (2011) A review of the demographic, clinical and psychosocial correlates of perceived control in three chronic motor illnesses. Disability and Rehabilitation 33:13-14, pages 1065-1088.
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Viv Brunsden & Rowena Hill. (2009) Firefighters’ experience of strike: An interpretative phenomenological analysis case study. The Irish Journal of Psychology 30:1-2, pages 99-115.
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Adele Dickson, David Allan & Ronan O’carroll. (2008) Biographical disruption and the experience of loss following a spinal cord injury: An interpretative phenomenological analysis. Psychology & Health 23:4, pages 407-425.
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Brendan Gough, Nicky Weyman, Julie Alderson, Gary Butler & Mandy Stoner. (2008) ‘They did not have a word’: The parental quest to locate a ‘true sex’ for their intersex children. Psychology & Health 23:4, pages 493-507.
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Jonathan A. Smith & Mike Osborn. (2007) Pain as an assault on the self: An interpretative phenomenological analysis of the psychological impact of chronic benign low back pain. Psychology & Health 22:5, pages 517-534.
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Joanna M. Brocki & Alison J. Wearden. (2006) A critical evaluation of the use of interpretative phenomenological analysis (IPA) in health psychology. Psychology & Health 21:1, pages 87-108.
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