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Research Papers

MS and me: exploring the impact of multiple sclerosis on perceptions of self

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Pages 1208-1217 | Received 26 Mar 2011, Accepted 01 Nov 2011, Published online: 13 Dec 2011

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Victoria Bassett & Clair Hebron. (2023) The lived experience of physical exertion for persons with advanced multiple sclerosis: making connections with the world. Disability and Rehabilitation 0:0, pages 1-11.
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Holly Emery, Christine Padgett, Tamara Ownsworth & Cynthia A. Honan. (2022) A systematic review of self-concept change in multiple sclerosis. Neuropsychological Rehabilitation 32:8, pages 1774-1813.
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Michal Soffer. (2022) The social construction of multiple sclerosis in Israel: a cultural reading of illness narratives. Disability and Rehabilitation 44:13, pages 3154-3164.
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Elizabeth Devon Eldridge-Smith, Megan Loew & Lara M. Stepleman. (2021) The adaptation and validation of a stigma measure for individuals with multiple sclerosis. Disability and Rehabilitation 43:2, pages 262-269.
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Jessica Moore, Fiona J. R. Eccles & Jane Simpson. (2020) Post-diagnostic lived experiences of individuals with essential tremor. Disability and Rehabilitation 42:20, pages 2894-2902.
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Brynn C. Adamson, Matthew D. Adamson, Melissa M. Littlefield & Robert W. Motl. (2018) ‘Move it or lose it’: perceptions of the impact of physical activity on multiple sclerosis symptoms, relapse and disability identity. Qualitative Research in Sport, Exercise and Health 10:4, pages 457-475.
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Thomas M. Wright & Litza A. Kiropoulos. (2017) Intimate relationship quality, self-concept and illness acceptance in those with multiple sclerosis. Psychology, Health & Medicine 22:2, pages 212-226.
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Kerry Mutch, Abigail Methley, Phil Moore & Anu Jacob. (2014) Life on hold: the experience of living with neuromyelitis optica. Disability and Rehabilitation 36:13, pages 1100-1107.
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Articles from other publishers (27)

Holly Emery, Ingrid van der Mei, Christine Padgett, Tamara Ownsworth, Therese Burke, Lauren Giles & Cynthia A. Honan. (2023) The multiple sclerosis self-concept change scale: Development and validation of a new measure. Multiple Sclerosis and Related Disorders 79, pages 104955.
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Gizem Yağmur YALÇIN, Ayşe BESER & Murat KÜRTÜNCÜ. (2022) Evaluation of the Relationship Between Socio-demographic Characteristics and Social Support with Adherence to Treatment in Patient with Multiple Sclerosis. International Journal of Disabilities Sports and Health Sciences 5:2, pages 75-82.
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Jorge Emanuel Martins, Joana Simões, Marlene Barros & Mário Simões. (2022) Pre-Molecular Assessment of Self-Processes in Neurotypical Subjects Using a Single Cognitive Behavioral Intervention Evoking Autobiographical Memory. Behavioral Sciences 12:10, pages 381.
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Brynn Adamson, Matthew Adamson, Dominique Kinnett-Hopkins & Robert Motl. (2022) Medicalization of Exercise Through Vigilance, Productivity, and Self-Care: A Secondary Data Analysis of Qualitative Interviews Among Those With Multiple Sclerosis. Adapted Physical Activity Quarterly 39:4, pages 399-423.
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Hikari Ando, Rosanna Cousins & Carolyn A. Young. (2021) Understanding quality of life across different clinical subtypes of multiple sclerosis: a thematic analysis. Quality of Life Research 31:7, pages 2035-2046.
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Stine Torp Løkkeberg & Gunnar Thoresen. (2021) Experiences of quality of life in people with Multiple Sclerosis who are in a wheelchair. Nursing Open 9:4, pages 2217-2226.
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Seada A Kassie, Jannat Alia & Lynda Hyland. (2021) Biopsychosocial implications of living with multiple sclerosis: a qualitative study using interpretative phenomenological analysis. BMJ Open 11:8, pages e049041.
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Litza Kiropoulos, Natalie Ward & Vanja Rozenblat. (2019) Self-concept, illness acceptance and depressive and anxiety symptoms in people with multiple sclerosis. Journal of Health Psychology 26:8, pages 1197-1206.
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Mandip Dosanjh, Jane Alty, Carol Martin, Gary Latchford & Christopher D. Graham. (2020) What is it like to live with a functional movement disorder? An interpretative phenomenological analysis of illness experiences from symptom onset to post‐diagnosis. British Journal of Health Psychology 26:2, pages 325-342.
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Claire Cook & Pirjo Vuoskoski. (2021) ‘I just want someone to rub some life into them!’: the lived experience of impaired sensation in the feet related to multiple sclerosis. British Journal of Neuroscience Nursing 17:Sup1, pages S48-S54.
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Robert Kohls. 2021. Scholarly Publication Trajectories of Early-career Scholars. Scholarly Publication Trajectories of Early-career Scholars 133 149 .
Emanuela Calandri, Federica Graziano, Martina Borghi, Silvia Bonino & Elena Cattelino. (2020) The Role of Identity Motives on Quality of Life and Depressive Symptoms: A Comparison Between Young Adults With Multiple Sclerosis and Healthy Peers. Frontiers in Psychology 11.
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Jane Desborough, Crystal Brunoro, Anne Parkinson, Katrina Chisholm, Mark Elisha, Janet Drew, Vanessa Fanning, Christian Lueck, Anne Bruestle, Matthew Cook, Hanna Suominen, Antonio Tricoli, Adam Henschke & Christine Phillips. (2020) ‘It struck at the heart of who I thought I was’: A meta‐synthesis of the qualitative literature examining the experiences of people with multiple sclerosis. Health Expectations 23:5, pages 1007-1027.
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I. Vachkov, M. Odintsova & O.A. Tristan. (2020) Features of Experiencing a Spiritual Crisis and Attitudes to Self in Persons with Spinal Injury. Counseling Psychology and Psychotherapy Консультативная психология и психотерапия 28:3, pages 42-64.
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Jennifer Chamberlain-Salaun, Kim Usher & Jane Mills. (2020) Outsiders in the Experts’ World: A Grounded Theory Study of Consumers and the Social World of Health Care. SAGE Open 10:1, pages 215824402090342.
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Emanuela Calandri, Federica Graziano, Martina Borghi & Silvia Bonino. (2019) Young adults’ adjustment to a recent diagnosis of multiple sclerosis: The role of identity satisfaction and self-efficacy. Disability and Health Journal 12:1, pages 72-78.
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Rafiyah Khan, Alan Uren, Luke Canham, David Cottrell, Marcus J. Drake & Nikki Cotterill. (2018) What Are the Participants’ Perspectives of Taking Melatonin for the Treatment of Nocturia in Multiple Sclerosis? A Qualitative Study Embedded within a Double-Blind RCT. Multiple Sclerosis International 2018, pages 1-9.
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Shala Ghaderi Berntsson, Anne-Marie Landtblom & Gullvi Flensner. (2017) Cerebellar ataxia and intrathecal baclofen therapy: Focus on patients´ experiences. PLOS ONE 12:6, pages e0180054.
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Karen Strickland, Allison Worth & Catriona Kennedy. (2017) The liminal self in people with multiple sclerosis: an interpretative phenomenological exploration of being diagnosed. Journal of Clinical Nursing 26:11-12, pages 1714-1724.
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Zumrut Gedik, Oya Sorias & Egemen Idiman. (2015) Do coping styles mediate the relationship between disability status and psychosocial loss in people with relapsing remitting multiple sclerosis?. Journal of Health Psychology 22:6, pages 707-721.
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A. Soundy & T. Elder. 2017. Nutrition and Lifestyle in Neurological Autoimmune Diseases. Nutrition and Lifestyle in Neurological Autoimmune Diseases 117 125 .
Maciej Wilski & Tomasz Tasiemski. 2017. Multiple Sclerosis: Bench to Bedside. Multiple Sclerosis: Bench to Bedside 43 55 .
M. Wilski, T. Tasiemski & A. Dąbrowski. (2015) Body Esteem Among Women with Multiple Sclerosis and its Relationship with Demographic, Clinical and Socio-Psychological Factors. International Journal of Behavioral Medicine 23:3, pages 340-347.
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Andy Soundy, Carolyn Roskell, Tracey Elder, Johnny Collett & Helen Dawes. (2016) The Psychological Processes of Adaptation and Hope in Patients with Multiple Sclerosis: A Thematic Synthesis. Open Journal of Therapy and Rehabilitation 04:01, pages 22-47.
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Joanna Blundell Jones, Sue Walsh & Claire Isaac. (2014) “Putting One Foot in Front of the Other”: A Qualitative Study of Emotional Experiences and Help-Seeking in Women with Multiple Sclerosis. Journal of Clinical Psychology in Medical Settings 21:4, pages 356-373.
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Chrisma Pretorius & Ninon Joubert. (2014) The experiences of individuals with Multiple Sclerosis in the Western Cape, South Africa. Health SA Gesondheid 19:1.
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Jacqui Steadman & Chrisma Pretorius. (2014) The impact of an online Facebook support group for people with multiple sclerosis on non-active users. African Journal of Disability 3:1.
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