Citations (36)
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Ann Ekdahl, Siv Söderberg & Malin Holmström Rising. (2023) Striving for moments of easier breathing despite being trapped in breathlessness: meanings of feeling well for women with chronic obstructive pulmonary disease stage III or IV. International Journal of Qualitative Studies on Health and Well-being 18:1.
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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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Catharina Melander, Päivi Juuso & Malin Olsson. (2022) Women’s experiences of living with lipedema. Health Care for Women International 43:1-3, pages 54-69.
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Christopher Meek, Gogem Topcu, Nima Moghaddam & Roshan das Nair. (2021) Experiences of adjustment to secondary progressive multiple sclerosis: a meta-ethnographic systematic review. Disability and Rehabilitation 43:22, pages 3135-3146.
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Shahla Biglar Chopoghlou, Nasrin Hanifi & Nasrin Jafari Varjoshani. (2020) A comparative study of uncertainty and coping strategies of patients with multiple sclerosis for members and nonmembers in peer groups. Health Care for Women International 41:3, pages 354-367.
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Sema D. Yılmaz, Haluk Gumus, Faruk O. Odabas, Halil E. Akkurt & Halim Yılmaz. (2017) Sexual Life of Women with Multiple Sclerosis: A Qualitative Study. International Journal of Sexual Health 29:2, pages 147-154.
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Kim Walder & Matthew Molineux. (2017) Occupational adaptation and identity reconstruction: A grounded theory synthesis of qualitative studies exploring adults’ experiences of adjustment to chronic disease, major illness or injury. Journal of Occupational Science 24:2, pages 225-243.
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Malin Olsson, Lisa Skär & Siv Söderberg. (2011) Meanings of being received and met by others as experienced by women with MS. International Journal of Qualitative Studies on Health and Well-being 6:1.
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Articles from other publishers (28)
Libby Byrne. (2023) Unless Something Goes Wrong: Making Art to Understand and Mitigate the Risk of Therapeutic Inertia in the Treatment of Multiple Sclerosis. Journal of Patient Experience 10, pages 237437352311515.
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Ashley Polhemus, Sara Simblett, Erin Dawe Lane, Benjamin Elliott, Sagar Jilka, Esther Negbenose, Patrick Burke, Janice Weyer, Jan Novak, Marissa F. Dockendorf, Gergely Temesi & Til Wykes. (2023) Experiences of health tracking in mobile apps for multiple sclerosis: A qualitative content analysis of user reviews. Multiple Sclerosis and Related Disorders 69, pages 104435.
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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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Georgina Newton, Amy Griffith & Andy Soundy. (2020) The experience of fatigue in neurological patients with Multiple Sclerosis: a thematic synthesis. Physiotherapy 107, pages 306-316.
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Yasuko Igai. (2020) Concept analysis of dignity‐centered care for people with chronic progressive disease. Japan Journal of Nursing Science 17:2.
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Chloe Parton, Terri Katz & Jane M Ussher. (2017) ‘Normal’ and ‘failing’ mothers: Women’s constructions of maternal subjectivity while living with multiple sclerosis. Health: An Interdisciplinary Journal for the Social Study of Health, Illness and Medicine 23:5, pages 516-532.
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Libby Byrne. (2018) Healing in the Absence of a Cure. Journal of Patient Experience 6:1, pages 7-10.
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Angeliki Bogosian, Myfanwy Morgan & Rona Moss-Morris. (2019) Multiple challenges for people after transitioning to secondary progressive multiple sclerosis: a qualitative study. BMJ Open 9:3, pages e026421.
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Félix Bravo-González & Arturo Álvarez-Roldán. (2019) Esclerosis múltiple, pérdida de funcionalidad y género. Gaceta Sanitaria 33:2, pages 177-184.
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Hanneke van der Meide, Truus Teunissen, Pascal Collard, Merel Visse & Leo H Visser. (2018) The Mindful Body: A Phenomenology of the Body With Multiple Sclerosis. Qualitative Health Research 28:14, pages 2239-2249.
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Joanna Blundell Jones, Sue Walsh & Claire Isaac. (2017) The Relational Impact of Multiple Sclerosis: An Integrative Review of the Literature Using a Cognitive Analytic Framework. Journal of Clinical Psychology in Medical Settings 24:3-4, pages 316-340.
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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
.
Gullvi Flensner & Gudrun Rudolfsson. (2016) Learning to fly with broken wings - forcing a reappraisal of time and space. Scandinavian Journal of Caring Sciences 30:2, pages 403-410.
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Andrew Soundy, Carolyn Roskell, Rachel Adams, Tracey Elder & Helen Dawes. (2016) Understanding Health Care Professional-Patient Interactions in Multiple Sclerosis: A Systematic Review and Thematic Synthesis. Open Journal of Therapy and Rehabilitation 04:04, pages 187-217.
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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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Louise Bager, Hanne Konradsen & Pia Sander Dreyer. (2015) The patient's experience of temporary paralysis from spinal anaesthesia, a part of total knee replacement. Journal of Clinical Nursing 24:23-24, pages 3503-3510.
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Leire Ambrosio, Juana Maria Senosiain García, Mario Riverol Fernández, Sagrario Anaut Bravo, Sara Díaz De Cerio Ayesa, María Eugenia Ursúa Sesma, Neus Caparrós & Mari Carmen Portillo. (2015) Living with chronic illness in adults: a concept analysis. Journal of Clinical Nursing 24:17-18, pages 2357-2367.
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Eva Benzein, Cecilia Olin & Carina Persson. (2015) ‘You put it all together’ - families' evaluation of participating in Family Health Conversations. Scandinavian Journal of Caring Sciences 29:1, pages 136-144.
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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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Cynthia L. Murray, Michelle Ploughman, Chelsea Harris, Stephen Hogan, Michelle Murdoch & Mark Stefanelli. (2014) The Liberation Procedure Decision-Making Experience for People With Multiple Sclerosis. Global Qualitative Nursing Research 1, pages 233339361455141.
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Sally Hartley, Maggie McArthur, Michaela Coenen, Maria Cabello, Venusia Covelli, Joanna Roszczynska-Michta, Tuuli Pitkänen, Jerome Bickenbach & Alarcos Cieza. (2014) Narratives Reflecting the Lived Experiences of People with Brain Disorders: Common Psychosocial Difficulties and Determinants. PLoS ONE 9:5, pages e96890.
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Hannah Rose Wilkinson & Roshan das Nair. (2013) The psychological impact of the unpredictability of multiple sclerosis: a qualitative literature meta-synthesis. British Journal of Neuroscience Nursing 9:4, pages 172-178.
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Malin Olsson, Lena Stafström & Siv Söderberg. (2013) Meanings of Fatigue for Women With Parkinson’s Disease. Qualitative Health Research 23:6, pages 741-748.
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Åsa Audulv, Kenneth Asplund & Karl-Gustaf Norbergh. (2011) The influence of illness perspectives on self-management of chronic disease. Journal of Nursing and Healthcare of Chronic Illness 3:2, pages 109-118.
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Crossref
Laura DennisonLucy Yardley, Angela Devereux & Rona Moss-Morris. (2010) Experiences of adjusting to early stage Multiple Sclerosis. Journal of Health Psychology 16:3, pages 478-488.
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Andrew D. Campbell, Paula T. Ross, Arno K. Kumagai, Jennifer G. Christner & Monica L. Lypson. (2010) Coming of Age With Sickle Cell Disease and the Role of Patient as Teacher. Journal of the National Medical Association 102:11, pages 1073-1078.
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Malin OlssonLisa Skär & Siv Söderberg. (2010) Meanings of Feeling Well for Women With Multiple Sclerosis. Qualitative Health Research 20:9, pages 1254-1261.
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