Citations (41)
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Emilie Wawrziczny, Aubane Corrairie & Pascal Antoine. (2021) Relapsing-remitting multiple sclerosis: an interpretative phenomenological analysis of dyadic dynamics. Disability and Rehabilitation 43:1, pages 76-84.
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Elaine Schembri Lia & Angela Abela. (2020) The couple relationship when the female partner has an acquired physical disability. The History of the Family 25:2, pages 265-286.
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Sibel Öztürk & Nuray Dayapoğlu. (2019) Women with Multiple Sclerosis and Marital Adjustment: A Sample from Turkey. The American Journal of Family Therapy 47:3, pages 137-147.
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Kerry Mutch, Abigail Methley, Shahd Hamid, Perry Moore & Anu Jacob. (2017) If they are OK, we are OK: the experience of partners living with neuromyelitis optica. Disability and Rehabilitation 39:13, pages 1279-1286.
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Arielle M. Silverman, Aimee M. Verrall, Kevin N. Alschuler, Amanda E. Smith & Dawn M. Ehde. (2017) Bouncing back again, and again: a qualitative study of resilience in people with multiple sclerosis. Disability and Rehabilitation 39:1, pages 14-22.
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Pavol Mikula, Iveta Nagyova, Martina Krokavcova, Marianna Vitkova, Jaroslav Rosenberger, Jarmila Szilasiova, Zuzana Gdovinova, Johan W. Groothoff & Jitse P. van Dijk. (2014) Coping and its importance for quality of life in patients with multiple sclerosis. Disability and Rehabilitation 36:9, pages 732-736.
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Articles from other publishers (35)
Camilla Holden, Peter Hewitt & Rachel Tams. (2023) Striving to Limit the Impact: Parenting an Adult Child Who Has Multiple Sclerosis—A Grounded Theory Study. International Journal of MS Care 25:6, pages 259-265.
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Charlotte Manceau, Emilie Constant, Elodie Brugallé, Emilie Wawrziczny, Céline Sokolowski, Bérengère Flinois, Guillaume Baille, Luc Defebvre, Kathy Dujardin & Pascal Antoine. (2022) Couples facing the “honeymoon period” of Parkinson's disease: A qualitative study of dyadic functioning. British Journal of Health Psychology 28:2, pages 366-382.
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Evelyn Palmer, Emily Kavanagh, Shelina Visram, Anne-Marie Bourke, Ian Forrest & Catherine Exley. (2022) When should palliative care be introduced for people with progressive fibrotic interstitial lung disease? A meta-ethnography of the experiences of people with end-stage interstitial lung disease and their family carers. Palliative Medicine 36:8, pages 1171-1185.
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Anne Parkinson, Crystal Brunoro, Jack Leayr, Vanessa Fanning, Katrina Chisholm, Janet Drew, Jane Desborough & Christine Phillips. (2022) Intertwined like a double helix: A meta‐synthesis of the qualitative literature examining the experiences of living with someone with multiple sclerosis. Health Expectations 25:3, pages 803-822.
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Elizabeth J. Halstead, Justin Stanley, Damian Fiore & Kim T. Mueser. (2021) Impact of Cognitive Impairment on Adults with Multiple Sclerosis and Their Family Caregivers. International Journal of MS Care 23:3, pages 93-100.
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Cathy Bulley, Gillian Baer, Dawn Mahal, Christina H Buckton, Stewart Donald, Keith Lugton, David Gillespie & Brendan McCormack. (2021) Supporting families and carers of people living with multiple sclerosis: a rapid realist review and realist evaluation. International Journal of Care and Caring 5:2, pages 263-282.
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Rachel McCauley, Regina McQuillan, Karen Ryan & Geraldine Foley. (2021) Mutual support between patients and family caregivers in palliative care: A systematic review and narrative synthesis. Palliative Medicine 35:5, pages 875-885.
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Isabella C. Bertschi, Fabienne Meier & Guy Bodenmann. (2021) Disability as an Interpersonal Experience: A Systematic Review on Dyadic Challenges and Dyadic Coping When One Partner Has a Chronic Physical or Sensory Impairment. Frontiers in Psychology 12.
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Yael Hochman, Einav Segev & Miriam Levinger. (2019) Five Phases of Dyadic Analysis: Stretching the Boundaries of Understanding of Family Relationships. Family Process 59:2, pages 681-694.
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Victoria Wood & Susan L. Kasser. (2020) Spousal support and self-determined physical activity in individuals with multiple sclerosis: A theory-informed qualitative exploration. Disability and Health Journal 13:1, pages 100835.
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Elisabet Eriksson, Maria Wejåker, Anna Danhard, Annika Nilsson & Marja-Leena Kristofferzon. (2019) Living with a spouse with chronic illness – the challenge of balancing demands and resources. BMC Public Health 19:1.
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Caroline Kilty, Corina Naughton & Aine de Roiste. (2019) Constraints and ethical tensions in the area of young-onset dementia. British Journal of Nursing 28:21, pages 1380-1386.
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Leslie Beth Herbert, Kristine Zerkowski, Sarah O’Brien, Kathryn Volpicelli Leonard & Amrita Bhowmick. (2019) Impact on interpersonal relationships among patients with multiple sclerosis and their partners. Neurodegenerative Disease Management 9:3, pages 173-187.
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Sandra L. Neate, Keryn L. Taylor, George A. Jelinek, Alysha M. De Livera, Chelsea R. Brown & Tracey J. Weiland. (2019) Taking active steps: Changes made by partners of people with multiple sclerosis who undertake lifestyle modification. PLOS ONE 14:2, pages e0212422.
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Damien Appleton, Noelle Robertson, Laura Mitchell & Rosie Lesley. (2018) Our disease: a qualitative meta-synthesis of the experiences of spousal/partner caregivers of people with multiple sclerosis. Scandinavian Journal of Caring Sciences 32:4, pages 1262-1278.
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Lauren Killner & Andrew Soundy. (2018) Motivation and experiences of role transition in spousal caregivers of people with multiple sclerosis. International Journal of Therapy and Rehabilitation 25:8, pages 405-413.
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Sandra L. Neate, Keryn L. Taylor, George A. Jelinek, Alysha M. De Livera, Chelsea R. Brown & Tracey J. Weiland. (2018) Psychological Shift in Partners of People with Multiple Sclerosis Who Undertake Lifestyle Modification: An Interpretive Phenomenological Study. Frontiers in Psychology 9.
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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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Emilie Wawrziczny, Pascal Antoine, Francine Ducharme, Marie-Jeanne Kergoat & Florence Pasquier. (2016) Couples' experiences with early-onset dementia: An interpretative phenomenological analysis of dyadic dynamics. Dementia 15:5, pages 1082-1099.
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Chiara Rollero. (2016) The Experience of Men Caring for a Partner With Multiple Sclerosis. Journal of Nursing Scholarship 48:5, pages 482-489.
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