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Research Papers

Being in- or out-of-sync: Couples' adaptation to change in multiple sclerosis

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Pages 196-206 | Accepted 01 May 2009, Published online: 15 Dec 2009

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Dilek Demirtepe-Saygılı. (2021) Multiple sclerosis experiences of couples: Examination of patient and partner perspectives. Journal of Health Psychology 27:9, pages 2079-2090.
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Sarah M. Bannon, Victoria A. Grunberg, Heena R. Manglani, Ethan G. Lester, Christine Ritchie & Ana‐Maria Vranceanu. (2022) Together from the start: A transdiagnostic framework for early dyadic interventions for neurodegenerative diseases. Journal of the American Geriatrics Society 70:6, pages 1850-1862.
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Emanuela Calandri, Federica Graziano, Martina Borghi & Silvia Bonino. (2021) The future between difficulties and resources: Exploring parents' perspective on young adults with multiple sclerosis. Family Relations 71:2, pages 686-706.
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Ada-Katrin Busch & André Fringer. (2022) Psychosocial Impact of Multiple Sclerosis on Couples: Relationship Between Anxiety, Depression, and Stress Communication of Both Partners. Journal of Primary Care & Community Health 13, pages 215013192211191.
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Maiken Schjerlund, Hanne Agnholt, Lærke Rohr Gregersen, Tina Heilesen & Mona K. Pedersen. (2020) Cognitive impairment in patients with chronic kidney disease—Next of kin's experiences. Journal of Renal Care 47:2, pages 87-95.
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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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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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Elizabeth D’Arrigo‐Patrick, Sarah K. Samman & Carmen Knudson‐Martin. (2020) Moving from “I” to “We”: A Grounded Theory Analysis of Couple Therapy with Liver Patients and Their Partners. Family Process 59:4, pages 1517-1529.
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Elizabeth J Halstead, Victoria M Leavitt, Damian Fiore & Kim T Mueser. (2020) A feasibility study of a manualized resilience-based telehealth program for persons with multiple sclerosis and their support partners. Multiple Sclerosis Journal - Experimental, Translational and Clinical 6:3, pages 205521732094125.
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Anna Ovšonková, Edita Hlinková, Michaela Miertová & Katarína Žiaková. (2020) Selected social aspects in the life of patients with multiple sclerosis. Kontakt 22:2, pages 104-110.
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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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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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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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Riley Bove, Allison McHenry, Kerstin Hellwig, Maria Houtchens, Neda Razaz, Penelope Smyth, Helen Tremlett, A. D. Sadovnick & D. Rintell. (2016) Multiple sclerosis in men: management considerations. Journal of Neurology 263:7, pages 1263-1273.
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Nadine LacroixM. serv. sM. serv. s, Normand BoucherPh.D.Ph.D. & Patrick VilleneuvePh.D.Ph.D.. (2016) Participation sociale et sclérose en plaques : Réalité particulière. Service social 62:2, pages 94.
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Karen Strickland, Allison Worth & Catriona Kennedy. (2015) The experiences of support persons of people newly diagnosed with multiple sclerosis: an interpretative phenomenological study. Journal of Advanced Nursing 71:12, pages 2811-2821.
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Christina Samios, Kenneth I. Pakenham & Jill O’Brien. (2014) A Dyadic and Longitudinal Investigation of Adjustment in Couples Coping with Multiple Sclerosis. Annals of Behavioral Medicine 49:1, pages 74-83.
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A.-K. Busch, R. Spirig & W. Schnepp. (2014) Bewältigung der Multiplen Sklerose in der PartnerschaftCoping with multiple sclerosis in partnerships. Der Nervenarzt 85:6, pages 727-737.
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Michele Messmer Uccelli. (2014) The impact of multiple sclerosis on family members: a review of the literature. Neurodegenerative Disease Management 4:2, pages 177-185.
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Liselott ?restedt, Carina Persson & Eva Benzein. (2014) Living as a family in the midst of chronic illness. Scandinavian Journal of Caring Sciences 28:1, pages 29-37.
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Nic Hughes, Louise Locock & Sue Ziebland. (2013) Personal identity and the role of ‘carer’ among relatives and friends of people with multiple sclerosis. Social Science & Medicine 96, pages 78-85.
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Elizabeth S. Knaster, Kathryn M. Yorkston, Kurt Johnson, Kara A. McMullen & Dawn M. Ehde. (2011) Perspectives on Self-Management in Multiple Sclerosis. International Journal of MS Care 13:3, pages 146-152.
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Yára Dadalti Fragoso, Alessandro Finkelsztejn, Maria Cristina B. Giacomo, Liliana Russo & Wesley Soares Cruz. (2010) The effect of multiple sclerosis on the professional life of a group of Brazilian patients. Arquivos de Neuro-Psiquiatria 68:6, pages 914-917.
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Kathryn M. Yorkston, Michelle S. Bourgeois & Carolyn R. Baylor. (2010) Communication and Aging. Physical Medicine and Rehabilitation Clinics of North America 21:2, pages 309-319.
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