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Research Article

The family of the multiple sclerosis patient: A psychosocial perspective

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Pages 83-89 | Published online: 11 Mar 2010

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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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Helena Gauffin, Gullvi Flensner & Anne-Marie Landtblom. (2015) Being parents with epilepsy: thoughts on its consequences and difficulties affecting their children. Neuropsychiatric Disease and Treatment 11, pages 1291-1298.
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Articles from other publishers (22)

Irene Gil-González, María Ángeles Pérez-San-Gregorio, Jesús Funuyet-Salas, Rupert Conrad & Agustín Martín-Rodríguez. (2023) Significance of Post-Traumatic Growth and Mental Health for Coping in Multiple Sclerosis Caregivers. Healthcare 11:10, pages 1390.
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Dimitris Sokratous, Charalambos C. Charalambous, Eleni Zamba Papanicolaou, Kyriaki Michailidou & Nikos Konstantinou. (2023) Investigation of in-phase bilateral exercise effects on corticospinal plasticity in relapsing remitting multiple sclerosis: A registered report single-case concurrent multiple baseline design across five subjects. PLOS ONE 18:3, pages e0272114.
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Ilham Raji, Ibtissam El Harch, MohammedE. A. Ragala, Mohamed Berraho & MohammedF Belahsen. (2023) impact of therapeutic education programs on the quality of life of patients with multiple sclerosis: Protocol of a systematic reviews. Journal of Education and Health Promotion 12:1, pages 264.
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Barbara Kołecka & Aleksandra Kołecka. (2022) Formy wsparcia pacjenta i rodziny w sytuacji choroby o zróżnicowanym przebiegu. Studia Edukacyjne:65, pages 137-147.
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Saskia Elkhalii-Wilhelm, Anna Sippel, Karin Riemann-Lorenz, Christopher Kofahl, Jutta Scheiderbauer, Sigrid Arnade, Ingo Kleiter, Stephan Schmidt & Christoph Heesen. (2022) Experiences of persons with Multiple Sclerosis with lifestyle adjustment–A qualitative interview study. PLOS ONE 17:5, pages e0268988.
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Beatrice Lee & Fong Chan. (2022) The Development and Psychometric Validation of the Brief Disability-Related Stress Scale in Individuals With Multiple Sclerosis . Rehabilitation Counseling Bulletin, pages 003435522210871.
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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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Maria Luca, Nerea Ortega-Castro & Francesco Patti. (2021) Paediatric Multiple Sclerosis: A Scoping Review of Patients’ and Parents’ Perspectives. Children 9:1, pages 11.
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Marialaura Di Tella, Virginia Perutelli, Giuseppina Miele, Luigi Lavorgna, Simona Bonavita, Stefania Federica De Mercanti, Lidia Mislin Streito, Marinella Clerico & Lorys Castelli. (2021) Family Functioning and Multiple Sclerosis: Study Protocol of a Multicentric Italian Project. Frontiers in Psychology 12.
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Shashank Ghai, Elisabeth Kasilingam, Roberta Lanzillo, Masa Malenica, Vincent van Pesch, Niamh Caitlin Burke, Antonio Carotenuto & Rebecca Maguire. (2021) Needs and Experiences of Children and Adolescents with Pediatric Multiple Sclerosis and Their Caregivers: A Systematic Review. Children 8:6, pages 445.
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Saúl Reyes, Sebastian Suarez, Kimberley Allen‐Philbey, Alison Thomson & Gavin Giovannoni. (2020) The impact of social capital on patients with multiple sclerosis. Acta Neurologica Scandinavica 142:1, pages 58-65.
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Sofía García-Sanjuán, Manuel Lillo-Crespo, María José Cabañero-Martínez, Miguel Richart-Martínez & Ángela Sanjuan-Quiles. (2019) Experiencing the care of a family member with Crohn’s disease: a qualitative study. BMJ Open 9:10, pages e030625.
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Nuray Dayapoğlu & Mehtap Tan. (2017) The care burden and social support levels of caregivers of patients with multiple sclerosis. Kontakt 19:1, pages e17-e23.
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Neda Razaz, K. S. Joseph, Ruth Ann Marrie & Helen Tremlett. 2017. Health Issues in Women with Multiple Sclerosis. Health Issues in Women with Multiple Sclerosis 63 72 .
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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Heidrun Golla, Stephanie Mammeas, Maren Galushko, Holger Pfaff & Raymond Voltz. (2015) Unmet needs of caregivers of severely affected multiple sclerosis patients: A qualitative study. Palliative and Supportive Care 13:6, pages 1685-1693.
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Neda Razaz, Helen Tremlett, W. Thomas Boyce, Martin Guhn, KS Joseph & Ruth Ann Marrie. (2015) Impact of parental multiple sclerosis on early childhood development: A retrospective cohort study. Multiple Sclerosis Journal 21:9, pages 1172-1183.
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Marita P McCabe, Katherine J Ebacioni, Rex Simmons, Elizabeth McDonald & Lisa Melton. (2015) Unmet education, psychological and peer support needs of people with multiple sclerosis. Journal of Psychosomatic Research 78:1, pages 82-87.
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Maren GalushkoHeidrun GollaJulia StruppUte KarbachClaudia KaiserNicole ErnstmannHolger PfaffChristoph OstgatheRaymond Voltz. (2014) Unmet Needs of Patients Feeling Severely Affected by Multiple Sclerosis in Germany: A Qualitative Study. Journal of Palliative Medicine 17:3, pages 274-281.
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S. Vitiello. 2013. Aspetti psicologici nella sclerosi multipla. Aspetti psicologici nella sclerosi multipla 195 206 .
Józef Opara, Krystyna Jaracz & Waldemar Brola. (2012) Burden and quality of life in caregivers of persons with multiple sclerosis. Neurologia i Neurochirurgia Polska 46:5, pages 472-479.
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Rex D. Simmons. (2010) Life issues in multiple sclerosis. Nature Reviews Neurology 6:11, pages 603-610.
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