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Research Article

Spiritual well-being of the individual with amyotrophic lateral sclerosis

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Pages 337-341 | Published online: 10 Jul 2009

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Christina L. Rush, Ethan G. Lester, Heena Manglani, Emily Woodworth, Ottavio Vitolo, Maurizio Fava, James D. Berry, Kate Brizzi, Suma Babu, Elizabeth C. Lindenberger, J. Randall Curtis & Ana-Maria Vranceanu. (2023) Resilient together-ALS: leveraging the NDD transdiagnostic framework to develop an early dyadic intervention for people with amyotrophic lateral sclerosis and their informal care-partners. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24:7-8, pages 719-726.
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Anna Maksymowicz-Śliwińska, Dorothée Lulé, Krzysztof NieporĘcki, Katarzyna Ciećwierska, Albert C. Ludolph & Magdalena Kuźma-Kozakiewicz. (2023) The quality of life and depression in primary caregivers of patients with amyotrophic lateral sclerosis is affected by patient-related and culture-specific conditions. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24:3-4, pages 317-326.
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Kerstin Stieber Roger & Andrew Hatala. (2018) Religion, spirituality & chronic illness: A scoping review and implications for health care practitioners. Journal of Religion & Spirituality in Social Work: Social Thought 37:1, pages 24-44.
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Francesco Pagnini. (2013) Psychological wellbeing and quality of life in amyotrophic lateral sclerosis: A review. International Journal of Psychology 48:3, pages 194-205.
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Francesco Pagnini, Christian Lunetta, Gabriella Rossi, Paolo Banfi, Ksenija Gorni, Nadia Cellotto, Gianluca Castelnuovo, Enrico Molinari & Massimo Corbo. (2011) Existential well-being and spirituality of individuals with amyotrophic lateral sclerosis is related to psychological well-being of their caregivers. Amyotrophic Lateral Sclerosis 12:2, pages 105-108.
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Joanna Epton, Robert Harris & Crispin Jenkinson. (2009) Quality of life in amyotrophic lateral sclerosis/motor neuron disease: A structured review. Amyotrophic Lateral Sclerosis 10:1, pages 15-26.
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Geraldine Foley, Paul O'Mahony & Orla Hardiman. (2007) Perceptions of quality of life in people with ALS: Effects of coping and health care. Amyotrophic Lateral Sclerosis 8:3, pages 164-169.
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Hiroshi Mitsumoto, Mark Bromberg, Wendy Johnston, Rup Tandan, Ira Byock, Mary Lyon, Robert G. Miller, Stanley H. Appel, Josh Benditt, James L. Bernat, Gian Domenico Borasio, Alan C. Carver, Lora Clawson, Maura. L. Del Bene, Edward J. Kasarskis, Susan B. Legrand, Raul Mandler, Jane Mccarthy, Theodore Munsat, Daniel Newman, Robert L. Sufit & Andrea Versenyi. (2005) Promoting excellence in end‐of‐life care in ALS. Amyotrophic Lateral Sclerosis 6:3, pages 145-154.
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Articles from other publishers (13)

Lorenza Palazzo, Sara Pompele, Marta Rossi, Gabriella Rossi, Simona Spinoglio & Ines Testoni. (2022) Facing Muscular Dystrophy During Covid-19 Pandemic: The Role of Support Associations and Spirituality. Pastoral Psychology 71:2, pages 217-231.
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Motataianu Anca, Andone Sebastian, Radu Cristina, Bajko Zoltan, Barcutean Laura, Balasa Adrian, Voidazan Septimiu, Stoian Adina & Maier Smaranda. (2020) Predictors of Depression in Caucasian Patients with Amyotrophic Lateral Sclerosis in Romania. Brain Sciences 10:8, pages 470.
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Hawa O. Abu, Christine Ulbricht, Eric Ding, Jeroan J. Allison, Elena Salmoirago-Blotcher, Robert J. Goldberg & Catarina I. Kiefe. (2018) Association of religiosity and spirituality with quality of life in patients with cardiovascular disease: a systematic review. Quality of Life Research 27:11, pages 2777-2797.
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Annerieke C. van Groenestijn, Esther T. Kruitwagen-van Reenen, Johanna M. A. Visser-Meily, Leonard H. van den Berg & Carin D. Schröder. (2016) Associations between psychological factors and health-related quality of life and global quality of life in patients with ALS: a systematic review. Health and Quality of Life Outcomes 14:1.
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Mary R. O'brien & David Clark. (2015) Spirituality and/or religious faith: A means for coping with the effects of amyotrophic lateral sclerosis/motor neuron disease?. Palliative and Supportive Care 13:6, pages 1603-1614.
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Sébastien Montel, Laurence Albertini & Elisabeth Spitz. (2011) Coping strategies in relation to quality of life in amyotrophic lateral sclerosis. Muscle & Nerve 45:1, pages 131-134.
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A. Chiò. 2010. Handbook of Disease Burdens and Quality of Life Measures. Handbook of Disease Burdens and Quality of Life Measures 3511 3539 .
Abbey R. Roach, Alyssa J. Averill, Suzanne C. Segerstrom & Edward J. Kasarskis. (2009) The Dynamics of Quality of Life in ALS Patients and Caregivers. Annals of Behavioral Medicine 37:2, pages 197-206.
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Janet E. McLeod & David M. Clarke. (2007) A review of psychosocial aspects of motor neurone disease. Journal of the Neurological Sciences 258:1-2, pages 4-10.
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Paul H. Gordon & Hiroshi Mitsumoto. 2007. Motor neuron disorders and related diseases. Motor neuron disorders and related diseases 389 424 .
V. Havet. (2006) Prise en charge psychologique du patient atteint de sclérose latérale amyotrophique (SLA) et de sa famille. Revue Neurologique 162, pages 301-307.
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V. Havet. (2006) Évaluation psychologique et psychopathologique du patient atteint de sclérose latérale amyotrophique (SLA). Revue Neurologique 162, pages 164-172.
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Marilyn Trail, Naomi D. Nelson, John N. Van, Stanley H. Appel & Eugene C. Lai. (2003) A study comparing patients with amyotrophic lateral sclerosis and their caregivers on measures of quality of life, depression, and their attitudes toward treatment options. Journal of the Neurological Sciences 209:1-2, pages 79-85.
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