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Articles

Impact of patient suffering on caregiver well-being: The case of amyotrophic lateral sclerosis patients and their caregivers

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Pages 457-466 | Received 26 Apr 2011, Accepted 09 Aug 2011, Published online: 25 Nov 2011

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Claudia Zanini, Maddalena Fiordelli, Julia Amann, Mirjam Brach, Armin Gemperli & Sara Rubinelli. (2022) Coping strategies of family caregivers in spinal cord injury: a qualitative study. Disability and Rehabilitation 44:2, pages 243-252.
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Francesco Tramonti, Paolo Bongioanni, Rebecca Leotta, Irene Puppi & Bruno Rossi. (2015) Age, gender, kinship and caregiver burden in amyotrophic lateral sclerosis. Psychology, Health & Medicine 20:1, pages 41-46.
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Ralf Stutzki, Markus Weber, Stella Reiter-Theil, Urs Simmen, Gian Domenico Borasio & Ralf J. Jox. (2014) Attitudes towards hastened death in ALS: A prospective study of patients and family caregivers. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 15:1-2, pages 68-76.
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Antonella Mossa, Masako Mayahara, Chuka Emezue & Olimpia Paun. (2023) The Impact of Rapidly Progressing Neurodegenerative Disorders on Caregivers. Journal of Hospice & Palliative Nursing.
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Davide Gentili, Giovanna Deiana, Vanna Chessa, Annalisa Calabretta, Elisabetta Marras, Costanzo Solinas, Carmelo Gugliotta & Antonio Azara. (2023) Quality of Life in Amyotrophic Lateral Sclerosis Patients and Care Burden of Caregivers in Sardinia during COVID-19 Pandemic. Healthcare 11:11, pages 1641.
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Ling Lian, Minying Zheng, Ruojie He, Jianing Lin, Weineng Chen, Zhong Pei & Xiaoli Yao. (2022) Analysing the influencing factors on caregivers’ burden among amyotrophic lateral sclerosis patients in China: a cross-sectional study based on data mining. BMJ Open 12:9, pages e066402.
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Laura Gallego‐Alberto, Rosa Romero‐Moreno, María Márquez‐González, Richard Schulz, Isabel Cabrera, Javier Olazarán‐Rodríguez & Andrés Losada. (2021) Compassion in dementia caregiving: Psychometric properties of the Caregiving Compassion Scale in Spanish caregivers. Health & Social Care in the Community 30:5.
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Manjusha G Warrier, Priya Treesa Thomas, Arun Sadasivan, Saraswati Nashi, Seena Vengalil & A. Nalini. (2022) Development of Guidelines for Spouses Engaged in Home-Based Care of Persons With Motor Neuron Disease From Indian Context. Journal of Patient Experience 9, pages 237437352210775.
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Barbara Bassola, Silvia Cilluffo & Maura Lusignani. (2020) Going inside the relationship between caregiver and care‐receiver with Amyotrophic Lateral Sclerosis in Italy, a Grounded Theory study. Health & Social Care in the Community 29:4, pages 1083-1090.
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Juyeon Oh, Jung-A Kim & Min Sun Chu. (2021) Family Caregiver Suffering in Caring for Patients with Amyotrophic Lateral Sclerosis in Korea. International Journal of Environmental Research and Public Health 18:9, pages 4937.
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James Grogan & Zachary Simmons. (2020) Telemedicine for the Care of Neuromuscular Disorders. Current Treatment Options in Neurology 22:6.
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Antonio Geraldo Abreu Filho, Leila Salomão Plata Cury Tardivo, Acary Souza Bulle Oliveira & Helga Cristina Almeida da Silva. (2019) Brazilian Nursing and Psychology students' visits to patients with amyotrophic lateral sclerosis: prospective analysis. Arquivos de Neuro-Psiquiatria 77:11, pages 782-791.
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Hyeon Sik Chu, Young Ran Tak & Seung Hyun Kim. (2018) Factors Influencing Psychosocial Well-Being in Family Caregivers of People with Amyotrophic Lateral Sclerosis. Journal of Korean Academy of Nursing 48:4, pages 454.
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Jessica de Wit, Leonhard A Bakker, Annerieke C van Groenestijn, Leonard H van den Berg, Carin D Schröder, Johanna MA Visser-Meily & Anita Beelen. (2017) Caregiver burden in amyotrophic lateral sclerosis: A systematic review. Palliative Medicine 32:1, pages 231-245.
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Anna Marconi. (2017) Psychological Intervention in Amyotrophic Lateral Sclerosis: Suggestions for Clinical Practice. Journal of Psychology & Clinical Psychiatry 8:2.
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Susan Bergin & Carole Mockford. (2016) Recommendations to support informal carers of people living with motor neurone disease. British Journal of Community Nursing 21:10, pages 518-524.
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Huub Creemers, Sandra de Morée, Jan H Veldink, Frans Nollet, Leonard H van den Berg & Anita Beelen. (2016) Factors related to caregiver strain in ALS: a longitudinal study. Journal of Neurology, Neurosurgery & Psychiatry 87:7, pages 775-781.
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Dezhi Chen, Xiaoyan Guo, Zhenzhen Zheng, Qianqian Wei, Wei Song, Bei Cao, Rui Huang, Rong Yang & Huifang Shang. (2015) Depression and anxiety in amyotrophic lateral sclerosis: Correlations between the distress of patients and caregivers. Muscle & Nerve 51:3, pages 353-357.
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Marilyn E. Miller. 2014. A Comprehensive Guide to Geriatric Rehabilitation. A Comprehensive Guide to Geriatric Rehabilitation 120 123 .

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