Respite Care Services for Patients With Amyotrophic Lateral Sclerosis and Their Families From the Perspective of Home Care Nurses
Author:
Affiliation:
1. Gunma University, Maebashi-shi, Japan
2. Gunma University Hospital, Maebashi-shi, Japan
Abstract
Publisher
SAGE Publications
Subject
Public Health, Environmental and Occupational Health,Community and Home Care,Leadership and Management
Link
http://journals.sagepub.com/doi/pdf/10.1177/1084822315599953
Reference22 articles.
1. Burden, depression, and anxiety in caregivers of people with amyotrophic lateral sclerosis
2. Existential well-being and spirituality of individuals with amyotrophic lateral sclerosis is related to psychological well-being of their caregivers
3. The need for support services for family carers of people with motor neurone disease (MND): views of current and former family caregivers a qualitative study
4. Motor Neurone Disease family carers’ experiences of caring, palliative care and bereavement: An exploratory qualitative study
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1. Perceptions of people with motor neurone disease, families and HSCPs: a literature review;British Journal of Community Nursing;2022-04-02
2. The impact of respite care from the perspectives and experiences of people with amyotrophic lateral sclerosis and their care partners: a qualitative study;BMC Palliative Care;2022-02-28
3. Supportive needs of informal caregivers of people with amyotrophic lateral sclerosis in Switzerland: a qualitative study;Palliative Care and Social Practice;2022-01
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