Development of Guidelines for Spouses Engaged in Home-Based Care of Persons With Motor Neuron Disease From Indian Context
Author:
Affiliation:
1. Department of Psychology, Christ University, Bangalore, India
2. Department of Psychiatric Social Work, NIMHANS, Bangalore, India
3. Sampurna Montfort College, Bangalore, India
4. Department of Neurology, NIMHANS, Bangalore, India
Abstract
Funder
Indian Council of Medical Research
Publisher
SAGE Publications
Subject
Health Policy,Health (social science),Leadership and Management
Link
http://journals.sagepub.com/doi/pdf/10.1177/23743735221077535
Reference36 articles.
1. Who's there and who cares: age as an indicator of social support networks for caregivers among people living with motor neurone disease
2. Experiences of burden, needs, rewards and resilience in family caregivers of people living with Motor Neurone Disease/Amyotrophic Lateral Sclerosis: A secondary thematic analysis of qualitative interviews
3. From symptom onset to a diagnosis of amyotrophic lateral sclerosis/motor neuron disease (ALS/MND): Experiences of people with ALS/MND and family carers – a qualitative study
4. From first symptoms to diagnosis of amyotrophic lateral sclerosis: perspectives of an Irish informal caregiver cohort—a thematic analysis
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Palliative care needs and utilisation of specialist services for people diagnosed with motor neuron disease: a national population-based study;BMJ Open;2024-08
2. Family Perspectives on Key Elements of Good Home Palliative Care in South and Southeast Asia: A Scoping Review;Home Health Care Management & Practice;2024-01-28
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