Living with tracheostomy ventilation for motor neurone disease: a qualitative study of family member perspectives

Enhanced psychological, social, and practical support is urgently needed for families caring for someone with tracheostomy ventilation for MND. Greater awareness of its long-term impact, realistic home assessments, and structured support networks are essential.

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Publication Details

Journal
Disability and Rehabilitation
Published
2025-10-15
DOI
https://doi.org/10.1080/09638288.2025.2574536
Primary Topic
Family and Patient Care in Intensive Care Units
Type
article
Field-Weighted Citation Impact
0.00
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article

Living with tracheostomy ventilation for motor neurone disease: a qualitative study of family member perspectives

Nicola Turner, Christina Faull, Martin R. Turner, Eleanor Wilson et al.
Disability and Rehabilitation
Family and Patient Care in Intensive Care Units
article

Living with tracheostomy ventilation for motor neurone disease: a qualitative study of family member perspectives

Nicola Turner, Christina Faull, Martin R. Turner, Eleanor Wilson, Scott Davidson, Jonathan E. Palmer
article en

Abstract

Enhanced psychological, social, and practical support is urgently needed for families caring for someone with tracheostomy ventilation for MND. Greater awareness of its long-term impact, realistic home assessments, and structured support networks are essential.

Disability and Rehabilitation
University of Nottingham (GB), University of Leicester (GB), NHS Greater Glasgow and Clyde (GB), University of Oxford (GB), University Hospitals Plymouth NHS Trust (GB)
Openalex Percentile: Top 58%
Family and Patient Care in Intensive Care Units
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