Abstract
Neurological bilateral upper limb weakness can result in self-feeding difficulties and reliance on carers. Mealtimes become time consuming and frustrating. This exploratory inquiry examined the experiences, of users of a feeding device. Method: Semi-structured interviews were conducted either by telephone or administered via email to explore quality of life, changes to independence, benefits/limitations, and psychological impact of the equipment. Findings: Thematic analysis gave rise to five themes: Independence, emotions, impact on life, motivation and limitations. Conclusion: This exploratory inquiry has contributed new qualitative evidence to the knowledge and understanding of users' experiences of a manual feeding device. Users report that the need for assistance/support is reduced and their quality of life, independence and freedom improved. Time and resources savings for the family, carers and staff appear to result in a more equal relationship between user and carer.
Original language | English |
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Pages (from-to) | 1-5 |
Number of pages | 5 |
Journal | American Journal of Occupational Therapy |
Volume | 72 |
Issue number | 3 |
DOIs | |
Publication status | Published - 6 Mar 2018 |
Bibliographical note
© 2016 American Occupational Therapy Association . This is an author-produced version of a paper accepted for publication in American Journal of Occupational Therapy.Keywords
- Feeding devices
- independence
- quality of life