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Our disease: a qualitative meta‐synthesis of the experiences of spousal/partner caregivers of people with multiple sclerosis
Author(s) -
Appleton Damien,
Robertson Noelle,
Mitchell Laura,
Lesley Rosie
Publication year - 2018
Publication title -
scandinavian journal of caring sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.678
H-Index - 66
eISSN - 1471-6712
pISSN - 0283-9318
DOI - 10.1111/scs.12601
Subject(s) - psychological intervention , psychology , qualitative research , argument (complex analysis) , nursing , health professionals , medicine , health care , sociology , social science , economics , economic growth
Purpose To provide a unique and conceptually comprehensive account of the lived experiences of caregiving spouses/partners of people with multiple sclerosis, which can be used to better enable health professionals to provide appropriate support services. Method A systematic review of qualitative studies reporting the experiences of caregiving spouses/partners was conducted. Relevant articles were identified and analysed using a meta‐ethnographic synthesis. Results Twenty studies met eligibility criteria, of which 18 were included in the final meta‐synthesis. Six major concepts were identified: Acceptance and Appreciation , Commitment , Becoming the Carer, Living with Loss, Shifting Sands and Setbacks with Services . A model of carer experience is presented as a line of argument to synthesise the findings. Suggestions are made regarding the types of supportive interventions that might be effective for spousal carers. Conclusion The findings increase our understanding about the experiences of partners caring for people with multiple sclerosis. Spousal carers can adapt to the challenges associated with change and loss, and have the potential to develop appreciation, acceptance and hope. Services need to be sensitive to the fluctuating demands placed upon carers and be flexible in their support.