Supportive and Palliative Care Needs Identified By Multiple Sclerosis Patients and Their Families

Document Type

Journal Article

Faculty

Faculty of Computing, Health and Science

School

School of Nursing, Midwifery and Postgraduate Medicine / WA Centre for Cancer and Palliative Care

RAS ID

9280

Comments

Wollin, J. A., Yates, P. M., & Kristjanson, L. J. (2006). Supportive and palliative care needs identified by multiple sclerosis patients and their families. International journal of palliative nursing, 12(1). 20-26. Available here

Abstract

Aim: To identify the supportive needs of individuals with multiple sclerosis (MS) and their families. Design, Sample and Method: In-depth interviews were carried out with people living with MS in the community, their family members and health professionals. The data were transcribed verbatim and recurring themes identified. Findings: The analysis of interviews revealed four themes: disbelief and devastation; losses and forced life choices; tracking down services and information; and sadness and relief. Conclusion: Given the duration, range of symptoms and distress often associated with MS, the findings of this research raise the important question of the role of palliative services in supporting the person with MS and his/her family.

DOI

10.12968/ijpn.2006.12.1.20392

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Link to publisher version (DOI)

10.12968/ijpn.2006.12.1.20392