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Loss and change: experiences of people severely affected by multiple sclerosis

Department of Palliative Care and Policy, King’s College London, London, polly.edmonds{at}kcl.ac.uk

Bella Vivat

Department of Palliative Care and Policy, King’s College London, London and School of Health Sciences and Social Care, Brunel University, Uxbridge

Rachel Burman

Department of Palliative Care and Policy, King’s College London, London

Eli Silber

Department of Neurology, King’s College Hospital, London

Irene J Higginson

Department of Palliative Care and Policy, King’s College London, London

This study aimed to explore important issues for people severely affected by multiple sclerosis (MS). Individual interviews were conducted with 23 people with MS (PwMS) and 17 informal carers, the data relating to 32 PwMS. Information was obtained about 19 females and 13 males, with a mean age of 55, median time from diagnosis was 14.5 years, and physical disabilities ranged from mild to severe, although fifteen patients had severe disabilities. Twenty-six of the 32 individuals were unable to walk, 24 were catheterised, and 18 had considerably impaired or no upper limb function. Personal issues in relation to loss and change, particularly in terms of losses of or changes in physical abilities, including maintaining mobility, independence, relationships and social role were raised commonly in response to an open-ended question about what issues were important in living with MS. Coping with MS requires individuals to deal with the losses and changes brought about by their illness. Our study suggests that even patients who have had MS for many years and are now severely affected continue to experience loss and change. We recommend that attention be given to emotional support which specifically addresses three main areas of dealing with loss and change for people that are severely affected - physical issues, independence and relationships. Palliative care providers may have expertise in managing loss that could be useful for these patients in partnership with neurological services.

Key Words: change • independence • loss • mobility • multiple sclerosis • palliative care • relationships

Palliative Medicine, Vol. 21, No. 2, 101-107 (2007)
DOI: 10.1177/0269216307076333


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