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American Journal of Alzheimer's Disease and Other Dementias logoLink to American Journal of Alzheimer's Disease and Other Dementias
. 2001 May-Jun;16(3):177–182. doi: 10.1177/153331750101600306

Long-term consequences of the Alzheimer's caregiver role: A qualitative analysis

Nancy J Karlin 1, Paul A Bell 2, Jody L Noah 3
PMCID: PMC10833982  PMID: 11398567

Abstract

A qualitative analysis was performed on responses of 51 participants to open-ended questions about the experience of being family caregivers for a loved one affected by Alzheimer's disease. Participants had been in the caregiver role for at least eight years. Results indicated a pattern of adapting successfully or unsuccessfully to the caregiver role, experiencing initial caregiver burden, finding relief in social support when available, and longterm distress or long-term positive change. Memories and feelings were strong about individuals and institutions that had been helpful or indifferent many years earlier as the caregivers struggled to cope with their unplanned predicament.

Keywords: Alzheimer's disease, caregiving, caregivers' role, family caregivers

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Contributor Information

Nancy J. Karlin, Department of Psychology, University of Northern Colorado, Greeley, Colorado.

Paul A. Bell, Department of Psychology, Colorado State University, Boulder, Colorado.

Jody L. Noah, Department of Psychology, University of Northern Colorado, Greeley, Colorado.

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