The final, formatted version of the article will be published soon.
ORIGINAL RESEARCH article
Front. Glob. Womens Health
Sec. Aging in Women
Volume 5 - 2024 |
doi: 10.3389/fgwh.2024.1461626
This article is part of the Research Topic The Impact of the COVID-19 Pandemic on Older Women’s Health and Well-Being View all articles
Social Worlds of Appalachian Women Caregivers of Older Relatives Living with Dementia
Provisionally accepted- Virginia Tech, Blacksburg, United States
Rationale: Over 11 million people in the United States provide care for an older family member with dementia, with this responsibility primarily falling on daughters and wives. In Appalachia, a mountainous region in the U.S characterized by close families, family members were crucial to ensuring that care needs were met for people living with dementia during the COVID-19 pandemic. However, we know little about the well-being of family caregivers during the public health crisis. Guided by a Limited Future Time Perspective postulate, which posits that as people age they begin to prioritize emotionally meaningful relationships over instrumental goals, we asked how dementia caregiving changes the social lives of family caregivers situated within kin networks; and how a public health crisis (i.e., COVID-19 pandemic) affects caregivers who are already at risk for social isolation and feelings of loneliness. Methods: Participants were recruited from a regional health care system and four Area Agencies on Aging. In our longitudinal study we invited family caregivers to be interviewed at multiple time points over a 4-year period. The sample for this study was women caregivers interviewed (N=27; age range 32-81, m=63). Interviewers followed a semi-structured protocol with questions designed to elicit descriptions about a.) changes in formal and informal support over time, b.) the person living with dementia’s symptoms and disease progression, and c.) how the pandemic affected caregivers’ and persons living with dementia’s social worlds. Findings: We found three types of caregivers: (1) caregivers who had social lives interdependent with their relative with dementia, (2) caregivers and persons living with dementia whose social lives were restricted due to dementia symptoms and caregiving demands, and (3) caregivers and their relative living with dementia who maintained separate social lives. Dementia symptoms more than social distancing measures contributed to caregivers’ shrinking social worlds particularly for those with interdependent social lives despite living amongst kin. Conclusions: This study is important in understanding how women in Appalachia fared during a pandemic in the context of dementia caregiving. This research supports the need for respite services and dementia care training for respite workers.
Keywords: Dementia, Appalachia, Pandemic (COVID-19), Activity restriction, Respite
Received: 08 Jul 2024; Accepted: 31 Oct 2024.
Copyright: © 2024 McCann, Roberto, Savla and Blieszner. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Brandy R. McCann, Virginia Tech, Blacksburg, United States
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.