“欢迎来到我们的世界”:痴呆症患者在COVID-19大流行之前和期间的经历

Melissa Harris-Gersten, Florence U Johnson, Josie Granner, S. Hastings
{"title":"“欢迎来到我们的世界”:痴呆症患者在COVID-19大流行之前和期间的经历","authors":"Melissa Harris-Gersten, Florence U Johnson, Josie Granner, S. Hastings","doi":"10.21926/obm.neurobiol.2303178","DOIUrl":null,"url":null,"abstract":"People diagnosed with dementia are experts on living with the disease, yet their perspectives are often overlooked in research and practice. The pandemic has amplified health inequities among older adults, but the impact of the pandemic on the lived experience of people living with dementia remains unclear. This qualitative study used a series of 2 virtual focus groups with people living with dementia (N = 7) to explore challenging situations and emotions experienced by community-dwelling people living with dementia prior to and during the pandemic. Focus group transcripts were analyzed using narrative thematic analysis with themes finalized through consensus among a 3-member coding team. Two themes with corresponding subthemes emerged: humanizing dementia (subthemes: early experiences with cognitive impairment, health care experiences, overstimulation, activism, tools to live well with dementia) and “welcome to our world” (subthemes: loss, stress, health impacts). Participants faced challenges prior to and during the pandemic that impeded their ability to live well with the disease. In the midst of the disruption of the pandemic, society saw a glimpse of what it was like to live with dementia due to restrictions that limited access to supports, resources, routines, and socialization. Despite significant barriers, people living with dementia identified many strategies to humanize their experience including the use of humor, activism, and social support. Insights of people living with dementia in this study can be used to inspire a shift in the narrative of dementia as a disability to one of strength, ability, and living well.","PeriodicalId":74334,"journal":{"name":"OBM neurobiology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"“Welcome to Our World”: Experiences of Persons Living with Dementia Prior to and During the COVID-19 Pandemic\",\"authors\":\"Melissa Harris-Gersten, Florence U Johnson, Josie Granner, S. Hastings\",\"doi\":\"10.21926/obm.neurobiol.2303178\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"People diagnosed with dementia are experts on living with the disease, yet their perspectives are often overlooked in research and practice. The pandemic has amplified health inequities among older adults, but the impact of the pandemic on the lived experience of people living with dementia remains unclear. This qualitative study used a series of 2 virtual focus groups with people living with dementia (N = 7) to explore challenging situations and emotions experienced by community-dwelling people living with dementia prior to and during the pandemic. Focus group transcripts were analyzed using narrative thematic analysis with themes finalized through consensus among a 3-member coding team. Two themes with corresponding subthemes emerged: humanizing dementia (subthemes: early experiences with cognitive impairment, health care experiences, overstimulation, activism, tools to live well with dementia) and “welcome to our world” (subthemes: loss, stress, health impacts). Participants faced challenges prior to and during the pandemic that impeded their ability to live well with the disease. In the midst of the disruption of the pandemic, society saw a glimpse of what it was like to live with dementia due to restrictions that limited access to supports, resources, routines, and socialization. Despite significant barriers, people living with dementia identified many strategies to humanize their experience including the use of humor, activism, and social support. Insights of people living with dementia in this study can be used to inspire a shift in the narrative of dementia as a disability to one of strength, ability, and living well.\",\"PeriodicalId\":74334,\"journal\":{\"name\":\"OBM neurobiology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-08-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"OBM neurobiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21926/obm.neurobiol.2303178\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"OBM neurobiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21926/obm.neurobiol.2303178","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

被诊断患有痴呆症的人是与这种疾病一起生活的专家,但他们的观点在研究和实践中往往被忽视。大流行加剧了老年人之间的卫生不平等,但大流行对痴呆症患者生活经历的影响仍不清楚。这项定性研究使用了一系列痴呆患者(N = 7)的2个虚拟焦点小组,以探索在大流行之前和期间居住在社区的痴呆患者所经历的挑战性情况和情绪。使用叙事主题分析对焦点小组记录进行分析,主题是通过3人编码团队的共识确定的。出现了两个具有相应分主题的主题:使痴呆症人性化(分主题:早期认知障碍经历、保健经历、过度刺激、行动主义、与痴呆症一起生活的工具)和"欢迎来到我们的世界"(分主题:损失、压力、健康影响)。参与者在大流行之前和期间面临着各种挑战,这些挑战阻碍了他们与疾病共存的能力。在大流行的混乱中,社会一瞥了痴呆症患者的生活,因为限制了获得支持、资源、日常活动和社会化的机会。尽管存在重大障碍,但痴呆症患者确定了许多使其经历人性化的策略,包括使用幽默、行动主义和社会支持。在这项研究中,对痴呆症患者的见解可以用来激发人们将痴呆症作为一种残疾的叙述转变为一种力量、能力和生活得很好的叙述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
“Welcome to Our World”: Experiences of Persons Living with Dementia Prior to and During the COVID-19 Pandemic
People diagnosed with dementia are experts on living with the disease, yet their perspectives are often overlooked in research and practice. The pandemic has amplified health inequities among older adults, but the impact of the pandemic on the lived experience of people living with dementia remains unclear. This qualitative study used a series of 2 virtual focus groups with people living with dementia (N = 7) to explore challenging situations and emotions experienced by community-dwelling people living with dementia prior to and during the pandemic. Focus group transcripts were analyzed using narrative thematic analysis with themes finalized through consensus among a 3-member coding team. Two themes with corresponding subthemes emerged: humanizing dementia (subthemes: early experiences with cognitive impairment, health care experiences, overstimulation, activism, tools to live well with dementia) and “welcome to our world” (subthemes: loss, stress, health impacts). Participants faced challenges prior to and during the pandemic that impeded their ability to live well with the disease. In the midst of the disruption of the pandemic, society saw a glimpse of what it was like to live with dementia due to restrictions that limited access to supports, resources, routines, and socialization. Despite significant barriers, people living with dementia identified many strategies to humanize their experience including the use of humor, activism, and social support. Insights of people living with dementia in this study can be used to inspire a shift in the narrative of dementia as a disability to one of strength, ability, and living well.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
1.00
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信