Digital outreach in online dementia discourse

Boyd H. Davis, M. Maclagan, C. Pope
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Abstract

Introduction: The rapid online expansion of social media can decrease social isolation for both caregivers and persons with dementia (PWD) through the digital communities they create. Background: PWD and their caregivers are increasingly turning to social media to express their own concerns and offer advice to each other. Material analyzed: Multimodal methods were used to analyze three online sites – two caregiver sites and one site for PWD. The sites are StoryCall, a video archive recorded by South Carolina caregivers about caring for US veterans with dementia; Molly and Joey, a video series of Joey’s interactions with his mother Molly, who had Lewy body dementia; and Dementia Diaries, oral diaries transcribed by volunteers. Results: The topics discussed online by people who wish to advise caregivers often differ from the issues and topics that most concern or interest caregivers. Persons with dementia openly shared that they still wished to live as well as possible and wanted to be seen as real people. Implications and conclusions: Through social media, PWD remind themselves and others that they are more than their condition; similarly, caregivers of PWD educate themselves and others through sharing experiences and asking questions.
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在线痴呆症话语中的数字外展
导读:社交媒体的快速在线扩展可以通过护理人员和痴呆症患者创建的数字社区减少他们的社会孤立。背景:残疾人士及其照顾者越来越多地利用社交媒体来表达自己的担忧,并相互提供建议。资料分析:采用多模式方法分析三个在线网站-两个护理者网站和一个PWD网站。这两个网站分别是StoryCall,这是一个由南卡罗来纳州护理人员录制的关于照顾患有痴呆症的美国退伍军人的视频档案;《莫莉和乔伊》(Molly and Joey)系列视频,记录了乔伊与患有路易体痴呆的母亲莫莉(Molly)的互动;痴呆日记,由志愿者记录的口头日记。结果:在线讨论的主题,谁希望建议照顾者往往不同的问题和主题,最关心或感兴趣的照顾者。痴呆症患者公开表示,他们仍然希望生活得尽可能好,并希望被视为真正的人。影响和结论:通过社交媒体,残疾人提醒自己和他人,他们不仅仅是他们的状况;同样,残疾人士护理人员也通过分享经验和提问来教育自己和他人。
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来源期刊
Journal of Interactional Research in Communication Disorders
Journal of Interactional Research in Communication Disorders Social Sciences-Linguistics and Language
CiteScore
0.40
自引率
0.00%
发文量
3
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