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'I am making a difference': Understanding advocacy as a citizenship practice among persons living with dementia

机译:“我有所作为”:了解痴呆症生活人员的公民身份的宣传

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In recent years, persons living with dementia have started advocating to have a more active role in shaping policies and interventions that impact their quality of life. In order to meaningfully involve and engage persons living with dementia in decision-making processes, community partners, providers, planners, as well as researchers and healthcare practitioners need to have a better understanding of their experience of living with dementia. Focusing on the lived experiences of dementia and advocacy enables the understanding that persons living with dementia can be agents of change with purpose and intent and helps us think beyond common stereotypes associated with dementia. Despite the valuable efforts of advocates to create this paradigm shift, there is limited research documenting their experiences of advocacy. Using the citizenship perspective, this study explores the experience of advocacy through semi-structured interviews with three persons living with dementia in Vancouver, Canada, focusing specifically on their motivation to advocate and the challenges they have faced along the way. Findings suggest a number of ways through which advocates living with dementia position themselves as social citizens. Consistent with the dimensions of social citizenship, participants suggested that advocacy (i) gave them a sense of purpose; (ii) helped them express their solidarity with the wider community of people living with dementia; (iii) facilitated their fight for freedom against stigma and discrimination; and (iv) enabled them to grow and evolve over time. Supporting individuals' meaningful engagement and advocacy helps acknowledge the agency and autonomy of persons living with dementia and their identity as social citizens. Taking this approach is imperative to facilitate community partnerships with persons living with dementia and their engagement in the development of relevant policy and practices aimed at creating dementia-friendly communities.
机译:近年来,痴呆症的人开始倡导在塑造影响他们生活质量的政策和干预方面具有更积极的作用。为了有意义地涉及和参与在决策过程中患有痴呆症的人,社区合作伙伴,提供者,规划者以及研究人员和医疗保健从业者需要更好地了解他们与痴呆症生活的经历。专注于痴呆症和倡导的生活经历使得理解痴呆症的人可以是具有目的和意图的变化的代理,并帮助我们超越与痴呆症相关的常见刻板印象。尽管倡导者创造了这一范式转变的宝贵努力,但研究了他们对宣传经验的有限研究。本研究采用公民身份观点,通过加拿大温哥华痴呆症的三人探讨了倡导的经验,专注于他们对倡导的动机以及他们沿途所面临的挑战。调查结果表明了许多方式,通过痴呆症定位自己作为社会公民的倡导者。与社会公民身份的维度一致,参与者建议宣传(I)给了他们一种宗旨; (ii)帮助他们表达他们的团结与痴呆症的更广泛的人群; (iii)促进他们争取与耻辱和歧视的自由; (iv)使他们能够随着时间的推移而增长和发展。支持个人的有意义的参与和宣传有助于承认痴呆症和他们身份的原子能机构和自主权作为社会公民。采取这种方法必须促进与痴呆症的人的社区伙伴关系以及他们在制定旨在创造痴呆型社区的相关政策和做法的参与。

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