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Improved chance associated with oral hpv among people with type 1 diabetes in comparison with the population-results from the countrywide registry-based, cohort review.
Further regression analyses revealed that the results for constructive cyber defending were the inverse of those obtained for aggressive defending. Defending self-efficacy was positively associated with constructive defending and negatively associated with aggressive defending. Moral disengagement was negatively associated with constructive defending and positively associated with aggressive defending. These results address the perplexing issue of why moral disengagement has been related to defending in some studies and not in others. As with most measures of defending, the general cyber defending measure confounds constructive and aggressive defending. Given the paucity of support from the welfare state, the lion's share of care for American seniors with memory loss is shouldered by their spouses who tend to be older and sometimes are frail themselves. Previous research has bifurcated attention to either accounts from diagnosed individuals or carers rather than understanding the experience within a socio-relational context of sometimes half-century long relationships. The present study was a qualitative investigation of 11 community-dwelling dyads (N = 22) living in the Greater Boston Area to understand how married heterosexual couples experience Alzheimer's. They were predominately white, highly educated individuals with mild to moderate AD and their spouses. Grounded theory methodologies were used to collect, code, and analyze all narrative study data. The data from these spousal dyads reveal that most couples approached AD as a joint challenge and were committed to maintaining their prior roles and lives for as long as possible, including shared outlooks, approaches, and activities. By showing how some couples navigate AD together rather than separately, these data provide an important counter narrative to the burden-based framing of AD in our social imagination. Regardless of perceptions of relationship closeness, all dyads employed strategies to live life positively with Alzheimer's. Despite being a highly privileged sample, or an "ideal type," these data reveal the importance of studying AD as a coupled or family event; that is, a social and relational matter, rather than simply an individual medical problem. They also highlight the importance of relationship-centered care in meeting families "where they are" in terms of existing social roles. Universalizing all AD experiences leads to an over-reliance on reductionist tropes such as "stress" and "burden" and exacerbates the very real threat to social disenfranchisement. An understanding of how older adults conceptualize healthy aging is important for the development of policies, programs, and services designed to promote health; this understanding must reflect the ethno-cultural diversity of the population. This pilot study aimed to examine Canadians' definitions of healthy aging and ethno-cultural variations in these definitions. The baseline data for a sub-sample (n = 535) of the Canadian Longitudinal Study on Aging (CLSA) Tracking Cohort (n = 21,241) were examined. Narrative responses to an open-ended question on healthy aging were analyzed using a previously developed coding system. The most common themes for all the ethno-cultural groups were "lifestyle", "physical activity", and "attitude"; other themes varied by ethno-cultural background. These findings demonstrate that older Canadians from various ethno-cultural backgrounds define healthy aging differently. These variations must be taken into consideration for developing culturally sensitive programs to promote healthy aging among all Canadians. Theorizing on healthy (or 'successful') aging must envision it as a subjective and multidimensional concept. The ending of a story provides clarity by framing separate encounters within an overall plot. It can intensify focus and feeling, as limited time creates a sense of preciousness. The end additionally calls for new beginnings, as places are vacated for other stories to be told. It is a generative space as new conversations can evolve. The 'end' of an academic story contains opportunities for beginnings and vibrant encounters, and academics may be able to explore the richness within an expansive and generative spaces by having the 'end in sight.' Resistance to physical decay and the desire to keep youthful looks are not new in human history. Rapamycin manufacturer Today, however, anti-aging discourse intensifies the longing to reshape one's body and stop the ravages of time. Aging is often portrayed as a personal accountability, a sign of moral responsibility, and even disease, which affects older women disproportionately. In order to adjust to contemporary beauty standards, many older women decide to undergo various rejuvenation procedures. However, few studies on the outcomes of such cosmetic interventions in relation to aging, acceptance and self-perception exist. This article addresses American writer Erica Jong's concerns about the aging body and surgical anti-aging interventions. As spokeswoman of the American post-war generation, the author shows how facial rejuvenation procedures generate conflicting feelings, and reminds her readers that older women continue to be doubly marginalized in today's youth- and beauty-driven society. 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.
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