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Wyświetlanie 1-2 z 2
Tytuł:
‘NO ONE KNOWS ANYTHING’: KINSHIP CAREGIVERS AND THEIR EXPERIENCES WITH SOCIAL SERVICES IN POLAND
Autorzy:
GRZELKA, MICHALINA
SZOSTAKOWSKA, KATARZYNA
Powiązania:
https://bibliotekanauki.pl/articles/1036257.pdf
Data publikacji:
2019-12-31
Wydawca:
Uniwersytet im. Adama Mickiewicza w Poznaniu
Tematy:
aging
caregiving
disability
family
gender
Opis:
This paper provides a window into the ways kinship caregivers of elderly persons and people with disabilities describe their experiences with social services in Poland. Kinship caregivers in Poland, the majority of whom are women, often struggle with inadequate access to social services dedicated to people with disabilities and the elderly. One of the major issues faced by caregivers who try to secure these services, are complex rules and regulations which frequently make it very difficult to access information and assistance. By the way of critical discourse analysis, this paper examines letters by and interviews with kinship caregivers in Poland. These two data sets present the problems faced by kinship caregivers of elderly persons and people with disabilities who are frequently left frustrated by their interactions the social services system and its gatekeepers. Therefore, the authors hope that this study will provide policymakers responsible for social policy in Poland with some useful insights and suggestions.  
Źródło:
Society Register; 2019, 3, 4; 97-114
2544-5502
Pojawia się w:
Society Register
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
I don’t have this huge backlog of good feeling for her: Role-relational trajectories in interview accounts of caring for a relative with dementia
Autorzy:
Kruk, Bartłomiej
Powiązania:
https://bibliotekanauki.pl/articles/2135340.pdf
Data publikacji:
2020-12-01
Wydawca:
Uniwersytet im. Adama Mickiewicza w Poznaniu
Tematy:
role-relationships
dementia caregiving
family
gender
membership categorization analysis
Opis:
Caring for a family member with dementia involves multifaceted relational issues linked to the construction of caregiving as an emotional, symbolic and morally sanctionable practice inscribed in kin relations and dominant femininity (Paoletti 2007). As the disease disrupts taken-for-granted expectations for a person with dementia and the entire family, this qualitatively new situation necessitates the (re)negotiation of kin roles and responsibilities (Peel 2017; Purves 2011). By applying conversation analysis and membership categorization analysis to an audio-taped open-ended interview with an American female caregiver, this paper investigates in-depth how she discursively navigates complex familial role-relational trajectories while assisting her mother with dementia. The study examines the situatedness of role vis-á-vis self-other relations with assumptions about categories within the membership categorization devices ‘family’ and ‘gender’ being critical to this process. It documents how the participant contextualizes care experience not only in the standardized relational pair ‘daughter-mother’ but brings into focus a broader constellation of historical, contemporaneous or hypothetical aspects of kinship ties (e.g., with her parents, siblings or children), each of which invokes distinct expectations, responsibilities and loyalties which sometimes competing with other relations. The study thus exposes certain commonsense propositions concerning normative family role-relationships which function as powerful benchmarks for making life choices, interpreting one’s experiences, and morally evaluating oneself and others while providing care to kin with dementia.
Źródło:
Yearbook of the Poznań Linguistic Meeting; 2020, 6, 1; 183-220
2449-7525
Pojawia się w:
Yearbook of the Poznań Linguistic Meeting
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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