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Demenca in družinski odnosi : magistrsko delo
ID Bogataj, Karmen (Author), ID Kejžar, Anamarija (Mentor) More about this mentor... This link opens in a new window

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Abstract
Pričujoča naloga govori o vplivu demence na svojce oseb z demenco. V prvem delu naloge je predstavljen teoretičen pregled oblik demence ter pogledov nanje. Večja pozornost je namenjena spremenjenim odnosom v družini s starim človekom, komunikaciji s starimi ljudmi ter z osebami z demenco ter skrbi zanje, izpostavljeni so izzivi družinskih oskrbovalcev starih ljudi. Zadnje poglavje teoretičnega dela je namenjeno pregledu omrežja pomoči, ki je v Sloveniji dostopno svojcem ljudi z demenco. V empiričnem delu naloge je predstavljena izpeljana kvalitativna raziskava, za namen katere sem intervjuvala svojce oseb z demenco. Raziskovalna vprašanja so se navezovala na pomen znanja o demenci, vplivu demence na odnose z osebo z demenco in druge družinske odnose ter službe, s katerimi so svojci sodelovali. Ugotovitve kažejo, da so svojci demenco v glavnem poznali že pred diagnozo družinskega člana ter da jim je znanje olajšalo razumevanje in doživljanje sprememb, ki jih je demenca prinesla. Skrb za osebo z demenco je na družino vplivala povezovalno (sodelovanje), nekateri svojci so poročali tudi o nestrinjanjih glede izvajanja skrbi. Več svojcev je poročalo, da so tekom demence z družinskim članom vzpostavili večjo povezanost (ta je manj temeljila na govoru in bolj na drugih oblikah komunikacije, čutilih). Svojci so sodelovali z zdravstvenimi delavci, zasebnimi službami in društvi. Večkrat so od njih pričakovali več informacij in konkretnejšo pomoč, kot so jo dobili. Največ informacij so dobili od zdravnikov, knjig in socialnih omrežij. Pokazala se je potreba po podporni službi, ki bi združevala svojce in institucije, jim nudila znanje o demenci in praktični izvedbi skrbi ter jih tudi podprla, da ob skrbi za osebo z demenco ne pozabijo na skrb zase.

Language:Slovenian
Keywords:demenca, družinski odnosi, omrežje pomoči, znanje, obremenjenost
Work type:Master's thesis/paper
Typology:2.09 - Master's Thesis
Organization:FSD - Faculty of Social Work
Place of publishing:Ljubljana
Publisher:[K. Bogataj]
Year:2024
Number of pages:160 str.
PID:20.500.12556/RUL-155514 This link opens in a new window
UDC:616.892.3-055.5/.7:364
COBISS.SI-ID:205162499 This link opens in a new window
Publication date in RUL:05.04.2024
Views:439
Downloads:66
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Secondary language

Language:English
Title:Dementia and Family Relationships
Abstract:
The master's thesis focuses on the impact of dementia on family members of individuals with dementia. The first part of the thesis provides a theoretical overview of different forms of dementia and perspectives on them. Special attention is given to the changed dynamics within families with elderly individuals, communication with the elderly and individuals with dementia, and caregiving for them. The challenges faced by family caregivers of elderly people are highlighted. The final chapter of the theoretical part addresses the support network available to family members of people with dementia in Slovenia. The empirical part of the thesis presents a qualitative research study conducted through interviews with family members of individuals with dementia. The research questions focused on the importance of knowledge about dementia, the impact of dementia on relationships with the affected individual and other family members, and collaboration with services they interacted with. Findings indicate that family members were mostly familiar with dementia before the diagnosis of a family member, and that this knowledge facilitated their understanding and acceptance of the changes brought about by the disease. Caregiving for individuals with dementia had a unifying effect on the family, although disagreements regarding caregiving practices arose. Most family members reported an increased sense of connection with the individual with dementia over the course of the disease, which relied less on verbal communication and more on other forms of communication and senses. Family members collaborated with healthcare professionals, private services, and associations, but often expected more information and concrete assistance than they received. They obtained the most information from doctors, books, and social networks. The study revealed a need for a support service that would bring together family members and institutions, provide knowledge about dementia and practical caregiving support, and also encourage self-care among family members while caring for a person with dementia.

Keywords:dementia, family relationships, support network, knowledge, caregiving burden

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