Global ETD Search

21	Transpersoners upplevelser av vårdmöten : En litteraturöversikt / Transgender persons experiences of healtcare encounters : A literature review Nordström, Wilma, Svenlin, Carl-Johan January 2023 (has links) Bakgrund: Transpersoner lider i högre utsträckning av psykisk ohälsa i jämförelse med övrig befolkning. I enlighet med lagar och konventioner har alla människor rätt till jämlik och adekvat vård. Sjuksköterskor behöver bred kompetens för att kunna ge hälsofrämjande och likvärdig vård. Trots det upplevs svårigheter att behandla transpersoner på grund av otillräcklig utbildning och kunskap. Syfte: Syftet var att beskriva transpersoners upplevelser av mötet med vårdpersonal. Metod: En litteraturöversikt baserad på tolv kvalitativa vetenskapliga originalartiklar. Litteratursökningarna genomfördes i databaserna Cinahl Complete och PubMed. Resultat: I resultatet framkom fyra kategorier; att bli felkönad, människa inte vara transperson, betydelsen av kunskap eller okunskap hos vårdpersonal och vårdmiljöns betydelse. Transpersoner upplevde att deras könsidentitet var dominerande i mötet med vårdpersonal oavsett sökorsak. Upplevelsen av att inte få adekvat vård eller bemötande på grund av kompetensbrist var också tydlig. Sammanfattning: Bemötande har stor betydelse för hur transpersoner upplever sin vård. Positiva upplevelser av mötet med vårdpersonal var trygghetsingivande och stärkande medan negativa upplevelser var diskriminerande och icke hälsofrämjande. En ytterligare påverkande faktor var vårdmiljön. / Background: Transgender people suffer to a greater extent from mental illness in comparison to the rest of the population. In accordance with laws and conventions, everyone has the right to equal and adequate care. Nurses need broad competence to be able to provide health-promting and equivalent care. Despite that, difficulties are experienced in treating transgender people due to insufficient education and knowledge. Aim: The aim was to describe transgender persons experiences of healthcare encounters. Method: A litterature review based on twelve original qualitative scientific articles. The litterature search was carried out in the databases Cinahl Complete and PubMed. Results: Four categories emerged in the results; to be misgendered, human not just a transgender person, the importance of knowledge or lack of knowledge of healthcare staff and the importance of the healtcare environment. Transgender people felt that their gender identity was dominant in the encounter with healthcare professionals, regardless of the reason for seeking health care. The experience of not receiving adequate care or treatment due to lack of knowledge was also clear. Summary: The healthcare encounter has a great significance for how transgender people experience their care. Positive experiences of the encounter with healthcare personnel were reassuring and empowering, while negative experiences were discriminatory and did not promote transgender persons health. An additional factor that influenced the impression was the health care enviroment. Transgender persons Health care staff Knowledge Lack of knowledge Treatment Health care environment Experience Transpersoner Vårdpersonal Kunskap Kompetensbrist Bemötande Vårdmiljö Upplevelse Nursing Omvårdnad
22	From the "rising tide" to solidarity: disrupting dominant crisis discourses in dementia social policy in neoliberal times MacLeod, Suzanne 26 March 2014 (has links) As a social worker practising in long-term residential care for people living with dementia, I am alarmed by discourses in the media and health policy that construct persons living with dementia and their health care needs as a threatening “rising tide” or crisis. I am particularly concerned about the material effects such dominant discourses, and the values they uphold, might have on the collective provision of care and support for our elderly citizens in the present neoliberal economic and political context of health care. To better understand how dominant discourses about dementia work at this time when Canada’s population is aging and the number of persons living with dementia is anticipated to increase, I have rooted my thesis in poststructural methodology. My research method is a discourse analysis, which draws on Foucault’s archaeological and genealogical concepts, to examine two contemporary health policy documents related to dementia care – one national and one provincial. I also incorporate some poetic representation – or found poetry – to write up my findings. While deconstructing and disrupting taken for granted dominant crisis discourses on dementia in health policy, my research also makes space for alternative constructions to support discursive and health policy possibilities in solidarity with persons living with dementia so that they may thrive. / Graduate / 0452 / 0680 / 0351 / macsuz@shaw.ca social determinants of health social exclusion crisis discourse Alzheimer's Alzheimer Society of Canada Suzanne MacLeod Susan Strega Donna Jeffery poststructural poststructuralism admission to long-term care funding for long-term care acute care aging demographic BC Psychogeriatric Association biomedical British Columbia Canada Health Act collective social responsibility competition corporate profit corporatization deresponsibilization elder friendly elderly citizens family caregivers Foucault found poetry genealogy of power knowledge incompetent Ministry of Health moral economics pharmaceutical bed blocker stigmatized tsunami absent-person action plan aging population alternative discourse apocalyptic demography appropriate archaeology archaeology of knowledge archaeological British Columbia burden Canada caregiver charity charitable collective collective car community community care condition of possibility conditions of possibility corporate counter-discourse dementia dementia care dementia policy dementia social policy dependent depoliticize discourse discourse analysis disruptive discourse economic burden economics economy elder emergency epidemic exclusion fear-monger Foucauldian found poem genealogy genealogical health authority health care health care staff health care system health policy document healthy lifestyle home and community care homogenization homogenize hospital imaginaries imaginary incapable individual responsibility individualism knowledge long-term care material effect materiality of discourse media moral panic national strategy neoliberal neoliberalism neoliberal rationality not prepared object objectification other person-centered people living with dementia person living with dementia persons living with dementia person with dementia poem poetic representation poetry policy policies political politics power power knowledge power relations private privatize privatization productivity of dominant discourse public health care residential care resistance responsibility responsibilization rising tide safety net shift costs to caregivers responsibility social policy imaginary social well-being social work social worker solidarity specialized stakeholder state stigma subject matter expert taxpayer threat unprepared unproductive voluntary volunteer wait time wave social policy
23	From the "rising tide" to solidarity: disrupting dominant crisis discourses in dementia social policy in neoliberal times MacLeod, Suzanne 26 March 2014 (has links) As a social worker practising in long-term residential care for people living with dementia, I am alarmed by discourses in the media and health policy that construct persons living with dementia and their health care needs as a threatening “rising tide” or crisis. I am particularly concerned about the material effects such dominant discourses, and the values they uphold, might have on the collective provision of care and support for our elderly citizens in the present neoliberal economic and political context of health care. To better understand how dominant discourses about dementia work at this time when Canada’s population is aging and the number of persons living with dementia is anticipated to increase, I have rooted my thesis in poststructural methodology. My research method is a discourse analysis, which draws on Foucault’s archaeological and genealogical concepts, to examine two contemporary health policy documents related to dementia care – one national and one provincial. I also incorporate some poetic representation – or found poetry – to write up my findings. While deconstructing and disrupting taken for granted dominant crisis discourses on dementia in health policy, my research also makes space for alternative constructions to support discursive and health policy possibilities in solidarity with persons living with dementia so that they may thrive. / Graduate / 0452 / 0680 / 0351 / macsuz@shaw.ca social determinants of health social exclusion crisis discourse Alzheimer's Alzheimer Society of Canada Suzanne MacLeod Susan Strega Donna Jeffery poststructural poststructuralism admission to long-term care funding for long-term care acute care aging demographic BC Psychogeriatric Association biomedical British Columbia Canada Health Act collective social responsibility competition corporate profit corporatization deresponsibilization elder friendly elderly citizens family caregivers Foucault found poetry genealogy of power knowledge incompetent Ministry of Health moral economics pharmaceutical bed blocker stigmatized tsunami absent-person action plan aging population alternative discourse apocalyptic demography appropriate archaeology archaeology of knowledge archaeological British Columbia burden Canada caregiver charity charitable collective collective car community community care condition of possibility conditions of possibility corporate counter-discourse dementia dementia care dementia policy dementia social policy dependent depoliticize discourse discourse analysis disruptive discourse economic burden economics economy elder emergency epidemic exclusion fear-monger Foucauldian found poem genealogy genealogical health authority health care health care staff health care system health policy document healthy lifestyle home and community care homogenization homogenize hospital imaginaries imaginary incapable individual responsibility individualism knowledge long-term care material effect materiality of discourse media moral panic national strategy neoliberal neoliberalism neoliberal rationality not prepared object objectification other person-centered people living with dementia person living with dementia persons living with dementia person with dementia poem poetic representation poetry policy policies political politics power power knowledge power relations private privatize privatization productivity of dominant discourse public health care residential care resistance responsibility responsibilization rising tide safety net shift costs to caregivers responsibility social policy imaginary social well-being social work social worker solidarity specialized stakeholder state stigma subject matter expert taxpayer threat unprepared unproductive voluntary volunteer wait time wave social policy

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