The experiences of caregives caring for children diagnosed with acute leukemia

dc.contributor.advisorSekudu, Johannah
dc.contributor.emailmakopanomothiba@gmail.comen
dc.contributor.postgraduateMothiba, Makopano Sara
dc.date.accessioned2013-09-09T12:14:38Z
dc.date.available2012-11-12en
dc.date.available2013-09-09T12:14:38Z
dc.date.created2012-04-17en
dc.date.issued2011en
dc.date.submitted2012-11-06en
dc.descriptionDissertation (MSW (Health Care))--University of Pretoria, 2011.en
dc.description.abstractBeing informed that your child has a form of childhood cancer such as acute leukemia can be devastating for any primary caregiver. The sudden changes that occur affect the receiver of this bad news to the extent that their world becomes focused on the sick child at the expense of the other family members. This study originated from the researcher’s need to gain insight into the experiences of caregivers looking after children diagnosed with acute leukemia. The caregiver could be the legal guardian of the child, the biological mother or the child’s grandmother. The aim of the study was to explore the caregivers’ daily experiences while they look after these sick children. The objectives also involved providing a broad overview of literature on acute leukemia as a childhood condition, exploring the experiences of caregivers for children diagnosed with acute leukemia and drawing conclusions and recommendations for improved social work intervention specifically for these caregivers. To explore the experiences of caregivers, the researcher conducted a phenomenological study as part of the qualitative research approach. The participants in the study were recruited by means of availability sampling when they brought their children for treatment. The data was collected by means of in-depth interviews in which ten (10) caregivers shared their experiences. The researcher was able to gain insight into the experiences of the caregivers while they were caring for the patients diagnosed with acute leukemia. The findings revealed that, while some of the participants had a good support system, others had far less support. Consequently they yearned for the support and physical presence of their family. The researcher found that the participants lived far away from the hospital, which hindered the family from making regular visits to the hospital. This disrupted the family system, because the focus fell mostly on the sick child. There were also major financial implications in caring for a sick child, and the participants’ children are all recipients of a welfare social relief grant. Copyrighten
dc.description.availabilityRestricteden
dc.description.departmentSocial Work and Criminologyen
dc.description.facultyHumanities
dc.identifier.citationMothiba, MS 2011, The experiences of caregives caring for children diagnosed with acute leukemia, MSW dissertation, University of Pretoria, Pretoria, viewed yymmdd < http://upetd.up.ac.za/thesis/available/etd-11062012-114031 / >en
dc.identifier.otherF12/4/562/gmen
dc.identifier.upetdurlhttp://upetd.up.ac.za/thesis/available/etd-11062012-114031/en
dc.identifier.urihttp://hdl.handle.net/2263/31404
dc.language.isoenen
dc.publisherUniversity of Pretoria
dc.rights© 2011, University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoriaen
dc.subjectUCTDen
dc.subjectLeukemiaen
dc.subjectAcuteen
dc.subjectExperiencesen
dc.subjectAcute lymphocytic leukemiaen
dc.subjectAcute myeloid leukemiaen
dc.subjectTreatmenten
dc.subjectSocial workeren
dc.subjectCaregiveren
dc.subjectHospitalen
dc.subjectFamily
dc.titleThe experiences of caregives caring for children diagnosed with acute leukemiaen
dc.typeDissertationen

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