dc.contributor.author |
Joseph Osafo |
|
dc.contributor.author |
Birthe Loa Knizek |
|
dc.contributor.author |
James Mugisha |
|
dc.contributor.author |
Eugene Kinyanda |
|
dc.date.accessioned |
2021-01-10T11:55:47Z |
|
dc.date.available |
2021-01-10T11:55:47Z |
|
dc.date.issued |
2017 |
|
dc.identifier.issn |
17448603 |
|
dc.identifier.uri |
https://combine.alvar.ug/handle/1/49183 |
|
dc.description.abstract |
Home-based care for HIV patients is popular in contexts severely affected by the epidemic and exacts a heavy toll on caregivers. This study aimed at understanding the experiences of caregivers and their survival strategies. A total of 18 caregivers (3 males and 15 females) were interviewed using a semi-structured interview guide, and thematic analysis was used to analyse the data. Analysis suggests that the caregivers are burdened with insecure provisions for food and difficulties in accessing health care. They however survived these strains through managing their relationships, sharing burden with care-recipients, social networks and instrumental spirituality. These findings are discussed under two major themes: 1). Labour of caregiving and 2). Survivalism. Home-based care presents huge opportunities for community response to the HIV/AIDS epidemic in African settings. It is however burdensome and thus should not be left for families alone to shoulder. There is therefore an urgent need for protecting home-based care for HIV children in Uganda. Implications for improving and strengthening social interventions in home-based care of HIV/AIDS in the Ugandan context are addressed. |
|
dc.description.sponsorship |
Medical Research Council (MC_UP_1204/10) United Kingdom |
|
dc.description.sponsorship |
Medical Research Council (MR/L004623/1) United Kingdom |
|
dc.publisher |
BioMed Central |
|
dc.relation.ispartof |
Globalization and health |
|
dc.subject |
Caregivers |
|
dc.subject |
Children with HIV |
|
dc.subject |
Experiences |
|
dc.subject |
Uganda |
|
dc.subject.mesh |
Acquired Immunodeficiency Syndrome/nursing |
|
dc.subject.mesh |
Caregivers/psychology |
|
dc.subject.mesh |
Child |
|
dc.subject.mesh |
Cost of Illness |
|
dc.subject.mesh |
Developing Countries |
|
dc.subject.mesh |
Female |
|
dc.subject.mesh |
HIV Infections |
|
dc.subject.mesh |
Health Services Accessibility |
|
dc.subject.mesh |
Home Nursing |
|
dc.subject.mesh |
Humans |
|
dc.subject.mesh |
Male |
|
dc.subject.mesh |
Qualitative Research |
|
dc.subject.mesh |
Social Support |
|
dc.subject.mesh |
Surveys and Questionnaires |
|
dc.subject.mesh |
Uganda |
|
dc.title |
The experiences of caregivers of children living with HIV and AIDS in Uganda:a qualitative study |
|
dc.type |
journal article |
|
dc.identifier.doi |
10.1186/s12992-017-0294-9 |
|
dc.identifier.pmid |
28899415 |
|
dc.identifier.mag |
2754996295 |
|
dc.identifier.pmc |
PMC5596491 |
|
dc.identifier.lens |
065-182-696-780-920 |
|
dc.identifier.volume |
13 |
|
dc.identifier.issue |
1 |
|
dc.identifier.spage |
72 |
|
dc.identifier.epage |
72 |
|
dc.subject.lens-fields |
Public health |
|
dc.subject.lens-fields |
Health care |
|
dc.subject.lens-fields |
Qualitative research |
|
dc.subject.lens-fields |
Social policy |
|
dc.subject.lens-fields |
Psychological intervention |
|
dc.subject.lens-fields |
Health services research |
|
dc.subject.lens-fields |
Acquired immunodeficiency syndrome (AIDS) |
|
dc.subject.lens-fields |
Medicine |
|
dc.subject.lens-fields |
Thematic analysis |
|
dc.subject.lens-fields |
Gerontology |
|