|Institution:||University of Fort Hare|
|Full text PDF:||http://contentpro.seals.ac.za/iii/cpro/DigitalItemViewPage.external?sp=1015356|
Informal caregiving denotes care that is provided by a family member or friend rather than by a professional who is reimbursed for services. Assuming a caregiving role can be stressful and burdensome. The effects of caregiving on the caregiver's health are moderated by individual differences in resources and vulnerabilities, such as socioeconomic status, prior health status, and level of social support. This work describes the determinant of psycho-social well-being of informal caregivers of physically challenged children in southwest of Nigeria. This study is guided theoretically by Ryff”s psychosocial well-being theory, The study adopted expo facto research design. Multistage samplings involving the use of random and purposive techniques were used to select 812 respondents who are informal caregivers. Social support questionnaire, Social support satisfaction level, Ryff’s psychological well-being scale were used. Findings indicated that social support predicted psycho-social well-being of informal caregivers of physically challenged children. Social support and satisfaction level combine together have impact on psycho-social well-being of informal caregivers of physically challenged children. More also, socio-economic factors such as occupation, educational level and income also predict psycho-social well-being of informal caregivers. Finally, marital status and gender also contribute to well-being of caregivers. It was therefore, recommended that social inclusion should be pursued with de-institutionalization of children with disability. Parents of children with disability should be encouraged to form support group and as well as encouraging fathers of children with disability to take an active part in ensuring their children with disability well-being. More also, there is need to empower informal caregivers through training and education. More importantly governments at the three levels ( Federal, State and local) should assist caregivers at ensuring their own and that of their children with disability well-being through improvement on various existing social welfare services in the country.