Experiences of the caregivers on the healthcare and psychosocial services available for cerebral palsy children in Mangochi district in Malawi.

Background: Children with cerebral palsy require multidisciplinary and holistic care to manage their medical needs and maximise their developmental and educational potential. Exploring experiences of caregivers on healthcare and psychosocial services available for children with cerebral palsy is key in addressing gaps existing in provision of quality health care and psychosocial services both at community and hospital settings. Methods: We conducted a qualitative exploratory descriptive study. Twelve caregivers of children with cerebral palsy were interviewed face-to-face using interview guides at Mangochi district. Twelve caregivers of children with cerebral palsy were interviewed face-to-face using interview guides at Mangochi district. Purposive and snowball sampling were used to select the study participants. Results: The findings of the study showed that some of the participants received inadequate information related to the etiology and prognosis of cerebral palsy, alternative treatments, and information related to childcare at home. There was also a lack of follow-up and home visits by health care workers. The majority of participants received informal psychosocial support from their relatives and friends. However, there was lack of formal psychosocial services, such as counselling services, unavailability of support groups, and lack of assistive devices. Challenges encountered by children with cerebral palsy and their caregivers were related to inadequate finances, transport challenges, and lack of basic needs, which resulted in the inability to provide necessities to children with cerebral palsy and inability to take their children to the hospital for regular physiotherapy services. In addition, caregivers face physical strain and burden during care. Conclusion: The study found that there was inadequate provision of health care and psychosocial services to children with cerebral palsy. The study recommends the provision of comprehensive cerebral palsy information to caregivers, the formation of support groups, conducting outreach clinics and home visits to children with cerebral palsy, and provision of assistive ambulation devices by healthcare professionals and the department of social welfare.