By Ali Lukomo
The community in Kamuli has been strongly warned against linking disability in children with witchcraft, with advocates urging parents to seek medical attention rather than turning to traditional healers.
This vital message was delivered during a one-day health camp organized by the Spina Bifida and Hydrocephalus Association Uganda (SHAU) at Kitayunjwa Health Three.
SHAU, a non-governmental organization formed by parents of children suffering from Spina Bifida and Hydrocephalus, conducted the camp to provide much-needed medical care and education.
Children with hydrocephalus and Spina Bifida received treatment, while others were referred to specialized hospitals such as those in Mbale.
Jackline Ahimbisibwe, SHAU’s Eastern Region Coordinator, speaking to our correspondent, affirmed their commitment to Kamuli for a period of five years.
During this time, the organization will tirelessly sensitize the community about Spina Bifida and Hydrocephalus, conditions that affect children, and establish effective pathways for disseminating crucial health information.
Ahimbisibwe highlighted a prevalent and dangerous misconception. “Usually, mothers who deliver these children develop fears that maybe they were bewitched, and others end up going to witch doctors,” she explained.
She sharply contrasted this with the medical reality, stating that these birth defects usually affect the fetus as early as four weeks into pregnancy, long before any perceived “bewitchment.”
Reinforcing this critical message, Musota Ali, working with one of SHAU’s sister organizations, emphatically warned parents against consulting witch doctors. “Instead of thinking their children were bewitched, parents should go to specialists for proper treatment,” he urged, stressing the importance of evidence-based medical care.
Looking ahead, the Spina Bifida and Hydrocephalus Association Uganda is committed to a comprehensive awareness campaign. They plan to work closely with local leaders, cultural leaders, political leaders, religious leaders, and technical staff in Kamuli. This collaborative effort aims to raise awareness about the importance of promoting children’s rights, especially for those living with debilitating conditions like Spina Bifida and Hydrocephalus. The message is clear: understanding and medical intervention, not superstition, are the rightful paths to supporting these vulnerable children.
