Cerebral palsy in Nigeria: One woman's mission to help her daughter and others

In Nigeria, a country faced with numerous health challenges, cerebral palsy remains one of the most prevalent neurological disorders affecting children. At the heart of efforts to confront and mitigate the impacts of this condition is the remarkable story of one woman's relentless mission to not only support her daughter but also extend a helping hand to others grappling with the implications of cerebral palsy. Cerebral palsy is a permanent movement disorder that appears early in childhood. Symptoms include poor coordination, stiff muscles, weak muscles, and tremors. There may be problems with sensation, vision, hearing, swallowing, and speaking. The severity of symptoms varies among individuals: some may experience minor challenges with movement, while others may be entirely unable to move and require lifelong care. Various factors, including infections and injuries during pregnancy, premature birth, and lack of oxygen to the brain, can lead to the development of cerebral palsy. Despite advancements in healthcare, families in Nigeria often face significant challenges in securing appropriate care due to limited resources, lack of specialized healthcare providers, and widespread stigma associated with the disorder. Amid these daunting conditions, one woman has emerged as a beacon of hope for many. After her daughter was diagnosed with cerebral palsy, she embarked on a journey to not only seek the best possible care for her child but also to destigmatize the condition and advocate for better support systems for affected families. Recognizing the profound challenges faced by other parents navigating the complexities of cerebral palsy, she founded a non-profit organization dedicated