One Baby. One Family. A Movement.
The Festus Fajemilo Foundation started as an initiative towards a very passionate drive to save the life of the then baby Festus — born in the year 2004 to Mr. and Mrs. Fajemilo and diagnosed to have hydrocephalus with no access to treatment and support.
The discovery of several other children with similar impairments prompted Festus's parents to initiate a self-funded Parents Support Group in 2008, which evolved into the incorporation of FFF as a formal not-for-profit disability-focused organisation.
As the Foundation identified, engaged, and provided support to more children with Spina Bifida and Hydrocephalus (SBH) and their families in Lagos State and beyond, the need to strengthen the human and institutional capacity of the Foundation became more imminent.
The demand for more advocacy, raising of public awareness, capacity-building of stakeholders, and provision of support services to children and their families required more financial, human, material, and technical resources — which could only be achieved through the strategic repositioning of the Foundation to become a trusted leading champion for advocacy and support service provision for children and adults with SBH in Nigeria and beyond.




