FFF with the support of Shine – Spina bifida • Hydrocephalus • Information • Networking • Equality U.K. organized a 2-day virtual training (July 22nd – 23rd, 2021) on Continence Management for 38 Nursing staff from four public tertiary health facilities LASUTH, UCH, OAUTHC Ile-Ife & LUTH…..
Author: Fesfaj Admin
Equality
We believe all human beings are created equally irrespective of age, gender, religion, race and socio-cultural background
World Spina Bifida and Hydrocephalus Day
This is an annual event to celebrate people living with these conditions globally recognizing their immense contributions to the society. The aim is to raise awareness and understanding about Spina Bifida and Hydrocephalus. On this day, we also advocate and promote the rights of persons with these conditions. The theme for this year is WSBHDAY20- UNITED IN TIMES OF COVID-19Join …
Support Group
Festus Fajemilo Foundation currently holds support group activities at two locations in Nigeria. The locations are within the premises of Lagos state university teaching hospital (LASUTH) Ikeja, Lagos and Obafemi Awolowo University teaching hospital complex (OAUTHC), Ile-Ife.
NOLB Project
NOLB project is a 20-month project from July 2017 – February 2019 and is funded by the International Disability Alliance (IDA) & International Federation for Spina Bifida and Hydrocephalus (IF).
Public Awareness
We increase public awareness and education
Safe Drinking Water Act
The Safe Drinking Water Act (SDWA) is the principal federal law in the United States intended to ensure safe drinking water for the public. Pursuant to the act, the Environmental Protection Agency (EPA) is required to set standards for drinking water quality and oversee all states, localities, and water suppliers who implement these standards. SDWA applies to every public water …
Cultivating hope in Haiti
Helping rebuild a country after a massive natural disaster.
Our History
The Festus Fajemilo Foundation began in 2006, and is named after a boy who developed hydrocephalus two months after he was born. Festus’ parents found it hard to get any information and support, and his condition worsened, seriously limiting his development and requiring continuous and complex care.
Festus Fajemilo Foundation
…Promoting Disability Inclusion