FFF provides localised support, education, and empowerment by bringing together people affected by Spina Bifida & Hydrocephalus and their families.
Living with Spina Bifida or Hydrocephalus — or caring for someone who does — can feel isolating. FFF's Support Group exists to change that. It is a safe, welcoming space where affected individuals and their families come together, share experiences, and find strength in one another.
Through regular meetings at hospital venues in Lagos and Ile-Ife, FFF fosters a community of unconditional acceptance, practical knowledge, and genuine hope.
The support group offers far more than a meeting. It is a source of knowledge, courage, and connection for every family that walks through the door.
Connect with others who truly understand. Share your journey, listen to theirs, and find mutual encouragement among members who walk the same path.
Access information, ideas, resources, and lived experience that leads to deeper understanding of SBH conditions — information that is hard to find elsewhere.
Leave behind the fear of judgment. Our group offers a space of full acceptance — where every family, every child, and every struggle is welcomed without condition.
Learn and reinforce practical coping strategies from facilitators and fellow members — building resilience for the everyday challenges of living with SBH.
Develop hope by hearing from members who are thriving — living well with SBH. Their journeys show what is possible and remind every family that a better life is within reach.
Simply being heard and understood has profound therapeutic power. Our meetings create space for emotional healing through story-sharing, prayer, and communal care.
FFF support group meetings are held at two hospital venues in Lagos and Ile-Ife. All meetings are free and open to affected individuals, carers, and family members.
Waiting Area behind Family Medicine Block
LASUTH, Ikeja, Lagos
Neurosurgery Clinic (SOP), Department of Surgery, Phase IV
OAUTHC, Ile-Ife, Osun State
Joins us today! Share & feel loved.
Contact Us to Attend →Every meeting is a structured yet warm gathering — designed to make newcomers feel welcome and regulars feel at home.
Every session opens with a warm welcome. New members are introduced and every attendee — family member or patient — is made to feel they belong.
A medical professional or FFF facilitator shares practical information about managing Spina Bifida and Hydrocephalus — from treatments to daily care routines.
Members share personal stories, challenges, and victories. This is the heart of the meeting — where real connection happens and hope is exchanged.
Attendees ask questions, seek guidance, and are connected to appropriate medical or social support services where needed.
Each session closes with encouragement, upcoming announcements, and a reminder that every family is part of a community that never leaves them behind.
FFF's support group is connected to a broader international network of Spina Bifida and Hydrocephalus organisations. You are joining a global family — one committed to ensuring no one faces these conditions alone.
View Community Network →The FFF Support Group relies on the generosity of donors to continue bringing families together. Your gift helps cover meeting facilitation, health education sessions, and outreach to new families.
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