Empowering Lives, Raising Awareness, Fighting Stigma
About Us – Epilepsy Foundation of Nigeria
The Epilepsy Foundation of Nigeria (EFN) is a non- profit organization dedicated to raising awareness, providing medical support, and advocating for the rights of people living with epilepsy across Nigeria. We are committed to eliminating stigma, ensuring access to life-saving medications, and empowering individuals and caregivers with the knowledge and resources they need.
With a mission to transform lives, we work to create a society where epilepsy is understood, treated, and accepted without discrimination.
Our Mission
To improve the lives of Nigerians affected by epilepsy by:
Our Vision
Epilepsy in Nigeria – The Facts
Over 4 million Nigerians live with epilepsy.
80% of cases in Nigeria do not receive proper treatment due to lack of awareness, stigma, and inadequate healthcare access.
1 in 3 people with epilepsy face discrimination in schools, workplaces, and communities.
Many epilepsy-related deaths occur due to mismanagement of seizures and lack of access to affordable medication.
Join Us in Making a Difference!
At EFN, we believe that no one should suffer in silence. Through our initiatives, we are working to bridge the healthcare gap, break social stigma, and provide hope for individuals and families affected by epilepsy.
Whether through donations, volunteering, advocacy, or partnerships, you can be part of the
movement to change lives and end epilepsy stigma in Nigeria.
Follow Us across social media
Together, we can create a future where epilepsy is no longer feared but understood. Thank you for your support!
Our Programs & Initiatives
Epilepsy Foundation of Nigeria
At the Epilepsy Foundation of Nigeria (EFN), we are committed to creating a future where epilepsy is understood, treated, and accepted without stigma. Through education, advocacy, medical support, and community engagement, we empower people living with epilepsy, caregivers, and the public to take action.

Education & Awareness Campaigns
Lack of awareness and stigma remain the biggest barriers for people living with epilepsy in Nigeria. Our campaigns are designed to educate, challenge misconceptions, and foster a society of understanding and support.

Don’t Label Me Campaign
Many people living with epilepsy are wrongly labeled as cursed, possessed, or incapable of leading a normal life. The “Don’t Label Me” campaign aims to break these stereotypes and show that epilepsy does not define a person’s worth or abilities.


Have You Seen Epilepsy?
The “Have You Seen Epilepsy?” campaign highlights the hidden struggles of those living with epilepsy. Not all seizures involve convulsions—some may be as subtle as staring spells, confusion, or brief blackouts. Many people suffer in silence, fearing judgment or lack of understanding.
What This Campaign Does:
- Educates health workers, teachers, and the general public on the different types of epilepsy.
- Uses real-life video documentation and patient stories to show what epilepsy truly looks like.
- Encourages early diagnosis and medical intervention, helping people seek treatment before symptoms worsen.
Impact So Far
Individuals educated through community outreach and social media engagement.
Workshops held in 250+ communities, focusing on schools, workplaces, and religious institutions.
Testimonies from individuals who have been able to live more confidently after the campaign.
Warriors Unite Initiative – Mental Health & Epilepsy Support
Living with epilepsy often comes with anxiety, depression, and isolation. The “Warriors Unite” Initiative provides a safe space for people with epilepsy and their families to come together, share experiences, and learn coping strategies.
Key Features:
- Community gatherings & support groups where people can freely talk about their experiences.
- Guest talks by neurologists and mental health experts to discuss seizure management and emotional well-being.
- Workshops on stress management, mindfulness, and self-care to promote mental health resilience.
So far, Warriors Unite has reached over 5,000 individuals through in-person and virtual sessions, creating a growing network of epilepsy warriors across Nigeria.
Caregiver Resources & Community Support
Caring for someone with epilepsy can be overwhelming. Many caregivers lack the knowledge, emotional support, and resources needed to help their loved ones manage the condition effectively.
How We Support Caregivers:
- Caregiver Training Programs – Teaching families how to handle seizures, administer first aid, and provide emotional support.
- Online and In-Person Support Groups – Connecting caregivers with others facing similar challenges.
- Resource Guides & Workshops – Providing updated information on epilepsy management, nutrition, and mental health.
Our caregiver network has supported over 1,500 families, ensuring that no one faces epilepsy alone.
Join the Movement – Be Part of the Change!
The fight against epilepsy stigma and lack of resources starts with awareness and action.
Here’s how you can help:
- Donate to support epilepsy treatment and education.
- Volunteer to help with awareness campaigns and community outreach.
- Partner with us to expand epilepsy care and advocacy across Nigeria.
Together, we can create a Nigeria where epilepsy is no longer misunderstood, untreated, or feared. Thank you for this mission!
Medication & Financial Support for Patients
In Nigeria, 80% of people with epilepsy do not receive the treatment they need due to high costs, lack of availability, and stigma. The Epilepsy Foundation of Nigeria works to bridge this gap by providing financial assistance and access to anti-seizure medications.
Our Medical Support Programs Include:
- Free and subsidized anti-epileptic drugs (AEDs) for those who cannot afford them.
- Partnerships with hospitals and pharmacies to ensure continued medication supply.
- Emergency financial support for low-income families facing urgent medical needs.
- Mobile health clinics bringing medical aid to underserved communities.
Over 2,500+ patients have already received medication assistance, reducing seizure frequency and improving quality of life.
Would you like to support this initiative?
