1 in 26 will be diagnosed with epilepsy in their lifetime
Its prevalence is more than autism, cerebral palsy, multiple sclerosis, and Parkinson’s combined
We serve Northern California from Fresno County to the Oregon Border
LIVING WITH EPILEPSY
A free Community Education Conference
Adult Support Group
Youth Art Therapy Fall
Family Sail Day
Adolescent Support Group
Adult Support Group
Youth Art Therapy Fall
Adolescent Support Group
Parent/Caregiver Support Group
Adult Support Group
Youth Art Therapy Fall
Living with Epilepsy Community Education Conference
Adolescent Support Group
Spanish Support Group
Adult Support Group
Youth Art Therapy Fall
Gala 2023
Adolescent Support Group
Parent/Caregiver Support Group
Adult Support Group
Adolescent Support Group
Adult Support Group
SUPPORT GROUPS
Providing community and support
for all affected by epilepsy
Support groups meet weekly for adults with epilepsy, weekly for adolescents, twice a month for parents/caregivers, and monthly for Spanish speakers.
Recently diagnosed? Looking for help?
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Give Back
You can support the foundation in many ways, including attending our events to raise awareness, holding a fundraiser in your community, or via financial support.
We can’t do it without you! Volunteer with us to give back to your community and to support our goal of serving all those with epilepsy. We love our volunteers!
Donations to EFNC directly support free programs and services for individuals and families affected by epilepsy. Your support will help positively impact the lives of the nearly 180,000 people living with epilepsy in Northern California.
It’s free, easy, and fast to donate a vehicle. Fill out the online form or call 1-888-205-3420. You will be contacted to schedule a free pick-up. Your car donation makes a difference; you get a tax deduction.
The stories behind the challenges faced by our community–their experiences and courage dealing with the reality of living with seizures.
I learned that perseverance is necessary for taking on the unknown. Sometimes in life, we aren’t dealt the cards we want, but what matters most is how you play them.
Epilepsy Warrior
The most dreaded question was, “What is the craziest thing you’ve ever done?” […] I found a voice, fulfillment, and that’s the craziest thing I’ve ever done.”
Filmmaker
As scary as living with epilepsy can be, I don’t fear it anymore, knowing that I have a community of people who understands me.
Board of Directors, EFNC
Thank you to our proud sponsors!
