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Welcome!

The Epilepsy Foundation of Northern California is a 501(c)(3) charitable organization leading the fight to stop seizures, find a cure and overcome the challenges created by epilepsy.

 

The Spectrum of Epilepsy..
Share Your Personal Story Here
 
Kathy's Story
My story is about being a survivor. At the age of two I was adopted making no information available of when or...
 
Amy's Story
My daughter, Madison, began having seizures some time in December 2009, a couple of weeks before her 6th birth...
 
Stacie's Story
Below is a short story that I wrote several years ago about my experiences to help inspire others in challengi...
 
Michelle's Story
What started out as outbursts of laughter for Emily ended up being epilepsy. I spoke to the nurse at her doct...
 
Tami's Story
I never knew much about epilepsy, still really dont. Ryan, my 18 year old son, started having seizures a coup...
 
Aimee's Story
Our ride on this wild ride called Epilepsy began on February 21st 2004 when our 5 month old son began having s...
 
Bill's Story
When I was three or four years old, I remember awaking to my parents rushing my sister to the Emergency Room. ...
 
Carolina's Story
There was never a time when I thought I could be the next one to be affected by epilepsy.   A normal...
 
Neva's Story
I have been involved in many areas of the Epilepsy Foundation for the past 20 years.

In Novemb...
 

Upcoming Events
Conference Call: Intractable Seizures
02/01/2012
Learn More

Epilepsy Pipeline Update Conference-Family and Friends
02/04/2012
Register Now

» See all upcoming events

» See Support Group listings


Tools & Resources

Seizure Action Plan

Day Care

Childs Guide

Education and DayCare

Learning and School Performance

Health Insurance Application

Childrens Storybooks

Click HERE for other helpful forms and resources.

Welcome to Epilepsy Foundation of Northern California
2012 Epilepsy Awareness Stroll Emerging Therapies - upcoming conference!- EFNC Facebook Page
We're gearing up for our 20th Annual Epilepsy Awareness Stroll! Come join us on Saturday, May 12, 2012 and help raise support and awareness for those with epilepsy and their families. Click here for more info.
 The Epilepsy Therapy Project, which seeks to advance new therapies for people living with epilepsy, will be hosting a "Family Day" conference on Saturday, February 4, 2012.
 
 

Now over 1000 EFNC members on Facebook!


Add your email and stay updated on Foundation news and events!

EFNC does not solicit emails to other organizations and includes an opt-out option.

Act Now! Please Support Resolution 298 Epilepsy Video Series
 
 
 
 
 
 
 



Please urge your member of Congress to sign the "Dear Colleague" letter and become a co-sponsor of H. Res 298.
 
It's simple and easy! You can send a message directly to your member asking for their support.  Consider personalizing your message by adding your own story about living with epilepsy.
 
Thanks for your support!

 
For our video series by doctors talking about the many different issues that affect people with epilepsy click here.