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About Us

Our Mission

Our mission is to lead the fight to overcome challenges of living with epilepsy and to accelerate therapies to stop seizures, find cures, and save lives.

The Epilepsy Foundation Oregon (EFOR) is the principal advocate for the epilepsy community in Oregon.

Over 42,900 people in Oregon are living with epilepsy or seizure related conditions.

Epilepsy Foundation Oregon is a chapter of the National Epilepsy Foundation of America, and works closely with the National Foundation to develop and implement programs and services for people with epilepsy in Oregon.

A volunteer advisory board of professionals and community leaders provide leadership to Epilepsy Foundation Oregon. EFOR hosts a Professional Advisory Board of healthcare professionals that advise and support the organization.

EFOR’s office is located in Portland, OR.

 

Our Programs

Funding supports the following uncompensated programs and services provided to people with epilepsy and their families:

Camp Discovery
Annual youth summer camp

Community Action Network (C.A.N.) Program
Community Volunteer Program

Community Education & Training
For public, police, teachers, nurses and employers

Teen, Adult, Parent Support Groups
Support groups for people with epilepsy and their families

Employment Assistance Programs
Support for employment transition

Public Education Programs
Fall conferences about epilepsy

Teens Speak Up! (TSU)/Public Policy Institute (PPI)
Advocacy and government relations

SUDEP Oregon
Support for people bereaved by SUDEP and other epilepsy-related deaths