Epilepsy Foundation Oregon

EFA Oregon logo in front of Mt. Hood
Over 43,000 People in Oregon are Living with Epilepsy

The Epilepsy Foundation Oregon provides programs and services that support people and families impacted by epilepsy. With the strength of a national organization and network of epilepsy experts, EFO provides national scope and local impact.


From ground breaking research to SUDEP support, local educational programs and a 24/7 Helpline, Epilepsy Foundation Oregon is here to serve you.


We are leading the fight to END EPILEPSY® in Oregon by supporting and mobilizing the epilepsy community through educational activities, direct services, advocacy, as well as research to accelerate therapies to stop seizures, find cures, and save lives. The Foundation also seeks to educate the general public to better understand epilepsy and seizure disorders, including knowing proper seizure first aid.

How to Contact Our Staff

Email us at oregon@efa.org

Connect with us

Programs & Resources

Topgolf Hillsboro


The Epilepsy Foundation Oregon is excited to bring you the Take a Swing at Epilepsy event at Top Golf in Hillsboro! Join us on Sunday, March 10, 2024 for a day of fun, food, and community at this premier entertainment destination while showing your support for the 3.4 million people living with the challenges of epilepsy. We appreciate our partners helping to raise awareness for epilepsy alongside 100% of event proceeds support programs, client services, advocacy and more!


Register Here


PACES - Adult Self-Management

PACES in epilepsy logo


Over the course of multiple weekly sessions, participants develop coping and goal-setting strategies that improve overall and discrete aspects of quality of life, epilepsy self-management, and address anxiety and depression. The program’s structure has been validated by randomized, controlled trials in multiple states. Its framework and curriculum, delivered via facilitated group sessions, is proven effective.


Contact Jaritza Garcia at jgarcia@efa.org for more information about how to get involved.

Camp Discovery


Camp Discovery is an annual summer camp where children experience archery, rock climbing, canoeing, hiking, swimming, arts/crafts, campfire games and much more. Thanks to our sponsors and generous donors, Camp Discovery is free of charge to all campers living with epilepsy and one sibling. Additional siblings may attend for a minimal charge of $150 per sibling. Volunteer opportunities are also available. Please see below for Frequently Asked Questions.


Camp Discovery will be held, July 28th-31st, 2024, at Camp Magruder in Rockaway Beach, Oregon.


Registration information will be posted Spring 2024.



Where is Camp Magruder – “Camp Discovery”?

Camp Magruder is located in Rockaway Beach, OR on the Oregon coast.
Address: 17450 Old Pacific Hwy Rockaway Beach, OR 97136

Where will my child stay while at camp?

Campers will stay in one of Camp Magruder's cabins. the cabins are enclosed and have bunk beds in each cabin. Camp directors are responsible for cabin assignments. All participants should bring their own blankets, sleeping bags, pillows, toiletries, towels, etc.

What if my child is on medication or needs medical attention?

There are registered nurses on site to provide basic first aid and medication given to campers. These nurses have reviewed the Camper Application Forms sent in by camper parents or guardians. ALL medication will be turned over to the nurses (volunteers and campers) upon arrival and only the camp nurses will distribute the medication to campers.

Medical Information:

Please provide your first day of medication to your child prior to arriving at Camp Discovery. Please don’t forget to pick up your medication when you pick up your child on the last day of Camp Discovery. There are epilepsy doctors on call during Camp Discovery for nurse consultation. In the case of emergencies, the registered nurses will determine whether to call 911 or not. In case of an emergency, injured or sick children will be taken to the nearest hospital as determined by the nurse, EMT or doctor.

Can I call my child?

Phone use by campers is typically prohibited. Messages for Camp Directors can be left on the camp voicemail and will be relayed to the group leader at mealtime. The land line number is (503) 355-2310.

What should my child bring to camp?

Bring enough of the supplies listed below to last for four days, plus extra just in case. Send clothes appropriate for all types of weather including enough warm clothing. It is best to label everything with your child’s name just in case it is misplaced. Remember, you or your child will be out in the rustic setting of the natural forest. Video game players are not suggested as the experience of Camp is non-electronic.


If you have any additional questions, please contact Jaritza Garcia at jgarcia@efa.org. 

Upcoming Events

Topgolf Hillsboro

5505 Northeast Huffman Street
Hillsboro, OR
United States

The Epilepsy Foundation Oregon is excited to bring you the Take a Swing at Epilepsy event at Top Golf in Hillsboro! Join us on Sunday, March 10, 2024 for a day of fun, food, and community at this
Parent Support Group - Pacific Standard Time

United States

This group supports parents and provides a place to share experiences, provide encouragement, and provide support for each other through this epilepsy journey. The goal is to help parents/caregivers

Support Our Story

With your help, we can continue to raise awareness by sharing stories from the epilepsy community. Your tax deductible donation to the Epilepsy Foundation can change lives for the better.

Contact Us


16409 SE Division St Ste 216 PMB 1115 Portland, OR 97236

Mailing Address

16409 SE Division St Ste 216 PMB 1115 Portland, OR 97236

Local Contacts

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