Each year hundreds of people attend our free conferences to learn about treatments, medication and social issues relating to epilepsy. Conferences are held in Portland, OR in the Spring and Bend, OR each November. Check out the upcoming schedule for an event near you.
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SUDEP Oregon is a support, education and awareness program for people in the Northwest impacted by Sudden Unexpected Death in Epilepsy. SUDEP Oregon is composed of a network of family members and friends who have lost loved ones to epilepsy.
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When epilepsy is diagnosed, it affects the whole family. Sometimes the practical problems of daily living – from insurance, to jobs, to medical care – may seem overwhelming. At other times, it helps just to talk to people who understand what its like to live with epilepsy.
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The CAN Volunteer program provides opportunities for people with epilepsy, their family members and friends to support the programs and services offered by Epilepsy Foundation Oregon.
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Speak Up Speak Out (SUSO) is an advocacy program designed to promote involvement by people with epilepsy, their families and friends in government and legislative activities.
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The annual summer camp is held in July each year. Children will experience archery, rock climbing, canoeing, hiking, swimming, arts/crafts, campfire games and much more.
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In a continuous effort to bring knowledge and education to the community about epilepsy, EFOR staff and volunteers conduct Seizure Recognition and Response trainings.
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Through federal legislation in 2008, Epilepsy Centers of Excellence (ECoE) were established in four regions and sixteen sites around the country to better serve veterans living with epilepsy.
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