Our research aims to help every person impacted by this heartbreaking condition.
The number of people affected by epilepsy is greater than the populations of Chicago and Boston combined.
470,000 children in the US currently live with the potentially devastating effects of epilepsy.
Learn how this college student battles epilepsy stigma by advocating like a champion.
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Featuring performances by Nils Lofgren, Miguel Cervantes, and Musicality
CURE is founded by Susan Axelrod.
CURE co-sponsors the National Institutes of Health Conference – the first of its kind to focus on a cure for epilepsy.
CURE establishes the first Sudden Unexpected Death in Epilepsy (SUDEP)-targeted research program.
CURE establishes the first-ever Prevention of Epilepsy After Traumatic Brain Injury Award.
CURE takes up another unprecedented initiative by publishing its State of Research in Epilepsies Report.
CURE launches the Infantile Spasms (IS) Research Initiative to accelerate the understanding of IS and adaption of innovative therapy into the clinic.
CURE launches a new signature program, the Epilepsy Genetics Initiative (EGI) creating a culture of personalized medicine for people with epilepsy.
Our mission is to find a cure for epilepsy, by promoting and funding patient-focused research. We identify and fund cutting-edge research, challenging scientists worldwide to collaborate and innovate in pursuit of a cure for epilepsy.
Since being founded in 1998, CURE has been at the forefront of epilepsy research, raising more than $60 million to fund research and other initiatives.
The answers are out there, and we’re determined to find them.
We are Citizens United for Research in Epilepsy (CURE) - the leading nongovernmental agency fully committed to funding research in epilepsy.
Our organization was founded by Susan Axelrod and mothers of children with epilepsy who joined forces to spearhead the search for a cure.