Predicting who will develop epilepsy after infection with malaria may now be possible.
Learn how stigma impacts those with epilepsy and what you can do about it.
Receive email alerts about epilepsy research discoveries.
CURE’s epilepsy research focus.
Get updates on our weekly podcast, launching this month.
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.
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.