The latest CURE Epilepsy impact report is here. 

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Dear CURE Epilepsy Community Member,
I’m proud to present our latest issue of Researching to CURE Epilepsy ([link removed]) , our semi-annual report that highlights our work and the work of our incredible team of determined and dedicated researchers, the impact CURE Epilepsy-funded research has had, and encouraging stories from the epilepsy community that inspire us.
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In this issue you will see:
* The impact of our $4 million, multi-site Infantile Spasms Initiative which launched our work in cutting-edge team science.
* A summary of the research awarded in 2020 and currently underway in the areas of genetics, the mechanisms of epilepsy, SUDEP and more.
* An interview with Libby and Victor Boyce who lost their son, Cameron, to SUDEP, and who find hope through the promise of research.
* A recap of events that helped sustain our work and amazing the people who made it possible.

Our unrelenting pursuit of a cure is motivated by members of our community, like you. We promise not to stop until we achieve our shared vision: a world without epilepsy.

With gratitude,

Beth Lewin Dean, CEO
CURE Epilepsy
Our mission is to find a cure for epilepsy, by promoting and funding patient-focused research. CURE Epilepsy is a non-profit 501(c)(3) tax-exempt organization. Our tax identification number is 36-4253176.
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