Dear CURE Epilepsy Community Member,
I’m proud to present our latest issue of Researching to CURE Epilepsy, 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 |
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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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