CURE Epilepsy

CURE Epilepsy CURE Epilepsy is a nonprofit organization dedicated to finding cures for epilepsy.

CURE Epilepsy's mission is to fund breakthrough research that will transform the lives of people living with epilepsy as we lead the search for a cure. We are the leading nongovernmental agency fully committed to funding research in epilepsy. CURE Epilepsy has been at the forefront of epilepsy research, raising more than $90 million to fund innovative research and other initiatives that will lead

the way to a cure for epilepsy. CURE Epilepsy funds grants for young and established investigators and has awarded more than 285 cutting-edge projects around the world to date.

A little rain can't stop Ella's Race! 🌦️ After a grey morning, the sun came out over La Grange, Illinois to greet the El...
09/03/2026

A little rain can't stop Ella's Race! 🌦️ After a grey morning, the sun came out over La Grange, Illinois to greet the Ella's Race runners as they prepared to start the race. 👟

Over 400 friends, families, and community members came together for a day of joy, smiles, snacks, and running for a great cause - to find a cure for epilepsy. This year's race raised over $87,000 for CURE Epilepsy!

We're so honored to be a part of the Cunneen's amazing celebration of community, resilience, and hope year after year. 💜

09/02/2026

This month on the Seizing Life podcast 🎙️renowned neurologist and former NINDS Director Dr. Walter Koroshetz discusses the future of epilepsy research and the critical role of federal funding in driving scientific breakthroughs.

From identifying hundreds of genetic causes of epilepsy to the promise of gene editing, genomic therapies, closed-loop brain stimulation, and beyond, Dr. Koroshetz shares why there’s more hope than ever for people living with epilepsy and their families.

He also offers an inside look at today’s research landscape, the importance of supporting early-career scientists, and why collaboration across government, nonprofits, academia, and industry is essential to advancing epilepsy treatments and, ultimately, cures.

💜 Listen now to hear why the next decade could transform epilepsy care and what it will take to keep progress moving forward: https://bit.ly/460X11S

National Service Dog Awareness Month is here! 🐕‍🦺 Kick off the celebration  with the paws-itively heartwarming tail of C...
09/01/2026

National Service Dog Awareness Month is here! 🐕‍🦺 Kick off the celebration with the paws-itively heartwarming tail of CURE Epilepsy intern, Channing, and her canine companions Georgie and Bishop. In Channing's own words...

"I had my first seizure when I was nine. After having my second seizure, I was diagnosed with epilepsy."

"My family held out hope for years that I would gain control, that I would respond to medication, that I would grow out of it."

"But that hope was crushed after a video EEG revealed a lifelong diagnosis of juvenile myoclonic epilepsy, and our world turned upside down."

"Three years later, we found ourselves in Atlanta, Georgia at Canine Assistants getting matched with my first seizure response dog, Georgie, and my world was turned around once again."

"The bond you build with your dog is simply unmatched. My bond with Georgie was incredible, just like it is with the dog I have now."

"My current service dog, Bishop, is Georgie's great nephew. Bishop is different than Georgie because he is a seizure alert dog. He gives me the same alert that an aura might, but I don't have an aura. So, Bishop is my aura."

"He had some big paws to fill. But, knock on wood, Bishop has never missed a seizure alert."

A supportive community, a determined family, and one inspiring young girl. Learn how Ella’s Race motivated Barbara Kelle...
08/31/2026

A supportive community, a determined family, and one inspiring young girl. Learn how Ella’s Race motivated Barbara Keller to make an IRA gift to CURE Epilepsy and help advance critical epilepsy research. 💜

Read her story in our Impact Report here: https://bit.ly/3UnEpGK

Mohan resides in the Darjeeling region in West Bengal, India. As a person living with epilepsy in this area, he has a un...
08/28/2026

Mohan resides in the Darjeeling region in West Bengal, India. As a person living with epilepsy in this area, he has a unique perspective on tradition, science, community, and acceptance. Here is a snippet of the story he sent to us:

"Every individual encounters a time in life when they begin to paint vibrant pictures of their future. That moment arrived for me as well, a time when I was brimming with energy, dreams, and genuine excitement."

"The year was 2016, a year permanently marked in my mind. After years of intense familial and personal hardships and financial struggles, I was finally mapping out a secure, prosperous future. I harbored a fierce desire to bring lasting joy to the faces of my aging parents, to prove my potential, and to find true success. I was stepping out into the warm sunshine of boundless possibilities, where the future seemed ready to embrace me."

"But destiny had a different script for me perhaps. One regular morning, while sitting down for a Morning Meal with my family and watching a football match, unprecedented and unaware the first terrifying sudden storm of a seizure violently struck me. It triggered, the entire room spun out of control. Within seconds I could understand what was happening, my sensory organs failed, my consciousness snapped, and a total blackout ensued."

"When I finally awoke on a hospital bed, the first image that greeted me was the absolute terror, shock, and despair written across my family’s faces. The bright future I was preparing to chase vanished instantly into a thick fog of uncertainties. This single, unannounced electrical tempest shattered all my plans and expectations in one clean, devastating swipe."

"From that fateful day forward, my battle was no longer about scaling a career-graph or achieving conventional success ; it transformed into an existential fight for survival against the random electrical storms within my own brain. Every single day since, I have been fighting an invisible battle, where no physical weapons are drawn and no tangible enemy stands before me. It is a lonely warfare where the battlefield is my own Brain and the adversary is a microscopic flaw within my nervous system."

"To those observing from a safe distance, this condition is easily dismissed as mere “shaking” or a temporary “fit.” But in truth, it is an agonizing ordeal that completely destroys the body and spirit, leaving one entirely fractured from within."

Find his full story here: https://www.cureepilepsy.org/personal-stories/mohan-raj-thakuris-story/

The impact of our research grants will be felt for years to come. Research lines supported by CURE Epilepsy are continui...
08/27/2026

The impact of our research grants will be felt for years to come. Research lines supported by CURE Epilepsy are continuing to progress and past grantees are now mentoring the next generation of epilepsy scientists.

Recently, we released a survey to past grantees about the transformative impact of our funding over time. Check out our latest Annual Report to see what three of them had to say: https://bit.ly/4zCq6y5

Our Annual Report 2025-2026 is here! We hope you take pride in the progress you’ve fueled, celebrate the power of commun...
08/25/2026

Our Annual Report 2025-2026 is here! We hope you take pride in the progress you’ve fueled, celebrate the power of community, and enjoy our collective accomplishments. 🙌

Thank you for making our work possible. 💜 Check out the full report here: https://bit.ly/3UQOE6p

This month's Epilepsy Research Newsletter featured the following articles:💊 Seizure Relapse in New Onset Epilepsy: It is...
08/24/2026

This month's Epilepsy Research Newsletter featured the following articles:

💊 Seizure Relapse in New Onset Epilepsy: It is Not Always Drug Resistance https://bit.ly/4hQk5rj

🧠 Inflammation May Drive Rare Epileptic Syndrome: https://bit.ly/4zsGrp5

📄 Progress Report on New Epilepsy Treatments: A Summary of the Eighteenth Eilat Conference on New Antiepileptic Drugs and Devices (EILAT XVIII): https://bit.ly/46deLXK

Get these updated delivered right to your inbox every month! Subscribe here: https://bit.ly/4xVLQn5

Infantile spasms (IS) are a medical emergency. That's why we helped to create the Infantile Spasms Action Network (ISAN)...
08/20/2026

Infantile spasms (IS) are a medical emergency. That's why we helped to create the Infantile Spasms Action Network (ISAN), a powerful coalition of advocacy groups, medical experts, and families raising awareness to improve early diagnosis and lifelong outcomes for children impacted by IS.

This year marked the 11th annual Infantile Spasms Action Network Workshop in Silver Spring, MD. We heard updates on infantile spasms research, diagnosis, and outcomes, while planning for Infantile Spasms Action Week, happening in December.

A huge thank you to our Governance partners, TSC Alliance and Dup15q Alliance.

There is still time to register to join us for our next Pipeline of Progress webinar! Learn about the latest research re...
08/20/2026

There is still time to register to join us for our next Pipeline of Progress webinar! Learn about the latest research regarding therapeutic devices for epilepsy, including transcranial electrical stimulation, transcranial magnetic stimulation, and focused ultrasound. Register now here: https://bit.ly/3QWq0A5

The Pipeline of Progress series is generously supported by independent educational grants from Lundbeck, Stoke Therapeutics, uniQure, and Xenon Pharmaceuticals Inc. and produced by CURE Epilepsy.

This webinar is the second in our Pipeline of Progress series, created especially for people living with epilepsy and the loved ones who support them.This int...

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420 N. Wabash Avenue, Suite 650
Chicago, IL
60611

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Wednesday 8:30am - 5pm
Thursday 8:30am - 5pm
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