More research. Better treatments. Family support.
Helping those with epilepsy until there’s a day without epilepsy.
The Logan Jett Research Foundation helps improve the lives of everyone touched by epilepsy, funding research for treatment options while working toward a cure, and providing a network of resources and support.
We believe in better days… we believe in hope.
Maybe you’re a patient or a caregiver, a family with a child or another loved one who has epilepsy, or someone who might know a person battling epilepsy and wishes to donate. Whatever category you fall into, we’re glad you’re here.
HERE’S HOW WE SUPPORT OUR EPILEPSY COMMUNITY
Special Thank You to Our Sponsors
Patients are often reluctant to admit their condition -- even to close family, friends or co-workers -- because there's still a great deal of stigma and mystery surrounding the disease that plagued such historical figures as Julius Caesar, Edgar Allan Poe and Lewis Carroll. And when people affected by epilepsy are reluctant to expose their condition, the public remains in the dark about it - a tragic irony that has made patient care and raising funds for research more than challenging.
- Lynda Resnick, Vice Chair and Co-Owner at The Wonderful Company
Logan’s Story
When our son was diagnosed with Polymicrogyria and Epilepsy at 3 months old, our world changed forever. We had no idea the journey that we were beginning to embark upon.
We also had no idea the changes with which we would consider ourselves blessed.
Epilepsy affects our son's life in extremely negative ways. It affects all of our lives in extremely negative ways. But...we have also been set on a path of great hope and inspiration that never would have been possible without ALL of the circumstances that are part of this journey.
While we never expected the twists and turns that we have traveled, we are learning to not only accept them, but to embrace all that life has to offer through them.
We're letting go of fear and relying on our faith.
We're learning that you don't always have to be bold, but you do have to be real.
And we will only effect change by inspiring those around us to do the most good they can do.
We're not researchers and we're not doctors, but it's time we start driving our efforts toward making a difference in the lives of those that suffer with epilepsy, just like our son. We're only going to change the world of epilepsy, by changing the world through epilepsy. We're here to help create connections, spur hope and spark a desire in those who want to be part of something larger than any single one of us.
One step at a time, we hope to one day see a world without seizures. How are we going to do that? With the help of each one of you, celebrating tiny triumphs and spreading giant hope.