Seizures are shared.
So is relief.

With fewer seizures, families finally have the ability to live more in the moment. Discover real patients and their stories.


There’s really no better way to describe Grace. You’ll see it in every inch of her, but especially in her resilience. Because at just 5 years old, Grace has spent most of her life having close to 400 seizures a day.

See Grace's Story

I love you, Mommy.

Words any mother would love to hear, but for Jen, they mean even more. Because for years, her son Cameron’s frequent seizures made it difficult for him to interact with his family.

See Cameron's Story

A little bit of independence.

That may seem like a common thing for most parents to want for their children. For Jon, it was different. He was only 4 years old when he was diagnosed with Lennox-Gastaut syndrome. He and his parents spent years trying multiple treatments and searching for anything that might help.

See Jon's Story

A whole new world

For so long, Aaron’s parents were his whole world. Relentless seizures and unanswered questions left their family secluded for nearly 20 years. It wasn’t until age 19 that Aaron finally received a Lennox-Gastaut syndrome diagnosis.

See Aaron's Story

Hope for the future

Steven’s childhood was tough for him, his mom, Annette, his dad, Steve, and his younger brother, Michael. Seizures dominated their lives. Without a proper diagnosis, Steven was treated through trial and error by many different doctors.

See Steven’s Story

Growing up

It took 20 years to get a Dravet diagnosis for Zach. For him and his mom, Leslie, those years were frustrating—just waiting for answers, waiting for relief, waiting to grow up. Once they received that diagnosis, a whole world of connections and information opened up to them—which ultimately led to EPIDIOLEX.

See Zach’s Story