A college student with epilepsy offers advice on not only how to survive, but also thrive.

After losing her son to a rare form of epilepsy called NORSE, or New Onset Refractory Status Epilepticus, Nora Wong set out to get answers from doctors and researchers. When she found little informati

This month onSeizing Life Jon Tuteur shares his journey with adult-onset epilepsy. From his first seizure at age thirty, through his epilepsy diagnosis, treatment, and eventual brain surgery, Jon di

This week onSeizing Life Dr. Laura ODwyer joins us to talk about the fastest growing segment of people living with epilepsy in the United States older adults. Dr. ODwyer explains why adults are

This month onSeizing Life author Laura Beretsky shares her decades-long journey with epilepsy, from diagnosis at age 6, through college, parenting, fighting discrimination in the workplace, and ulti

This month onSeizing Life a nurse and mother shares her young sons journey from the onset of focal seizures to a devastating diagnosis of Rasmussens Encephalitis to a life-changing brain surgery.

This month onSeizing Life we explore artificial intelligence as it relates to epilepsy care, how its impacting epilepsy diagnosis and treatment today, and what it promises for the future.

This week onSeizing Lifewe revisitjust a few of the incredible guests and conversations from 2020. In a challenging year, we, like so many across the country, had to adjust to working remotely. And

This week on Seizing Life Annette Adkins, who has lived with intractable epilepsy since 2014, discusses the impacts of epilepsy on her professional and personal life, and how it led her to participat

This week on Seizing Life we speak with two rare epilepsy organizations, The KCNT1 Epilepsy Foundation and The Cute Syndrome Foundation, in an episode recorded at Epilepsy Awareness Day at Disneyland