Isabella, living with LGS
Taking FINTEPLA since 2020
Family stories
Families affected by LGS fight for better seizure control each and every day.
Hear from real caregivers about the kind of treatment success that is worth fighting for.
Rick and Cynthia reflect on the day that Olivia’s pediatric neurologist suggested FINTEPLA.
Tracy shares her hopes for Devon’s future after being on FINTEPLA for 3 years.
Melissa explains what life is like now that Isabella's seizures have reduced.
The Bertolino family celebrates Scarlett's positivity and individuality after adding FINTEPLA to her treatment plan.
Asaiah's family talks about his favorite activities and how FINTEPLA has had an impact on day-to-day life.
Ezekiel's parents and caregivers talk about standing up for Ezekiel and starting FINTEPLA.
Scarlett, living
with LGS
WHAT DO SEIZURE-FREE MOMENTS MEAN TO YOUR FAMILY?
Tell us how FINTEPLA has helped your family turn seizure-free moments into meaningful memories. Your experience may inspire other families in the LGS community.


ONWARD® is here to help with your questions
Clinical Nurse Educators and Care Coordinators are ready to help with personalized resources, education, and more.

Think FINTEPLA could help your loved one?
Download the Patient Brochure to learn more.


