Feb 2023 / CHARITY MATTERS PODCAST
CURE Epilepsy Founder, Susan Axelrod, appears as a guest on the Charity Matters podcast to discuss her journey as a parent to a child with epilepsy and how that experience lead to her, and other parents, creating CURE Epilepsy.
Jan 2023 / CHILD LIFE ON CALL PODCAST
CURE Epilepsy Boar Chair, Kelly Cervantes, appears on the Child Life on Call podcast to share how her family sought to empower themselves in the face of their daughter Adelaide’s epilepsy, her work with CURE Epilepsy, and much more.
Dec 2022 / REACHMD
In hopes of learning more about how the brain changes due to aging in patients with childhood-onset epilepsy, a new study was funded that may suggest some interesting findings. So what do we need to know from the results of this study? To dive into this topic, Dr. Andrew Wilner is joined by Dr. Bruce Hermann, Emeritus Professor at the University of Wisconsin School of Medicine and Public Health, and Dr. Shlomo Shinnar, Professor Emeritus of Neurology and Pediatrics at Albert Einstein College of Medicine.
Dec 2021 / MORNING CHAVA PODCAST (PREVIOUSLY KNOWN AS MIRACULOUS MAMAS)
Board Chair and Seizing Life host, Kelly Cervantes, talks about what it’s like to be a miraculous mama.
Nov 2021 / NPR’S PODCAST WHAT’S HEALTH GOT TO DO WITH IT
CURE Epilepsy CEO, Beth Dean, along with community advocate and mom Nora Hennessy spoke with Dr. Joseph Sirven about epilepsy and living with epilepsy on NPR’s What’s Health Got to Do with It podcast.
Oct 2018 / GLOBE NEWSWIRE
An online charity auction, to fund epilepsy research, features autographed items and concert experiences donated by Rock & Roll Hall-of-Famers, country music legends, and musical theater stars.
Dec 2016 / BUSINESSWIRE
Citizens United for Research in Epilepsy (CURE) and Lundbeck announced the launch of the CURE Education Enrichment Fund Scholarship Program, which is a one-time scholarship (up to $5,000) for people who are living with epilepsy, family members and caregivers.
SUDEP
Aug 2016 / THE NEW YORK TIMES
Sudden Unexpected Death in Epilepsy (SUDEP) was largely undiscussed between medical professionals, including neurologists, and thus patients were not warned of the dangers or what could put them at risk. It was not until CURE Epilepsy asked what was being done to address SUDEP that the federal government took action.
