In this episode, What the EF podcast chats with the queen of epilepsy advocacy, Tiffany Kairos, and ask the questions that can’t be answered in a doc’s office. Like…what does a marriage look like when epilepsy enters after the wedding day? Available on: YouTube, Spotify, Apple, Google Podcasts, Amazon Music, & Audible … Read More
Here’s something to tell your boss–the primary sponsor of the American Disability Act also has epilepsy! What the EF podcast chats with Tony about his vigorous fight to get the ADA passed and his mind-blowing journey with seizures. Available on: YouTube, Spotify, Apple, Google Podcasts, Amazon Music, & Audible Stay connected to … Read More
In this episode, What the EF podcast talks to Jared Muscat about why he wouldn’t let epilepsy stop him from doing his favorite thing: surfing. Water safety is tricky when it comes to seizures, and Jared shares how to stay safe without giving up your passion—no matter what it is. What the … Read More
In this episode, What the EF podcast tackles an audience-requested topic: SUDEP. There are so many questions, and Dr. Kim Pargeon guides through all of them. Available on your favorite streaming service! YouTube, Spotify, Apple, Google Podcasts, Amazon Music, & Audible Stay in touch with What the EF by following us on … Read More
What the EF podcast kicks off Seizen 3 with Jennifer Reyes on her strategies for the awkward convos at work about seizures or needing accommodations (which are legally required but hard to ask for). Grab a pen because you’ll want to write these tips down! Available on: YouTube, Spotify, Apple, Google Podcasts, … Read More
A Seizure Action Plan is a personalized document that provides information on how others can respond on how to respond on your behalf during a seizure. Here we’ll share how a seizure action plan can give you back some control.
Lisa Lindahl is the inventor of the sports bra. ‘Nuff said. Lisa’s mom said that epilepsy meant she had zero expectations of Lisa accomplishing anything. Instead, Lisa paved the way for female entrepreneurs and people living with epilepsy. We chatted with this icon about how much things have changed—and what still needs … Read More
Mia L. van der Kop shares her perspective as both a researcher and a patient in an article published in the highly regarded scientific journal, Epilepsia. Read an excerpt here.