What the Ef?! is the podcast that says out loud what everyone else with epilepsy is thinking: WTF is happening right now?! Hosted by Landis Wiedner, this show unpacks the unfiltered, often hilarious, sometimes heartbreaking realities of life with epilepsy. Each week, Landis brings together neurologists, advocates, celebrities, caregivers, and everyday people to share raw stories, expert insights, and those “you-can’t-make-this-up” epilepsy moments no one talks about—but everyone should.
It’s equal parts education, community, and comic relief. Whether you’re living with seizures, supporting someone who is, or just curious to learn more, this show creates an approachable, stigma-busting space where laughter and real talk fuel change.
⚡ Epilepsy • Seizures • Awareness • Advocacy • WTF moments ⚡
Special thanks to SK Life Science and Neurelis for sponsoring 2024 and supporting conversations that matter.
Disclaimer: This podcast is for informational and entertainment purposes only. Nothing shared here should be taken as medical advice. Always consult your physician or qualified healthcare provider for diagnosis and treatment.
Hosted on Acast. See acast.com/privacy for more information.
What the Ef?! is the podcast that says out loud what everyone else with epilepsy is thinking: WTF is happening right now?! Hosted by Landis Wiedner, this show unpacks the unfiltered, often hilarious, sometimes heartbreaking realities of life with epilepsy. Each week, Landis brings together neurologists, advocates, celebrities, caregivers, and everyday people to share raw stories, expert insights, and those “you-can’t-make-this-up” epilepsy moments no one talks about—but everyone should.
It’s equal parts education, community, and comic relief. Whether you’re living with seizures, supporting someone who is, or just curious to learn more, this show creates an approachable, stigma-busting space where laughter and real talk fuel change.
⚡ Epilepsy • Seizures • Awareness • Advocacy • WTF moments ⚡
Special thanks to SK Life Science and Neurelis for sponsoring 2024 and supporting conversations that matter.
Disclaimer: This podcast is for informational and entertainment purposes only. Nothing shared here should be taken as medical advice. Always consult your physician or qualified healthcare provider for diagnosis and treatment.
Hosted on Acast. See acast.com/privacy for more information.
The first thing Brian remembers after his first seizure is a boot smashing through his semi-truck windshield—strangers pulling him from the wreckage as his world changed forever. After a misdiagnosis, years of drug-resistant epilepsy, and 30 seizures a month, Brian found the strength to keep fighting. With cutting edge brain technology—and with the steady support of his loved ones—he’s celebrating seven months seizure-free and a brand-new chapter.
Follow on socials for more convos and clips!
YouTube: @WhatTheEfPodcast
Insta: @whattheefpodcast
TikTok: @what.the.ef.podcast
Shout out to community partners Epilepsy Foundation of America, Danny Did Foundation & Epilepsy Alliance America AND our sponsors Neurelis and SK life science! Thank you for keeping this community going!
Learn more about Legacy Bridges Foundation that helped Brian through recovery: https://www.legacybridgesfoundation.org/
Hosted on Acast. See acast.com/privacy for more information.
