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.
So, what's it like being married to someone with epilepsy? Steve and I get real about our relationship—how we met, the challenges we’ve faced, and the moments that make it all worth it. From seizure depression to the Kid Decision (to have kids or not?), and yes, even who gets the last French fry, we’re sharing it all.
Appreciate these folks giving this podcast their "I do's": Epilepsy Foundation of America, Neurelis, and SK life science.
Hosted on Acast. See acast.com/privacy for more information.
