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.
This week’s episode is one you’ll want to take notes on. Ayesha Akhtar, VP of Health Equity at the Epilepsy Foundation of Greater Chicago, isn’t just talking about change—she’s handing out the blueprint.
If you’ve ever wondered, “What can I actually do to make a difference for people with epilepsy?”—Ayesha’s got answers (and a few challenges you just might want to take on). Find out how education, advocacy, and community power can close the gaps—and how you can be part of it.
📲 Don’t forget to subscribe & follow on YouTube, Instagram and TikTok for extra clips and community convos!
Big thanks to community partners Epilepsy Foundation of America, Danny Did Foundation, and Epilepsy Alliance America AND sponsors Neurelis and SK life science for keeping this community going strong.
Hosted on Acast. See acast.com/privacy for more information.
