What the Ef?! Podcast Por What the EF arte de portada

What the Ef?!

What the Ef?!

De: What the EF
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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.

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Episodios
  • 5 Tips in 5 Minutes on Surviving the Holidays!

    5 Tips in 5 Minutes on Surviving the Holidays!
    Dec 16 2025

    Every year, my brain has a fun holiday tradition of doling out seizures. Like my epilepsy is Santa but with a very dark sense of humor.


    So this year I came up with 5 strategies to (hopefully) mitigate the holiday seizen. From bathrooms to booze to holiday blues--I'm hoping these tips help!


    Tune into this 5-minute What the Elf?! episode and let me know if any of these work for you!


    But above all, remember no matter how many strategies we put in place, seizures are not our fault. They happen when we do everything "right." So please be kind to yourself. I promise you are not alone in this.


    Thank to you the amazing support we had in 2025 from sponsors Neurelis & SK life science and community partners Epilepsy Foundation of America, Danny Did Foundation, and Epilepsy Alliance America!

    Hosted on Acast. See acast.com/privacy for more information.
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    6 m
  • I Didn’t Know I Could Ask My Doctor That with Dr. Claude Steriade

    I Didn’t Know I Could Ask My Doctor That with Dr. Claude Steriade
    Oct 28 2025

    Ever sit in your doctor’s office like, “Wait… what did you just say?” Dr. Claude Steriade, an epileptologist at NYU, is here to translate the medical jargon and hand over her playbook for better communication with your doc.


    She shares the *one magical thought* she wishes every patient could have, explains autoimmune epilepsy (the sneaky diagnosis that hides in plain sight), and shows how to ask for the right tests.


    Oh, and don’t miss her 3 game-changing tips for making conversations with your doctor way less awkward.


    Follow on YouTube, Instagram and TikTok for extra clips and community convos!


    Shout out to community partners Epilepsy Foundation of America, Danny Did Foundation, Epilepsy Alliance of American AND our sponsors Neurelis and SK life science! Thanks for helping bridge the communication gap in the epilepsy world!

    Hosted on Acast. See acast.com/privacy for more information.
    Más Menos
    48 m
  • *LIVE* from Lisbon! Backstage Pass to the International Epilepsy Congress

    *LIVE* from Lisbon! Backstage Pass to the International Epilepsy Congress
    Oct 14 2025

    What happens when thousands of epilepsy nerds take over Lisbon? Tune in for chats with people from all over the world–Argentina, UK, Australia, Colombia, Kenya and more! Convos about the ethics of AI in epilepsy treatment, the move from pediatric to adult care, to how gut health affects seizures.


    Turns out, the biggest conference in the world isn’t just about science—it’s about connection, curiosity, and a whole lot of hope. 🌍💜


    Subscribe YouTube, follow Instagram and TikTok for extra clips and community convos!


    Shout out to community partners Epilepsy Foundation of America, Danny Did Foundation, and Epilepsy Alliance America AND our sponsors Neurelis and SK life science! Thank you for supporting the epilepsy sphere!

    Hosted on Acast. See acast.com/privacy for more information.
    Más Menos
    43 m
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