Ever heard of a rescue med but not sure wtf it really means? Join Dr. Becker, a top epileptologist at Ohio State’s Comprehensive Epilepsy Center, as she explains rescue meds, how to use them, and how to talk to your doctor about them. And check out how Dr. Becker and her team are revolutionizing epilepsy treatment through cutting-edge research and compassionate care.Take this survey about rescue meds, enter your email, and you'll be entered to win epilepsy merch!

https://www.surveymonkey.com/r/WTEFThank you to our Community Partner Epilepsy Foundation of America and sponsors Neurelis and SK life science for making conversations like this possible.

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Growing up, Anna faced relentless bullying and doubt from both peers and teachers because of her seizures. But instead of letting the stigma define her, she transformed her pain into power. Now a Community Outreach Specialist for her local Epilepsy Foundation of Wisconsin, Anna is a source of inspiration 🌟 and support 🤝, ensuring that no one feels alone on their epilepsy journey.

Tune in to hear how Anna flipped the script, owned her epilepsy, and became a beacon of hope (and hilarity). 💪

Thank you to our Community Partner Epilepsy Foundation of America and Sponsors SK life science and Neurelis for making conversations like this possible.

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Jessica Chappell started as a clerk for a local store and is now a business analyst for that same corporation. Despite facing discrimination for her epilepsy, she used it as fuel to climb higher. Dreams of being a cop were sidelined, and she now trains law enforcement on seizure safety. Tune in and hear how to turn haters into motivation.

Available on: YouTube, Spotify, Apple, Amazon Music, & Audible (links in @whattheefpodcast bio)

Thank you SK Life Science and Neurelis for being our stepping stones!

Check out @strobealert for strobe light reviews of movies and TV!

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Kate Kostolansky, founder of Char Bear Keeps Dancing, and Dr. Christina Briscoe, pediatric epilepsy fellow, share insights on infantile spasms and epilepsy, emphasizing the importance of advocacy and education. Their conversation highlights the need for more support and resources for affected families. Join the discussion on hope and self-care!

Get a bear and book! Or donate them to a children's hospital!

https://www.charbearkeepsdancing.com/

Resources Kate and Chris mentioned for infantile spasms:

Epilepsy Foundation of America

https://www.epilepsy.com/

Infantile Spasms Action Networkhttps://infantilespasms.org/

Pediatric Epilepsy Research Consortium (PERC)https://pediatricerc.com/

Thank you Neurelis and SK life science for the bear hugs!

What the EF podcast is also available on: YouTube, Spotify, Apple, Amazon Music, & Audible

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Tune in for singer-songwriter Tiana Goss's inspiring journey, as she navigates a new epilepsy diagnosis while chasing her dreams! From dazzling The Voice to lighting up LA stages, her passion and talent always shine bright. As she prepares to grace the stage at the Cam for a Cause Gala this weekend, Tiana is a true testament to turning setbacks into comebacks!

Like, subscribe, and follow  @WhatTheEFPodcast !Thank you SK life science and Neurelis for rocking out with us!

Check out Tiana's music: www.tianagossmusic.com

What the EF is available on: YouTube, Spotify, Apple, Amazon Music, & Audible

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Meet Jeff Baltes, the epitome of resilience and humor! From relocating for accessible transportation to the horrendous hurdles of health insurance and employment, Jeff's story will have you laughing, crying, and cheering him on! Tune in for a rollercoaster of emotions!Available on: Spotify, Apple, Amazon Music, Audible, and more!Thank you Neurelis and SK life science for battling through this hellscape with us!For the resources Jeff mentioned, check out Epilepsy Foundation of Greater Chicago: https://epilepsychicago.org/(Click on "How Can We Help?" tab)

Check out Jeff's informational (and funny) YouTube page:

https://www.youtube.com/@jeffonthebrain

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NEW! Epi-Gem Episodes featuring gems in the Epilepsy Community! Starting with the *must-have* seizure training in schools! Meet Collin, our seizure educator extraordinaire, sharing how it transformed his school days. With Sarah, our inclusive education advocate, we dish out practical tips to bring seizure training to YOUR school. Tune in for the scoop on why it's crucial and how to make it happen!

Empowering People’s Independence, Epilepsy Serviceshttps://www.epiny.org/epilepsy/Empowering People’s Independence, Camp EAGRhttps://www.epiny.org/epilepsy/camp-eagr/Epilepsy Alliance America – Seizure First Aid Traininghttps://www.epilepsyallianceamerica.org/seizure-safety/seizure-first-aid-training-for-school-personnel-your-way/Epilepsy Alliance America – Epilepsy Summer Campshttps://www.epilepsyallianceamerica.org/programs-services/camp-programs/

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