Diagnosed at just six days old, kinda makes Paige Wade the OG of epilepsy. As an adult, her seizures subsided until two popped up, taking away her driver's license. Paige teaches second grade, and her students weren't the only ones getting dropped off by their moms. (Awkward.)

Paige opens up about how losing her independence led to depression—and how she slowly climbed her way back. Now a thriving content creator, she shares the mindset shifts and daily habits that helped her heal, including her focus on nutrition, movement, and mental health. Tune in for three powerful strategies Paige used to reclaim her life and her sense of self.

Check out Paige's Insa: @changewithpaige

Shout out to these folks for making convos like this possible!

Community partners Epilepsy Foundation of America and ⁨the Danny Did Foundation⁩ and sponsors Neurelis and SK life science

​​When Sarabjeet Bhutani was diagnosed with epilepsy as a child, she understood the secrecy that came with it. The cultural stigma in her community ran so deep, that for decades Sarabjeet stayed silent. And when her daughter was also diagnosed at age 10, the cycle continued. (If only they were born in Gen Z!)

But that all changed when Pree had a seizure in front of her school. (Can’t hide that, right?) From then on, Pree would dedicate her life to talking openly about it. Becoming an advocate, speaking at congressional hearings, and lobbying for seizure first aid legislation.

In this episode we talk about the blurred lines between privacy and shame. And how one daughter’s courage inspired her mother to help break a generational silence.

Shout out to Community Partners Epilepsy Foundation of America and the Danny Did Foundation as well as sponsors SK life science and Neurelis!

Live from the National Epilepsy Walk in D.C., Landis Wiedner and Miles Levin hit the National Mall with one big question: What do you wish more people knew about epilepsy? The answers were real, raw, and sometimes even funny!What do YOU wish more people understood? Comment below and join the conversation!Thank you Community Partner Epilepsy Foundation of America and sponsors Neurelis and SK life science for making convos like this possible.

JP Severin thought his epilepsy was controlled—until his seizures decided to make a comeback right in the middle of his career and dad life. JP shares what it’s like when your kids witness your seizures, the emotional aftermath, and the challenge of accepting what’s beyond his control.

With humor and heart, JP dives into the weird wisdom seizuresbring, and how life’s unpredictability can reshape perspective on gratitude and empathy.

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

When Nancy Iida’s son went off to college, she had to face a hard truth: she couldn’t control his seizures. That lesson deepened when her daughter was diagnosed with cancer and she herself battled Lyme disease.

Through it all, Nancy turned to art as a way to create peace in a life filled with uncertainty. In this episode, she shares how she’s learned to let go, find balance, and embrace the practice of resilience and laughter.

Check out Henry's Heroes Foundation: https://henrysheroesfoundation.org/

Thank you to our Community Partner Epilepsy Foundation of America and Sponsors SK life science and Neurelis for supporting peace in the epilepsy world!

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.

What happens when your epilepsy meds turn against you? Mere Davis found out the hard (and very painful) way. On her way to an epilepsy walk, a bad case of medication toxicity caused her to pass out, faceplant on the sidewalk, and start a long journey of medical treatment.

In this episode, Mere shares her story with wit and wisdom, breaking down what medication toxicity is, how to avoid it, and why you should always watch your step (literally).

A big shoutout to our Community Partner the Epilepsy Foundation of America and Sponsors SK life science andNeurelis for keeping the lights on and the mics hot so we can have important convos like this one.

Ever felt dismissed by a doctor? Author Ilana Jacqueline gets it. In this episode, she shares what medical gaslighting is, how to spot it, and *three game-changing tips* to stand your ground in the doctor’s office. She opens up about her own medical journey and how it led her to become a self-advocacy pro.

If you’ve ever struggled to feel heard in the doc’s office, tune into this convo and order Ilana’s book “Medical Gaslighting” for even more guidance.

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

When Dr. Amee Shah’s epilepsy, long under control, returned, she faced a tough question: should she share her story? After keeping seizures a secret her whole life, she chose to open up. While many people were supportive, others were not – even requesting Amee to take down social media posts about her epilepsy. Instead of letting that hold her back, Amee turned it into fuel for advocacy, becoming a public voice for epilepsy awareness. In this episode, she shares the cultural challenges of being vulnerable and the power of owning your story.Learn more about seizure pillows that we talk about in this episode here: https://www.dannydid.org/selecting-a-device/Thank you to our Community Partner, the Epilepsy Foundation of America, and Sponsors SK life science and Neurelis for standing up to stigma with us.

How do you turn epilepsy into a motivator for growth and success? Justice Bartley, a former NBA player development coach, takes us courtside to share his journey from high school basketball to the NBA coaching staff—all while navigating life with epilepsy. Hear how Justice found the right support, embraced accountability, and transformed challenges into life lessons.

Plus, a sneak peek at his stealth startup and his mission to empower athletes with epilepsy with the 1in26 Athlete Foundation. 

Thank you to our Community Partner Epilepsy Foundation and Sponsors SK life science and Neurelis for making slam dunk convos like this possible.