They say laughter is the best medicine - unless you're diagnosed with something that sounds like a meme.

Mike lives with FAP, short for Familial Adenomatous Polyposis - a rare genetic disorder that guarantees colon cancer without drastic surgical intervention. In this unfiltered and laugh-out-loud conversation, Mike opens up about the brutal realities of living without a large intestine, the mental toll of life-altering surgery at 18, and the deeply personal decision to write a memoir titled A Bump in the Road. From rows of shark-like baby teeth to an ostomy bag that looked like Rudolph’s nose, Mike takes us through the gritty details of his medical journey. But what starts as a conversation about disease turns into something much bigger: a story of resilience, perspective, and finding purpose on the other side of pain. Plus, a passionate pitch for bidets, because we all know bidets are for kings. 

Check out Mike's book!

Turns out, the most dangerous thing on TV in the ‘90s wasn’t violence—it was Pikachu. In December, 1997, nearly 700 kids in Japan were rushed to the hospital after watching a single episode of Pokémon. No, this isn’t an urban legend—it actually happened, and it was electrifying (lol). This week, Jer walks the fellas headfirst into the wild, true story of the Pokémon seizure panic, how Pikachu literally short-circuited a nation, and why poor ol’ Porygon got wrongfully canceled before being canceled was cool.

We break down the science of photosensitive epilepsy, uncover how a cartoon nearly led to a nationwide media meltdown. Justice for Porygon. Blame Pikachu. 

You can watch this entire episode over on YouTube!

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Taylor Arbeau is a firecracker. A passionate photographer, musician, and former Special Olympics athlete, she also happens to live with Down syndrome — mosaic Down syndrome, to be exact (yeah, we had no clue what that was either). In this candid convo, Taylor drops truth bombs about growing up “different,” discovering self-love, and calling bullshit on assumptions people make about her. She opens up about dating, her dreams of becoming a mom, and the unexpected ways Down syndrome has shaped her art and identity.

This episode is all heart and zero pity. It’s a celebration of difference, determination, and the power of proudly being yourself — even if you might have a tiny bit of road rage.

Follow Taylor’s work on Instagram:

Photography: @beausphotos3

Music: @taylorandmusic.3

Jeremie met Terry where all deep, life-altering connections begin: half-naked in a sauna, trying not to die of heat stroke. What started as a sweaty convo about testosterone turned into one of the most jaw-dropping pain stories we’ve ever heard. Terry's been battling chronic pain since the age of nine thanks to a rare hip disease that left his femur more hammerhead shark than ball-and-socket. He’s survived countless surgeries, dealt with decades of ignorance around pain management, and got hit by a car after finally getting relief from his first hip replacement. Oh yeah—he’s also the President of the Chronic Pain Association of Canada. This episode is for anyone who's ever been told they're “too young” for real pain, who’s had their suffering questioned, or who just wants to hear a badass 64-year-old tell it like it is—with a body that creaks louder than a haunted house and a sense of humour sharper than a surgical scalpel.

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Falling asleep is easy—until it becomes the hardest part of your day. Recorded live in Toronto, this episode dives into the unpredictable world of narcolepsy type 1 with Heather, a traditional Chinese medicine practitioner living with both narcolepsy and cataplexy. From sleep-deprived misdiagnoses to lucid hallucinations and arms that give out mid-laugh, Heather walks us through the reality behind the disorder’s misunderstood pop culture image. She opens up about losing her spontaneity, finding community, and redefining rest, all while navigating a healthcare system still catching up. It’s funny, eye-opening, and more than a little dreamlike.

When a hospital nurse's error leads to a life-threatening hemorrhage, Tracy's fight for survival and answers begins. This week, Tracy shares her unbelievable journey through misdiagnosis, two kidney transplants, and a near-fatal medical error that led her to become a fierce patient safety advocate. From a childhood illness that unknowingly attacked her kidneys to a shocking turn of events post-transplant, Tracy's story is a testament to resilience and the critical importance of self-advocacy in healthcare.

You can watch this entire episode over on YouTube!

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When the map doesn’t match the terrain, sometimes you just make your own path. Natalia Bartlomowicz was born with a rare congenital condition so unique it doesn’t even have a name—just a stack of medical files and a body doctors still can’t quite predict. In this episode, she opens up about navigating childhood surgeries, a 16-hour operation in Boston, and the emotional toll of being called a “medical mystery.” From discovering she has two uteri to building a safe space for youth with chronic illness, Natalia’s story is one of resilience, radical self-advocacy, and finding strength in the unexpected. She talks dating, dignity, and how the healthcare system can better treat patients as people. It’s a heartfelt ride through one woman’s no-name diagnosis—and the superpower she’s made of it.

Links:

together-we-thrive.ca

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You can’t outgrow puberty—but maybe we can outlearn how we teach it. This week, Jer and Tay explore a topic often overlooked: puberty education for youth with disabilities. Social worker and doctoral student Jennalyn Suda breaks down how trauma-informed frameworks can radically reshape how we approach this formative stage, especially for students who face additional barriers. From the sensory challenges of menstruation to the cultural and cognitive complexities that shape understanding, Jennalyn sheds light on the gaps in traditional education. The boys dive into awkward memories, laugh about the lessons they never learned, and highlight how shifting the conversation from shame to empowerment might just be the change we need.

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When you go in for testicular cancer surgery, do they offer you a scrotal facelift while they're down there? We ask the important questions. This week is a wild ride through Taaha's diagnosis in grade 12. Taha talks about the pressure to be strong for his family, how the other testicle "kicks up into overdrive" to pick up the slack, and the incredible nurses who inspired him to change his life's path. Now a registered nurse and a fierce advocate for the Canadian Cancer Society, Taaha is using his experience to help others and expose the staggering out-of-pocket costs that come with our "free" healthcare system.

You can watch this entire episode over on YouTube.

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When the cost of survival outweighs the cost of death, something has gone deeply wrong. In this sobering and eye-opening episode, Mitch, living with cerebral palsy and chronic pain, shares his harrowing journey through a Canadian healthcare and social system that he argues is failing its disabled citizens. From the challenges of inadequate education and inaccessible post-secondary programs, to the emotional toll of societal stigma and the bureaucratic obstacles in pursuing intimacy, Mitch exposes the gaps that leave many disabled individuals isolated, under-resourced, and overlooked. He bravely discusses everything from systemic failures and addiction to sex work and survival strategies — reminding us how much dignity and independence are shaped by equity, not charity.

You can watch this entire episode over on YouTube.

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