What happens when your body is slowly losing its ability to breathe, but your brain is busy building the future of technology? This week, the fellas (and a very helpful Brock) sit down with Chouaieb (Cho), an AI Black Belt at Google who is quite literally using technology as a personal savior. Cho lives with Ulrich Congenital Muscular Dystrophy (UCMD), a rare condition that has left his diaphragm functioning at just 16% capacity. For Cho, the "AI revolution" isn't about deepfakes or taking jobs - it's about cloning his own voice so he can keep telling stories to his three kids after his inevitable tracheostomy. We dive into the raw logistics of "engineering a life": from why he has to basically dehydrate himself just to sit through a podcast, to the nightmare of calling 50 hotels just to find one with a bed that fits a medical lift. It’s a conversation about "Career Pivots," the BS "Saint or Pity" binary society forces on disabled people, and why Cho identifies more as an entrepreneur than a patient.

Connect with Cho:

LinkedIn: https://linkedin.com/in/nemri

Instagram: @choe_nemri

Mentorship & Advocacy:

FREE Mentorship (Disabled in Tech): https://cal.com/nemri/disability

Professional Paid Mentorship: https://mentorcruise.com/mentor/chouaiebnemri/

Cho’s Accessibility Projects:

* Airbnb Accessibility Analyzer: https://github.com/cnemri/airaccess

* WheelAir: A repository of airline wheelchair policies: https://wheelair.netlify.app/

You can watch this entire episode over on YouTube: https://www.youtube.com/playlist?list=PL0EVgIbBQOxtKJ4qjAlfeutzZRfCGV8nb

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What do you do when your own tongue starts "shedding" like a snake and your doctor tells you to just "eat a banana"? Imagine waking up and seeing the world through 90s TV static, while your muscles literally stretch and tear like gum when you yawn. Làyla joins the boys to break down the reality of living with Refractory Myasthenia Gravis (MG), a version of the illness so stubborn it requires constant infusions just to keep her stable. From the terrifying moment she realized her jaw was atrophying, to the bizarre neurological world of Visual Snow Syndrome, Làyla shares it all with a level of humor and confidence that is honestly infectious.

You can watch this entire episode over on YouTube: https://www.youtube.com/playlist?list=PL0EVgIbBQOxtKJ4qjAlfeutzZRfCGV8nb

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What happens when your abdomen decides it's tired of the basement and wants to move into the penthouse suite? This week, we sit down with Jude, who was born with a rare birth defect called Congenital Diaphragmatic Hernia (CDH). In plain English: they had a hole in their diaphragm (the dinner-plate-sized muscle that keeps your "upstairs" and "downstairs" separate) and their organs decided to throw a housewarming party in their chest cavity. We're talking a spleen, liver, and bowels all fighting for real estate where their lungs were supposed to grow. Jude is living proof that even if you start life with your organs in the wrong room, you can still build a hell of a house.

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What happens when a "Professional Knower" gets hit with a disease that has absolutely zero f*cking answers? Broadcasting legend and former CBC host Gill Deacon spent her life demanding answers for the public, but in 2022, her own body became the ultimate mystery. From her heart feeling like a "motorized toy" to wearing a wool toque 24/7 just to feel a semblance of warmth, Gill takes us through the 20-month wilderness of Long COVID. In this episode, we dig into the "stew of symptoms" that forced a high-functioning pro into bed rest and the radical neuroplasticity workshop that eventually helped her "climb out" and reclaim her life.

Gill’s new book, A Love Affair with the Unknown, is available now.

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Imagine being 21 years old, trapped in a two-week coma, completely unable to move or speak, while your sister leans over your bed and confesses her deepest darkest secret to you, and you hear the whole thing.

This week, we sit down with Melanie, who at 21 years old, went from a "parking lot" migraine on the 401 to a life-saving brain surgery that left her in a two-week coma . But Melanie wasn't just "asleep"—she describes a vivid, "locked-in" experience where she heard every secret her friends whispered and saw her aunt’s birthday wishes in brushstrokes of pink and purple. Melanie shares her "heritage moment" journey of proving every ableist professor wrong by becoming the first legally blind person to graduate from teachers' college in Ontario, despite the system betting she wouldn't make it to Christmas. Melanie’s story is a masterclass in why you should never tell a "determined" woman what she can’t do.

Check out the incredible work Melanie does: https://connect4life.ca/

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Briefing the President one day, forgetting how to cook bacon the next. What happens when a high-achieving powerhouse (Harvard grad, Wall Street alum, and Obama White House staffer) suddenly loses her most prized asset: her mind? Marisa Renee Lee joins the boys to get brutally honest about her "dumpster fire" journey with Long COVID. From the visceral pain of biting through a night guard in her sleep to the terrifying moment her larynx was 70% blocked while on a "restorative" trip to Greece, Marisa’s story is a raw look at identity, ego death, and the absolute chaos of a body in revolt. We dive into the controversial intersection of vaccine injury and infection, the skepticism Black women face in the U.S. healthcare system, and the three questions that forced her to reframe her life as "currently disabled".

For all things Marisa - https://www.marisareneelee.com/about

You can watch this entire episode over on YouTube.

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You know that irrational fear that a simple sore throat or a gym injury might actually be something way worse? Well, for Scott, that nightmare became a reality in the most terrifying way possible. At 35, Scott was living the dream as an elite, nationally ranked college soccer coach. He was unstoppable—until he wasn't. After feeling under the weather which doctors initially dismissed as a minor illness turned out to be Group A Strep, which rapidly evolved into Necrotizing Fasciitis (the media loves to call it "flesh-eating disease," but Scott sets the record straight). He woke up a month later from a coma to discover he had become a quadruple amputee. It’s a story about losing your body, finding your heart, and the resilience it takes to keep playing the game.

Scott's book 'Play From Your Heart' is available now for pre-order: https://librarytalespublishing.com/products/play-from-your-heart

You can watch this entire episode over on YouTube.

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It’s been eight years since Marnie first sat down with the fellas, and let’s just say… things haven’t exactly slowed down. Back in 2018, Marnie was a 23-year-old trying to navigate her mother’s sudden and terrifying diagnosis of paranoid schizophrenia. Now, at 31, she’s back in the studio to give us the raw, unfiltered update on what happens after the diagnosis. Marnie takes us through the absolute rollercoaster of the last few years. From her mom’s near-death experience involving a ruptured bowel (and the subsequent delusions that the doctors harvested her organs) to the detective work required to figure out why her mom is buying furniture for imaginary tenants. We get deep into the heavy stuff: the crushing anxiety of wondering if you’re going to inherit your parent’s illness, the guilt of moving across the country to save your own sanity, and the weird, heartbreaking reality of "parenting your parent" before you’ve even had kids of your own.

Check out Marnie’s podcast:

Giddy Up: https://open.spotify.com/show/5FjHKJoPzNOehPX2B1qr1X?si=fe429e23dec640c0

Instagram: @gidddyyyup

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