This week is what the kids would refer to as Gnar Gnar. We sit down with Ashleigh to talk about her traumatic experience of giving birth to her second child. She suffers "3rd world country type injuries" due to several complications. We're talking about things like gestational diabetes pumping sugars into the baby to create an unborn Hodor. A baby with a broken shoulder from birth. A pelvic organ prolapse (specifically a bowel and a bladder prolapsing into Ashleigh's vagina) and more. Jeremie could barely hold it together, so if you already are squeamish with birth stuff, good luck. Massive shoutout to Ashleigh for being a powerhouse and holding down the fort.
Chris Muise might sound like a cool country rock star. But no, he's a reporter living with a hella rare disease. This episode is chalk full of big words. Vasculitis! Aosinophils! Wrestlemania! Chris lives with a variation of a disease that only effects 1 in 6,000,000. Take a moment and read that again. Childhood Churg Straus Syndrome comes in stages and each one is as awful as the next. Buckle up for a wild story heartwarming story of a wandering billionaire making dreams come true near the end of the episode!
Meet Lainie! Three years ago she found a small bald spot on her head. Since that date, she has lost every single hair on her head cyclically at least twice! This week we take a deep dive into the world of Alopecia! Lainie gives us the rundown on life as a balding woman and the wild treatments in order to deal with her situation. Rogaine anyone? Who is the newfie Jew? The MADMAX look is so in right now. Also is it a wig? Or is that her hair? Brian makes a shocking discovery.
What consists of a good death? According to Caitlin Doughty, It is staring down your death fears—whether it be your own death, the death of those you love, the pain of dying, the afterlife (or lack thereof), grief, corpses, bodily decomposition, or all of the above. Accepting that death itself is natural, but the death anxiety of modern culture is not. Caitlin is a mortician, activist, and funeral industry rabble-rouser. We dive deep into the different ways in which the world deals with death. From raking hot bones out of an oven to vultures ceremoniously eating human remains to wrapping bodies in a shroud and burying it three feet under the earth, there are many options for us to plan our death. This episode is not to be missed!
This week we come to you from Jeremie's ultra slick looking private hospital room! Everyone's favourite Sickboy host (obviously) was rushed to the ER after doing his best "death in a Quinten Tarantino film" impression by spewing movie FX amounts of blood out of his mouth with every cough. Don't worry, he's okay! Plus it gave us an opportunity to sit down and talk about the latest in weird and wild health news! From cures to HIV, to dudes eating their own body parts, to horrifyingly disgusting hospital food and beyond!
There is much to be done about hate extremism in the world today. But what can we do about Love Extremism? Ethan Lipsitz is on a mission to spread more love. Especially after his experience with brain cancer. What started as a terrifying seizure in his bed one night quickly turned into a scenario where he and his healthcare team needed to race against the clock to remove as much of a tumour as they could. Buckle up for a wild story and some extreme love!
The sun is always shining in beautiful LA, but it seems to shine even brighter at Justin Baldoni’s house. This week we sit down with easily one of the most genuine and charming humans we’ve ever met. Justin is an American actor, director and filmmaker. His latest film ‘Five Feet Apart’ is about to put Cystic Fibrosis on the motha f***in’ MAP! This beautiful and endearing film tells the story of Seventeen-year-old Stella who spends most of her time in the hospital as a cystic fibrosis patient. Her life is full of routines, boundaries and self-control -- all of which get put to the test when she meets Will, an impossibly charming teen who has the same illness. This week we talk about the process of creating a film that will simultaneously speak to the masses and the cystic fibrosis community, The power of vulnerability, Being the most true and authentic version of yourself, and more. Huge shout out to our supporters on Patreon for this conversation wouldn’t have been possible if it weren’t for you.
Visit http://patreon.com/sickboy to support!
When Derric came out to his Dad, his father disapprovingly told him that he was going to get AIDS. Derric grew up in the Bible Belt, West Virginia, where in a lot of places being gay is still unaccepted. So a couple years later, when Derric tested positive for HIV, he was devastated. Opening up about his diagnosis was extremely challenging and within a short amount of time he moved west to be in a more accepting and supportive community. Derric's story is incredibly important because living with HIV and being gay is still wracked with stigma, which makes it hard for Derric to talk about it. By sharing his story he hopes that people living with similar challenges feel less alone and we know that this will resonate deeply with a lot of our listeners. Thank you, Derric for being vulnerable and open with us, you're a beautiful human being!
This week we take a deep dive into the past and present of nurse practitioner Verena Rizg. A conversation that taps into the nuances and complexities of faith vs culture when approaching grief. The boys finally get schooled on the difference between LPN, RN and Nurse practitioner (turns out LPN does not stand for Lower Paid Nurse, sorry dad) and a very much needed dive into how race effects both giving and receiving care.
This week we sit down with Estelle Thomson. Good friend and Nova Scotia yoga instructor and artist. We spend a solid 10 minutes beating around the bush and awkwardly avoiding the topic at hand... The death of Tommy, Estelle's two year old son. It's a perfect example of how so many of us are effected by the inability to know how to broach the tough subject of death. Estelle is a power house of a woman who has so much to teach the world about life, loss, and how to face the harsh realities of death. Thank you Estelle. Thank you Tommy.
Christa Angell is not related to Criss Angel but she knows a pretty gnarly magic trick. Like being born with her bladder on the outside of her body! AKA Bladder Exstrophy. We dive into full bladder reconstruction using sections of large intestine, self catheterizing, life long pelvic issues, acupuncture and Ayurvedic practices. But most importantly a full blown ASMR session near the end.
Aren Morris has spent a career changing the lives of a bunch of snot nosed kids from Sackville. She was basically Jeremie's Robin Williams and he was her Matt Damon. This ex drama teacher/competitive improv coach is moving through life dealing with a crippling case of Rheumatoid Arthrisis. From beautiful physiotherapists to highly aggressive rub & tugs this conversation goes ALL over the map with laughs and love.
In July of 2017 Molly was newly engaged to her partner of six years and beginning to think about starting a family. One day, out of nowhere, she felt a weird pain in her left breast. She instinctively reached her hand to the site of the pain and felt an obvious lump protruding from her side. Breast Cancer wasn't the first thing to cross her mind... she was only 29...
On this week we talk about Molly's experience being diagnosed, her physical treatment, and, even more importantly, Mammalgrams... they're like the animal crackers of boob exams...
This week is FULL of laughs, but don't get it wrong. Diabetes is not funny. Kylie joins the fellas in Halifax to drop knowledge on nearly 350 people about what life with diabetes is like. From the adorable sing songs at diabetes camp, to the most expensive liquids in the world, to Brian's Kale addiction, to giving yourself herpes, to shoving dirty needles into boys fingers, we this episode dives deep. Grab some Cineplex popcorn and an extra large coke and enjoy!
Tanya is your friendly neighbourhood family doc, or at least she was. She's been on leave for a good chunk of time because she's nasty boo boo in her blood. Leukaemia to be specific. This week we learn how cancer doesn't discriminate - doctors get it too! How being a doc can prepare you, in a way, for whats to come with cancer treatment. And we also find out that Brian really needs to deal with that twin brother health card identity fraud ordeal.
It might sound like a Lord Of The Rings character... however Tetralogy of Fallot is actually a combination of four congenital abnormalities in the heart. Sophie literally started from the bottom, now she here. And by bottom, we mean she was born in literally the worst rated hospital in her home country. A wild journey has brought her to where she is today! An exceptional young women with a funny foreign accent ;)
To follow Sophie's story check out her blog:
Mylene is like a real life stretch armstrong! Although this may sound like a super power, it most certainly is not. Loose joints may help with flexibility but this is just a small part of life with Ehlers-Danlos Syndrome. From chronic pain, to insomnia, to jacked up adrenalin levels, the fellas and Mylene dive in deep into life with EDS!
Meet Laura! A part time mad food scientist, story telling, should be rapper living in New York. She lives with a rare genetic skin disorder called genetic skin disorder. Sure her skin is flakey and dry but it goes SO much deeper than just that. Horribly painful, constantly sloughing off, hours upon hours of daily maintenance. This week Laura leads the fellas through the meaning of Spoon Theory, stories of a painful childhood into adulthood, the difference between pain tolerance and threshold and much much more.
Alexis was born missing a large portion of her left arm. This didn't stop her from following her dreams of having her own successful YouTube cooking show. Nor did it stop her from doing anything she damn well pleases! Live from SAIT the fellas and Alexis have a giggle filled conversation about disability, naming your limbs, the benefit of having a stump for a kitchen tool, sex, stump biting and more.
Sh*t happens. And so does menopause! This week the fellas tap back into their female anatomy knowledge with the help of Shirley Weir, the founder of the online community Menopause Chicks. Her goal? Empowering women to navigate perimenopause and menopause with confidence and ease! Did you know that menopause isn’t just for old ladies? Did you know that the ovaries are different than the eggs? Of course you do. You’re not some dodo like Jer-Bear.
How does one live while born with huge hole in their infant heart? When your heart fails how do you survive?! Medical advancements have come a long ass way! The fellas sit down this week with Callie, a west coast gal who has had countless surgeries to fix a broken heart. Not through love loss, just through a congenital heart defect.
Unlike Bob Marley, Oliver went through with removing a hunk of one of his cancer ridden digits. Unfortunately that didn't stop the cancer. From fingernail, to lymph and beyond Oliver has the "Bad" skin cancer. Was it from a mole? Too much sun? Well, chances are it was hereditary. Oliver is a well spoken dude who continuously drops knowledge on the fellas in this weeks episode.
"This is going to get really intimate, really fast." This week we are talking about the vagina! Specifically a painful vagina. Michelle has spent her whole life experiencing an extremely sensitive and painful vulva. From excruciating "Q-tip tests", to discomfort from tampons, to the near impossibility of sex, it's been a rough road to recovery. The good news is, PVD can be treated! And spoiler alert - this episode has a happy ending.
What is it like to have a 4 year old living with complex medical issues? Tough as sh*t. But Kaiti is a BAMF Mother! Her beautiful little daughter Layla was once considered a "Floppy baby". She is unable to hold her neck up, sit, stand, walk, talk. After a 2.5 year search between Ontario and BC she was accepted to the Undiagnosed Disease Network at UCLA and were able to finally walk away with a diagnosis. She has PCH2d. It's a progressive, life limiting diagnosis. Parenting a first born is never easy. But nothing can prepare someone for parenting a first born who may die before their 5th birthday.
Tracy is not pregnant. She may look pregnant, but she for sure is not. So don't ask her how far along she is. Don't touch her belly and exclaim "Ohhhh he's gonna be a soccer player". So why does she look pregnant? Why does her pee look like coca-cola? Why does she need blood thinners or have countless blood transfusions? Because Tracey lives with a rare life threatening disease called Paroxysmal nocturnal hemoglobinuria (PNH).