Symptomatic: A Medical Mystery Podcast

Suffering from inexplicable sores & excruciating pain since he was 5 years old, August searched to uncover what plagued so many years of his life and threatened his mobility. His dreams of a musical theater career quickly faded away as his condition worsened, so August decided to challenge the constant silencing of his symptoms and fight the cause of the irreversible physical damage.

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If you’re looking for more information on Behcet’s, you can check out the American Behcet’s Disease Association by heading to www.behcets.com. You can also find August Rocha on Instagram & TikTok @WithLoveAugust.

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Kam is rapidly losing her motor skills as she’s attacked by an unknown & unseen disease. In a matter of months, she goes from starring on her high school soccer team to struggling to make it up the stairs. Bouncing between doctors and facing countless misdiagnoses, Kam never wavers in her chase to uncover what is threatening to take away her mobility.

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For more information on GNE Myopathy go to CureGNEM.org and check out the first ever GNE myopathy clinic at UC Irvine’s neuromuscular center led by one of Dr. Korb’s colleagues. You can also find Kam Redlawsk on Instagram & Twitter @KamRedlawsk.

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Diagnosed at a young age, Antoinette has dealt with Sickle Cell all her life. It’s not until she’s older that she realizes her Sickle Cell is unlike any case her doctor has seen before. With deliberating symptoms and multiple crises, Antoinette turns to her doctor for a life changing diagnosis.

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To find out more information on Sickle Cell disease visit the Sickle Cell Disease Association of America at sicklecelldisease.org.

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Kyle was in the ER for a break or sprain almost every month. The injuries were too frequent & too severe to be written off as Kyle just being an active kid. There was something larger at work here. Doctors found a growth on Kyle’s spine that thrusts him onto a rollercoaster ride trying to find the source of the problem before permanent damage is done.

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To find out more information on EDS visit the Ehlers-Danlos Society at ehlers-danlos.com or listen to Dr. Bluestein’s podcast - Bendy Bodies with the Hypermobility MD - wherever you get your podcasts.

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Shelby was a freshman in college when she got mono - something that, though draining, is very common in school-age kids. But her mono wasn’t like anything her friends or family had ever seen before. As her condition turns life-threatening, stumped doctors search for answers before it is too late for her or her unborn child.

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To find out more information on POTS, visit StandingUpToPOTS.org.

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Zach was your average 11-year-old who loved pizza, sports, and going fishing with his Dad until an incident at a baseball game changed his life forever. As an illness quickly takes hold and wreaks havoc on his body, it’s a race against the clock to figure out what’s happening and save Zach’s life.

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To find out more information on Sepsis, visit Sepsis.org.

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As a young teenager, Athena began experiencing pimple-like abscesses in various areas of her body. For years, doctors attributed the painful lesions to poor hygiene, shaming Athena into internalizing and enduring her chronic inflammatory condition in silence. Pushing through pain, embarrassment and self-blame, Athena meets a young doctor who finally gives her hope - and a name - for her disorder.

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If you’re looking for more information on Hidradenitis Suppurativa, you can check out the Hidradenitis Suppurativa Foundation by heading to HS-Foundation.org. You can also explore Athena Gierbolini’s work with Hope for HS.

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Nyobie grew up knowing there was something different about her body. As a young woman, she was plagued by unexplained symptoms doctors initially dismissed as part of puberty. But persistent pain and swelling in her arms and legs were just the beginning of her battle. After 19 years of being silenced and misled, Nyobie finally found a life-changing doctor - and diagnosis.

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If you’re looking for more information on Lupus, you can check out the Lupus Foundation of America by heading to Lupus.org. You can also learn more about Nyobie Gordon-Rick and the work of National Health Educator Leticia Ocaña.

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Nearly half of all Americans suffer from a chronic illness and many struggle for an accurate diagnosis. Welcome to “Symptomatic: A Medical Mystery Podcast,” a brand new podcast from iHeartRadio. Each week, host Lauren Bright Pacheco (Happy Face, Murder in Oregon) unravels the medical mystery of a patient’s baffling symptoms and explores how their lives were turned upside down in search of answers.

From the first signs of trouble, through a swirl of misdirection and failed treatment attempts, to the final relief at a confirmed diagnosis - these are their stories.

Listen to the first episode of “Symptomatic: A Medical Mystery Podcast"on October 10th, 2022.

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