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Videos

June 4, 2024

Is There a Cure for Sleeping Beauty Syndrome?

Is There a Cure for Sleeping Beauty Syndrome? #kls #sleepingbeautysyndrome #raredisease #medicalpodcast

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May 31, 2024

Living with KLS: The Realities Behind Sleeping Beauty Syndrome

Living with KLS: The Realities Behind Sleeping Beauty Syndrome #kls #sleepingbeautysyndrom #narcolepsy #raredisease

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May 28, 2024

Understanding the Difference Between Narcolepsy and Sleeping Beauty Syndrome?

Understanding the Difference Between Narcolepsy and Sleeping Beauty Syndrome? #narcolepsy #kls #raredisease #sleepingbeauty

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May 21, 2024

Is Jordan Syndrome More Common Than You Think?

Is Jordan Syndrome More Common Than You Think? #jordansyndrome #raredisease #podcast #shorts

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May 14, 2024

The Dangers of Comparing Children's Development Milestones

The Dangers of Comparing Children's Development Milestones #miestones #rarediseases #podcast

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May 7, 2024

The Journey of Diagnosis: Understanding Jordan Syndrome

Join us on a fascinating journey as we delve into the world of Jordan syndrome with Michelle and her daughter. Discover the unique challenges and triumphs faced by individuals living with this ultra-rare neurological disorder. Don't forget to hit subscribe for more insightful discussions on medical conditions like this! #medicalpodcast…

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April 25, 2024

Donate Life Month! Revisit with Molly!

Join us for an inspiring discussion with Molly, a living liver transplant recipient, as she shares her journey during Donate Life month. Find out how a close friend changed her life through organ donation and learn how you can make a difference at registerme.org. Subscribe for more heartwarming stories and…

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April 23, 2024

Understanding the Autism Spectrum: Breaking Stereotypes and Promoting Awareness

Understanding the Autism Spectrum: Breaking Stereotypes and Promoting Awareness #autism #asd #autismdad #shorts

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April 21, 2024

My Life Battling Sleeping Beauty Syndrome (KLS) | Bethany's Incredible Story

Have you heard of Kleine Levin Syndrome (KLS) or "Sleeping Beauty Syndrome"? In this captivating episode of The Medical Maze podcast, we sit down with Bethany, who bravely shares her journey living with this extremely rare condition that causes her to sleep for weeks at a time. Bethany discusses the…

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April 21, 2024

April is Autism Awareness/Acceptance Month: A Father's Powerful Story of Severe Autism

As April comes to a close, we at The Medical Maze podcast honor Autism Awareness/Acceptance Month with a raw and unflinching look at the often misunderstood world of severe autism. Join us as we sit down with Phil, the father of 11-year-old Dominic, who bravely shares his family's heart-wrenching journey.…

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March 30, 2024

How My Child's Diagnosis Transformed My Faith

How My Child's Diagnosis Transformed My Faith #faith #medical #raredisease #shorts

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March 18, 2024

How my Parents Helped Save my Son's Life with Ice Baths

How my Parents Helped Save my Son's Life with Ice Baths #pma #raredisease #disease #medicalpodcast

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March 13, 2024

Understanding the Origins and Traits of a Rare Condition

Understanding the Origins and Traits of a Rare Condition #PMA #raredisease #medicalpodcast

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March 7, 2024

Understanding the symptoms of Sickle Cell

Understanding the symptoms of Sickle Cell #sicklecell #sicklecelldisease #raredisease #medicalpodcast

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March 1, 2024

Owning Your Own Business with Sickle Cell

Owning Your Own Business with Sickle Cell #sicklecell #businessowner #shorts #podcast #raredisease

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Feb. 27, 2024

Coping with Sickle Cell

Coping with Sickle Cell #sicklecell #disease #raredisease #sicklecellanemia

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Feb. 25, 2024

Living with Sickle Cell Disease: A Personal Journey

Living with Sickle Cell Disease: A Personal Journey #sicklecell #sicklecelldisease #sicklecellanemia #raredisease #diagnosed #medicalmaze

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Feb. 19, 2024

337,000 People have this RARE Disease

337,000 People have this RARE Disease #pku #raredisease #illness #shorts #podcast

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Feb. 18, 2024

My Son Has a Rare Brain Cancer No One's Heard Of

In this powerful and moving episode of The Medical Maze podcast, host Don-Ellen Ray has an intimate conversation with her cousin Brooke Abner about her son Jackson's courageous battle with a rare brain tumor called Pilomyxoid Astrocytoma. Brooke vulnerably shares the heartbreaking challenges and miraculous triumphs her family has faced…

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Feb. 18, 2024

She Lives with Razor Blades in Her Blood: One Woman’s Raw Story of Battling Sickle Cell Disease

Can you imagine living every day with shards of glass slicing through your veins? That’s the agonizing reality for my courageous guest Cameron, who shares her deeply personal story of fighting sickle cell anemia since birth. Even the slightest weather change or emotional stress can trigger grueling, week-long hospitalizations filled…

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Feb. 13, 2024

Symptoms of PKU in Children

Symptoms of PKU in Children #pku #developmentaldelay #shorts #podcast #raredisease Dan Ellmer, who was diagnosed with the rare inherited metabolic disorder phenylketonuria (#PKU) as a child. He shares his remarkable story of living with this condition that causes intellectual disability if undiagnosed. Dan explains what PKU is, how it's screened…

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Feb. 7, 2024

Understanding PKU. How Missing Enzyme Impacts Protein Breakdown #shorts

Understanding PKU. How Missing Enzyme Impacts Protein Breakdown #raredisease #genetics #disability #healthpodcast #chronicillness #invisibleillness #advocacy #epigenetics #publichealth #enzymedisorders

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Feb. 4, 2024

I Can't Have Protein or My Brain Stops Working: Living with PKU

We speak with Dan Ellmer, who was diagnosed with the rare inherited metabolic disorder phenylketonuria (#PKU) as a child. He shares his remarkable story of living with this condition that causes intellectual disability if undiagnosed. Dan explains what PKU is, how it's screened for at birth in some countries, why…

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Dec. 6, 2023

Looking Forward to 2024

Looking Forward to 2024 #heresto2024 #surgery #newyear #podcast #update #Rarediseases

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