Medical Stories

Medical Stories Emmy-winning docuseries. Behind every diagnosis, there’s a powerful story worth sharing.

Disclaimer: Medical Stories and all content provided are intended solely for informational purposes and should not be construed as medical advice. Always consult with a qualified healthcare professional for personalized guidance regarding your health. Reliance on any information presented here is at your own discretion and risk.

06/18/2026

Emma’s parents knew something was different with her when she was still a toddler.

While other kids ran at daycare, Emma could only walk. She’d wake up in the middle of the night screaming that her legs were in pain. And she had to get a root canal at age 3.

It wasn’t until later that Emma was diagnosed with X-linked hypophosphatemia, or XLH, a rare genetic disorder that weakens an individual’s bones and teeth.

Emma’s mother, Bridget, walks us through the ups and downs of trying to get Emma’s diagnosis, and how it led to her daughter finally getting to enjoy life as a teenager.

Watch Emma's journey here: https://youtu.be/BmELK9LKVEc?t=38. And follow us for more inspiring stories.

This episode also features in-depth commentary from renowned expert Jill Simmons, MD, Professor of Pediatrics, Vanderbilt University School of Medicine.

06/15/2026

Julie was dead for about five minutes before her husband saved her life.

Julie has HFpEF, a form of heart failure. The National Institutes of Health say it’s more common in women than men and accounts for at least half the cases of heart failure in women.

Today, Julie is in the best shape of her life and doing better than ever. She tells Medical Stories how she’s adapted to her condition, and how it even brought her closer to her husband, Gregg.

Watch Julie's story here: https://youtu.be/zF5ub8oKLNE?t=38

This episode also features in-depth commentary from renowned experts Clyde W. Yancy, MD, MSc, Chief of Cardiology, Northwestern Medicine, Bluhm Cardiovascular Institute, and Jane Wilcox, MD, Associate Chief of Cardiology, Northwestern Medicine, Bluhm Cardiovascular Institute.

06/11/2026

As a child, Nina battled constant health problems, including deformities in her hand and trouble with her spine. But it wasn’t until she was a teenager that she experienced a life-threatening emergency.

Nina suffered an aortic dissection, in which her aorta tore open, causing blood to split apart the artery.

Thankfully, doctors were able to save her life, but that was just the beginning of her ordeal, as she needed a transplant to prevent her from being hospitalized again.

Nina details how challenging her experience was, while also highlighting how her mom helped her endure the recovery process, even inspiring her to pursue a new dream.

Watch Nina's story here: https://youtu.be/wLEuC4j4y_s?t=36

Thank you to our collaborators, Aortic Hope and Think Aorta US, for helping us raise awareness of this condition. With their help, we're able to share Nina's story today.

This episode also features in-depth commentary from renowned expert James Black, MD, Professor of Surgery at Johns Hopkins University and Chief of Vascular Surgery at Johns Hopkins Hospital.

06/08/2026

As a cardiologist in Vero Beach, Florida, Howard was used to treating heart problems. But he was caught off-guard when he developed his own heart condition.

Howard has atrial fibrillation (AFib), an irregular and rapid rhythm in the upper chambers of the heart. It can lead to complications like stroke or heart failure, according to the Mayo Clinic.

Medical Stories documents how because of his background, Howard’s journey with AFib was unique – as well as the cutting-edge procedure that helped treat his condition.

Watch Howard's story right here: https://youtu.be/05-8p2Lp_iA?t=38

This episode also features in-depth commentary from renowned expert Vivek Reddy, MD, Director of Electrophysiology, Mount Sinai Fuster Heart Hospital.

06/07/2026

When Roxana first found a lump in her breast, she dismissed it as just another harmless cyst. But her situation soon took a turn for the worse.
Roxana was diagnosed with breast cancer, the same disease that her mother died of. Luckily, because it was caught early, she was able to undergo effective treatment. But it still took a toll on her, affecting her schooling as well as her fertility.

As Roxana shares her experience, she emphasizes the importance of her loved ones, whether it was her breast cancer support group, or her brother, Ronney.

We're sharing her story today as part of National Cancer Survivors Day, an opportunity to honor survivors and inspire others who have been recently diagnosed.

Watch Roxana's story here: https://youtu.be/-Ti5dlmwHsA?t=38

This episode also features in-depth commentary from renowned experts Carmen Calfa, MD, Breast Medical Oncologist Sylvester Comprehensive Cancer Center, and Mandy Hathaway, MD, Medical Oncologist University Cancer & Blood Center.

06/04/2026

Methi knew something was wrong when the hives on her body wouldn’t go away. And it would be nine years before she found relief.

Methi has chronic spontaneous urticaria (CSU), a condition in which red, itchy welts develop randomly all over her body, according to the Cleveland Clinic. The hives caused so much pain that she remembers “wishing I could scratch with a cheese grater.”

For almost a decade, Methi lived in despair, searching in vain for a treatment that would help her. But not only did she find relief, she also found a way to use her experience to give back to others.

Watch Methi's story here: https://youtu.be/DmmYEyAOUrM?t=37

This episode also features in-depth commentary from renowned expert Jonathan Bernstein, MD, Professor of Clinical Medicine, University of Cincinnati College of Medicine.

06/01/2026

Going back to the classroom after COVID was a challenge for lots of kids, but for Sam, it was even tougher – because he found that his classmates now towered over him.

Sam had growth hormone deficiency (GHD), which prevented him from developing like others his age. It wasn’t long before Sam started feeling isolated from his classmates because of his condition, and his mom, Meagan, realized something needed to be done.

Medical Stories sits down with Sam and Meagan as they relate how they discovered Sam’s deficiency – and the treatment that helped them address it.

Thank you to our collaborator, The MAGIC Foundation, for helping us raise awareness of this condition. With their help, we're able to share Sam's story today.

Watch Sam's story here: https://youtu.be/5meWgeoYBPU?t=35

This episode also features in-depth commentary from renowned expert Jose David Gamez, MD, Pediatric Endocrinologist, Driscoll Children's Hospital.

05/29/2026

Lauren knew something was different during her second pregnancy.

She had strange symptoms like enlarged feet and excessive sweating, but her doctors blamed it on diabetes. It wasn’t until after she gave birth that she learned she had acromegaly, caused by a tumor in her brain.

Acromegaly is a rare illness triggered by the pituitary gland in the brain that can cause the hands, feet, and other parts of the body to become larger than normal.

Luckily, Lauren’s diagnosis wasn’t a death sentence. Thanks to new treatments and the support of her husband, Lauren found a way to manage her disease – and even give back to the acromegaly community.

Watch Lauren's story right here: https://youtu.be/fwlHUCh5T5w?t=41

This episode also features in-depth commentary from renowned expert Wenyu Huang, MD, PhD, Endocrinologist, Northwestern Medicine.

05/28/2026

Rick was enjoying his retirement in Sarasota, Florida, when he started having severe leg pain.

After initial testing forced him to investigate further, he learned he had prostate cancer, the second-most common cancer in men in the U.S., according to the American Cancer Society.

But during his treatment, Rick not only kept a positive attitude – he found a way to give back that became his new purpose in life.

Watch Rick's story by clicking here: https://youtu.be/HtkzE-Y-PUw?t=41

This episode also features in-depth commentary from renowned expert Kosj Yamoah, MD, PhD, Chair, Department of Radiation Oncology, Moffitt Cancer Center.

05/26/2026

Sam’s parents, Tausha and Doug, noticed a lump on his neck one day that concerned them. A short while later, they learned he has pediatric acute lymphoblastic leukemia (pALL), a cancer of the blood and bone marrow, according to the National Cancer Institute.

But Sam’s case surprised his doctors as well, as he’s the first person with Down syndrome to have this type of disease.

That made Sam’s treatment twice as hard for both him and his family. But Tausha and Doug were still overwhelmed by the outpouring of support as their community rallied around their son.

Watch Sam's story by going here: https://youtu.be/arxRjqZkAI0?t=38

This episode also features in-depth commentary from renowned expert Luke Maese, DO, Pediatric Oncologist, Primary Children's Hospital, University of Utah Health.

Address

12000 Biscayne Boulevard
Miami, FL
33181

Telephone

+18666810204

Website

Alerts

Be the first to know and let us send you an email when Medical Stories posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Business

Send a message to Medical Stories:

Shortcuts

Share

Category