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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.

03/13/2026

Follow us and share to help spread kidney health awareness.

In celebration of kidney health and the millions living with kidney disease, this week we’re amplifying real human stories that remind us why early detection matters.

Kidney disease is often silent in its earliest stages, showing little to no symptoms until significant damage has occurred. Simple blood and urine tests can make all the difference.

Share this post to spread awareness about kidney disease. And watch the stories of Jeff and B.T., two individuals diagnosed with kidney diseases, by going here: https://shorturl.at/Dhfn9

03/11/2026

After 30 years in the Air Force, B.T. thought retirement would mean slowing down. Instead, he faced chronic kidney disease, a silent condition that progressed to end-stage kidney failure.

After beginning home dialysis, B.T. still found ways to live his life fully: exercising daily, restoring cars, and embracing life with perspective and purpose.

Follow us for more & watch B.T.’s full story here: https://shorturl.at/E3gnL

03/09/2026

Jeff was blindsided when a routine physical uncovered something far more serious: IgA nephropathy, a rare kidney disease that often has no symptoms until the damage is already done.

What started as an unexpected test result became a lifelong journey of monitoring, treatment, and faith. But Jeff is using his story to raise awareness so others can be diagnosed earlier and protect their kidney health.

March 12 is World Kidney Day, a day to raise awareness about kidney health and the importance of early detection. We’re highlighting stories like Jeff’s this week to shine a light on kidney diseases and the people living with them.

Follow us for more & watch Jeff’s full story here: https://shorturl.at/A1ttd

03/06/2026

Sumaira is a former dancer who experienced strange symptoms like vision loss and nerve pain before she was finally diagnosed with neuromyelitis optica (NMOSD), a rare autoimmune disease.

While at first the condition left Sumaira debilitated, she refused to let it define her life, eventually deciding to start a foundation (The Sumaira Foundation) to raise awareness and support research for this rare disease.

March is NMOSD Awareness Month, a time to educate, advocate, and amplify the voices of those living with this rare disease.

Follow us for more & watch Sumaira’s full story here: https://tinyurl.com/37cnwbh4

03/04/2026

Follow us for rare disease stories that matter.

Neuromyelitis optica spectrum disorder, or NMOSD, is a rare autoimmune disease that can lead to blindness, paralysis, or life-threatening complications. Because it's a rare condition, it is often misdiagnosed or misunderstood.

People living with NMOSD face unpredictable attacks on their body that can permanently change their lives. Like Courtney, Sumaira, and Deshon, many must rebuild their futures after devastating setbacks.

NMOSD Awareness Month is dedicated to education, early diagnosis, and advancing research. During this month, we stand with those with the disease, as well as caregivers and advocates working toward better treatments and ultimately, a cure.

Share this post for awareness & watch our story highlighting NMOSD here: https://tinyurl.com/37cnwbh4

03/02/2026

These three inspiring individuals are living with neuromyelitis optica spectrum disorder (NMOSD), a rare autoimmune disease.

Courtney is a violinist and music teacher who lost her vision but never lost her love for music.

Sumaira is an advocate and foundation founder. She turned her diagnosis into a mission to raise awareness and fund research.

Deshon is a young fighter and community leader. He faced rapid paralysis and vision loss yet continues to push forward with strength and faith.

March is NMOSD Awareness Month, a time to elevate patient voices and spotlight the urgent need for early diagnosis and treatment.

Follow us for more about NMOSD & watch the stories of Courtney, Sumaira, and Deshon by going here: https://tinyurl.com/37cnwbh4

02/27/2026

After losing his naval aviation career because he was diagnosed with Wilson disease, a rare genetics disorder, Cory found new purpose in love, learning, and hope for the future.

Like Cory, over 300 million people around the world are living with rare diseases. February 28 is Rare Disease Day, so we’re highlighting stories like Cory’s this week to raise awareness for the rare disease community.

Follow us for more & watch more rare disease stories, including Cory’s, by going here: https://shorturl.at/qCQil

02/25/2026

For most people, cuts and scrapes on your skin are nothing to worry about, but for Luke and his family, they’re potentially deadly.

Luke has WHIM syndrome, which affects his immune system’s ability to fight infections. The condition has impacted three generations of Luke’s family, including his son and his mother, but with vigilance, treatment, and hope, they continue to live full, active lives together.

WHIM syndrome is a rare disease, with only about 100–200 cases in the U.S. Rare Disease Day is this Saturday, February 28. Let’s raise awareness, support research, and stand with families facing rare conditions.

Follow us for more & check out more rare disease stories, including Luke’s story, by clicking here: https://shorturl.at/qCQil

02/23/2026

Growing up, Charlie experienced most of the world in a protective bubble – because of a rare condition he had.

Charlie was born without T cells due to congenital athymia, meaning he lacked a functioning immune system. For the first few years of his life, he was only rarely allowed outside to enjoy occasional car rides.

But today, he’s thriving, finally able to play, connect, and simply be a kid.

Rare Disease Day is on February 28, a day to shine a light on the 300 million people worldwide living with rare conditions and the families who stand beside them. This week, we’re highlighting rare disease stories like Charlie’s to spread awareness and inspire action.

Follow us for more & watch more stories about rare diseases, including Charlie’s story, by going here: https://shorturl.at/qCQil

02/20/2026

Georgia, a lifelong California resident, loves tending to her farm and staying active on her land.

But after years of suffering shortness of breath that was getting worse and worse, Georgia learned she had a heart condition called mitral valve regurgitation.

But she found new hope through a minimally invasive heart valve treatment.

In honor of American Heart Month, we’re sharing stories that educate, inspire, and empower.

Follow us for more & watch Georgia’s full story here: https://shorturl.at/89qN4

02/18/2026

Heart disease was never a concern of Georgia’s, whose parents lived into their 90s with few health problems. So it came as a shock when she was diagnosed with a heart ailment known as mitral valve regurgitation.

While in the beginning Georgia feared the worst, with the support of her family and a life-changing procedure, she’s back to living her life the way she intended.

Follow us for more & watch Georgia’s full story here: https://shorturl.at/89qN4

02/16/2026

Follow us for more stories that raise awareness and inspire hope.

American Heart Month is a time to educate, advocate, and shine a light on heart conditions that impact millions of people every year, including heart valve disease.

One of those people is Georgia, who has mitral valve regurgitation (MVR), one of the most common valve conditions. It can cause shortness of breath, fatigue, and heart failure if left untreated.

We stand with anyone going through heart disease, treatment, or recovery, and the families supporting them every step of the way.

Watch Georgia tell her story of battling MVR here: https://shorturl.at/89qN4

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