Medical Stories

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

02/14/2026

Happy National Donor Day!

Today, we honor the life-saving power of organ and stem cell donation, and the people whose generosity makes second chances possible.

Jordan is a heart transplant recipient, whose life was saved after an unexpected medical emergency led to an urgent transplant call in the middle of the night.

Walter is an acute myeloid leukemia (AML) survivor, whose journey included intensive chemotherapy, a relapse, and ultimately a life-saving stem cell transplant made possible by a donor’s selfless gift.

Two different journeys. One shared truth: donations save lives.

Join us in honoring donors and their families by sharing this post and spreading awareness.

Watch their full transplant journeys at the links below.

Jordan's story: https://tinyurl.com/4m4jbuk8
Walter's story: https://tinyurl.com/4rd3txcn

02/12/2026

Jordan is a father, husband, and heart transplant recipient who refused to give up, even when his heart function dropped to just 9%.

Through emergency surgery, a device known as an LVAD, and a breakthrough clinical trial, Jordan’s journey is a powerful reminder of hope, resilience, and the life-saving impact of organ donation.

Follow us for more & watch Jordan’s full story here: https://tinyurl.com/3fytx583

02/10/2026

This week, we’re highlighting two people who have gone through heart transplants.

First, we have Glenn, a husband, father, grandfather, and longtime New Yorker who faced heart disease for decades before receiving the gift of a new heart.

And we also meet Jordan, a devoted husband, father, and golf course superintendent. With the support of his wife and daughter, Jordan was able to navigate heart failure and ultimately a life-saving heart transplant.

Stay tuned this week to learn more about their powerful journeys. And don’t forget to watch their full stories here: https://tinyurl.com/3fytx583

02/09/2026

Share this post with someone you know to show your support for AMD & Low Vision Awareness month!

People like Nita remind us that vision loss doesn’t have to define a life. During AMD & Low Vision Awareness Month, we’re sharing her story to raise awareness, encourage regular eye exams, and highlight the hope made possible through early detection and treatment.

Nita is living proof that with support, care, and creativity, life can still be full and meaningful. Click below to check out her full story on our YouTube.

In this episode, Medical Stories visits Nita, a craftswoman living out her retirement in Florida with her husband, Dave. Nita suffers from age-related macula...

02/04/2026

Nita was diagnosed with age-related macular degeneration (AMD), a leading cause of vision loss in adults over 50.

But with proper treatment and the support of her husband, she continues to create, adapt, and thrive.

Follow us for more & watch Nita’s full story here: https://tinyurl.com/59xrnbek

02/02/2026

In Sarasota, Florida, Nita spends her time creating beach-inspired crafts alongside her husband, Dave.

While she lives with age-related macular degeneration (AMD) in both eyes, which severely affects her vision, it hasn’t stopped her from doing what she loves, or from living life to the fullest.

February is AMD/Low Vision Awareness Month, so we’re highlighting Nita’s story in honor of this month.

Follow us for more & watch Nita’s full story here: https://shorturl.at/183En

month

01/29/2026

Kira’s journey with Alagille syndrome includes years of treatment, a liver transplant, and ongoing recovery, showing strength, perspective, and determination every step of the way.

Often beginning in infancy, Alagille syndrome is a rare genetic condition that impacts things like growth, nutrition, and overall health.

Follow us for more & check out Kira’s full story here: https://tinyurl.com/59xrnbek

01/27/2026

When she was just a baby, Kira was diagnosed with Alagille syndrome, a rare genetic condition that affects the liver and how the body processes bile.

Her whole life, she’s faced liver disease, clinical trials, a transplant, and major surgeries, yet continues to move forward with resilience and hope.

Follow us for more & watch Kira’s full story here: https://tinyurl.com/59xrnbek

01/25/2026

Today is International Alagille Syndrome Awareness Day. Share this post with someone to spread awareness about this condition.

Alagille syndrome is a rare genetic condition, affecting about 1 in 30,000 children, that most often impacts the liver but can affect many parts of the body. While there is no cure, advances in treatments and research are changing what the future looks like for individuals with the disease.

Meet Kira. Her journey is a reminder of the strength of this community and the hope that continues to grow through awareness, connection, and innovation.

Follow us to learn more about Kira and Alagille syndrome, and watch her journey here:

Alagille syndrome is a very rare genetic condition occurring in 1 in 30,000 children that are born. When doctors discovered Kira's serious liver issues, gene...