Medical Stories

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...

01/23/2026

Today, we recognize BPDCN Awareness Day! Share this post with someone you know to spread awareness about BPDCN.

Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare and aggressive blood cancer that often first appears as skin lesions before affecting the blood, bone marrow, or lymph nodes. Because it can look like other conditions, diagnosis is often delayed, making awareness critical.

For Robert, it all started when he noticed a strange spot on his skin, which eventually led to a BPDCN diagnosis. But through treatment, a bone marrow transplant, and the support of his family, he continues to move forward with hope.

By sharing stories and supporting research, we can help improve understanding, diagnosis, and outcomes for those living with BPDCN.

Want to learn more? Watch Robert’s journey with BPDCN here: https://shorturl.at/mzkDh

01/22/2026

Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare blood cancer, often first showing up on the skin

Robert’s diagnosis led to treatment, remission, and a life-saving bone marrow transplant, with his wife, Valerie, and his son, Ross, by his side every step of the way.

BPDCN Awareness Day is this Friday, January 23. Learn more about Robert’s diagnosis by following us & watching his full story here: https://shorturl.at/mzkDh

01/19/2026

When Robert first noticed something unusual on his skin, it started him on a journey that changed everything.

He was eventually diagnosed with blastic plasmacytoid dendritic cell neoplasm (BPDCN), a rare blood cancer. But through treatment, remission, and a life-saving bone marrow transplant, Robert found the strength to persevere, especially when his son, Ross, stepped up in the biggest way.

BPDCN Awareness Day is January 23, a day to raise awareness, share hope, and support those affected by this rare blood cancer.

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