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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.

04/16/2026

Sandra is a woman living with Pompe disease, a rare genetic disorder that can degrade a person's muscles.

Although her diagnosis changed everything, it didn’t affect her resolve to keep fighting.

Follow us for more & watch Sandra’s full story here: https://shorturl.at/6TtVs

04/15/2026

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Pompe disease is a rare, genetic neuromuscular disorder that causes progressive muscle weakness due to a buildup of glycogen in the body’s cells.

Today, during International Pompe Day, we're raising awareness for those with the disease as well as their families and friends helping them live with this life-changing condition. Sloths represent Pompe awareness because muscle weakness and slowed movement are key symptoms of the disease.

Thousands of people worldwide are living with Pompe, many still searching for answers.

Share this post for Pompe awareness & go here to watch the story of Sandra, who was diagnosed with Pompe late in life: https://shorturl.at/6TtVs

04/13/2026

What started as unexplained symptoms became a decade-long journey for Sandra to get a proper diagnosis. But now that she knows what’s ailing her, she’s determined not to let it slow her life down.

Sandra has Pompe disease, a rare genetic disorder that can cause progressive muscle weakness.

International Pompe Day is April 15, a time to raise awareness about Pompe disease and the importance of early diagnosis and treatment. We're highlighting Sandra’s story this week in honor of the Pompe community.

Stay tuned for more & watch Sandra’s full story here: https://shorturl.at/6TtVs

04/10/2026

Alyssa is a mom, entrepreneur, and triathlete. She built businesses, raised three amazing children, and trained hard, until her diagnosis of Cushing’s disease changed everything.

But she doesn’t let that stop her.

Follow us for more & watch Alyssa’s full story here: https://tinyurl.com/55uy4x83

04/08/2026

Share this post to help raise awareness for Cushing’s disease and the importance of early diagnosis.

Alyssa is a mom of three, an entrepreneur, and a former competitive triathlete. When rapid weight gain, fatigue, brain fog, and muscle weakness took over her body, she knew something wasn’t right.

After months of testing, she was diagnosed with Cushing’s disease, caused by a pituitary tumor producing excess cortisol.

As part of Cushing's Awareness Day, we're sharing Alyssa's story again. Thousands of people, just like Alyssa, are living with Cushing’s disease, and many more are likely undiagnosed. The longer a diagnosis is delayed, the longer recovery can take.

Through surgeries, medical therapy, and holistic care, Alyssa continues to fight, and today, she’s training again.

Follow us for more powerful stories & watch Alyssa’s full story here: https://tinyurl.com/55uy4x83

04/06/2026

Alyssa is a triathlete and mother of 3 whose body started changing in ways she couldn’t explain. She eventually found the answer when she was diagnosed with Cushing’s disease, a rare hormonal disorder caused by excess cortisol.

April 8 is Cushing’s Awareness Day, a time to raise awareness about this rare condition. So this week, we’re highlighting Alyssa’s story.

Follow us for more & watch Alyssa’s full story here: https://tinyurl.com/55uy4x83

04/03/2026

Janelle was always the active one, chasing grandkids around the yard, hosting family, and never slowing down.

Then her legs stopped cooperating.

The falls started.

And everything changed.

Janelle was diagnosed with a rare autoimmune disease called LEMS. There’s no cure, but that doesn’t mean there’s no hope.

Follow us for more & watch Janelle’s full story here: https://shorturl.at/2rc74

04/01/2026

A devoted grandmother, wife, and lifelong fitness lover, Janelle has had to learn to navigate life with a rare autoimmune disease called LEMS.

Her life looks different today, but her resilience has never been stronger.

Follow us for more & check out Janelle’s full story here: https://shorturl.at/2rc74

03/30/2026

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Today is Lambert-Eaton Myasthenic Syndrome (LEMS) Awareness Day, a day to raise awareness for a rare autoimmune disease that weakens the connection between nerves and muscles and is often misdiagnosed.

Janelle is a wife and a grandmother of five. She’s also a fitness lover and a fighter. After years of always being active, she began experiencing unexplained weakness, falls, and fatigue. In 2019, she was diagnosed with LEMS, a rare condition that can impact mobility, independence, and quality of life.

Unfortunately, there is no cure, but with treatment, faith, family, and resilience, Janelle continues to move forward every day.

Share this post to spread awareness & watch her full story here: https://shorturl.at/2rc74

03/28/2026

He ran 15 miles the morning he learned had cancer.

Now, Kenny’s running toward hope, for himself and others living with multiple myeloma.

Share his story to spread awareness about multiple myeloma & watch his full journey here: https://tinyurl.com/2umf24jb

03/27/2026

Meet Kenny! As an active, long-distance runner, whose friends considered him the healthiest guy in the room, Kenny enjoyed pushing his limits, improving his stamina, and staying strong through miles of running in the mountains of North Carolina.

But when he learned he had multiple myeloma, everything changed.

With the help of the people by his side, Kenny found the strength to go the distance in his battle against the disease.

We’re excited to share Kenny’s story as part of Multiple Myeloma Awareness Month.

Follow us for more & watch Kenny’s full story here: https://tinyurl.com/2umf24jb

03/26/2026

Share this post to spread awareness about multiple myeloma.

Multiple myeloma is a blood cancer that begins in plasma cells, a type of white blood cell. About 543,000 people are living with the disease worldwide. Today, on International Myeloma Action Day, we’re highlighting their struggle.

Follow us for more, and check out the story of Kenny, a long-distance runner who was diagnosed with multiple myeloma, by going here: https://tinyurl.com/2umf24jb

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