Anyone With A heart

Anyone With A heart Johnny's Heart Organ Donor Page Johnny Boatman, a beloved father, husband, and decorated U.S. Army veteran, is in critical need of a heart transplant.

His friends and family have come together to launch the “anyone with a he❤️‍rt…” campaign to raise awareness of his urgent condition and to encourage people facing difficult decisions to consider a Directed Heart Donation that could save Johnny’s life. At 58, Johnny Boatman has dedicated over 25 years of his life to serving this country, earning the Bronze Star Medal and retiring as a Lt. Colonel

from the Illinois National Guard. As the creator of Operations First Choice, a Chicago-based program helping youth aged 7-17, and currently serving in a leadership role at the Department of Defense, Johnny's impact on his community and country is immense. Despite his active and healthy lifestyle as a former Division I football player for the University of Mississippi (Ole Miss!), Johnny has been diagnosed with hereditary ATTR (hATTR) amyloidosis, a rare condition affecting only an estimated 50,000 people worldwide. This progressive disease has led to congestive heart failure, and now Johnny’s only chance at survival is a heart transplant. He remains hospitalized, waiting on the transplant list for his miracle. Directed Heart Donation is rare but can be life-saving. The "anyone with a heart..." campaign aims to raise awareness, not just for Johnny but for others in need of directed organ donations. The Boatman family, who have quietly faced Johnny's illness for the past year, are now asking for help in spreading the word about his urgent need for a heart transplant.

“We are waiting for a miracle,” says the family. “Johnny has always had a big, loving heart. Now, he needs a new one to continue being the amazing husband, father, and leader he is. We ask everyone to share his story and raise awareness for Directed Heart Donation. Anyone with a heart can make a difference.”

❤️How You Can Help❤️
- Share Johnny’s story on social media and encourage others to do the same.
- Raise awareness about Directed Heart Donations, which can save lives.
- Help Johnny and others like him by spreading the message of hope and support.

📊 One in 25 Black Americans have the gene which can contribute to developing a life threatening disease you may have nev...
08/05/2026

📊 One in 25 Black Americans have the gene which can contribute to developing a life threatening disease you may have never heard of....Hereditary Amyloidosis.

Join VCU Health Facts & Faith Fridays, Center and VCU Health Pauley Heart Center to learn more about Genetic .

Johnny Boatman and Quan will speak on the patient and caregiver experience.

Webinar event: August 21st at 3pm ET

Register here: https://bit.ly/4wD4vUl

Phi Beta Sigma Fraternity Inc Alpha Kappa Alpha Sorority Incorporated

Learn more about the living kidney and liver donation could save someone's life and the quality of their life.
07/29/2026

Learn more about the living kidney and liver donation could save someone's life and the quality of their life.

If you're considering donating an organ, learn about the process, whether you might be eligible, and the importance of notifying your family that you want to donate.

❤️‍🩹 Grateful doesn't quite cover it. 🙏🏾Johnny Boatman and Quan joined 's Patient Day this year, where the focus was on ...
07/20/2026

❤️‍🩹 Grateful doesn't quite cover it. 🙏🏾

Johnny Boatman and Quan joined 's Patient Day this year, where the focus was on couples navigating life with a family member's rare disease. 💙

Johnny lives with ATTR CM V122i hereditary Amyloidosis, and days like this remind me how much stands between his diagnosis and his quality of life today. Namely, people.

🔬 Scientists who spend years in labs so families like ours get more ordinary days together.

🗣️ Researchers who took the time to ask us real questions, not just clinical ones.

🫶🏾 People who could easily stay behind the data but choose to sit across the table from the patients they're working for.

That's the kind of company BridgeBio is building, one where patient voices actually shape the science. ✨

To everyone doing that work, thank you for showing up for Johnny, for us, and for every family living with a rare disease. ❤️‍🩹

07/02/2026

Mike Lane (founder of ) and Johnny Boatman spoke at Harlem, NY's Beatrice Lewis Senior Center for their 'Harlem Hearty" Series.

They shared their patient journey with Hereditary Amyloidosis to increase awareness of the gene, disease, early warning flags, and treatment therapies.

1 in 25 African Americans have the V122i gene for Hereditary Amyloidosis. Knowing your status could save the lives of your family lineage.

Johnny's goal is to help others learn of the disease early to lower their chances of long hospital stays, organ transplant or worse....

Many thanks to Diane Butts for the video and pics from the event.

A diagnosis of Hereditary Amyloidosis will change your life, however it doesn't stop you from LIVING! ❤️‍🩹An early   CM ...
06/27/2026

A diagnosis of Hereditary Amyloidosis will change your life, however it doesn't stop you from LIVING! ❤️‍🩹

An early CM diagnosis will give you more treatment options to live a full and quality life.

We are grateful for Johnny Boatman's heart and kidney donor, making it possible for him to have a second chance at quality life.

Amyloidosis Research Consortium Amyloidosis Alliance

Quan Boatman discusses how ATTR-CM affected her husband and why they now advocate for earlier awareness and treatment.

❤️‍🩹 Learn more about Hereditary Amylodosis via the Amyloidosis Research Consortium Webinar Series.
05/22/2026

❤️‍🩹 Learn more about Hereditary Amylodosis via the Amyloidosis Research Consortium Webinar Series.

Conversations and presentations about living with and caring for those impacted by V122I Hereditary ATTR Amyloidosis

Today, Johnny Boatman supported the Amyloidosis Army and Mike Lane  at Harlem's Harlem Healthy Hearts program with Mt. S...
05/21/2026

Today, Johnny Boatman supported the Amyloidosis Army and Mike Lane at Harlem's Harlem Healthy Hearts program with Mt. Sinai Hospital.

The Amyloidosis Army had the privilege of joining Dr. Icilma Ferguson MD FACC FASPC and her Harlem Healthy Hearts program of Mount Sinai Hospital. Her team, led by Nancy Thomas, did an impressive job educating the community in Harlem about Amyloidosis and provided FREE genetic testing on site. Patie...

Thank you to VCU Health Hume-Lee Transplant Center and VCU Health Pauley Heart Center for the annual Heart-A-Versary! Ou...
05/21/2026

Thank you to VCU Health Hume-Lee Transplant Center and VCU Health Pauley Heart Center for the annual Heart-A-Versary!

Our (new) hearts are full of joy to thank everyone for another year.

Let's not forget we are also honoring the donors and donor families for their precious gift. ❤️

Check out Johnny Boatman on the podcast Gift of Life Episode 107 The Organ Transplant Podcast from Gift of Life on Amazo...
05/12/2026

Check out Johnny Boatman on the podcast Gift of Life Episode 107 The Organ Transplant Podcast from Gift of Life on Amazon Music.

URL: https://bit.ly/4eHJa62



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