The Children's Heart Foundation

The Children's Heart Foundation Funding the most promising congenital heart defect research so that Heart Warriors everywhere can live longer, healthier lives.
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The Children's Heart Foundation was founded in 1996 and is the country's leading organization solely dedicated to funding congenital heart defect (CHD) research. Our vision is a world in which everyone born with a congenital heart defect has the chance to live a long, healthy life, and that eventually, CHDs will be eradicated altogether. That's why we are dedicated to funding research to advance the diagnosis, treatment, and prevention of CHDs. With the help of our volunteers and supporters, we are making great progress. Since The Children's Heart Foundation began funding CHD research more than 25 years ago, survival rates, longevity, and quality of life have dramatically improved for CHD patients. Because of this, The Children's Heart Foundation has added important research focus on developmental, transitional, and long term care needs affecting the millions of Americans with CHDs who now live longer lives. The research we fund positively impacts all CHD patients.

April is   and it's the perfect time to celebrate the HEART of The Children’s Heart Foundation— our volunteers! ❤️On beh...
04/01/2026

April is and it's the perfect time to celebrate the HEART of The Children’s Heart Foundation— our volunteers! ❤️

On behalf of The Children’s Heart Foundation, thank you to all of our amazing volunteers. Your support helps us fulfill our critical mission. Whether you donate your money, give your time, or help fundraise, people like you are at the heart of the work we do!

Today is the final day of Women's History Month and we're proud to celebrate the incredible women who help drive our mis...
03/31/2026

Today is the final day of Women's History Month and we're proud to celebrate the incredible women who help drive our mission forward. ❤ Meet Jessica Zink, a dedicated volunteer whose passion and impact continue to inspire our community.

When asked, "How do you use your voice, platform, or expertise to make an impact?", she shared: "As a congenital heart surgery physician assistant, I have the privilege of caring for patients and families during some of the most challenging moments of their lives. I use my expertise and platform to advocate for greater awareness of congenital heart disease, support families navigating complex medical journeys, and champion the importance of continued research. Through my work with our local chapter of the Children’s Heart Foundation and in sharing my clinical perspective and experiences, I hope to help bridge the gap between the medical community and the public, and inspire greater support for the advancements that will improve outcomes for children with congenital heart defects."

During Women's History Month, we take the opportunity to spotlight some of the extraordinary women leaders here at The C...
03/31/2026

During Women's History Month, we take the opportunity to spotlight some of the extraordinary women leaders here at The Children's Heart Foundation. ❤ Today we're highlighting Beth Sewell, an amazing and volunteer.

When asked, "Why is continued research so important for the future of CHD care?", Beth answered: "When I get asked this question it always takes me back to when Maddie was having her first surgery. I was talking with one of the cardiologists regarding Maddie’s future and what that would look like. He made the comment that if she had been born 15 years before we might have been told to take her home and enjoy the very short time we would have with her. He explained that research is always improving and I thought, if it had improved that much in the past 15 years, what would the next 15 years of research bring? That was such a powerful statement that gave us endless hope for our precious baby." 💝

During Women's History Month, we take the opportunity to spotlight some of the remarkable women driving change. ❤ Today ...
03/30/2026

During Women's History Month, we take the opportunity to spotlight some of the remarkable women driving change. ❤ Today we're honoring Shaira Whittle, an incredible Mom and leader of the Rocky Mountain region for The Children’s Heart Foundation.

When asked "Why is continued research so important for the future of congenital heart disease care?", Shaira said:

"Continued research is not just important—it is absolutely vital for the future of congenital heart disease care. Because no child should have to suffer, and no parent should ever have to endure the unimaginable pain of losing their child.

We have to believe in a future where “Heart Angels” are no longer a reality, where loss is no longer part of this story. A future where every Heart Warrior not only survives, but truly thrives—living full, healthy, and limitless lives.

Research is hope. It is progress. It is the path forward that turns heartbreak into healing and possibility. And until that future becomes reality, we cannot stop pushing, advocating, and fighting for every single child and every single family."

Today is  ! ❤🩺 We appreciate all of the doctors who care for babies, children, and adults with congenital heart defects ...
03/30/2026

Today is ! ❤🩺 We appreciate all of the doctors who care for babies, children, and adults with congenital heart defects and who give hope to families everywhere.

Do you or your child have a favorite doctor? Tell us about them in the comments below! 👇❤️‍🩹

We're thrilled to announce our 2026 Congenital Heart Walk incentives! ❤ This year's collection features some fantastic s...
03/27/2026

We're thrilled to announce our 2026 Congenital Heart Walk incentives! ❤ This year's collection features some fantastic special edition 30th anniversary items to recognize your incredible fundraising efforts supporting The Children's Heart Foundation.

🎁 $250 Level - Dog Leash or Socks
🎁 $500 Level - Baseball Cap
🎁 $1,000 Level - Sweatshirt or Pickle Ball Set
🎁 $2,500 Level - Quarter Zip
🎁 $5,000 Level - Backpack or Chair

Visit http://chfwalk.org to register to walk and start fundraising today!

*Gifts are not cumulative; only one item is awarded to each fundraiser, with the exception of t-shirts. All registered participants who raise at least $100 will receive a 2026 Event T-Shirt on walk day. Fundraiser may select one item at or below the level achieved. You must be registered as a participant to earn gifts.

Ahead of   on March 30th, we'd like to send a special thank you to the esteemed doctors from across the country who serv...
03/26/2026

Ahead of on March 30th, we'd like to send a special thank you to the esteemed doctors from across the country who serve on our Medical Advisory Council (MAC). ❤ Our MAC oversees our research granting process and helps ensure that we fund the most promising and impactful research each year. We're so grateful to each of them for lending their time and talents to support our mission. Meet them here: https://www.childrensheartfoundation.org/about-us/medical-advisory-council.html

On this   we're sharing Eli's story. He shares his   journey with us below."My story began in a way no one expected. I w...
03/25/2026

On this we're sharing Eli's story. He shares his journey with us below.

"My story began in a way no one expected. I was born in Taipei, Taiwan. Not long after I was born, my body started to struggle. I became cold, my color began to change, and breathing didn’t come easily. While others thought everything was fine, one doctor listened closely and knew something wasn’t right. Within hours, I was fighting for my life.

A medical team rushed me to National Taiwan University Hospital, where doctors discovered I had a congenital heart condition called Transposition of the Great Arteries, along with coarctation of the pulmonary artery.

At just one day old, I underwent a nine hour open heart surgery.

The first few weeks of my life were spent in the ICU. I was surrounded by doctors, machines, and constant care. My family could only visit me during certain hours, waiting and hoping as I fought to recover.

Eventually, I grew strong enough to go home, but my journey was just beginning.
My early months were filled with medications, checkups, and careful monitoring. There were moments of uncertainty, but also moments of steady progress. At six months old, I had another cardiac catheterization, and my doctors continued to watch my heart closely as I grew.

Recently, I had another cardiac catheterization to better understand the pressure in my heart. At first, doctors thought it might be caused by scar tissue. Instead, they found extra tissue in my pulmonary artery. The good news is that my heart can likely stay as it is for now, strong and stable without needing immediate intervention.

Today, I’m thriving. I love musical theater, history, singing, video games, and pretty much all the things teenage boys like to do.

You might not know everything my heart has been through just by looking at me. I run, workout, and live life like any other kid. The only visible reminder is a scar on my chest, a symbol of everything I’ve overcome.

My heart may be different, but it is strong. And my story is still being written." ❤

The Children's Heart Foundation is partnering with the Izak Szymczak Research Fund to support research that focuses on d...
03/23/2026

The Children's Heart Foundation is partnering with the Izak Szymczak Research Fund to support research that focuses on durable mechanical support in patients with single-ventricle congenital heart disease. ❤

The 2025 Izak Szymczak Research Fund Award​, administered through The Children’s Heart Foundation​, has been awarded to Dr. Mark Rodefeld (Indiana University) for his research on, ""Fontan Pump: Wireless Charge and Control System Development"".

Dr. Rodefeld’s work aims to move the Fontan pump closer to full implantability by developing a wireless charging, control, and monitoring system—eliminating external hardware and helping improve quality of life for patients while easing the daily burden on families and caregivers.

Together, we’re investing in research that brings hope and transforms care for CHD patients.

"Spring: a lovely reminder of how beautiful change can truly be."Happy Spring everyone! 🌷☔️
03/21/2026

"Spring: a lovely reminder of how beautiful change can truly be."

Happy Spring everyone! 🌷☔️

This  , we're proud to share women who are doing incredible things ❤ Koko's Candles is owned and operated by Janeen Koko...
03/20/2026

This , we're proud to share women who are doing incredible things ❤ Koko's Candles is owned and operated by Janeen Kokodynski in Scottsdale, Arizona. After losing her one month old son Matthew to a congenital heart defect ( ) in 2005, Janeen worked tirelessly with The Children’s Heart foundation to fundraise while also creating awareness. In 2017, she combined her love of candle making with her commitment to this nonprofit and Koko’s Candles was born.

At Matthew's funeral, hammered pewter hearts were passed out. These hearts were slightly misshapen and imperfect - just like Matthew's. When Janeen launched her company, she knew she wanted to incorporate these hearts into her candle line. Before each candle is poured, a small heart is placed at the bottom. After the candle has burned, you may remove the heart and place it in your change purse or pocket to serve as a reminder that you are loved.❤

A portion of the profits from each candle is donated to The Children's Heart Foundation. Shop here: https://kokoscandles.com/

"Being a mother to a kiddo with a significant medical condition means you never stop advocating and raising funds for a ...
03/19/2026

"Being a mother to a kiddo with a significant medical condition means you never stop advocating and raising funds for a better tomorrow, for science that means they could possibly outlive you. When your kiddo is thriving, it looks from the outside like everything is normal. My constant wish is for many many many more years that look normal!"

THIS is why we walk ❤ Register for a Congenital Heart Walk near you and help fund the groundbreaking research of tomorrow: http://chfwalk.org/

Address

5 Revere Drive One Northbrook Place Suite 200
Northbrook, IL
60062

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

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