Our mission is to eliminate the reason we exist.
Our purpose is personal. We’ve all been directly impacted by CHD in one way or another, and we are relentless in our pursuit to solve it in our lifetime.
Medical Advisory Board
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Board of Directors
Tyler Thayer
Co-Founder & President
Tyler is originally a Nolensville native. After completing his undergraduate and Master’s degrees in Architecture at the University of Tennessee in Knoxville, he and his wife Erica moved back home to Nolensville. Tyler didn’t know anything about CHD until his son, Calvin, was born with a complex congenital heart defect. He now runs his own architecture design firm, Paradym Studio, and is acting President of Project Heart. He is passionate about promoting awareness and raising funding for CHD research.
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Erica Thayer
Co-Founder & Vice-President
Erica Thayer is the Co-Founder of Project Heart, along with her husband Tyler Thayer. Together they have 3 children: Calvin, who was born with CHD, Adelaide, and Rosemary. Erica works part-time as an Audiologist in Franklin and full-time as a homemaker and homeschooling mom.
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Dr. Thomas Doyle
Board Director
Dr. Thomas Doyle is the Ann and Monroe Carell Professor of Pediatrics, and Clinical Director of the Division of Pediatric Cardiology at the Monroe Carell Jr. Children’s Hospital at Vanderbilt. Dr. Doyle graduated from the University of Arizona School of Medicine in 1987. He completed his Pediatric Residency at the University of Maryland in 1990, and then stayed an additional year at the University of Maryland to act as Chief Resident. It was during his residency that he developed a passion for pediatric cardiology. This interest led to a Pediatric Cardiology Fellowship training at Yale University. Upon completion of his pediatric cardiology training, Dr. Doyle accepted a position as an interventional cardiologist at Vanderbilt University Medical Center. He was the first trained pediatric interventional cardiologist in the state of Tennessee and introduced numerous new techniques to the State including percutaneous PDA closure, vascular stent implantation, and device closure of atrial and ventricular septal defects. Over the subsequent 30 years, Dr. Doyle, along with his partners Dr. Nicholson and Dr. Janssen, have built the largest pediatric interventional cardiology program in the state. Dr. Doyle’s research interest lies in the design and development of novel devices to improve the care of children with congenital heart disease.
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Brianna Shank
Board Director
Brianna is a pediatric cardiac ICU nurse with 12 years of experience specializing in the care of children with congenital heart disease. She is passionate about the critical research being done to advance the treatment of CHD and improving outcomes.
A mother of four and dedicated healthcare professional, she works on the front lines providing critical care to vulnerable young patients, ensuring each child receives exceptional medical support during their treatment journey.
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Connor Shank
Board Director
Connor is an entrepreneur through and through. Having started multiple companies over the past 15 years with two exits, he believes in technology’s ability to solve real-world problems. Drawing from his experience building and scaling commercial solutions, he’s especially interested in how innovation can transform healthcare outcomes.
Connor is an advocate for Artificial Intelligence and is developing innovative solutions to guide organizations to support main street and mid market companies in the coming years.
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Staff
Brittany Southwood
Major Gifts Officer
Originally from Kentucky, I made my way to Nashville to build a career in Business Development within the commercial construction industry. Now, I’m excited to channel those skills into making a difference by supporting groundbreaking research. I’m thrilled to be part of the Project Heart mission to grow a heart!
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Help us grow the cure for CHD.
The alternative isn’t an option. All existing treatments for CHD just delay the inevitable. By the age of 12, children with complex CHD will have had three open-heart surgeries and face more surgeries as they get older. Most people with complex CHD who survive to adulthood will die in their 40s. They won’t even see their children grow up.