Why we exist

Because no child should die from a detectable and treatable heart condition

Where Our Mission Began

Simon’s Heart was founded in memory of Simon Sudman, a seemingly healthy baby who died in his sleep. Many said SIDS. Fortunately, our pediatricians were curious and said, "Babies don't just die. Go get your hearts checked."

Mom was diagnosed with Long QT Syndrome - an arrhythmia that has been linked to SIDS deaths. This is just one of the types of conditions that cause sudden cardiac arrest and death in children, teens and young adults.

We started offering free heart screenings to prevent other parents from losing children to detectable and treatable heart conditions. The video below tells the rest.

Mission & Vision

Mission

To prevent sudden cardiac arrest and death in children, teens, and young adults.

Vision

A world where children don’t die from detectable and treatable heart conditions.

Our Values

Curiosity

We ask questions and seek answers that lead to prevention.

Integrity

We ground our work in transparency, science, and compassion.

Empathy

We serve families, educators, and communities with care.

Innovation

We use creativity to make detection a priority and prevention engaging.

Collaboration

We partner with medical experts, schools, lawmakers, and allies to create change.

Our Value Proposition

It took almost two decades for us to realize it. We created a suite of tools that makes the
prevention of sudden cardiac arrest and death more efficient and effective.

HeartBytes

Protecting the hearts of every student, requires a change to the standard of care, and ownership from the medical community.

So, we built the first digital screening platform and pediatric cardiac registry of seemingly healthy kids. Now, research is more accessible.

CPR Jukebox

Why is the CPR table usually empty at public events? Do students even know the song Stayin Alive? The answers to these questions led to the creation of the CPR Jukebox.

We don't need to be licensed to save a life. We just need a song, a ball, and some rhythm.

GotAED

Many youth facilities don't have the money to purchase an automated external defibrillator (AED). This is unacceptable and dangerous.

In minutes, an organization can launch a campaign to start raising funds for a reduced-price (brand new) AED device.

Governance

Staff & Board

Simon’s Heart is the collaborative effort between a small and mighty staff, dedicated board members and medical professionals, volunteers and students.

Transparency & Accountability

We are committed to using every donation responsibly and transparently. Annual reports, audits, and impact summaries are available to show how your support directly saves lives.

Jake Berman

“I attended a heart screening at Colonial Middle School when I was ten. I was in the marching band and liked to hike and rock climb. I was diagnosed with Wolff Parkinson White Syndrome. After my procedure, I kept doing the same things.”

Whitney Jones

Whitney’s commitment to heart health advocacy began at 10 years old when she and her mother, Rayna, were diagnosed with Long QT Syndrome during a Simon’s Heart screening at Downingtown West High School. Despite the diagnosis, Whitney pursued her passion for cheerleading and continued to thrive in the sport through her college years at St. Joseph’s University. After graduating, Whitney joined Stryker Instruments as the Senior Specialist for Off-Site Meeting and Events, where she skillfully orchestrates events that promote health and medical innovation. Further extending her impact, Whitney is an active member of the Simon’s Heart Young Professionals Committee, while her mother Rayna contributes her expertise on the Board of Directors.

Katie Asper

“I attended a heart screening at Upper Dublin High School when I was ten. I played soccer. I was diagnosed with Wolff Parkinson White Syndrome and had an ablation to fix the problem. I attend Temple University.”

Matthew Green

“I attended a heart screening in Mason, Ohio, when I was ten. I participated in baseball, basketball, and diving. I was diagnosed with an atrial septal defect. I had surgery to repair the hole and started wearing a protective shirt during activity. I am graduating from Miami University.”

Valerie Krawitz

“I attended a heart screening at Colonial Middle School when I was ten. I played baseball, soccer, and track. I was diagnosed with Long QT Syndrome and an atrial septal defect. I had heart surgery to repair the hole and I take medicine for the Long QT. I can’t play competitive sports like I once did, but found other activities. Next year, I’m attending Penn State University.”

Drew Harrington

“I attended a heart screening at Radnor High School when I was ten. I played lacrosse, tennis, and basketball. I was diagnosed with Wolff Parkinson White Syndrome. I used to feel my heart beat really fast, but just assumed it was fine. Coincidentally, on Simon’s 7th birthday, I had a procedure called an ablation. Today, my heart is fine and I attend the University of Richmond.”

Alaysia Keeley

“I attended a heart screening at Norristown High School when I was ten. I played softball and enjoyed going to the mall with my friends. I was diagnosed with Long QT Syndrome. I had to stop playing sports and drinking soda. Now, I take medication and live a normal life.”

Kyle McCabe

“I attended a heart screening at Norristown High School when I was ten. I played baseball, basketball, and football. I was diagnosed with Long QT Syndrome. I stopped playing sports to protect my heart, but I still manage to have fun.”

Melissa Fair

“I attended a heart screening at Colonial Middle School when I was ten. I loved dancing and hanging out with my friends. I was diagnosed with Partial Anomolous Pulmonary Venous Return and Atrial Septal Defect. The doctor told me that my life would have been cut short if I hadn’t found out. I’m graduating from Penn State University this year.”

Zach Steffens

“I attended a heart screening at Stillman Elementary School in Tenafly, N.J., when I was fourteen years old. I love running, Tae Kwon Do, and Armenian cultural dancing. I was diagnosed with a rare congenital defect called ALCAPA (Anomalous Left Coronary Artery from the Pulmonary Artery). I had open-heart surgery and recovered well. One month later, I suffered a cardiac arrest and an automated external defibrillator (AED) saved my life. I now have an implantable cardioverter defibrillator (ICD) and am healthier than ever. I will be attending The College of New Jersey and majoring in biomedical engineering.”

Annie FitzPatrick

“I went into sudden cardiac arrest at a local convenience store when I was 19 years old. My heart stopped and the only reason I am alive today is because an AED was readily available. I was diagnosed with Long QT Syndrome shortly after and was introduced to Darren and Phyllis with Simon’s Heart. I have been an active volunteer ever since. I went on to graduate Cum Laude from Drexel University with a double major in Business Analytics and Marketing and now work at a leading chemical company.”

Maeve Quinn

"I had a sudden cardiac arrest during softball tryouts at my high school. I was 15 years old. Thanks to the quick thinking of my coach and athletic trainer, they started doing CPR and using an AED immediately. This helped save my life. I had an implantable defibrillator surgically placed in case this happens again. I volunteer to educate people on the importance of screenings, learning CPR and the use of AEDs. Anyone can save a life like mine! I am planning on going to college for nursing."