Our Children Rarely Die

Published in the Huffington Post

Rare is defined as seldom occurring or found, uncommon. There are only 24 known manuscripts of the Magna Carta. There are only 4,480 black rhinos left on the face of the earth. This past Thanksgiving, the Grand Canyon was filled by an inversion cloudthat only happens once every 10 years.

Rare can make things intriguing and desirable. It can turn people into collectors. If, however, the word is used to describe a medical condition, it gives us permission to be dismissive and turn away.

Last month, Patrick Awosogba, a freshman basketball player at Rutgers University, collapsed and died. A newspaper article reporting his death stated “although rare, the condition [that caused his death] is the most frequent cause of sudden death in young people.”

Ten years ago, my son, Simon, died from an undetected heart condition. Ever since, I’ve heard this claim. Heart conditions that lead to sudden cardiac arrest (SCA) and death in children are rare. But is it?

The particular condition that took the life of Patrick is called hypertrophic cardiomyopathy. It is estimated to exist in one out of every 500 people. I’m wondering, if one out every 500 rhinos on earth were black, would they still be considered rare? Probably not.

I decided to check out the National Organization for Rare Disorders (NORD). It maintains a rare disease database. I didn’t find cardiomyopathy. I also didn’t find Long QT Syndrome. That’s the “rare” condition that I was diagnosed with after Simon died. This condition exists in anywhere from 1:2,000 to 1:7,000 people, and is responsible for up to 15 percent of all sudden infant deaths (SIDS). There are about ten conditions that can lead to sudden cardiac arrest in children.

So why do people think kids dying of SCA is a rare event? There are two reasons. First, we don’t know how many kids die from SCA because we’ve haven’t been tracking it. The American Academy of Pediatrics suggests the number is 2,000. I have seen other groups that put the number anywhere at 7,000.

The good news is that in October 2013, the US established a registry to track sudden death in the young. This registry is being piloted in ten states and will gather comprehensive data on the deaths of children between the ages of 0 to 24. This is great start, but when the World Wildlife Federation is counting the black rhino population, do they just focus on 20 percent of the grasslands in Africa?

The other reason is that some medical experts pretend that we know the number, and that it is low. These researchers used Internet searches and insurance death records to track the number of student athlete sudden deaths, and then marketed it as an official U.S. registry. That’s not very “expert-ish,” and it’s a little misleading to us laypeople. Isn’t there a more scientific and reliable way?

Patrick died at college playing basketball. His death made the paper. My son, Simon, didn’t. They both died of sudden cardiac arrest, but only one was counted. Our statistics are already off by 50 percent. That’s an F.

Let’s make sure that our children are counted as closely as the black rhino. Let’s make sure our research in this area is as meticulous as the process of authenticating a copy of the Magna Carta. Before we casually throw around a term, let’s make sure that sudden death really is as rare as inversion clouds in the Grand Canyon.

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."