Op Ed – Don’t Judge a Book

This past week, many parents in the Greater Philadelphia area learned what I learned almost ten years ago – sudden cardiac arrest isn’t just an adult thing. It takes the lives of thousands of children every year.

Two students, an eighth grader from Harrington Middle School in Mount Laurel, and a first grader from Andrew Jackson Elementary in Philadelphia, collapsed and died from cardiac arrest.

In 2005, my son, Simon, died suddenly. He was a baby so most people told me it was SIDS.  Our pediatrician, however, was a bit wiser. She said, “get your hearts checked because babies don’t just die.”  Following her advice, we got tested. My wife, Phyllis, was diagnosed with a heart condition called Long QT Syndrome. It’s an arrhythmia that is linked to 15% of all SIDS deaths.

My heart breaks for these two families. The obvious reason is that there is a gaping void in their life now. It may narrow over time, but it will always be there. There is nothing more painful or unjust than losing a child. We all know that life is unfair, but its not supposed to be this unfair.

The less obvious reason is that I’ve dedicated the last nine years of my life to raising awareness about sudden cardiac arrest in children so that other parents wouldn’t have to take this path. I wanted them to be smarter so they could do a better job of protecting their children. Apparently, I failed. I let these families down.

Now, they’re walking in my shoes wondering how, in the 21st century, their child can die from detectable and treatable heart condition. Think about that. It’s not a rare disease. We don’t need billions of dollars to find a cure. We have the technology. We have the treatments. We just need to look. We need to be a little curious, like my pediatrician was nine years ago.

The Journal of American Board of Family Medicine published a study in 2012 showing that 72% of all students that died from SCA reported having symptoms from the underlying heart conditions.  I’ve met students who reported symptoms, like a racing heart or fainting. They were later diagnosed with heart conditions. Prior to their diagnosis, their symptoms were dismissed as drinking too much soda and being dehydrated, respectively. The signs were there. We almost let those kids down. We need to be a little more curious . . . a little wiser.

Sudden cardiac arrest is what happens when the heart stops beating, suddenly and unexpectedly. It is not a heart attack.  That’s what happens when blood can’t get to the heart. The conditions that cause sudden cardiac arrest in children come in two varieties: structural and electrical.

If the heart is too big or the valves are in the wrong place, the heart can’t work properly.  Alternatively, the heart rhythm can get interrupted because of an electrical abnormality.  All of these conditions are mostly genetic. They can be detected and treated.

Here are the warning signs:  (1) fainting or seizures during or immediately after exercise; (2) unexplained shortness of breath; (3) dizziness during exercise; (4) extreme fatigue; (5) a racing heart.  Also, parents should be aware if a family member has died suddenly and unexpectedly before the age of 50.

So, what’s next? The experts will debate the merits of making heart screenings a standard of care, while we continue to provide free eye and ear exams to students in schools. The lawmakers will debate the merits of placing AED devices in schools, even though each is already equipped life saving measures like fire alarms, sprinkler systems and security systems. However, starting tomorrow, we, the parents, can be more diligent and less dismissive about the warning signs of the underlying conditions.

My seemingly healthy baby, who was average height and weight and scored an 8 and 9 on his APGAR tests, had an undetected heart condition.  These two boys, energetic and vibrant students, described as “one of the kids everybody knew,” and “shy, funny and loveable” had undetected heart conditions. The answers may be right in front of us. We just need to look.

As children, we learned not to judge a book by its cover. Remember, we need to look at what’s on the inside. It’s time to realize that this saying applies to our children’s hearts too.

 

 

 

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."