Simon’s Club Member of the Week – Katie Asper

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Karen Asper, a nurse affiliated with Abington Hospital, volunteered to work at Simon’s Fund’s free heart screening at Upper Dublin high school on September 23rd, 2012. As the day wore on, Karen learned that space had opened up at the ‘sold out’ screening and she went home to pick up her children to be screened. Like most parents who bring their children to screenings, Karen expected to be in and out. Like 1% of these parents – or 1 in 100 – Karen was stunned when she learned that her daughter had a heart condition.

The EKG had shown that daughter Katie, 14, had Wolff Parkinson White Syndrome (WPW), a disorder that can run in families. Although Katie had never complained of any symptoms, such as dizziness or a racing heart, during a stress test, when her heart was stressed to a rate of 190, the Wolff Parkinson White still showed up on the monitors. This indicated that the condition could put Katie in danger. Ironically, at the time, some of Karen’s days were being spent working in Abington’s cardiac stress lab giving stress tests.

People with WPW have an extra electrical circuit in their heart, which can cause their heart rate to go too high. The gravity of a person’s WPW depends on which pathway is affected by the aberrant circuit. Katie’s doctors could not determine which pathway was impacted without performing invasive electrophysiological tests. Her mother found this untenable, “I was having a hard time intervening with an invasive procedure when Katie was not symptomatic,” she explains.

The uncertainty was taking its toll on Katie, causing her to visit the nurse more at school and feel apprehensive. Karen found herself regularly quizzing the cardiologists in her stress test lab, until finally she got the advice that spurred her to action. Dr. Andy Fireman advised her to stop thinking like a nurse and instead think like a mom about how she would feel if something happened to Katie. His advice, combined with Katie’s upcoming mission to Belize, where she wouldn’t have access to advanced medical care, finally made the decision easy.

Almost nine months to the day after her initial heart screening, Katie underwent the testing and a cardiac ablation at Children’s Hospital of Philadelphia. Her family was told after the procedure that they had made the right choice; had the doctor have known in advance which pathway was aberrant, ablation to remedy it would definitely have been recommended. An EKG and echocardiogram shortly thereafter showed no sign of WPW.

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."