(Written by her parents)

Becca Basketball

Becca’s Basketball Photo

HEARTFELT cardiac screening saved Rebecca’s life!

Rebecca ran cross-country, played JV  basketball, and ran long distant track for Esperanza High School. In the summer after her freshman year, a girl’s sister on her cross-country team, Morgan, died suddenly on the tennis court from cardiac arrest. This event plus shortness of breath that Rebecca felt frequently when running longer distances in cross-country (her doctor told her it was sports induced asthma and gave her an inhaler to use), troubled her often.  She suspected that something else might be wrong. That fall, HEARTFELT cardiac screening was offered at her high school campus and Rebecca felt the urge to be checked. The screening was easy and didn’t take long. After her screening, Rebecca was told by Heartfelt Cardiac Projects that an abnormality was detected, and referred her to a cardiologist for further testing.

Becca Cross Country Esperanza

Becca’s Cross Country Photo

Rebecca was diagnosed with Hydrotropic Cardiomyopathy (HCM). This is a
thickening of the middle wall (septum) between the heart chambers that makes the
lower left ventricle smaller and harder for blood to get through especially during
extreme exercise. At the time Rebecca was running up to 6 miles a day in cross-
country. The shortness of breath and tightness she was feeling in her chest wasn’t
from asthma; it most likely was from not enough blood being pumped through her
heart! Her cardiologist told her to stop organized sports immediately. He ran her
through several stress tests and found her heart working fine under normal
conditions. If her heart continued to pump extremely in sports, she may have
suffered cardiac arrest.

Becca Cross Country OC Invitational

Becca’s Cross Country OC Invitational Photo

We are so thankful we discovered this through HEARTFELT cardiac screening.  Rebecca’s life has changed. It’s been hard for her to give up competitive sports. She has found alternative ways of exercise through Pilates, yoga, and hiking. Her cardiologist has her on a low dosage beta-blocker medication but no further medical attention is needed other than yearly heart checkups.

HCM is genetic. Our family has been genetically tested and neither her brother nor
sister has HCM. We also know that Rebecca can pass this along to her kids but now
that this gene has been identified, it possibly could be “spun out” of Rebecca’s DNA
so it may not affect her future children.

Becca Bday

Becca’s Birthday Photo

This diagnosis has also inspired Rebecca to inform others about this screening. She
learned that statistically 3 other people at her school could have HCM and not know
it. The following spring after her diagnosis, Rebecca spoke to every sports team at
Esperanza High School encouraging them to get tested at the HEARTFELT cardiac
screening held at the same time as the spring sport’s physicals. Supporting
HEARTFELT cardiac screening is very important to Rebecca. Many thanks to Holly,
the founder of HEARTFELT cardiac screening, for all her kindness and
encouragement during this scary time!

Dawn & Mark,
Rebecca’s mom  & dad

Learn more about heart screenings at:

Heartfelt Cardiac Projects

~ ~ ~ ~ ~




A message from Holly Morrell, Executive Director, Heartfelt Cardiac Projects

On July 14, 2012, I survived emergency open-heart surgery by only 90 seconds.  I believe my life was spared in order for me to continue my life’s work — saving others from Sudden Cardiac Arrest (SCA).  

SCA kills a high-school athlete every three days and 450,000 people each year.  It is the number-one killer of women and the number-one killer in the U.S.  I am living with a heart disease that has killed six members of my family.

Through my nonprofit organization, PHFE Heartfelt Cardiac Projects, I have spent the past 14 years providing community cardiac screenings for early detection of heart disease and other cardiac conditions that can lead to sudden death.  I have provided comprehensive cardiac evaluation to over 30,000 people across the United States, free of charge or at just a fraction of what it would cost them any other way.  It has been both a privilege and an indescribable blessing to have had the opportunity to save and/or protect the lives of hundreds of people, who would not have access to or money for these screenings.

I cannot do this alone.  I need your help!

I must raise funds for PHFE Heartfelt Cardiac Projects to continue the service of this life-saving organization.


by making a tax-deductible donation

so I can continue to screen more people and save more lives.


Thank you . . . from the bottom of my heart.

~Holly Morrell


 Please take five minutes to view this video

profiling four young kids recently saved by Heartfelt screenings

and to learn more about my personal story.


For more information, visit Heartfelt Cardiac Projects at:

HEART STORY by Scott Popjes



As I made my way from the kitchen back into the den my heart suddenly started to race, and a sudden tightness in my chest and shortness of breath, quickly followed.  I had grown accustomed over the years to the palpitations associated with PVC’s (Pre-Ventricular Contractions), but unlike PVC’s, which were usually isolated to one or two beats, this racing rhythm kept going.  It wasn’t long before I became lightheaded and my vision started to tunnel, like I was looking at the world through a paper towel roll.   I leaned up against the wall in nervous anticipation of what would happen next.

My heart “story” didn’t start at that moment.   It started about 24 years earlier when, during a high school basketball physical, a heart murmur was detected.   After seeing multiple doctors and having multiple echocardiograms (ECHO) I was diagnosed with mitral valve prolapse (MVP).   This discovery ended my high school athletic pursuits, but at the time no other limitations were placed on my activity.   I continued with an active lifestyle – weight training, racquetball, pickup basketball games, softball, flag football.

Reflecting back now I can remember having a random fluttering feeling in my chest, a sensation similar to what I imagine butterflies would feel like flying around inside my chest.  But it happened infrequently and I didn’t think much of it and didn’t say anything about it.  For more than 5 years life went on.

When I was 22 my dad was diagnosed with Hypertrophic Cardiomyopathy (HCM), a genetic heart disorder that affects 1 in every 500 people. Once my dad was diagnosed, it was recommended that I stop my strenuous activity and get screened as soon as possible.   So off to the doctor I went, and sure enough, since that initial diagnosis of mitral valve prolapse in high school my septum had thickened and I was diagnosed with HCM.

Even though I experienced no noticeable symptoms associated with HCM my lifestyle changed.  It had to or I would run the risk of a symptom of the disease: sudden cardiac death.  So no more burst activity.  No more competitive sports.  Shortly after the diagnosis, my cardiologist recommended I enroll in a research study for HCM that was underway at the National Institutes of Health (NIH) in Bethesda, MD.  And for a number of years I made an annual trek to Bethesda to be examined – Electrocardiogram (ECG), Chest X-ray, ECHO – and given medication.   At the time there was never any mention of me needing an Implantable Cardioverter Defibrillator ICD.

I remained asymptomatic and lived a reasonably active lifestyle for the next 3 or 4 years.   I moved to California for career pursuits and everything seemed stable.  Then, while driving home from the gym with a friend, my heart started to race, I became short of breath and my vision started to tunnel.  I immediately pulled over and my friend summoned an ambulance.  They took me to the hospital and after a few hours of monitoring and observation I was released.   California was a very long way from the NIH in Bethesda so I immediately contacted a cardiologist / electrophysiologist who had been recommended to me.  The doctor arranged for a holter monitor for a few days.  As a result of the monitor it was determined that I had Supraventricular Tachycardia (SVT) and Atrial Flutter, rhythm abnormalities, but not the dreaded ventricular tachycardia.

For a few months I tried medication to control the SVT and atrial flutter.  But it didn’t fully suppress the irregular rhythm.  The next step was a radiofrequency ablation  for Atrial Fibrillation (A-Fib).    That procedure was a success and everything went back to normal… for a while.

About 9 months later I started to have more palpitations and a racing heart beat.   Once again, I was put on a holter monitor.  This time the results were different.  It showed episodes of ventricular tachycardia (V-Tach), a much more serious concern.   At that time I was given two options, medication or an ICD.  Due to my family history and risk stratification I was a candidate for an ICD.  But the thought of having the device implanted in my chest was a bit frightening.   The only other option was a potent anti-arrhythmia drug called Amiodarone.   So after some discussion my doctor and I agreed to try the Amiodarone.

While the Amiodarone was effective in keeping my heart stable, it’s potentially toxic side effects gnawed at the back of my mind.  Over time the drug can build up in a patient’s system and start affecting the liver, the eyes, the thyroid.  I was still young and realized I’d have to be on this drug for the rest of my life.  I couldn’t help but wonder what that kind of exposure could end up doing to me.  Would the side effects over time be too great?   I also couldn’t help but think about having an errant rhythm that the drug couldn’t control.  If that ever happened there was no other “safety net” that could prevent sudden cardiac arrest. I was beginning to think that this drug was not the ideal long-term treatment plan for my situation.

By late 1999 I became more comfortable with the thought of getting an ICD.  More and more, it seemed like the best long-term choice for me.  The decision was made and in December 1999 I had my ICD implanted.   And almost 8 years later, on that Friday evening in 2007 I was happy I did.

As I slid down the wall to the floor with my heart racing and my vision tunneling, I called out to my wife and braced myself for the ICD shock I was certain was about to hit me.  But it didn’t come.  Instead, smaller “pulses” known as ATP delivered pacing therapy to my heart as the first level of defense against a dangerous rhythm.  Within seconds my heart rate returned to normal and the symptoms disappeared.    My wife was already on the phone with my doctor’s office, and shortly thereafter I transmitted the data from my ICD using my Medtronic Carelink remote monitor.  The episode was confirmed as V-Tach at a rate in excess of 200 beats per minute and that it was terminated by the ATP therapy.  That day I was thankful that I had the ICD implanted in my chest, because without it the outcome may have been very different.

It’s now 2013 and I have had an ICD implanted in my chest for almost 14 years.   I live with the peace of mind of knowing that if my heart ever does go into a dangerous, irregular rhythm that my ICD will do its best to correct it and keep me alive.

Screening through echocardiogram detected the HCM and made me aware of my heart disease.   Careful monitoring detected the potentially life-threatening rhythms and led to me having an ICD that has since intervened and probably saved my life.  While the journey hasn’t always been the easiest (open heart surgery, inappropriate ICD shocks) it’s nothing compared to the consequences of having a heart condition and not knowing about it until it’s too late.

Get screened.  It’s easy, it doesn’t hurt, and it only takes a few minutes of your time. And who knows, it may end up saving your life.







Heart Murmur:

Hypertrophic Cardiomyopathy (HCM):

Echocardiogram (ECHO):

Electrocardiogram (EKG):

Mitral Valve Prolapse (MVP):

Supraventricular Tachycardia (SVT):

Radiofrequency Ablation for Atrial Fibrillation (A-Fib):


Implantable Cardioverter Defibrillator (ICD):

Amiodarone (Drug):



  • Heart disease is the leading cause of death for women in the United States.
  • Heart disease kills more women than all cancers combined.
  • Heart disease is the cause of death of approximately 26% of women who die each year  ~  That’s one in every four women.
  • 64% of women who die suddenly of coronary disease have no previous symptoms, and in many cases their deaths may have been prevented had they had access to cardiac screenings early on (American Heart Association 2010).

64 Percent of woment


Early detection saves lives!

Heartfelt Cardiac Projects

provides affordable heart screenings to the public.

Make arrangements to have your heart screened today!

Find out how:


Did you know that . . .

Sudden Cardiac Arrest (SCA)

kills more than 1,000 people a day,

that’s one person every 90 seconds,

a number greater than the number of deaths each year

from breast cancer, lung cancer, stroke or AIDS?




Early Detection Saves Lives!

Heartfelt Cardiac Projects

offers affordable heart screenings to the public.

Have your heart screened today!






“Carry out a random act of kindness,

with no expectation of reward,

safe in the knowledge that one day

someone might do the same for you.”

~Princess Diana


Give the gift of peace of mind.

Provide an affordable heart screening for someone today.

Contact Heartfelt Cardiac Projects to find out how:




Early detection saves lives!

If you would like to be screened at our Mission Viejo, California event,

please click link below: