Home / 2020 / Discovering CHD on a Soccer Field

Discovering CHD on a Soccer Field

Friday, November 20, 2020

By Jordan Marada

My name is Jordan Marada and I am a southern California native. At the early age of 4, my mother introduced me to a soccer ball after playing for many years herself.

Both of my parents helped coach my recreational soccer team before I was quickly recruited by a competitive club team at age 9. I played competitively from an early age and was continuously motivated by the passion and love for the sport, the friendships, and the dream I had of being a professional soccer player!

I was recruited and committed to play in college, where I began to peak in my career. During my Junior year at the University of Southern California in 2012-2013, our team wore heart rate monitors during daily training sessions. These quickly alerted my coaches and team doctors that there was something abnormal with my heart. My heart rate was ridiculously high for my fitness level and age. I was sent to the team cardiologist where I underwent multiple tests. Shortly after the testing, I was diagnosed with a bicuspid aortic valve.

The diagnosis did not slow me down one bit and my doctor was pleasantly surprised by how strong my heart was. I continued to play soccer and yearly check-ups were required to make sure there were no changes, as the bicuspid valve can begin to leak or become faulty or calcified.

After my 4-year college career and a healthy heart, I knew that was not the end of my soccer career! I was recruited by a professional club in the Czech Republic in 2016 where I played two seasons. My time in Europe was incredible—I met so many new friends and teammates and had the time of my life continuing to play the sport I love.

After my European adventure, I was extremely excited to play in my hometown of Orange County for a brand-new team, the LA Galaxy Orange County Women’s Team. In the summer of 2019, we won a National Championship in Calgary, Canada. During that incredible summer, I was approached by an agent who offered me a contract to play in Japan.

I was wrong after thinking my pro career was coming to an end. I was on a plane two weeks later heading to Japan where I scored the game-winning goal in my Japanese playing debut!

Although I have been blessed to play my sport without a serious injury for many years, I unfortunately ruptured my Achilles tendon during a training session upon my return home from Japan this past January. I underwent surgery that month, and I am continuing to recover well as I look forward to what is next in my career.

I am currently working for a professional men’s soccer team in Orange County, CA, called Cal United Strikers FC. I work as the team's Operations & Community Relations Manager and have been learning so much from the other side of the sport. I also enjoy mentoring and coaching young and upcoming athletes and encouraging them that no dream is too big!

After my diagnosis, there is no doubt that I have felt the stress, anxiety, and worry of knowing that I do not have a “normal” heart. I am thankful for the opportunity to share my story and look at my defect as a unique and special trait I carry with me.

My lasting words of encouragement: Attack each day with positivity, joy, and gratefulness! You can overcome any obstacle by viewing your “defect” as an opportunity for your strength to shine through. You are stronger than you think!


Note: Always make sure to check with your ACHD cardiologist before beginning any exercise routine.


Add yours below.


The opinions expressed by ACHA bloggers and those providing comments on the ACHA Blog are theirs alone, and do not reflect the opinions of the Adult Congenital Heart Association or any employee thereof. ACHA is not responsible for the accuracy of any of the information supplied by the ACHA bloggers.

The contents of this blog are presented for informational purposes only, and should not be substituted for professional advice. Always consult your physicians with your questions and concerns.

Connect with ACHA

Join us in our mission to empower the congenital heart disease community by advancing access to resources and specialized care that improve patient-centered outcomes.

Enter your name, email and state to get started. If you choose to, you can provide more information to us in the next step for more tailored communications! We'll never, for any reason, share your personal information. Already get ACHA emails? We’ve got you! You do NOT need to fill out this form.

*By sharing your information, you consent to receiving emails from ACHA.

  • {{ m }}
{{ validation.firstError('basic.FirstName') }}
{{ validation.firstError('basic.LastName') }}
{{ validation.firstError('basic.Email') }}
{{ validation.firstError('basic.State') }}