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The Man with a Big Heart

by Nicole Stenzel on Thursday, Sep 03, 2020

Gerald David Stenzel, or “Jerry,” as he was better known, was born October 14, 1966, in Wells, Minnesota to Dominic and Evangeline Stenzel—who had a small farming operation and raised their 11 (yes, 11) children on the farm outside that same small town in Minnesota. Jerry had what he always described as a “normal” childhood—at least, as normal as it can be with 10 siblings—when, in fact, Jerry and his childhood were anything but normal.

Shortly after he was born, it was discovered that Jerry had a congenital heart defect. His tricuspid valve had not fully developed: diagnosis tricuspid atresia. Jerry was whisked away a few hours down the highway to Mayo Clinic, where surgeons performed a shunt operation to save his life.

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CHD and Finding “The One”

by Lauren Bednarz on Thursday, Nov 29, 2018

My husband, Chris, and I have been together 10 years and married almost seven. Some days I still can’t believe I found my soulmate and very best friend. I’m so grateful and blessed to have him in my life.

When I was born 31 years ago I was supposedly a healthy baby girl, but at 10 weeks old and in heart failure, I was diagnosed with complex congenital heart defects: tricuspid atresia, hypoplastic right ventricle, and ventricular septal defect. Medical technology to help save us complex CHDers was still so “new,” and my parents were living moment to moment never dreaming that 31 years later I would be happily married and living a wonderful full life despite all the challenges I have faced.

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Travel Must-Knows of a Heart Warrior

by Jara Weinkauf on Friday, Dec 15, 2017

Travelling is one of my favourite things to do in my free time. But as life has it, exploring the world with a congenital heart disease can be slightly different than usual.

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It All Started With A Stretch

by Ellen Greenberg on Friday, Feb 26, 2016

For the last two years, I have been dealing with chronic migraines—the worst kind. My cardiologist is not sure why I am living with this type of chronic pain. I know that many of us CHDers live with chronic pain. My neurologist is bewildered as to what to do for me—due to my multiple congenital heart defects—and common migraine medications have been difficult to administer.

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Half a Century with Half a Heart

by Tracey Grasty on Thursday, Jan 28, 2016

Sometimes I get scared I will be all alone. I'm scared my parents will leave me all alone because they are in their 80s. I need to have a Fontan revision sometime in the near future, but I'm scared I won't do well, or I will have to go it all alone because—let's face it—my mom won't fly, she has health issues of her own, and my dad, who is older than her, needs to keep her safe.

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I’m Just Jen

by Jennifer Gooden on Tuesday, Jan 12, 2016

I am not a heart hero. I am not a cardiac warrior. I am not a congenital heart survivor. I am not quite sure why it a plucks my nerve when people call me brave, strong or some combo of cardiac champion.

I am just Jen. I am me.

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Disclaimer

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.