Episode 2

Tetralogy of Fallot: What Every Parent Needs to Know

There is a moment that changes everything.

A baby is born. And something is wrong. The lips are blue. The oxygen is low. And within hours a parent is handed a diagnosis they cannot yet pronounce. A name they will spend the rest of their lives learning to carry.

Tetralogy of Fallot.

It is one of the most common complex congenital heart defects in the world. It accounts for approximately ten percent of all congenital heart disease cases. And yet most people, including most new parents sitting in that hospital room for the first time, have never heard of it until it becomes their reality.

That is what this episode is about.

In Episode 002 of Small Hearts, Loud Voices, we break down exactly what Tetralogy of Fallot is. Not in cold medical language. Not in a way that makes you feel more lost than when you started. But in plain, human, honest terms that every parent, caregiver, and advocate deserves to have access to.

You will learn what the four defects are and what they mean for your child's heart. You will hear the story of a family navigating a Tetralogy of Fallot diagnosis from the very first moment. You will receive encouragement for the road ahead, because this journey is long and hard and you deserve to feel held inside of it. And you will leave with something you can actually do today to support the CHD community.

If you are a parent who just received a Tetralogy of Fallot diagnosis, this episode was made for you. If you are a CHD survivor living with the long term effects of congenital heart disease, this episode was made for you. If you are a nurse, a teacher, a neighbor, or a stranger who wants to understand what families living with CHD are actually going through, this episode was made for you.

Congenital heart disease affects one in every one hundred births. Tetralogy of Fallot alone accounts for tens of thousands of new diagnoses every single year. These are not rare children. They are everywhere. In your neighborhood. In your child's classroom. In cardiac units right now waiting for surgeries that will change the course of their lives.

They deserve a world that knows their name.

About the Podcast

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Small Hearts, Loud Voices
Facts, stories, and encouragement for every family touched by congenital heart disease.

About your host

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Adrian Adair

Adrian Adair is the founder of Heartbeat Forward, a federally recognized 501(c)(3) nonprofit dedicated to congenital heart disease awareness, support, and advocacy for children and families living with CHD.
He did not come to this work by accident. He came to it because he believes congenital heart disease is the most overlooked crisis in children's health today. One in one hundred babies is born with it. It affects more children every year than all childhood cancers combined. And most people have never heard of it until it walks into their own family.
Adrian is the author of The Quiet Majority, a book about why congenital heart disease deserves to be seen, and a tireless voice for the children and families navigating a diagnosis the world moves too fast to notice.
Small Hearts, Loud Voices is his commitment to changing that. Every episode is built around one CHD fact, one child's story, one word of encouragement, and one call to action. No filler. No noise. Just truth, humanity, and purpose for every family touched by congenital heart disease.
He believes the children living with CHD are not statistics. They are not diagnoses. They are whole, extraordinary people with hearts that keep beating against every odd. And they deserve a world that knows their name.
Visit heartbeatforward.org to learn more about the mission.