Teneritas · Heartbeat Forward Press

Books on Congenital Heart Disease

Written for families, survivors, and every heart touched by CHD — two books that refuse to let congenital heart disease be invisible.

Congenital heart disease is the most common birth defect in the world, affecting 1 in 100 children born each day. These books exist because the CHD community deserves stories, truth, and words that make them feel less alone.

The Quiet Majority — a book about congenital heart disease by Adrian Adair, cover art by Marco Moreci. Shows a baby sleeping in a golden bassinet.
Now Available

Publisher: Teneritas, 2026

Format: Paperback · Digital

Cover Art: Marco Moreci

Book One

The Quiet Majority

Why Congenital Heart Disease Deserves to Be Seen

Congenital heart disease affects nearly 40,000 babies born in the United States every year. Yet despite being the most common serious birth defect in the world, CHD remains radically underfunded, widely misunderstood, and nearly invisible in the public conversation about children's health. The Quiet Majority is a call to change that.

Written by CHD advocate and author Adrian Adair, this book cuts through the silence with clarity and conviction. It examines why congenital heart disease has been overlooked by mainstream medical advocacy, what the research funding gap actually costs CHD survivors and their families, and why the estimated 2.4 million Americans living with CHD deserve far more than they have been given. This is not a clinical textbook. It is an argument — passionate, evidence-informed, and deeply human — for why CHD must be seen.

"The quiet majority has been waiting long enough. Their stories, their surgeries, their daily lives living with repaired and unrepaired hearts — these matter."

  • The history of congenital heart disease research and why awareness has lagged behind other conditions
  • A clear examination of the CHD funding gap and its real-world consequences for survivors
  • The full scope of CHD: from simple defects to complex single-ventricle hearts
  • Why pediatric heart disease advocacy needs new voices, new channels, and new urgency
  • A vision for a world in which every CHD family is informed, supported, and seen
  • CHD Advocacy
  • Heart Defect Awareness
  • Pediatric Cardiology
  • Patient Advocacy
  • Public Health
  • Congenital Heart Disease
CHD Survivors Adults and teens living with a congenital heart condition who want their experience named and validated
CHD Families Parents, siblings, and caregivers searching for language that honors the weight of their journey
Advocates Community leaders and nonprofit workers building the next generation of CHD awareness
Healthcare Professionals Nurses, cardiologists, and social workers seeking a patient-centered perspective on CHD
Order on Amazon
Letters to the Waiting Room — a book for CHD families by Adrian Adair, illustrated by Marco Moreci. Shows hands holding a handwritten letter in a hospital waiting room.
Now Available

Publisher: Teneritas, 2026

Format: Paperback · Digital

14 Letters · Full Collection

Book Two

Letters to the Waiting Room

For Every Family Touched by Congenital Heart Disease

The hospital waiting room is one of the loneliest places in the world. It is where CHD families sit with fear they cannot put into words — waiting for surgical outcomes, waiting for news, waiting for a future they cannot yet see. Letters to the Waiting Room walks into that room and sits beside you.

This collection of 14 original letters is addressed directly to the people who live with congenital heart disease every day: the parents pacing during open-heart surgery, the CHD survivor learning to carry their diagnosis into adulthood, the sibling who grew up in the background of someone else's medical crisis, the caregiver who has run out of words. Each letter is a direct, honest, and deeply personal act of witness. Not advice. Not a clinical framework. A letter.

Author Adrian Adair — himself immersed in CHD advocacy as the founder of Heartbeat Forward — writes from a place of genuine closeness to the CHD experience. These letters do not minimize what CHD families carry. They honor it.

"There are things you have been waiting for someone to say. This book is an attempt to say them — without flinching, without false comfort, without leaving you alone."

  • The parent whose child is in surgery right now
  • The CHD survivor entering adulthood with an unfinished heart
  • The family who just received a prenatal CHD diagnosis
  • The caregiver who has forgotten how to rest
  • The sibling who grew up in the shadow of CHD
  • The CHD community mourning someone who did not survive
  • The medical team who holds CHD hearts in their hands every day
  • And more — a complete, intimate collection for every season of the CHD journey
  • CHD Family Support
  • Heart Surgery
  • Pediatric Heart Disease
  • CHD Grief
  • Caregiver Support
  • CHD Survivor
  • Congenital Heart Disease
New CHD Parents Families who have just heard the words "congenital heart defect" for the first time
CHD Adults Grown CHD survivors navigating healthcare, identity, and an uncertain future
Bereaved Families Those who have lost someone to CHD and need their grief witnessed
Support Communities CHD support groups and hospital chaplains seeking healing reading for families
Order on Amazon

About the
Author

Adrian Adair is an actor and CHD advocate based in Los Angeles, California. He is the founder of Heartbeat Forward, a federally recognized 501(c)(3) nonprofit dedicated to congenital heart disease awareness, family support, and the next generation of CHD advocacy. His books are published under Teneritas, a literary imprint committed to stories that matter. Adair's writing and advocacy have reached thousands of CHD families across the United States, and he continues to grow Heartbeat Forward's programs — from care packages and scholarship support to resource guides for every age and stage of the CHD journey.

Every small heart deserves a loud voice.

Both books are available now in paperback and digital format through Amazon. Share them with a CHD family. Leave one in a hospital waiting room. Let someone know they are not alone.

The Quiet Majority Letters to the Waiting Room