Book 1 — Personal Memoir

I Missed the Signs

For years, my body was sending messages I refused to hear. Fatigue that I called laziness. Swelling I blamed on travel. A diagnosis I thought was manageable — until it wasn't. This is that story.

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Paperback Available

Why I Wrote This

The book I wish had existed when I needed it most

Nobody tells you what kidney disease actually feels like from the inside. The medical community gives you lab numbers. Family gives you worry. The internet gives you worst-case statistics. What I needed was a real person telling me what it felt like to walk through it — day by day, decision by decision — and what happens when you wait too long to take it seriously.

I was that person who minimized, rationalized, and delayed. I was the one who thought "I'll deal with it after this trip" and "it's probably just stress." The signs were there for years. I missed them — or more accurately, I chose not to see them. That cost me in ways I am still accounting for today, sitting in a dialysis chair three days a week.

I wrote this so you wouldn't have to find out the hard way. Whether you've just been diagnosed with CKD, or you're watching someone you love ignore symptoms that concern you, this book is the conversation I wish someone had forced me to have earlier.


Who This Book Is For

If you recognize yourself here, this is your book

The Newly Diagnosed
You just got your CKD diagnosis and have no idea what this means for your life. You need a real person's account, not a pamphlet.
The Denier
You have symptoms. You've been putting off the appointment. Something in this book will recognize you.
The Caregiver
Your spouse, parent, or friend is sick and won't listen. Read this so you can understand what they're going through — and how to reach them.
The Dialysis Patient
You're already in the chair. You need to know someone else has been here and kept living — fully, with purpose and plans.

From the Book

A passage from Chapter 1

Excerpt — Chapter 1: The First Sign I Ignored

The doctor said my creatinine was elevated. I heard the word "elevated" and nodded like I understood what that meant. I didn't ask what creatinine was. I didn't ask what elevated meant for someone my age. I didn't ask what the next step was.

I smiled, said thank you, and made a mental note to look it up later. I never looked it up. I had a flight to catch.

That was 2019. By 2022 I was on dialysis.


The MAVTG Book Series

Recommended reading order

01
You are here
I Missed the Signs
The personal story. Start here if you want to understand what kidney disease feels like before the diagnosis you ignored becomes the one that defines you.
02
Michael's Big Kidney Journey
What happens after diagnosis. Treatment decisions, dialysis life, keeping your identity while your body is being managed by machines.
03
Day One: Understanding Kidney Disease
The plain-language clinical guide. Use this alongside your nephrologist — every term, every decision point, every question you should be asking.

About the Author

Written from the inside

Michael Moore during a hemodialysis session
Written from the chair — three days a week.

Michael Moore was diagnosed with Stage 5 Chronic Kidney Disease after years of ignoring the warning signs. He has been on dialysis three days a week for over six years — Monday, Wednesday, and Friday, four hours each session. He is on the national kidney transplant waitlist.

This book was not written by a doctor. It was written by a patient who lived it — who missed every sign, paid the price, and decided the experience was worth putting on paper so others don't have to learn the hard way.

I Missed the Signs is Michael's first published book. It is available now on Amazon in Kindle, paperback, and hardcover.

Kindle $9.99 (ASIN B0GR1ZC6X2)  ·  Paperback $14.99 (ASIN B0HBN4PYH7)  ·  Hardcover $21.00 (ASIN B0HC2R7GN1)


Ready to read it?

Available now on Amazon in Kindle, paperback, and hardcover. Your story doesn't have to look like mine — but reading this one might help you write a better ending to yours.

Get the Paperback — $14.99 → Kindle — $9.99 → Hardcover — $21.00 →

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Medical Disclaimer: This book is a personal memoir and does not constitute medical advice. The experiences described are the author's own. Always consult a qualified nephrologist or healthcare provider for diagnosis, treatment decisions, and medical guidance specific to your situation.