As a child, I was haunted by a recurring nightmare of a doctor joyfully skipping down the street toward my house. He was there to take me from my family and add me to his “collection.” He always carried a string of balloons, each holding a child I recognized but couldn’t place. I knew we were always connected. When he reached my door, my mom would bring me to him, and he would “plug” a string into my chest, turning me into a balloon like kids, watching from the other side.

I spent my early years battling cancer. I didn’t know I had cancer at the time, just that I was there for “testing”—as if something “bad” was inside of me. I remember playing with other children in the hospital, bonding over shared experiences and IVs. At the time, I didn’t realize how these moments would later connect.

Years later, in my mid-20s, my mom shared that all the children I’d played with in the hospital—my friends—had died. I was the only survivor. One day, while journaling, I realized the children in my dream weren’t just a coincidence. They were the same children I had spent time with. I remembered playing with them and, later, playing alone after they were gone. My hospital had contacted Make-A-Wish, expecting me to die soon, and granted me one last wish. But I didn’t die. Unlike them, I survived.

That’s when I realized the dream was connected to my mortality. When the dreams appeared, the children weren’t physically present, meaning they were watching over me from the afterlife. I wasn’t fully on their side or this one—I was in between. It highlighted how close to death I had been and the guilt I felt for being the only one who survived.

For years, I struggled with survivor’s guilt. I couldn’t understand why I was spared. When I was diagnosed again and survived, the guilt intensified. Why am I alive?

Now, approaching my 30th anniversary of survival, I think about my friends and their families who have been gone for 30 years. My birthday typically represents grief, but last year I decided to live for them. Through me, they have life. Though I don’t know their names, I know they’re watching me, proud of who I’ve become.

I dedicate the rest of my life to living for them, knowing they’re always watching over me, experiencing it with me. This website, my life, my adventures, everything—is dedicated to them and their families. As the lone survivor, everything I have is for them. Through me, their memories live on.

This blog is dedicated to my fellow roommates at Oscher’s Pediatric Oncology in New Orleans, Louisiana, from 1995-1997, and their families. I have never forgotten your faces. Everything I do, everything I accomplish, is for you.

May you continue to know peace, and may peace continue to know you.

Outside of those I knew personally, I also dedicate this website to all families, children, and young adults who have ever faced chronic illness—those here and those who have passed. I send you positive vibes and best wishes for you to live your best dreams.

Imerman Angels

Imerman Angels is an organization I came across years later, after my second diagnosis. They provide one-on-one peer mentoring for free to cancer survivors, their caregivers, and even people with a genetic mutation who haven’t had cancer. While I didn’t use this resource during either of my cancer journeys, I can 100% acknowledge how vital it would have been—not just for me, but for my family as well. Especially my mom, who truly had no idea if what she was doing was the right choice. [I do hope she knows she chose right.]

There’s no “guidebook” for “what to do when you or your child has cancer,” but Imerman Angels provides support that’s as close as possible to what each person is experiencing. And while no cancer journey is the same, they strive to match you with someone who truly understands what it’s like to face a cancer diagnosis.

[Jonny did his big one.]

Because no one should fight cancer alone.

Donate to Imerman Angels

Oschers Pediatric Oncology

It’s clear that without this place and their treatment, I wouldn’t be here. While they couldn’t save all of us, they saved me. And without that advanced treatment and care, I wouldn’t be here today. Children facing a cancer diagnosis should have all the resources they need to beat it and fight back, so they too can live a fulfilling life.

Together, we stand strong for every child’s future.

Donate to Oschers Children’s Oncology

Make-A-Wish Foundation

My wish to Disney World was supposed to be one of my final memories of this life—and one of the last memories my family would have of me. Even now, at the age I am today, that wish and trip to Disney World remain a pivotal moment in my life. I remember so much from that trip, especially the special treatment I received, which allowed me to truly experience the magic of Disney. I wasn’t a sick child — I was just a child in the happiest place on Earth.

I still remember it like it was yesterday: running around the parks with my siblings, seeing Mickey, Minnie, and the princesses, being called up on stage during the magic show, meeting Shamu, feeling the stingrays at SeaWorld, riding the Jurassic Park-themed strollers, even the Jaws ride at Universal Studios, and having dinner at the Japanese Hibachi Grill at Epcot. I remember all of it—and what I don’t remember is actually being sick. That’s what the Make-A-Wish Foundation provides to children and families battling life-threatening illnesses: a chance to just be a family, and a child—creating pleasant memories instead of focusing on the challenges of hospital life.

Donate to Make A Wish Foundation

If any of this page touches you, or even rings true to a journey you or someone you know has navigated, I ask that you donate to one of these three organizations, to help support not only children and young adults, but also families who are navigating such a devastating disease. 


All three, organization that changed my life forever — Literally.