Owen's story...

On May 2, 2020, at 2:02 PM, our world changed forever when we met Owen. From the start, his curious blue eyes seemed to take in everything, as if he was already trying to figure out how the world worked.

With sandy blonde hair and a big personality, his first words—“Hi!” quickly followed by the oh-so-random but unforgettable “Lasagna”—had us in stitches. (For context, that’s straight out of his favorite show Go, Dog, Go! on Netflix.)

From the beginning, he wasn’t your average kid. While most toddlers were glued to the aquarium glass, Owen was busy trying to understand light switches, door hinges, and anything remotely “techy.”

As Owen grew, his personality became as vibrant as his smile. Patient, persistent, and overflowing with love, he has this way of making everyone feel special. One thing about Owen? If you promise him something, he’ll remember. (Seriously, don’t try to wiggle out of it.)

His mix of stubbornness and laser-sharp focus is unmatched, and whatever he sets his mind to, he doesn’t stop until it’s done. He’s a little builder at heart, always working with his hands, tinkering, and creating. And when it comes to his family, his love runs deep. He calls us his “friends” and treasures every cuddle and hug like they’re the best part of his day.

But then, one day, everything changed. A lump appeared…

Owen Watson, currently being treated for B-Cell Acute Lymphoblastic Leukemia at OSHU.

A lump emerged...

The journey to discovering Owen’s B-Cell Acute Lymphoblastic Leukemia was like being trapped on a rollercoaster that just wouldn’t stop. At first, it seemed innocent enough—just a few ear infections. Antibiotics became part of our routine, and we tried to roll with it, thinking it was just one of those phases kids go through.

Then, a lump appeared on Owen’s neck. It was small at first, barely noticeable, but it didn’t stay that way. It grew, and with it, our worries. Pediatricians and even ER doctors reassured us it was nothing serious—probably just related to the ear infections. “Give it time,” they said.

So, we waited. And hoped.

Unexpected collapse...

Owen’s snoring—eerily similar to his dad’s pre-tonsillectomy days—finally pushed us to see an ENT. The doctor seemed concerned about his swollen lymph nodes but wasn’t overly alarmed. They suggested a follow-up six weeks later.

So, we waited some more.

But just two weeks later, our worry turned to full-blown panic. Owen suddenly collapsed, letting out a scream of pain that shattered any sense of calm we’d managed to hold onto. At first, the doctors thought it was a toddler’s fracture—a relatively common and usually minor bone crack. We latched onto that explanation, hoping it was just a bump in the road.

But it wasn’t. The fracture was a distraction, a red herring. The real issue was still lurking, undiagnosed and growing more dangerous by the day.

So, we waited even longer.

Worst fears confirmed...

Finally, the local ENT noticed something we couldn’t ignore: Owen’s swollen lymph nodes were multiplying. That observation fast-tracked us to a specialist at OHSU Doernbecher Children’s Hospital. What followed was a whirlwind of tests—a blur of pokes, scans, and nervous conversations, all barely concealing the fear that was growing in the pit of our stomachs.

The call came at a moment we’ll never forget. Owen had just scaled a play structure, his little face beaming with pride. He was so happy, so full of life. When we told him we had to go back to the hospital, he protested, “No, Daddy, but I feel better now.” His words, so innocent and full of hope, cut us to the core.

When we were admitted, our worst fears were confirmed. Owen’s condition was worse than we could have imagined, his little body already bearing the weight of an illness we hadn’t even realized was there. His rapid decline pushed us into a reality we weren’t ready for—a path we’d never have chosen. Yet, here we were, starting a long and grueling battle.

One that, thankfully, came with hope for recovery.

But nearly a year later, nothing could have prepared us what were were going to discover...

Owen's life will be shortened — even if he survives Leukemia.

What started as elevated liver enzymes in Owen’s blood forced us to pause his treatment and switch to a newer medication called Blinna. At first, we hoped this would help ease some of the side effects he’d been experiencing. But then we began noticing subtle, troubling changes—he struggled to climb stairs, had difficulty standing up from the ground, and moved with an awkwardness that wasn’t like him.

Our oncologists were quick to point out the drop-foot he was developing, initially attributing it to the side effects of Dexamethasone and Vincristine. And in a way, they were right. But the real cause turned out to be far more sinister.

Even with the switch to Blinna, which should have lessened his muscle weakness, the drop-foot got worse. That’s when we were referred to a physical therapist. What we expected to be a straightforward appointment turned into a moment that broke us.

Owen couldn’t climb stairs by himself.
He couldn’t engage his core muscles enough to jump, even slightly.
He needed help with effortless activities for a 4-year-old.

The therapist knew something was very wrong. She ordered a CK (creatine kinase) blood test. When the results came back, the CK levels were off the charts—above 10,000.

And just like that, the pieces fell into place, but in the most devastating way possible. Given Owen’s age, his symptoms, and the test results, it was almost certain: Owen had Duchenne Muscular Dystrophy.

Almost two weeks later, genetic testing confirmed it.

Duchenne is a cruel, relentless disease. It eats away at the muscles, robbing a person of their strength bit by bit until it takes away their heart or lungs, too.

There’s no cure.
No treatment to stop it.

All we can do now is give Owen the best life we possibly can. To fill his days with love, joy, and moments that will make him feel invincible, even when the odds seem impossible.

Owen's combined diagnosis' is extremely rare.

The rarity of cases like this comes down to how uncommon it is for both conditions to happen at the same time, combined with the fact that if there is other cases, they’re not widely reported in any medical literature. This makes his treatment plan even trickier since Owen's leukemia treatments could actually make his DMD worse.

What is B-Cell Acute Lymphoblastic Luekemia?

B-Cell Acute Lymphoblastic Leukemia (B-ALL) is a type of cancer that starts in the blood and bone marrow. It happens when the body produces too many abnormal white blood cells that can’t do their job right. This throws everything off, making it harder to fight infections, transport oxygen, or control bleeding.

What is Duchenne Muscular Dystrophy?

Duchenne Muscular Dystrophy (DMD) is a condition that causes muscles to weaken and lose function over time. It mostly affects boys and happens because of a genetic issue that disrupts the protein muscles need to stay strong. As kids with DMD get older, everyday tasks like walking, breathing, and even heart function deteriorate.

Owen Watson, currently being treated for B-Cell Acute Lymphoblastic Leukemia at OSHU.

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currently being treated for B-Cell Acute Lymphoblastic Leukemia at OSHU.