Jonny's Journey. A Path to a New Beginning.

Jonny's Journey. A Path to a New Beginning. Meet Jonny, who was born with a rare metabolic disorder called OTC Deficiency.

Follow his journey ahead as we look to give him a new beginning with a Liver Transplant.

One year with many wins and lots of love. 💚Yesterday, July 25, we celebrated one full year since Jonny received his live...
07/27/2026

One year with many wins and lots of love. 💚

Yesterday, July 25, we celebrated one full year since Jonny received his liver transplant.

It’s hard to believe we’ve already reached this milestone. Looking around yesterday at all the smiling faces, laughing kids, and people who have loved and supported us through this journey, I couldn’t help but feel incredibly grateful.

Jonny told me it was “the best day of my life.” That sentence alone made every bit of it worth it. Charlie rated it as “the best day of the year.” 😂 He has slightly higher expectations in life, but I’ll happily take that review too.

To everyone who came, sent messages, or simply thought of us—thank you. It meant more than you’ll ever know.

As if the week couldn’t have gotten any better, Jonny and I were also at SickKids on Monday for his one-year transplant follow-up.

The results couldn’t have gone better.

Before transplant, surviving was all we knew.

Our lives revolved around appointments, bloodwork, medications, admissions, advocating, educating, and constantly preparing for what might happen next. It was exhausting and, at times, heartbreaking. Looking back now, I realize just how much of my life was spent simply trying to keep my little boy safe.

Today, for the first time in a very long time, I truly feel like we’re beginning to step out of survival mode and into living.

Over the last couple of days, I’ve also taken a few quiet moments to myself to reflect. I found myself offering thanks in a way that’s difficult to explain.

To Jonny’s donor…

A family’s worst day became the reason our family gets to have all of these beautiful days. It’s such a complicated emotion to hold so much gratitude while knowing it came at the cost of another family’s unimaginable loss.

It still feels surreal that my son was the one who received this incredible gift.

In Canada, 4,344 people were waiting for an organ transplant at the end of 2025, including 646 people waiting for a liver. During that same year, 212 Canadians died while waiting for a transplant, 86 of them while waiting for a liver.

Those numbers are heartbreaking and remind me just how important organ donation truly is.

I will never be able to fully express my gratitude to Jonny’s donor, their family, and every single member of the transplant team at SickKids. They have not only given Jonny a future, they’ve given me one too.

They’ve slowly allowed me to let go of the obsessive anxiety that surrounded Jonny’s health for so many years and given me the ability to finally see a future that is bright for my boy.

One year ago, we were praying for a miracle.

Today, we’re living it.

Forever grateful. 💚

🎉 One-Year Liverversary Celebration Update 🎉We’re getting so excited for Saturday!We want to keep this day exactly how J...
07/22/2026

🎉 One-Year Liverversary Celebration Update 🎉

We’re getting so excited for Saturday!

We want to keep this day exactly how Jonny would want it—light, easy, fun, and surrounded by people who simply want to celebrate this incredible milestone with us. No expectations, no formalities… just a great afternoon together.

If you’re reading this, you’re welcome to join us! 💚

Here’s what we’ve got planned:
🎈 Street party out front
🏰 Bouncy castle
🪑Chair
🎮 Bring your Nintendo Switch or a controller if you’d like to jump into some gaming.
🔫 And don’t forget your favourite Nerf gun—we’re planning an epic battle in the forest!

One important update:
We’re moving the start time to around 3:30 p.m.

Charlie’s final baseball game has been scheduled for approximately 1:00–1:30 p.m., and after missing his championship game last year while we were in the thick of Jonny’s transplant, there’s no way I’m missing this one. ❤️

Thank you all for loving our family and walking this journey with us. We can’t wait to celebrate not only Jonny’s incredible first year with his new liver, but also the people who have supported us every step of the way.

See you Saturday! 💚
:::writing

An Update on Jonny’s Journey 💚It’s been a little while since our last update, and honestly… that’s a good thing. Around ...
06/28/2026

An Update on Jonny’s Journey 💚

It’s been a little while since our last update, and honestly… that’s a good thing. Around here, no news truly is good news.

Jonny celebrated his 11-month liverversary on the last day of school. It’s hard to believe how quickly time has passed. The weeks leading up to it were a whirlwind with year-end school activities, field trips, and even a few unexpected vet visits after our cat Toby used up a couple of his nine lives by getting hit by a car. Thankfully, he’s recovering well and is back where he belongs—at home with us.

The best news of all is that Jonny’s bloodwork continues to look great. Time and time again, his body is showing us that it’s accepting this incredible gift. We head back to SickKids toward the end of July for his next follow-up, but for now, we’re incredibly grateful for how well he’s doing.

In just a few weeks, on Saturday, July 25, we’ll be celebrating Jonny’s 1-Year Liverversary. What a milestone. 💚

If you’re reading this, we’d love for you to celebrate with us. Please head over to the event posted on this page for all the details. Whether you’ve followed Jonny’s journey from the beginning or joined along the way, we’d love to share this special day with you.

As summer begins, I’m looking forward to spending quality time with my boys. Last summer was spent recovering, living between hospital rooms and the same four walls. This year, we’re hoping to make memories, enjoy the little things, and soak up every moment together.

Thank you for continuing to cheer Jonny on. Every milestone is a reminder of how far he’s come, and we never take this gift for granted. 💚

💚 A Little Life Update 💚First and foremost — it’s McHappy Day 🍟A day that hits close to home for our family. Our journey...
05/06/2026

💚 A Little Life Update 💚

First and foremost — it’s McHappy Day 🍟
A day that hits close to home for our family. Our journey would have looked very different without RMH, and we’ll always carry that gratitude with us. Dinner made easy today, and for a cause that truly matters.

Now for a bit of a plot twist…
My guy somehow managed to land himself with a broken wrist in two spots 🫠
So we’re rocking a cast for the next 4 weeks. Because why not keep things interesting around here.

In between all of that, we celebrated a big milestone — 9 months post-transplant — alongside Jonny’s youngest cousin Logan’s first birthday.

And to top it all off… today is Toby’s 6th birthday 🎉
So many milestones.

Always something over here… but always so much to be grateful for. 💚

💚 A Morning of Emotion & Gratitude 💚I was able to open the envelope we received from Jonny’s donor’s family at our last ...
04/16/2026

💚 A Morning of Emotion & Gratitude 💚

I was able to open the envelope we received from Jonny’s donor’s family at our last clinic appointment.

It was from his donor’s mother.

I don’t think there are words strong enough for what that feels like. Opening something written by another mother, someone who has experienced unimaginable loss. It carries a weight and a connection that is hard to describe.

There’s an immediate recognition there. Not of circumstances, but of love. Of grief. Of what it means to be a mother holding both heartbreak and the need to reach out across it.

Our transplant team does encourage families to remain confidential, especially in these early stages, and I am still sitting with that guidance while also trying to process what this connection means in my own heart.

Although this is deeply personal for my family, this page has always been an outlet for me through this journey. Through the fear, the waiting, the healing, and everything in between, I have felt supported and less alone here.

So sharing this part of our story, even something this intimate feels like the only way I know how to process it right now. 💚

I’ll share the note I wrote in response below.

To the family of our donor,

There are some moments in life that split everything into a before and an after. The day my son received a liver transplant, thanks to your daughter was one of those moments.

It’s impossible to put into words the weight of what your family has given us. A new liver is not just a second chance at life. For my son, it’s a chance at a different life. One not defined by fear, restrictions, or constant monitoring. One with possibility.

My son was born with a rare condition. For the past many years, he has lived a life few could understand. One that looked stable from the outside, but underneath was full of complexity and vigilance. Every single day was a balancing act. Strict diets. Dozens of medications. Exhaustive check-ins. Constant bloodwork.
He lived a life of limitations. No overexertion. No stress. Every bike ride, swim, illness, school test, emotional breakdowns or even jumping on the trampoline came with risk. Constant worry. I watched him like a hawk. I had to. The risks were too great.

Recently everything shifted. Many unexplained hospital admissions in a matter of months. No clear reason. Just this reality we’d always been warned about. His condition is unpredictable. It was heartbreaking to watch him go through it, knowing this rare condition was doing things that doctors couldn’t always explain. This was proof that his condition was shifting, and not in our favor. The uncertainty became unbearable.

After many talks with specialists, I made a decision that no parent takes lightly, to move toward transplant. To give him a chance at a better quality of life. And just as we were preparing ourselves for the unknown, your family made a decision in the midst of the unimaginable.

Your daughter’s gift saved my child’s life and the lives of others too. I don’t know if I’ll ever truly be able to express how much it means that you chose to let your child live on in others. But I want you to know this: because of you, I’ll get to hold my son longer and most importantly with less fear. I’ll get to see him laugh freely. He’ll get to just be a kid, a teen, a man, someone who can grow into his own life, not one I am constantly managing moment by moment.

What your daughter has given reaches far beyond my son’s health. It has changed our entire family. For so long, we lived in a constant state of survival, where every decision, every moment, was shaped by his condition.

Because of your daughter’s gift, that weight has lifted in a way I don’t know how to fully describe. I am no longer living every moment on edge, watching for signs, trying to stay one step ahead of illness, making emergency room visits and carrying fear with me at all times. I have been able to step out of that constant state of vigilance and begin to breathe again.

I can be more present with both of my children. With joy, with calm, and with a sense of peace that we haven’t felt in a very long time. I am not just managing each day anymore, I am finally able to enjoy it. That is something your daughter has given not just to my son, but to me as a mother, and to us as a family.

In the process of searching for a living donor for my son, we had someone step forward with the intention of helping him, she chose to continue forward and ultimately donated a portion of her liver to someone else. So in a way, your daughter’s gift didn’t just change one life, it became part of something even bigger. Her gift helped create a path that allowed another life to be saved as well. It’s a reminder that this kind of love and selflessness doesn’t stop in one place. It continues on, reaching people we may never meet.

We are about to celebrate nine months since this incredible gift, and he is doing better than I ever could have hoped. He is a resilient, funny, and a strong boy who loves riding his bike, being outdoors, fishing, Lego, gaming and spending time with people he loves. Seeing him begin to enjoy those simple parts of childhood more freely has been something I don’t think I’ll ever take for granted.

I also want to thank you for the photos you shared. They are so incredibly meaningful to us. I will frame them and display them proudly in our home, as a beautiful reminder of her and the piece of her that now lives on in our hearts.

I hope you know that the love you poured into your daughter now lives on through my son. I carry that with me every single day. And when I hold him, I feel both of them. Your daughter and my son woven so perfectly together in the most sacred, quiet way.

There is no way to thank you enough. But please know that your daughter’s life and legacy will never be forgotten in our home. We are honouring her every single day.

With all my heart, from one mother to another, I honour you and your daughter.
A forever grateful mother of one of your daughter’s gifts.

🏡 Home Again 🏡We made it home safely, caught the early train, and were back just in time for Jonny to make it to fencing...
04/07/2026

🏡 Home Again 🏡

We made it home safely, caught the early train, and were back just in time for Jonny to make it to fencing last night!

His appointments went well, and everything is continuing to look reassuring. We’re so thankful to keep hearing that his new liver is doing exactly what it’s meant to do.

In other news…

I was handed something that completely stopped me in my tracks. An envelope addressed to Jonny from his deceased donor’s family.

I always thought there was about a year before any kind of exchange like this happened, knowing how important that first year is post-transplant. So to receive this now… I wasn’t expecting it.

My mind is racing. My heart kind of stopped in that moment.

It’s sitting here, unopened. And I know I’ll open it I just need to find the right time, the right space, and maybe the strength to take it all in.

Stay tuned… 💚

🚆 Back to Toronto We Go 🚆Departed for Toronto. Late, of course (train life 😅), but still grateful to be on the rails ins...
04/05/2026

🚆 Back to Toronto We Go 🚆

Departed for Toronto. Late, of course (train life 😅), but still grateful to be on the rails instead of the highway this Easter long weekend.

Tomorrow morning we’ll be back in the halls of SickKids for Jonny’s clinic appointment. Bloodwork first thing, followed by a routine ultrasound to make sure his incredible gift is still doing exactly what it’s meant to do in my sweet boy.

As always, your prayers, well wishes, and good vibes mean the world to us. We carry them with us into every appointment. 💚

On a side note, April is Organ Donation Awareness Month, and it holds such a deep place in our hearts. Because of one selfless decision, one family’s unimaginable loss turned into a gift to allow Jonny here, thriving, and living a life that once felt so uncertain.

Organ donation doesn’t just save lives.
It changes entire families!

We are living proof of that every single day.

d.

Having walked a similar road with Jonny, this story brings back all the emotions. The fear, the waiting, and the overwhe...
03/24/2026

Having walked a similar road with Jonny, this story brings back all the emotions. The fear, the waiting, and the overwhelming gratitude for a second chance. No family should have to go through it, but the strength these kids show is truly incredible.

Organ donation saves lives. Plain and simple. 💚

02/28/2026

💚 Rare Disease Day 💚

Rare Disease Day hits differently for us.

Before transplant, our world revolved around OTC Deficiency. The rare metabolic disorder that brought us onto this path. A condition where the body cannot properly clear ammonia from the bloodstream. Something invisible… until it’s not.

For years, we lived watching for subtle signs. Headaches, nausea, unusual fatigue, confusion, personality shifts. Things that might look minor to most people, but in someone with OTC can signal rising ammonia levels and the risk of a life threatening crisis. Bloodwork wasn’t optional. It was urgent.

Seven months ago, that chapter closed in a way we once only hoped for. Jonny’s transplant ended the daily battle with OTC. His new liver gave him freedom from the constant risk we carried for so long.

But today isn’t about closing the book.
It’s about awareness.

Because there are families still living in that hyper-vigilant space. Families counting grams of protein. Families rushing for ammonia checks. Families needing doctors, teachers, and communities to recognize symptoms quickly.

I’m sharing a short 2 minute video today to help others understand what to look for and when ammonia levels should be checked.

Rare doesn’t mean unlikely.
Rare doesn’t mean unimportant.
And rare families deserve loud support. 💚



https://www.facebook.com/share/v/18DJGebWM5/?mibextid=wwXIfr

💚 7 Months Since the Gift of Life 💚Today marks 7 months since Jonny received his new liver. A life changing gift we will...
02/26/2026

💚 7 Months Since the Gift of Life 💚

Today marks 7 months since Jonny received his new liver. A life changing gift we will never take for granted.

It’s been a month filled with life in the best way.

School trips.
School skating.
And even giving jiu-jitsu a try.

Seven months of healing.
Seven months of hope.
Seven months closer to the life we fought so hard to reach. 💚

Month by month, we are learning what normal looks like again. Our new normal.

And it is beautiful.

Address

London, ON

Website

https://www.giftoflife.on.ca/resources/pdf/transplant/PRELOD_Brochure_April_2023.pdf,

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