Josiah is a vibrant 5-year-old boy who has already endured more than many do in a lifetime. His journey began before he was even born when, at my 20-week ultrasound, doctors detected a congenital heart defect—a large ventricular septal defect, essentially a hole in his heart. Initially, the plan was to monitor him after birth and potentially place a pulmonary artery band to help stabilize him while waiting for his heart to grow enough for corrective surgery.
However, within hours of his birth, it became clear that his little heart was struggling. He showed immediate signs of heart failure and feeding difficulties. It was terrifying to watch our newborn fight so hard. He was quickly airlifted to Halifax for surgery to place the pulmonary artery band. Although the procedure helped, his heart remained too weak, and he required more medications just to sustain basic functions. At only three months old, we received devastating news— his heart could not be repaired. The only option left was a transplant.
This was May 2020, a time when the world was grappling with the peak of the COVID-19 pandemic. We had no choice but to uproot our lives and move to Toronto to wait for a new heart. My husband, Aaron, and our two-year-old son, Emmett, joined us in August 2020 and remained with us until we returned home in May 2022. It was an incredibly difficult journey, but staying together as a family gave us strength.
Josiah is thriving & his family’s future is filled with possibility.
Josiah
More Than Music: A Legacy of Compassion
Message from the Chairman
I’ve often said that music has the power to change lives, but nothing compares to what I’ve seen through my Foundation.
When we started this journey nearly 40 years ago, I never imagined it would become what it is today. I just knew there were families out there who were scared, exhausted, overwhelmed and needed help urgently.
Over the years, I’ve met parents who were hanging on by a thread, kids waiting for a miracle, and communities coming together in ways that still leave me speechless. The stories stay with me—and so do the faces.
This work is deeply personal to me. Every child we help and every family we support, reminds me that what we do matters—not just in numbers or
milestones, but in moments. In the quiet courage of a mom sleeping in a hospital chair. In the relief of a dad hearing, “We found a match.” In the joy of a kid getting to go home.
I’m so proud of how far we’ve come, and I’m even more inspired by what’s ahead. As we gear up for our 40th anniversary, I’m thinking a lot about legacy—not just mine, but ours. Everyone who’s donated, championed, or shared our mission has helped build something that’s going to last.
From the bottom of my heart, thank you for believing in us and for standing beside the children and families who need it most.
With sincere appreciation,
David Foster, OC, OBC Founder and Chairman
David Foster Foundation
Every child we help and every family we support, reminds me that what we do matters
Hope in Action: A Mid-Year Reflection from the CEO Message
from the Chief Executive Officer
As we move through the second half of the year, I want to take a moment to reflect on the extraordinary generosity, resilience, and compassion that define our David Foster Foundation community.
This has been one of our busiest years to date. The demand for assistance has never been higher and because of your continued support, we’ve been able to respond with the same heart, urgency, and commitment that have guided this Foundation for nearly four decades.
From urgent transplants to longawaited homecomings, families across the country are finding hope and healing because of you. Behind
every statistic is a story: a child given the chance to grow up, parents given strength in their most vulnerable moments, and communities rallying to ensure no family faces transplant care alone.
As we look ahead to the fall and begin to lay the groundwork for our 40th anniversary in 2026, I am reminded that this Foundation was built on the belief that every child deserves a chance at life and every family deserves to be supported through the unimaginable.
Your support makes this possible. Thank you for being part of this mission and for helping us create more tomorrows and brighter
futures for transplant children and their families.
With gratitude,
HCol Michael Ravenhill Chief Executive Officer
David Foster Foundation
Honourary Colonel
Canadian Armed Forces
410 Tactical Fighter Squadron
From Reflection to Action: Helping Families in Need
Message from SVP, Fund Development
Ihope your summer with friends and family is going well. Hard to imagine that we are over halfway through the calendar year, the home stretch. For me, and I am sure it is the same for many of you, it is time to reflect regarding how I, just one player in a world of some 8 .062 billion (2023), can assist in making the World a better place, (Michael Jackson-2009), for the less fortunate.
Clearly, singularly, making the World a better place, helping those who need it the most, is honourable, but not realistic. Being a contributor, no matter the amount, a piece of the puzzle, is very doable and the responsibility of each of us. On pages 8-9, the statistics are overwhelming regarding the need of Canadian families, from coast to coast, who are applying to the
Foundation for financial assistance for non-medical expenses, like rent, food, accommodations, vehicle, regular every day family expenses, as their child is going through the life-saving pediatric organ transplant process. It is safe to consider the statistics as they speak volumes.
As I have mentioned in previous newsletters, 100% of your donation to the Foundation goes directly to support families, not a penny to administration,
How to
1. Mail your cheques to David Foster Foundation, 212 Henry Street, Victoria BC V9A 3H9
2. Please call 1-877-777-7675
With sincere thanks, John Danson SVP, Fund Development David Foster Foundation
make a donation to the Foundation:
3. Online through PayPal at davidfosterfoundation.com
4. Electronic funds transfer— please email info@davidfosterfoundation.com and thus the total amount of your donation is eligible for a full tax receipt. “And now you know the rest of the story”—Paul Harvey.
Standing with Families, Every Step of the Way
Message from Director of Family Relations
As we share this summer edition of our newsletter, I’m proud to reflect on two stories that speak to the heart of what we do at the Foundation.
The first is Josiah’s. His transplant journey, featured in this newsletter, is a powerful reminder of how quickly life can change—and how critical timely support is for families facing the unimaginable. From the uncertainty of his diagnosis to the life-altering moment a donor was found, Josiah’s story highlights not only his own resilience but also the strength and love of his entire family.
This year, we also deepened our support for children living with transplants by funding three major
pediatric transplant camps across Canada. These programs offer something truly special: connection, belonging, and the freedom to just be a kid among others who understand. You can read more about these camps and the memories made on pages 6-7.
Thank you for continuing to stand with us. Your support helps ensure families like Josiah’s never have to face this journey alone.
With gratitude
Aleea Dahinden Director of Family Relations
David Foster Foundation
The David Foster Foundation
Children living with transplants at Camp Kivita.
THE LONGEST WAIT
The hardest part of daily life in Toronto was the unknown. We never knew when the call would come, making it impossible to plan one day to the next. We couldn’t leave the city, couldn’t visit family, and were confined to a two-hour radius of SickKids Hospital at all times. Even when my grandmother passed away, I could only attend her funeral virtually.
The anxiety was suffocating, especially at night. My husband and I would lay awake for hours, staring at each other, waiting. We had heard that most transplant calls happen in the middle of the night, so we mentally prepared ourselves for that moment. But as the months passed, we watched other families come and go—some friends who were listed after us received their hearts and went home, while we remained behind. It wasn’t our time yet.
Despite the uncertainty, we found solace in our little community at Ronald McDonald House. The other families there became our saving grace, filling the void left by our own families. We celebrated small victories together, supported each other through setbacks, and formed lifelong friendships. One of the most memorable days was when the PACU team arranged a trip to the aquarium for the children—a rare and cherished escape from the hospital routine.
For my husband, faith and prayer got him through. For me, the anxiety became overwhelming, and I eventually reached out for medication to cope. It was a daily battle to hold onto hope while watching our son struggle.
THE CALL THAT CHANGED EVERYTHING
Then, on a cold March day in 2022, everything changed. I was reheating leftovers for lunch when my phone rang. The voice on the other end delivered the news we had been waiting for: a heart was available for Josiah. We had to be at the hospital within two hours to begin pre-transplant testing.
The hours leading up to the surgery felt surreal. We had spent so long preparing for this moment, but nothing could truly prepare us. That night, surgeons worked tirelessly to give Josiah a second chance at life. By the time I saw him at 7 AM, he was sleeping in the cardiac critical care unit. Exhausted, I returned to Ronald McDonald House for a short nap.
When I came back around lunchtime, I was stunned—just hours after his transplant, Josiah was already rolling over onto his hands and knees, determined to move. It was a moment of sheer relief and disbelief. His strength before
Above: Josiah at age two.
Below: The brothers in camo jackets in Newfoundland to meet distance family members for the first time.
the surgery had carried him through it, and his recovery was nothing short of remarkable.
Before the transplant, Josiah had wanted to run and play like any two-year-old, but his oxygen levels wouldn’t allow it. His lips would turn purple, and we’d have to force him to sit still to recover. But now, for the first time, he could move without limits. Seeing him run and play without turning blue was one of the first moments we knew everything had changed.
HOMECOMING AFTER 680 NIGHTS
Just three days after surgery, Josiah was discharged from SickKids. We stayed in Toronto for eight more weeks for monitoring, but on May 5, 2022, after 680 nights away, we finally walked through our front door. It felt like winning the lottery.
Friends and family were waiting for us, and they had filled our fridge and cupboards to welcome us home. The transition back to “normal” life was strange at first. For two years, the four of us had shared a bedroom, and suddenly, Josiah and Emmett had their own rooms again. They were inseparable, as if they had never spent a moment apart. The best part was the freedom—being able to hop in the car and go wherever we wanted, seeing family and friends again after so long.
A FUTURE WE ONCE FEARED WOULDN’T COME
Now, at 5 years old, Josiah is preparing to start Kindergarten—a milestone I once feared he would never reach. His immune system remains suppressed due to the anti-rejection medications he will take for life, but he no longer requires a feeding tube—an incredible victory for us all. His routine heart checkups, alternating between Halifax and Toronto, have become adventures rather than burdens, as we make them as fun as possible for him.
None of this would have been possible without an organ donor and the unwavering support of the David Foster Foundation. Throughout our time in Toronto, they ensured we never had to worry about financial burdens. They covered our living expenses, helped with household costs back home, and continued supporting us until we were able to find new jobs. That kind of generosity is something we will never forget.
If you ever find yourself in a situation like ours, know that you are not alone. There are organizations and people out there who will go above and beyond to help.
Above: Josiah with his mother just moments before his transplant. Below: Josiah with his brother in their backyard tree house a week after returning home.
An Incredible Summer to Remember…
At the David Foster Foundation, we know that healing extends beyond hospital walls. This summer, we were proud to support three incredible camps that give transplant kids, and in some cases, their families, the chance to connect, grow, and just be kids.
In 2025, we continued our long-standing support of Kidney Camp and Campfire Circle (formerly Camp Kivita), and for the first time, funded Heart Transplant Family Camp in Alberta. These programs are more than just summer getaways—they’re powerful, life-shaping experiences that create community, build resilience, and offer joy that lasts long after the campfire burns out.
Campfire Circle | Ontario
Formerly Camp Kivita, this much-loved transplant camp entered an exciting new chapter in 2025. The original leadership team at Kivita transitioned the camp to Campfire Circle, an organization known for its exceptional medical programming and stunning camp facilities. Originally created for children with cancer, Campfire Circle recently expanded to welcome kids with a range of serious medical conditions, including those who have undergone transplants.
With a fully staffed medical team and hospital-grade infrastructure, Campfire Circle offers a safe, vibrant environment where kids can participate in everything from ropes courses to canoing to leadership certification programs. Their in-hospital programming also runs year-round, providing creative play and emotional support to families navigating life before and after transplant.
Heart Transplant Family Camp | Alberta
This was the first year the Foundation supported Heart Transplant Family Camp, and it quickly became clear what a powerful, needed program it is. Launched in 2011 and run
1. New friendships, shared laughs, and memories to last a lifetime —the heart of transplant camp.
2. From soccer fields to campfires, kids get the chance to just be kids again.
3. Campers together at Enfant Merci.
4. Confidence grows with every adventure, from the water to the woods, kids are able to discover what they’re capable of at each of the transplant camps.
Supporting Transplant Kids at Camp!
entirely by volunteers, this camp brings together heart transplant recipients and their families from across Alberta, BC, Saskatchewan, and Manitoba.
What makes this camp unique is its full-family format—parents, siblings, and caregivers all attend together. The programming is thoughtfully tailored for all ages and includes education sessions, support groups, peer mentorship, and a touching memorial for organ donors. One of the most anticipated events? A wildly joyful 50-a-side soccer game that spans generations.
Kidney Kids Camp | British Columbia
Hosted at Camp Latona in partnership with COTS (Children’s Organ Transplant Society) and the Kidney Foundation of Canada (BC & Yukon Branch), Kidney Kids Camp offers a five-day outdoor adventure for children aged 10–18 who are living with kidney disease or who have received transplants.
Our continued support helped provide campers with a safe, medically supported space to enjoy swimming, hiking, archery, water-skiing, and more.
WHY IT MATTERS
For many transplant children and families, these camps are a highlight of the year. They provide moments of freedom, belonging, and joy in the midst of what can often be an overwhelming medical journey.
Supporting these programs is one of the many ways the David Foster Foundation helps children and families feel not just supported— but uplifted. These are the kinds of memories that last a lifetime.
I think our son has forgotten he has a family at home, lol. We have lost him to camp forever.
Thank
you!
—Lindsay, Camp Mom
Photo credit: Suzanne Teresa Photography
Working Together Through Every
In 2024, the David Foster Foundation supported 92 families whose children were waiting for or recovering from life-saving solid organ transplants.
With your trust and generosity, in July of 2025 we’ve now helped 1,560+ families across Canada since our inception.
This work isn’t just about one moment. It’s about showing up through all of them—assessment, surgery, recovery, and the long road after.
AT A GLANCE— 2024 IMPACT
Where Families Are in Their Journey
Families greatest time of need usually comes at the critical first six months after transplant, when medical needs are high and time off work is common, however the Foundation helps families through all stages of their child’s transplant journey.
97 flights booked to reach medical care
3,100 nights of accommodation funded for 43 families
Organ Types Supported in 2024
• Liver and kidney transplants had the largest volume of stages funded, as these are more common transplanted organs.
• Heart transplants families needed the most help before surgery while listed and waiting.
• Multi-organ and lung transplants often required longer-term, complex support.
29 received life-saving organ transplants in 2024
Children helped at every stage of their transplant journey
The Foundation supports families who are waiting for a transplant, to over a year post-transplant.
Step of the Transplant Journey . . .
The Hidden Costs of Care— Housing & Travel Support
When a child needs a transplant, care often means leaving home, sometimes for weeks, sometimes for months, and even sometimes for years.
Thanks to you, 43 families had a safe place to stay while accessing care in Toronto, Edmonton, or Vancouver
Behind every night funded is a child in need, a parent trying to stay strong, and a family holding onto hope.
Flight Support Across Canada
With only a few pediatric transplant hospitals in Canada, travel is often unavoidable. In 2024, the Foundation booked 97 flights, ensuring kids reached care without delay.
TOP ROUTES FLOWN
3,100 TOTAL NIGHTS of accommodation
90% OF NIGHTS at Ronald McDonald Houses
36% of nights used by JUST 5 FAMILIES
HOUSING IN 2024 WHY THIS MATTERS
Average Stay: 72 NIGHTS Longest Stay: 365 NIGHTS
8+ Charlottetown, Toronto 6 each Saskatoon & Winnipeg Prince George Vancouver 4 each & Regina
Families Across Canada
We supported families from every province. Top regions: Ontario Alberta British Columbia 37 18 17 Families Families Families
TO THE FAMILIES: Your strength is why we do this
TO THE HOSPITALS AND SOCIAL WORKERS: Your partnership makes this possible.
TO OUR DONORS: You turn barriers into bridges for families in medical crisis. Thank you for being part of this journey.
More Than a Piano—
A Gift to be Cherished, a Cause to be Proud of
Donor Spotlight: George Vassallo & Christine Cole
At the David Foster Foundation, we are continually inspired by the generosity and compassion of the donors who make our mission possible. This summer, we are proud to highlight the incredible support of George Vassallo and Christine Cole—long-time friends of the Foundation and cherished members of our donor family.
George and Christine first joined us at the Night on Broadway Gala in 2022 at Toronto’s Hotel X. From the moment they arrived, their warmth and commitment to helping children and families in need were unmistakable. That evening, they participated in our live auction and made a remarkable contribution to the Foundation’s mission, purchasing a very special piece of musical history.
Earlier this year, their custom Yamaha grand piano, a symbol of that unforgettable night was delivered to their home after a six-day journey from Los Angeles to Toronto. This exquisite piano has a history as remarkable as its new owners. From the hands of Grammy Award–winning producer David Foster, this instrument has played a role in the performance of some of the most beloved songs of our time and has taken center stage at dozens of major events featuring some of the most accomplished performers in the world.
What makes this piano truly one-of-a-kind is not just its sound or elegance, but its legacy. Its gold interior has been personally signed by over 45 world-renowned artists, entertainers, and celebrities. It is a piece of musical history, a symbol of hope, and now, a cherished investment to be enjoyed for years to come.
George and Christine's generosity didn’t stop there. They have continued to support the Foundation’s work through our Los Angeles event and other initiatives, helping ensure that families facing life-threatening pediatric illness receive the support they need, when they need it most.
At the David Foster Foundation, we are continually inspired by the generosity and compassion of the donors who make our mission possible.
George Vassallo, Christine Cole and their custom Yamaha grand piano.
THANKS TO ALL OUR PARTNERS
Life Legacy Members
Suzanne and Walter Scott Foundation
Richard J. Stephenson
& Dr. Stacie J. Stephenson
Jim & Sandi Treliving
Argyros Family Foundation
Kyle MacDonald & John Franklin
Cheryl and Haim Saban
AWIN Group of Dealerships
Paragon Gaming
John and Bonnie Buhler Foundation
TELUS
The Anschutz Foundation
Newton Glassman Charitable Foundation in partnership with Catalyst Capital Group
Legacy of Service, Compassion & Community
Volunteer Spotlight: Jamie Pearce A
For nearly four decades, Jamie Pearce has been a vital part of the David Foster Foundation’s story. His steady leadership, generous spirit, and commitment to service have made a lasting difference in the lives of children and families across Canada.
Jamie began volunteering with the Foundation in 1988 while serving as a young constable with the Victoria Police Department. He signed up to help at one of the very first David Foster celebrity softball events, unaware that it would mark the beginning of a lifelong relationship with the Foundation and its mission.
Over the past 38 years, Jamie’s involvement has continued to grow. He has participated in the Tour de Rock as both a rider and a support team member, served on the steering committee, and taken on leadership of transportation and security for major fundraising events. He has also helped coordinate police organizations across the country to provide skilled officers as volunteer drivers and event security. These efforts have helped reduce costs and ensure that more funding is directed where it is needed most: to children and families.
Jamie’s dedication to public service extends far beyond his work with the Foundation. Over a 30-year career in policing, including 10 years in senior leadership as an Inspector, he was deployed to Kosovo for nine months as a peacekeeper. There, he led an international team responsible for the protection of high-risk political figures, international judges and prosecutors, and individuals involved in war crimes tribunals.
Now retired, Jamie is enjoying life with more time for family, friends, travel, and continued community involvement. “I’ve had the privilege of working with some of the very best volunteers, celebrities, participants, and the Foundation’s incredible team,” he reflects. “Each event is emotional, inspiring, and deeply meaningful.”
Jamie has watched the Foundation grow from a local initiative into a nationally recognized organization that has supported over 1,500 families. He remains proud to be part of a team that brings people together in cities and communities across Canada with one shared goal: to support families facing life-threatening pediatric illness and help give them more time together.
Jonathon D. Fischer Foundation
Greenwood Gaming & Entertainment
The Dennis & Phyllis Washington Foundation
The Slaight Family Foundation
Joan & Paul Waechter
Walter & Maria Schneider
Jim Pattison
James Wilson & Vivian Roy S.G. Cunningham
The Waugh Family Foundation Aird & Berlis LLP ALLVISION
National Partners
National Post
Community Partners
Boston Pizza Foundation
DeerFields Clinic
Gib-San Pools
Oak Bay Beach Hotel
StayWell Suites
RBC Wealth Management
Tom Lee Music
GAIN
Flytographer
Jamie Pearce (centre) with John Danson and Marty Schubert at Simply Spectacular, Cabo 2023.
