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Sonia went into the hospital expecting to have her heart valve replaced. She planned to return to her teaching job just two weeks later. But when her heart could no longer keep up after surgery, what began as a routine procedure quickly became a fight for her life. Within months, Sonia was facing heart failure, failing lungs, and the need for a heart and double lung transplant. In this episode, Candice sits down with Sonia to explore her extraordinary journey through months in hospital, the uncertainty of waiting for a life-saving transplant, and the emotional toll of facing a future she never imagined. Sonia shares what it was like to learn that she needed not one, but three new organs, and how she grappled with fear, grief, and the possibility that she might not survive. As the months in hospital passed, Sonia began to find ways to reconnect with herself. Through sewing, crafting, decorating her hospital room, and creating moments of comfort, she found ways to hold on to her identity beyond being a patient. With the support of her family, friends, healthcare team, and an incredible hospital wedding, Sonia discovered what kept her fighting: love, connection, and the determination to live the years her mother and sister never had the chance to experience. Sonia also speaks candidly about life after transplant, including the trauma that can linger long after surgery, the nightmares and emotional challenges of recovery, and the difficulty of finding a community of people who truly understand what she has experienced. As a patient advocate, her journey has deepened her belief that support, connection, and being heard are essential parts of healing. This is a conversation about more than survival. It is about rebuilding an identity when illness takes so much away, learning to live with the lasting effects of medical trauma, and finding hope even when the future feels uncertain. Sonia reminds us that while we cannot always control what happens to us, we can find meaning in the people we love, the experiences we share, and the chapters still waiting to be written. Links and Resources Click here for more information about living organ donation. Click here for more information about living kidney donation Click here for more information about living liver donation Click here for information Sessions for potential donors Click here to learn more about the Kidney Foundation’s Peer Support Program Click here for mental health support from Canadian Mental Health Association Connect with the Podcast or Learn More About Organ Donation Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a National Board Member for the Kidney Foundation of Canada and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. Thanks for spending your time with us. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

At 27, Layla discovered they had been living with only one functioning kidney. After their kidney function rapidly declined, they found themselves navigating kidney failure, dialysis, and a life that looked very different from the one they had imagined. But their journey would lead to a life-changing gift: a kidney transplant from their mother, who travelled all the way from Iran to donate. In this episode, Candice sits down with Layla to explore their journey from diagnosis to transplantation, including the emotional challenges of living with kidney disease as a young adult. Layla shares what it was like to move from Iran to Canada, discover their kidney condition, and adjust to the realities of dialysis while trying to maintain a sense of independence and connection with friends. Together, Layla and Candice reflect on the importance of peer support, the spoon theory and the challenges of accepting help. Layla opens up about the complicated emotions surrounding their mother’s decision to donate, including the fear of putting her through surgery and the guilt of accepting such an extraordinary gift. Through therapy and reflection, Layla began to understand the transplant as an opportunity for healing, love, and connection. Layla also shares how life changed after transplant, from the freedom to travel and enjoy everyday moments to the deeper meaning of calling the transplanted kidney “our kidney.” Whether you are navigating kidney disease, considering living donation, or supporting someone through transplantation, this conversation is a powerful reminder that hope can be found in connection, accepting help, and learning to embrace the love that others offer. In This Episode What it was like to navigate kidney disease as a young adult while trying to maintain friendships, work, and independenceHow peer support through the Kidney Foundation helped Layla feel understood and less aloneWhat the spoon theory means.Why Layla chose in-centre hemodialysis and how building support systems helped them manage their healthThe emotional challenges of accepting a kidney donation from their motherHow therapy helped Layla work through guilt, fear, and the complicated emotions surrounding living donationWhy Layla calls the transplanted kidney “our kidney” and how the transplant became part of a deeper healing journeyHow living with kidney disease taught Layla to accept uncertainty and appreciate the presentWhy accepting help and love can be an important part of finding hope Links Click here for more information about living organ donation. Click here for more information about living kidney donation Click here for more information about living liver donation Click here for information Sessions for potential donors Click here to learn more about the Kidney Foundation’s Peer Support Program Connect with the Podcast or Learn More About Organ Donation Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a National Board Member for the Kidney Foundation of Canada and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. Thanks for spending your time with us. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

In this special episode, Candice sits down with Tyler, a double living organ donor whose journey began with donating blood and eventually led him to donate both a portion of his liver and a kidney. Tyler first became interested in living donation after years of donating blood and wondering about the direct impact his donations could have. He decided to anonymously donate part of his liver to someone he had never met, ultimately becoming a living liver donor at UHN’s Ajmera Transplant Centre. But his story didn’t end with one donation. Tyler decided to pursue anonymous kidney donation as well. Then, an extraordinary series of connections changed everything. Years earlier, Tyler had met a couple while on vacation. Through a series of remarkable coincidences, he later discovered that they were connected to people in his own family—and eventually learned that the woman he had met was experiencing kidney failure and needed a transplant. Tyler had already begun the process of becoming an anonymous kidney donor. He wondered whether his donation could instead be directed to her. After going through the necessary testing, they discovered they were a match. Together, Tyler and Candice talk about the emotional experience of anonymous donation, family concerns, recovery from two very different surgeries, and what it means to see the impact of a donation unfold over time. Tyler also reflects on the idea that one donation can affect far more than a single recipient—from a recipient’s spouse and children to the people waiting behind them on the transplant list. Whether you are considering living donation, have been touched by transplantation, or simply want to hear a remarkable story about generosity and human connection, this conversation is a powerful reminder that one decision can change far more lives than we may ever see. In This Episode ● How Tyler’s journey into living donation began with blood donation ● Why he decided to anonymously donate part of his liver to a stranger ● How Tyler and his family navigated the fear and uncertainty surrounding donation ● Why Tyler decided to pursue a second donation—a kidney ● The incredible series of coincidences that connected Tyler with his kidney recipient ● The difference between recovering from liver and kidney donation ● The ripple effect of living donation and how one donation can impact an entire family ● What Tyler wishes more people understood about living donation ● Why he believes one decision can have a much greater impact than we may ever see Links Click here for more information about living organ donation. Click here for more information about living kidney donation Click here for more information about living liver donation Click here for information Sessions for potential donors Katie’s story: https://youtu.be/f6lIYM9fiCU?si=q7eE3_VCCGhha-Qx  Yorkville Run / Team Transplant: https://bit.ly/teamtransplant26  Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a National Board Member for the Kidney Foundation of Canada and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

In this special episode, Candice sits down with Kevin Gosling, the first person in Canada to anonymously donate part of his liver to a stranger, made possible at UHN’s Ajmera Transplant Centre. More than 20 years later, his decision continues to shape the future of living organ donation. Kevin shares how a simple question—What about people who don't have someone to donate for them?—led him on a journey that challenged medical norms, changed hospital policies, and ultimately created what many now call "The Gosling Effect." Together, they discuss the barriers he faced, the emotional moments that stayed with him, the ripple effect of one selfless act, and why he believes ordinary people are capable of extraordinary generosity. Whether you're curious about living donation, have been touched by transplantation, or simply need a reminder of the good that exists in the world, this conversation is one you won't forget. In This Episode How Kevin first learned that living donation to a stranger was possibleWhy he refused to accept "we don't do that" as an answerThe challenges of becoming Canada's first anonymous living liver donorThe ethical questions and medical concerns behind a historic firstThe support of family throughout the donation journeyReceiving a letter from the recipient's family for the first timeThe origin of the "Gosling Effect" and its lasting impactWhy anonymous donation comes from a different kind of motivationA powerful analogy about saving a life and taking a leap of faithKevin's hopes for the future of transplantation and organ donation Links Learn more about living organ donation: www.livingorgandonation.ca  Living Organ Donation at UHN: UHN Ajmera Transplant Centre Information Sessions for potential donors: givelifeuhn.eventbrite.ca  Becoming a living donor: https://www.uhn.ca/Transplant/Pages/become_living_donor.aspx Liver Canada: Transforming the future of liver health | Liver Canada   Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a board member for the National Kidney Foundation and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. Thanks for spending your time with us. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

Growing up with kidney disease can feel isolating, but as this episode reminds us, you are never alone. In this episode of the Living Transplant Podcast, host Candice Coghlan sits down with longtime friend, advocate, transplant recipient and dragon boat coach Jess Bailey. Diagnosed with kidney disease as a child, Jess shares what it was like navigating school, friendships, dialysis and two kidney transplants while learning to embrace being different. Jess opens up about the realities of life after transplant, why a transplant is "a long-term temporary solution," and how community, peer support and sport have helped shape her journey. Together, Candice and Jess discuss the power of the Kidney Paired Donation Program, the importance of living donation, and the incredible impact that nurses, healthcare teams and fellow transplant recipients can have along the way. The conversation also explores the Transplant Games, dragon boating, survivor's guilt, adapting to dialysis, and why hope remains at the heart of the transplant community. Whether you're living with kidney disease, waiting for a transplant, supporting someone you love, or simply curious about organ donation, this episode is a reminder that there is always a community ready to welcome you. In This Episode Growing up with kidney disease and dialysisNavigating childhood and high school while feeling "different"Receiving a first kidney transplant as a child that lasted nearly 24 yearsLife after transplant and managing lifelong medicationsWhy transplant is not a cureFinding belonging through dragon boating and the Transplant GamesThe importance of peer support and patient communitiesAdvice for newly diagnosed kidney patientsUnderstanding the Kidney Paired Donation ProgramThe generosity of living organ donorsHope for the future of transplantation and medical innovationGratitude for healthcare teams and transplant nurses Links Learn more about living organ donation: www.livingorgandonation.ca Living Organ Donation at UHN: UHN Ajmera Transplant Centre Information Sessions for potential donors: givelifeuhn.eventbrite.ca  Becoming a living donor: https://www.uhn.ca/Transplant/Pages/become_living_donor.aspx Kidney Foundation of Canada: https://kidney.ca/  Kidney Paired Donation Program: https://blood.ca/en/organs-tissues/living-donation/kidney-paired-donation-program  Canadian Transplant Association and the Canadian Transplant Games: https://www.canadiantransplant.com   Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a board member for the National Kidney Foundation and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. Thanks for spending your time with us. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

What actually makes someone a “match” for organ transplant? And how close are we to a future where transplant compatibility becomes even more personalized? In this episode of Living Transplant Podcast, host Candice sits down with Jeff Kiernan from UHN’s HLA Lab to explore the hidden world of transplant immunology — the science that helps determine donor compatibility, monitor antibodies, and support long-term transplant success. Jeff breaks down what HLA is, why the idea of a “perfect match” is often misunderstood in solid organ transplant, and how new innovations are helping highly sensitized patients access life-saving organs. From molecular matching and immune response prediction to the future of organ preservation and personalized transplant care, this conversation offers a fascinating behind-the-scenes look at the science shaping the future of transplantation. Candice also reflects on her own experience as a kidney transplant recipient and what it means to live with the realities of sensitization, second transplants, and long-term graft survival. Whether you’re a transplant recipient, donor, healthcare professional, or simply curious about the incredible science happening behind the scenes, this episode shines a light on the people and technology working every day to help patients live longer, healthier lives. In This Episode:What HLA actually means and why it mattersThe truth about “perfect matches” in organ transplantHow antibodies affect transplant compatibilityWhy highly sensitized patients face additional challengesThe future of molecular matching and predictive transplant scienceHow UHN teams collaborate across transplant programsInnovations in organ preservation and perfusion technologyThe behind-the-scenes role of Medical Laboratory Technologists (MLTs) Links How UHN’s Transplant Immunology Lab matches patients with donor organs, stem cells: https://www.uhn.ca/corporate/News/Pages/uhn-transplant-immunology-lab-hla-matching.aspx Learn more about living organ donation: www.livingorgandonation.ca  Living Organ Donation at UHN: UHN Ajmera Transplant Centre Information Sessions for potential donors: givelifeuhn.eventbrite.ca  Becoming a living donor: https://www.uhn.ca/Transplant/Pages/become_living_donor.aspx CBS Highly Sensitized Patient Program: https://professionaleducation.blood.ca/en/organs-and-tissues/programs/highly-sensitized-patient-hsp-program  Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a board member for the National Kidney Foundation and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. Thanks for spending your time with us. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

Discover Maigen’s powerful story of becoming a living liver donor during the uncertainty of COVID-19—and how one spontaneous “why not?” turned into a life-saving decision. In this episode of Living Transplant, Maigen shares how a lighthearted comment between family became the beginning of an extraordinary journey. Rooted in love, resilience, and a deep sense of care for others, her story highlights the emotional and physical realities of living donation, the strength of family bonds, and the perspective shift that comes with giving a part of yourself to save a life. From navigating the transplant process during a global pandemic to redefining her relationship with her body and her future, Maigen offers an honest and inspiring look at what it truly means to be a living donor. In this episode, we explore: Maigen’s spontaneous decision to become a living liver donor during the early days of COVID-19How a simple “why not?” mindset led to a life-changing journeyThe realities of donor testing, including unexpected challenges like rapid weight lossNavigating transplant logistics and emotional stress during a global pandemicThe importance of communication, advocacy, and support systems throughout the processWhat recovery really looks like—and how quickly life can begin to feel “normal” againThe evolving meaning of her transplant scar—from insecurity to a badge of honourThe impact of donation on family relationships, identity, and future outlookAdvice for potential donors and caregivers navigating uncertaintyLinks  Learn more about living organ donation: www.livingorgandonation.ca  Living Liver Donation at UHN: UHN Ajmera Transplant Centre Information Sessions for potential donors: givelifeuhn.eventbrite.ca  Becoming a living donor: https://www.uhn.ca/Transplant/Pages/become_living_donor.aspx Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a board member for the National Kidney Foundation and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. Thanks for spending your time with us. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

In this powerful episode of Living Transplant, Fadia shares her deeply personal journey through kidney disease, receiving a living donor transplant from her sister, and now navigating a return to dialysis. With honesty and vulnerability, she reflects on the evolution of her mindset—from a “go, go, go” approach to one rooted in acceptance, rest, and self-compassion. Fadia opens up about the realities of invisible illness, balancing motherhood and a demanding career in education, and the emotional complexity of asking for and receiving help. She also speaks to the power of community through the ACB Organ Health Committee, and how advocacy, culturally safe care, and representation are critical in improving outcomes for Black patients. This episode is a reminder that transplant is not a cure, but part of a lifelong journey. Fadia’s story encourages listeners to slow down, speak up, and redefine what strength truly looks like. Key TopicsLiving donor kidney transplant and sibling donationReturning to dialysis after transplantRedefining “balance” and embracing restInvisible illness and “you don’t look sick”Motherhood, career, and chronic illnessThe importance of support systems and asking for helpPatient advocacy and being the expert of your own bodyNavigating the healthcare system and medical mistrustCultural safety and equity in organ donation and transplantationThe impact of community: ACB Organ Health Committee Links Learn more about living organ donation: www.livingorgandonation.ca Living Kidney & Liver Donation at UHN: UHN Ajmera Transplant Centre Information Sessions for potential donors: givelifeuhn.eventbrite.ca  Becoming a living donor: https://www.uhn.ca/Transplant/Pages/become_living_donor.aspx ACB Organ Health Committee & Green Table Talk: https://www.youtube.com/@acborganhealth   Black Health Alliance: https://blackhealthalliance.ca Kidney Foundation of Canada – Living Donation https://kidney.ca/Get-Involved/Be-a-Living-Donor Trillium Gift of Life Network – Organ Donation in Ontario https://www.giftoflife.on.ca Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a board member for the National Kidney Foundation and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. Thanks for spending your time with us. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

What happens after transplant—when the surgery is over and real life begins? In this episode of Living Transplant, we’re joined by Eugenia Chan, a pharmacist from the Transplant Outpatient Pharmacy (TOP) at UHN, to explore the critical (and often unseen) role pharmacy teams play in a patient’s lifelong transplant journey. Unlike a typical pharmacy, TOP is fully integrated into the transplant program—supporting over 5,000 patients each year from the moment they leave the hospital and throughout their lives. From medication management to financial navigation, this team is a constant, trusted connection for patients. Together, we unpack how this specialized care improves outcomes, reduces complications, and helps patients feel less alone in what can be an overwhelming experience. In This Episode, We Cover: Why transplant pharmacy is differentHow TOP provides continuous, specialized care that goes far beyond dispensing medications.Medication adherence made easierThe impact of blister packaging, delivery across Ontario, and proactive dose management in helping patients stay on track, catching complications earlyHow frequent check-ins and strong patient relationships help pharmacists identify side effects and concerns before they become serious.Navigating medication fearsHonest conversations about side effects, what to expect, and how care teams adjust treatment to fit each patient’s needs.What transplant patients need to know about over-the-counter medications, supplements, and everyday risks.Breaking down financial barriersHow medication reimbursement specialists help patients access coverage, reduce out-of-pocket costs, and navigate complex insurance systems.The future of transplant pharmacyInnovations like blister pack automation, refill reminders, and text-based systems designed to make care even more accessible. Links and Resources Learn more about the UHN Transplant Outpatient Pharmacy (TOP): https://www.uhn.ca/Transplant/TOP Learn more about living organ donation: www.livingorgandonation.ca Living Kidney & Liver Donation at UHN: UHN Ajmera Transplant Centre Information Sessions for potential donors: givelifeuhn.eventbrite.ca  Becoming a living donor: https://www.uhn.ca/Transplant/Pages/become_living_donor.aspx Kidney Foundation of Canada – Living Donation https://kidney.ca/Get-Involved/Be-a-Living-Donor Trillium Gift of Life Network – Organ Donation in Ontario https://www.giftoflife.on.ca Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a board member for the National Kidney Foundation and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. Thanks for spending your time with us. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

Emma didn’t see herself as brave — she simply saw a problem and knew she could help. At 79 years old, Emma became a living kidney donor for her husband after he began dialysis. But the path to donation wasn’t straightforward. After initially being turned away during her first evaluation due to concerns about blood sugar levels, Emma refused to give up. She advocated for herself, gathered medical evidence from her family doctor, and wrote a heartfelt letter asking for a second chance to be assessed. That persistence led her to the Toronto General Hospital Living Donor Program, where she was ultimately approved to donate. In this episode, Emma shares the deeply personal journey of advocating for herself, navigating the evaluation process, and donating a kidney to the person she has spent her life with. She reflects on why she never felt fear about the surgery, how dialysis affected their lives together, and why she believes more people should consider living donation — regardless of age. Now recovering just weeks after surgery, Emma is already looking ahead to what matters most: more time together, traveling again, and enjoying the life they’ve built side by side. Her message is simple but powerful: if you are healthy and willing to help, one kidney can change someone’s life. Links and Resources Learn more about living organ donation: www.livingorgandonation.ca Living Kidney & Liver Donation at UHN: UHN Ajmera Transplant Centre Information Sessions for potential donors: givelifeuhn.eventbrite.ca  Becoming a living donor: https://www.uhn.ca/Transplant/Pages/become_living_donor.aspx Kidney Foundation of Canada – Living Donation https://kidney.ca/Get-Involved/Be-a-Living-Donor Trillium Gift of Life Network – Organ Donation in Ontario https://www.giftoflife.on.ca Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a board member for the National Kidney Foundation and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. Thanks for spending your time with us. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

In this special International Women’s Day bonus episode of the Living Transplant Podcast, we sit down with Dr. Irene Kim — abdominal transplant surgeon, Director of the Transplant Center at Cedars-Sinai, and the Esther and Mark Schulman Endowed Chair in Transplant Medicine. Beyond her many titles, Dr. Kim is also a mentor, a leader, and a mother. In this thoughtful and deeply human conversation, she reflects on the realities of balancing a demanding surgical career with family life, the mentors who shaped her journey in transplant medicine, and the lessons that come with leadership. Dr. Kim shares why motherhood has been one of the most humbling roles in her life, how strong support systems make success possible, and why mentorship doesn’t have to be gendered. She also opens up about how personal experiences with illness can reshape the way physicians connect with their patients. The episode closes with a powerful reflection inspired by author J.D. Salinger — a reminder that in a world constantly pushing us to do more and be more, sometimes the most meaningful realization is simply knowing when we already have enough. In honour of International Women’s Day, this conversation celebrates the women leading, caring, mentoring, and shaping the future of medicine and our communities. Links and Resources Cedars-Sinai Medical Center: https://www.cedars-sinai.org J.D. Salinger, The Catcher in the Rye: https://www.amazon.com/Catcher-Rye-J-D-Salinger/dp/0316769487 LinkedIn: https://www.linkedin.com/in/irene-kim International Women’s Day: https://www.internationalwomensday.com/ UHN Women: https://www.uhn.ca/corporate/AboutUHN/UHNWomen  Learn more about living organ donation: www.livingorgandonation.ca Living Kidney & Liver Donation at UHN: UHN Ajmera Transplant Centre Information Sessions for potential donors: givelifeuhn.eventbrite.ca   Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a board member for the National Kidney Foundation and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. Thanks for spending your time with us. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

What really happens when someone decides to become a living kidney donor? In this episode of Living Transplant, Candice sits down with UHN living donor kidney coordinator Melinda Skadorwa to unpack the full donor journey — from the first health questionnaire to surgery day and beyond. Melinda shares how she found her way into transplant nursing, what a typical (and often unpredictable) day looks like, and the most common fears and misconceptions she hears from potential donors. The conversation explores the emotional and logistical realities of donation, including financial barriers, white coat anxiety, and the importance of strong support systems. Listeners will also learn how innovative programs like Kidney Paired Donation and List Exchange are helping more Canadians receive life-saving transplants — even when donors and recipients aren’t compatible. Whether you’re considering donation, supporting someone who is, or simply curious about how living donation works, this episode offers an honest and compassionate look behind the scenes. What You’ll Learn in This Episode: How Melinda’s path led her into transplant careWhat living donor coordinators actually doStep-by-step overview of the living donor evaluation processCommon myths and fears about kidney donationLife after donation: recovery and long-term outlookHow Kidney Paired Donation expands transplant access across CanadaThe unique impact of non-directed (anonymous) donorsBarriers donors may face — including financial and system challengesEmotional supports available for living donorsAdvice for anyone thinking about becoming a donor Links and Resources Learn more about living organ donation: www.livingorgandonation.ca Living Kidney Donation at UHN: UHN Ajmera Transplant Centre Kidney Paired Donation Program: Kidney Paired Donation Program Financial Support for Living Donors: https://www.eventbrite.ca/e/financial-support-for-living-organ-donors-tickets-60824861799?aff=ebdsoporgprofile Information about Becoming a Living Kidney Donor: https://www.eventbrite.ca/e/information-for-potential-living-kidney-donors-tickets-62066475499?aff=ebdsoporgprofile  Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a board member for the National Kidney Foundation and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. Thanks for spending your time with us. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

In this episode of the Living Transplant Podcast, host Candice Coghlan speaks with Dr. Blayne Sayed, transplant and hepatobiliary surgeon at SickKids and UHN, about the complexity and emotional depth of pediatric liver transplantation. Dr. Sayed shares what makes children’s liver surgery uniquely challenging, how families navigate the transplant journey, and why long-term relationships between care teams and families matter so deeply. They explore the powerful role of living liver donation, advances in transplant science and immune research, and emerging technologies like organ perfusion that may improve outcomes and expand the donor pool. Dr. Sayed also discusses the future of transplant care — including reducing immunosuppression, protecting organs from injury, and building stronger transition supports for children growing into adult care. Did you know that when a child needs a liver donor, both donor evaluation and surgery take place at UHN — a powerful reflection of our strong partnership in pediatric living donor transplantation. Key Takeaways Pediatric liver transplantation involves highly complex, technically demanding surgery on very small patients.Families often face a long and emotionally intense journey from diagnosis to transplant.Living liver donation is a critical lifeline for children and helps reduce wait times and risk.Strong collaboration between SickKids and UHN supports seamless donor evaluation and surgery.Long-term relationships between transplant teams and families are central to pediatric care.Research into liver injury and immune response may help reduce rejection and improve long-term outcomes.New organ perfusion technologies could allow organs to be treated and optimized before transplant.Some liver transplant recipients may eventually be able to safely minimize or stop immunosuppression.Better transition programs are needed to support teens moving from pediatric to adult transplant care.Innovation in transplant science is accelerating and holds real promise for children. Connect with the Podcast or Learn more about Organ Donation Click here for more information about living organ donation. Click here to learn more about liver transplantation Click here to hear stories about living organ donors and recipients Click here to learn more about Sick Kids liver transplant program Centre for Living Organ Donation on Instagram Ajmera Transplant Centre on Instagram Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a board member for the National Kidney Foundation and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. Thanks for spending your time with us. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

In this heartwarming episode of the Living Transplant podcast, we welcome Bianca and Joseph to share the incredible journey of their daughter, Camilla. Initially born healthy, Camilla’s persistent jaundice led to a life-changing diagnosis of biliary atresia at just four weeks old. After a failed Kasai procedure, the family was thrust into survival mode at SickKids Hospital, facing the terrifying reality that their infant daughter needed a liver transplant to survive. Joseph recounts the emotional process of becoming his daughter’s living donor, transforming a time of immense fear into a story of profound sacrifice and paternal love.  The couple opens up about the unique challenge of having two family members in surgery simultaneously and the unforgettable relief of their reunification during recovery. Now nearly three years post-transplant, Camilla is a thriving toddler, hitting every milestone. Bianca discusses how they navigate “mom guilt,” the importance of normalizing Camilla’s transplant scar, and the vital role of the “poop chart” in early diagnosis. Their story is a testament to the resilience of families, the power of advocacy, and the miracle of organ donation. Connect with the Podcast or Learn more about Organ Donation Click here for more information about living organ donation. Click here for more information about living kidney transplantation.  Click here for more information about Polycystic Kidney Disease.  Ajmera Transplant Centre on Instagram Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a board member for the National Kidney Foundation and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. Thanks for spending your time with us. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

In this powerful episode of The Living Transplant Podcast, host Candice Coghlan is joined by Kamika Sylvester, RN — nurse, patient advocate, nonprofit founder, and tech entrepreneur — for a deeply honest conversation about racism in healthcare, patient advocacy, and reimagining what truly equitable care can look like. Kamika shares her journey as a patient first, navigating a life-altering diagnosis at just 18 years old, and how that experience shaped her path into nursing, advocacy, and systems change. Together, Candice and Kamika unpack why mistrust exists in healthcare for many racialized communities, how bias and burnout impact both patients and providers, and why dignity and listening must be at the centre of care. Listeners will also learn Kamika’s practical ABCDs of Advocacy, a simple but powerful framework to help patients and families navigate complex healthcare systems with confidence: A – Adjust your attitude B – Bring backup C – Have concise conversations D – Keep detailed documentation The conversation also explores: Why representation in healthcare teams matters for patient outcomesHow burnout affects healthcare providers — especially those from racialized communitiesWhat real cultural safety looks like beyond “checkbox” trainingHow healthcare leaders, providers, and allies can use their privilege to create meaningful changeWhat a truly inclusive, reimagined healthcare system could look likeThis episode is essential listening for patients, caregivers, healthcare professionals, and anyone committed to building a more just, compassionate, and equitable healthcare system. Links Centre for Living Organ Donation Ajmera Transplant Centre Code Melanin – Supporting Black, Indigenous, and racialized healthcare professionals and addressing burnout The Black Birth Project – Advancing equity in maternal and birth outcomes Green Table Talk (ACB Organ Health Committee) – Community conversations on organ health and equity Each episode, we share patient stories about organ donation from transplant recipients and living donors, along with insights and education from leading medical experts. Whether you’re a patient, a caregiver, a donor, or simply curious about the world of organ transplantation, you’ll hear expert advice and inspiring journeys of hope, resilience, and second chances. About our Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre. She is also a board member for the National Kidney Foundation and a kidney transplant recipient. After she was diagnosed with kidney failure in her early 20s, she was on dialysis until receiving a transplant from her mother. Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at [email protected]. Thanks for spending your time with us. The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.