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Published by Living Transplant: Patient Stories | Organ Donation | Medical Experts with Candice Coghlan. Supported by the Ajmera Transplant Centre, Toronto General Hospital, UHN
Living Transplant: Patient Stories | Organ Donation | Medical Experts is a podcast that takes you behind the scenes at the transplant program at Toronto General Hospital with the goal to educate, inspire and fuel your passion about transplant, with your host, Candice Coghlan, an Education & Outreach Coordinator at the Centre for Living Organ Donation at the UHN Ajmera Transplant Centre and a kidney transplant recipient.
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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 livingorgandonation@uhn.ca . 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 possible Why he refused to accept "we don't do that" as an answer The challenges of becoming Canada's first anonymous living liver donor The ethical questions and medical concerns behind a historic first The support of family throughout the donation journey Receiving a letter from the recipient's family for the first time The origin of the "Gosling Effect" and its lasting impact Why anonymous donation comes from a different kind of motivation A powerful analogy about saving a life and taking a leap of faith Kevin'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 livingorgandonation@uhn.ca. 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 dialysis Navigating childhood and high school while feeling "different" Receiving a first kidney transplant as a child that lasted nearly 24 years Life after transplant and managing lifelong medications Why transplant is not a cure Finding belonging through dragon boating and the Transplant Games The importance of peer support and patient communities Advice for newly diagnosed kidney patients Understanding the Kidney Paired Donation Program The generosity of living organ donors Hope for the future of transplantation and medical innovation Gratitude 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 livingorgandonation@uhn.ca. 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 matters The truth about “perfect matches” in organ transplant How antibodies affect transplant compatibility Why highly sensitized patients face additional challenges The future of molecular matching and predictive transplant science How UHN teams collaborate across transplant programs Innovations in organ preservation and perfusion technology The 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 livingorgandonation@uhn.ca. 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-19 How a simple “why not?” mindset led to a life-changing journey The realities of donor testing, including unexpected challenges like rapid weight loss Navigating transplant logistics and emotional stress during a global pandemic The importance of communication, advocacy, and support systems throughout the process What recovery really looks like—and how quickly life can begin to feel “normal” again The evolving meaning of her transplant scar—from insecurity to a badge of honour The impact of donation on family relationships, identity, and future outlook Advice for potential donors and caregivers navigating uncertainty Links 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 livingorgandonation@uhn.ca. 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 Topics Living donor kidney transplant and sibling donation Returning to dialysis after transplant Redefining “balance” and embracing rest Invisible illness and “you don’t look sick” Motherhood, career, and chronic illness The importance of support systems and asking for help Patient advocacy and being the expert of your own body Navigating the healthcare system and medical mistrust Cultural safety and equity in organ donation and transplantation The 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 livingorgandonation@uhn.ca. 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 different How TOP provides continuous, specialized care that goes far beyond dispensing medications. Medication adherence made easier The impact of blister packaging, delivery across Ontario, and proactive dose management in helping patients stay on track, catching complications early How frequent check-ins and strong patient relationships help pharmacists identify side effects and concerns before they become serious. Navigating medication fears Honest 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 barriers How medication reimbursement specialists help patients access coverage, reduce out-of-pocket costs, and navigate complex insurance systems. The future of transplant pharmacy Innovations 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 livingorgandonation@uhn.ca. 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 livingorgandonation@uhn.ca. 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 livingorgandonation@uhn.ca. 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 care What living donor coordinators actually do Step-by-step overview of the living donor evaluation process Common myths and fears about kidney donation Life after donation: recovery and long-term outlook How Kidney Paired Donation expands transplant access across Canada The unique impact of non-directed (anonymous) donors Barriers donors may face — including financial and system challenges Emotional supports available for living donors Advice 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 livingorgandonation@uhn.ca. 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 Donatio n 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 livingorgandonation@uhn.ca. 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 Donatio n 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 livingorgandonation@uhn.ca. 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 outcomes How burnout affects healthcare providers — especially those from racialized communities What real cultural safety looks like beyond “checkbox” training How healthcare leaders, providers, and allies can use their privilege to create meaningful change What a truly inclusive, reimagined healthcare system could look like This 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 livingorgandonation@uhn.ca. 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 Crystal Hardy, a First Nations patient, researcher, and advocate whose lived experience with dialysis and kidney transplantation deeply informs her work in Indigenous kidney health. Crystal shares her journey through kidney failure, dialysis, and transplant — not just as a patient navigating a complex healthcare system, but as a researcher working to transform it. She reflects on the moment she realized that life on dialysis could still be full of purpose, the importance of feeling seen within healthcare, and how cultural safety, trust, and community connection directly impact health outcomes. Together, Candice and Crystal explore the systemic barriers First Nations patients face, including geographic isolation, under-referral for transplant, cultural mismatch in care, and inadequate navigation and relocation supports. Crystal introduces the Indigenous Kidney Health Project, explaining how Indigenous storywork and the Two-Eyed Seeing framework are being used to identify gaps in kidney care and reimagine more equitable, culturally congruent systems. This episode is a moving, insightful conversation about advocacy, food sovereignty, patient partnership, and hope — and a reminder that kidney care must meet people where they are, honour who they are, and listen to the stories they carry. What You’ll Learn in This Episode How Crystal’s lived experience as a dialysis and transplant patient shaped her research and advocacy Why feeling seen and heard is foundational to culturally safe kidney care The real-world barriers First Nations patients face when accessing dialysis and transplantation Why Indigenous patients are referred for transplant significantly less often — and what needs to change What the Indigenous Kidney Health Project is and why patient voices lead the work How Two-Eyed Seeing blends Indigenous knowledge with biomedical research The role of food sovereignty and traditional foods in kidney health Why connection, purpose, and peer support are essential on the kidney journey How healthcare systems can move from “cultural training” to truly individualized, respectful care Key Takeaways Kidney disease is a lifelong journey — transplantation is not a cure, but a transition Cultural safety is not a checklist; it is built through trust, listening, and relationships Geography and relocation create profound inequities in access to kidney care Indigenous patients must be partners and leaders in research about their care Food, culture, language, and community are inseparable from health outcomes Purpose and peer connection can be life-sustaining during dialysis and transplant journeys Systemic change is possible — and already beginning — when patients are centered Notable Quotes “I was my own best case study.” “I see you.” “You can’t reform the system if you don’t know what people are actually living through.” “Transplant isn’t a cure — it’s a different way of living with care.” About the Guest Crystal N. Hardy is a First Nations kidney patient, researcher, and advocate whose work focuses on Indigenous kidney health, cultural safety, and equitable access to transplantation. Drawing from her own experiences with dialysis and transplant, Crystal leads research that centers Indigenous voices, storywork, and patient partnership to address systemic gaps in kidney care. If you are a First Nations patient, caregiver, or healthcare provider interested in supporting or participating in the Indigenous Kidney Health Project, Crystal welcomes connection, please reach out to cnhardy@lakeheadu.ca About the 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 kidney transplant recipient and board member of the National Kidney Foundation. Diagnosed with kidney failure in her early 20s, Candice spent time on dialysis before receiving a living donor kidney transplant from her mother. Resources & Links Learn more about living organ donation: www.livingorgandonation.ca Living Kidney Donation at UHN: UHN Ajmera Transplant Centre Living with Kidney Disease Thunder Bay Event Recording: Living with Kidney Disease Crystal Hardy Story 1:49:56 CanSOLVE CKD Indigenous People’s Engagement & Research Council Get In Touch Have questions, comments, or ideas for a future episode? Email the Centre for Living Organ Donation at livingorgandonation@uhn.ca Disclaimer: The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General Hospital or the University Health Network.
In this episode of the Living Transplant podcast, host Candice Coghlan turns the microphone on the show’s very own producer, Amy Schluter. Amy is a podcast host and producer, an entrepreneur, a mom of three and now a 25-year kidney transplant recipient. As we celebrate this incredible milestone of twenty-five years since her kidney transplant, Amy joins Candice for a heartfelt, funny, and deeply honest conversation about her unexpected diagnosis at 25, the life-changing gift from her sister, and what it’s like to build a full, vibrant life in the decades that follow. It’s a journey defined by resilience, creativity, and the joy of living life to the fullest. A transplant isn’t a cure, but there have been significant advances over the last 25 years. Amy takes us back to the year 2000, discussing the technological landscape of transplantation at the time and how laparoscopic surgery was a groundbreaking procedure for her donor, her sister Kelly. Candice and Amy discuss the evolution of transplant care, from the early days of "Timex watch" medication reminders to the modern era of health tech. Listeners will hear inspiring stories about Amy’s high-risk pregnancy with twins, the messy, emotional realities of recovery, including a memorable blender explosion and her hopes for the future, from organ cloning dreams to simply staying healthy to watch her kids grow. Whether you’re newly diagnosed, newly transplanted, or decades into your journey, a caregiver or a medical professional, this conversation offers inspiration, humour, and a unique perspective drawn from decades of lived transplant experience. It’s a powerful testament to the longevity and quality of life possible after transplantation. Key Takeaways: The 25-Year Milestone: Amy reflects on living longer with her transplant than without it. Pregnancy and Twins: A look at the rare and high-risk journey of carrying twins as a transplant recipient and the medical curiosity it sparked at St. Michael's Hospital. Technological Advancements: How transplant surgery and aftercare have evolved over the last two decades. Balancing Act: Insights on managing a career as a serial entrepreneur and podcast producer while prioritizing health and family. Mental Resilience: Overcoming the trauma of diagnosis and the importance of community support. Links and Resources Chef Over Your Shoulder Podcast Bespoke Productions Kidney Foundation Peer Support Pregnancy & Kidney Disease Transplant Pregnancy Registry Connect with the Podcast or Learn more about Organ Donatio n Click here for more information about living organ donation. Click here for more information about living kidney transplantation. 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 livingorgandonation@uhn.ca. 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, Dr. Edward Cole shares his extensive experience in nephrology and kidney transplantation. With a career spanning over fifty years at the University Health Network, Dr. Cole has witnessed the trajectory of transplant medicine from its infancy to its advacned state today. He reflects on the future of nephrology, including potential innovations in transplantation and the significance of mentorship in shaping the next generation of healthcare professionals. In This Episode, We Cover: The Early Days: What transplant medicine looked like in 1975 versus today. The Game Changers: How drugs like Cyclosporine revolutionized survival rates. The Science of Matching: Understanding HLA antigens and the breakthrough of the Paired Donation Program. Future Horizons: Xenotransplantation and the dream of eliminating anti-rejection medication. Hard Truths: Dr. Cole’s candid advice on patient advocacy and the realities of a medical career. Connect with the Podcast or Learn more about Organ Donatio n 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 livingorgandonation@uhn.ca. 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 conversation, Yitzi Gal discusses the significance of practicing failure through improvisation and mistakes in a safe environment, emphasizing the need to differentiate between minor errors and life-threatening situations. He highlights the importance of emotional resilience and the ability to assess risks in everyday life. Key Takeaways We need to practice failure in a safe space. Mistakes should not be equated with life-threatening situations. Emotional training is essential for risk assessment. Not every failure leads to significant consequences. Understanding the context of mistakes is crucial for growth. Teaching students about failure prepares them for real life. Practicing in a controlled environment builds confidence. Life lessons often come from making mistakes. Differentiating between minor and major risks is vital. Emotional health is impacted by our perception of failure. Links and Resources Improv for Anxiety One Man’s Solution for Crushing Anxiety: Improv Play with Fire Improv Brene Brown TED Talk: The Power of Vulnerability Internal Family Systems (IFS) – Richard Schwartz The Power of Addiction and The Addiction of Power: Gabor Maté at TEDxRio+20 Connect with the Podcast or Learn more about Organ Donatio n Learn more about Living Organ Donation Learn more about Kidney Transplantation 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 livingorgandonation@uhn.ca. 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 Living Transplant , we sit down with Dr. Susy Hota, an infectious diseases physician and medical director of Infection Prevention and Control at UHN. Dr. Hota takes us inside the world of C. difficile infections and the remarkable, life-changing treatment known as fecal microbiota transplantation (FMT). From her early fascination with microbiology to leading pandemic preparedness at one of Canada’s largest hospitals, Dr. Hota shares her journey, insights from the frontlines of COVID-19, and how collaboration and relationships underpin every breakthrough in healthcare. We then explore the gut microbiome — the “hidden organ” inside us — and how FMT offers new hope for patients living with recurrent C. diff. Dr. Hota also demystifies the donor process, potential risks, and the exciting future of microbiome research that could transform how we treat everything from gut disorders to mental health. Key Takeaways Hope and healing: Even for those with chronic or recurrent infections, there are innovative treatments that can restore quality of life. Relationships matter: Whether in outbreak response or research, collaboration is key to success in healthcare. Your gut is an ecosystem: FMT is changing how we think about disease — focusing on restoring balance, not just killing bacteria. The future is bright: As microbiome science advances, new possibilities are emerging for treating conditions far beyond infection. About our Guest Dr. Susy Hota is the Division Head of Infectious Diseases at UHN and Sinai Health and the Medical Director of Infection Prevention and Control at UHN. She has been a leader in pandemic preparedness, infection control, and innovative treatments such as fecal microbiota transplantation. Her work bridges clinical care, research, and systems-level leadership to improve safety and health outcomes for patients across Canada. Connect with the Podcast or Learn more about Organ Donatio n Learn more about Living Organ Donation Learn more about Kidney Transplantation Learn more about Dr. Hota’s research and fecal transplantation 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 livingorgandonation@uhn.ca. 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, host Candice Coghlan sits down with Sasha, a social worker at Toronto General Hospital, to discuss the vital intersection of mental health, addiction recovery, and organ transplantation. Sasha shares her journey into social work, her experience supporting patients in the Alcohol Liver Disease Program, and how stigma can affect those living with alcohol-related liver disease. The conversation dives deep into the realities of recovery, relapse prevention, financial barriers, and the emotional toll of transplant life — for both patients and families. Sasha emphasizes compassion, honesty, and the importance of recognizing addiction as a health condition, not a moral failing. Together, Candice and Sasha explore the meaning of resilience, the need for peer and mental health support, and the small acts of kindness that make a lasting impact in healthcare. Key Takeaways Addiction is a health condition and should be treated with empathy and understanding. Mental health support is just as critical as physical care in the transplant process. Family and caregivers play an essential role in a patient’s recovery journey. Financial challenges and access to mental health care remain major barriers for many patients. Peer support networks are transformative but still lacking for liver transplant patients. Honesty and emotional validation are key tools for social workers supporting transplant patients. It’s okay to not feel okay — emotional lows are part of the transplant journey. Resources & Links Learn more about Living Organ Donation Learn more about Living Liver Donation Learn more about Mental Health supports available Centre for Living Organ Donation on Instagram Ajmera Transplant Centre on Instagram About the Podcast Each episode of Living Transplant shares real stories from transplant recipients, living donors, and healthcare experts. Whether you’re a patient, caregiver, or simply curious about organ donation, you’ll hear honest conversations about resilience, hope, and the life-changing power of organ transplantation. About the Host Candice Coghlan is the Education & Outreach Coordinator at the Centre for Living Organ Donation at UHN’s Ajmera Transplant Centre, a kidney transplant recipient, and a board member for the National Kidney Foundation. Contact Have questions? Comments? Ideas for an episode? Please reach out to the Centre for Living Organ Donation at livingorgandonation@uhn.ca. 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 deeply moving episode of The Living Transplant Podcast, host Candice Coghlan sits down with Mary, a liver transplant recipient whose story embodies courage, vulnerability, and self-advocacy. Mary opens up about her struggles with addiction, mental health, and identity, sharing how her liver transplant became a turning point toward healing — both physically and emotionally. She discusses the often-overlooked connection between mental and physical health, the stigma surrounding addiction, and the life-changing power of receiving an accurate diagnosis after years of being misunderstood. This honest and heartfelt conversation reminds us that healing doesn’t end with surgery — it continues with self-discovery, support, and breaking the silence around mental health. Key Takeaways Mental and physical health are deeply interconnected — both deserve equal attention. Addiction and mental health struggles are health issues, not moral failings. Advocacy starts small: asking for help is an act of bravery, advocacy is crucial in navigating the healthcare system Receiving a transplant can awaken gratitude, but also complex emotions that deserve space and care. A proper diagnosis can completely change a person’s quality of life. Breaking the stigma around mental health begins with open, honest conversations. Community and compassion are powerful forces in recovery. Mental health challenges often go unseen and misunderstood. Organ donation is a life-changing gift that impacts families. Everyone struggles with something; it's important to talk about it. Links and Resources More information about living organ donation More information about living liver transplantation Centre for Living Organ Donation on Instagram Ajmera Transplant Centre on Instagram Canadian Mental Health Association About Our Guest Mary R. — Liver transplant recipient and mental health advocate. Her story highlights resilience, hope, and the importance of treating the whole person, not just the body. Connect with the Podcast or Learn more about Organ Donatio n 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 livingorgandonation@uhn.ca. 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.
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