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Explore every episode of the podcast Living Transplant: Patient Stories | Organ Donation | Medical Experts

Dive into the complete episode list for Living Transplant: Patient Stories | Organ Donation | Medical Experts. Each episode is cataloged with detailed descriptions, making it easy to find and explore specific topics. Keep track of all episodes from your favorite podcast and never miss a moment of insightful content.

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TitlePub. DateDuration
From Blood Donation to Double Living Donor: Tyler’s Kidney and Liver Donation Story17 Sep 202600:36:09

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.


The Gosling Effect: How One Anonymous Liver Donor Redefined What’s Possible in Transplant Medicine25 Jun 202600:43:27

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.



Never Lose Hope: Jess Bailey on Community, Dragon Boats and the Gift of Life11 Jun 202600:43:40
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 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.

Beyond the Perfect Match: How HLA Science Is Changing Transplant28 May 202600:34:47

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.




Eight Weeks for a Lifetime: Maigen’s Journey as a Living Liver Donor07 May 202600:37:26

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.


You Don’t Look Sick: Fadia on Invisible Illness, Advocacy, Redefining Life on Dialysis, and the Transplant Journey16 Apr 202600:38:06

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.


Behind Every Transplant: Inside Toronto General's Outpatient Transplant Pharmacy02 Apr 202600:38:18

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.

A Second Chance for Love: Emma’s Determination to Donate a Kidney at 79 | Patient Stories, Organ Donation and Medical Experts19 Mar 202600:29:44

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.



International Women’s Day: Dr. Irene Kim on Motherhood, Mentorship & Transplant Leadership08 Mar 202600:16:45

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.



Guiding the Gift: Behind the Scenes with a Living Kidney Donor Coordinator 05 Mar 202600:37:08

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.

One Liver for Life: Pediatric Liver Transplants | Patient Stories, Organ Donation and Medical Experts19 Feb 202600:46:58

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 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.

A Toddler Transplant: How Daddy's Liver Saved Camilla's Life | Patient Stories, Organ Donation and Medical Experts05 Feb 202600:54:05

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 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.


Reimagining Healthcare: Advocacy, Equity, and Dignity with Kamika Sylvester, RN | Patient Stories, Organ Donation and Medical Experts22 Jan 202600:52:34

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.



“I See You”: Indigenous Kidney Health, Cultural Safety, and Reimagining Care | Patient Stories, Organ Donation and Medical Experts08 Jan 202600:44:05

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.



Amy's Reflections from the First 25 Years of a Kidney Transplant Journey | Patient Stories, Organ Donation and Medical Experts18 Dec 202500:40:16

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 Donation

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.



Fifty Years of Kidney Transplantation: Nephrologist Dr. Cole's Perspective on Revolutions in Renal Care | Patient Stories, Organ Donation and Medical Experts04 Dec 202500:36:08

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 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 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.


Yes And… The Joy of Imperfection | Patient Stories, Organ Donation and Medical Experts20 Nov 202500:40:10

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 Donation

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.




The Hidden Organ: The Ecosystem of the Gut & Fecal Transplants | Patient Stories, Organ Donation and Medical Experts06 Nov 202500:38:16

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 Donation

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.


A Social Worker’s Perspective: Understanding Addiction, Recovery, Transplant Care | Patient Stories, Organ Donation and Medical Experts27 Oct 202500:30:43

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.


Mary’s Journey: Healing Beyond Transplant | Patient Stories, Organ Donation and Medical Experts09 Oct 202500:35:50

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 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 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.




Twice the Gift: Megan’s Double Anonymous Living Donor Story | Patient Stories | Organ Donation | Medical Experts25 Sep 202500:33:43

In this inspiring episode, host Candice Coghlan speaks with Megan Owen-Evans, a rare double anonymous living organ donor. Megan has given both a kidney and part of her liver—gifts offered not to family or friends, but to complete strangers in need.


Together, they explore what motivates someone to step forward for such extraordinary acts of altruism, the recovery journey, and the myths and misconceptions around anonymous donation. Megan also shares how her experiences as a donor inspired her advocacy work, including pushing for paid leave for living donors through the Living Donor Circle of Excellence.


This conversation highlights not only the bravery of living donors but also the ripple effects their generosity creates in workplaces, families, and communities.


Episode Highlights

Megan’s journey from childhood experience to becoming a living donor

Discovering the option of anonymous kidney and liver donation

What recovery was really like after both surgeries

Misconceptions about living and anonymous donation—and how to address them

Writing letters to her recipients and the emotional connections that followed

How Megan helped shape workplace policy to remove financial barriers for donors

Why living donors see their gift as life-changing not just for recipients, but for themselves


Takeaways

Living donors undergo thorough medical and psychological screening to ensure safety.

Recovery from kidney and liver donation is often faster and easier than many assume.

Community support and employer recognition play a vital role in making donation possible.

Altruism can be a powerful force that reshapes not only individual lives but also public policy.

Every act of donation—whether blood, organs, or advocacy—creates ripples of hope.


Links and Resources

Click here for more information about the Living Donor Circle of Excellence

Click here to watch videos of living organ donors and recipients of living 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 living liver transplantation

Click here to watch videos of living organ donors and recipients of living donation

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.



Psychopathy, Altruism and the Gift of Life: Neuroscience with Dr. Abigail Marsh | Patient Stories | Organ Donation | Medical Experts17 Sep 202500:36:25

In this episode, Dr. Marsh explains the neuroscience of altruism, from the role of the amygdala to genetic influences on empathy. Through Dr. Marsh’s donor stories and research insights we explore the spectrum of altruism and psychopathy. She reveals how the amygdala, the brain region tied to emotional responses, plays a pivotal role in altruistic behavior. Remarkably, research shows that altruistic kidney donors often have larger amygdala sizes compared to the average person.


Dr. Marsh also reveals the genetic factors that shape empathy and altruistic tendencies, while challenging the misconception that altruism is irrational or abnormal. She contrasts the media’s frequent focus on negative aspects of human nature with the lived experiences of donors, who describe profound feelings of honor and fulfillment after giving the gift of life.


Throughout the conversation, personal stories from living organ donors underscore the importance of community support for both donors and recipients. Dr. Marsh emphasizes the power of education and awareness to dispel myths about donation and highlights that altruism is not only a natural human trait but also one that can be nurtured and encouraged in all of us.


Links and Resources

Dr. Marsh’s Website

Dr. Marsh’s TedTalk

The Fear Factor, by Dr. Marsh

Dr. Marsh LinkedIn


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 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.

This Journey is for Life27 Feb 202501:06:46

 In this episode of the Living Transplant podcast, host Candice Coghlan is joined by Loi Nguyen; a father, outdoorsman, and all around very positive person. Loi is living with polycystic kidney disease. We discussed his journey from diagnosis to kidney modality options, to the call that came in that changed his life: that there was a living kidney donor ready to donate a kidney to him through the paired exchange program. 

We're later joined by Christine Bruce, the Senior Director of Laboratory Medicine at UHN. Not only is Christine the Director of the program, which is incredibly instrumental in all parts of transplant, but she is also an anonymous kidney donor. After reading an email we sent out about Living Donation Week, Christine made the decision that she would fill out her health history form and wait six months to see if she was still passionate about the opportunity to become a donor. And when she decided she was, her path to transplant was unique, as she went from a practitioner to a patient. Please enjoy.  

The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

For more information about living organ donation, please visit www.livingorgandonation.ca

For more information about living kidney transplantation, please visit: https://www.uhn.ca/Transplant/Living_Donor_Program/Pages/living_kidney_donor.aspx

For more information about Polycystic Kidney Disease, please visit https://www.endpkd.ca/ 

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 Other Side of the Hug29 Nov 202400:59:03

In this episode of the Living Transplant podcast, host Candice Coghlan is joined by Winne Jerome who talks to us about her journey as a living donor to her sister through the Kidney Paired Donation Program, making that decision after having a premature newborn baby at home. She spoke about how when she found out she was able to donate a kidney to a stranger, so her sister would receive a kidney from a stranger, the excitement was too much to hold. We are later joined by Darlene Jagusic, a registered nurse who spent time supporting the Living and Deceased Donation Program in Saskatchewan, as well as being a critical care nurse in B. C. and Saskatchewan for many years. She is now the Program Manager for the Kidney Paired Donation and Highly Sensitized Patient Program at Canadian Blood Services.

We discuss hope for those waiting, the details and intricacies of the Kidney Paired Donation Program, and the gratitude we have for organ donors. Please enjoy.  

The views and opinions expressed in this episode do not necessarily reflect the offical policy or position of Toronto General or University Health Network. 

For more information about kidney transplantation, please visit: https://www.uhn.ca/Transplant/Kidney_Transplant_Program 

For more information about the Kidney Paired Donation Program, please visit: https://www.blood.ca/en/organs-tissues/living-organ-donation/kidney-paired-donation 

To watch Winnie & Fadia's story on Great Actions, please visit: greatactions.ca 

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.

Take What You Need, Save My Baby06 Sep 202400:57:16

In this episode of the Living Transplant postcast, host, Candice Coghlan was joined by Stephanie Dyriw, a living liver donor to her son. Stephanie was put in a situation no parent could ever imagine, when her healthy, three and a half year old son crashed into liver failure with no warning. Within days, Stephanie and the UHN team worked tirelessly to get the testing done in partnership with SickKids to test to find if she would be a match, and thankfully, within mere days, Stephanie became a living liver donor to her son, saving his life. We are later joined by Dr. Nazia Selzner, a transplant hepatologist and Medical Director of the Living Donor Liver Transplant Program at the Ajmera Transplant Centre, and Dr. Cynthia Tsien, Education Director of the Ajmera Transplant Centre. We spoke about diversity, equity and inclusion in transplant, both for professionals and for patients and families. We discussed how equity, diversity, and inclusion in transplant medicine are crucial to ensuring all patients have fair access to life saving treatments, regardless of their background, leading to better overall health outcomes, and how for professionals, fostering an inclusive environment enhances teamwork, broadens perspectives, and improves decision making, ultimately advancing the field and providing more comprehensive care. Please enjoy.

The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

For more information about Great Actions Leave a Mark, please visit greatactions.ca

For more information about living liver transplant, please visit https://www.uhn.ca/Transplant/Liver_Transplant_Program 

To register for the Diversity, Equity and Inclusion in Transplant conference, please visit https://deiintransplant.com/ 

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.

We are a Resilient Group15 Aug 202401:00:29

In this episode of the Living Transplant podcast, host, Candice Coghlan, was joined by Manuel Escoto, the Patient, Family, Donor Partnerships and Knowledge Mobilization Director at CDTRP, the Canadian Donation and Transplantation Research Program alongside Sadia Baig, the Programs Coordinator at the Kidney Foundation of Canada, Ontario branch. What is the common thread between the three of us you might be thinking? Well, all of us are not only working in the field of transplant, donation and chronic illness, but we're all living with kidney disease diagnosed at a young age.

We speak about being diagnosed with a chronic disease, the mental and physical roller coasters, working in a professional field that we also have a personal connection to, what it's like to connect with others who are going through something similar, and the importance of advocacy and having a strong network of support. Join the three of us as we dive into these topics in a unique episode where the people with lived experience are also the experts in the field. Please enjoy.

The views and opinions expressed in this episode do not necessarily reflect the offical policy or position of Toronto General or University Health Network. 


For more information about kidney transplantation, please visit www.livingorgandonation.ca 

For more information about CDTRP, please visit https://cdtrp.ca/en/ 

For more information about the Kidney Foundation of Canada, please visit www.kidney.ca 

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.

It's Not Outrageous: Jillian Best's Epic Swim Across Lake Ontario04 Jul 202401:01:30

In this episode of the Living Transplant podcast, host Candice Coghlan was joined by Jillian Best, the first organ transplant recipient and one in only 72 people to ever swim across Lake Ontario in all of recorded history. Jillian trained, swam and built her mental fortitude so she could swim across Lake Ontario in 18 hours and 36 minutes. She finished the historic 52 kilometer crossing to raise money for the transplant unit who saved her life and her mother's. We are later joined by Dr. Marie Faughnan, a Lung Specialist and HHT specialist at St. Michael's Hospital. As an avid cycler and physician, Dr. Marie was healthy and ready when a colleague of hers experienced liver failure and was in need of a life saving liver transplant. She asked herself, why not me? She went through the process of going from a physician to a patient and became a living liver donor to save her colleague's life. Throughout this episode, we talk about perserverence, commitment, sacrifice and doing hard things with extreme bravery. Please enjoy. 

The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

For more information about living liver donation, please visit www.livingorgandonation.ca

For more information about Jillian Best's swim across Lake Ontario, please visit https://www.thestar.com/news/canada/q-a-londoner-jillian-best-relives-her-historic-swim-across-lake-ontario/article_5b953b74-c9eb-5944-bb0f-88add77d74d8.html 

To listen to Dr. Marie Faughnan's story and other living donors and recipients, please visit www.greatactions.ca 

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.

I Don’t Want to Just Survive, I Want to Live06 Jun 202400:58:52

In this episode of the Living Transplant podcast, host Candice, was joined by Dawn Ethier, a police officer and mother of four. Dawn had thyroid cancer over 10 years ago. The cancer was treated, but she was left with hypoparathyroidism, which caused horrible side effects, changed her lifestyle, and took a lot of time away from her family, her work, and her life. Dawn did a lot of research, and with her advocacy and ingenuity, brought the idea of a parathyroid transplant to her doctors, who eventually found Dr. Karen Devon, an endocrine surgeon at UHN's Sprott Department of Surgery.  With only one other recorded case of this exact transplant in scientific literature, Dr. Devon was inspired by Dawn to do homework, connect with specialists around the world, and several years later, cured Dawn's hypoparathyroidism following a ground-breaking North American first procedure at UHN's Ajmera Transplant Centre. This changed Dawn's life, her family's life, and changed the future for patients.

The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

For more about Dawn’s story, and the team behind this North American first, please visit https://uhnfoundation.ca/stories/north-american-first-transplant-offers-mother-of-four-a-future-now/

For more information about Ajmera Transplant Centre, please visit https://www.uhn.ca/Transplant

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.

My Mom is My Person02 May 202400:55:17

In this episode of the Living Transplant podcast, host Candice Coghlan was joined by Kelsey Hannah, an OR nurse and mother who went on a journey of health and wellness to lose weight to save her mother's life by donating a portion of her liver to her. We talked about her journey of self reflection, empowerment, dedication, and what it felt like to juggle life while the clock ticked down getting closer to her mother needing that gift of life of a liver transplant.

We were later joined by Chantal Wiggins, a Transplant Coordinator at the Ajmera Transplant Centre in the Living Donor Liver Program. We spoke about the processes that donors have to go through to ensure their health and safety, memorable moments in her career, and what it feels like to get to be part of a team that truly saves lives.

The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network. 

To learn more about living liver donation, please visit https://www.uhn.ca/Transplant/Living_Donor_Program/Pages/living_liver_donor.aspx 

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.

A Piece of Me in Heaven04 Apr 202400:56:52

WELCOME TO SEASON 5! In this episode, host Candice Coghlan was joined by Vanessa Tait, a Cree woman from O-Pipon-Na-Piwin Cree Nation who put her heart and soul into supporting her father, Kenneth, through his kidney health journey. She uprooted their lives to move from her father's home community of O-Pipon-Na-Piwin Cree Nation, over 700km north of Winnipeg, to the city to access dialysis, as there were no hemodialysis machines and no capacity to do home dialysis, with the lack of access to large amounts of water needed. While in Winnipeg, Vanessa was his primary caregiver. We spoke about their journey together, the medical barriers they and many other First Nations patients face, and the decision for Vanessa to give the gift of life, a kidney to her father, despite his chances of survival being long so he could live his days out in community, surrounded by loved ones. 

We were later joined by Dr. Michael Anderson from the Urban Indigenous Community in Toronto. He is Mohawk Bear Clan and mixed European with family roots in Tyendinaga Mohawk Territory. He practices surgical oncology in palliative care medicine and is the strategic lead for Indigenous Health at the University Health Network. We spoke about ethical Indigenous community healthcare research partnerships, grief, healing, and Indigenous conceptualizations of death and dying.

This episode is dedicated, in loving memory to Vanessa's "daddio", Kenneth.

The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network. 

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.

*** CONTENT WARNING***
 A note to our listeners, this episode comes with a content warning as we discuss death, dying, and palliative care. We also discuss barriers to care for Indigenous communities. This is simply to empower you, our audience, with the knowledge that you may need to make healthy decisions about how or if you should consume this podcast content.  If you need resources or support, you can visit the Hope for Wellness helpline, which offers immediate help to all Indigenous people across Canada, available 24/7 with immediate support and crisis intervention. You can call the toll free helpline at 1 855 242 3310, or you can connect to the online chat at hopeforwellness.ca. You can also reach out to the Bereaved Families of Ontario Organization at www.bereavedfamilies.net or call them at 416 440 0290.  

For more information about the UHN Indigenous Health Program, please visit: https://uhnfoundation.ca/stories/fostering-a-healthier-relationship-to-improve-access-to-high-quality-care-for-indigenous-communities/ 

To watch Vanessa Tait's documentary, Gift to Give please visit: https://gem.cbc.ca/gift-to-give/s01 

To watch Vanessa Tait's Great Actions Leave a Mark interview, please visit: www.greatactions.ca 

To learn more about living kidney donation, please visit: https://www.uhn.ca/Transplant/Living_Donor_Program/Pages/living_kidney_donor.aspx 

Grateful for the Little Things12 Oct 202300:38:34

In this episode, host, Candice, is joined by Melissa Sidhu who works in healthcare, is a passionate volunteer and living liver donor to her brother over 10 years ago. We spoke about her journey as a donor, relationships with loved ones, how to find tiny moments of joy and gratitude throughout this episode.

You will also hear clips from members of the transplant community sharing their gratitude.

The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General or University Health Network.

To learn more about living liver donation, please visit https://www.uhn.ca/Transplant/Living_Donor_Program/Pages/living_liver_donor.aspx

To listen to all of our submissions of gratitude, please visit https://drive.google.com/drive/folders/13Di_gaucmChOR7tDB873mGsCQAgh9zkD?usp=sharing 

To read messages of gratitude, please visit bit.ly/LDW23TX

I Choose Life28 Sep 202300:47:53

In this episode, host Candice Coghlan sat down with Afsana Lallani, a cat lover and nursing graduate who made a public social appeal to find a living liver donor to save her life. They talk about being young and living with a chronic illness, facing death and how a supportive community can make all the difference. They are later joined by Dilshad Lallani, Afsana’s mother, caregiver and a pediatric nurse practitioner. She speaks about the family journey in supporting someone on the transplant waitlist, being an emotional support and what it was like being a nurse practitioner living through the process with her daughter on the verge of death. 

The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General Hospital or University Health Network.

For more information about PSC, please visit https://www.liver.ca/patients-caregivers/liver-diseases/primary-sclerosing-cholangitis/ 

For more information about finding a living donor, please join one of the Centre's free virtual Finding a Living Donor Webinars, by registering at http://givelifeuhn.eventbrite.ca 

Pressure for Change14 Sep 202300:58:29

In this episode, we're celebrating Living Donation Week. Host, Candice was joined by Sylvie Charbonneau, past president of the Kidney Foundation of Canada, advocate, change maker, and living kidney donor to her son. We were also joined by Dr. Joseph Kim, Director of the Kidney Transplant Program at the Ajmera Transplant Center. We discussed barriers and changes that need to be made to increase access to organ donation as a whole across Canada and how we can support others to receive and give the gift of life.

For more information about living kidney donation, please visit https://www.uhn.ca/Transplant/Kidney_Transplant_Program 

For more information about the ODTC Collaborative, please visit https://profedu.blood.ca/en/organs-and-tissues/practices-and-guidelines/current-projects/odtc-projects 

If you have questions, please reach out to us at livingorgandonation@uhn.ca

The views and opinions in this episode do not necessarily reflect the official policy or position of Toronto General Hospital or University Health Network.

Ajmera Transplant Centre's 2nd Annual Education & Research Conference31 Aug 202301:33:40

In this episode, host Candice, takes you behind the scenes of the Ajmera Transplant Centre's 2nd Annual Education and Research Conference, to hear about incredible science, clinical, and research aspects of transplantation. Hear from the following:

Samrat Ray: Expanding the transplant pancreas donor, using an ex vivo perfusion model.

Adriana Roberta: Determining the impact of certain mismatches, which are located in the DQ Loco and the development of chronic rejection.

Javier Solera: The severity of COVID 19 Omicron variant and Omicron specific immune responses in solid organ transplant patients.

Lakshmi Kugathasan: Systematic review and network meta analysis research in induction therapy in heart transplantation.

Bonnie Chao: Machine learning approaches to processing and interpreting ex vivo lung radiographs and predicting transplant outcomes.

Dr. Laura Donahoe: Improving the quality of lung transplantation through a technical skills simulation program for surgical lung transplant fellows. 

Christina Lam: Fibrinogen like protein 2 molecule and how it influences the development of thymic regulatory T cells. 

Luckshi Rajendran: The Toronto management of initially unresectable liver metastasis for colorectal cancer  in a living donor liver transplant program.

For more information about the Ajmera Transplant Centre's program, please visit www.uhntransplant.ca 

For more information about Dr. Laura Donahoe's Take-Home Surgical Anastomosis Simulation Model, please visit: https://pubmed.ncbi.nlm.nih.gov/37202320/ 

If you have questions, please reach out to us at livingorgandonation@uhn.ca

The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General Hospital or University Health Network.

I've done this before, I can do it again.17 Aug 202300:52:13

In this episode, host Candice Coghlan was joined by Justin Poy, a father, entrepreneur, and businessman who has lived with multiple types of renal replacement therapy since the age of 10, including three kidney transplants, hemodialysis, peritoneal dialysis, as well as home dialysis. Justin spoke about mental health, resiliency, parenting with a chronic illness, and how to appreciate each day. Later we were joined by Dr. Samantha Anthony, the first person to hold the title of Health Clinician Scientist in Canada, Transplant and Regenerative Medicine Center, Department of Social Work, Child Health Evaluative Science Research Institute at SickKids. Together, we explored the medical journey and tools to support children, youth, and families created from the perspective of those who live with it. We also spoke about post traumatic growth and the whole family journey. 

For more information about peer support, please visit https://kidney.ca/support 

For more information about living kidney donation, please visit www.livingorgandonation.ca

For more information about Dr. Samantha Anthony's work, please visit https://lab.research.sickkids.ca/anthony/anthony-lab/ 

If you have questions, please feel free to reach out to us at livingorgandonation@uhn.ca

The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General Hospital or University Health Network.

 

Playing with New Lungs03 Aug 202300:54:08

In this episode, host Candice Coghlan sat down with Tara Lisabeth, who received not one, but two double lung transplants at a young age. She spoke about life with cystic fibrosis, what it felt like to take deep breaths and how transplant gave her the opportunity to walk down the aisle and get married. Later we were joined by Dr. Marcelo Cypel, the Surgical Director for the Ajmera Transplant Centre at UHN and UHN ECLS Program, among many other accolades, who also performed Tara's first double lung transplant. He spoke to us about innovations to expand the donor pool and create more viable lungs for transplant with therapies like light based therapy to inactivate hepatitis C virus, a universal blood type, lung preservation and repair with Ex Vivo, and what it is like leading and being part of a team who has now celebrated the 3000th lung transplant.

For more information about Cystic Fibrosis, please visit: https://www.uhn.ca/Transplant/Lung_Transplant_Program/Pre-Transplant/Pages/cystic_fibrosis.aspx 

For more information about the UHN Lung Transplant Program, please visit: https://www.uhn.ca/Transplant/Lung_Transplant_Program 

For more information about the Ex Vivo Lung Perfusion System, please visit: https://uhnfoundation.ca/stories/out-of-body-experience/ 

The views and opinions expressed in this episode do not necessarily relfect the official policy or position of Toronto General Hospital or University Health Network.

 

I've Learned to Walk 3x in My Life08 Jul 202300:47:10

In this episode, host Candice Coghlan sat down with Shilpa Raju, an epidemiologist who finished her degree while battling cancer. She survived the cancer, however unfortunately the side effects from her treatment caused severe lung damage, resulting in her need for a double lung transplant. Shilpa spoke about being a young person battling illness and trying to keep a sense of normalcy and positivity through her day to day. Later, we were joined by Dr Mamatha Bhat, a staff hepatologist and clinician scientist at UHN's Ajmera Transplant Program and University of Toronto's division of gastroenterology. She speaks to us about machine learning and AI implications for health care and how it is going to revolutionize the world of transplant and beyond.

To learn more about Dr. Bhat's research in Artificial intelligence, machine learning and deep learning in liver transplant visit:  https://pubmed.ncbi.nlm.nih.gov/37208107/ 

For information about living organ donation visit www.livingorgandonation.ca or www.uhntransplant.ca 

You can also reach out to us directly at livingorgandonation@uhn.ca 

The views and opinions expressed in this episode do not necessarily reflect the official policy or position of Toronto General Hospital or University Health Network.

Waiting for the Science to Catch Up22 Jun 202300:52:01

Host Candice Coghlan is joined by Darryl Wallis, who was diagnosed with Hollow Visceral Myopathy at age one. He grew up in and out of hospitals and unable to eat, but about 16 years ago, he received a multi-organ transplant including a liver, bowel, stomach and pancreas, which gave him his life back. He was able to have a family and become a pharmacist and a few years ago, Darryl's son was diagnosed with the same disease. He also received a multi-organ transplant by the same surgeon, Dr. Anand Ghanekar, who is our expert guest. Dr. Ghanekar's practice focuses on abdominal organ transplantation. He joins us to discuss the rarity of multi-organ transplants and the privilege it is to have the opportunity to restore somebody from certain death to almost a normal life, and the personal connection he has to the success of his patients.

To learn more about the multi organ transplant program visit https://www.uhn.ca/Transplant/Pages/default.aspx 

Want to register your consent to be an organ donor when you pass? Want to see if you are a registered organ donor? Visit www.beadonor.ca and don't forget to tell your family about your wishes.

You can also reach out to us directly with any questions at livingorgandonation@uhn.ca

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.

The Rest of Your Sight Life08 Jun 202301:03:35

Host Candice Coghlan is joined by Amber Needham and her living eye stem cell donor, Kathy O'Toole. They discuss how Amber lost her eyesight twice from unique situations. Amber, Kathy and Candice talk about their remarkable journey as Amber went from 2020 vision to blindness and how she was given a second chance with sight when Kathy donated stem cells from her eye. They are later joined by Amber's ophthalmologist, Dr. Clara Chan, who talks about fascinating innovation in science with stem cell transplants, the healing properties of amniotic membranes, and how her work is a lesson in humanity and the strength of patients. 

To purchase Amber's book, The Blind Girl Sees, visit: https://www.amazon.ca/Blind-Girl-Sees-Seeing-Through/dp/1039136869 

To learn more about Amber's charity work visit: https://uhnfoundation.ca/stories/amber-needham-rides-toward-vision-care-for-all/ 

If you are interested in learning more about stem cell donation you can visit:

https://www.blood.ca/en/stemcells/donating-stemcells/stemcell-eligibility-and-registration 

https://www.uhn.ca/PatientsFamilies/Health_Information/Health_Topics/Documents/Living_Donor_Corneal_Limbal_Stem_Cell_Transplant.pdf 

Or reach out directly to us at livingorgandonation@uhn.ca

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.

I Got My Voice Back25 May 202301:04:12

Host Candice Coghlan is joined by Ivica, an opera singer who loves baking, teaching others, and above all else, his family. Ivica discusses his journey with kidney failure and how his brother stepped forward to be his donor, giving him back the strength to sing beautifully. Later we're joined by Margot Mitchell, a retired social worker who worked at UHN for over 20 years. She speaks of the importance of good mental health and how we can all move through grief to gratitude. 

To listen to more of Ivica's singing, check out @onetenorthreekidneys 

If you are looking to connect with Peer Support, visit the Kidney Foundation at https://kidney.ca/Support/Peer-Support 

UHN's Coping with a Transplant manual https://www.uhn.ca/PatientsFamilies/Health_Information/Health_Topics/Documents/Coping_with_a_Transplant.pdf 

Or reach out directly to us at livingorgandonation@uhn.ca to connect with someone to share experiences.

The views and opinions expressed in this interview do not necessarily reflect the offical policy or position of Toronto General Hospital or the University Health Network.

The Queen of My Heart Function11 May 202300:47:42

Host Candice Coghlan is joined by Charles Cook, an incredibly brave and vibrant person who is a heart and kidney transplant recipient. After far too many close cases with death, Charles has implemented the life motto of ‘keep bangin’. Charles and Candice are later joined by the one of a kind cardiologist, Dr. Heather Ross who is highly decorated with awards like Canadian Geographic’s top 100 Explorers and the Order of Canada. She talks about football, her childhood, Testing Your Limits and why the patient journey to her, is more than just treating the disease.

With special guest Millie, the Myers parrot.

To read more about Charles’ journey, visit: https://www.keepbangin.com/

To read more about Dr. Heather Ross & Testing Your Limits, visit: https://uhnfdn.ca/tyl/

For more information about the ACB Organ Health YouTube Channel, visit: https://www.youtube.com/channel/UCFFz8hoKUxTYltN1aX8nghA 

The views and opinions expressed in this interview do not necessarily reflect the official policy or position of Toronto General Hospital or the University Health Network.

BONUS: Great Actions Leave a Mark - Paul27 Apr 202300:24:59

In September, 2022, we launched Great Actions Leave a Mark, a national, multi-year public awareness campaign about living organ donation and transplantation. It has images and videos of living kidney and liver donors and recipients from across Canada. This week you will hear another story from a great actions model about their journey with living organ donation.

In this episode, host Candice was joined by Paul. Paul’s partner was diagnosed with kidney failure and told him about the three possible paths he could go down. Paul acted without hesitation, thinking he would be a good candidate. After vigorous testing, Paul and his partner found out he was a wonderful match, and they had a successful transplant. 

The views and opinions expressed in this interview do not necessarily reflect the official policy or position of Toronto General Hospital or the University Health Network. 

To submit or share your story, please reach out to us at livingorgandonation@uhn.ca

To view the Great Actions Leave a Mark campaign, please visit www.greatactions.ca 

BONUS: Great Actions Leave a Mark - Ian13 Apr 202300:17:54

In September 2022, we launched Great Actions Leave a Mark, a national, multi-year public awareness campaign about living organ donation and transplantation. It has images and videos of living kidney and liver donors and recipients across Canada. 

In this episode, Host Candice is joined by Ian Goodall-George, who self proclaimed himself as the poster child for boring, but is anything but that. Ian is an anonymous, non directed kidney donor, meaning he stepped forward to donate a kidney to a stranger, just out of the goodness of his heart. 

The views and opinions expressed in this interview do not necessarily reflect the official policy or position of Toronto General Hospital or the University Health Network. 

To submit or share your story, please reach out to us at livingorgandonation@uhn.ca

To view the Great Actions Leave a Mark campaign, please visit www.greatactions.ca 

BONUS: Great Actions Leave a Mark - Ashley30 Mar 202300:22:08

In September 2022, we launched Great Actions Leave a Mark, a national, multi-year public awareness campaign about living organ donation and transplantation. It has images and videos of living kidney and liver donors and recipients across Canada. 

In this episode, Host Candice is joined by Ashley, a world traveller and horseback rider who donated a kidney to a stranger through the Kidney Paired Donation program. 

The views and opinions expressed in this interview do not necessarily reflect the official policy or position of Toronto General Hospital or the University Health Network. 

To submit or share your story, please reach out to us at livingorgandonation@uhn.ca

To view the Great Actions Leave a Mark campaign, please visit www.greatactions.ca 

To learn more about the Kidney Paired Donation program, please visit https://www.blood.ca/en/about-us/media/kidney-paired-donation/backgrounder-kidney-paired-donation-program#:~:text=The%20national%20Kidney%20Paired%20Donation%20(KPD)%20program%20is%20an%20interprovincial,become%20a%20living%20kidney%20donor. 

BONUS: Great Actions Leave a Mark - Craig16 Mar 202300:26:16

In September, 2022, we launched Great Actions Leave A Mark, a national, multi-year public awareness campaign about living organ donation and transplantation.  It has images and videos of living kidney and liver donors and recipients across Canada. In the coming weeks, you'll hear stories from great actions models about their journey with living organ donation.

In this episode, Host Candice interviewed Craig Settee, a family man and marathon runner who donated a kidney to his brother just over ten years ago.

The views and opinions expressed in this interview do not necessarily reflect the official policy or position of Toronto General Hospital or the University Health Network.

To submit your story, please reach out to us at livingorgandonation@uhn.ca

To view the Great Actions Leave a Mark campaign, visit www.greatactions.ca 

To learn more about organizations discussed in this podcast please visit:
Ajmera Transplant Centre: https://www.uhn.ca/Transplant 
CanSolve CKD: https://cansolveckd.ca/ 
BC Transplant: http://www.transplant.bc.ca/
Transplant Manitoba: https://www.transplantmanitoba.ca/ 
TAP: https://transplantambassadors.ca/ 
Living Donor Circle of Excellence: https://www.livingdonorcircle.com/partner/cst 
PRELOD: https://www.giftoflife.on.ca/resources/pdf/PRELOD_Online_Brochure_April_2022_FINAL.pdf 
Hope Air: https://hopeair.ca/ 

 

BONUS: Great Actions Leave a Mark - Jaime02 Mar 202300:21:28

Bonus Episode: Great Actions Leave a Mark - Jaime

In September, 2022, we launched Great Actions Leave A Mark, a national, multi-year public awareness campaign about living organ donation and transplantation.  It has images and videos of living kidney and liver donors and recipients across Canada.

In the coming weeks, you'll hear stories from Great Actions models about their journey with living organ donation.

In this episode, host Candice is joined by Jaime Watt, whose partner donated a kidney to him. 

The views and opinions expressed in this interview do not necessarily reflect the official policy or position of Toronto General Hospital or the University Health Network.

To submit your story, please reach out to us at livingorgandonation@uhn.ca

To view the Great Actions Leave a Mark campaign, visit www.greatactions.ca 

BONUS EPISODE: Remember This Living Donation - Len16 Feb 202300:07:57

Bonus Episode: Remember This Living Donation - Len

During Living Donation Week 2021, we partnered with the podcast, Remember This, with host Amanda Cupido to highlight first person living organ donation stories submitted through an online app. In this episode, Len shares his story as a double anonymous, non-directed living donor, which means he donated a portion of his liver to a stranger, then he donated a kidney to a stranger!

The views and opinions expressed in this interview do not necessarily reflect the official policy or position of Toronto General Hospital or the University Health Network.

To submit your story, please reach out to us at livingorgandonation@uhn.ca

For more information about Living Liver Donation visit https://www.uhn.ca/Transplant/Living_Donor_Program/Pages/living_liver_donor.aspx

BONUS EPISODE: Remember This Living Donation - Glenna02 Feb 202300:05:25

Bonus Episode: Remember This- Glenna

During Living Donation Week 2021, we partnered with the podcast, Remember This, with host Amanda Cupido to highlight first person living organ donation stories submitted through an online app. In this episode, Glenna shares her journey as a non-directed, living anonymous donor, meaning she donated 62% of her liver to a stranger! Enjoy!

The views and opinions expressed in this interview do not necessarily reflect the official policy or position of Toronto General Hospital or the University Health Network.

To submit your story, please reach out to us at livingorgandonation@uhn.ca

For more information about Living Liver Donation visit https://www.uhn.ca/Transplant/Living_Donor_Program/Pages/living_liver_donor.aspx

BONUS EPISODE: Remember This Living Donation - Katie19 Jan 202300:12:47

During Living Donation Week 2021, we partnered with the podcast, Remember This, hosted by Amanda Cupido to highlight first person living organ donation stories submitted through an online app. In this episode, Katie shares her journey as a living liver donor to her husband Simon and its impact on their family. Enjoy!

To submit your story, please reach out to us at livingorgandonation@uhn.ca

For more information about Living Liver Donation visit https://www.uhn.ca/Transplant/Living_Donor_Program/Pages/living_liver_donor.aspx

BONUS EPISODE: Remember This Living Donation - Palma05 Jan 202300:18:26

Bonus Episode: Remember This- Palma
During Living Donation Week 2021, we partnered with the podcast, Remember This, with host Amanda Cupido to highlight first person living organ donation stories submitted through an online app. In this episode, Palma shares her journey as a living liver donor to her cousin Jess. Enjoy!

The views and opinions expressed in this interview do not necessarily reflect the official policy or position of Toronto General Hospital or the University Health Network. 

To submit your story, please reach out to us at livingorgandonation@uhn.ca

For more information about Living Liver Donation visit https://www.uhn.ca/Transplant/Living_Donor_Program/Pages/living_liver_donor.aspx

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