Advertise on podcast: Kidney Transplant Conversations ~ Patient, Donor & Caregiver Edition

In this powerful and deeply human episode of Kidney Transplant Conversations, filmmaker Donald Griswold shares the extraordinary story behind his documentary film "Abundant," a cinematic exploration of one of the rarest and most profound acts of generosity: non-directed living kidney donation. Donald, a first-time filmmaker at age 59 after a career in medical marketing, was drawn into the kidney donation world through research that revealed both a profound need and an untold story. What he discovered was not just a medical process, but a community defined by courage, empathy, and transformation. Abundant brings these stories to life through an innovative fusion of live storytelling, professional dance, and visual art, creating an immersive emotional experience that goes far beyond traditional documentary filmmaking. The film features real donors who step onto the stage to share aspects of their personal journeys: why they chose to give part of themselves to a stranger, and how that decision reshaped their identity and sense of purpose. Their stories reveal the transition from a mindset of scarcity to one of abundance. Donald explains that Abundant was designed not just to inform, but to inspire and to open conversations, demystify donation, and empower patients and families to see new possibilities. With screenings across the country and a streaming release planned for March 2026, the film represents innovative advocacy rooted in storytelling, emotional connection, and human truth. Abundant is ultimately a testament to what becomes possible when ordinary people embrace extraordinary generosity, and how one story can change countless lives. Available for streaming March 26, 2026 at www.AbundantMovie.com, Abundant invites viewers to share the film and start the first step toward transplant and living donation.  Resources: Website: https://AbundantMovie.com  Streaming from: https://stuff.io (commencing March 26)    About Donald Griswold:  Donald Griswold - "Abundant" Writer, Director, and Producer, has lived in the Dallas, Texas area most of his life. ABUNDANT is his first documentary feature film, completing a life-long dream of being a filmmaker.  Donald graduated from the University of North Texas with a Bachelor of Arts in Radio, Television and Film, specializing in film writing. Donald has written and directed narrative, comedic and business scripts for video and audio. Donald’s experience includes writing, directing, and producing a wide range of video productions ranging from full-length DVD concepts to television commercials. He also has ghost written a memoir for a notable figure in the field of engineering. Storytelling has always had great meaning to Donald. “At the heart, I am a writer first.  And I’ve spent a lifetime learning the subtleties of telling a layered story.  In fiction, I love tools like implication and context to allow the audience to play a part in understanding a story for themselves.  But with filmmaking… Wow!  there are so many ways to evoke emotion and connection with the audience.  There are so many layers you can touch and create to effect that immersion and I enjoyed working in all of them!  These are all reasons why I had to base my first feature film in the actual world of storytelling.” Donald also writes works of fiction and non-fiction, and he published his first novel, Dying Light in 2017. In 2018, Donald opened Maitri River Productions, a non-fiction media production business to make media that inspires social change. ABUNDANT  is the first production of Maitri River Productions.  As a storyteller, Donald has appeared in Oral Fixation, the critically acclaimed Dallas-based storytelling show. In 2015, his story for the show Push the Envelope was voted by the public as Best in Show, and he performed the story in the annual Best of Season show. Donald has also produced Word of Mouth, a live storytelling series that hosted shows in Dallas and Atlanta. Donald is a long-time supporter of the arts in Dallas. He supports museums, local artists, and live performance, especially ShakespeareDallas.

As our understanding of APOL1-Mediated Kidney Disease (AMKD) grows, so does the need for greater awareness. National APOL1-Mediated Kidney Disease (AMKD) Awareness Day is observed annually on the last Tuesday of April.  In this episode of Kidney Transplant Conversations, we share an inspiring story of resilience, advocacy, and hope. Sharron Rouse opens up about her personal journey with kidney disease — a journey that began with a diagnosis of lupus nephritis, only to later discover she was actually battling FSGS (focal segmental glomerulosclerosis), a condition sometimes linked to the APOL1 gene variant that is found in around 35% of people of African ancestry.  In a heartfelt conversation with host Rolf Taylor, Sharron discusses the shock of her diagnosis, the challenges of navigating unclear answers, and the life-changing gift of a kidney transplant from her sister. As the founder of Kindness for Kidneys International, Sharron is now a tireless advocate, raising awareness about the genetic factors influencing kidney health. She emphasizes the importance of early diagnosis, the critical role of research into APOL1-related kidney disease, and the urgent need for greater awareness in communities of African descent. Tune in to hear how Sharron’s story offers hope to kidney warriors everywhere, highlights the life-saving potential of genetic testing, and makes a powerful case for early intervention. This episode is both inspiring and a call to action for greater education, early screening, and community empowerment. Kindness for Kidneys Website: https://www.kindnessforkidneys.org/ APOL1-Mediated Kidney Disease (AMKD) Awareness Day: https://www.kidneyfund.org/amkd-day-proclamation  Should I get tested for the APOL1 gene? https://www.kidney.org/kidney-topics/apol1-mediated-kidney-disease-amkd  (c) Project Advocacy 2025

In part 2 of our discussions with Liz, Grace & Shelley, we invite our guests to reflect on six specific questions about their experiences of giving and receiving, and the world of kidney donation.     1. One thing that has been most wonderful about this experience     2. One thing that has been most surprising    3. One thing that has been really difficult    4. One way that you have changed personally because of this experience    5. One thing you wish you could change (magic wand question)     6. One call to action for listeners. We delve into the remarkable stories of how Shelley, Liz, and Grace were connected through the life-saving act of kidney donation. Shelley, a special education teacher in Portland, Oregon, shares her journey of seamlessly becoming a donor, while Liz, a transplant recipient from Chicago, recounts her renewed zest for life and the accountability inspired by her "kidney sisters." Grace, a hospice nurse from the small island of Kauai, reflects on the joy and challenges of living far from her recipient and the emotional impact of reading a heartfelt letter of gratitude. Through candid conversations, these women discuss the surprising ease of the donation process, the profound relationships formed, and the ripple effects of their decisions. They also highlight the struggles of shifting societal perceptions of organ donation and emphasize the importance of becoming advocates for this life-changing cause. Tune in to hear about their transformative experiences and the shared mission of encouraging others to consider donation, making a lasting impact on the lives of many in need. (c) Project Advocacy 2024

S2 E5. Giving thanks for kindness, science and cooperation during Thanksgiving week. A kidney paired donation story. Liz, Grace & Shelley - Part 1    What if you saw a billboard asking for a volunteer to donate a kidney and “share your spare” to save someone’s life? What if it just made immediate sense to you, and you found yourself saying yes? Meanwhile, Liz was in urgent need of a kidney transplant. She had been unwell as a child and her kidneys had failed, just as the first kidney transplants were being pioneered. Now, 40 years later, Liz needed a new transplant. Her cousin, Grace, had volunteered to donate, and was figuring out how to make this happen from her remote location 5,000 miles away – on the Pacific Island of Kauai. Grace wasn’t a good match for Liz, but a great match for someone else. And Shelley was a near-perfect match for Liz. Somehow, they needed to plan an exchange and give Liz her best possible future health.  Today’s episode is a reunion for three people whose lives intersected in a beautiful and remarkable way. Grace, Liz, and Shelley share their stories and perspectives, and pull back the curtain on the incredible benefits of living kidney paired donation (KPD) and the important role of vouchers. Shelley, a special education teacher from Portland, takes us through her decision-making process to become a kidney donor after seeing a billboard advertisement, including the role played by the National Kidney Registry in her journey. Liz, a four-time transplant recipient and a patient healthcare entrepreneur from Chicago, discusses her life-changing moments associated with her transplants, starting from the age of 11. Grace, a hospice nurse from the Hawaiian Islands, reveals the emotional moments leading up to her decision to donate a kidney and the challenges faced due to her geographic location. The episode further explores the scientific advancements in kidney transplants, the impact of living donations, and the importance of organizations like the National Kidney Registry in facilitating these life-saving processes. The National Kidney Registry is one of the world’s leading kidney exchange organizations. Please visit  https://www.kidneyregistry.com/  for more information.  And tune in to Part 2 next time, where the trio reflect on their experiences, and comment on what could be improved in the world of kidney transplants, and why more people should step forward to donate. © Project Advocacy 2024

Welcome to the latest episode of Kidney Transplant Conversations, where we continue our exploration of the Transplant Games of America in San Diego. This inspiring event, bringing together organ donors, recipients, and their families, marks a joyful reunion after the challenges posed by the pandemic. The San Diego games also celebrates it's uniquely diverse local population, including contributions from indigenous and latino artists.  Join us as we dive into the heart of the games, starting with the Fun 5K run along San Diego's picturesque waterfront. We meet participants who share their personal transplant stories and the significance of this gathering. Their journeys reflect themes of hope, gratitude, and the powerful impact of organ donation.  We also explore the vibrant activities inside the convention center, meeting organizations like Life Force and the Chris Klug Foundation, which provide invaluable support and information. Unique performances and cultural events further enrich the experience, celebrating life and community. For those inspired to join this incredible community, discover how you can get involved with the Transplant Games and learn more about living kidney donation. Listen in to feel the positivity and unity that define this remarkable event. For educational purposes only. Not intended as medical advice.  (c) Project Advocacy 2022 - 2024 Chris Klug Foundation    https://www.chrisklugfoundation.org/  Living Donation info:    https://www.kidneyregistry.com/  Transplant Games of America  https://www.transplantgamesofamerica.org/copy-of-teams

With members of Team North Carolina as our guide, we delve into the vibrant world of the Transplant Games of America. Discover the rich history of these games, which began in 1978 in England and have since evolved into a significant event for transplant recipients and donor families in the U.S. Hosted by the Transplant Games of America, this bi-annual event brings together thousands of participants, fostering a sense of community and showcasing the spirit of life after transplant. Join us as we explore the experiences of attendees at the San Diego games, where diversity and inclusion are celebrated, and where families find a place to honor their loved ones who have given the gift of life. From the competitive spirit of sports events like basketball and pickleball to the heartwarming connections made through pin trading, there's something for everyone at the Transplant Games. Hear personal stories from Team North Carolina members, including their journey of camaraderie, competition, and advocacy. Learn how these games provide a platform for education, awareness, and the sharing of personal journeys, inspiring others to become organ donors and support this life-changing cause. Tune in to experience the magic of the Transplant Games and the uplifting reminder of the power of community and the resilience of the human spirit. (c) Project Advocacy 2022 - 2024  Find your local team attending the Transplant Games of America  https://www.transplantgamesofamerica.org/copy-of-teams

In this compelling episode of Kidney Transplant Conversations, Valen Keefer joins us to share her extraordinary journey through the world of organ transplantation. From a young age, Valen faced the challenges of living with a chronic illness, navigating the complexities of kidney and liver transplants. Her story is one of resilience, advocacy, and empowerment. Valen discusses her impactful docuseries, "Letters of Hope," which chronicles her experiences and serves as a resource for both patients and caregivers. She highlights the importance of finding one's voice in the healthcare journey and the vital role caregivers play in the process. As a passionate advocate, Valen talks about her mission to educate and inspire others, emphasizing the significance of organ donation and the need for accurate portrayals in media. Her upcoming recognition at the Donate Life Hollywood Inspire Awards underscores her commitment to raising awareness and fostering understanding. Tune in to learn more about Valen's remarkable story, the power of community, and how individuals can live a full life post-transplant. Discover how her experiences are helping to shape a brighter future for those in the transplant community. (c) Project Advocacy 2022-2024 Link: Letter of Hope Docuseries https://valenkeefer.com/letters-of-hope-docuseries  Link: Valen Keefer Website https://valenkeefer.com/

In this heartwarming episode of "Kidney Transplant Conversations," host Rolf Taylor sits down with Shana Pereira, a remarkable woman who received both a kidney and heart transplant on Christmas Day. Shana shares her extraordinary journey, beginning with the discovery of her kidney failure on a previous Christmas Eve, and the numerous challenges she faced along the way to receiving her transplants. Despite the odds stacked against her, Shana's story is one of resilience, hope, and the power of a strong support network. With the help of her devoted friends and compassionate doctors, she navigated through the complexities of finding donors and battling additional health issues, including heart failure and a potential cancer diagnosis. Shana's faith and determination, combined with the love and prayers of those around her, culminated in a true Christmas miracle. Her inspiring tale is a testament to the strength of the human spirit and the belief in something greater than oneself. Join us as we explore the twists and turns of Shana's incredible journey, offering hope and encouragement to anyone facing their own life challenges. (c) Project Advocacy 2022 - 2024

Mike was just seven years old when he lost his father to kidney disease, and many years later he learned that he was at an advanced stage of the inherited condition called polycystic kidney disease (PKD), and his kidneys were slowly failing. 2019 was a very challenging year and Mike experienced multiple medical issues. He knew he needed a transplant, and that the waitlist was long and with no guarantees.  Mike started researching how to go about receiving a kidney from a living donor, and he came across resources from “The Big Ask, The Big Give,” a program of The National Kidney Foundation. Asking for a kidney can be awkward, and using social media is a whole different world for someone who never used Facebook, so Mike needed a champion. In this episode he shares how before he asked for a kidney, he had to ask for help, and navigate the pandemic at the same time.  Meanwhile, Mike’s niece Andrea had never thought very much about donating an organ until she heard Uncle Mike’s story. In the second part of this episode, Andrea shares with us how she came to the realization that she could do something significant to help. She also discusses how gifting a kidney has opened up a new and unexpected richness in her life, including her involvement with Kidney Donor Athletes, and a recent trip to Mount Kilimanjaro.  FULL TRANSCRIPT ⬇ With host and series producer Rolf Taylor.  Resources mentioned during this episode:  The Big Ask, The Big Give, NKF   www.kidney.org/transplantation/livingdonors  Kidney Donor Athletes    www.kidneydonorathlete.org/  Kidney Transplant Conversations is underwritten by Veloxis Pharmaceuticals, Inc. All views and opinions expressed in the podcast reflect those of the participants and do not necessarily represent the views and opinions of Veloxis Pharmaceuticals, Inc. Excerpts “I’m not very media savvy, let’s put it that way. I don’t do any social things on the internet because I’m an old guy. They said find someone to be your champion. My daughter-in-law volunteered for this project.” – Mike “What happened to me was a miracle because if you look at kidney transplants for people my age, it’s really low, when I got my transplant, I was 69.”  – Mike “The next words she said were “I’m approved as a donor for Uncle Mike. It just came out of the blue! We had no idea that she went through all these tests. She didn’t want anyone to know in case she could not help.”  – Mike “It has been one of the best things that I have done in my life. I’m just so grateful for the doctors and for science and for all the support that I was able to find. I was so blessed to be able to give this gift.”  – Andrea  © Project Advocacy, 2022 - 2023

In the previous episode we heard Darryl’s story, how he needed a kidney transplant because of kidney cancer. This week we meet Jim, who responded to “The Big Ask,” and donated a kidney to his close friend Darryl. Jim shares with us his side of the story, explaining why doing this for his “brother” was so important to him, and he describes his overall experience of making “The Big Give.” And Dr. Adam Bregman joins us to talk about his experience with kidney transplant patients using resources from programs such as “The Big Ask, The Big Give” to help find their own living donor. He also explains how a kidney from a living donor tends to last longer. We also explore the subject of health disparities in kidney disease and discuss some of the root causes. FULL TRANSCRIPT ⬇ With host and series producer Rolf Taylor. Resources mentioned during this episode: The Big Ask, The Big Give, National Kidney Foundation                www.kidney.org/transplantation/livingdonors Kidney Transplant Conversations is underwritten by Veloxis Pharmaceuticals, Inc. All views and opinions expressed in the podcast reflect those of the participants and do not necessarily represent the views and opinions of Veloxis Pharmaceuticals, Inc. © Project Advocacy, 2022-2023

In our last episode, the first of several episodes celebrating National Donate Life Month, we sat down with Jennifer Martin from the National Kidney Foundation and learned about “The Big Ask, The Big Give”, a program dedicated to helping people with chronic kidney disease find their living kidney donor. In this episode we meet military veteran Darryl Shaw, a kidney cancer survivor who also served multiple tours of duty. Darryl’s family members helped champion a successful campaign to raise funds for a kidney transplant, funding that helped his eventual living donor complete the initial compatibility tests. Darryl now volunteers as a mentor with programs such as “The Big Ask, The Big Give” from NKF, sharing his experiences and giving encouragement. He can offer perspectives from the point of view of ESKD patient who received a kidney from a friend and colleague, as well as being someone who opted for home dialysis and overcame many medical challenges. Darryl is now studying for his master’s degree in Pastoral Counseling, and he plans to continue in service to the kidney patient community. With host and series producer Rolf Taylor. FULL TRANSCRIPT ⬇️  Resources mentioned during the podcast: Every April is National Donate Life month  www.donatelife.net/ndlm/ The Big Ask, The Big Give, NKF  www.kidney.org/transplantation/livingdonors The National Foundation for Transplants  www.transplants.org Mighty Cause  www.mightycause.org We thank the participants and advisors who help make Kidney Transplant Conversations possible. Kidney Transplant Conversations is underwritten by Veloxis Pharmaceuticals, Inc. All views and opinions expressed in the podcast reflect those of the participants and do not necessarily represent the views and opinions of Veloxis Pharmaceuticals, Inc. © Project Advocacy, 2022

Every year, April is National Donate Life Month. This is an annual time for increasing awareness of the importance of registering as an organ donor or saving a life by being a living donor. And for kidney transplants, living donation offers the best possible outcomes for recipients.   But asking someone to give a kidney can be daunting, and the process can be a challenge. For the next episodes of Kidney Transplant Conversations, we will be hearing from support organizations such as the National Kidney Foundation (NKF), the National Living Donor Assistance Center (NLDAC), and TransplantFirst Academy (TFA) about programs supporting living donation. We’ll also talk with healthcare providers about their professional perspectives, and hear from living donor recipients about their experiences. This week, Jennifer Martin from the National Kidney Foundation tells us all about their program “The Big Ask, The Big Give”, a comprehensive resource which includes webinars and workshops, and makes mentors available by phone. the National Kidney Foundation website link is www.kidney.org/transplantation/livingdonors and you can also call them on 1.855.653.2273. With series producer and host Rolf Taylor.  Other resources mentioned in this episode include: National Donate Life Month www.donatelife.net/ndlm/; The Johns Hopkins Living Donor Champion Program https://www.hopkinsmedicine.org/transplant/patient_information/live-donor-program.html; National Living Donor Assistance Center www.livingdonorassistance.org/.  Kidney Transplant Conversations is underwritten by Veloxis Pharmaceuticals, Inc. All views and opinions expressed in the podcast reflect those of the participants and do not necessarily represent the views and opinions of Veloxis Pharmaceuticals, Inc. © Project Advocacy, 2022    LINK TO TRANSCRIPT (PDF) ⬇️

Our first guest on this episode is counseling psychologist Dr. Camilla Nonterah, who discusses the importance of understanding and supporting transplant patients from both biological and psychosocial perspectives. She also reflects on the impact COVID is having on the mental health of transplant patients. During this episode we also hear from Barbara, John and Ed from the Florida Organ Transplant Association, who share with us their observations and concerns about the challenges of living alongside COVID as a transplant recipient. Dr. Nonterah is Assistant Professor of Health Psychology at the University of Richmond in Virginia. A counseling psychologist by training, Dr. Nonterah is an expert in the psychosocial aspects of chronic illness by examining health disparities and health equity, health behaviors, treatment seeking, and mental health associated with end-stage organ disease and solid organ transplantation. She is also a proponent of positive psychology.  The Florida Organ Transplant Association's mission is to support the transplant community through forums to provide information and financial support for patients, caregivers and organ donor families, educate the community at large on the importance of organ donation, and fund transplant research. With podcast producer and host Rolf Taylor. About Dr. Camilla Nonterah: https://psychology.richmond.edu/faculty/cnontera/ About Florida Organ Transplant Organization: https://www.floridaorgantransplant.org/ We thank the participants and advisors, and our underwriters, who helped create this podcast.  Kidney Transplant Conversations is underwritten by Veloxis Pharmaceuticals, Inc. All views and opinions expressed in the podcast reflect those of the participants and do not necessarily represent the views and opinions of Veloxis Pharmaceuticals, Inc. © Project Advocacy, 2022  LINK TO TRANSCRIPT (PDF) ⬇️

20 years ago, a young Benji Lafitte had his promising basketball career cut short by kidney failure, and he would go on to depend on dialysis for the next two decades. After almost giving up on the transplant process, an old basketball rival persuaded Benji to engage again with a transplant center. Benji joins us on this episode of Kidney Transplant Conversations to share his long journey to transplant with us, and he also remembers with gratitude his friend and mentor Chris Osbourne, the individual who had helped him try for a transplant again. Chris was another kidney transplant recipient, but he hesitated to get vaccinated, and his life was recently lost to the COVID-19 pandemic. We discuss some of the misinformation that can contribute to vaccination decisions, and Benji highlights the importance of never giving up on yourself and your health. With series producer and host Rolf Taylor.  This episode of Kidney Transplant Conversations is dedicated to the memory of Chris Osbourne. Kidney Transplant Conversations is underwritten by Veloxis Pharmaceuticals, Inc. All views and opinions expressed in the podcast reflect those of the participants and do not necessarily represent the views and opinions of Veloxis Pharmaceuticals, Inc. © Project Advocacy, 2022  LINK TO TRANSCRIPT (PDF)  ⬇️

We talk with kidney transplant surgeon Dr. Robert Montgomery about his own experience of receiving a heart transplant three years ago. This led him to a new understanding of the challenging “new normal” for patients after a transplant, which involves multiple medications and many new responsibilities. We also discuss the evolving impacts of the ongoing COVID-19 pandemic on an estimated 10 million people with compromised immune systems. Dr. Montgomery talks about his health equity leadership role at NYC Langone, where intentional policies are helping to foster diverse hiring and retention of health workers from underrepresented groups. He also shares some of the ways that the institute is improving health outcomes in transplantation, through research into disparities and understanding of their root causes, particularly social determinants. With podcast host Rolf Taylor. About Dr. Montgomery: https://nyulangone.org/news/life-death-life-death-life-dr-robert-montgomery  We thank the participants and advisors, and our underwriters, who helped create this podcast.  Kidney Transplant Conversations is underwritten by Veloxis Pharmaceuticals, Inc. All views and opinions expressed in the podcast reflect those of the participants and do not necessarily represent the views and opinions of Veloxis Pharmaceuticals, Inc. © Project Advocacy, 2022  DOWNLOAD TRANSCRIPT (PDF) ⬇️