Kidney Transplant Conversations features diverse voices and experiences of donating, receiving, and caring for this gift of life. Each new episode features interviews with patients, caregivers, advocates, donors, healthcare providers, and community leaders We invite you to subscribe and let Kidney Transplant Conversations keep you connected, informed and inspired with a constant flow of new thoughts and ideas. Send suggestions for guests and topics to: rolf.taylor@projectadvocacy.com
Episodes
Wednesday Feb 09, 2022
Wednesday Feb 09, 2022
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
Tuesday Jan 25, 2022
Tuesday Jan 25, 2022
We are joined by history maker Dr. Velma Scantlebury, who became the first Black female transplant surgeon in the US in 1989. In a wide-ranging discussion we ask whether all the current talk about health equity is resulting in real action, and we explore several current examples of intentional change. Firstly, the “Boldly Against Racism” Campaign at the American Society of Transplant Surgeons (ASTS); secondly, the updated Hippocratic Oath at Columbia University Vagelos College of Physicians and Surgeons, clearly centering health equity, diversity, and inclusion; and thirdly the recent recommendations affecting the way that kidney function calculations (eGFR) are made. Dr. Scantlebury also shares her concerns that patients with fewer resources are being disadvantaged by the burden of appointments required in preparing for a transplant and this may extend how long patients are kept on dialysis, acting as a potential barrier to transplantation.
Velma P. Scantlebury, M.D, FACS, recently retired from Christiana Care’s Kidney Transplant Program where she served as the Associate Director, and Director of Outpatient Clinics. She currently holds the position of Professor of Surgery at Texas Christian University (TCU) and University of North Texas Health Science Center (UNTHSC) and Medical School, in Forth Worth Texas. Dr. Scantlebury also serves as a medical advisor to various organizations and healthcare professionals. She has been named to both the “Best Doctors in America” and “Top Doctors in America” lists multiple times.
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
Resources and links
About Dr. Velma Scantlebury: https://vpscantleburymd.com/
ASTS Boldly Against Racism Campaign: https://asts.org/about-asts/boldly-against-racism-campaign#.YZKxAL3MLa4
Columbia University Vagelos College of Physicians and Surgeons Hippocratic Oath: https://www.youtube.com/watch?v=AujwxJNZtp8
Time to Eliminate Health Care Disparities in the Estimation of Kidney Function: https://www.nejm.org/doi/full/10.1056/NEJMe2114918
Monday Jan 03, 2022
Monday Jan 03, 2022
Not everyone lives close to a hospital. In this podcast we discuss two potential challenges in managing chronic kidney disease and kidney transplants: the first is care when you live a long distance from specialist care, and the second is potential financial barriers. Our guest in this episode, Dr. Silas Prescod Norman, tells us about some very real ways that his hospital center has worked proactively to address both barriers, and with tangible results.
Silas Prescod Norman, M.D., M.P.H is a nephrologist at the University of Michigan, working in the transplant program since 2002, and he currently serves as the co-Medical Director for kidney and pancreas transplant and Medical Director of the Transplant Multidisciplinary Ambulatory Clinics, which see more than 18,000 patient visits annually. Dr. Norman has made numerous contributions to the transplant program including the development of outreach satellite clinics to allow patients greater access to transplant opportunities, the focus of today’s episode.
Dr. Norman also serves with and volunteers for a number of organizations related to kidney transplantation, including the National Kidney Foundation of Michigan, The American Kidney Fund, and MOTTEP, the Minority Organ Tissue Transplant Education Program and more recently became an advisor to this podcast, representing the American Society of Transplantation.
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, 2021
Tuesday Oct 19, 2021
Tuesday Oct 19, 2021
In this episode we meet Dr. Joyce Trompeta, A Nurse Practitioner (NP) specializing in transplantation, and an Associate Professor in the school of medicine, at the University of California, San Francisco where she conducts outcome research in the department of surgery.
Dr. Trompeta discusses several areas of interest, including her concerns about disparities impacting Asian American, Pacific Islander and Latino populations; her work in Hawaii; how younger Latinos with kidney disease are facing unique challenges relating to immigration; and her travels to Japan, where stigma and cultural beliefs have limited organ transplantation, but where the younger generations are now leading change with a little help from Kumamon, Japan’s most popular bear.
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, 2021
Wednesday Sep 08, 2021
Wednesday Sep 08, 2021
How the UNC Chapel Hill Latino Transplant Clinic is increasing access through culturally competent care. UNC Chapel Hill Latino Transplant Clinic, Part 2
Featuring Transplant Social Worker Daniela Matz and clinic founder Dr. Pablo Serrano.
In our last episode we met José and Xiomara Flores and heard about their five-year journey from kidney disease diagnosis to their live donor transplant, which took place at the University of North Carolina Transplant Latino Transplant Clinic. The clinic is the culmination of a very intentional vision, a strategic decision to integrate a Latino-focused Transplant Clinic within the Abdominal Transplant Division at UNC Chapel Hill. Since being established in 2018, they have gone on to demonstrate how workforce diversity and cultural competency go hand in hand in the delivery of quality care.
In today’s episode, transplant social worker Daniela Matz and clinic founder Dr. Pablo Serrano look back on Jose and Xiomara’s story, share with us insights into how the clinic works, and how they have been able to reduce renal transplant disparities.
All views and opinions expressed in this podcast reflect those of the participants.
We thank the participants and advisors who helped create this podcast, and our underwriter, Veloxis Pharmaceuticals.
© Project Advocacy, 2021
Resources relevant to Episodes 2 & 3 of Kidney Transplant Conversations:
Welcome to Infórmate
El objetivo de ésta página bilingüe es educar a los hispanos / latinos acerca de la donación de riñón en vida.
The goal of this bilingual page is to educate Hispanics / Latinos about living kidney donation.
National Kidney Foundation:
La información más importante sobre la enfermedad renal.
Provides lots of great information about kidney disease from prevention to transplant, including living donation.
https://www.kidney.org/espanol
American Kidney Fund
Nuestra misión es ayudar a las personas a combatir la enfermedad de los riñones y vivir una vida más sana.
Information plus financial assistance opportunities.
https://www.kidneyfund.org/en-espanol/
National Foundation for Transplants
Cómo eliminar las barreras financieras para los donantes vivos.
Removing financial barriers to transplantation.
https://transplants.org/resources/
Children’s Organ Transplant Association:
Recaudación de fondos y apoyo para niños y adultos jóvenes con poliquistosis renal.
Fundraising and support for children and young adults with polycystic kidney disease.
Monday Aug 23, 2021
Monday Aug 23, 2021
In this episode we’ll hear from José a patient, and Xiomara, his wife and donor, as they describe the challenges they experienced in their quest for a kidney transplant, and the joy they have felt since then. We’ll also hear from transplant social worker Daniela Matz, who assisted them.
The Census Bureau estimates that there are over 60 million Hispanics and Latinos living in the United States, and the Latinx population is the fastest growing minority. As many as 40 million are speaking Spanish as their first language. Although Hispanics and Latinos are more likely to experience kidney failure compared to other Americans, they are less likely to access kidney transplant as a solution, the resulting disparity means more years on dialysis, reduced quality of life, reduced life expectancy, and increased healthcare expenses.
Part of the problem is the waitlist for a transplant, there simply aren’t enough organs to go around. If a living donor can be found, then that is a gamechanger. But here we find another disparity – because the process of live donor kidney transplantation can often elude our minority populations.
To address some of these issues, in 2018 Dr. Pablo Serrano established the Latino Transplant Clinic at the University of North Carolina (UNC) Division of Abdominal Transplantation, in Chapel Hill, NC, with the aim of providing culturally competent and culturally sensitive care.
August is National Minority Donor Awareness Month (NMDAM).
Founded in 1996 by the National Minority Organ Tissue Transplant Education Program (MOTTEP) to bring heightened awareness to donation and transplantation in multicultural communities. For more information and shareable resources please visit:
https://www.donatelife.net/nmdam/
All views and opinions expressed in this podcast reflect those of the participants.
We thank the participants and advisors who helped create this podcast, and our underwriter, Veloxis Pharmaceuticals.
© Project Advocacy, 2021
Resources relevant to Episodes 2 of Kidney Transplant Conversations
Welcome to Infórmate
El objetivo de ésta página bilingüe es educar a los hispanos / latinos acerca de la donación de riñón en vida.
The goal of this bilingual page is to educate Hispanics / Latinos about living kidney donation.
http://informate.org/
National Kidney Foundation:
La información más importante sobre la enfermedad renal.
Provides lots of great information about kidney disease from prevention to transplant, including living donation.
https://www.kidney.org/espanol
American Kidney Fund
Nuestra misión es ayudar a las personas a combatir la enfermedad de los riñones y vivir una vida más sana.
Information plus financial assistance opportunities.
https://www.kidneyfund.org/en-espanol/
National Foundation for Transplants
Cómo eliminar las barreras financieras para los donantes vivos.
Removing financial barriers to transplantation.
https://transplants.org/resources/
Children’s Organ Transplant Association:
Recaudación de fondos y apoyo para niños y adultos jóvenes con poliquistosis renal.
Fundraising and support for children and young adults with polycystic kidney disease.
www.cota.org
Thursday Jun 10, 2021
Thursday Jun 10, 2021
Episode 1: Impact of Pandemic, & Meeting People Where They Are
Welcome to Kidney Transplant Conversations. The COVID-19 pandemic has everyone asking a lot of questions, especially transplant recipients, and those waiting for a transplant. In this episode we discuss the impact of the pandemic, talk about masks and vaccines, and how the pandemic is impacting people with immunosuppression. To explore these subjects, we welcome two guests to the podcast. Firstly, living donor recipient Risa Simon, who will share insights from the transplant patient’s point of view, and then Daryle Blackstock, PA-C, who will talk about the importance of meeting people where they are.
All views and opinions expressed in this podcast reflect those of the participants.
We thank the participants and advisors who helped create this podcast, and our underwriter, Veloxis Pharmaceuticals.
© Project Advocacy, 2021
Links to resources mentioned in this episode:
Kinsey's Kidney Adventure by Nadine Morsi
Medical Apartheid by Harriet Washington