Podcasts about National Kidney Foundation

What does feeling truly seen and supported mean in your health care? For many LGBTQIA+ people with kidney disease, the answer isn't simple. Jess Walters is a mixed-media artist, Board Certified Patient Advocate, and independent scholar living with a kidney transplant. Marissa is the Patient Programs Director at the National Kidney Foundation (NKF) and a social worker working to make kidney care more inclusive. Together, they share what supportive care and community look like and why they matter. In today's episode we heard from: Jess Walters (they/them) is a mixed-media artist, Board Certified Patient Advocate (BCPA), and independent scholar from Charlottesville, Virginia. They are a multiply-neurodivergent, queer, nonbinary person with Alport syndrome, a rare genetic disorder which caused late-onset deafness and kidney failure at age 29. In 2018, after undergoing two months of peritoneal dialysis, Walters received a kidney transplant from a living donor at the University of Virginia, where they currently serve as an inaugural FusionLab Arts Research Fellow at the Center for Health Humanities and Ethics in the School of Medicine. Their research focuses on the intersections of art and health, navigating accommodations in cultural arts spaces to promote individual and community wellbeing by including disabled, neurodivergent, and chronically ill participation and perspectives. They regularly participate in Kidney Patient Summits with the National Kidney Foundation and have served as a member of their Diversity & Health Equity Advisory Committee for 4 years. Marissa Argentina, LMSW is a licensed social worker who has been in the field of nephrology since 2010. She has worked for the National Kidney Foundation since 2015 and has been working on the NKF Peers program 2017. She is currently the Patient Programs Director at the National Kidney Foundation. She had previously worked as a dialysis center social worker in the Bronx, NY.   Additional Resources: The Impact of Unequal Care for LGBTQ+ Kidney Patients NKF Online Community: LGBTQIA NKF Peers Jess Walters Art Rivanna Area Queer Center New City Arts Initiative   Do you have comments, questions, or suggestions? Email us at NKFpodcast@kidney.org. Also, make sure to rate and review us wherever you listen to podcasts.  

Kent Bressler speaks with Rachel Claudine and Dr. Sandy Gilbert from the National Kidney Foundation. They explore the groundbreaking KidneyCARE Study, a pioneering patient-centered research initiative designed to gather vital data directly from individuals living with various stages of kidney disease. Rachel shares her personal journey with Lupus Nephritis, emphasizing the significance of patient stories in advancing kidney health research. Dr. Gilbert highlights the study's aim to capture real-world patient experiences, offering insights into disease progression and treatment efficacy. Discover how this innovative registry is set to transform kidney care and empower patients, while also discovering how you can contribute to this vital research. For more information on the KidneyCARE Study and to participate, visit kidneycarestudy.org. About Our Guests: Sandy Gilbert, PhD is the Senior Director of Patient Outcomes Research at the National Kidney Foundation (NKF), where she manages the KidneyCARE (Community Access to Research Equity)™ Study. Since joining NKF in 2024, she has focused on developing and overseeing this pioneering national kidney disease patient registry – the first to integrate patient-reported data with clinical data from electronic health records (EHRs). Rachel Claudin, BS, CCLS is the Patient-Centered Research Director at the National Kidney Foundation (NKF). Her main work for the past three years has been focused on the advancement of the KidneyCARE Study. As a person living with Lupus Nephritis, she is excited for the patient- entered data collected by the Study to increase and improve kidney care research. Previous to the NKF, Rachel worked in hospital and hospice settings advocating for patients utilizing the shared decision-making model of healthcare. For more information on Kidney Solutions and to join our supportive community, visit kidneysolutions.org Host: Kent Bressler Producer: Jason Nunez Remember to keep breathing, and don't miss the next amazing episodes of Kent's Kidney Stories!

In this episode, Melanie shares some reflections of her time at the National Kidney Foundation's sping meeting for healthcare professionals. She gives a summary of the educational sessions she gave, moderated and some other highlights from this high profile national kidney health meeting for professionals.    Submit a question for Melanie to answer on the podcast! Connect with The Kidney Dietitian! Work with Us! |  Instagram | Facebook | Pinterest | Facebook Group | Newsletter www.thekidneydietitian.org All information in this podcast is meant for educational purposes only and should not be used in place of advice from a medical professional.  

Jennifer Cramer-Miller is a writer, speaker, and joy seeker. She's the Minnesota Board Chair for the National Kidney Foundation, and a Donate Life Ambassador for LifeSource. She's also the author of the award-winning memoir, Incurable Optimist: Living with Illness and Chronic Hope, which is available now. On today's show, Annmarie and Jennifer discuss kidney failure, unconditional love, and how the stories of our lives seldom unfold quite how we plan. Episode Sponsors Excelsior Bay Books – A locally owned & independent bookstore. Our atmosphere is casual and inviting with a comfy seating area in the center of the store. We have an interesting mix of titles and can special order anything not on the shelves. Our children's section is outstanding! All books and toys are hand-picked for quality and fun. We also offer a great selection of reading accessories (lights, bookmarks, book plates), puppets, puzzles, notecards, and educational gifts and toys. And we are dog-friendly. Come in and browse, or shop online at excelsiorbaybooks.net. Big Hill Books – The happiest bookstore in Minneapolis. Big Hill Books welcomes you to Bryn Mawr, one of the most charming and eclectic neighborhoods in the Twin Cities. As a general interest bookstore, we offer an engaging, inclusive inventory of titles and a bright, airy space for customers to sit, read and relax. Our feline friends, Goose and Addie, are also available for some complimentary lap time. Visit Big Hill Books and help us build a community in which "we all do better when we all do better." Find us online at bighillbooks.com. Authors and Titles Mentioned in This Episode: Incurable Optimist: Living with Illness and Chronic Hope, by Jennifer Cramer-Miller Kelly Corrigan recently featured Jennifer Cramer-Miller's story on Thanks for Being Here. Here's a trailer for Steel Magnolias, a film which you should not watch if you do not want to cry. Here's the opening credits for ThirtySomething which ought to be streaming somewhere – I'd love to see if it still holds up. Bruce Springsteen singing Thunder Road in Barcelona – fantastic! Follow Jennifer Cramer-Miller: Instagram: @jennifercramermiller Facebook: @JenniferCramerMiller Twitter: @JenniferCramerMiller LinkedIn: @jenniferCramerMiller Learn more at jennifercramermiller.com and join her monthly-ish newsletter here. Buy Jennifer's book here. Jennifer Cramer-Miller's Awards and Recognition: International Impact Book Award, Family + Medical Book Excellence Award Winner, Family  BookFest Award Winner, Transformational Memoir + Relationships & Family 2024 IPPY E-Book Award: Gold Winner 2024 Next Generation Book  Finalist, Memoir + Cover Design National Indie Excellence Book Award - Inspiration + Medical + Non-Fiction Living Now Award Bronze Medal: Health and Wellness Readers' Favorite Award: Gold Medal - Non Fiction Publishers Weekly, starred review "...a knockout memoir..." *Also, here's a link to donatelife.net if you want to learn more about organ donation and kidney.org if you'd like more about kidney health. Photo Credit: Belu Photography **Writing Workshops and Wish Fulfillment:  If you liked this conversation and are interested in writing abroad, consider joining Annmarie and co-leader Athena Dixon for a writing retreat in Italy in September, 2025. You can travel to a beautiful place, meet other wise women, and write your own stories. We'd love to help you make your wishes come true.  As of this moment, we only have 2 spots left. This will sell out. Act now and join us! Or for women interested in an online Saturday morning writing circle, message Annmarie to learn more. Learn more about your ad choices. Visit megaphone.fm/adchoices

Jennifer Cramer Miller from the National Kidney Foundation tells us about an exciting advancement in lab-grown organs.

There's a common misconception that people on home dialysis can't have pets. But that's just a myth. Professor Cameron Wolfe, a transplant infectious disease specialist at Duke University, along with Keith Plummer, a transplant recipient with home hemodialysis experience, and Brittany Dickerson, an in center hemodialysis patient with experience in peritoneal dialysis are here to share how you can safely manage treatments while living with pets. Professor Cameron Wolfe is a Transplant Infectious Disease specialist at Duke University.  He was a previous Chair of the Disease Transmission Advisory Committee (DTAC), working with the federal transplant administration to ensure safe and successful transplantation in the US.  Cameron is the current secretary of the Infectious Disease section of The Transplantation Society, an international society representing transplant professionals and patients globally.  His research focusses on safe transplantation for patients and donors living with HIV and hepatitis, and managing respiratory viruses and emerging pathogens. Keith Plummer was diagnosed with kidney cancer in 2010, coming out of surgery with one kidney functioning at 20 percent. Thanks to a great Nephrologist and a lot of hard work, he was able to hold off dialysis for close to a decade. Keith was on home hemodialysis for 4 years before receiving a transplant 1.5 years ago. Keith first got involved with advocacy about 6 years ago as he lobbied for the TRSA, making many visits to the state capitol to fight for industry and employees. Over his time on dialysis, Keith have moved from part time to being fully retired which has given more time to advocate. He is an advocate for the DPC and has participated in the last four fly-ins in Washington DC. He has been advocating with the NKF for the past 2 years and look forward to helping kidney patients in New York and across America. Brittany Dickerson is a dedicated mother, motivational speaker, and compassionate life coach living with Polycystic Kidney Disease (PKD). She uses her kidney failure battle to educate and help others regarding kidney disease and transplantation. Through partnership with the National Kidney Foundation, Brittany has had the opportunity to mentor others and to be a guest for the National Kidney Foundation Podcast channel. Her dedication to kidney awareness has led her to pursue becoming a National Kidney Foundation Advocate. Brittany uses her voice to spread a powerful message of perseverance and hope. Brittany's goal is to continue making an impact on individuals facing adversity, offering guidance, support, and being a shining example of strength in the face of hardship.   Additional Resources: Safe Living After Transplant Find Support with NKF Peers   Do you have comments, questions, or suggestions? Email us at NKFpodcast@kidney.org. Also, make sure to rate and review us wherever you listen to podcasts.

Community DC Host Dennis Glasgow visits with the Executive Director for the National Kidney Foundation Michele Anthony to talk about the latest happenings and an upcoming Gala, plus Stacy Warr joins us to talk about her own personal journy and relationship with the NKF of Washington DC. 

Hello cold cold Wichita!   Grab a warm bowl of soup and pull up a chair to the Wichita Dinner Table!   We are excited to have a special guest just in time for Valentine's Day. We welcome Chef Josh Rathbun with Lottē to discuss the restaurant along with Rathbun's work with the National Kidney Foundation.   We're blessed to have the whole gang back. Put down that snow shovel and prepare to laugh, cry, roll your eyes with me, The Kansas Gastronomist, DJ Carbon, Annette Lawless and Live Local.

High phosphorus (hyperphosphatemia) is a common complication caused by chronic kidney disease. Join us for this NKF Live to learn more about why this happens and how to successfully manage high phosphorus in CKD. During this program, you will hear a kidney doctor, a clinical pharmacist, and a person living with high phosphorus discuss important information to know about when managing high phosphorus.   Dr. Jay Wish is Professor of Clinical Medicine at Indiana University School of Medicine in Indianapolis and Chief Medical Officer for Outpatient Dialysis at Indiana University Health.  He is past president of the National Forum of ESRD Networks, served on the Board of Directors of the Renal Physicians Association and the American Association of Kidney Patients and was the recipient of the latter's Visionary Award in 2005. He has over 150 articles, reviews, and book chapters published, particularly in the areas of ESRD quality oversight/improvement, accountability, anemia management and vascular access. Dr. Katie Cardone is an associate professor at Albany College of Pharmacy and Health Sciences in Albany, NY. She is a clinical pharmacist with a clinical practice and research program focused on improving care in patients with kidney disease in outpatient nephrology and dialysis. She co-led the publication of pharmacy practice standards for pharmacists caring for people with kidney disease. She is a member of the Board of Pharmacy Specialties Ambulatory Care Pharmacy Council and is a fellow of the National Kidney Foundation, the American Society of Nephrology, and the American College of Clinical Pharmacy. Quenton Turner Gee has been on in-center hemodialysis for about 2 years. He was diagnosed with Stage 4 CKD in 2020. After a battle with COVID-19, it quickly progressed to end-stage kidney disease. Since starting on dialysis, he's been advocating for mental health and policies improving access to transplants and kidney innovations.   Additional Resources: Phosphate Lowering Agents High Phosphorus Information NKF Peers   Do you have comments, questions, or suggestions? Email us at NKFpodcast@kidney.org. Also, make sure to rate and review us wherever you listen to podcasts.

Nearly 90,000 people are waiting for a kidney transplant but there are not enough kidneys to meet this need. Altruistic kidney donors, or those who give anonymously, are relatively rare, but their numbers are growing and their impact is profound. Today we hear from one such remarkable individual, Daniel Emerson, Digital Marketing Director of National Kidney Foundation, who chose to give the gift of life to a stranger.   Dan Emerson is the Director of Digital Marketing at the National Kidney Foundation. Starting in 2018, he has worked to engage with the kidney community and provide them with resources and information to support them on their health journey. In June of 2024, Dan donated his kidney to an anonymous recipient through a non-directed donation. He lives in upstate New York with his husband and son.   Additional Resources: Dan's Story   Do you have comments, questions, or suggestions? Email us at NKFpodcast@kidney.org. Also, make sure to rate and review us wherever you listen to podcasts.  

In this episode of BioTalk, Bill Tompkins, President and CEO of the Montgomery County Economic Development Corporation (MCEDC), discusses the strategies driving Montgomery County's position as a leading bioscience hub. Bill highlights MCEDC's role in reinforcing the region's standing as the third-largest bioscience cluster in the U.S. and shares insights into the new Institute for Health Computing. He also introduces two new venture funds—the Technology Innovation Fund and the Founders Fund—designed to accelerate innovation and support local entrepreneurs. Bill outlines MCEDC's priorities for the upcoming year, emphasizing economic growth, investment opportunities, and fostering collaborations that make Montgomery County a thriving ecosystem for business and life sciences. Bill Tompkins is the President and Chief Executive Officer of the Montgomery County Economic Development Corporation (MCEDC), based in Rockville MD. He leads a team of twenty-five diverse professionals who work to fulfill the mission of making Montgomery County one of the best, most diverse and equitable places to be in business in the country. Bill was previously Executive Vice President and Chief Operating Officer and has been with MCEDC since January of 2019. Bill has a seasoned background in marketing, business operations, strategic planning, and nonprofit management, with most of his career serving as a senior executive in the media and entertainment industries with Fortune 500 companies. Bill also ran a consulting practice which advised companies on strategic business opportunities and brand transformation strategies. From May 2014 until August 2015, Bill was Vice President, Advertising and Marketing at The Philadelphia Tribune. He made a strategic investment in The Tribune to help ensure the long-term sustainability of Black media in the US. In July 2012, he was named President and CEO of the National Newspaper Publishers Association, a Washington based organization, which represents over two hundred Black owned and operated newspapers across the nation. Bill joined the Eastman Kodak Company in 2000 as Chief Marketing Officer for the Entertainment Imaging Business unit and became Vice President and General Manager of the Motion Picture Film Group while also serving as a corporate vice president. Prior to Kodak, Bill spent nineteen years from 1982 until 2000 at The Washington Post Newspaper in a variety of executive positions. His most recent position there was Vice President of Marketing with most of his career spent in the Advertising and Circulation Departments. Bill has been in active leadership positions on several nonprofit Boards including the Mosaic Theater Company of DC where he is Treasurer and the former Chair of the Board, Rockville Economic Development (REDI), Worksource Montgomery and the Advisory Boards of the Universities at Shady Grove and Montgomery Moving Forward. He was previously Chairman, National Kidney Foundation, National Capital Area, member, Board of Directors, California Chamber of Commerce, the Advertising Council, the Studio Theatre, The Washington Convention and Visitors Association, The Boys and Girls Clubs of Greater Washington, the American Black Film Festival Advisory Board, and The Helen Hayes Awards Committee. He is also a member of the Executive Leadership Council, and a graduate of Leadership Washington. Bill is a member of the Economic Club of Washington, the Executive Leadership Council, and a graduate of Leadership Washington. Bill received his MBA from the Harvard Business School where he was a General Motors Fellow and received his BA in Economics, magna cum laude from Tufts University. Editing and post-production work for this episode was provided by The Podcast Consultant (https://thepodcastconsultant.com).

In this episode, we explore micronutrient considerations for persons living with chronic kidney disease, including risks, medications, laboratory monitoring and tips for completing effective nutrition screening and assessments in this patient population. Melissa Prest DCN, RDN, LDN, is the founder and owner of Kidney Nutrition Specialists based in Seattle, WA. Her past experience includes working as the Foundation Dietitian for the National Kidney Foundation of Illinois and in a dialysis center providing medical nutrition therapy for individuals treated with renal replacement therapy. This episode was recorded on 11/13/24 and is hosted by Christina M. Rollins, MBA, MS, RDN, LDN, FAND, CNSC.  

Because of medical advances, kidney failure is no longer a death sentence. Today, those with kidney failure have treatment options like dialysis and kidney transplantation. Unfortunately, many aren't aware that home hemodialysis or peritoneal dialysis treatments are available. What is peritoneal dialysis and who can benefit from it? Today, Britney Dickerson, dialysis patient, and Jenny Wilson, Davita's regional director of home dialysis in New York City, are here to break it down. Jennie Wilson, MSN, RN has been working in Home Dialysis for over a decade and currently oversees several centers in the New York Metro Area that provide training and care to home dialysis patients. Her interest in population health and healthy equity has led to her passion for educating patients on their dialysis modality options. She has partnered with the National Kidney Foundation on various projects to share the clinical and lifestyle benefits of home dialysis. Brittany Dickerson- I am a dedicated mother, motivational speaker, and compassionate life coach living with Polycystic Kidney Disease (PKD). I use my kidney failure battle to educate and help others regarding kidney disease and transplantation. My personal journey has fueled my passion for helping others navigate life's challenges with courage and grace. Through partnership with the National Kidney Foundation, I have had the opportunity to mentor others and to be a guest for the National Kidney Foundation Podcast channel. My dedication to kidney awareness has led me to pursue becoming a National Kidney Foundation Advocate. I use my voice to spread my powerful message of perseverance and hope. My goal is to continue making an impact on individuals facing adversity, offering guidance, support, and being a shining example of strength in the face of hardship.    Do you have comments, questions, or suggestions? Email us at NKFpodcast@kidney.org. Also, make sure to rate and review us wherever you listen to podcasts.

On this edition of Score Values, Alex Kuhn chats with Jackie Burgess-Bishop of the National Kidney Foundation of Illinois.

We've told many stories with the folks from the National Kidney Foundation to support events like the Kidney Walk on October 6th at UMBC. But, when you meet Sam Cosby and hear his inspiring journey, you might want to do more than just walk and run. Are you a match? The post Samuel Cosby tells Nestor about his need for a new donor kidney and NKF Kidney Walk on October 6th at UMBC first appeared on Baltimore Positive WNST.

Today, those with kidney failure have multiple treatment options like dialysis and kidney transplants; however, many aren't aware of treatments like home hemodialysis. What is home hemodialysis, and who could benefit from it? Learn all that and more on today's episode. Jennie Wilson, MSN, RN has been working in Home Dialysis for over a decade and currently oversees several centers in the New York Metro Area that provide training and care to home dialysis patients. Her interest in population health and healthy equity has led to her passion for educating patients on their dialysis modality options. She has partnered with the National Kidney Foundation on various projects to share the clinical and lifestyle benefits of home dialysis. Bell Maddux was first diagnosed with MPGN when she was fifteen years old. She went through college, got married and started her career before she became eligible for transplant. She was fortunate to receive a living donation from her father without having to be on dialysis. Then, after 10 years with her father's kidney, Bell started in-center dialysis, and switched to home-hemodialysis in 2021. Bell is optimistically awaiting “the call” for a deceased donor, but in the meantime, she stays busy with her husband raising their two children, 7 and 12. She is a Peer Mentor and Patient Advocate with the National Kidney Foundation and has an 18-year career as a digital producer for a NY advertising agency.   Additional Resources: https://www.medicare.gov/care-compare/; https://homedialysis.org/; https://www.kidney.org/atoz/content/homehemo; https://www.kidney.org/peers; https://healthunlocked.com/nkf-dialysis#utm_source=nkf_webpage&utm_medium=w   Do you have comments, questions, or suggestions? Email us at NKFpodcast@kidney.org. Also, make sure to rate and review us wherever you listen to podcasts.

In a rut? Dealing with overwhelm? Do you simply want to get back to being a better version of yourself? This episode is for YOU! Listen as Maria breaks down ways to set achievable goals and conquer procrastination in just 28 days. You'll hear practical ways to reset yourself both physically and personally. Also, special guest Neko Northington joins Maria to talk about Kidney Disease and the important work that National Kidney Foundation is doing to ensure that families will have a place to turn when they need answers, drive innovation in transplantation and get more loved ones off the kidney transplant wait list. Learn more at: www.kidney.org. See omnystudio.com/listener for privacy information.

In a rut? Dealing with overwhelm? Do you simply want to get back to being a better version of yourself? This episode is for YOU! Listen as Maria breaks down ways to set achievable goals and conquer procrastination in just 28 days. You'll hear practical ways to reset yourself both physically and personally. Also, special guest Neko Northington joins Maria to talk about Kidney Disease and the important work that National Kidney Foundation is doing to ensure that families will have a place to turn when they need answers, drive innovation in transplantation and get more loved ones off the kidney transplant wait list. Learn more at: www.kidney.org. See omnystudio.com/listener for privacy information.

According to some sports media, nearly 300 million people watch the sport of MMA. On this episode of The PVDcast, I am joined by Allen Levine, CEO and promoter of Coliseum Combat Zone MMA. This new MMA company has their inaugural event scheduled for September 14. Allen and I will discuss the match card and many other aspects of the event. This includes supporting the National Kidney Foundation through the event due to Allen's experience with chronic kidney disease. We will wrap up our conversation chatting about Allen's sports show, Pittsburgh Sportsline. Don't forget to rate, review and subscribe to the show & new episodes of The PVDcast drop every Thursday!

On today's special episode of Hot Topics and Kidney Health we're sharing audio from a recent webinar hosted by National Kidney Foundation on kidney xenotransplantation. Stay tuned to hear from the experts and learn about the latest updates on animal-to-human transplantation.   Dr. Tatsuo Kawai is a professor of surgery at Harvard Medical School and the A. Benedict Cosimi Chair in Transplant Surgery at Massachusetts General Hospital. He is also director of the Legorreta Center for Clinical Transplantation Tolerance. He was awarded the Martin Research Prize at MGH in 2009 and the New Key Opinion Leader Award by the Transplantation Society in 2010 for this work. In the field of xenotransplantation, he has collaborated extensively with eGenesis over the past five years, achieving over two years of survival for genetically edited kidney xenografts in nonhuman primates, which was published in Nature in 2023. In March 2024, he successfully performed the world first kidney xenotransplantation from the pig with 69 genomic edits in a living patient with end stage renal disease.  Vineeta Kumar MD, FAST, FASN  is the lead nephrologist for the Living Kidney Donor and Incompatible Kidney Transplant programs at the University of Alabama in Birmingham. She is an expert in kidney transplantation, living kidney donation, incompatible kidney transplant, kidney paired donation and cardiovascular outcomes after kidney transplantation. Peter Reese, MD, PhD, is an NIH-funded transplant nephrologist and epidemiologist. His research focuses on: a) developing effective strategies to increase access to solid organ transplantation; b) improving the process of selecting and caring for living kidney donors; c) determining outcomes of health policies on vulnerable populations with renal disease, including the elderly; d) testing strategies to improve important health behaviors such as medication adherence; and e) transplant ethics. He was a recipient of a Presidential Early Career Award for Scientists and Engineers, was elected member of the American Society of Clinical Investigation, and was a Greenwall Faculty Scholar in bioethics. He is a past chair of the Ethics Committee for the United Network for Organ Sharing (UNOS), which oversees organ allocation and transplant regulation in the US, and is an Associate Editor for the American Journal of Kidney Diseases. He co-led the THINKER, USHER, MYTHIC, and SHELTER trials involving transplanting HCV-infected donor organs into uninfected recipients. His work has been generously funded by foundations and the NIH, including a K-24 to support mentoring.   Do you have comments, questions, or suggestions? Email us at NKFpodcast@kidney.org. Also, make sure to rate and review us wherever you listen to podcasts.  

It's Episode 14 of The Nephron Segment! Join us as we chat with Dr. Mehmet Sukru Sever and Dr. Rasha Rashan and discuss disaster nephrology and kidney care during crises. To summarize Dr. Sever tells us "disasters are inevitable. And All countries around the globe are at risk of disasters, either natural or man made." We discuss what we might learn from prior disasters, what do expect in the future, and what we should do, as a nephrology community, to prepare for the worst. Nephrons: Matthew Sparks, Samira FaroukGuests:  Mehmet Sukru Sever, Rasha Rashan1:44: Marmara earthquake (1999)2:35: Bingöl earthquake (2003)2:44: Bam earthquake (2003)2:57: Médecins Sans Frontières (MSF)4:07: Some of Dr. Sever's Papers4:35: "Destructive Disasters, trauma, crush injury, and beyond" 9:42: Kidney News 2024 Special Section 13:10: "Disasters & Kidney Care: Pitfalls and Solutions" (Nature Reviews Nephrology 2023)16:31: "An Overlooked, Possibly Fatal Coronavirus Crisis: A Dire Need for Kidney Dialysis" (New York Times 2020) 19:23: "Nephrology Care in Challenging Circumstances: A Patient's Perspective" (Kidney News 2024)19:59: Syrian refugee crisis22:08: Refugees & asylees in the United States25:49: National Kidney Foundation's "Emergency Resources" 26:35: Announcement: ASN, ISN, ERA Collective Effort (2023) 29:06: "Planet Sets Record for Hottest Day Twice in a Row" (2024)29:12: A review of CKD of unknown etiology (CKDu)29:49: UEFA Euro 2024

Melanie spent a week in Long Beach, CA at the annual National Kidney Foundation this month. She shares her reflections about the state of kidney stone nutrition at national level.     Submit a question for Melanie to answer on the podcast! Connect with The Kidney Dietitian!  Instagram | Facebook | Pinterest | Facebook Group | Newsletter www.thekidneydietitian.org All information in this podcast is meant for educational purposes only and should not be used in place of advice from a medical professional.  

Losing a kidney transplant can feel very overwhelming. Today we're here with Anthony Tuggle, a former NKF board member, to hear how he's coping with losing a transplant and learn what's next for him.   Anthony Tuggle is the Afiniti President of Customer Operations, and a former Board Member of the National Kidney Foundation and of NKF Serving Alabama, Georgia and Mississippi. Tuggle is responsible for expanding global contact center operations, accelerating business development, overseeing product deployment and engaging clients to generate value for enterprises, customers and employees. Prior to joining Afiniti, Tuggle served as Vice President – Customer Care, Sales and Service Centers at AT&T where he led more than 30,000 sales leaders and has built a culture that fosters a passion for winning. He models a "find-a-way" mindset in his approach to leadership and inspires his team to embrace the importance of agility. Tuggle is the acclaimed author of I'm Better Not Bitter: My Personal Journey - Kidney Transplant Recipient's Story of Winning in Business & Life and Moving Forward, which shares how he has overcome obstacles, is self-motivated, and creates a work culture of success. Notably, Tuggle led efforts in his local community as the 2018-2020 Chairman of the Atlanta Kidney Walk, which raised more than $500,000 for NKF. He also has partnered with AT&T to raise more than $200,000 to date.   Additional resources: NKF Peers   Do you have comments, questions, or suggestions? Email us at NKFpodcast@kidney.org. Also, make sure to rate and review us wherever you listen to podcasts.

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Pattie Dash joins Lauren in Episode 50 of “How'd Her Career Get There?” where she reflects on her career path through the nonprofit sector. Her trajectory was marked by continual growth, fueled not only by the support of mentors but also by the strong foundation and moral lessons instilled by her parents. Recognizing her potential, these mentors guided her journey, nurturing her talents and empowering her to advocate for roles that sparked her curiosity. Her story highlights the profound impact of mentorship and self-belief in forging a fulfilling career path. Through newfound confidence, Pattie's narrative imparts invaluable lessons for anyone navigating their professional journey. Links for topics mentioned during the episode: National Kidney Foundation for MD & DE: https://www.kidney.org/offices/nkf-serving-maryland-delaware Upcoming Events for National Kidney Foundation: https://www.kidney.org/events Sante Event: https://support.kidney.org/event/2024-sante-giving-back-for-kidney-disease/e538425 Upcoming National Kidney Foundation Walks: https://www.kidneywalk.org

In this enlightening episode, Dr. Dustin Portela, a board-certified dermatologist, is joined by Leah Adams, a stage 1A melanoma survivor and skin cancer awareness advocate. Together, they dive into the world of skin cancer awareness, prevention, and early detection. Leah interviews Dr. Portela about the importance of understanding different types of skin cancer, debunking common myths, and sharing essential resources for those affected. Along the way, they emphasize the critical role of self-care, regular skin checks, and the power of social support groups. Leah Alexis Adams received her Bachelor's of Science from Ohio University in Child and Family Studies with a minor in Psychology. She then received her dual Master's degree in Social Science Administration and Nonprofit Management from Case Western Reserve University. Leah is the Program Manager for the National Kidney Foundation's Northern Ohio office. She has been with the organization for almost 5 years. In her role, Leah manages the planning and implementation of all NKF programs in the Northern OH territory to support kidney patients, caregivers and raise awareness in her community, and educate healthcare professionals. Some personal things to note about Leah is that she is an avid runner who has ran 3 full marathons, she loves to hike in her local Ohio Metroparks and state parks and she loves to travel whenever she has the opportunity. When she is off the clock you can find her advocating about skin cancer, sun safety and sharing her (stage IA) and her father's (stage IV metastatic) story of melanoma to anyone who is willing to listen and learn. Through sharing her story with melanoma on social media/online, she has had the privilege and opportunity to work with multiple brands in the sun safety space, has been featured on local news stations, magazines and has been a guest on a variety of podcasts. Follow Leah on Instagram  Key Points Covered: Dr. Dustin Portela's Journey into Dermatology: Shares his path from a curious middle schooler dissecting frogs to becoming a board-certified dermatologist. Discusses why he chose dermatology for its blend of procedural and medical treatments. Breaking Down Skin Cancer: Explains the three primary types: basal cell carcinoma, squamous cell carcinoma, and melanoma. Highlights the varying levels of risk and common characteristics of each type. Melanoma Awareness: Leah shares her personal story as a stage 1A melanoma survivor, providing insights into the challenges of early detection and treatment. They discuss the ABCDEs of melanoma identification and how individuals can empower themselves through self-exams. Prevention and Early Detection Strategies: Dr. Portela emphasizes the importance of sun protection from an early age. Encourages monthly skin checks, particularly for those with family histories or increased risk. Managing and Treating Skin Cancer: Outlines the treatment process for different types of skin cancer, emphasizing surgical excision and Mohs micrographic surgery. Discusses how sentinel lymph node biopsies are used in managing melanoma. Support and Resources: Suggests reliable resources such as the Skin Cancer Foundation and local support groups. Highlights how organizations like Outrun the Sun raise funds for critical research and connect people. Myths and Misconceptions: Dr. Portela debunks myths surrounding sunscreen, emphasizing its role in reducing skin cancer risk. Explains how the misconception of sunscreen causing cancer is harmful and unfounded. Final Takeaways: Leah and Dr. Portela encourage everyone to prioritize their skin health by using sunscreen, seeking regular skin checks, and fostering healthy lifestyle habits. They underscore the power of social support and research advancements in improving melanoma outcomes. Support the Dr. Dustin Podcast and my mission to take free dermatology care to underserved communities through my mobile clinic.  You can support us by shopping for skincare through the links below Skinbetter Science: My favorite premium skincare line Shop Skinbetter Science Discounts on Neutrogena, EltaMD and more on the Aire Skin Store

Kidney donor Michele Love tells Nestor her story of giving life and invites you to Sante for the National Kidney Foundation on May 8th at The Baltimore Museum of Industry. The post Kidney donor Michele Love tells Nestor her story of giving life and invites you to Sante for NKF first appeared on Baltimore Positive WNST.

(AURN News) – In observance of National Kidney Month, Black Health Matters and the National Kidney Foundation have united forces to bring the pressing issue of kidney health within the African American community to the forefront. According to the National Kidney Foundation, Black individuals face a staggering fourfold increased risk of developing kidney failure compared to other racial groups. One in three kidney failure patients in the United States is Black. Nationwide, 33% of adults are susceptible to kidney disease. Diabetes emerges as the primary culprit behind kidney failure, closely followed by high blood pressure, according to the organization. The data is sobering: more than 42% of Black adults grapple with high blood pressure, a significant contributing factor to kidney dysfunction. There is a critical need for comprehensive outreach initiatives, early detection programs, and culturally sensitive healthcare interventions tailored to the unique needs of the African American community. We must remember that behind each statistic lies a personal narrative of struggle, resilience, and the unyielding quest for equitable access to quality healthcare. Far too many African Americans in our country are not treated fairly or taken seriously by medical professionals. Learn more about your ad choices. Visit megaphone.fm/adchoices

Diagnosed with a rare autoimmune kidney disease at just 22 years old, Jennifer has since undergone four kidney transplants. Now, she uses her platform as Board Chair of the National Kidney Foundation in Minnesota, Donate Life America volunteer and author of Incurable Optimist: Living with Illness and Chronic Hope to advocate for organ donation and kidney disease prevention. Listen to Jennifer's remarkable journey on this episode of Let's Talk Hope.

Kidney transplant recipient and survivor Vaunita Goodman talks transplant, her new second life, love of sailing and the value of National Kidney Foundation at State Fare in Catonsville on "A Cup Of Soup Or Bowl Week" for The Maryland Food Bank. The post Crab Cake Row: Vaunita Goodman talks transplant, new life & the value of National Kidney Foundation first appeared on Baltimore Positive WNST.

Sarah chats with two super neat physicians, Dr. Niralee Patel & Dr. Sharmeela Saha, about kidneys! Learn more about what it takes to become a kidney doctor and how it's a multi-disciplinary profession. Bonus points if you can remember what foods are high in potassium (hint: think beyond bananas)! Guest email contacts: niralee.patel@uc.edu and sharmeela.saha@uc.eduHelpful links:                                                                                                                                                          PKD[F] is polycystic kidney disease [foundation] | https://pkdcure.org/                        Dialysis | https://www.kidney.org/atoz/content/dialysisinfo                                                      NKF is the National Kidney Foundation | https://www.kidney.org/                                Nephrology MSSP, NepSim & more are offered for UCCOM students! 

It's hard to keep up with all the new diets that cycle through news outlets and social media. Do you know which ones are right for you and your kidney health? On this episode, you will hear from experts on how to find the diet that's right for you and how to stick to it.   Amanda Hays, MS, RDN, LD is a Registered Dietitian Nutritionist in Austin, TX with over a decade of experience serving thousands of people across all stages of chronic kidney disease. As the owner of Relish Nutrition Therapy, she specializes in taking the most powerful, research-based medical nutrition therapy recommendations and practically implementing them into real life without sacrificing the joy of food. She believes a healthy diet starts with a healthy relationship with food and that everyone with kidney disease deserves access to quality care and support. . Jane DeMeis, MS, ODCP became involved with the National Kidney Foundation when she was diagnosed in 2018 with stage 4 kidney disease. She was the Director of Education and Organizational Development for U R Medicine Home Care. She is now a certified Kidney Coach. She has supported local cooking classes with recommendations for kidney friendly meals. She works with patients who have just been diagnosed with CKD at either level 3 b or 4 and have been given a diet to follow and need help on how to manage their eating and living with CKD diagnosis.    Additional Resources  Nutrition and Kidney Health Kidney-Friendly Recipes   Do you have comments, questions, or suggestions? Email us at NKFpodcast@kidney.org. Also, make sure to rate and review us wherever you listen to podcasts.

In this episode, Dr. Suzette Sutherland and Dr. Alana Desai from the University of Washington discuss the management of urinary tract stones in pregnant patients, considerations for ureteroscopy, and consequences of radiation exposure in the fetus. First, the doctors underscore the importance of ultrasound as the first line imaging modality to minimize fetal exposure to radiation. Dr. Sutherland and Dr. Desai also delve into nausea and pain management options, recommended diets for prevention of stone formation during pregnancy, and the necessity of involving a multidisciplinary team in such cases. The episode concludes with a remarkable case study from Dr. Desai's experience. --- SHOW NOTES 00:00 - Introduction 02:06 - Incidence and Risk Factors of Kidney Stones in Pregnancy 03:29 - Physiological Changes and Stone Formation in Pregnancy 07:04 - Diagnosing Kidney Stones in Pregnancy 13:08 - Expectant Management vs. Intervention 14:41 - Managing Pain and Nausea in Pregnant Patients with Kidney Stones 17:13 - Decompression Methods for Kidney Stones in Pregnancy 23:13 - Ureteroscopy as a Preferred Intervention 26:05 - Case Description from Dr. Desai 30:04 - Considerations for Ureteroscopy in Pregnant Patients 31:14 - Preventing Kidney Stones in Pregnancy --- RESOURCES Lyon, M., Sun, A., Shah, A., Llarena, N., Dempster, C., Sivalingam, S., Calle, J., Gadani, S., Zampini, A., & De, S. (2023). Comparison of Radiation Exposure for Pregnant Patients Requiring Intervention for Suspected Obstructing Nephrolithiasis. Urology, 182, 61–66. https://doi.org/10.1016/j.urology.2023.09.023 Thongprayoon, C., Vaughan, L. E., Chewcharat, A., Kattah, A. G., Enders, F. T., Kumar, R., Lieske, J. C., Pais, V. M., Garovic, V. D., & Rule, A. D. (2021). Risk of Symptomatic Kidney Stones During and After Pregnancy. American journal of kidney diseases : the official journal of the National Kidney Foundation, 78(3), 409–417. https://doi.org/10.1053/j.ajkd.2021.01.008

In this episode, Dr. Suzette Sutherland and Dr. Alana Desai from the University of Washington discuss the management of urinary tract stones in pregnant patients, considerations for ureteroscopy, and consequences of radiation exposure in the fetus. First, the doctors underscore the importance of ultrasound as the first line imaging modality to minimize fetal exposure to radiation. Dr. Sutherland and Dr. Desai also delve into nausea and pain management options, recommended diets for prevention of stone formation during pregnancy, and the necessity of involving a multidisciplinary team in such cases. The episode concludes with a remarkable case study from Dr. Desai's experience. --- SHOW NOTES 00:00 - Introduction 02:06 - Incidence and Risk Factors of Kidney Stones in Pregnancy 03:29 - Physiological Changes and Stone Formation in Pregnancy 07:04 - Diagnosing Kidney Stones in Pregnancy 13:08 - Expectant Management vs. Intervention 14:41 - Managing Pain and Nausea in Pregnant Patients with Kidney Stones 17:13 - Decompression Methods for Kidney Stones in Pregnancy 23:13 - Ureteroscopy as a Preferred Intervention 26:05 - Case Description from Dr. Desai 30:04 - Considerations for Ureteroscopy in Pregnant Patients 31:14 - Preventing Kidney Stones in Pregnancy --- RESOURCES Lyon, M., Sun, A., Shah, A., Llarena, N., Dempster, C., Sivalingam, S., Calle, J., Gadani, S., Zampini, A., & De, S. (2023). Comparison of Radiation Exposure for Pregnant Patients Requiring Intervention for Suspected Obstructing Nephrolithiasis. Urology, 182, 61–66. https://doi.org/10.1016/j.urology.2023.09.023 Thongprayoon, C., Vaughan, L. E., Chewcharat, A., Kattah, A. G., Enders, F. T., Kumar, R., Lieske, J. C., Pais, V. M., Garovic, V. D., & Rule, A. D. (2021). Risk of Symptomatic Kidney Stones During and After Pregnancy. American journal of kidney diseases : the official journal of the National Kidney Foundation, 78(3), 409–417. https://doi.org/10.1053/j.ajkd.2021.01.008

You may have heard the buzzword superfoods but what are they and do they have special qualities? Board-certified renal dietitian, Jen Hernadez is here to break it down.   In this episode we spoke with, Jen Hernandez RDN, CSR, LDN- Jen Hernandez is a registered dietitian and a certified specialist in renal nutrition. She has served the kidney community in dialysis clinics as well as with the National Kidney Foundation of Hawaii to help spread awareness of kidney disease and strive for prevention with early detection and interventions. In 2018, Jen founded Plant-Powered Kidneys. Jen uses her virtual private practice to help people in all stages of kidney disease, from stage one through transplant, to provide evidence-based nutrition guidelines and recommendations. The clients and students of Plant-Powered Kidneys learn and implement the fundamentals to keep their kidney function so that they can delay or even prevent kidney failure and the need for dialysis.   Additional Resources  Superfoods  Superfoods Blog   Do you have comments, questions, or suggestions? Email us at NKFpodcast@kidney.org. Also, make sure to rate and review us wherever you listen to podcasts.  

The Filtrate:Joel TopfSwapnil HiremathSophia AmbrusoAC GomezJosh WaitzmanJennie LinNayan AroraThe CurbsidersMatt F. Watto (@DoctorWatto)Paul Nelson Williams, America's primary care physician (@PaulNWilliamz)With Special Guest:JD Foster (@KidneyVet)Sayed Tabatabai (@TheRealDoctorT) Nephrologist in Austin and the author of These Vital SignsMichelle Rheault (@rheault_m) Chief of Pediatric Nephrology at the University of Minnesota and lead author of the DUPLEX TrialEditor:Joel TopfShow Notes:Lily toxicity in the cat (PubMed)Surgeons perform kidney transplants in cats amid rising demand for advanced pet care (ABC News)Treatment of ibuprofen toxicity with serial charcoal hemoperfusion and hemodialysis in a dog (PubMed)Nephrology in Veterinary Medicine (Kidney 360)Star Wars Society of San Antonio (FaceBook)These Vital Signs (Amazon)Dr Tabatabai read a short story called The Handholder, here is the original tweet thread for that story (ThreadReader)The pearl not the patient (PubMed)Late Braking and High Impact Clinical Trial press releaseMENTOR, Rituximab or Cyclosporine in the Treatment of Membranous Nephropathy, was in 2019 not 2017 (NEJM)KALM-1, A Phase 3 Trial of Difelikefalin in Hemodialysis Patients with Pruritus, was in 2019 not 2017 (NEJM)Sophie's number one pick: Efficacy and safety of sparsentan versus irbesartan in patients with IgA nephropathy (PROTECT): 2-year results from a randomised, active-controlled, phase 3 trial (Lancet)Patients in the sparsentan group had a slower rate of eGFR decline than those in the irbesartan group. eGFR chronic 2-year slope (weeks 6–110) was −2·7 mL/min per 1·73 m2 per year versus −3·8 mL/min per 1·73 m2 per year (difference 1·1 mL/min per 1·73 m2per year, 95% CI 0·1 to 2·1; p=0·037); total 2-year slope (day 1–week 110) was −2·9 mL/min per 1·73 m2 per year versus −3·9 mL/min per 1·73 m2 per year (difference 1·0 mL/min per 1·73 m2 per year, 95% CI −0·03 to 1·94; p=0·058).Clinical Trial Considerations in Developing Treatments for Early Stages of Common, Chronic Kidney Diseases: A Scientific Workshop Cosponsored by the National Kidney Foundation and the US Food and Drug Administration (AJKD)AC Gomez's Pick: MDR-101-MLK Update: Operational Immune Tolerance Achieved in Living Related HLA-Matched Kidney Transplant Recipients (ASN-Online.org) Josh's Pick: A Phase 2 Trial of Sibeprenlimab in Patients with IgA Nephropathy (NEJM)Nayan's Pick: The EnAKT LKD Cluster Randomized Clinical Trial (JAMA Internal Medicine) The Freely Filtered simultaneous release (NephJC)Freely Filtered is now a verb. Swap's Pick: Strategies for the Management of Atrial Fibrillation in PatiEnts Receiving Dialysis (SAFE-D) (ASN-Online.org)Joel's Pick: AYAME Study: Randomized, Double-Blind, Placebo-Controlled Phase 3 Study of Bardoxolone Methyl in Diabetic Kidney Disease (DKD) Patients (ASN-Online.org)Reata is a no-show to the 2012 ASN Kidney Week (PBFluids)Michelle's Pick: Sparsentan versus Irbesartan in Focal Segmental Glomerulosclerosis. The DUPLEX Study (NEJM)DUET: A Phase 2 Study Evaluating the Efficacy and Safety of Sparsentan in Patients with FSGS (PubMed)

While chronic kidney disease diagnosis is rare in children, its effects are profound. Furthermore, there's so much scientists don't know about kidney function. Keia Sanderson is hoping to change that. She specializes in chronic kidney disease treatment in pediatric patients and discusses avenues to advance treatment and prevention. This podcast gives her the perfect platform to explain How kidney disease is especially challenging to identity in children because chronic kidney disease stages are often asymptomatic in pediatric patients, Why preterm babies are vulnerable to certain conditions because of the development timing of the nephrons, and Why it's important to identity intervention measures before dialysis and kidney transplantation provide the only recourse. Keia Sanderson, MD, is an assistant professor of medicine in the Division of Nephrology and Hypertension at the University of North Carolina School of Medicine. Her job is a mix of teaching, clinical work, and research. In her clinical work, she takes care of children with kidney disease at all stages, including kids who receive transplants. Her current research is focused on kidney outcomes in children with complex medical histories, in particular children who've been born prematurely. She says that the challenge is oftentimes the asymptomatic nature of kidney disease in children. Therefore, she and other clinicians are often meeting kids with disease states that are irreversible and are turning toward dialysis treatment and transplantation.  Dr. Sanderson gives listeners a special focus on the risks from preterm birth. Because preterm babies tend to have less nephron development, the nephrons that are present have to work overtime and are subject to hyper filtration. But because doctors have been able to identify this as a critical time, they are looking at ways to better manage preterm infant treatment. For example, what medications are they receiving that could affect kidney development? How are we feeding infants in this active development stage? How are we handling their oxygenation? While a clear pathway is not yet evident, she is hopeful she and other researches will find one. Currently, she's hoping to develop mathematical models to make better predications about the risk levels for different babies. For more information, see the UNC Kidney Center, the National Kidney Foundation, and talk to your primary doctor. Available on Apple Podcasts: apple.co/2Os0myK 

Dr. Staci Leisman is a board certified internist and nephrologist who practices nephrology at Mount Sinai Hospital. She is also an accomplished educator in the Icahn School of Medicine at Mount Sinai. 
Dr. Leisman received her B.A. in English Language and Literature from Yale University, where she graduated magna cum laude and was inducted into Phi Beta Kappa. She received her M.D. from Washington University in St Louis, where she was one of 8 recipients of the Distinguished Scholar Award. She completed her residency in Internal Medicine and fellowship in Nephrology at Mount Sinai Medical Center. As a fellow, she completed research in transplant immunology in the laboratory of Dr. Peter Heeger, which resulted in a Young Investigator Award from the American Society of Transplantation and two oral presentations at the American Transplant Congress. During her fellowship, she co-first authored and was a contributing author on numerous papers. 
Dr. Leisman's clinical duties include caring for patients on dialysis at an outpatient dialysis facility, as well as attending on the inpatient renal service at Mount Sinai Hospital. 
Dr. Leisman has been extensively involved in teaching throughout her career. She currently teaches students at all levels of medical education, including medical students, residents and fellows.  She is the course director for the Human Physiology course in the medical school, and holds a secondary appointment in the Department of Medical Education, where she is a co-director for the medical school curriculum. In her capacity as an educator, she has won numerous awards including Teacher of the Year at North General Hospital, the Edward Ronan Student Council Award at the Icahn School of Medicine, the Institute for Medical Education's Excellence in Teaching Award, the Student Council Lifetime Achievement Award, the JOWMA Outstanding Achievement Award, and the Gold Humanism in Medicine Award. She has been selected for membership in the Institute for Medical Education as a Master Educator. 
Dr. Leisman also serves on the International Association of Medical Science Educators' educational scholarship committee, and serves on the editorial board of Advances in Chronic Kidney Disease, the Journal of the National Kidney Foundation. She is the Deputy Education Director for the Kidney Self Assessment Program (KSAP), the preeminent board preparation tool published by the American Society of Nephrology. _______________________________________________________ Become a JOWMA Member! www.jowma.org  Follow us on Instagram! www.instagram.com/JOWMA_org  Follow us on Twitter! www.twitter.com/JOWMA_med  Follow us on Facebook! https://www.facebook.com/JOWMAorg/ Stay up-to-date with JOWMA news! Sign up for the JOWMA newsletter! https://jowma.us6.list-manage.com/subscribe?u=9b4e9beb287874f9dc7f80289&id=ea3ef44644&mc_cid=dfb442d2a7&mc_eid=e9eee6e41e

Kent talks to Lauren Drew, who gave her kidney to a stranger and became a kidney advocate. Lauren works at the National Kidney Foundation and helps shape policies for kidney patients and donors. Listen to this episode to hear Lauren's inspiring story and learn how to support the kidney community. If you have questions regarding items discussed during this episode or would like more information about Kidney Solutions weekly Support Group, contact Kent at kent.bressler@kidneysolutions.org For more information about Kidney Solutions, visit us at www.kidneysolutions.org Host: Kent Bressler Producer: Jason Nunez

KCBS Radio's Foodie Chap Liam Mayclem is here to discuss this Weekend's events from Halloween In The Castro to WhiskyFest.

Let's listen to the inspiring journey of Judge Derek Mosley, a true advocate for empowering the youth and promoting civil discourse, whose path to the law was ignited by a character he saw on LA Law. Explore how Judge Mosley uses social media to share impactful Black history stories, inspiring future generations to rise against adversity. Find out the significance of leading by example, as Judge Mosley encourages young people to see him as a role model and act upon their dreams, when you listen to this episode.Tune in to learn how his passion for law and inspiring others led him to create the METAL Program, providing students with invaluable insights into various career opportunities and discover the program's impact as students get the chance to meet professionals from different fields, fostering a sense of curiosity and ambition. Join Judge Derek Mosley in embracing a "we" mindset instead of an "I" perspective, fostering meaningful change in our communities.Episode Highlights:12:25 - No matter if you're Black, White, Asian, Latino, no matter what your background is, if you don't eat, you are going to die. You can be as opposite as you think we are, but we have to eat to survive. So, why not let's get together and eat as humans and just talk and get to know each other? When you do that, you realize you have more in common than what separates you, and that's been going on from day one.14:29 - When I was going to school, Martin Luther King is about the extent of Black people you learned about, and you learned a little bit about slavery and then Black history. So, if you knew nothing about Black people, you would think our entire diaspora was slavery and Martin Luther King.18:29 - I think it's important for my daughters to see it because they know how important it is to me that it's important to them because now they're doing it. They do the same thing. Connect with Becky Dubin JenkinsLinkedInConnect with Judge Derek MosleyLinkedInGuest Bio:Derek Mosley graduated from Marquette University Law School in 1995. After graduation he served as an Assistant District Attorney for Milwaukee County from 1995-2002. As an Assistant District Attorney, he represented the State of Wisconsin in over 1,000 criminal prosecutions. In 2002, Mr. Mosley was appointed Municipal Court Judge in Milwaukee. At the time of his appointment, he was the youngest African-American to be appointed judge in the State of Wisconsin. For ten years Mr. Mosley served as the Chief Judge of the Milwaukee Municipal Court. In 2023, Mr. Mosley became the Director of the Lubar Center for Public Policy Research and Civic Education at Marquette University Law School.Judge Mosley routinely speaks both nationally and internationally about Unconscious Bias and Black History. Also, as a kidney transplant recipient, he is an ardent supporter of Donate Life Wisconsin, the National Kidney Foundation, and Versiti (formerly the Blood Center of Wisconsin). He currently serves as a Donate Life Hollywood advisor to the television and movie industries to promote accurate depictions of organ donation and transplant on television and in movies. In his spare time, Judge Mosley is a local Milwaukee foodie, and served as a 2022 James Beard Judge for the James Beard Foundation.

“Your dad just shot your mom; you've got to go back [to college].” In this episode, Jimmie McMillian, Senior Corporate Counsel at Indianapolis Motor Speedway,  joins Derrin Slack for a conversation about overcoming obstacles and leaving a legacy. After failing out of college, Jimmie's life changed forever when he found out his father shot his mother three times. As he sat in the hospital wondering if she would survive, he made a decision that would affect the rest of his life. As he shares his story, you'll hear what he did next, and why he continues to live every day with a desire to be great. Additional Resources: More on PeopleForward Network Follow PeopleForward Network on LinkedIn Check out the original episode Learn more about National Kidney Foundation of Indiana Indianapolis Motor Speedway Connect with Jimmie Mcmillian  

Every Wednesday on MPR News with Angela Davis, you can listen to conversations about health and wellness.  MPR News host Angela Davis revisits highlights from three recent conversations. An infectious disease doctor and pediatric nurse talk about vaccine fatigue as the new COVID-19 booster rolls out. Plus, the increasing number of children who are nearsighted and how to prevent and treat kidney disease.  Guests:  Dr. Greg Poland is an internal medicine physician at the Mayo Clinic in Rochester, Minn., and an infectious disease expert. He's founder and director of the Mayo Vaccine Research Group and the Editor-in-Chief of the medical journal Vaccine.  Sheyanga Beecher is a pediatric nurse practitioner with Hennepin HealthCare. She's also medical director of the mobile pediatric clinic, which has provided thousands of vaccines against COVID-19 and childhood diseases, along with basic health care. Dr. Mary Gregory is a board-certified optometrist based in Monticello, Minn., who specializes in children's vision and learning. Dr. Derek Horkey is an ophthalmologist with St. Paul Eye Clinic who does comprehensive eye care for adults. He has additional expertise in treating glaucoma. Dr. Naim Issa is a nephrologist treating people with kidney disease and kidney transplants at Mayo Clinic in Rochester, Minn. where he's also an associate professor at Mayo Clinic School of Medicine. Jennifer Cramer-Miller has lived with kidney disease since her early 20s. Her memoir “Incurable Optimist: Living with Illness and Chronic Hope” describes her four kidney transplants, including a kidney from her mother and from a 25-year-old anonymous donor. She serves as board chair of the National Kidney Foundation (serving Minnesota).   Subscribe to the MPR News with Angela Davis podcast on: Apple Podcasts, Google Podcasts, Spotify or RSS.  Use the audio player above to listen to the full conversation. 

Our book choices often relate back to current events—whether it's women's rights, LGBTQIA+ equality, BIPOC empowerment, climate change, etc. So, we decided to create Popping Off the Page, special spin-off episodes that highlight the people who are trying to make the world a better place. On this episode, we interview Christina Davis from National Kidney Foundation. As you know, kidney health is near and dear to Maritza's heart, so we chat with Christina about the upcoming Authors Luncheon, a 35-year-old fundraiser uniting best-selling authors and tens of thousands of literary enthusiasts. Authors for this year's luncheon include Lee Child, Anita Gail Jones, Lauren Groff, Mac Barnett, and Shawn Harris.

(0:00-20:58) Opening RCST discussing fun with KU football numbers (20:59-38:56) Voice of the Jayhawks Brian Hanni (38:57-1:00:36) Lie Detector Test (1:00:37-1:15:46) Greg Ostertag from the National Kidney Foundation (1:15:47-1:24:49) Lance Leipold's recent comments (1:24:50-End) Kansas City Star's Jesse Newell

A contributor writes, “I said no to massage to a patient after fresh dialysis. When would it be OK to work on this person?” Seems like a simple question. But it's not. We know a fair amount about kidney disease and about dialysis. And here's a surprise: The interface between massage therapy and people using dialysis has sparked a lot of conversation in research and medical circles. What are people saying—and learning—about massage therapy for dialysis users? Better listen to this episode of I Have a Client Who . . .   Sponsors:     Books of Discovery: www.booksofdiscovery.com       Host Bio:                    Ruth Werner is a former massage therapist, a writer, and an NCBTMB-approved continuing education provider. She wrote A Massage Therapist's Guide to Pathology, now in its seventh edition, which is used in massage schools worldwide. Werner is also a long-time Massage & Bodywork columnist, most notably of the Pathology Perspectives column. Werner is also ABMP's partner on Pocket Pathology, a web-based app and quick reference program that puts key information for nearly 200 common pathologies at your fingertips. Werner's books are available at www.booksofdiscovery.com. And more information about her is available at www.ruthwerner.com.                                      Recent Articles by Ruth:          “Working with Invisible Pain,” Massage & Bodywork magazine, November/December 2022, page 36, http://www.massageandbodyworkdigital.com/i/1481961-november-december-2022/38   “Unpacking the Long Haul,” Massage & Bodywork magazine, January/February 2022, page 35, www.massageandbodyworkdigital.com/i/1439667-january-february-2022/36. “Chemotherapy-Induced Peripheral Neuropathy and Massage Therapy,” Massage & Bodywork magazine, September/October 2021, page 33, http://www.massageandbodyworkdigital.com/i/1402696-september-october-2021/34.           “Pharmacology Basics for Massage Therapists,” Massage & Bodywork magazine, July/August 2021, page 32, www.massageandbodyworkdigital.com/i/1384577-july-august-2021/34.           Resources:    Pocket Pathology: https://www.abmp.com/abmp-pocket-pathology-app   Çeçen, S. and Lafcı, D. (2021) ‘The effect of hand and foot massage on fatigue in hemodialysis patients: A randomized controlled trial', Complementary Therapies in Clinical Practice, 43, p. 101344. Available at: https://doi.org/10.1016/j.ctcp.2021.101344.   Dialysis: Types, How It Works, Procedure & Side Effects (no date). Available at: https://my.clevelandclinic.org/health/treatments/14618-dialysis (Accessed: 6 September 2023).   Diane Mastnardo, B.S. et al. (2016) ‘Intradialytic Massage for Leg Cramps Among Hemodialysis Patients: a Pilot Randomized Controlled Trial', International Journal of Therapeutic Massage & Bodywork: Research, Education, & Practice, 9(2), pp. 3–8. Available at: https://doi.org/10.3822/ijtmb.v9i2.305.   Habibzadeh, H. et al. (2020) ‘Effects of Foot Massage on Severity of Fatigue and Quality of Life in Hemodialysis Patients: A Randomized Controlled Trial', International Journal of Community Based Nursing and Midwifery, 8(2), pp. 92–102. Available at: https://doi.org/10.30476/IJCBNM.2020.81662.0.   Hemodialysis - NIDDK (no date) National Institute of Diabetes and Digestive and Kidney Diseases. Available at: https://www.niddk.nih.gov/health-information/kidney-disease/kidney-failure/hemodialysis (Accessed: 6 September 2023).   I have a person who is on dialysis 3 times per week requesting massage therapy. We are taught that it is contraindicated in school. Is it safe for a person receiving dialysis to receive massage? (2014) National Kidney Foundation. Available at: https://www.kidney.org/blog/ask-doctor/i-have-person-who-dialysis-3-times-week-requesting-massage-therapy-we-are-taught-it (Accessed: 6 September 2023).   Kidney disease and massage - Ask Our Experts / Dr. John Agar, Nephrologist (2012a) Home Dialysis Central. Available at: https://forums.homedialysis.org/t/kidney-disease-and-massage/2745 (Accessed: 6 September 2023).   Kidney disease and massage - Ask Our Experts / Dr. John Agar, Nephrologist (2012b) Home Dialysis Central. Available at: https://forums.homedialysis.org/t/kidney-disease-and-massage/2745 (Accessed: 6 September 2023).   Kidney Disease Statistics for the United States - NIDDK (no date) National Institute of Diabetes and Digestive and Kidney Diseases. Available at: https://www.niddk.nih.gov/health-information/health-statistics/kidney-disease (Accessed: 6 September 2023).   Lai, M.-Y. et al. (2006) ‘Fever with acute renal failure due to body massage-induced rhabdomyolysis', Nephrology Dialysis Transplantation, 21(1), pp. 233–234. Available at: https://doi.org/10.1093/ndt/gfi158.   Lazarus, E.R. et al. (2020) ‘The effects of an olive-oil massage on hemodialysis patients suffering from fatigue at a hemodialysis unit in southern India - a randomized controlled trial', Journal of Complementary & Integrative Medicine, 18(2), pp. 397–403. Available at: https://doi.org/10.1515/jcim-2019-0338.

Episode #69: with Jennifer Cramer-MillerYou know those articles and memes that are everywhere reprimanding us about what NOT to say to a friend who is going through a hard time of any kind? Jennifer is here today to say THE OPPOSITE of that. She's urging us to stop being afraid of saying the wrong things to friends with chronic illness, or friends dealing with anything else. Your friends will never say the perfect thing! WE will sometimes say the "wrong thing" to our friends. And I agree with Jennifer that we need to leave so much more room for people to say the imperfect thing and then let it go.Meet Jennifer Cramer-MillerJennifer is an author, speaker, and four-time kidney transplant recipient. Diagnosed with an incurable autoimmune disease at 22 and then experiencing the weight and relief of four transplants has given Jennifer a way of seeing life and the people in it that I could not wait to share with listeners.Jennifer's memoir, Incurable Optimist: Living with Illness and Chronic Hope  is available now where books are sold. She also has lots of essays all over the place but some examples—  Zibby Mag, Brevity,  Grown & Flown, Star Tribune, and Minnesota Physician— some of which were started in our ModernWell Writing Group! Find Jennifer on her website, and on Instagram, Twitter, and Facebook. A few links mentioned in the episode:The National Kidney Foundation for information on becoming a living donorThe Good Life: Lessons from the World's Longest Scientific Study of Happiness by Robert Waldinger M.D. and Marc Schulz Ph.D The guest spot I mentioned was on The Untitled Gen-X Podcast where we did a deep dive into Steel Magnolias Let's connect over all things friendship! Here's my Substack newsletter about friendship & more Dear Nina website with show notes and a guide to pitching yourself as a guest Instagram & TikTok Twitter JOIN the Dear Nina Facebook group Ask an anonymous question

Kidney failure is sometimes called a silent killer, since symptoms aren't noticeable until they're life threatening. About one in seven people have chronic kidney disease, or about 15 percent of Americans, and many of them don't know it.Treatments for kidney failure have improved — drugs, dialysis and kidney transplants are more successful than they used to be. But more than half of people who start dialysis still die within five years.MPR News host Angela Davis talks with a doctor about the need for prevention and early treatment, and a Minnesotan who lived through four kidney transplants.Guests Dr. Naim Issa is a nephrologist who treats people with kidney disease and kidney transplants at Mayo Clinic in Rochester, Minn. He's also an associate professor at Mayo Clinic School of Medicine.Jennifer Cramer-Miller has lived with kidney disease since her early 20s and has received four kidney transplants, including a kidney from her mother and from a 25-year-old anonymous donor. She serves as board chair of the National Kidney Foundation (serving Minnesota). She's just out with a new memoir, “Incurable Optimist: Living with Illness and Chronic Hope.”Subscribe to the MPR News with Angela Davis podcast on: Apple Podcasts, Google Podcasts, Spotify or RSS. Use the audio player above to listen to the full conversation.   

At the National Kidney Foundation, we believe that everyone who needs a kidney should get a kidney. To make this dream a reality, we've launched the Transplants for All Initiative. What is this initiative and how will it make a difference in the lives of people with kidney disease? In today's episode special guests Morgan Reid, NKF's Transplant Policy & Strategy Director and Haley Jenson, NKF's Transplant Programs Director explain this and more.   Morgan Reid Morgan Reid is the Director of Transplant Policy & Strategy for the National Kidney Foundation, implementing strategies and creating patient-centric policies that promote equitable kidney transplantation access. A kidney transplant recipient herself, with personal experience as a chronic kidney disease, kidney failure, and dialysis patient, she has a deep passion for improving organ donation and transplant processes.   Haley Jensen  Haley Jensen, MPH MBA, is Director of Transplant Programs for the National Kidney Foundation. She is responsible for leading growth and strategy for transplant educational programs, as well as overseeing organization-wide initiatives to ensure Transplants for All through research, innovation, awareness, and professional education. Haley is a kidney transplant recipient with years of volunteer advocacy and peer mentorship experience. She is passionate about ensuring every patient has the opportunity to receive the gift of life.   Additional resources:  Transplants for All Resources Transplants for All Blog    Do you have comments, questions, or suggestions? Email us at NKFpodcast@kidney.org. Also, make sure to rate and review us wherever you listen to podcasts.  

Philadelphia's music scene has produced some of the most notable acts in hip-hop and R&B. Case in point Freeway and Julian King. This year, Freeway is celebrating the 20th anniversary of his debut album: Philadelphia Freeway. He's also using his platform to better his life as a spokesperson and health ambassador for the National Kidney Foundation and the organization he founded, the Freedom Thinkers Academy. Next up, Julian King comes from the same institution, the High School for Creative & Performing Arts (CAPA), as some of your favorite musicians like Boyz II Men and Jazmin Sullivan. And today he has leaped to national stages such as John Legend's team on NBC's The Voice and writing and performing the theme song for the Emmy® Nominated film “All Boys Aren't Blue.” Freeway and Julian ARE Philly.