KidneyTalk - An Online Radio Show By Renal Support Network

Most people cannot imagine life on dialysis for even a year"Vanessa Evans has lived it for nearly three decades. Diagnosed at 12, she has seen it all: transplant, loss, in-center care, and home hemodialysis. But her story is not what you would expect. In this episode, she shares with Lori what really changed everything"and why she is now helping other people who have kidney failure choose a dialysis treament that works for them.

Eddie Z, is a talented musician and producer who has been the driving force behind some of Charlotte, North Carolinas most iconic music venues. But his conversation with Lori is more than just music talk. Eddie opens about his personal journey, sharing the challenges he has faced with kidney disease and the unexpected transformations that have reshaped his outlook on creativity and purpose. It is a story about hitting rock bottom and finding a new way to rise. Tune in to hear the pivotal moment that turned everything around for Eddie and what it took for him to come back stronger than ever.

In this two-part conversation, Lori Hartwell and nephrologist Jim McCabe, MD dig into one of the most challenging parts of hemodialysis: fluid management. Why is it still so difficult to get it right and what is missing that could make the patient experience better? As they explore the gaps patients face every treatment, a well-known but underused technology comes into focus raising a simple question: if better solutions exist, why arent we using them?

In this two-part conversation, Lori Hartwell and nephrologist Jim McCabe, MD dig into one of the most challenging parts of hemodialysis: fluid management. Why is it still so difficult to get it right and what is missing that could make the patient experience better? As they explore the gaps patients face every treatment, a well-known but underused technology comes into focus raising a simple question: if better solutions exist, why arent we using them?

Could your gut be quietly shaping the future of your kidney health? On this episode of Kidney Talk, host Lori Hartwell welcomes renowned kidney specialist Dr. Johnson and kidney disease survivor Bettye Mashack for a fascinating conversation about the overlooked link between gut health and kidney disease. From surprising science to real-life patient experiences, this conversation challenges conventional thinking and offers new hope for people at every stage of kidney disease. You may never think about probiotics, sugar, or good and bad bacteria the same way again.

Feeling tired and washed out? It could be more than fatigue. Lori Hartwell and Dr. Todd Minga, Vice-President of Clinical Research and Medical Affairs at Akebia Therapeutics uncover how anemia and kidney disease intertwine"and why understanding this hidden link could change how you manage your health.

On this episode of KidneyTalk, Lori Hartwell chats with Dr. Ken Sutha, a pediatric nephrologist who understands kidney disease in a way few doctors can"because he has lived it.

What if the key to freedom was not found in a cure, but in a choice? Ridishanae (Nae) Shaw shares how she redefined life, love, and independence in her kidney journey. Hear her story in the latest KidneyTalk® podcast episode.

On this episode of KidneyTalk, Lori Hartwell chats with Shelby McClure, whose kidney journey is anything but ordinary. Shelby has experienced nearly every form of dialysis"each with its own challenges, breakthroughs, and life lessons. From peritoneal dialysis in the quiet hours of the night to the self-discipline of home hemodialysis, Shelbys story is packed with unexpected turns, personal revelations, and a powerful transplant experience that changed everything "tune in to hear the full story.

In a joint interview, Krystal Bilodeau, a Home Therapies RN at FMCNA, and Brian Hutchinson, who is currently undergoing peritoneal dialysis, talk with Lori about fluid management, sodium intake, and dietary choices. Brian shares his personal experiences with treatment and reveals his familys favorite kidney-friendly meals. Meanwhile, Krystal explains the training process for peritoneal dialysis and outlines what it entails.

Living with kidney disease is not easy, but its a journey shared by many. In a compelling exchange between KidneyTalk® host Lori Hartwell and Jennifer Cramer Miller, author of Incurable Optimist: Living with Illness and Chronic Hope, striking parallels emerge in their respective multiple kidney transplant experiences. So, grab a seat, relax, and tune in to their engaging discussion as they delve into the art of cultivating optimism, drawing insights from their expertise on the subject.

In this episode of Kidney Talk, Lori welcomes Dr. Richard Johnson - renowned nephrologist, author of Comprehensive Clinical Nephrology, and a pioneer in kidney disease research. Together, they dive into the fascinating connection between gut health and chronic kidney disease, exploring how good bacteria can support kidney function. Dr. Johnson shares insights on probiotics like Renadyl, leaky gut syndrome, and how gut imbalances might impact people who are on dialysis or have elevated creatinine levels. This enlightening conversation uncovers why gut health matters more than we ever imagined.

In this episode, Lori talks with nephrologist Dr. Arun Malhotra about what inspired him to pursue nephrology and dives into an important discussion about the connection between chronic kidney disease (CKD) and high potassium, also known as hyperkalemia. They cover symptoms to watch for, the role of diet, how to manage potassium levels, and the importance of working closely with healthcare providers.

Austin Lees journey with kidney disease began before he was even born. Lori first met Austin when he traveled from DC as a teenager to attend the Renal Teen Prom. Overcoming anxiety and depression, Austin has transformed into a powerful advocate for others facing similar challenges. Tune in to discover how he turned adversity into empowerment and continues to inspire his peers.

Much like our host Lori, Michael Jiuliano faced the challenges of kidney disease from a young age. In a spirited and heartfelt conversation, they delve into their childhood experiences"navigating numerous treatments and hospital stays, and the impact these had on their relationships with peers. Listen in to learn how these early encounters not only shaped their lives but forged a resilience that continues to define them today.

In this podcast, Lori Hartwell chats with Dr. Paul Kimmel, a prominent nephrologist, to explore the valuable insights found in his book, The Bodys Keepers: A Social History of Kidney Failure and Its Treatments. Together, they examine the history of kidney disease, addressing the emotional challenges faced by patients, the significant advancements in treatment, and the continuing inequities in kidney care. This discussion underscores both the progress achieved in the field and the persistent gaps that remain, offering a thorough overview of how far we have come and the journey that still lies ahead.

Dr. Frita Fisher, who is triple board-certified in Nephrology, Internal Medicine, and Pediatrics, engages in a discussion with Lori Hartwell about the role of phosphorus and its impact on overall health. Join them as they explore what phosphorus is, why it is present in many foods, and why people with kidney disease are more likely to experience elevated phosphorus levels. They also cover the symptoms and health risks associated with high phosphorus levels, as well as both traditional and emerging treatment options to help maintain normal phosphorus levels for improved well-being.

Dialysis technicians serve on the front lines every day. Dwelyn Williams is president of the National Association of Nephrology Technicians/Technologists. He had his first experience with kidney disease at 16 years old when his mother needed dialysis. It inspired him to help care for not only his mother but for others who suffer from kidney failure. For 20 years, Dwelyn has remained dedicated to honing his skills, traveling where he is needed and learning how to best care for people. Listen in to hear about a day in the life of a dialysis technician. Who knows, maybe you will be inspired to become a professional technician in the renal field.

Have you ever encountered a financial or healthcare internet scam? Advocate Karol Franks and Lori discuss the latest trending scams, key signs to identify potential scams, what to do if you believe you have been a victim, and most importantly, tips to avoid becoming one.

Kidney disease is a chronic condition, in addition there are five stages. How you are going to feel from day to day and through each of the stages can have a negative impact your mental wellness. Felicia Speed, PhD, LMSW, VP of Social Work Services, Fresenius Kidney Care and Lori discuss coping strategies and other options that are available to help.

As we live longer thanks to technological advances, we reach years in age where we need more assistance. Many of us will need to take care of aging loved ones and may need to learn about, understand and deal with dementia and Alzheimer's. Jacqueline Marcell, author of Elder Rage - Take my father - Please, talked to Lori about the difficulties that come with taking care of aging parents. She shares her own experiences with love and humor and shares early warning signs to identify Alzheimer's, tips on how to take the car keys away and how to handle anger outbursts.

Barriers to innovation for people who are on dialysis is a hot issue. While Medicare is a great source of comfort and provides access to necessary treatments, it does face challenges with its existing payment structure that hinder access to new, innovative treatments. Dr. Jeffrey Silberzweig, a nephrologist, and Lori discuss recent breakthroughs and delve into the advantages and disadvantages of the current payment system, while also exploring potential solutions. This show promises to ignite a lively discussion on the impact of payment practices on innovation in kidney care.

Centers for Medicare and Medicaid Services (CMS) implements quality initiatives for Medicare beneficiaries on dialysis. CMS uses these measures to see how the dialysis facility is performing. Dawn Curtis, VP of Clinical Quality, Fresenius Medical Care and Lori discuss the measures dialysis clinics look at and how the kidney care team uses them as a benchmark to provide adequate care for people on dialysis.

Joy Araujo, a source of inspiration for her peers, has won the RSN annual essay contest on multiple occasions. Through her heartfelt and insightful essays, Joy has touched the hearts of readers, sharing her life experiences and imparting wisdom as only she can. Lori, too, has faced her own set of challenges growing up with kidney disease. Together, these seasoned warriors offer insights on how they have conquered kidney disease, how writing helps cope with emotions and the opportunity to gain valuable insights from these talented storytellers. Don't miss out on this exciting dialogue.

Home dialysis nurses educate their patients about how to safely do their treatments at home and overcome the barriers and fears associated with taking on their own care. Learn what the day is like for a nurse and why their job is so rewarding. Casey Shuler, RN, talks about what inspired her to pursue a career in the field of kidney care and why she is so passionate about it. You may just want to join her!

When caring for patients over the course of several years, nephrologists often get the opportunity to develop relationships with them. The experience is a lot like family, says Michael Kraus, MD, Associate Chief Medical Officer at Fresenius Kidney Care. Tune in as he talks with Lori about what attracted him to the rewarding career of kidney care. He will share the details of the typical workday of a nephrologist and offer insight into day-to-day responsibilities. He will also give advice to medical school students who may be interested in becoming nephrologists.

Jennifer McClung was diagnosed with kidney disease at a young age. After receiving a kidney transplant Jennifer started to put on extra weight and needed to make a change. She managed to lose the weight and along the way developed lifestyle changes to keep it off. Listen in to hear what worked for her and tips that can help make your own weight loss journey a success.

The journey of a single mom with kidney disease is a testament to unwavering determination as they navigate a career, medical appointments, treatments and the emotional toll, all the while nurturing and supporting their family. Mauricia Ambrose is a mother, a real estate investor and an author. Mauricia is also on peritoneal dialysis and shares how she gets things done, introduced her illness and treatment to her son and includes him in the process.

When you are in high school the list of things to worry about usually include getting good grades and getting the chance to talk to your crush, not kidney disease. Lori sits down with the RSN Administrative Coordinator, Isela King, who was diagnosed with IgA Nephropathy while in high school to talk about what it was like to be diagnosed at a young age, her experience volunteering at the Renal Teen Prom, and how her experience with RSN influenced both her educational and career path.

The inclusion of oral phosphate lowering drugs in the dialysis payment bundle starting in January 2025 is a significant change that has sparked debates and discussions within the kidney community. Lori and Jeffrey Silberzweig, MD delve into this topic along with a brief history and evolution of the bundled payment system. They discuss the pros and cons of this action and potential limitations on medication choices for patients. While bundling care encourages healthcare providers to consider overall value and efficiency in their treatment approaches it can prevent individualized treatment plans for delivery of patient care.

Lori and Cher, both kidney transplant recipients, have dealt with kidney disease for the majority of their lives. They also share a deep respect for the environment. Listen in to hear some tips, and what they have learned from their experiences with recycling medical and dialysis supplies and medications.

If itching is causing you discomfort or keeping you up a night, this show is for you! Itchy skin, medically referred to as pruritus, is a common and often distressing condition. The uncomfortable sensation can range from a mild annoyance to a severe, incessant itch, leading to scratching that may exacerbate the issue. Managing pruritus often involves identifying the underlying cause before finding a treatment that works. Listen in to hear Nidhi Sukul, MD and Lori discuss what might be the cause, questions to ask your doctor and a new treatment option.

Have you ever had a surprise medical bill? One where you do not even recognize the name of the doctor? The No Surprises Act is here to protect you. Patricia Kelmar, a consumer protection advocate, explains what you need to know about unexpected medical bills and steps you can take to protect yourself. Listen in to hear what to look out for, how to respond and who to call if you need help.

Music Producer, artist David Rush was diagnosed with kidney failure and doctors told him that he would need a kidney transplant or dialysis to survive. That is when he decided to take matters into his own hands and use his platform as a music artist and producer to raise awareness for kidney disease, home dialysis and organ donation. Rush teamed up with Pitbull to create a song called All Night which became a viral hit and helped raise awareness for kidney disease and organ donation. Today we learn more about his journey, his work and how he shares his experience with Lori of doing home dialysis while keeping up with a busy work and family schedule.

Making decisions about kidney failure treatment options can be daunting. Your lifestyle and other considerations play a huge part in the evaluation process. Where do you start? In this podcast, Lori and Dori Schatell, Executive Director at Medical Education Institute (MEI), discuss a new tool that can help you decide which treatment best suits your needs.

Deciding to be a living kidney donor comes with considerations like job stability and earning a paycheck, yet they shouldn™t be obstacles. Dr. John Gill, MS, shares how the American Society of Transplantations Living Donor Circle of Excellence can remove this barrier by educating companies on how they play a role in this decision. Their unique program paves the way for corporate discussions and pledges to support employees who choose to give the gift of life.

In this episode, Lori is joined by Dr. Meredith Stensland, Assistant Professor of Research in Psychology at The University of Texas Health Science at San Antonio. Dr. Stensland talks about her research on pet therapy in dialysis centers and the benefits that both patients and staff can experience with this service. Puppy love is contagious, so cuddle up with your furry friend and listen along!

People on dialysis spend a lot of time interacting with their social workers. These professionals are in the perfect position to help people learn more about kidney transplantation and the evaluation process at a transplant center. Anna Rutherford, MSW, a dialysis social worker, and Lori discuss what is involved and clue you in on things you may want and need to know.

Dawn Edwards is a 31-year kidney-disease survivor who has served her peers and the community as a mentor and educator for more than 25 years. Today she talks to Lori Hartwell, also a long-time kidney-disease survivor, about her journey from her diagnosis to the current day as she works toward undergoing a kidney transplant. Listen in to learn how kidney care has evolved and how both of these powerful women have learned to cope and thrive in spite of chronic kidney disease.

Nathan Gutierrez was born with the physical disability spina bifida. He has been restricted to a wheelchair since birth. The disease led to kidney failure to transplantation, yet he never let his disability interfere with his amazing accomplishments. He shares with Lori how he came to understand how his challenges are not who he is and how he has been able to live the life he was meant to live. Listen and be inspired to overcome your obstacles and live your best life.

Anyssa Dang authored the book so her younger brother could understand what he is going through. Kidneys for Kids helps kids who are diagnosed with kidney disease (and their siblings) understand what the doctors are telling them about their condition and helps them process their feelings. Listen in to learn how this book can empower children living with kidney disease diagnoses.

Dialysis social workers are the lifeline to those dealing with the emotional, financial, and transportation demands of kidney disease. Anna Rutherford, LMSW, is Senior Manager of Social Work Services at Fresenius Kidney Care. She is dedicated to helping her patients cope, adjust, and reach the goals they set for themselves to realize their best quality of life. Listen in as she talks about her role working in a dialysis clinic as she helps her patients thrive.

For everyone, food is the number one topic! What to eat? The renal diet is complicated, and it changes throughout the different stages of kidney disease. A renal dietitian can make a big difference to people who are either struggling with, or are new to a renal diet. Anne Moselle, MS, RD, CHWC, shares how she helps people get excited about the foods that can help them have good outcomes and maintain good health. Listen in to hear renal-recipe-adjustment tips for go-to dishes for people on dialysis. You will get hungry, and might even find yourself thinking about becoming a renal dietitian!

Thirty years ago, John Larsen entered the dialysis healthcare field and never looked back. As a Patient Care Technician (PCT), John lives on the front lines at the dialysis clinic where he works. From start to finish, PCTs play an essential role at dialysis treatment centers. They spend a great deal of quality time with their patients and have a unique opportunity to develop special relationships with them. Listen in to what motivates John and keeps him engaged in his rewarding career.

For Molly Reehl, CDN, working as a technician was the first step in a career in dialysis. She loved caring for patients and felt valued by them, and she wanted to provide them with more care. To fulfill her dream to become a dialysis nurse, Molly worked full-time while attending school and raising a family. She remains passionate about providing care for patients, and her future has no limits. Listen in to hear Mollys inspiring story. We are so grateful for her dedication.

Discussion about transplants and urinary tract infections.

Lori and Dr. Kam Kalantar-Zadeh, Professor of Medicine and Public Health at UC Irvine School of Medicine, discuss each stage and what you can to help delay the progression of the illness.

Listen in as Edmund Lawler, a journalism teacher and author, tells Lori the story of one extraordinary visionary in the world of medical science. More than seven decades ago, Edmunds great uncle, Dr. Richard Lawler, reached beyond the science of his time to perform the first human kidney transplant ever in this country. It was June 17, 1950, when Dr. Lawler performed the groundbreaking surgery. Learn why the doctor™s effort was criticized, the outcome of the transplant and how the medical community reacted.

Does thinking about dinner make you want to turn and run to the nearest greasy spoon? Lori and Caitlin Harris, RD, know cooking can be daunting when you have kidney disease. Let them give you the scoop on how they make cooking fun, fast and fabulous! Their joy is contagious as they share how making even small changes in how you think about food can mean big payoffs for your taste buds and your health too! Listen in, and soon you will be on your way to serving up some of their favorite renal-friendly recipes.

When you have kidney disease people who stay ahead of the game do the best. At any given time, close to 40 percent of people on the UNOS kidney transplant list are inactive. Lori and Lazaro Cherem, MD, discuss why patients become inactive and what you need to do to make sure your status is current, so you do not miss a kidney offer. A kidney transplant is not a cure and requires ongoing monitoring to ensure the kidneys health, so you never have to end up back on the transplant list. Listen to a robust conversation about the advanced testing options that are now available, and what direction doctors need to look at to avoid potential problems that may jeopardize your future health.

Germs seize every opportunity to invade your body. The infections that follow can endanger your life, especially if you have kidney disease. Bloodstream Infections are one of the leading causes of death for people on dialysis. Listen in as Lori and Crystal Grate, RN, CNN, Director of Infection Prevention at Fresenius Medical Care, discuss the warning signs and what actions to take if you suspect you have an infection.

People on dialysis sometimes require rehabilitation in a skilled nursing home as they recuperate from surgery, medical emergencies or are unable to care for themselves. When this happens, they have to travel from their nursing facility to a dialysis clinic which can interrupt their recovery. Lori and Alice Hellebrand, RN, Chief Nursing Officer at Dialyze Direct, discuss the option of dialyzing in a skilled nursing facility with trained personnel. Learn how this benefits all people involved and reduces the burden of having to be transported to receive lifesaving care.

When you are an infant, the last thing you need is a new heart. But that is exactly what Trent Sullivan, aka, Sully, needed when he was just 5 months old. He got one, but it would not be his only transplant. At age 18, he needed a new kidney, as well. Lori sits down with this Walking Miracle to find out what kept him going throughout his early years and what he does now to enjoy the life he was given.

It is important to incentivize new therapies so companies will invest and bring products to market. Kathy Lester, JD, MPH, talks with Lori about how Medicare is working to create policies to spark innovation. About 90 percent of people on dialysis have access to Medicare. But ESRD treatment options only become available when payment is available to support them. When funding is not available, new innovations, even those approved by the FDA, will not become available to patients. Tune in to learn what you can do to ensure we have access to new therapies and medical equipment in the future.

Walk into a store this time of year and you can bet you will see the glittering holiday dcor on display. But how long will you have to search to find the gifts that your friends with kidney disease will truly appreciate? Sit back and relax as your personal shopping guides Lori Hartwell and Cher Thomas discuss what items they would like to see wrapped up this holiday season just waiting to please those special people in your life.

Should you change your diet when you are first diagnosed with any early stage of kidney disease? What foods can contribute to kidney disease or help maintain your existing kidney function? How can understanding your lab values help? Registered dietitian Beth Shanaman and nutrition and fitness manager Katy Wilkens, MS, RD, share insights into these issues and their diet recommendations when you are diagnosed with kidney disease.

Elizabeth Barnett is a partner and public policy expert for Avenue Solutions. She represents Kidney Care Partners, an advocacy coalition dedicated to improving care for people who have kidney disease. Elizabeth discusses with Lori the CKD Improvement and Treatment Act of 2021 S1971/HR 4065 that was introduced last year by both the House and the Senate. Listen in to learn how the bill will improve innovations and the quality of care for those with kidney disease.

For Gail Dewald, RN, CNN, passion for her work is evident as she explains a day in her life as a nephrology nurse working with people who have kidney disease. Many things have changed throughout her career, but her dedication to those with kidney disease remains the same. Listen in to hear about innovations in kidney care and the insight she has gained during her 30-plus years in the field.

Do you know what to do when disaster strikes? Depending on the damage your community sustains, your local dialysis clinic can be closed for a day or two to a couple of months. You have a lot of support available around you, but do you know who to call for help? Listen in as Bob Loeper, Vice President of Disaster Response Fresenius Medical Care, North America, shares what patients and caregivers can do to be prepared and ensure that the needs of people who require dialysis to live are met.

Jessica Frysz is a young woman who has beat a lifetime of odds. She has learned to flourish despite having dealt with kidney disease since she was a baby. While on dialysis for 28 years and having a kidney transplant, Jessica focused on her ambitions and dreams. Listen in to be inspired by this courageous young woman.

George Franklin III is president of the Transplant Quarter Century Club and a contributing writer of Because of Organ Donation, a book by Brenda E. Cortez. George had a kidney transplant more than 45 years ago. Listen in to learn his secret for keeping his gift of life healthy and strong.

Dr. Victor Gura is an associate clinical professor of medicine at the Geffen School of Medicine at UCLA. He and his company, Wearable Artificial Organs, Inc., were issued a patent for "combination wearable and stationary dialysis systems." Dr. Gura has worked 21 years in Italy and London, and finally in the United States to develop the devices. Initial clinical trials have already been conducted in Seattle, Washington. Tune in to this show to learn about the results of the trials and what the next steps are to make this invention a reality.

Kidney disease is difficult enough without suffering needlessly. Many over-the-counter medications are harmful to the kidneys. What can you do to take control of pain without causing more damage? If you, or someone you know has kidney disease, it is especially important to be in the know about options to relieve pain. Lori and nephrologist Dr. Mary J. Godinich discuss the side effects of medications and the differences between over-the-counter pain relievers and some safe alternatives.

Getting listed for a kidney transplant can be a daunting process. Do you know your dialysis social worker can help with the process and prepare you for what is to come? Felicia Speed, Vice President of Social Work Services for Fresenius Kidney Care, shares tips to help you prepare for your kidney transplant. Listen in to learn how to overcome difficulties and barriers.

Tricia McCarley, a nurse practitioner with Fresenius Kidney Care, sits down with Lori to discuss dialysis lab values and why you should care. Listen in to learn what the different tests show, how your own body processes may affect the results, and which lab values you may be able to control.

Innovations in treating kidney disease were just beginning when Dr. Steven Rosansky, aka Dr. Ro, a nephrology specialist in Columbia, SC, first started his practice. He was drawn to this medical specialty because it gave him the opportunity to really do something to help his patients. In this interview, Lori and Dr. Ro put a kidney disease diagnosis into perspective. Listen in to learn the differences between each of the five stages of kidney disease, plus what you might be able to do to slow the progression of the disease and preserve more of your own kidney function.

What is artificial intelligence (AI), and does it apply to kidney care? Dr. George Aronoff, Chief Medical Officer and Co-inventor at Dosis, has over 30 years of experience in nephrology. He explains how AI-based anemia medication dosing is personalized and precisely based on the patients own demonstrated response. This can potentially lead to maintaining or improving a patients outcome. Be in the know about AI and take part in your anemia management.

Calciphylaxis is a bone and mineral condition that can occur in people who have kidney disease or are on dialysis. Kidneys regulate many things including minerals which can cause the buildup of calcium causing painful wounds that are very susceptible to infections. Dr. Smeeta Sinha and Dr. Sagar Nigwekar explain the warning signs of calciphylaxis, ways to manage phosphorus and what treatments are currently available. Listen in to this show to learn more and about a new clinical trial to find an alternative therapy for calciphylaxis.

Art therapy has been shown to be an effective way to help children and their families cope with having a chronic illness such as kidney disease. It helps to ease the mental and emotional stress that often accompanies their battle with illness. Plus, it allows them to forget about the pain, even for a while, and just relax. Board Certified Art Therapists Raja Aossey and Kathy Peal explain the process, its benefits and how parents can connect with an art therapist or child life specialist for their child.

The Comprehensive Immunosuppressive Drug Coverage for Kidney Transplant Patients Act that passed in congress in 2020 extends Medicare coverage for anti-rejection drugs from 36 months to the life of the transplant. Troy Zimmerman, Special Projects Director, National Kidney Foundation worked closely with congress to bring this bill to fruition. He explains the details of the bill, when it goes into effect and who will benefit by the new law.

There is an APP for everything. And luckily, there is one to help monitor what is needed to keep your transplanted kidney healthy. Transplant surgeon Dr. David Axelrod is the Kidney, Pancreas, Living Donor Transplant Surgical Director at the University of Iowa. He explains how to get the most from using the APP for post-transplant care. Listen in to learn how to do your part to keep your kidney healthy.

Kidney transplant recipients deal with taking anti-rejection meds for life. Talaris is developing an alternative to immunosuppression. Nancy Krieger, MD, Talaris Therapeutics Chief Medical Officer, explains how this new treatment will work and how it differs from what is currently prescribed. She also talks about how you can learn more about the clinical trials that are available.

Beth Witten, LCSW is an expert in insurance issues. She shares with Lori the basics of Medicare, what is covered and how to save money on drug prescriptions. Listen in to hear answers the most common questions people who have kidney disease have about navigating the complicated process. You don™t want to miss this show.

VidaFuel CEO Bette Parolini and her team envisioned how the gratifying experience of snacking equals the importance of nutrition. The result is delicious! VidaFuel™s innovative snacks for the renal diet include both sweet and savory options. Products also include tasty protein drinks. Things are just getting started, so expect more treats and flavors soon. If you are on dialysis and love chocolate or potato chips, or need a tasty protein supplement, don™t miss this show.

Wendy Rodgers, M.Ed, MPH, and RSN Chairman of the Board, is a kidney transplant recipient and lupus survivor. Lupus is a systemic autoimmune disease that assaults healthy tissues and organs. Males are less likely to develop the disease, but they often experience more severe symptoms. And symptoms may vary because lupus can affect different parts of the body. Listen in to learn about the symptoms and the causes of lupus, and the treatment innovations that are on the horizon.

Michelle Pace, RN, a kidney care advocate manager at Fresenius Kidney Care, will talk about the benefits of transitioning from in-center to home dialysis. Listen in as she explains the options that exist, and how they can add more freedom and flexibility to your diet and lifestyle.

Do you know the difference between a bacterial infection and a virus? Are you aware of the different symptoms of each one? And do you know when an illness is contagious? These are important distinctions that determine the precautions anyone should take to avoid contracting an illness or passing it along to others. Listen in as Michael Kraus, MD, Associate Chief Medical Officer at Fresenius Kidney Care and Lori Hartwell discuss the good bacteria, the bad bacteria, and the ugly virus.

Assessing your kidney transplant health and making sure you keep that organ as long as possible is essential. Transplant Nephrologist Dr. Philippe Gauthier and Lori Hartwell discuss the evaluation of how doctors determine kidney rejection. Innovations in monitoring are now available that can help doctors prevent rejection so you can maintain the gift of life.

John Butler, President and CEO of Akebia, has been involved in the field of kidney health since 1991, and has seen many innovations. He is also the elected Chair of Kidney Care Partners, the largest kidney care coalition in the nation comprised of patient advocates, dialysis professionals, care providers, researchers, and manufacturers. John feels a personal connection to the kidney community. His purpose-driven mission is to better the lives of all people impacted by kidney disease. Listen in to learn about the current innovations in kidney disease treatments and what is on the horizon.

At age 10, Valen Keefer was diagnosed with polycystic kidney disease. By age 18, after spending a year in the hospital, she needed a kidney transplant. As if that was not enough, in 2016, Valens chronic sepsis led to her need for a liver transplant. Now in her 30s, Valen shares her inspiring story of survival navigating many health hurdles.

How do you go about finding a living kidney donor? Karol Franks began her journey with advocating for a kidney for her daughter in the late 1990s. She provides insight in to what is involved in searching for a kidney and ways to get started. She shares with Lori what is involved and the steps needed to start the process of kidney donation.

How has Covid-19 affected organ procurement organizations (OPOs)? Are kidney transplantations and donations still taking place? Today, Lori talks with Kristine Neal, Director of Communications for South Carolinas OPO, We Are Sharing Hope SC. Listen in to this show to learn how the pandemic has altered the experiences of transplant recipients and prospective donors, and learn what OPOs are doing to help ensure the Gift of Life continues.

It is a given that anyone with a weakened immune system is more vulnerable to the Covid-19 virus than the general public. If you are waiting for a kidney transplant, or have had one, you will want to listen to this informative podcast. Lori, and transplant nephrologist Dr. Rafael Villicana, Medical Director of the Loma Linda Transplant Center, have a candid conversation on what you can expect and do to protect yourself during the Covid-19 pandemic.

RSN and Lori Hartwells good friend Stacy Hoblitzell takes over the helm of the KidneyTalk Podcast show today for an intriguing look into the life and inspirational kidney disease journey of RSN founder and President Lori Hartwell.

In this time of Covid-19, healthcare professionals are very stressed, and both staff and people who require dialysis care need to be supportive of one another. To increase the supply of comfort and empathy, the executive committee of the Coalition for Supportive Care of Kidney Patients is working to get the right words to dialysis clinic personnel. Listen in to this show to learn coping mechanisms at this critical juncture to help alleviate anxiety.

Now more than ever it is important to avoid a hospital stay. Some hospitals are already at or near capacity and many are concerned about shortages ahead of expected coronavirus cases. You can help yourself and your local healthcare system by making sure that you remain as healthy as possible. Learn about the most common causes of hospitalization in people requiring dialysis and what to do to stay safe.

Jennifer Parker, RDN, CSR, LDN, is the Lead Dietitian at Fresenius Kidney Care. Today we learn from her about the new renal diet guidelines that are soon to be released. Jennifer and Lori discuss how you can stick to your recommended diet and still enjoy meals. Listen in to this show to find out what is back on the "good" list, and more.

Tim Atkins grew up with kidney disease. His 41 years on dialysis has not stopped Tim from visualizing his dreams and passionately pursuing them. His adventurous lifestyle, while on home dialysis, has taken him to many places. While enjoying a career in broadcast radio, Tim lived in the Virgin Islands and traveled across the U.S. in an RV with his dialysis machine in tow. Listen in to hear why home hemodialysis works so well for Tim, as he shares his tips to success for living the dream.

People who need dialysis often spend so much time at a clinic that they, and the staff, view each other as friends instead of maintaining a professional relationship. Eileen Rhodes, Patient Services Director at the ESRD Network 18, shares why this can lead to crossing important boundaries. Maintaining a high level of care requires everyone to stay on the same page and understand the boundaries of a patient/staff relationship. Lori and Eileen discuss this topic in detail and offer tips for everyone in a clinical setting to remember. Tune in to learn how to advocate for yourself, as a patient in these situations and, if necessary, start resolving these issues.

Lisa Summers met Dan, on an online dating site and soon discovered she was in fact a perfect match for him. Dan learned that he had kidney disease and would need to start dialysis treatments. Lisa educated herself about kidney disease, and would go on to become health advocate for Dan, and so much more. Listen in to hear about her journey through the process, including giving the gift of life.

Robin Russell, MS, RD, LD, is the Fresenius Regional Lead Dietitian at North Texas Region, Great Plains Group. Today she talks with Lori about all-things sodium. People who are on dialysis know the struggles of controlling thirst and managing fluid. Sodium intake has a lot to do with successfully keeping thirst at bay. Robin shares with Lori the difference between table salt, monosodium glutamate (MSG) and all the many other ingredients you will find in food. Listen in to learn all of this, plus some sodium free alternatives.

Holidays can be challenging for those with kidney disease. Watching portion sizes and indulging in tempting treats in moderation is key. But so is keeping a focus on the enjoyable foods that are within the renal diet instead of thinking about the foods to be avoided. Lori and Lubna will discuss some delicious main course choices and sides that satisfy special dietary needs such as stuffing a turkey with apples and serving brie as a lower phosphorus cheese option. Listen in to learn all this and more and enjoy those holiday parties and meals!

Americas Got Talent superstar Angelica Hale says, "Never give up and keep on dreaming. Keep on believing in yourself. No matter what you are going through, you can still achieve your dreams and reach your goals." Angelica faced several challenges as a toddler and had a kidney transplant at the age of four. She went on to win runner up in the 12th season of Americas Got Talent five years later. Like Lori Hartwell, Angelica overcame so much at a young age and yet came out on top. Listen in to hear her incredible story, and learn how she remembers to take her transplant meds and copes with life after a transplant. And dont miss her exciting plans for the future!

Anyone who receives a kidney transplant has an important role to play to prevent their body from rejecting the new organ. What can you do to increase the life expectancy of your new kidney? Dr. Stanley C. Jordan is the Director of Nephrology and Transplant Immunology at Cedars-Sinai Medical Center and a pioneering kidney transplant researcher. Lori has known him since her childhood. From the beginning of his career, he was fascinated by immunology research and wanted to understand how it could be applied to problems with transplant rejection. In this episode of KidneyTalk, Dr. Jordan delves deeply into the role of antibodies"how they affect who is able to receive a transplant and how long that kidney can remain healthy. Dr. Jordan shares with Lori what transplant recipients must do to keep their new kidney healthy. Listen in to hear about new immunology therapy and the treatment advances that can prevent transplant rejection and help people keep their gift of life.

As someone who has had kidney disease since age 2 back in 1968, Lori Hartwell has witnessed many exciting medical breakthroughs throughout her life. Today she speaks with Geoffrey Block, MD, vice president, nephrology, at Reata Pharmaceuticals, about some of those breakthroughs. Dr. Block is part of a team researching a new, regenerative medicine to improve kidney function in those with rare forms of kidney disease such as Alport Syndrome, autosomal dominant polycystic kidney disease (ADPKD), and focal segmental glomerulosclerosis (FSGS). Listen in to this show to hear the encouraging results of the team™s published clinical research.

Dr. Rafael Villicana, medical director of kidney transplants at Loma Linda Medical Center, and Lori Hartwell, are both well-acquainted with the kidney transplant process. Listen in to this show to learn about how to become listed to receive a kidney transplant. During the interview, Lori and Dr. Villicana will talk about the requirements and timelines for both living and deceased donor transplants and walk you through the process of getting the tests they require. You™ll also hear about scenarios that may prevent you from becoming listed.

Nephrology nursing is a unique specialty. Because kidney failure requires a great deal of maintenance, nephrology nurses really get to know their patients and often have long-term relationships with them. They learn each patients specific needs and unique indicators for when they do not feel well or are out of sorts, or when they are doing well and should keep up the good work. Tamara Kear, PhD, RN, CNS, CNN has over 30 years of experience as a nephrology nurse and has held a variety of roles within this specialty. In 2020, she will become the Executive Director of the American Association of Nephrology Nurses to help lead the future. Today Lori and Tamara discuss the role of the nephrology nurse and why Lori Hartwell admires and appreciates all they do. Nephrology Nurses week is Sept. 8 " 15, 2019. We would like to say thank you for choosing this career and for making a difference in so many lives.

Everyone has a book in them, so how do you get it out? Adversity introduces you to yourself and everybody has a unique perspective. Especially when you have experienced a life contending with a chronic illness. Your distinctive point of wisdom can help someone else struggling to live a fulfilling life with the same illness. But where do you start? Henriette Ivanans and Lori Hartwell each have a successful book under their belts. Listen to these two accomplished authors for tips on how to tell your story and reach those who need to hear it.

A beloved animal is your best friend. To hear a doctor say you have to give up your pet in order to get a kidney transplant is a nightmare. There are mixed messages in the healthcare community about having a pet and receiving a kidney transplant. Dr. Rafael Villicana, the Kidney Transplant Medical Director of Loma Linda Medical Center and Lori Hartwell discuss the general precautions to take to keep your furry and feathered friends and prevent the risk of infection. Learn what you need to do and which animals need an extra level of care so transplant recipients can stay healthy.