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Renal Health Disparities

2026-02-09T15:42:50-05:00February 9th, 2026|Categories: eNews, Quality of Life, Resources, Staying Healthy, Treatment, What Causes Kidney Disease|

The word “disparity” is defined as a difference in level or treatment, especially, one that is seen as unfair. No matter what race, creed, or color, all patients should be treated fairly and equally! Many patients cannot advocate for themselves—this can also be a problem/obstacle. This article focuses on information about renal health disparities. The DPC Education Center’s intention is to always be a valuable resource. The information below is retrieved from: Health Publishing, Harvard Medical School (health.harvard.edu). Many people are surprised to learn that kidney disease does not affect everyone equally. In Reno and across the United States, chronic kidney [...]

Habichuelas tiernas horneadas con parmesano

2026-01-09T14:36:10-05:00January 5th, 2026|Categories: Recipes, Spanish Materials, Staying Healthy, The Kidney Citizen|

Receta enviada por: JoEllen Ford, MS, RD, LDN Tiempo de preparación: 5 min Tiempo de cocción: 15 min Tiempo total: 20 min Porciones: 4 Ingredientes: 1 libra (aprox. 450 g) habichuelas tiernas (o judías verdes) frescas 2 cucharadas aceite de oliva 2 cucharadas queso parmesano rallado 2 cucharadas pan rallado japonés (panko) ¼ cucharadita sal ½ cucharadita ajo en polvo Instrucciones: Precaliente el horno a 400 °F (200 °C). En un tazón grande, mezcle todos los ingredientes hasta que las habichuelas tiernas (o judías verdes) estén bien cubiertas con el resto de los ingredientes. Distribuya las habichuelas o judías en [...]

2025 State Medigap Wins & 2026 Priorities

2026-01-09T14:31:53-05:00January 5th, 2026|Categories: Costs for Treatment, Dialysis, Kidney Transplant, Resources, The Kidney Citizen|

Elizabeth Lively, DPC Eastern Region Advocacy Director Pamela Zielske, DPC Western Region Advocacy Director DPC will continue to build on this momentum in the state Medigap arena in the 2026 legislative session. Our state advocacy directors are currently planning on advancing Medigap legislation in Georgia, Massachusetts, Michigan, Nebraska, Ohio, and Utah. How can you help? We are always looking for DPC Patient Ambassadors to share their stories by writing letters to legislators, testifying at committee hearings, and participating in Action Alerts that are emailed to our members. Building strong relationships with legislators through the legislative process [...]

Living Fully: My Journey with Peritoneal Dialysis

2026-01-09T14:20:35-05:00January 5th, 2026|Categories: Dialysis, In-Center Hemodialysis, Kidney Transplant, Peritoneal Dialysis, Quality of Life, Staying Healthy, Support, The Kidney Citizen, Treatment|

Dwan Dobson, DPC Patient Ambassador When I was first diagnosed with kidney failure in 2005, it felt like my life had been turned upside down overnight. One day I was working two jobs as a teacher and tutor at a detention center, and the next, I was in the hospital learning that my kidneys had stopped working. Like so many others, I didn’t know what to expect, but I was determined to stay positive and keep moving forward. At first, I began emergency dialysis through a chest port. Once I adjusted, I transitioned to peritoneal dialysis (PD) at [...]

Choosing the Right Path: My Journey with Home Hemodialysis

2026-01-09T14:01:19-05:00January 5th, 2026|Categories: Dialysis, Home Hemodialysis, In-Center Hemodialysis, Kidney Transplant, Quality of Life, Support, The Kidney Citizen, Treatment|

Amber Gardner, DPC Patient Ambassador When I was diagnosed with kidney failure in 2023, it came as a shock. I had gone to the doctor for high blood pressure, but soon learned that my kidneys were failing. Suddenly, I was faced with decisions that would affect every part of my life – which treatment option to choose, how to adjust my routine, and what this diagnosis meant for my future. With a background in journalism, research has always been second nature to me. I spent hours learning about dialysis – comparing hemodialysis (HD), done through the arm or [...]

Turning Trials into Triumph: A Journey with Kidney Disease

2026-01-09T13:48:41-05:00January 5th, 2026|Categories: Diagnosis of Kidney Disease, Dialysis, In-Center Hemodialysis, Kidney Transplant, Peritoneal Dialysis, Quality of Life, Support, The Kidney Citizen, Treatment, What Causes Kidney Disease|

Alethea Walls, DPC Board Member I've learned that living with kidney disease doesn't mean life stops - it just means you learn to live it differently. My journey with kidney disease began at just 14 years old. I was diagnosed with rapidly progressive glomerulonephritis (RPGN), and my life changed overnight. While most teenagers were navigating high school and part-time jobs, I was learning about my treatment options. I started with peritoneal dialysis, then transitioned to hemodialysis. Each option came with its own adjustments, but I wasn't going to let this stop me. As soon as I turned 16, [...]

Nocturnal Home Hemodialysis (HHD): Kidney Replacement Therapy with Less Impact on Daily Life

2026-01-09T13:23:02-05:00January 5th, 2026|Categories: Diagnosis of Kidney Disease, Dialysis, In-Center Hemodialysis, Kidney Transplant, Mental Health, Peritoneal Dialysis, Quality of Life, Support, The Kidney Citizen, Treatment, What Causes Kidney Disease|

Brigitte Schiller, MD, FACP, FASN, SVP, Medical Officer: Home Therapies, Global Medical Office, Medical Affairs, Fresenius Medical Care Important progress has been made in the delivery of dialysis. The “one size fits all” approach with standard thrice-weekly in-center hemodialysis shifts toward personalized care, emphasizing quality of life, independence, and symptom management tailored to each person’s clinical and personal needs. Kidney replacement therapy at home is a critical ingredient in this effort. While kidney transplantation remains the gold standard of end-stage kidney disease (ESKD), most people require dialysis before receiving a transplant. As patients await transplantation, selecting the appropriate [...]

Staying Hopeful Through the Wait

2026-01-09T13:12:47-05:00January 5th, 2026|Categories: Diagnosis of Kidney Disease, Dialysis, In-Center Hemodialysis, Kidney Transplant, Mental Health, Peritoneal Dialysis, Quality of Life, Support, The Kidney Citizen, Treatment, What Causes Kidney Disease|

Hasan Artharee, DPC Board Member Polycystic kidney disease (PKD) runs in my family. I watched my grandmother go through dialysis when I was young, and later my mother during my college years. So, when I was diagnosed with PKD at 22, I understood what the future might hold. The diagnosis came after my blood pressure kept rising and I needed medication. My doctors checked my kidneys and found that PKD was affecting my blood pressure and other systems. They told me that based on my family history, I'd probably need dialysis or a transplant by my 40s. For [...]

Finding My Path Through Treatment Options

2026-01-09T13:00:21-05:00January 5th, 2026|Categories: Dialysis, Home Hemodialysis, In-Center Hemodialysis, Kidney Transplant, Peritoneal Dialysis, Quality of Life, Support, The Kidney Citizen, Treatment|

Cheri Rodriguez Jones, DPC Board Secretary I was seven years old when doctors diagnosed me with a rare kidney disease. The 1980s and 90s didn't offer much in terms of treatment – just managing symptoms and preserving kidney function as long as possible. Hospital visits became routine. At 19, after some tests, my doctor called with surprising news: "You need to start dialysis." While unexpected, I'd always known dialysis was coming eventually. By then I was already a mother to my infant son. Discovering What Worked for Me The medical team recommended peritoneal dialysis so I could do [...]

DPC Advocacy Day 2025: When Patients Lead, Policy Listens

2025-10-10T15:58:59-04:00October 1st, 2025|Categories: Quality of Life, Resources, Staying Healthy, The Kidney Citizen, Treatment|

Yolonda Brisbane, DPC Grassroots Manager From July 12–15, 2025, the nation’s capital was infused with a powerful sense of purpose and unity as Dialysis Patient Citizens (DPC) welcomed 36 extraordinary Patient Ambassadors—dialysis patients, transplant recipients, and family members of those living with or lost to End Stage Renal Disease (ESRD)—to Washington, D.C. for our Annual Congressional Advocacy Day. Our time together began with preparation and purpose. Patient Ambassadors entered a space of belonging that offered state-of-the-art meeting rooms and delicious kidney-friendly meals—nourishing both body and spirit. This setting became the heart of meaningful conversations, new friendships, and genuine camaraderie. [...]

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