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Greetings from San Antonio Texas

2024-03-28T20:58:43-04:00December 17th, 2021|Categories: Dialysis, The Kidney Citizen|

By Natalie Zuniga, DPC Board Member, pictured here with her husband, Eddie Zuniga My name is Natalie Zuniga and I survived the 2021 Texas ice storm with my spouse, Eddie Zuniga, who is also a dialysis patient! I have been a dialysis patient for over three years and my husband has been a dialysis patient for eight years. At first, we thought it was a death sentence and we were not going to live much longer, and we gave up. But then, by hard work and education through Dialysis Patient Citizens and our nutritionist, Mary, we are now striving [...]

Travel Lovers, Don’t Let Dialysis Slow You Down

2024-03-28T20:58:46-04:00December 17th, 2021|Categories: Home Hemodialysis, Peritoneal Dialysis, Quality of Life, The Kidney Citizen, Treatment|

By Vanessa Evans, Sr. Manager, Patient Communities and Advocacy at Fresenius Medical Care North America and DPC Board Member Brenda and Bernie Alvey are the consummate camper travelers, crisscrossing the United States and taking in sights from the St. Louis Arch to the Grand Canyon. But their camper has a few unusual features, including two recliners, extra outlets, and a homemade stand to accommodate Brenda’s portable home hemodialysis equipment. The Alveys have always loved traveling, but they thought their trips had come to an end when Brenda was diagnosed with Membranoproliferative Glomerulonephritis (MPGN), an autoimmune disease that destroys kidney [...]

Improving Equity in Dialysis Treatments and Transplants

2024-03-28T20:58:50-04:00December 7th, 2021|Categories: Dialysis, eNews, Kidney Transplant, Treatment|

Earlier this month the U.S. Department of Health & Human Services (HHS) announced that it is seeking comments on future rulemaking to support the President’s executive orders to advance health equity and improve health outcomes for people in need of dialysis treatment and transplants. HHS Secretary, Xavier Becerra stated, “We want to hear from diverse stakeholders, especially the patients and their families. Your feedback is essential to our work in ensuring equal access to vital resources.” HHS acknowledged that both Black and Latino individuals are more likely to have kidney failure than white individuals in the United States (almost 4 times [...]

One Step Closer to a Wearable Artificial Kidney

2024-03-28T20:59:02-04:00August 11th, 2021|Categories: Dialysis, eNews, Home Hemodialysis|

For the past 20 years, Victor Gura, MD, FASN, an associate clinical professor of medicine at the Geffen School of Medicine at UCLA, has been working on a wearable artificial kidney, or WAK. Gura has been through multiple iterations - from prototype 1.0, which weighed over 200 pounds, to prototype 2.0, which weighed 11 pounds and was tested in clinical trials in Italy, London, and Seattle, to the latest version, WAK 3.0. Weighing in at just 2 pounds and powered by a rechargeable battery, WAK 3.0 was issued patent number 10,993,183 for a combination wearable and stationary dialysis system. The description [...]

Ask Your Nephrologist: What is happening to my skin and nails?

2024-03-28T20:59:08-04:00May 19th, 2021|Categories: Dialysis, Kidney Transplant, Physical Health, The Kidney Citizen|

Keith A. Bellovich, DO There is a broad range of skin manifestations when having to depend on dialysis. Skin disorders can affect a patient's quality of life and can negatively impact their mental and physical health. Itching (uremic pruritus) is by far the most common complaint that patients suffer. But dry skin (xerosis cutis) and skin discoloration are also common complaints in patient with severe loss of kidney function. Dry skin is caused by reduction in the size of sweat glands and atrophy of sebaceous or oil producing glands. Dry skin increases the susceptibility to infections and this is aggravated by [...]

There Is No Place Like Home

2024-03-28T20:59:12-04:00April 19th, 2021|Categories: Home Hemodialysis, Peritoneal Dialysis, The Kidney Citizen|

By Shaminder Gupta, MD, Nephrologist End Stage Renal Disease (ESRD) is a life changing diagnosis and impacts both the patient and the family. While waiting for renal transplantation, renal replacement therapy (RRT) is required to sustain life. RRT, also known as dialysis, can be provided either in-center or at home. Home therapies can either be via peritoneum (PD) or via fistula (HHD). Patients are concerned about their own abilities to provide this life sustaining therapy on their own. This is natural and should be anticipated as a barrier. Most of us, including medical professionals, would also share these apprehensions. Success at [...]

Participating in a Clinical Trial

2024-03-28T20:59:56-04:00August 21st, 2020|Categories: Additional Resources, Early Intervention, eNews, Home Hemodialysis, In-Center Hemodialysis, Kidney Transplant, Peritoneal Dialysis, Treatment, Webinar|

New medical treatments and products are continually being developed for people living with kidney disease. Part of the development process for high quality, scientific, and safe options is through research to test the treatment or product before it becomes available on the market. This phase of research is called a clinical trial or a clinical research project. People can volunteer to be part of a clinical trial if they meet the specific requirements for the study. You might consider participating in the research process for many reasons including if it has a personal meaning for you or if you want to [...]

Care Coordination Fixes One of the Biggest Flaws in the American Health Care System

2024-03-28T21:00:03-04:00July 6th, 2020|Categories: Diagnosis of Kidney Disease, In-Center Hemodialysis, The Kidney Citizen|Tags: , |

By Gloria Rohrer, DPC Patient Ambassador As a dialysis patient, it has become clear to me that one of the biggest flaws in the American health care system is the disjointed way care is often provided to patients. If patients have chronic conditions alongside other health complications, it can be exceedingly difficult to navigate the different doctors and hospitals we need in order to receive proper care. When seeing so many different doctors at various clinics and hospitals, patients like me can suffer adverse effects if all our treatments are not designed to address our full medical history, rather than a [...]

Reflections from 45 Years on Dialysis

2024-03-28T21:00:13-04:00May 2nd, 2020|Categories: Diagnosis of Kidney Disease, In-Center Hemodialysis, Pediatric Kidney Disease, The Kidney Citizen|Tags: , |

By Jack Reynolds, DPC Board Member I have survived on in-center hemodialysis for the last 45 years. I have also received Medicare for all those years to pay for most of my dialysis and other medical needs. I currently reside outside the village of Palmyra, Iowa. One of the first group of Patient Ambassadors to advocate in Washington, D.C. in 2005, I have visited Capitol Hill many times since. Because of the cost, time and effort it takes to keep a kidney patient healthy, I feel that it is important to be aware of issues and legislation that can impact our [...]

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