Dialysis Act would give patients more stability, options

2026-08-28T15:32:07+00:00August 28th, 2026|Categories: Medigap Coverage, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Promote Financial Security|

I was first diagnosed with kidney failure in 2005 and immediately started emergency dialysis. It was a shock, but I wasn’t about to let it stop me. I began peritoneal dialysis (PD) at home so I could keep working as a teacher and a detention center tutor. Even while managing treatment, I continued to show up for my students every day. After a successful kidney transplant in 2015, I got almost ten years of freedom from dialysis. But when my transplanted kidney began to fail again in 2023, I returned to PD late last year. I’m back on the transplant [...]

Lifesaving

2026-08-27T17:57:20+00:00August 27th, 2026|Categories: Medigap Coverage, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Promote Financial Security|

A recent Supreme Court decision allows private insurers to push new dialysis patients — those who take a frequent treatment for kidney failure to survive — off their plans they’ve worked hard to keep. It’s a direct assault on the lives of dialysis patients across America. Forcing patients off their private insurance immediately after diagnosis — often within months — is unjust. I’ve lived on dialysis for over four years, endured the pain of needles tearing through my skin twice daily, and fought to keep my dignity in a system that often prioritizes profits over people. I’ve been lucky; I [...]

DPC Patient Ambassador Spotlight – Pesh Patel

2026-08-26T15:06:40+00:00August 26th, 2026|Categories: Featured Spotlight, Get Involved, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Spotlight|

Check out our Patient Ambassador Spotlight, where we highlight members who elevate the voices of people with kidney disease. This month’s Spotlight is on Pesh Patel from Lafayette, New Orleans. In 2017, while working in Melbourne, Australia, Pesh became unable to walk three city blocks without stopping to catch his breath. He was rushed to the hospital, where he found out that one of his kidneys had never fully developed, and the other was only 2% functional. Pesh then spent 15 months on hemodialysis before receiving a transplant in 2018. Two and a half years later though, his body rejected [...]

A better life

2026-07-28T19:55:09+00:00July 19th, 2026|Categories: Increase Quality of Care, Innovation, Patient Ambassadors, Patient Stories in the News|

I was 16 when I started dialysis. I spent 17.5 years in treatment before receiving a transplant nearly 10 years ago. But a transplant isn’t a cure — it’s another type of treatment for my kidney failure, one that still requires lifelong medications, labs and procedures. Even with coverage, I’ve seen how hard it can be for patients to access treatments they need. Too many people I’ve met on this journey, including those in my local kidney support group, struggle to get therapies that could improve their quality of life, like treatments for pruritus, anemia, phosphorous control or infection prevention. [...]

Congress must support innovation for dialysis patients

2026-07-23T15:57:23+00:00July 18th, 2026|Categories: Increase Quality of Care, Innovation, Patient Ambassadors, Patient Stories in the News|

Editor: I spent seven years on dialysis — the only treatment outside of a transplant for kidney failure — before receiving a kidney transplant in 2023. Every day I spent hooked up to that machine was a reminder of how fragile life becomes when your kidneys fail. Before my diagnosis, I was healthy; I was an athlete and musician. But after my diagnosis, I lost my job and my employer insurance with it. Bills piled up fast. It wasn’t until a social worker helped me apply for Medicare and Medicaid that I got the coverage I needed .But I know [...]

DPC Patient Ambassador Spotlight – Adrian Ropp

2026-08-26T15:04:19+00:00July 14th, 2026|Categories: Get Involved, Increase Quality of Care, Innovation, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Spotlight|

Check out our Patient Ambassador Spotlight, where we highlight members who elevate the voices of people with kidney disease. This month’s Spotlight is on Adrian Ropp from Draper, Utah. Originally from Blackfoot, Idaho, Adrian was diagnosed with kidney failure in 2022 and his life changed drastically. So, it was no small feat that on the third anniversary of receiving his kidney transplant, Adrian was on Capitol Hill, advocating with his fellow patient ambassadors for Dialysis Patient Citizens’ 2026 Annual Advocacy Day. When Adrian went on dialysis in 2022, he quickly made friends with many fellow patients and saw firsthand how [...]

Support Kidney Care Access Protection Act

2026-07-14T16:51:30+00:00July 1st, 2026|Categories: Increase Quality of Care, Innovation, Patient Ambassadors, Patient Stories in the News|

To the editor: Kidney failure changed everything for me. I was already grieving the loss of my husband, daughter, and grandson when I learned my high blood pressure and diabetes had gone unchecked for years, leading to total kidney failure. Within weeks, I had to start dialysis. The first day, I sat in my car and cried. I wasn’t just scared for my health, I was terrified of the financial toll. I now rely on Medicare and Medicaid, but even then, I have to pay out of pocket for critical medications and vitamins. I want to work, but I can’t. [...]

Congress must strengthen Medicare for dialysis patients

2026-07-14T16:46:55+00:00June 30th, 2026|Categories: Increase Quality of Care, Innovation, Patient Ambassadors, Patient Stories in the News|

Editor: I was on dialysis — a treatment that kept me alive while my kidneys failed — for five years before receiving a kidney transplant. I was fortunate to keep private insurance for the first 30 months and then transition to Medicare along with New York’s supplemental coverage. Medicare’s approach to dialysis care falls short. There was little change in the treatments I received over the years. I, and many others like me, lacked access to innovative treatments that help control phosphorus, prevent itchy skin, manage anemia, and prevent potentially fatal infections. That’s because Medicare reimbursement for new drugs and [...]

Letters: Bill in Congress would help dialysis patients

2026-06-18T16:02:06+00:00June 17th, 2026|Categories: Medigap Coverage, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Promote Financial Security|

In 2017, while working in Melbourne, Australia, I became unable to walk three city blocks without stopping to catch my breath. Within hours of reaching the ER, I’d had two blood transfusions and was in the ICU. I found out one kidney had never fully developed, and the other was only 2% functional. I spent 15 months on hemodialysis before receiving a transplant in 2018. Two and a half years later, my body rejected it. In August 2024, I was back on dialysis. One in 3 Americans is at risk for kidney disease. That’s not a statistic lawmakers can afford [...]

New dialysis patients deserve continued coverage

2026-07-17T14:39:27+00:00June 15th, 2026|Categories: Medigap Coverage, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Promote Financial Security|

I was first diagnosed with kidney disease in 2001, shortly after the birth of my second daughter. What doctors thought was pregnancy-related high blood pressure turned out to be the start of kidney failure. For years, I tried to push forward, working full time and raising my girls, until my health declined sharply in 2010, and I went into a hypertensive crisis. I started peritoneal dialysis in 2011, which allowed me to keep working for a time. But, when I eventually had to switch to hemodialysis, the treatment completely drained me. My work hours dropped from full time to part [...]

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