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

2026-06-17T17:24:42+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 [...]

Protecting dialysis patients

2026-06-18T15:57:39+00:00June 14th, 2026|Categories: Medigap Coverage, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Promote Financial Security|

My sister and I have polycystic kidney disease and shared the same dialysis schedule for years. I’ve been on dialysis nearly 15 years, surviving heart surgery and breast cancer before receiving a kidney transplant last October. My sister was not so lucky. After losing private insurance through divorce, she refused disability, believing she couldn’t survive on those benefits. Our family paid out of pocket to keep her on dialysis. By the time she got coverage, she had already started to give up. Her transplant failed. She passed away two years ago. When dialysis patients feel abandoned by the system, they [...]

Dialysis patients deserve protection

2026-06-17T17:20:57+00:00June 12th, 2026|Categories: Medigap Coverage, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Promote Financial Security|

During my final year of college, I nearly died. What began as abdominal pain, misdiagnosed and mistreated, spiraled into sepsis that was shutting down my organs one by one. By the time I reached the hospital, I needed four units of blood and four hours of emergency dialysis before I could even have surgery. I was a college student on my parents' private insurance with no clue what the next steps were. That diagnosis changed everything. But instead of letting it define me, it drove me. I finished my degree, continued working full-time and became an advocate for what I [...]

LETTER TO THE EDITOR: Congress must restore protections for dialysis patients

2026-06-18T15:58:33+00:00June 12th, 2026|Categories: Medigap Coverage, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Promote Financial Security|

My husband Greg was diagnosed with end-stage renal disease in 2006. He spent nearly seven years on dialysis before receiving a kidney transplant in 2013. For over a decade, that transplant gave him his life back. Then, in late 2023, complications from COVID caused his transplant to fail, and in October 2024, he returned to dialysis. The second time has been far harder — not because anything is different, but because we already know this fight is physically, emotionally and financially draining. When Greg was first diagnosed, we had private insurance. We received a letter warning us that we were [...]

Letter to the Editor: Kidney disease

2026-06-11T15:33:33+00:00June 10th, 2026|Categories: Increase Quality of Care, Innovation, Patient Ambassadors, Patient Stories in the News|

I was not looking for kidney disease when it found me. It surfaced during a routine pre-op workup for a completely unrelated procedure. After advocating for myself and pushing for a follow-up, I was diagnosed with chronic kidney disease in 2021. I am not on dialysis yet, but I know it’s not a question of if but when. That reality drives me to advocate. I have friends in the dialysis community living this right now, and I watch them navigate a system that too often fails to keep pace with the treatments that could help them. Innovations in kidney care, [...]

Letter to the editor: Act would restore safeguard for patients

2026-06-17T17:30:06+00:00June 10th, 2026|Categories: Medigap Coverage, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Promote Financial Security|

I have been on hemodialysis for four years. My grandmother was also on dialysis. I started just a year or two after she did. So when I say kidney disease runs in my family, I mean it in the most personal way possible. Dialysis is exhausting. You sit for four to five hours at a time, sometimes dealing with staff who aren't always sensitive to what patients are going through. I am also managing more than just kidney failure. I am a below-the-knee amputee facing a second amputation, and that exhaustion becomes almost unbearable. I started on employer-sponsored private insurance [...]

Kidney disease help

2026-06-09T15:27:45+00:00June 7th, 2026|Categories: Increase Quality of Care, Innovation, Patient Ambassadors, Patient Stories in the News|

In 2020, COVID-19 caused my kidneys to fail. I spent five months in the hospital, four of them on a ventilator, and my wife was called and told to consider pulling the plug and letting me go. I survived, spent two years on peritoneal dialysis, and eventually received a lifesaving kidney transplant in 2023. Living through kidney failure opened my eyes to the fact that too many people don't know what help and resources are available to them, and that's because no one tells them. That has to change, and so does the way we support patients while they're on [...]

Kidney disease is devastating. Congress can help ease journey

2026-06-08T15:52:35+00:00June 5th, 2026|Categories: Medigap Coverage, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Promote Financial Security|

I never knew I was sick. I went to the doctor’s office for a routine procedure, and the lab results sent me straight to the hospital. That was how I learned my kidneys were failing. There was no warning and no symptoms. I was working at AT&T at the time and had private insurance that carried me through. I received a kidney transplant. I was fortunate. My wife worked, and I had faith, family and friends. Not everyone has these luxuries. Now, because of a recent Supreme Court ruling, private insurers can push newly diagnosed dialysis patients off their coverage [...]

Throw kidney disease patients a lifeline

2026-06-02T20:08:18+00:00June 2nd, 2026|Categories: Increase Quality of Care, Innovation, Patient Ambassadors, Patient Stories in the News|

I learned I had polycystic kidney disease just before my wedding. What followed was 13 years of dialysis, the loss of my husband before he could donate his perfectly matched kidney, and years of fighting through grief, illness and uncertainty. Kidney disease affects entire families. In my case, because polycystic kidney disease is genetic, multiple relatives have faced dialysis. That’s why I became an advocate, a social worker and an educator. I’ve spent years writing books and hosting “The Lisa Baxter Show” to help patients understand how to care for themselves and navigate treatment. Patients need more than dialysis. They [...]

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