Dialysis Patient Citizens News
Letter: Dialysis patients need Congress’ help
As a leader in the Kidney Foundation of Central Pennsylvania, I see how much financial concerns weigh on the hearts of kidney patients. People become overwhelmed by the out-of-pocket costs of dialysis treatment, and that stress can become too much, worsening health outcomes. We need to make it easier for dialysis patients to pay for treatment. They have productive lives to live – they just need the tools to live them. Private insurance is often a golden ticket for dialysis patients, helping cover most, if not all, [...]
Letter: Protect NH dialysis patients
Protect dialysis access To the Editor: All dialysis patients are required to have Medicare as their primary insurer after 30 months from when they start dialysis, but the law has always allowed us to keep our private insurance until then if we wanted. Now, a Supreme Court decision from 2022 may allow private insurers to reduce coverage of many life-saving dialysis services. Keeping coverage after starting dialysis provides stability during a very difficult time. After this ruling, dialysis patients may have to worry about the hassle of [...]
Letter: Give dialysis patients a hand
Dear editor, My father, Bill Robinson, passed away 10 years ago from complications related to End Stage Renal Disease (ESRD). Yet, he lived a relatively full, healthy and active life. Dialysis allowed him to continue living and working for 10 years. As his primary caretaker, I saw firsthand the problems afflicting kidney patients. I witnessed many patients struggling to pay for life-saving treatment, which can cost hundreds of thousands of dollars per year. Luckily, my father had private health insurance to cover the costs of his treatment. [...]
Letter: Help dialysis patients
When you start dialysis, which I was on for three years, there is a lot of uncertainty and fear. However, worrying about immediately changing health insurance plans after diagnosis hasn’t typically been a problem for most patients, because private insurance companies had to cover treatments for 30 months before the patient automatically joins Medicare. However, the U.S. Supreme Court issued a ruling last year that could potentially weaken long-standing protections that are essential for dialysis patients. This is highly concerning, because the last thing that new dialysis [...]
Protect insurance for dialysis
The life of a dialysis patient is one of constant uncertainty. I could not continue working when I started dialysis, as is the case for many other patients. Thankfully, my spouse’s private insurance helped cover the treatment costs. Without private insurance, I would have been on the hook for thousands of dollars. I also could have lost my amazing in-network doctors and the option for at-home dialysis. In short, I would have had a completely different journey through kidney failure. It is critical that kidney patients have [...]
Dialysis patients should not be singled out
Kidney failure is not a death sentence. With the right healthcare, Americans on dialysis can live energetic, productive lives. Unfortunately, paying for dialysis in America has become a Herculean task. Medicare only covers 80%, and the remaining 20% can cost thousands per year. Private insurance usually covers the first 30 months of dialysis before patients’ transition, by law, to Medicare. However, a Supreme Court decision last year could allow private insurance companies to deny certain treatments to dialysis patients and deplete their coverage during that period. I [...]
Protect dialysis patients from shocking bills
Last year I wrote to you about the shocking moment when my young daughter was diagnosed with kidney failure. Thankfully, I was able to be her part-time caregiver with the help of our primary physician through her dialysis treatment and the many health challenges she faced. The last thing dialysis patients should worry about is money. That’s why I’m writing to you again to share my concern about a recent U.S. Supreme Court ruling that allows insurance companies to weaken health coverage for dialysis patients and push [...]
Letter: dialysis funding
When your kidneys fail, dialysis is your hope for a better future. But affording dialysis can be a tricky ordeal because Medicare, which all dialysis patients are required to have as their primary provider after 30 months, only covers 80% of the treatment costs. For me, paying the other 20% was hard because, as someone under the age of 65, I had to pay high premiums for my supplemental plan. Unfortunately, paying for the coverage that saves patients' lives is about to become even more difficult. The [...]
Give dialysis patients time to plan
Kidney failure changed my life. I’ve learned a thing or two after spending 18 years on dialysis, receiving a kidney transplant, and spending years as an advocate for my fellow patients. In the initial 30 months of dialysis, dialysis patients have traditionally had the option to keep their private insurance in order to plan for their inevitable transition to Medicare. Planning proves especially important for patients who may no longer receive employer-provided insurance, since dialysis often prevents people from working. However, a recent Supreme Court decision may [...]
Letter: Congress must help dialysis patients
Since coming to Congress last year, Rep. Marie Gluesenkamp Perez has worked across party lines to help our community. I hope she’ll do so again by working to ensure that Washington’s kidney disease patients, of which I am one, can have access to proper insurance. After a Supreme Court ruling, private insurance companies may be able to weaken what they cover for dialysis patients. Previously, if someone had private insurance when they got diagnosed with kidney failure and started dialysis, they could keep their full coverage for [...]
Letter: We Must Protect Dialysis Patients
Those with a sudden and serious illness that requires immediate medical attention are called “crash” patients. My husband Raymond was a crash patient when he was diagnosed with End Stage Renal Disease, or kidney failure. Luckily, Raymond had private insurance, so he didn’t have to worry much about the cost of his life-saving dialysis treatments when he started. Eventually, dialysis patients transition to Medicare as their primary coverage within 30 months after beginning treatment. Yet now, a Supreme Court ruling from last year leaves room for private [...]
Dialysis Patient Citizens Applauds New Legislation Restoring Protections for Dialysis Patients
WASHINGTON, D.C. (December 20, 2023) -- Dialysis Patient Citizens (DPC), the leading advocacy organization for dialysis patients nationwide, today released the following statement applauding the introduction of the Restore Protections for Dialysis Patients Act by Representatives Mike Kelly (R-PA), Yvette Clark (D-NY), Neal Dunn (R-FL), Danny Davis (D-IL), John Joyce (R-PA), and Raul Ruiz (D-CA) to restore access to critical health insurance coverage for patients who choose it. “We applaud Representatives Kelly, Clark, Dunn, Davis, Joyce, and Ruiz for standing with dialysis patients by introducing this critical [...]
Happy Holidays from DPC
We want to wish you and your family a Happy Holiday, as well as a safe and healthy New Year. DPC offices will be closed for the holidays starting December 22 through January 1. We also want to take this opportunity to thank you for your continued support throughout 2023. Though the year posed some challenges, we appreciate you for helping us elevate the dialysis patient voice with policy makers. We are extremely grateful for all of your advocacy efforts, and we look forward to our continued [...]
Idaho Statesman: Dialysis
At the young age of 25 years old, I had to accept the fact that I would need dialysis treatment to survive. Like many Americans with kidney failure, I was too sick to continue working. I lost my employer-provided insurance soon after I stopped working. Since I did not immediately qualify for Medicaid, I was forced to pay the 20% of the bill that Medicare does not cover for 6 months. The costs were extensive, and I am still in the process of paying off that debt. [...]
Congress Must Help Kidney Patients
My wife was diagnosed with kidney failure in January of 2022. I was her primary caregiver until she passed away in June of this year. Now, I dedicate my time advocating for Americans with kidney disease. A pressing problem facing kidney patients in America is the difficulty paying for dialysis, which keeps patients alive. It can cost hundreds of thousands of dollars without insurance. When my wife started dialysis, we had Medicare, but Medicare only covers 80%. We have a private insurance plan to supplement Medicare, which [...]
Happy Thanksgiving from DPC Board, Staff, and Volunteers!
DPC would like to wish our many patient advocates, family, friends, and healthcare partners a happy Thanksgiving. We are grateful for all of these hard-working individuals and for their dedication to the kidney community, as well as their effort to help elevate the patient voice. This year, our patient advocates helped to secure passage of critical legislation at the federal level to help modernize the transplant system. We also worked hard to educate hundreds of policy makers about the importance of protecting dialysis patient access to private [...]
Dialysis
Ten years ago while working for an airline my life changed. I was diagnosed with kidney failure, and I learned I'd need dialysis to survive. Eight years of dialysis and a transplant later, I am writing now to advocate for kidney patients everywhere. For three years, I received dialysis in Dubai, United Arab Emirates. Despite initial difficulties, my dialysis care was relatively seamless. When I returned to the United States, Medicare required that I submit a plethora of paperwork. I had to pay out-of-pocket for more than [...]
DPC Expresses Outrage at CMS Indifference to Dialysis Patient Suffering
On October 27, 2023, the Centers for Medicare & Medicaid Services (CMS) issued its final rule updating payment rates and policies under the end-stage renal disease (ESRD) prospective payment system. This rule fails to address two serious problems currently facing dialysis patients, which DPC raised in its comment letter: workforce shortages and lack of access to innovative treatments. DPC’s statement on the Rule is available here.
Dialysis Patient Citizens Responds to Disappointing Final CMS Rule That Will Harm Patient Healthcare
WASHINGTON, D.C. (October 30, 2023) - Dialysis Patient Citizens (DPC), the nation’s largest patient-led, non-profit advocacy group for dialysis patients, released the following statement in response to the final rule issued by the Centers for Medicare and Medicaid Services (CMS) which only increases Medicare reimbursements for dialysis treatment centers by 1.6% and fails to properly fund access to new therapies. “The End Stage Renal Disease (ESRD) final rule released on Friday paints a chilling picture of an agency that is completely indifferent to the suffering of dialysis [...]
DPC Letter to CMMI on ESRD Treatment Choices Demonstration Issues
October 10, 2023 Dr. Elizabeth Fowler, Deputy Administrator Centers for Medicare & Medicaid Services 7500 Security Boulevard Baltimore, MD 21244 Re: ESRD Treatment Choices Demonstration Issues Dear Dr. Fowler: Last year, published research looking at CMMI’s ESRD Treatment Choices Model (ETC) indicated that the program is not having the effect that was hypothesized. Now, CMMI’s own evaluation contractor has echoed those findings. We urge CMMI to pause and reassess whether ETC was the best available policy intervention to promote home dialysis and transplantation, and consider alternatives. ETC imposes [...]