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Opinion: New bill would provide boon to dialysis care

2024-03-29T01:12:03+00:00August 10th, 2020|Categories: Patient Stories in the News|

Protecting patients in the U.S. has been at the top of the public mind since the start of the COVID-19 outbreak. Since March, people both here in Missouri and across the rest of the country have been taking steps to help curb the spread of the virus and keep each other safe, particularly those with other health issues that make them more susceptible to contracting the virus and having serious health problems as a result. Even with all we’ve done so far, however, there is still more we and our elected officials can do to protect high-risk Americans. One group [...]

DPC’s 2020 Annual Membership Survey is Live!

2024-03-29T01:12:03+00:00August 6th, 2020|Categories: 5-Star Ratings, Access to Transplant, Article, Care Coordination, Charitable Premium Assistance, Dental Coverage, Dialysis Funding, Get Involved, Immunosuppressive Drug Coverage, Innovation, Medicaid, Medicare Advantage, Medigap Coverage, Quality Incentive Program, Take Action, Transplant Donor Protection, Transportation Services, Treatment Options|Tags: |

Elevate the Voice of Patients with Kidney Disease and Their Caregivers Our 2020 Annual Membership Survey is live, and it will remain open until Friday, August 21. We are counting on your participation, as patient feedback helps to shape our public policy agenda and patient education priorities for the next year. This year we ask that both patients and caregivers take our survey. Rest assured your responses will remain completely anonymous. We only share the overall survey results with state and federal level policy makers, so they will better understand your needs, experiences, and preferences. Your feedback is crucial. Therefore, we will [...]

Action Alert – Help us Increase Patient Access to Immunosuppressive Medications

2024-03-29T01:12:03+00:00July 28th, 2020|Categories: Article, Immunosuppressive Drug Coverage, Medicare Advantage, News, Take Action|

The Comprehensive Immunosuppressive Drug Coverage for Kidney Transplant Patients Act (H.R. 5534, S. 3353) is gaining momentum in Congress, and we need your help continuing to get the word out. This bill was introduced by Representatives Ron Kind (D-WI) and Michael Burgess (R-TX), as well as Senator Bill Cassidy (R-LA). This legislation would extend Medicare coverage of immunosuppressive drugs beyond the current limit of 36 months for patients who are unable to obtain health insurance coverage elsewhere. Immunosuppressive medications play a critical role in preventing transplant recipients from rejecting a donor kidney. Right now, after dialysis patients receive a transplant, [...]

ESRD Community Honors the Legacy of Congressman John Lewis

2024-03-29T01:12:04+00:00July 27th, 2020|Categories: Medigap Coverage, News|

Our nation recently lost one of its most iconic and stalwart champions for justice in Congressman John Lewis. He dedicated his life to fighting for civil rights and social justice for all Americans, and his legacy will forever be remembered. Congressman Lewis was also one of the kidney community’s most consistent, trustworthy, and respected allies, and we join the nation in mourning his passing. Throughout his more than three decades in the U.S. House of Representatives, Congressman Lewis was a champion for patients with End-Stage Renal Disease (ESRD) and worked with them to increase access to treatment.  Specifically, he repeatedly introduced the Chronic Kidney Disease [...]

Letter to the Editor – BETTER Kidney Care Act

2024-03-29T01:12:04+00:00July 7th, 2020|Categories: Patient Stories in the News|

Since she was just three days old, my daughter has struggled with kidney failure. After over 30 years and three transplants, it’s become clear that more needs to be done to help kidney patients. Care coordination in particular needs a lot of attention. Without effective communication between doctors, things get harder for patients, and they can suffer serious health problems as a result. We’ve experienced this in my daughter’s care from the beginning. Medications and doses occasionally got mixed up when she was a baby, and recently a miscommunication between her doctors meant she was diagnosed with 40mg of one [...]

Dialysis Patient Citizens Files Lawsuit Against HHS Secretary Alex Azar and CMS Administrator Seema Verma Over New Regulation That Undercuts Dialysis Patient Access to Affordable, High-Quality Care

2024-03-29T01:12:04+00:00June 22nd, 2020|Categories: Care Coordination, Legal Defense, Medicare Advantage, News, Press Release|

WASHINGTON, D.C., (June 22, 2020) -- Today, Dialysis Patient Citizens (DPC) filed suit in the United States District Court for the District of Columbia against Health and Human Services Secretary Alex Azar, Centers for Medicare and Medicaid Services Administrator Seema Verma, the U.S. Department of Health and Human Services, and the Centers for Medicare and Medicaid Services in opposition to a discriminatory new federal regulation that will limit the ability of hundreds of thousands of End-Stage Renal Disease (ESRD) patients to access affordable, high quality treatment. “ESRD patients successfully fought to get Congress to pass bipartisan legislation that would ensure [...]

Letter: Helping Dialysis Patients

2024-03-29T01:12:04+00:00June 13th, 2020|Categories: Patient Stories in the News|

When my kidney issues started in 2009, I was fortunate enough to receive a donor kidney from my mother, which lasted until 2017. Unfortunately, new medications caused that kidney to fail and ultimately forced me to go on dialysis. Since starting dialysis I’ve worked with a great team at my local clinic that truly cares about me and even helps to coordinate dialysis treatments for me with other clinics when I travel for work. I’ve noticed recently, though, that I’ve had to play a bigger part in coordinating my own care when I see doctors outside of my clinic. Occasionally, [...]

Support New Kidney Care Act

2024-03-29T01:12:04+00:00June 12th, 2020|Categories: Patient Stories in the News|

While working in Abu Dhabi, I found out I had kidney disease and needed to begin dialysis. I was able to continue working abroad for a few more years, but a 2017 trip to the hospital showed me it was time to move back home. Since then, I’ve noticed that a better, more coordinated system is needed to help dialysis patients. Even when I had a care coordinator, I found the system never really worked for me. Whether it was managing medications, doctors’ appointments or even my attempts to get a kidney transplant, I always had to control the process [...]

Coordinated Care Bill Can Ensure Patients Receive Needed Treatment

2024-03-29T01:12:04+00:00June 10th, 2020|Categories: Patient Stories in the News|

Sadly, Paul Van Vooren passed away after this article was published. As a patient with Von Hippel-Lindau (VHL) who has undergone 65 surgeries, including a kidney transplant, and received dialysis treatments for over eight years, I know the importance of coordinate care for dialysis patients. My treatment for VHL sometimes requires me to travel hours to the Mayo Clinic in Rochester, MN. I also have my primary doctor in Sioux Falls that helps me maintain my active lifestyle, despite needing to rely on dialysis. From my conversations with other kidney patients, I know that isn’t the case. They also rely [...]

New Bill Offers Help for Georgia’s Dialysis Patients

2024-03-29T01:12:04+00:00June 4th, 2020|Categories: Patient Stories in the News|

Dialysis has forced me to make major adjustments, requiring me to make three weekly trips to the clinic for four-hour treatments while I continue my years-long wait for a kidney transplant.  I work hard to maintain my diet, get proper exercise, and stay on top of all of my treatments, but many dialysis patients can’t because they have diabetes or other serious conditions alongside kidney disease, and they need help coordinating their care.  A new bill working its way through Congress could help. The BETTER Kidney Care Act would allow all the doctors a dialysis patient sees to work together [...]

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