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About Hannah Bracamonte

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So far Hannah Bracamonte has created 605 blog entries.

CMS Proposes Changes to Medicare Payments for End-Stage Renal Disease

2024-03-29T01:10:14+00:00July 1st, 2021|Categories: Article, Improve Access to Care, Medicaid, Medicare Advantage, Quality Incentive Program|

On July 1, 2021, the Centers for Medicare & Medicaid Services (CMS) issued its ESRD Prospective Payment System (PPS) annual rulemaking. This proposed rule would update ESRD PPS payment rates, make changes to the ESRD Quality Incentive Program (QIP), and modify the ESRD Treatment Choices (ETC) Model for 2022. The proposed changes to the ETC Model policies aim to encourage dialysis providers to decrease disparities in rates of home dialysis and kidney transplants among ESRD patients with lower socioeconomic status, making the model the agency’s first CMS Innovation Center project to address health equity. The ETC model rewards ESRD facilities and [...]

Letters to the Editor

2024-03-29T01:10:14+00:00June 27th, 2021|Categories: Patient Stories in the News|

One certainty in life is that all of us will be tested by circumstances out of our control. For me, it was kidney failure, and since 2007 I've been on dialysis. I'm very blessed that I was able to receive this care, and that I've been able to live a healthy and happy life thanks to the support of a loving family. However, a lot of dialysis patients today can't afford the lifesaving treatments they need. That's why it is so important to pass the Jack Reynolds Memorial Medigap Expansion Act, a bill that would expand coverage for out-of-pocket costs [...]

Medigap expansion could clear major obstacle for kidney patients

2024-03-29T01:10:14+00:00June 24th, 2021|Categories: Patient Stories in the News|

After three difficult years on dialysis, I received a kidney transplant last fall through the Department of Veteran Affairs as a Marine Corps veteran. While I don't have dialysis treatments anymore, I keep touch with everyone I met at my dialysis center and find new ways to help patients. In these conversations, one topic seems to come up more than just about any other: high costs. Navigating Medicare, which many dialysis patients need for treatments, is a tricky and confusing process that gets more complicated if you don't have Medigap insurance to cover what Medicare doesn't. Sadly, that's the reality [...]

To the Editor: Medigap coverage important for people in need

2024-03-29T01:10:15+00:00June 21st, 2021|Categories: Patient Stories in the News|

To the Editor: As a single mom, starting dialysis required a lot of shuffling so I could attend treatments while juggling my responsibilities as a parent. Thankfully, it didn’t require big out-of-pocket payments to cover what Medicare couldn’t, since Michigan requires insurers to provide dialysis patients like me with access to Medigap. I know the reality is different for patients in my situation in other states, so I’m happy to see members of Congress from both parties working on the Jack Reynolds Memorial Medigap Expansion Act, which would expand “Medigap” coverage to dialysis patients under 65, so they don’t get [...]

Expanding Medigap coverage

2024-03-29T01:10:15+00:00June 21st, 2021|Categories: Patient Ambassadors, Patient Stories in the News, Spotlight|

I first started dialysis just over 20 years ago, and in that time I’ve done both home and in-center dialysis treatments in addition to receiving two kidney transplants. Along the way, I’ve been fortunate enough to have good coverage that kept my treatments affordable. As I’ve met other dialysis patients, I’ve realized just how rare that is. Many people with kidney disease receive their coverage through Medicare and if they are under 65, they can get hit with big bills that they have to pay out-of-pocket if Medicare doesn’t cover the whole cost of their treatment. No one should have [...]

Stay Up-to-Date on the Latest Kidney Care News with DPC’s New “Patient Stories” Page

2024-03-29T01:10:15+00:00June 18th, 2021|Categories: Article, Medicaid, Patient's Voice, Promote Financial Security|

Dialysis Patient Citizens wants to make it easier for you to stay up-to-date with the latest Letters to the Editor and Op-Eds written by our members. Head over to our new Patient Stories page to hear these members’ stories and how upcoming bills, such as the Jack Reynolds Memorial Medigap Expansion Act and the BETTER Kidney Care Act, would provide much needed assistance to patients. Check Out the Patient Stories Page

Dialysis Patient Citizens Statement Commemorating Juneteenth

2024-03-29T01:10:15+00:00June 17th, 2021|Categories: Article, Improve Access to Care|

WASHINGTON, D.C., (June 17, 2021) -- Dialysis Patient Citizens (DPC) today released the following statement recognizing Juneteenth and reaffirming its commitment to addressing healthcare disparities among kidney patients nationwide. “Today we commemorate Juneteenth, an important day in history that celebrates the emancipation of enslaved Americans and allows us an opportunity for reflection on both our nation’s history and how much further we have to go,” said DPC Board President Andrew Conkling. “Black Americans continue to face systemic inequalities in our country, including healthcare disparities that disproportionately hurt patients from communities of color. Too many patients with kidney disease experience firsthand unacceptable racial [...]

New bill would expand coverage to kidney patients who need it most

2024-03-29T01:10:15+00:00June 9th, 2021|Categories: Patient Stories in the News|

For 10 years, I acted as my father’s in-home dialysis provider, and having the chance to be there for him was one of the most rewarding experiences of my life. While he passed away last year, I’ve been able to channel that energy into helping and educating other patients who are in the same position he was. Caring for my father, along with my experiences as a nurse and my recent schooling to become a health education specialist, opened my eyes to a lot of disparities affecting our health system that have serious ramifications for dialysis patients. So many patients [...]

Both Sides of the Aisle Agree – We Need to Help Kidney Patients

2024-06-07T15:24:50+00:00June 9th, 2021|Categories: Advance Patient Choice, Dialysis Funding, Improve Access to Care, Increase Quality of Care, Innovation, Medicare Advantage, Medigap Coverage, Protect Patient Care|

On June 8, 2021, Senators Benjamin Cardin (D-MA) and Roy Blunt (R-MO) re-introduced The Chronic Kidney Disease Improvement in Research and Treatment Act (S.1971), a bipartisan, bicameral bill designed to not only raise awareness of chronic kidney disease (CKD) and end-stage renal disease (ESRD), but also improve understanding and access to treatment for patients, which includes the Jack Reynolds Memorial Medigap Expansion Act. The latest statistics from the Centers for Disease Control and Prevention estimates that more that 1 in 7 US adults (about 37 million people) have CKD and that as many as 9 out of 10 of those adults [...]

Opinion | Letter: Pass Kidney-care Bill

2024-03-29T01:10:15+00:00June 1st, 2021|Categories: Care Coordination, Patient Ambassadors, Patient's Voice, Spotlight|

By Kristi Flynn of Grovetown, GA I have struggled with kidney disease my entire life. I was diagnosed when I was 7, then started dialysis at 25 before finally receiving a kidney transplant in 2018. Throughout all of this, the role of coordinating care has fallen completely on me, a task I find particularly difficult because I am legally blind. Even within my transplant center, doctors can’t always communicate, and even more frustrating, occasionally change each other’s plans without consulting each other. With a more streamlined approach to care coordination, a lot of these problems could be relieved. Thankfully, Congress is [...]

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