About Hannah Bracamonte

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So far Hannah Bracamonte has created 731 blog entries.

DPC’s Letter to Dr. Mehmet Oz, Administrator at Centers for Medicare & Medicaid Services, on CMS-1846-P: CY 2027 Changes to the End-Stage Renal Disease (ESRD) Prospective Payment System, Acute Kidney Injury Dialysis (AKI) Payment, and ESRD Quality Incentive Program

2026-08-25T14:49:06+00:00August 24th, 2026|Categories: Advance Patient Choice, Comment Letter, Improve Access to Care, Increase Quality of Care, Promote Financial Security, Protect Patient Care|

August 24, 2026 The Honorable Mehmet Oz, Administrator Centers for Medicare & Medicaid Services 200 Independence Avenue, SW Washington, DC 20001 Re:       CMS-1846-P: CY 2027 Changes to the End-Stage Renal Disease (ESRD) Prospective Payment System, Acute Kidney Injury Dialysis (AKI) Payment, and ESRD Quality Incentive Program Dear Dr. Oz Dialysis Patient Citizens (DPC) offers comments on the above referenced Rule. DPC's membership, currently about 35,000, is restricted to kidney disease patients and their family members. DPC is a patient-led organization.  Our by-laws require that the President, Vice President and at least 51% of the Board be current dialysis patients.  The [...]

Dialysis Patient Citizens and the DPC Education Center Mourn the Passing of Arthur Hill

2026-08-20T13:22:26+00:00August 20th, 2026|Categories: Article, Board Members|

It is with a heavy heart that DPC and the DPC Education Center Board, staff, and volunteers learned of the passing of one of our Board members, Arthur Hill. Arthur worked as a distressed assets consultant for nearly 30 years before being diagnosed with kidney failure. From that point on, he applied his sharp analytical skills to exploring how advances in technology could be leveraged to help kidney patients and dedicated his time to patient advocacy. Arthur was instrumental in passing Indiana Senate Bill 215 (Public Law 28-2024), landmark legislation that reduced monthly Medigap premiums for dialysis patients under 65. [...]

NCSL 2026 Recap

2026-08-26T14:49:42+00:00August 3rd, 2026|Categories: Article, Medigap Coverage, News, Promote Financial Security, Protect Patient Care, State Advocacy|

The National Conference of State Legislators (NCSL) welcomed more than 7,000 attendees to its Legislative Summit in Chicago July 27-29. DPC was thrilled to participate in this bipartisan event as part of our legislative advocacy work at the state level. Megan Hashbarger, Senior Vice President of Government Relations, and State Advocacy Directors, Elizabeth Lively and Pamela Zielske, attended the event and shared updates on DPC’s critically important work in the states to increase access to affordable Medigap coverage. Over the course of the Summit, we heard numerous stories from attendees who have family members or friends facing kidney disease. Legislators or [...]

Advocacy Day 2026

2026-07-23T14:32:39+00:00July 20th, 2026|Categories: Advance Patient Choice, Article, Get Involved, Improve Access to Care, Increase Quality of Care, Innovation, Medigap Coverage, News, Patient Ambassadors, Policy Issues, Private Insurance Coverage, Promote Financial Security, Protect Patient Care|

During June 29th – 30th, DPC hosted our annual Advocacy Day in Washington, D.C. bringing together patients, family members, and care partners to meet with their Members of Congress to help elevate the dialysis patient voice. This year, 62 advocates attended our fly-in from 29 states, meeting with more than 90 Members of Congress and/or their staff. Advocates spoke with their Senators and Representative urging support for the Restore Act (H.R. 2199/S. 1173), which would allow patients to keep their private insurance coverage for the full 30-month transition period, and for the Kidney Care Access Protection Act (S. 2730 / H.R. 6214), [...]

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 [...]

Patient Advocates Head to D.C.

2026-06-24T15:39:03+00:00June 24th, 2026|Categories: About DPC, Get Involved, Improve Access to Care, Patient Ambassadors, Policy Issues, Promote Financial Security, Protect Patient Care, Take Action|

DPC is excited to welcome this year’s group of patient advocates to Washington, D.C. June 29th – 30th for our Annual Advocacy Day Event. Our advocates will be meeting with their representatives on the Hill to discuss two very important pieces of legislation for kidney patients:  S. 2730 / H.R. 6214 – The Kidney Care Access Protection Act and H.R. 2199 / S. 1173 – The Restore Protections for Dialysis Patients Act. If you have not yet done so, please take a moment to urge your representatives to co-sponsor these two bills. Access to innovation and private insurance are critical to [...]

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