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About Hannah Bracamonte

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So far Hannah Bracamonte has created 666 blog entries.

Happy Holidays and DPC’s Top 10 Accomplishments of 2019

2024-03-29T01:13:32+00:00December 20th, 2019|Categories: 5-Star Ratings, About DPC, Access to Transplant, Article, Care Coordination, Charitable Premium Assistance, Dental Coverage, Dialysis Funding, Immunosuppressive Drug Coverage, Innovation, Medicaid, Medicare Advantage, Medigap Coverage, Quality Incentive Program, Transplant Donor Protection, Transportation Services, Treatment Options|

Dialysis Patient Citizens wants to wish you and your family a Happy Holiday, as well as a safe and healthy New Year. Our offices will be closed for the holidays starting December 23 through January 1. We also want to take this opportunity to share our list of Top 10 Accomplishments for 2019, which would not have been possible without your support. Thank you again 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 collaboration in 2020 as we work together to improve dialysis [...]

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Trump Administration Proposes New Rules to Increase Accountability and Availability of the Organ Supply

2024-03-29T01:13:32+00:00December 17th, 2019|Categories: Uncategorized|

The U.S. Department of Health and Human Services (HHS) today took major steps to increase the availability of organs for the 113,000 Americans on waitlists for lifesaving organ transplants – 20 of whom die each day. As directed by President Trump in his July 10 Executive Order on Advancing American Kidney Health, the Centers for Medicare & Medicaid Services (CMS) is issuing a proposed rule to change the way organ procurement organizations (OPOs) are held accountable for their performance, and the Health Resources and Services Administration (HRSA) is issuing a proposed rule to remove financial barriers to living organ donation. This summer, [...]

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Advocacy Day Application Deadline Extended 1 Week

2024-03-29T01:13:32+00:00December 14th, 2019|Categories: Article, Get Involved, Take Action|

Good news—the deadline to apply for DPC's 2020 Advocacy Day in Washington, DC has been extended one week to Friday, December 20! We want to elevate the patient voice with policy makers with a strong and united group of advocates from all 50 states. Become a leader in your community by applying, and you could be the voice for dialysis patients with your state lawmakers in our nation’s capital.  We understand that the holidays are an especially busy time of year for many people, and we hope you will take some time in the next week to elevate the patient [...]

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DPC Board of Directors Elect New President

2024-03-29T01:13:32+00:00December 9th, 2019|Categories: Article, Board Members|

Andrew Conkling Andrew Conkling was elected as the new president for Dialysis Patient Citizens by DPC's Board of Directors, effective immediately. Conkling has served as DPC Vice President since 2016, participated in a number of DPC's Advocacy Days and met with lawmakers to discuss kidney disease issues from his home state of Alabama. He has also served as a DPC Patient Ambassador, clinic patient representative and done community outreach by sharing his personal experiences with young people. "It is an honor to be selected as DPC's Board President. I want to thank Jack Reynolds for his outstanding service as [...]

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DPC Meets with Oregon State Legislatures to Protect Patient Care

2024-03-29T01:13:32+00:00December 2nd, 2019|Categories: Article, Charitable Premium Assistance, Improve Access to Care, State Advocacy|

DPC staff standing in front of Oregon State Capitol In mid-November, DPC staff traveled to Salem, Oregon, to attend an informational hearing held by the Oregon House Committee on Health Care regarding outpatient dialysis treatment. The hearing focused on issues such as improving and expanding patient access to care while exploring ways in which to lower the cost of health care delivry for dialysis patients. While there, DPC staff also took the opportunity to meet individually with nearly all the Members of the House and Senate Health Committees or their staff. The goal of our meetings was to [...]

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Congressman Payne Jr. Comments on CMS Proposed Rule Regarding ESRD Treatment Choices Model Demonstration

2024-03-29T01:13:32+00:00November 20th, 2019|Categories: Treatment Options|

Congressman Donald Payne Jr. sent a letter to the U.S. Department of Health and Human Services (HHS) regarding the ESRD Treatment Choices Model Demonstration, which is the rule that pertains to increasing the number of home dialysis treatments and kidney transplants. Payne focused on the importance of protecting and prioritizing patient choice. Specifically, he explained that home dialysis is not always an optimal treatment option for patients due to a lack of caregiver support and the necessary space requirements needed for this treatment. Payne provides a unique perspective to the conversation on advancing kidney health in America. He has End-Stage Renal Disease [...]

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DPC’s Advocacy Day Application is OPEN! Apply by December 13, 2019

2024-03-29T01:13:33+00:00November 13th, 2019|Categories: Article, Get Involved, Take Action|

DPC is pleased to invite you to apply for our 2020 Advocacy Day! We are very fortunate that we are able to bring dialysis patients to Washington, D.C. each year to meet with their elected officials. This provides advocates like you with the unique opportunity to make your voice heard on behalf of dialysis patients from your state in order to improve dialysis care. Next year is no exception. We will meet with Members of Congress and their staff on Tuesday, June 2, 2020 with a comprehensive training the day before. We received over 100 applicants for our 2019 Advocacy Day, [...]

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DPC Fights for Patient Access in California

2024-03-29T01:13:33+00:00November 7th, 2019|Categories: Article, Charitable Premium Assistance, Improve Access to Care, Legal Defense, State Advocacy|

DPC is participating in a lawsuit against the state of California after a bill was passed by the Legislature that jeopardizes patient access to charitable assistance. The new law (known as Assembly Bill 290) was signed by California Governor Gavin Newsom last month. Conditions in the new law practically eliminates charitable assistance, which has helped thousands of low-income patients in California pay for their health insurance. The law will take effect January 1, 2020 unless the judge orders the delay DPC is requesting. DPC is fighting similar legislation in other states and will continue to protect dialysis patient access to [...]

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Patients and Advocacy Groups File Federal Lawsuit Against the State of California to Overturn AB 290

2024-03-29T01:13:33+00:00November 4th, 2019|Categories: Charitable Premium Assistance, Improve Access to Care, Legal Defense, Press Release, State Advocacy|

ORANGE COUNTY, Calif., Two kidney failure patients, together with two patient advocacy groups—the American Kidney Fund (AKF) and Dialysis Patient Citizens (DPC)—filed a federal lawsuit today in the U.S. District Court for the Central District of California against the State of California. The lawsuit, Doe vs. Becerra, asks the court to strike down AB 290, the newly enacted law that will do irreversible harm to dialysis and transplant patients who need charitable assistance to help them pay for health care. Filed against California Attorney General Xavier Becerra, California Insurance Commissioner Ricardo Lara, Shelley Rouillard, Director of the California Department of Managed Health Care, and Susan Fanelli, Acting Director of the [...]

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DPC Advocates for Patient Access to Private Health Insurance

2024-03-29T01:13:33+00:00October 30th, 2019|Categories: Article, Dialysis Funding, Improve Access to Care, Legal Defense, Private Insurance Coverage, Promote Financial Security|Tags: |

DPC filed an amicus brief in support of a lawsuit to protect patient access to private health insurance coverage. This is one of a number of lawsuits challenging discrimination by employer health plans in how they pay for dialysis. End-Stage Renal Disease (ESRD) patients are protected by the Medicare Secondary Payer Act (MSP), which permits ESRD patients to remain on their private health insurance plans for 30 months before they must enroll in Medicare. To protect this right from being chipped away, Congress prohibited health plans from making any distinctions in how they cover dialysis relative to how other treatments or diseases are [...]

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