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About Hannah Bracamonte

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So far Hannah Bracamonte has created 638 blog entries.

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 [...]

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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 [...]

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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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DPC Board Member Donnie Anderson Addresses CDC Infection Control Conference

2024-03-29T01:10:16+00:00May 12th, 2021|Categories: Innovation, News, Patient's Voice|Tags: |

Recorded for the 2021 Making Dialysis Safer for Patients Coalition Virtual Meeting DPC Board Member Donnie Anderson spoke on a panel entitled "COVID-19 from The Patient Perspective” at the CDC’s 2021 Making Dialysis Safer for Patients Coalition meeting. The virtual conference held in May was the Coalition’s fourth meeting to advance efforts to prevent bloodstream infections in dialysis patients. The conference facilitated information-sharing and idea generation among dialysis and infection prevention experts.

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Letters: Action Needed to Help Alabama Dialysis Patients

2024-03-29T01:10:16+00:00May 1st, 2021|Categories: Care Coordination, Patient Ambassadors, Patient's Voice, Spotlight|

By Cortney Beavers of Pell City, AL. One of the most difficult moments of my life was finding out that, despite being only 24 years old, my kidney was beginning to fail. After years of dialysis and a kidney transplant, I learned through my experiences in the health care system what needs to be improved. Doctors and nurses need a better care coordination framework to more effectively treat their patients. I had the benefit of working with terrific nurses and other providers who met my needs and communicated well between one another, but unfortunately that’s not the case for every [...]

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DPC Advocates Help Push State Legislation Forward

2024-03-29T01:10:16+00:00April 20th, 2021|Categories: Advance Patient Choice, Article, Medigap Coverage, State Advocacy, Transplant Donor Protection, Uncategorized|

State legislatures are in high gear during spring, and efforts by state legislators to support dialysis patients are in full swing this month. We’ve already had several legislative victories on living organ donor protection bills, while Medigap expansion legislation for the ESRD population has been introduced in multiple states. With support from multiple DPC Patient Ambassadors and Board Members sharing their personal stories on these two policy issues, DPC is making robust arguments for states to actively help improve the quality of life for End Stage Renal Disease (ESRD) patients. Kentucky, New Jersey, Maryland and Washington legislatures have already passed [...]

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New Year, New Administration Brings Changes to Medicare’s Kidney Demonstration Projects

2024-03-29T01:10:16+00:00April 14th, 2021|Categories: Article, Care Coordination, Dialysis Funding, Medicare Advantage, Protect Patient Care, Quality Incentive Program|

2021 was supposed to mark the beginning of three new Medicare programs to demonstrate innovations in kidney care, but a last-minute decision from the Center for Medicare and Medicaid Innovation has suspended two of them. This action unfortunately leaves about 50,000 dialysis patients with a nine-month gap in extra assistance they were receiving from a successful program that expired March 31. Here is the rundown on the current landscape of Medicare demonstration projects that impact dialysis patients. Demonstration projects are used by Medicare to test new models of care and/or new models of paying providers within Medicare’s traditional fee-for-service program. [...]

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National Minority Health Month

2024-03-29T01:10:16+00:00April 5th, 2021|Categories: Article, Improve Access to Care|Tags: |

April is also recognized as National Minority Health Month, in an effort to highlight and address the health disparities experienced in minority communities. This is especially prevalent among kidney and dialysis patients; Hispanic or Latino Americans 1.3 times more likely to have kidney failure than white Americans, Black or African Americans are almost 4 times more likely, American Indians and Alaska Natives are 1.2 times more likely, and Asian Americans are also at a higher risk. Additionally, the main risk factors for chronic kidney disease (CKD) disproportionately affect minorities. Diabetes, high blood pressure, heart disease, family history of kidney failure, diabetes, [...]

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Support New Kidney Care Act

2024-03-29T01:11:59+00:00April 1st, 2021|Categories: Care Coordination, Patient Ambassadors, Patient's Voice, Spotlight|

By Antonio Green of Virginia Beach, VA. 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, [...]

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April is Donate Life Month

2024-03-29T01:12:00+00:00April 1st, 2021|Categories: Access to Transplant, Article, Transplant Donor Protection|

Each April, National Donate Life Month encourages Americans to register as organ, eye, and tissue donors; to become educated about living donation (that includes living kidney donation!); and to honor those that have saved lives through the gift of donation. Over 100,000 children, men, and women are waiting for lifesaving organ transplants, with a new person added to the national transplant waiting list every 10 minutes. Here is some more information on the different types of transplant and what you can do to help. What are the different types of organ donation? Living donation – living donation is an opportunity [...]

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