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About Hannah Bracamonte

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So far Hannah Bracamonte has created 629 blog entries.

Kidney patients need protections restored

2024-05-21T16:30:13+00:00May 21st, 2024|Categories: Patient Stories in the News, Private Insurance Coverage|

I was 14 when my father was diagnosed with End Stage Renal Disease, or kidney failure. I witnessed the suffering, anxiety, and helplessness the disease brought upon my family. I also witnessed the financial burden of medical bills, which became unaffordable once my father was forced off of his marketplace insurance. Traditionally, private insurance companies cover dialysis for 30 months after an individual starts treatment, providing patients with the opportunity to focus on their health rather than worrying about their finances. However, a recent U.S. Supreme Court ruling weakens these protections, which could lead to more insurers kicking kidney failure [...]

DPC’s 2024 Advocacy Day

2024-05-23T14:34:34+00:00May 20th, 2024|Categories: Advance Patient Choice, Article, Get Involved, Improve Access to Care, Increase Quality of Care, Medigap Coverage, News, Patient Ambassadors, Private Insurance Coverage, Promote Financial Security, Protect Patient Care|

Earlier this month, DPC hosted our annual Advocacy Day in Washington, D.C. where we bring together patients, family members, and care givers to meet with their Members of Congress to elevate the patient story for dialysis patients. This year we had 65 advocates attend, representing 25 states, who had almost 80 Congressional meetings. Our patients spoke to Congressional offices asking them to support H.R. 6860 – The Restore Protections for Dialysis Patients Act and H.R. 5027 – The Chronic Kidney Disease Improvement in Research and Treatment Act. These two bills would allow dialysis patients access to private insurance and Medigap [...]

Buchanan Can Help Dialysis Patients

2024-08-20T18:54:19+00:00May 16th, 2024|Categories: Patient Stories in the News, Private Insurance Coverage, Spotlight|

I have kidney failure, and I need dialysis to survive. Dialysis is a treatment which removes excess water and toxins from my blood because my kidneys do not function naturally anymore. It has been a challenge, and my body is still getting used to the frequent treatment which wears down my body. Dialysis patients already worry enough about their physical condition. They should not have to worry about finances too. Sadly, they do. I was lucky to be retired and have sufficient coverage when I began dialysis, but I know people who struggle to pay. Some have private insurance, but [...]

Help dialysis patients

2024-06-27T14:47:14+00:00May 7th, 2024|Categories: Patient Stories in the News, Private Insurance Coverage, Spotlight|

End Stage Renal Disease (ESRD), commonly called kidney failure, changed my life. I was first diagnosed with kidney disease in 2014, and my kidneys totally failed in 2020 after a battle with covid-19. I relied on dialysis, the treatment which replaced my kidneys' blood-filtering function, from 2020 until August of 2023 when I received a kidney transplant. As an ESRD patient advocate lucky enough to have received a transplant, I feel obligated to call on Congressman French Hill to help future dialysis patients afford lifesaving dialysis care. He can do so by supporting the Restore Protections for Dialysis Patients Act. [...]

Support the Restore Protections for Dialysis Patients Act

2024-05-09T19:56:55+00:00May 6th, 2024|Categories: Patient Stories in the News, Private Insurance Coverage|

Kidney failure, or end-stage renal disease (ESRD), affects Americans of all ages. I was 14 years old when I received my diagnosis. I’ve been on dialysis for many years and have received two transplants in the process, but perhaps more stressful than dialysis has been paying for all my healthcare expenses. I’ve relied on private insurance for much of my ESRD journey. After my second transplant, I had private insurance that proved essential once my transplant failed and I needed to stay in the hospital. I eventually transitioned to Medicare, but did not qualify for Medicaid, and Medicare only pays [...]

Letter: Medicare failed us

2024-05-10T15:08:12+00:00May 6th, 2024|Categories: Dialysis Funding, Medicare Advantage, Patient Stories in the News, Staffing Shortages|

As a program coordinator for the Kidney Foundation of Central Pennsylvania, I have made it my life’s mission to help kidney patients manage their condition. I see or hear stories of the inadequate standards of care currently practiced at clinics, hospitals and specialist practices in this country. Many patients I talk to are frustrated and feel like they have been forgotten. We must do better. The problem lies in the lack of health care workers. A severe lack of funding makes it more difficult to hire and keep doctors, nurses and technicians. Much of the problem is demographic. With fewer [...]

Pass Restore in ‘24

2024-05-23T14:33:35+00:00May 6th, 2024|Categories: Article, News, Private Insurance Coverage, Promote Financial Security|

Becky's daughter Dianne relied heavily on her insurance coverage that paid to treat all of her complications and extended her time with her two children. Becky's story is why Congressman Mike Kelly is fighting for the entire kidney community to ensure access to coverage for all dialysis patients. Thank you Rep. Kelly for your efforts to Pass Restore in '24. Learn more about Private Insurance Coverage and view the video.

Rep. Van Drew, please help dialysis patients

2024-05-03T13:59:53+00:00May 2nd, 2024|Categories: Patient Stories in the News, Private Insurance Coverage|

At 20 years old, I was diagnosed with end stage renal disease (ESRD), or kidney failure. Two years later, I began receiving dialysis. I was employed upon diagnosis, but lost my job before beginning dialysis. I began dialysis on Medicare. Since Medicare only covers 80%, and my disability income disqualified me from Medicaid, I could not cover the remaining 20%. I went deep into medical debt just to survive. Six years of dialysis, a kidney transplant and 15 years later, I can now say that I am out of debt. I became a nurse, received an MBA, worked hard, and [...]

Dialysis Patient Citizens Issues Statement on Passing of Congressman Donald Payne Jr.

2024-04-24T20:19:10+00:00April 24th, 2024|Categories: Improve Access to Care, Increase Quality of Care, News, Policy Issues, Press Release, Promote Financial Security, Protect Patient Care|

Rep. Payne Received Dialysis Treatment and Supported DPC Advocacy Efforts WASHINGTON, D.C. (April 24, 2024) - Today, Dialysis Patient Citizens (DPC) Board President Andrew Conkling issued the following statement on the passing of Rep. Donald Payne Jr. (D-NJ). Rep. Payne received dialysis treatment, advocated for better care and insurance coverage for dialysis patients, and spoke at a DPC advocacy event in Washington, DC. “We are deeply saddened to learn of the passing of Congressman Payne, who was a true friend to Dialysis Patient Citizens and a tireless advocate for dialysis patients across the country,” said DPC Board President Andrew Conkling. “Despite [...]

DPC Seeks Information on Patients’ Experience With Itching

2024-04-24T16:12:21+00:00April 24th, 2024|Categories: Advance Patient Choice, Article, Increase Quality of Care, Innovation, Medicare Advantage, Treatment Options|

A couple of years ago, a new drug was approved to treat ESRD-related pruritis. Medicare approved an additional payment for the drug Korsuva for a period of 2 years. But, because of the short expiration date, very few nephrologists prescribed the medication, so even fewer dialysis facilities dispensed the drug. As a result, Korsuva never took hold to become the standard of care for pruritis. We’d like to know (1) Have experienced pruritis? (2) If so, did your clinicians tell you about Korsuva? We would like to convey patients’ experiences as we ask for Medicare to revisit coverage: what it’s like [...]

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