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About Hannah Bracamonte

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So far Hannah Bracamonte has created 605 blog entries.

Dialysis patients need Medigap expansion bill

2024-03-29T01:10:13+00:00September 8th, 2021|Categories: Patient Stories in the News, Spotlight|

It’s been 34 years since my brother donated his kidney to me and changed my life for the better. Now, we do what we can to support dialysis patients in our area and help people better understand just what challenges patients face every single day. For a lot of them, it all comes back to coverage. As a transplant recipient, it’s a major problem that I’ve experienced firsthand. Three years after my transplant, I lost the coverage I had and needed to turn to other plans that came with big out-of-pocket costs. Other patients across the country are in the [...]

Letter: Bill can ease costs

2024-03-29T01:10:13+00:00September 8th, 2021|Categories: Patient Stories in the News, Spotlight|

Starting dialysis 12 years ago at 28 completely changed my life. I had to begin going to a clinic for the hours-long treatments that dialysis involves, and the treatments, as well as their effects, forced me to end my career as an EMT. It was a difficult adjustment to make, but I’ve at least been fortunate enough to have supplemental insurance coverage through my wife’s work that helps to cover the cost of my treatments. Without that additional coverage, we’d have to find a way to make up for the 20 percent of the cost Medicare doesn’t pay for. Under [...]

Letter: Help for dialysis patients

2024-03-29T01:10:13+00:00September 8th, 2021|Categories: Patient Stories in the News|

Dialysis brings a lot of challenges, but one of the biggest is simply getting the coverage you need. The treatments make it very challenging for patients like me to work a traditional job, which means many of us do not have employer-sponsored insurance and rely on Medicare. If it doesn’t cover a specific medication or treatment, we have no choice but to pay out-of-pocket or get an expensive supplementary plan. That could change with a new bill called the Jack Reynolds Memorial Medigap Expansion Act. It would expand Medigap coverage to patients under 65 with end-stage renal disease, meaning more [...]

New Kidney Care Bills Vital for Expanding Coverage & Reducing Costs

2024-03-29T01:10:13+00:00September 3rd, 2021|Categories: Patient Stories in the News|

Starting dialysis seven years ago was a bit of a rude awakening. I had to accept that my day-to-day life had changed, and that I’d now need to devote significant time each week just to go through treatments. One of the most challenging parts of the process, though, was learning the ins and outs of the healthcare system. It was a difficult adjustment, but I’ve been lucky enough to have coverage that takes care of my dialysis treatments and the medications I need. However, I know through my conversations with other patients at my local clinic that the reality is [...]

LETTER: Expand Medigap and help dialysis patients get the care they need

2024-03-29T01:10:13+00:00August 29th, 2021|Categories: Patient Stories in the News|

I was only 19 years old when I was diagnosed with kidney disease. Because I was under 65, Medicare didn’t cover the full costs of treatments and medications throughout my 10 tough years on dialysis, and I was forced to make difficult choices between the care I needed and basic needs like groceries. A new bill, however, the Jack Reynolds Memorial Medigap Expansion Act, would change that by expanding Medigap coverage to dialysis patients under the age of 65. This bipartisan bill would make sure that every dialysis patient gets the healthcare coverage they need, which is why our leaders, [...]

2021 Annual Survey Last Call!

2024-03-29T01:10:13+00:00August 26th, 2021|Categories: 5-Star Ratings, Access to Transplant, Article, Care Coordination, Charitable Premium Assistance, Dental Coverage, Dialysis Funding, Immunosuppressive Drug Coverage, Innovation, Medicaid, Medicare Advantage, Medigap Coverage, Patient's Voice, Protect Patient Care, Quality Incentive Program, Take Action, Transplant Donor Protection, Transportation Services, Treatment Options|Tags: |

24 hours remain to complete our survey. Make sure to complete your survey for a chance at one of 10 remaining $100 gift certificates. Our 2021 Annual Membership Survey is live, and it will remain open until Friday, August 27. Your feedback helps to shape our public policy agenda and patient education priorities for the next year. This year we ask that both patients and caregivers take our survey. Rest assured your responses will remain completely anonymous. We only share the overall survey results with state and federal level policy makers, so they will better understand your needs, experiences, and [...]

Dialysis Patients Need Help. A New Medigap Bill is the Perfect Place to Start.

2024-03-29T01:10:13+00:00August 24th, 2021|Categories: Patient Stories in the News, Spotlight|

In 2004 my dad had his first dialysis treatment after flatlining from a heart procedure. We were not sure he would make it through the night as his organs were shutting down, but we were told that dialysis would help and at the time, we wanted to just do whatever was needed to save him. When my dad left the hospital, we were told that his kidneys would require dialysis in the future and his doctors would monitor him. Fast-forward to 2007, and we were informed that my dad would require dialysis three days a week for four hours at [...]

DPC Urges Medicare to Add Resources for Health Equity

2024-03-29T01:10:13+00:00August 19th, 2021|Categories: Comment Letter, Improve Access to Care, Medicare Advantage, Quality Incentive Program|

DPC has filed its letter commenting on this year’s Medicare ESRD Proposed Rule, which governs payments to dialysis facilities. The Centers for Medicare & Medicaid Services (CMS) heralded this year’s payment rules as undertaking new initiatives to reduce health disparities. DPC’s letter critiques these initiatives as insufficient and endorses alternative approaches. CMS is proposing to collect new data on racial disparities, and to stratify quality measures so that facilities serving disadvantaged patients no longer receive QIP payment reductions simply because patients are poor. DPC endorses these moves, but points to recent calls by experts to address disparities by supplementing payments to [...]

Action Alert – Support Care Coordination for Dialysis Patients

2024-03-29T01:10:13+00:00August 16th, 2021|Categories: Article, Care Coordination, Improve Access to Care, Take Action|

The BETTER Kidney Care Act (H.R. 4942/S. 2649) was reintroduced by Senators Young (R-IN) and Sinema (D-AZ), along with Representatives Blumenauer (D-OR), Butterfield (D-N), and Cardenas (D-CA). This bill would enhance access to care coordination services for thousands of patients across the United States currently living with End-Stage Renal Disease (ESRD). It could also help with services not covered by Medicare such as dental care and transportation. Coordinated care is essential for improving the overall care and health of ESRD patients. Specifically, better care coordination could mean help for patients with: scheduling doctors’ appointments, reviewing their medication regime, dealing with dialysis [...]

LETTER TO THE EDITOR: Medigap Bill A Welcome Change for Mississippi Dialysis Patients

2024-03-29T01:10:14+00:00August 12th, 2021|Categories: Patient Ambassadors, Patient Stories in the News, Spotlight|

Kristal pictured with her husband, Ernest Higgins. Photo by Cameron B. Potts My kidney transplant failing in 2017 changed my life. I went back on dialysis for the first time since 2012 and was spending more time in the hospital than I had before. Then, I lost my job and the insurance coverage it provided, and I had to go back on Medicare, which didn’t cover the whole cost of dialysis and forced me to pay up to 20 percent of the cost of my treatments. I’m not alone, either. Dialysis patients all over the country struggle to [...]

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