fbpx

HB 430 – Letter of Support

2024-03-29T01:10:09+00:00February 28th, 2022|Categories: Patient Ambassadors, Patient Stories in the News, Spotlight|

February 28, 2022 The Honorable Bart Rowland, Chair The Honorable Derek Lewis, Vice Chair House Banking & Insurance Committee Kentucky General Assembly 700 Capitol Avenue Frankfort, KY 40601 RE: HB 430 - SUPPORT Dear Chair Rowland, Vice Chair Lewis and Members of the Committee: My name is James O. “Hap” Strunk. I am a resident of Whitley City, serve as Chairman of the Kentucky Board of Embalmers & Funeral Directors, and also one of the more than 9,000 (i) Kentuckians with End Stage Renal Disease (ESRD). From my volunteer role as a Patient Ambassador for Dialysis Patient Citizens, I write [...]

Cover the Medigap

2024-03-29T01:10:11+00:00October 21st, 2021|Categories: Patient Stories in the News, Spotlight|

As a dialysis patient, one-time kidney transplant recipient, and a dialysis tech of 12 years, I’ve seen kidney care from just about every angle. I was fortunate to have insurance through my job which meant I didn’t have to deal with the out-of-pocket costs and hassle that sometimes come with Medicare, but that’s not true for everyone. Instead, they rely only on Medicare, and if it doesn’t cover certain costs, they can get stuck with a huge bill. Lawmakers can help change that by passing bills like the Jack Reynolds Memorial Medigap Expansion Act, which would open Medigap coverage to [...]

Dialysis patients need support from lawmakers

2024-03-29T01:10:12+00:00October 8th, 2021|Categories: Patient Stories in the News, Spotlight|

Dear Editor:   This December marks three years in my battle with kidney disease. My kidney failure diagnosis was hard to pin down, and without my husband, I am not sure I would still be here. My diagnosis came with a lot of things you’d expect: many hours spent in doctors’ offices and at dialysis treatment centers. What I didn’t know is that this diagnosis would also eventually put me in the hospital, with medical bills racking up the entire time  Of course, dialysis alone is expensive, especially when patients must pay for any costs that Medicare doesn’t cover. And, for many dialysis [...]

DPC Advocates Take Congress by Web Storm

2024-03-29T01:10:12+00:00September 21st, 2021|Categories: Article, Care Coordination, Get Involved, Improve Access to Care, Medigap Coverage, News, Patient Ambassadors, Policy Issues, Promote Financial Security, State Advocacy|

DPC held its annual Congressional Advocacy Day on September 21st, which was another great success! More than a hundred and fifty DPC Patient Ambassadors, Board members, staff and dialysis partners participated in nearly 200 Congressional meetings throughout the day to lobby on two important federal bills that would provide greater financial security and improve the quality of life for dialysis patients: The Jack Reynolds Memorial Medigap Expansion Act (H.R. 1676) would expand guaranteed issue rights to Medicare supplemental health insurance policies, known as Medigap, to all End Stage Renal Disease (ESRD) patients under age 65 in every state. Access to [...]

Alabama kidney patients need Congress to support Medigap Expansion Bill

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

Since I started dialysis in 2018, I’ve been lucky to have coverage that supplements Medicare and helps to keep my costs down. Even with that added coverage, though, I’ve noticed it is tough to afford all of the medicines I need. For patients without the additional coverage I have, that cost is even higher. When Medicare doesn’t pay for medication or dialysis treatment. That money comes out of their pocket, and the financial burden is just too much for some patients to take on. For the many dialysis patients like me with diabetes, the problem is even bigger because of [...]

Legislations would provide help for dialysis patients

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

I’ve lived on dialysis for 22 years, but there was a time when my kidney disease almost took my life. Through dialysis and a failed kidney transplant, though, I’ve done my best to stay upbeat and am excited to get another transplant kidney soon, hopefully. While it’s been a tough road, I’ve at least had the coverage I need to pay for my treatments. A lot of patients I’ve met only have Medicare, which doesn’t always cover their treatments and medications. Instead, they have to pay out-of-pocket costs as high as 20% of the cost of their treatments. Congress can [...]

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 [...]

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 [...]

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 [...]

Go to Top