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Congress: Please stand up for Minnesotans on dialysis

2024-09-17T18:33:04+00:00September 13th, 2024|Categories: Patient Stories in the News, Private Insurance Coverage|

When I was serving as my father’s caregiver through his dialysis treatments, I was struck by how difficult it can be to navigate the health insurance landscape. I was constantly on the phone with Medicare and the VA to ensure he was covered. Dialysis is an essential treatment that extends someone’s life and keeps them healthy, which is why it shouldn’t be hard to get proper coverage. Yet instead of becoming easier for patients, it’s getting even more complicated. The Supreme Court recently ruled that private insurers may no longer have to provide full coverage for dialysis treatments, even though [...]

Letter: ‘Requesting legislative action’

2024-09-17T18:20:12+00:00September 13th, 2024|Categories: Patient Stories in the News, Private Insurance Coverage|

I urge U.S. Rep. Jasmine Crockett (D-TX) to support the Restore Protections for Dialysis Patients Act. This legislation allows new dialysis patients to keep their private insurance, a critical financial lifeline, for their initial months of care. Dialysis is the only treatment for those awaiting a kidney transplant. However, a recent Supreme Court decision enables private insurers to weaken coverage in the first months of care, essentially pushing patients onto Medicare prematurely. This shift places enormous burdens on patients who need stability during a challenging time when they are often focused on just trying to keep their jobs. I was [...]

Indiana Governor Signs Affordable Medigap Access Legislation

2024-08-22T14:12:38+00:00August 16th, 2024|Categories: Article, Medigap Coverage, Protect Patient Care, State Advocacy|

In a major victory for under-age 65 dialysis patients in Indiana, Governor Eric Holcomb signed SB 215 in a formal bill signing ceremony on August 15, 2024. Attending this ceremonial bill signing was DPC Patient Ambassador Arthur Hill and DPC Eastern Region Advocacy Director Elizabeth Lively. Arthur’s impactful story of his dialysis journey elevated the voices of dialysis patients in Indiana, bringing the struggles of dealing with kidney failure to the forefront and influencing the hearts and minds of legislators to support SB 215. SB 215 becomes effective on December 31, 2024. This legislation provides access for under-age 65 dialysis [...]

DPC Advocates for Dialysis Patients at National Conference of State Legislators Summit

2024-08-22T14:12:44+00:00August 8th, 2024|Categories: Article, Medigap Coverage, Protect Patient Care, State Advocacy|

State legislators from across the nation convened in Louisville, Kentucky August 5-8 for the 50th National Conference of State Legislators Summit. As part of DPCs ongoing work in the states, DPC was on hand to share our critically important work on access to affordable Medigap coverage. Megan Hashbarger, VP of Government Relations, Yolonda Brisbane, Grassroots Manager, and Elizabeth Lively, Eastern Region Advocacy Director attended the event. We heard so many stories from interested state legislators who either a family member or friend dealing with kidney disease issues. Legislators from Arkansas, California, Georgia, Iowa, Kentucky, Maryland, Michigan, New Mexico, Ohio, Oklahoma and [...]

Americans should never be punished for having a debilitating illness

2024-07-30T19:21:34+00:00July 27th, 2024|Categories: Patient Stories in the News, Private Insurance Coverage|

Americans should never be punished for having a debilitating illness. Unfortunately, that’s what happens to people like me with illnesses such as End Stage Renal Disease (ESRD), otherwise known as kidney failure. ESRD changed my life. Paying for ESRD treatment, whether it was dialysis (the treatment which works in place of kidneys) or transplant, both of which I experienced, proved to be extremely difficult. I had to rely on Cobra, Medicare, and Medicaid, and I struggled to pay for life-saving treatment. For other ESRD patients, they face financial burdens because private insurers are allowed to kick them off their insurance. [...]

State Advocacy Update – Council of State Governments Meetings

2024-07-25T17:45:31+00:00July 25th, 2024|Categories: Advance Patient Choice, Article, Improve Access to Care, Increase Quality of Care, Medigap Coverage, News, Policy Issues, Promote Financial Security, Protect Patient Care, State Advocacy|

DPC’s two State Advocacy Directors have been busy advocating for dialysis patients this summer. Pamela Zielske, DPC’s Western Region Advocacy Director, attended the 77th Council of State Governments Annual Meeting in Portland, Oregon earlier this month. The event provided an outstanding opportunity to cultivate relationships with state legislators and attend policy sessions and legislative learning labs, including one hosted by Fresenius Medical Care on Improving Equity and Health Outcomes in Kidney Health Care. With legislators in attendance from 13 western states, the CSG West Meeting was a tremendous opportunity to elevate our advocacy work on behalf of dialysis patients with [...]

Restore Protections for Dialysis Patients Act needs NJ delegation’s support

2025-04-22T18:11:45+00:00July 22nd, 2024|Categories: Featured Spotlight, Get Involved, Patient Ambassadors, Patient Stories in the News, Private Insurance Coverage, Spotlight|

For most patients with End Stage Renal Disease (ESRD), or kidney failure, their diagnosis comes as a shock. One day, I was suddenly rushed to the ER and received the shocking diagnosis. I suddenly had to begin dialysis, the only treatment for ESRD outside of a kidney transplant. My life changed at that moment. I would now have to do almost daily dialysis treatments that can take several hours each time. I didn’t know how I was going to keep working and make ends meet. On top of that, I’ve had to deal with Medicare and Medicaid for my coverage [...]

Federal bill critical for dialysis patients

2024-07-23T17:29:03+00:00July 19th, 2024|Categories: Patient Stories in the News, Private Insurance Coverage|

COVID-19 changed the lives of all Americans. For me, a COVID-19 infection led to kidney failure. When the doctor diagnosed me with End Stage Renal Disease (ESRD), I could not believe it. Suddenly, I had to begin dialysis, the arduous and frequent treatment which replaces my kidneys. Dialysis allows me to live. Unfortunately, the health care expenses for dialysis patients can become overwhelming, especially since many of us have other health conditions. Fortunately, I began treatment on private insurance with a very low deductible, which kept me afloat. Dialysis became much less affordable once I transitioned to Medicare after 30 [...]

Supreme Court ruling puts decades-long patient protections at risk

2024-07-22T14:34:53+00:00July 19th, 2024|Categories: Patient Stories in the News, Private Insurance Coverage|

To the Editor: Chances are you know someone with End Stage Renal Disease (ESRD), or kidney failure. ESRD affects people of all ages and backgrounds. My kidneys failed despite the fact that I had a healthy lifestyle, and it was a hard pill to swallow. The only two treatments available for kidney failure are transplants — which are scarce — and dialysis, the treatment that removes extra fluid and waste products from your blood when your kidneys can’t. I received dialysis treatment for seven years before receiving a transplant in 2023. Dialysis is an expensive treatment. Thankfully, my Congressman, Paul [...]

Rep. Houchin needs to support act to help dialysis patients in Indiana

2024-07-23T17:42:42+00:00July 19th, 2024|Categories: Patient Stories in the News, Private Insurance Coverage|

Dialysis patients and families of the 9th Congressional District need your help. In 2022, the Supreme Court decided that group health plans do not violate the Medicare Secondary Payer Plan (MSP) law by changing the benefits for dialysis patients, which could force them into government coverage. This decision will place dialysis patients and their families in severe financial hardship, as Medicare only covers 80% of our health care expenses. Only recently did my state look at increasing patient access to private plans to help us cover the remaining 20%. In the meantime, we face restricted access to care and even [...]

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