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DPC Urges Medicare Agency to Withdraw Proposal That Could Weaken Protections for Transplant Patients

2024-03-29T02:08:06+00:00March 6th, 2014|Categories: Access to Transplant, Article, Comment Letter, Immunosuppressive Drug Coverage, Improve Access to Care|

Dialysis Patient Citizens (DPC) weighed in against a Medicare proposal that would complicate some transplant patients’ access to immunosuppressive drugs. Medicare Part D, like other private health plans, uses drug formularies to keep down costs. Formularies favor certain drugs over others in exchange for discounts. Patients are encouraged to ask their doctors to first prescribe medications on the formulary to take advantage of lower co-pays. Often a patient’s condition can be addressed by a drug on the formulary, but many transplant patients find that “first-line” immunosuppressive treatments aren’t effective or have serious side-effects. For this reason, DPC told CMS: “Immunosuppressive [...]

We Need to Hear From You!

2024-03-29T02:08:07+00:00February 7th, 2014|Categories: Article, Immunosuppressive Drug Coverage, Increase Quality of Care, Treatment Options|

DPC is currently working on two initiatives that require your input! First, the National Quality Forum is conducting a study of "Person-Centered Care" and is looking for patient input. DPC has volunteered to collect patient viewpoints on this subject, and we are inviting our members and other dialysis patients to share your experience with and insights into the care you've received. The National Quality Forum is an organization that endorses the standardized healthcare performance measures that are used by Medicare and other insurers to monitor quality. Its goal in this project is to figure out how to assess whether care is person-centered, which may [...]

DPC Thanks Texas for Allowing ESRD Patients to Purchase Medigap Plans

2024-03-29T02:08:07+00:00January 27th, 2014|Categories: Comment Letter, Medigap Coverage, State Advocacy|

Ms. Sara Waitt, General Counsel Texas Department of Insurance P.O. Box 149104 Austin, TX 78714-9104 Re: Minimum Standards for Medicare Supplement Policies Dear Ms. Waitt, As America’s largest patient-led organization representing dialysis patients, Dialysis Patient Citizens (DPC) works to improve the quality of life of all dialysis patients through education and advocacy. Today we are writing on behalf of over 37,000 dialysis patients in Texas, specifically those who use the Texas Health Insurance Pool for supplemental insurance. We would like to express our gratitude for the recent decision to extend an additional two-month guaranteed issue period from the date of [...]

For New Kidney Failure Patients Under 65: Is Medicare or an Exchange Plan the Better Insurance Option?

2024-03-29T02:08:07+00:00January 13th, 2014|Categories: Medicaid|Tags: |

Chronic Kidney Disease (CKD) patients who progress to end-stage renal disease (ESRD) before the age of 65 now have a new health insurance option—exchange health plans under the Affordable Care Act (ACA). Non-elderly patients who do not have, or will not be continuing, employer-sponsored insurance may be better off in an exchange plan depending on their financial circumstances. The reason for this is that the Affordable Care Act is more generous than Medicare in providing extra financial assistance to low-income individuals. Medicare Programs for Low-Income Patients Patient advocates have never considered Medicare to be a particularly generous health benefit, because it [...]

DPC Thanks California for Reinstating Nutritional Supplement Coverage

2024-03-29T02:08:07+00:00January 8th, 2014|Categories: Comment Letter, Medicaid, State Advocacy|

Ms. Pilar Williams, Chief Medical Supplies & Enteral Nutrition Benefits Branch, Pharmacy Benefits Division California Department of Health Care Services P. O. Box 997413, MS 4604 Sacramento, CA 95899-7413 Re: Proposed Policy Changes to Medi-Cal Enternal Nutrition Products Benefit Dear Ms. Williams, On behalf of the more than 50,000 people on dialysis in California, Dialysis Patient Citizens (DPC) would like to thank you and the state of California for restoring Medi-Cal coverage of enteral nutritional supplements for dialysis patients. With 30,000 members nationwide, DPC works to improve the quality of life of all kidney patients. Access to medically necessary oral [...]

DPC Encourages Coverage of Renal Dialysis in Exchange Plans

2024-03-29T02:08:07+00:00January 6th, 2014|Categories: Comment Letter, Promote Financial Security|Tags: |

Hon. Marilyn Tavenner, Administrator Centers for Medicare and Medicaid Services Department of Health and Human Services Hubert H. Humphrey Building 200 Independence Ave, SW Washington, D.C. 20201 Re: Coverage of Renal Dialysis in Exchange Plans Dear Administrator Tavenner: Dialysis Patient Citizens, America’s largest patient-led organization representing dialysis patients, is comprised of more than 26,000 dialysis and pre-dialysis patients and their families. We seek to ensure the patient point of view is considered by policy makers. We are writing to express our concerns about language we found in a spot-check of exchange plan documents that appears to permit disenrollment of patients [...]

Giving Tuesday: What Can We as Dialysis Patients Give?

2024-03-29T02:08:07+00:00December 6th, 2013|Categories: Immunosuppressive Drug Coverage, Patient's Voice, What is Kidney Disease?|Tags: |

By James Myers, DPC Patient Ambassador On the website for the Polycystic Kidney Foundation, there is an announcement about Giving Tuesday, December 3rd, 2013. It says you can give one of three ways: your voice, your time or your dollars. As a dialysis patient, I don’t know about you, but I don’t have any money. But two things that I have a lot of are voice and time, and I am more than happy to lend those to the cause of defeating PKD. I can honestly say that having an invisible fatal illness has colored every decision that I have [...]

HOPE Act Signed Into Law

2024-03-29T02:08:07+00:00December 1st, 2013|Categories: Access to Transplant, Article|Tags: |

After tireless efforts by DPC and others in the kidney community, President Obama signed the HIV Organ Policy Equity (HOPE) Act into law on November 21, 2013. The HOPE Act was introduced with strong bipartisan support in the House of Representatives by Rep. Lois Capps and Rep. Andy Harris and in the Senate by Sen. Barbara Boxer and Sen. Tom Coburn.  The HOPE Act legalizes the research of transplanting HIV positive organs into HIV positive recipients.  If this research proves this practice to be effective, the organ supply in the United States could increase by 500 organs per year.  Many of these organs [...]

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