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This guest post is part of the 2015 Cancer Policy Matters “The Imperatives for Quality Cancer Care: 20 Years Later” blog series. Although noted in the literature as early as the 1970’s, serving as the foundation for the 1982 establishment of The Wellness Community (now The Cancer Support Community) and certainly referenced in the 1995 NCCS […]
As part of our 20 Years Later blog series, NCCS CEO Shelley Fuld Nasso discusses the difference between palliative and end-of-life care, as well as barriers to palliative care in this video. The second principle from the Imperatives for Quality Cancer Care states, “Quality cancer care should be available in a health care system whose […]
The new #Oncology Care Model offers #cancer patients the hope of better care. @canceradvocacy @CMSinnovates https://t.co/uQA76ALOG3 — Shelley Fuld Nasso (@sfuldnasso) February 13, 2015 "What Does It Mean?" commentary by @drdonsdizon via @ASCO https://t.co/mr83TSTiYe clarity in doctor/patient communication — NCCS – National Coalition for Cancer Survivorship (@CancerAdvocacy) February 12, 2015 #WhatMattersMost – To be able […]
The National Coalition for Cancer Survivorship (NCCS) applauds the release by the Centers for Medicare and Medicaid Services (CMS) of the Oncology Care Model, a multi-payer program with the goal of providing cancer patients with higher quality, better coordinated care, at a lower cost. The Oncology Care Model builds on the current fee-for-service system for […]
On public television stations nationwide, the award-winning FRONTLINE series aired a program on February 10th based on the work of noted surgeon and writer, Atul Gawande. In addition to Gawande’s many clinical and surgical talents, he has the rare gift of writing articles and books for all of us, no matter what our level of […]
This month, as part of the 20 Years Later series, we are revisiting the second principle of the Imperatives for Quality Cancer Care: Access, Advocacy, and Accountability. The second principle states, “Quality cancer care should be available in a health care system whose standards and guidelines are developed in consideration of treating the whole person […]
Hard for clinicians to give up old practices, even when new evidence reveals that those practices offer little value: https://t.co/n3vFLx199y — Peter Ubel (@peterubel) February 6, 2015 "Dying Shouldn't Be So Brutal" new @nytopinion series on End-of-Life that I will also be writing for–soon, I hope. https://t.co/xughvb75Lh — TheresaBrown (@TheresaBrown) February 3, 2015 https://twitter.com/LlyOncOnCanvas/status/563019956565331968 We […]
NCCS submitted comments to the Food and Drug Administration (FDA) on the Draft Guidance: Framework for Regulatory Oversight of Laboratory Developed Tests (LDTs). We support the FDA’s efforts to develop a strong regulatory framework for LDTs and commend the agency for the open and transparent process it has pursued in developing the framework and receiving […]
I was honored to represent NCCS along with leaders in the health care community at the White House on Friday when President Obama announced his new Precision Medicine Initiative. Introducing the President was 19-year-old Harvard Student Elana Simon, who researched her own liver cancer and helped identify the genetic cause of the rare disease. The […]
This post is part of a special blog series: “The Imperatives for Quality Cancer Care: 20 Years Later.” Read more from this series. The first imperative states, “People with cancer have the right to a system of universal health care. This access should not be precluded because of preexisting conditions, genetic or other risk factors, […]
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Founder
Northeast Regional Cancer Institute
“Perhaps one of the most impactful collaborations in Dr. Brereton’s extraordinary career remains his early work and long friendship with Ellen Stovall. Through him, and in turn through the thousands of lives he has touched, Ellen’s work continues, and her mission lives on.”
—Karen M. Saunders
President, Northeast Regional Cancer Institute