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Tag Archive for: Patient Navigation

WCOE: Shared Decision-Making and Getting Doctors to Listen

March 9, 2015/in Cancer News, Cancer Policy Blog Care Planning, Quality Cancer Care, Survivorship Care NCCS News

Components of shared decision-making. #CTACSummit2015 pic.twitter.com/1yjm5MSwDC — Shelley Fuld Nasso (@sfuldnasso) March 3, 2015 Public meeting on breast cancer patient-focused drug dev. April 2, register now https://t.co/1OXRCdQvZM — NCCS – National Coalition for Cancer Survivorship (@CancerAdvocacy) March 2, 2015 "regard the cancer patient as autonomous individual who has the right 2B involved in decisions.." via […]

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Decision-Making in Cancer Care: Communication (INFOGRAPHIC)

February 27, 2015/in Cancer News, Cancer Policy Blog Care Coordination, Care Planning, Palliative Care, Quality Cancer Care, Survivorship Care NCCS News

The second principle of the Imperatives for Quality Cancer Care 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 with cancer. Health care plans must regard the cancer patient as an autonomous individual who has the right to be involved in decisions about […]

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Guest Post: Palliative Care in Oncology—We’ve Come a Long Way, Baby …But Let’s Not Rest on Our Laurels

February 26, 2015/in Cancer News, Cancer Policy Blog Care Planning, Clinical Guidelines, Palliative Care, Quality Cancer Care, Survivorship Care NCCS News

“The good physician treats the disease; the great physician treats the patient who has the disease.” -William Osler Since the creation of the National Cancer Act  in 1971, the medical establishment—and indeed our entire society—has taken up the powerful metaphor of a “war on cancer” as the approach to attacking and overcoming this dreaded disease.  This […]

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WCOE: New CMS Oncology Care Model Offers Hope, End of Life Planning, and ACA Questions Answered

February 13, 2015/in Cancer News, Cancer Policy Blog Access to Care, Affordable Care Act, Care Planning, Health Care Coverage, Palliative Care, Quality Cancer Care, Survivorship Care NCCS News

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 […]

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https://canceradvocacy.org/wp-content/uploads/2012/12/NCCS_Starburst_Thumbnail.jpg 125 125 actualize https://canceradvocacy.org/wp-content/uploads/2020/06/NCCA-Logo.png actualize2015-02-13 15:10:032015-02-13 15:10:03WCOE: New CMS Oncology Care Model Offers Hope, End of Life Planning, and ACA Questions Answered

Being Mortal Is Far From Being Morbid: Responding to FRONTLINE’s Profile of Surgeon Atul Gawande and End of Life Care

February 11, 2015/in Cancer News, Cancer Policy Blog Care Coordination, Care Planning, Palliative Care, Quality Cancer Care, Shared Decision-Making, Survivorship Care NCCS News

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 […]

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https://canceradvocacy.org/wp-content/uploads/2015/02/agawande.jpg 321 699 actualize https://canceradvocacy.org/wp-content/uploads/2020/06/NCCA-Logo.png actualize2015-02-11 16:58:102020-11-20 12:02:16Being Mortal Is Far From Being Morbid: Responding to FRONTLINE’s Profile of Surgeon Atul Gawande and End of Life Care

Revisiting the Second Principle of the Imperatives for Quality Cancer Care—Treating the Whole Person

February 6, 2015/in Cancer News, Cancer Policy Blog Care Coordination, Care Planning, Palliative Care, Quality Cancer Care, Survivorship Care NCCS News

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 […]

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https://canceradvocacy.org/wp-content/uploads/2015/01/20years.gif 500 500 actualize https://canceradvocacy.org/wp-content/uploads/2020/06/NCCA-Logo.png actualize2015-02-06 12:06:192015-02-06 12:06:19Revisiting the Second Principle of the Imperatives for Quality Cancer Care—Treating the Whole Person

Announcing a New Blog Series: “The Imperatives for Quality Cancer Care” 20 Years Later

January 25, 2015/in Cancer News, Cancer Policy Blog, NCCS News Access to Care, Affordable Care Act, Care Coordination, Care Planning, Health Care Coverage, Health Equity, Palliative Care, Payment Reform, Quality Cancer Care, Survivorship Care NCCS News

Read posts from the new blog series: “The Imperatives for Quality Cancer Care” 20 Years Later In 1995, NCCS published Imperatives for Quality Cancer Care: Access, Advocacy, Action, and Accountability (Imperatives), the culmination of an inclusive, community-based process.  Adopted at the First National Congress on Cancer Survivorship, the Imperatives represented the community’s first look at […]

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We’re Going Digital: Last Week to Order Cancer Survival Toolbox – Blood Cancer Programs in Audio CD

December 9, 2014/in Cancer News Care Coordination, Care Planning, Quality Cancer Care, Survivorship Care NCCS News

TIME’S RUNNING OUT: Cancer Survival Toolbox – Blood Cancer Programs – Free Shipping on Bulk Audio CD Orders The National Coalition for Cancer Survivorship (NCCS) is pleased to announce that the Cancer Survival Toolbox© is going fully digital! If you would like to order any audio CDs of the following blood cancer programs, please do […]

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NCCS Responds to Two Recent Articles Covering the Complexities of Transparency and Shared Decision-Making Issues

November 28, 2014/in Cancer News, Cancer Policy Blog Care Coordination, Care Planning, Clinical Guidelines, Payment Reform, Quality Cancer Care, Survivorship Care NCCS News

Two stories in last week’s New York Times illustrate the complexities of the changing healthcare marketplace.  They both describe discrete issues that beleaguer and hinder the transparency and shared decision-making that we at the National Coalition for Cancer Survivorship (NCCS) call for when patients need to make an informed decision about their care.  We comment […]

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Guest Post: Forgotten Survivors—Supporting the Needs of Patients with Advanced Cancers

November 18, 2014/in Cancer News, Cancer Policy Blog Care Coordination, Care Planning, Palliative Care, Quality Cancer Care, Survivorship Care NCCS News

Guest post by Lillie D. Shockney, RN, BS, MAS, Director of Johns Hopkins Breast Center and Cancer Survivorship Programs. On November 19, 2014, NCCS will present the Catherine Logan Award for Service to Survivorship to Lillie at the Focus on the Care evening reception in Washington, DC.  Though more and more cancer patients are being diagnosed […]

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Latest News

Brett Wilson – Navigating Childhood Cancer and Finding Purpose in Advocacy

September 13, 2023
Advocate Spotlight: Brett Wilson Brett Wilson's cancer experience started when she was just two years old. Her mother was concerned…
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Registration Open: 2023 State of Survivorship Survey Results Briefing | October 3

September 7, 2023
The National Coalition for Cancer Survivorship (NCCS) conducts an annual State of Survivorship Survey, in partnership with Edge…
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We did it! DIEP Flap Codes Saved

CMS Announces It Will Retain Breast Reconstruction Codes, A Reversal That Protects Patient Access to DIEP Flap Surgery

August 22, 2023
Yesterday, the Centers for Medicare and Medicaid Services (CMS) announced that it will retain procedure codes for breast cancer reconstruction,…
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Link to: Cancer Policy and Advocacy Team (CPAT)

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The NCCS Cancer Policy & Advocacy Team (CPAT) is a program for survivors and caregivers to learn about pressing policy issues that affect quality cancer care in order to be engaged as advocates in public policy around the needs of cancer survivors.

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Harmar Brereton, MD

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