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The fourth principle in the Imperatives for Quality Cancer Care states, “All people diagnosed with cancer should have access to and coverage for services provided by a multidisciplinary team of care providers across the full continuum of care. Health care plans should be held accountable for timely referral to appropriate specialists when symptoms of cancer […]
Over the weekend, I had the pleasure of attending and presenting at Stupid Cancer CancerCon in Denver, Colorado. Stupid Cancer is the largest US-based charity that comprehensively addresses young adult cancer through advocacy, research, support, outreach, awareness, mobile health, and social media. CancerCon is their yearly conference and social networking event for the young adult […]
SGR: Bipartisan Senate ends flawed Medicare payment formula https://t.co/9KQkuIFqDr — Alec Stone (@ONSAlec) April 15, 2015 What Is the ‘Doc Fix’? https://t.co/M4Iy0rh8K7 via @WSJPolitics — NCCS – National Coalition for Cancer Survivorship (@CancerAdvocacy) April 15, 2015 Living With Cancer: In and Out of the Closet https://t.co/dd3GxpPVVV via @nytimeswell — NCCS – National Coalition for Cancer […]
The National Coalition for Cancer Survivorship (NCCS) submitted comments to the House Energy and Commerce Committee on its 21st Century Cures legislative initiative. In our comments, we urged that the 21st Century Cures effort reflect a goal of ensuring delivery of appropriate treatment to each patient, based on a shared decision-making process. To achieve the […]
Data integration solution addresses one of the barriers associated with creating Care Plans for cancer survivors Journey Forward, a leader in survivorship care planning, and Electronic Registry Services (ERS), a leading provider of cancer registry software, today announced a successful implementation that enhances the use of patient data in after-care plans. Specifically, this enables data […]
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 […]
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 […]
Too Fast, or Too Slow? Public disagrees over pace of #FDA's new drug approvals https://t.co/gnvqJq56AH via @RAPSorg — ResearchAmerica (@ResearchAmerica) February 25, 2015 Everything I know about a good death I learned from my cat https://t.co/KeC5qEcynk — Shelley Fuld Nasso (@sfuldnasso) February 25, 2015 A Faster Way to Try Many Drugs on Many Cancers https://t.co/EFms6hYq3d […]
“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 […]
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 […]
Survivorship Champions is a program for all clinicians and researchers, both oncology and primary care, who are interested in improving survivorship care and primary care’s role in caring for cancer survivors.
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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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