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In recent months, there has been significant discussion among cancer patients, their physicians and other health care providers, and cancer organizations about the adequacy of the provider networks in their insurance plans. Cancer patients want assurances that they will receive quality care and can seek second opinions from those with expertise in their particular cancer. […]
This week the National Coalition for Cancer Survivorship (NCCS) joined colleagues in the Cancer Leadership Council (CLC)–a coalition that represents cancer patients, health care professionals, and researchers–in submitting comments on several standards for certification of qualified health plans as outlined in the 2015 Letter to Issuers in the Federally-facilitated Marketplace. The letter commends several recent […]
The National Coalition for Cancer Survivorship and the American Enterprise Institute (AEI) will co-host a symposium, “Putting the Cancer Patient First: Payment Reform in an Age of Personalized Cancer Care.” Friday, February 28, from 8:30 a.m. to 12:30 p.m. at the American Enterprise Institute Conference Center in Washington, DC. For those unable to attend, the event will be streamed […]
In a recent post published on the Health Affairs Blog, patient advocate Aubrey Hill writes about the impact of empathy in improving health outcomes. Hill, who draws on her experiences with the Colorado Coalition for the Medically Underserved, explores social and environmental factors that affect health and care, and suggests that the use of empathy in the […]
NCCS is following two important policy developments that will impact Medicare payments for physician services. Congress is making early steps to reform Medicare payments for physician services, and the Center for Medicare & Medicaid Innovation (CMMI) is seeking public input on refinements in Medicare payments to physician specialists. These steps to improve the Medicare payment […]
Several articles published on Tuesday, February 11, reported on a study in the British Medical Journal which finds death rates from breast cancer from all causes were the same in women who got mammograms and those who did not. The articles points out that the screening also had consequential effects when mammograms detected cancers that were too small […]
On February 8, a New York Times opinion piece published online describes a common situation where the disparities in communication and comprehension of clinical information from doctor to patient may have adverse consequences for patients. The author, Theresa Brown is an an oncology nurse, and she points out that not only can the miscommunication between a health […]
In his ASCO Connection commentary, “ The Awakening of the e-Patient: Are We Prepared to Engage?” Dr. Don Dizon confirms from the provider perspective what we at NCCS know to be true: patients want to be engaged in decision-making about their care, especially for a serious diagnosis like cancer. Dr. Dizon writes of the emergence […]
The empowered patient is a phrase that is often used to suggest a variety of activities that patients can engage in to allow their sense of access and control in certain situations to emerge. This sometimes overused phrase seems particularly interesting to people with cancer who often report that waiting for lab results is a […]
Today’s World Cancer Day calls attention to the fact that there are nearly 14 million people living in the United States today who have had a diagnosis of cancer. For the past 27 years, the National Coalition for Cancer Survivorship (NCCS) has advocated for issues related to the access, quality, and coverage of cancer related […]
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.
NCCS represents the millions of Americans who share a common experience – living with, through and beyond a cancer diagnosis. By sharing your story of how you have been touched by cancer, you are supporting the national cancer survivorship movement.
Together we can improve cancer care for survivors! Sign up to be the first to know about cancer policy issues and ways to take action
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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