Tag Archive for: care planning

WCOE: Life-saving End-of-life Discussions, New HHS Investment, When Seniors Talk to Med Students, and More

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What Caught Our Eye (WCOE) Each week, we recap the cancer policy articles, studies, and stories that caught our attention. "A nurse with fatal breast cancer says end-of-life discussions saved her life" #choosingwisely @NotesOnNursing https://t.co/cPhjYxPKGt — ABIM Foundation (@ABIMFoundation) September 29, 2015 How does cancer affect people from different populations and groups? This video explains […]

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Guest Post by Dr. Patricia Ganz: What Cancer Patients and Their Families Can Do to Coordinate Post-Treatment Care

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Twenty years later, the 9th Principle of the NCCS Imperatives for Quality Cancer Care could not be more relevant. Increasingly, patients are required to take more responsibility for their health, using knowledge and self-monitoring tools that have become an essential part of medical care, such as monitoring of blood pressure, physical activity, and weight-—to name […]

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Remembering Dr. Brent Whitworth, A Dear Friend and Compassionate Doctor

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Post by NCCS CEO Shelley Fuld Nasso Today marks three years since my dear friend, Dr. Daniel Brent Whitworth, passed away at the age of 43, 19 months after being diagnosed with advanced kidney cancer. I met Brent on the first day of orientation week at Rice University in 1987. We became fast friends, had the […]

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Caring for Cancer Survivors: A Primary Care Physician’s Perspective on the Last Twenty Years and the Road Ahead

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Over the past twenty years, the number of cancer survivors has grown substantially.  Survivors are also living longer, getting older, and have numerous medical conditions that require attention.  While survivors typically receive general medical care in primary care settings, the role of primary care providers (PCPs) in the long-term follow up of survivorship needs is […]

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Twenty Years Later Blog Series: Introducing the Ninth Principle of the Imperatives for Quality Cancer Care

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As part of our 20 Years Later blog series which examines progress in advancing the principles in the 1995 NCCS publication Imperatives for Quality Cancer Care: Access, Advocacy, Action, and Accountability (Imperatives), this month we will look at the ninth principle of Imperatives: “The responsibility for appropriate long-term medical care must be shared by cancer survivors, […]

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WCOE: Sept. 29 Chat About Side Effects, Friends at the End of Life, (Mostly) Living With A Brain Tumor, and More

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What Caught Our Eye (WCOE) Each week, we recap the cancer policy articles, studies, and stories that caught our attention. Join us on Sept 29 at 2pm ET for a chat about #cancer side effects & symptoms. Use #CTalk. https://t.co/oix4S5ISms — NCCS – National Coalition for Cancer Survivorship (@CancerAdvocacy) September 27, 2015 https://twitter.com/NikiBarrPhD/status/647408343598809088 Seeing is […]

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NCCS Submits Letters, Joins Cancer Leadership Council and C-P Alliance, in Comments to CMS on Proposed Revisions to Medicare Physician Fee Schedule

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NCCS submitted letters to the Centers for Medicare and Medicaid Services (CMS) on its proposed revisions to the Medicare physician fee schedule for calendar year 2016. In our letter, NCCS commended CMS for its efforts to enhance comprehensive care management for certain Medicare beneficiaries.  Through improvements in fee-for-service payments and various demonstration initiatives, CMS has made […]

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WCOE: How Chemo is Given, PCORI Hosts Twitter Chat About Cancer Side Effects, “Good Cancer,” How Mammography is Both Helping and Hurting, and Lung Cancer Incidence Increases in Never-Smokers

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What Caught Our Eye (WCOE) Each week, we recap the cancer policy articles, studies, and stories that caught our attention. How is chemotherapy given? In many different ways, as we explain: https://t.co/vqUOL5PBtc pic.twitter.com/tS2Xn8fiwe — National Cancer Institute (@theNCI) September 9, 2015 Sept 29 at 2pm ET: join our Twitter chat about #cancer side effects & […]

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Video Post: Advocate Marlene King Discusses Communicating End-of-Life Preferences and Quality of Life

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In 2008, Marlene King was diagnosed with ductal carcinoma. After treatment, the cancer seemed to be in remission, however in December 2011 the cancer returned in the same breast. She opted for a double mastectomy with expanders and implants. In late July 2012, she learned that her cancer had metastasized to her sternum, as well […]

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Video Post: Dr. Claire Snyder Discusses How Patient-Reported Outcomes Can Improve Cancer Care

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In March 2015, Dr. Claire Snyder participated in a panel discussion at the Cancer Policy Roundtable hosted by the National Coalition for Cancer Survivorship. The panel featured perspectives on how cancer patients and oncology professionals can work together to improve care planning and patient outcomes. Following the panel, Dr. Snyder sat down with us to […]

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