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Last week we noted two recent articles addressing palliative and end of life care issues, including an article written from the first-hand experience of Amy Berman, who is both a nurse and an individual living with cancer. In Amy Berman’s recent post on the Health Affairs Blog, she describes palliative care as the “best friend of the seriously ill.” […]
I attended two different events in Washington, DC this week where the focus was on end-of-life care and the challenges of ensuring that people have quality care and dignity at the end of their life. First was the U.S. Senate Special Committee on Aging roundtable meeting entitled, “Continuing the Conversation: The Role of Health Care Providers […]
“What We Can Learn by Listening to Older Adults” Chris Langston, a program director at the John A. Hartford Foundation, penned a recent Prepared Patient Blog post that resides on the Center for Advancing Health (CFAH) website. It refers to what many of us have learned from our work in patient advocacy which points to the dilemmas for the […]
If you already know of Amy Berman, have heard her story, or have been fortunate enough to have spent time with her, you will read more about what words like “patient centered” and “choosing wisely” look like when carried out to treat metastatic cancer. And you will also be exposed to issues that deal with the concept […]
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 […]
In a January 31st New York Times Op Ed, Drs. Rita Redberg and Rebecca Smith-Bindman of UCSF Medical Center report on how the increased uses of medical technologies for diagnosing, treating, and monitoring diseases like cancer, are contributing to unprecedented exposures to radiation. The consequences of these exposures is well documented, particularly for people diagnosed […]
The Institute of Medicine released a meeting summary today of a workshop that took place in February, “Partnering with Patients to Drive Shared Decisions, Better Value, and Care Improvements.” A short video capturing the key messages of the workshop, and including the voice of patients, has also been released. In an efficient health care system, […]
In a blog in Forbes, Peter Ubel asks, “Do Oncologists Lie to Their Patients About Their Prognoses?” Ubel shares a case study in which an oncologist gave a patient a false and overly optimistic estimate of his chance for remission. He says of the doctor’s action, “The oncologist’s behavior that day, the sudden switch from […]
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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