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In The New York Times article, “Coverage for End-of-Life Talks Gaining Ground,” Pam Belluck writes about efforts to reimburse physicians for having difficult but critically important discussions with patients about the kind of care they wish to receive at the end of life. “Five years after it exploded into a political conflagration over ‘death panels,’ […]
In Elana Gordon’s segment with NPR titled, “Hello, May I Help You Plan Your Final Months?” she reports on the work of Vital Decisions, a company that provides counseling via phone to beneficiaries of participating insurance companies in efforts to facilitate discussions about end-of-life care. Counselors often cold-call patients after attempts to reach them via postal […]
Several articles caught our eye this week about the complexities of our reimbursement system and the lack of incentives in our current system for the kind of care patients value and need – time with their physicians and help in coordinating their care among providers in a fragmented system. Coordinating care for people with cancer and […]
Yesterday, I stumbled across the Twitter chat #whentostop, hosted by the Oncology Nursing Society (ONS), addressing one of the most difficult questions anyone with cancer has to face: when is it time to stop treatment? I am new to Twitter chats, though I have lurked during the Healthcare Leader (#hcldr) and the Breast Cancer Social Media (#bcsm) chats and have been impressed […]
In “Breast Cancer Chemotherapy Varies Widely: Study Raises Questions About Early Treatment Choices,” Dr. Elaine Schattner, contributor to Forbes, directs readers to a recently released study that compares the risk of hospitalization between patients with early-stage breast cancer who received different chemotherapy regimens. The study also presented that the six most commonly administered chemotherapy regimens […]
Recently we were reminded of the importance of the Planning Actively for Cancer Treatment (PACT) Act, H.R. 2477 as we participated in the Lymphoma Research Foundation’s (LRF) Lymphoma Education and Advocacy Partners (LEAP) webinar focused on survivorship and care coordination. NCCS has identified the PACT Act as one of our primary public policy priorities as […]
In “Living with Cancer: Difficult Choices,” another installment in her series in The New York Times, Susan Gubar writes about the difficulty of deciding between treatment options when there is no obvious answer. Even patients who have a strong understanding of their disease may lack the expertise to evaluate different options, particularly when the options […]
On Wednesday, as part of the Merkin Series on Innovation in Care Delivery, the Brookings Institute held an event in their new MEDTalk format titled, Reinventing Patient-Centered Cancer Care. The MEDTalk event follows the popular TED Talk format, and it was designed to feature several short presentations that considered the challenges of delivering oncology care while enhancing the patient experience, […]
Three articles caught our eye at NCCS this week. The one that raises the most questions for us in terms of policy development is from our friend, Amy Abernathy, appearing as a blog post for the June 10th issue of The Hill. Her argument in support of patient-centered care is something we have advocated for […]
Cancer Policy Matters Guest Post by Tanisha Carino, Executive Vice President, Avalere Health The Affordable Care Act provides an unprecedented opportunity for millions to gain coverage through the exchange marketplace by enrolling in a qualified health plan (QHP) that covers essential health benefits and limits financial exposure to excessive out-of-pocket costs. More than 8 million […]
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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