Your generous year-end donation will be matched $1 for $1 DONATE
This month, as part of the 20 Years Later series, we are revisiting the fourth principle of the Imperatives for Quality Cancer Care: Access, Advocacy, and Accountability. Transcript: 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 […]
Dr. Walter F. Baile moderated a panel at the Spring 2015 Cancer Policy Roundtable that included many perspectives on how cancer patients and oncology professionals can collaborate in decision-making that will improve care planning and coordination. Following the panel, Dr. Baile sat down with us to discuss this issue further. In defining shared decision-making as […]
Marlene King was diagnosed with Ductal Carcinoma in Situ (DCIS) in 2008 at the age of 48, and she elected to have a lumpectomy, chemotherapy and radiation. After treatments the cancer seemed to be in remission. In 2011, the cancer returned and she decided it would be best to have to a double mastectomy and reconstructive surgery. However, one […]
This past weekend Kelsey Nepote of NCCS was honored to present a session on patient advocacy at the Stupid Cancer 2015 CancerCon event in Denver. As the largest oncology conference of its kind for the young adult cancer movement, CancerCon brought out hundreds of survivors at different points in the continuum of care, as well as caregivers and loved […]
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 […]
#Medicare, replacing the SGR forumula, and the need for quality measures via @sarahkliff https://t.co/LP8CmO69gX — NCCS – National Coalition for Cancer Survivorship (@CancerAdvocacy) April 6, 2015 Shirley Mertz spoke at FDA Pt-Focused Drug Development Mtng. https://t.co/t4sHSiWLWQ Passionate! pic.twitter.com/XdSDrTekx0 — MetastaticBCNetwork (@MBCNbuzz) April 3, 2015 Dr. Peter Ubel (VIDEO) "If we assume that we know what […]
CME Activity 4/17 at @HopkinsMedicine Kimmel Cancer Center "Cancer Survivorship: Improving Outcomes, Enhancing Care" https://t.co/kLaWwf9xjP — NCCS – National Coalition for Cancer Survivorship (@CancerAdvocacy) April 2, 2015 Palliative care integrated with oncology treatment is a lifeline to QOL for any age and any stage #hpm #CancerFilm https://t.co/XRRVLvCNDx — Rebecca Kirch (@RebeccaKirch) April 2, 2015 https://twitter.com/buffyjhamilton/status/583448116264882178 […]
This video post is part of the 2015 Cancer Policy Matters “The Imperatives for Quality Cancer Care: 20 Years Later” blog series. The third principle from the Imperatives for Quality Cancer Care states, “Standards of cancer care should be driven by the quality of care, not only by the cost of care, and should include participation in […]
This video post is part of the 2015 Cancer Policy Matters “The Imperatives for Quality Cancer Care: 20 Years Later” blog series. The third principle from the Imperatives for Quality Cancer Care states, “Standards of cancer care should be driven by the quality of care, not only by the cost of care, and should include participation in […]
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 […]
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
National Coalition for Cancer Survivorship
8455 Colesville Road | Suite 930 | Silver Spring, MD 20910
info@canceradvocacy.org | (877) NCCS-YES
Privacy Policy | Terms and Conditions
Copyright © 1995-2024 by the National Coalition for Cancer Survivorship
National Coalition for Cancer Survivorship, NCCS, Cancer Survival Toolbox, and related Logos are registered in the United States as trademarks of the National Coalition for Cancer Survivorship.
"*" indicates required fields
"*" indicates required fields
Be the first to hear about cancer policy and survivorship issues! Subscribe and receive the biweekly NCCS Health Care Roundup, invites to webinars and events, and more.
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