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The annual American Society of Clinical Oncology meeting is often followed by a flurry of announcements and news as developers of cancer drugs present results about their recent clinical trials. While news of new tools to help increase cancer survival rates is always welcome, many patient advocates attend the annual meeting with a focus on […]
Did A Study Overreach When It Said A Vaccine Prevents Leukemia? https://t.co/137H1AK7y5 — NPR Health News (@NPRHealth) May 27, 2015 Our hearts are saddened by the loss of AIS Member Chris Tannous. Read this beautiful tribute: https://t.co/fDrAt0ScfG pic.twitter.com/eTvGDfqqeY — Susan G. Komen (@SusanGKomen) May 29, 2015 The #Oncology Care Model is changing the nature of […]
This week, we learned the heartbreaking news that four cancer charities have been accused of misusing donor’s gifts, spent lavishly on inappropriate expenses, and did little to support the cancer patients they claimed to help. On behalf of our colleagues in the cancer community, and the millions of cancer survivors and caregivers, we find this breach […]
This month, as part of the 20 Years Later blog series, we are revisiting the fifth principle of the Imperatives for Quality Cancer Care: Access, Advocacy, and Accountability. This principle states: “People with cancer should be provided a range of benefits by all health care plans that includes primary and secondary prevention, early detection, initial […]
Living With Cancer: Patients on Our Own https://t.co/STkNQmCd2C SUsan Gubar's latest post via @nytimeswell — NCCS – National Coalition for Cancer Survivorship (@CancerAdvocacy) May 22, 2015 ASCO Updates Its Templates for Disease-Specific #Survivorship Care Plans https://t.co/NokdZl1NWr — Oncology Nursing News (@OncNursingNews) May 21, 2015 Healthcare too costly? Don't fear telling your doctor via @lisazamosky @latimes […]
This week NCCS joined a diverse group of advocacy groups in endorsing the bipartisan Medical Debt Relief Act of 2015 (H.R. 2362). Medical debts can remain on patients’ credit scores for up to seven years, even after they have been paid or settled, lowering his or her credit score and dramatically affecting the ability to […]
Reality: Living with Stage 4: The breast cancer no one understands, w/ insight from @jodyms, @fredhutch –https://t.co/xr1MZ5YG8L — Elaine Schattner MD, MA (@ESchattner) May 12, 2015 .@bagit4u We're participating and presenting the public policy advocacy workshop Aug. 16-20 Tucson #cancer #advocacy https://t.co/MlWtHF3QA4 — NCCS – National Coalition for Cancer Survivorship (@CancerAdvocacy) May 14, 2015 Great […]
Twenty years ago NCCS defined quality cancer care to include a full spectrum of necessary services for cancer patients. These included primary and secondary prevention, early detection, initial treatment, supportive therapies to manage pain, nausea, fatigue, and infections, long-term follow-up, psychosocial services, palliative care, hospice care, and bereavement counseling. This principle, and all of the […]
This month, as part of the 20 Years Later blog series, we are revisiting the fifth principle of the Imperatives for Quality Cancer Care: Access, Advocacy, and Accountability. This principle states: “People with cancer should be provided a range of benefits by all health care plans that includes primary and secondary prevention, early detection, initial […]
In another excellent piece in the The New Yorker entitled “Overkill,” Dr. Atul Gawande writes about what he calls an “avalanche” of unnecessary care Americans are receiving. With his characteristic mix of hard data, policy analysis, and personal stories, he describes the harms of overtreatment, to both individuals and the health care system. He writes, […]
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