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Coronavirus and Cancer Resources for Survivors

Cancer survivors have expressed concerns and questions about COVID-19, the coronavirus, and how they may be at higher risk due to their cancer history. Here are some resources about COVID-19 generally, and its impact for cancer survivors specifically. NCCS is seeking answers from public health experts on the coronavirus and its impact on cancer patients and survivors. Please leave a comment [...]
20years

Guest Post: Multidisciplinary Care Is the Hallmark of High Quality Care—So Why Doesn’t Everyone Get It?

The fourth principle in the Imperatives for Quality Cancer Care states, “All people diagnosed with cancer should have access to…
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NCCS Policy and Advocacy Manager Kelsey Nepote Attends and Presents at CancerCon: Takeaways and Steps for Moving Forward

Over the weekend, I had the pleasure of attending and presenting at Stupid Cancer CancerCon in Denver, Colorado. Stupid Cancer is the…
Patient-Care Team Communication

Join Us: “Patient-Care Team Communication: How Can the Survivor Prepare to Manage a Lifetime of Care?” Webinar

The National Coalition for Cancer Survivorship is hosting a free webinar titled, “Patient-Care Team Communication: How Can the…
20years

NCCS CEO Shelley Fuld Nasso Introduces the Fourth Principle of the Imperatives for Quality Cancer Care (VIDEO)

This month, as part of the 20 Years Later series, we are revisiting the fourth principle of the Imperatives for Quality Cancer Care:…
Dr. Walter F. Baile Offers

Dr. Walter F. Baile Offers Professional’s Perspective on Building the Relationship Between a Physician and a Patient

Dr. Walter F. Baile moderated a panel at the Spring 2015 Cancer Policy Roundtable that included many perspectives on how cancer patients…
Marlene King

Marlene King Discusses Living with Metastatic Breast Cancer and Collaborative Decision-Making with Her Oncologist

Marlene King was diagnosed with Ductal Carcinoma in Situ (DCIS) in 2008 at the age of 48, and she elected to have a lumpectomy,…
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NCCS Session at CancerCon 2015 Presents Two Types of Advocacy

This past weekend Kelsey Nepote of NCCS was honored to present a session on patient advocacy at the Stupid Cancer 2015 CancerCon event…
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WCOE: Making Informed Healthcare Decisions, Something We Can All Agree On, and the Power of Advocacy

  https://twitter.com/NotesOnNursing/status/590492825982214144 https://twitter.com/CancerAdvocacy/status/5916669871154012…
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WCOE: Bi-Partisan Bill Overhauls How Doctors Get Paid, Psychological Effects of Chemo, and the Art of Concealing Cancer

https://twitter.com/ONSAlec/status/588373432464715776 https://twitter.com/CancerAdvocacy/status/588398011803443200 https://twi…
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WCOE: Replacing the SGR Formula, Patient Advocate Speaks at FDA, and Dr. Peter Ubel talks Patient Needs

https://twitter.com/CancerAdvocacy/status/585110117261189120 https://twitter.com/MBCNbuzz/status/584062316418834432 https://tw…

Take Action

Link to: Survivorship Champions

Become a Survivorship Champion

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.

Learn More and Join »
Link to: Cancer Policy and Advocacy Team (CPAT)

Join CPAT

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.

Learn More and Join »
Link to: Survivor Stories

Share Your Story

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.

Share Your Story »

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