727 SEARCH RESULTS FOR: Cancer News

WCOE: Becoming a Caregiver, Homemade Cards From A Survivor, Quality of Life Talks, and Atul Gawande’s Latest

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Susan Gubar's Living With Cancer: Becoming a Caregiver https://t.co/OaEHabDNs0 via @nytimeswell — NCCS – National Coalition for Cancer Survivorship (@CancerAdvocacy) May 8, 2015 A cancer survivor designs the cards she wishes she’d received from friends and family: https://t.co/bKV9SFdVoV via @slate — NCCS – National Coalition for Cancer Survivorship (@CancerAdvocacy) May 8, 2015 It’s Not Just […]

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WCOE: The Cancer Care Continuum, Talking Cost with Your Doctor, Negotiating Costs, and Cervical Cancer Screenings’ “Great Success and Enduring Dilemma”

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The Cancer Care Continuum #CPAT15 pic.twitter.com/ve2yGApZFK — NCCS – National Coalition for Cancer Survivorship (@CancerAdvocacy) April 29, 2015 Dr. Mayer: Prior to receiving a survivorship care plan, patients must receive a written care plan. #CPAT15 — kelseynepote (@kelseynepote) April 29, 2015 If the doctor is unaware of your financial concerns, she's just going to think […]

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

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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 team of care providers across the full continuum of care. Health care plans should be held accountable for timely referral to appropriate specialists when symptoms of cancer […]

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NCCS Policy and Advocacy Manager Kelsey Nepote Attends and Presents at CancerCon: Takeaways and Steps for Moving Forward

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Over the weekend, I had the pleasure of attending and presenting at Stupid Cancer CancerCon in Denver, Colorado. Stupid Cancer is the largest US-based charity that comprehensively addresses young adult cancer through advocacy, research, support, outreach, awareness, mobile health, and social media. CancerCon is their yearly conference and social networking event for the young adult […]

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

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The National Coalition for Cancer Survivorship is hosting a free webinar titled, “Patient-Care Team Communication: How Can the Survivor Prepare to Manage a Lifetime of Care?” on Wednesday, April 29 from 3:00pm-4:30pm EDT as part of our Cancer Policy Advocate Training (CPAT) program. The CPAT program aims to train patient advocates on pressing cancer policy issues. […]

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

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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 […]

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

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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 […]

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

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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 […]

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NCCS Session at CancerCon 2015 Presents Two Types of Advocacy

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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 […]

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WCOE: Making Informed Healthcare Decisions, Something We Can All Agree On, and the Power of Advocacy

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  Few Consumers Are Using Quality, Price Information To Make Health Care Decisions https://t.co/jHm1W09icY — Amy Berman (@NotesOnNursing) April 21, 2015 Conversations w/ advocates @sfuldnasso "Payment reform should focus on quality, not quantity of patient care" @PhRMA https://t.co/xhpKTdG0tr — NCCS – National Coalition for Cancer Survivorship (@CancerAdvocacy) April 24, 2015 Why Many Doctors Don't Follow […]

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Link to: Survivorship Champions

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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.

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Link to: Cancer Policy and Advocacy Team (CPAT)

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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.

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