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Posts

Incremental Improvements Are Not Enough

October 1, 2014/in Cancer News, Cancer Policy Blog Care Planning, Palliative Care, Quality Cancer Care, Survivorship Care NCCS News /by actualize

Two years ago, the world lost an extraordinary person, my dear friend Dr. Brent Whitworth. He was a few days shy of his 42nd birthday when he learned of his diagnosis – stage IV kidney cancer – and he was devastated. He had surgery at a major cancer hospital and then entered a clinical trial […]

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0 0 actualize http://canceradvocacy.org/wp-content/uploads/2020/06/NCCA-Logo.png actualize2014-10-01 12:47:022014-10-01 12:47:02Incremental Improvements Are Not Enough

WCOE: “Why I Hope to Die at 75” and a New IOM Report on Quality and End of Life Preferences

September 19, 2014/in Cancer News, Cancer Policy Blog Care Coordination, Care Planning, Palliative Care, Quality Cancer Care, Survivorship Care NCCS News /by actualize

Are we finally ready to address the repeated recommendations in these series of reports and to make it possible for our healthcare system, providers of care, and our religious leaders to be more ready to assist people in making difficult decisions about how to die well? One of the articles that caught our eye this […]

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https://canceradvocacy.org/wp-content/uploads/2012/12/NCCS_Starburst_Thumbnail.jpg 125 125 actualize http://canceradvocacy.org/wp-content/uploads/2020/06/NCCA-Logo.png actualize2014-09-19 09:58:032014-09-19 09:58:03WCOE: “Why I Hope to Die at 75” and a New IOM Report on Quality and End of Life Preferences

WCOE: Paying Doctors to Talk About End-of-Life Care

September 5, 2014/in Cancer News, Cancer Policy Blog Access to Care, Care Coordination, Care Planning, Health Care Coverage, Palliative Care, Quality Cancer Care NCCS News /by actualize

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,’ […]

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https://canceradvocacy.org/wp-content/uploads/2014/09/ImageDoctor-and-PatThumbnail.gif 321 800 actualize http://canceradvocacy.org/wp-content/uploads/2020/06/NCCA-Logo.png actualize2014-09-05 14:55:302014-09-05 14:55:30WCOE: Paying Doctors to Talk About End-of-Life Care

WCOE: Patient Empowerment in Discussing End-of-Life Care

August 29, 2014/in Cancer News, Cancer Policy Blog Care Coordination, Care Planning, Palliative Care, Quality Cancer Care NCCS News /by actualize

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 […]

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The Difficult Question of When to Stop Treatment

August 15, 2014/in Cancer News, Cancer Policy Blog Care Coordination, Palliative Care, Quality Cancer Care, Survivorship Care NCCS News /by actualize

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 […]

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WCOE: Improving Quality for Patients by Delivering and Paying for Care Differently

August 1, 2014/in Cancer News, Cancer Policy Blog Palliative Care, Payment Reform, Quality Cancer Care, Survivorship Care NCCS News /by actualize

In two America Tonight segments entitled, “Is America treating cancer the wrong way?” Michael Okwu of Al Jazeera America delves into the cost of cancer care and an experiment in delivering care differently to reduce costs and improve quality for patients. Okwu interviews Dr. Arnie Milstein, director of the Stanford Clinical Excellence Research Center (CERC) […]

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https://canceradvocacy.org/wp-content/uploads/2012/12/NCCS_Starburst_Thumbnail.jpg 125 125 actualize http://canceradvocacy.org/wp-content/uploads/2020/06/NCCA-Logo.png actualize2014-08-01 14:48:452021-09-29 07:34:51WCOE: Improving Quality for Patients by Delivering and Paying for Care Differently

WCOE: Planning for Hospice, Difficult Conversations, and Second Opinions

July 25, 2014/in Cancer News, Cancer Policy Blog Care Planning, Palliative Care, Quality Cancer Care NCCS News /by actualize

As avid followers of Susan Gubar’s series in The New York Times on living with cancer, we read her most recent installment, “Living with Cancer: A Tour of Hospice” with interest. She described her fear of the pain, anxiety, and dementia that can accompany dying and her desire to avoid excessive treatment at the end of life. […]

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https://canceradvocacy.org/wp-content/uploads/2012/12/NCCS_Starburst_Thumbnail.jpg 125 125 actualize http://canceradvocacy.org/wp-content/uploads/2020/06/NCCA-Logo.png actualize2014-07-25 17:06:272020-10-21 11:04:34WCOE: Planning for Hospice, Difficult Conversations, and Second Opinions

Focus on the Care Video: Palliative Care and Living Well with Cancer

June 5, 2014/in Cancer News, Cancer Policy Blog Care Coordination, Care Planning, Palliative Care, Quality Cancer Care NCCS News /by actualize

Last week we noted two recent articles addressing palliative and end of life care issues, including an article written from the first-hand experience of Amy Berman, who is both a nurse and an individual living with cancer. In Amy Berman’s recent post on the Health Affairs Blog, she describes palliative care as the “best friend of the seriously ill.” […]

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WCOE: Amy Berman’s “Less Is More” Approach and End of Life Care

May 31, 2014/in Cancer News, Cancer Policy Blog Care Planning, Palliative Care, Quality Cancer Care, Survivorship Care NCCS News /by actualize

In the May 22nd Health Affairs online blog, “Living My Life My Own Way,” Amy Berman writes about what she knows firsthand and what she has learned from many years of professional experience.  And she writes and speaks about it so well, which is one of her many gifts.  She was diagnosed with inflammatory breast cancer in October […]

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https://canceradvocacy.org/wp-content/uploads/2012/12/NCCS_Starburst_Thumbnail.jpg 125 125 actualize http://canceradvocacy.org/wp-content/uploads/2020/06/NCCA-Logo.png actualize2014-05-31 10:29:552014-05-31 10:29:55WCOE: Amy Berman’s “Less Is More” Approach and End of Life Care

When Talking About the End of Life, Honesty and Words Matter

May 23, 2014/in Cancer News, Cancer Policy Blog Access to Care, Care Coordination, Care Planning, Health Care Coverage, Palliative Care, Quality Cancer Care NCCS News /by actualize

I attended two different events in Washington, DC this week where the focus was on end-of-life care and the challenges of ensuring that people have quality care and dignity at the end of their life. First was the U.S. Senate Special Committee on Aging roundtable meeting entitled, “Continuing the Conversation: The Role of Health Care Providers […]

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Latest News

Kara Kenan Advocate Spotlight

Kara Kenan: Helping Others is the Greatest Reward of Advocacy

August 3, 2022
“Nobody wins afraid of losing” rings true for Kara Kenan, a breast cancer survivor. It’s her favorite line from Chris Stapleton’s…
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Care and Career Support From Health Systems to Employers Webinar

Webinar – Care and Career Support: From Health Systems to Employers

August 3, 2022
NCCS hosted a webinar about the unique demands of caregiving in cancer and strategies that employers and health systems might engage…
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Bethany Ross

Bethany Ross: Advocating for Quality Cancer Care Through Storytelling

July 7, 2022
Advocate Spotlight July 2022 - Bethany Ross Bethany Ross is a four-year neuroendocrine cancer survivor, or “cancer badass,”…
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  • About
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    • Partnerships
    • Financial Information
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    • 2021 State of Cancer Survivorship Survey
    • 2020 State of Cancer Survivorship Survey
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Harmar Brereton, MD

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