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Cancer Nation (Formerly NCCS)
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        • About Us

        • Cancer Nation is the oldest cancer survivor-led non-profit organization in America. We advocate for quality cancer care for all touched by cancer.

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        • What is Advocacy?Learn about the different types of cancer advocacy, from personal advocacy to public interest advocacy.
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        • Public policy is government action, in the form of legislation, regulation, funding, and other actions. Public policy affects people with cancer and the cancer care system in many ways.

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        • Protecting Access to Medicaid for Cancer Survivors
        • Comprehensive Cancer Survivorship Act (CCSA)The CCSA is a large comprehensive bill introduced in Congress that aims to improve quality of care in all stages of a diagnosis.
        • Cancer Care Planning and Communications Act (CCPCA)CCPCA is a bill that would provide a billable Medicare service code for cancer care planning.
        • DIEP Flap AccessCancer Nation advocates for protection of access to DIEP Flap Breast Reconstruction Surgery for all breast cancer survivors.
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        • Whether you’re new to cancer advocacy or already have experience as an advocate, there are numerous ways you can get involved with Cancer Nation.

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        • Cancer Nation conducts an annual Cancer Nation Survivorship Survey, in partnership with Edge Research, to explore the cancer patient and survivor journey. This study captures a range of perspectives to better understand how Cancer Nation can support its mission to advocate for quality cancer care for all.

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        • 2023 Survivorship SurveyThe 2023 Survey explored the caregiver experience for the first time, and features new data on the effect of cancer treatment on employment.
        • 2022 Survivorship SurveyThe 2022 Survey found significant disparities in cancer care that impact people of color, young adults, women, and those with metastatic cancer, at higher rates.
        • 2021 Survivorship SurveyThe 2021 Survey demonstrated that when patients receive quality care, have excellent support, and have financial resources, they are more likely to have positive outcomes.
        • 2020 Survivorship SurveyIn the 2020 Survey, survivors reported that their care team is not helpful at addressing some common side effects of their cancer such as fatigue, anxiety, and depression.
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        • The Cancer Survivorship Checklist is designed to be a simple, straightforward tool patients and caregivers can use as a guide for information critical to their care wherever they are on the cancer care continuum.

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        • Cancer Nation provides a wide variety of resources for patients, caregivers, and health care professionals.

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text graphic, Cancer Nation Stovall Awards, white Cancer Nation logo on the left, Stovall Awards in light blue on the right

Ellen L. Stovall Award for Innovation In Patient-Centered Cancer Care

You are here: Home1 / Events2 / Ellen L. Stovall Award

The Stovall Award is a unique opportunity for patients and survivors to recognize pioneers who are transforming the cancer care system.

Each year, Cancer Nation honors two individuals or organizations — one health care professional* and one patient advocate or advocacy organization — whose commitment to innovations in patient-centered cancer care helps deliver better outcomes and a higher quality of life for those living with and beyond cancer. Cancer Nation created the Stovall Award to honor former CEO Ellen L. Stovall, a three-time survivor and visionary leader whose life and work reshaped what cancer care could (and should) be.

* Health care professional award co-presented by the American Society of Clinical Oncology.

Ellen L. Stovall

About Ellen L. Stovall

Learn more about Ellen’s decades-long advocacy to elevate patient voices and improve the cancer care system in America.

About Ellen About Ellen

2026 Stovall Award Winners

Cancer Nation is pleased to announce the 2025 winners of the Ellen L. Stovall Award for Innovation in Patient-Centered Cancer Care are Susan Leigh, BSN and Desirée A.H. Walker. They were recognized at the 2025 Igniting Hope Awards Reception on June 26, 2025. Learn more »

Read the Announcement »

Erin Cummings HeadshotErin Geddis Cummings, MSW, LCSW

Patient Advocate Award
“Few individuals have transformed a field as profoundly as Erin Geddis Cummings transformed Hodgkin lymphoma survivorship.”

— Sophia K. Smith, PhD, MSW, FAOSW, Chair, Hodgkin’s International, and
Kevin C. Oeffinger, MD, FASCO, Duke Cancer Institute

Erin Geddis Cummings, MSW, LCSW, will be honored posthumously with the 2026 Ellen L. Stovall Patient Advocate Award. Erin lived more than 50 years with and beyond Hodgkin lymphoma and built that lived experience into a life’s work supporting long-term survivors around the world.

In 2016, Erin co-founded Hodgkin’s International, a licensed clinical social worker’s answer to a gap she saw clearly: survivors who had been cured of Hodgkin lymphoma decades earlier were often left without guidance on the late effects of the treatments that saved their lives. Under her leadership, Hodgkin’s International grew into a global network of more than 800 survivors, delivering monthly newsletters, webinars, and evidence-based resources on late effects, screening, and long-term risk. In 2024, she brought that vision to life in person, organizing the first Hodgkin’s International Conference in Boston, where more than 100 survivors, clinicians, and researchers gathered to share best practices and elevate survivor and caregiver voices.
Erin Cummings meets with Rep. Mark DeSaulnier

Erin’s collaborations reached across Europe, North America, and Australia, connecting oncologists, survivorship researchers, and advocacy organizations including Blood Cancer United, the Lymphoma Research Foundation, the University of Cincinnati Cancer Center, and Duke Cancer Center for Onco-Primary Care. She was also a longtime partner of Cancer Nation’s Cancer Policy and Advocacy Training (CPAT) program, where her work helped bring the specialized needs of long-term survivors into policy and research conversations at the national level.

Erin died on February 24, 2026, from stomach cancer complicated by the long-term effects of the treatment she received as a child. She was 68. The community she built at Hodgkin’s International continues to carry her vision forward, connecting survivors and caregivers to the information, research, and quality care she spent her life fighting to make available to every long-term survivor. Read our memorial for Erin here.

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Bradley Zebrack headshot
Bradley J. Zebrack, PhD, MSW, MPH

Health Care Professional Award (Co-Presented by ASCO)
“Brad’s pioneering contributions to the field of AYA oncology and the psychosocial needs of this patient group represent a major innovation in the delivery of patient-centered care.”

— Patricia A. Ganz, MD, and Barbara Hoffman, JD,
Co-Founders, National Coalition for Cancer Survivorship

Bradley J. Zebrack, PhD, MSW, MPH, is a nationally recognized researcher, educator, and oncology social worker who has spent more than 25 years advancing the field of cancer survivorship. His research has shaped how the field understands quality of life, health disparities, supportive care, and the distinct needs of adolescents and young adults with cancer. He is a professor at the University of Michigan School of Social Work and one of the founding figures of adolescent and young adult (AYA) psychosocial oncology as a field of research.

Brad’s connection to Cancer Nation runs deep. Diagnosed with Hodgkin lymphoma in 1985 at age 25, he turned to the newly-founded NCCS (now Cancer Nation) for support and gave back almost immediately. In 1988, he and his then-fiancée Joanne Kelleher rode bicycles 11,000 miles around the perimeter of the United States over the course of a year, meeting with survivors, oncologists, nurses, social workers, and hospital administrators to advocate for medical and psychosocial support for people during and after cancer treatment, a novel concept at the time.

From left to right: Brad Zebrack and Joann Kelleher talk with Dr. Richard Karl at Moffitt Cancer Center, Tampa Florida, 1988.

The campaign raised more than $10,000 for NCCS and carried its message to communities across the country in the pre-internet era. Brad went on to serve on the NCCS Board of Directors from 1993 to 1998 and consulted on NCCS’s 1996 report, Imperatives for Quality Cancer Care: Access, Advocacy, Action and Accountability.

Brad earned his PhD in social work from the University of Michigan in 1999. During a postdoctoral fellowship with Patricia Ganz at UCLA, he developed quality-of-life questionnaires designed specifically for long-term cancer survivors and, later, for young adult survivors, tools now used widely across the field.

He has authored more than 170 peer-reviewed publications and 31 book chapters, mentored roughly 50 trainees, and holds fellowships with the American Psychosocial Oncology Society, the Society for Social Work and Research, and the Association of Oncology Social Work. His recent honors include the Rogel Scholar in Cancer Health Impact award from the University of Michigan Rogel Cancer Center (2025 to 2028), the Ruth McCorkle Excellence in Research Mentorship Award (2022), and the Archie Bleyer AYA Trailblazer Award (2025).

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Stovall 2022 Reception: Photo of Alicia Staley, Shelley Fuld Nasso, and Patricia Ganz, MD -- Photo by Leslie Kossoff/LK Photos

Past Stovall Award Recipients

Find out how Stovall Award winners have impacted the cancer care system and watch short films about their pioneering work.

Stovall Awardees Stovall Awardees

For questions about the Stovall Award, contact:

Karen Wilson, Development Manager

kwilson@canceradvocacy.org

About Ellen L. Stovall

Ellen and Annie SA

In more than two decades of service and leadership at the National Coalition for Cancer Survivorship (now Cancer Nation), Ellen L. Stovall crusaded for the delivery of quality cancer care to all Americans. As a cancer survivor of more than four decades, Ellen sought to design her own system of patient-centered care to address the serious late and long-term effects of her cancer treatment, including the treatment of a second cancer. In pursuing her own system of care, she focused on care that emphasized strong doctor-patient communication, coordination of care and symptom management, and full consideration of the evidence supporting treatment options.

Ellen considered herself a “lucky” cancer survivor because her advocacy for herself opened the door to some of the best of American cancer care, accompanied by some of the glitches and gaps in care that many experience. Ellen’s pursuit of her own quality cancer care informed NCCS efforts to improve the overall cancer care delivery and payment system. Ellen and her colleagues at NCCS pursued changes in public and private payment systems that would encourage cancer care professionals to provide patient-centered care through partnership with their patients and through redesign of their systems to honor the principles of patient-centeredness.

Events

  • Events
    • Igniting Hope Awards Reception
    • Ellen L. Stovall Award
      • 2026 Winners
      • Nominations
      • Awardees
      • Committees
    • Cancer Nation Policy Roundtable
    • Webinars

Latest News

Ringing the Bell Is Not the Finish Line: Desa-Rhea Jefferson on What Cancer Survivors Need Next

September 24, 2026
Desa-Rhea Jefferson survived liver cancer at 3 and thyroid cancer as an adult. She says ringing the bell is a starting point, not a finish line. Read more.
Read more
https://canceradvocacy.org/wp-content/uploads/Desa-Rhea-Jefferson_-Advocate-Spotlight-Blog-Banner.png 600 1200 Elleni https://canceradvocacy.org/wp-content/uploads/CancerNation_Logo_40Yrs_Stacked_TwoColor-scaled.png Elleni2026-09-24 11:10:172026-09-24 11:10:17Ringing the Bell Is Not the Finish Line: Desa-Rhea Jefferson on What Cancer Survivors Need Next
Image with Orchid background. Text reads: Cancer Nation Stovall Awards | 2026 Honorees | Patient Advocate Award - Erin Geddis Cummings, MSW, LCSW | Health Care Professional Award - Bradley J. Zebrack, PHD, MSW, MPH

Cancer Nation to Recognize Erin Cummings and Bradley J. Zebrack with 2026 Ellen L. Stovall Award

September 17, 2026
Cancer Nation is proud to announce the recipients of the 2026 Ellen L. Stovall Award for Innovation in Patient-Centered Cancer Care: …
Read more
https://canceradvocacy.org/wp-content/uploads/Stovall-Award-Honorees-2026-web-featured.jpg 675 1200 NCCS Staff https://canceradvocacy.org/wp-content/uploads/CancerNation_Logo_40Yrs_Stacked_TwoColor-scaled.png NCCS Staff2026-09-17 13:55:462026-09-22 13:46:42Cancer Nation to Recognize Erin Cummings and Bradley J. Zebrack with 2026 Ellen L. Stovall Award
a graphic flyer for an event with a light blue background. On the left, text reads Cancer Nation Survivorship Survey | WEB BRIEFING | Hear the findings from our first Survivorship Survey: Clinician Perspective. | Watch Now | on the right, a photo of a health care professional holding a clipboard.

Cancer Nation Releases Results from Survey of 600 Clinicians on Survivorship Care

September 16, 2026
Since 2019, Cancer Nation has conducted a Survivorship Survey of cancer survivors and caregivers to learn about their experiences with…
Read more
https://canceradvocacy.org/wp-content/uploads/Clinician-Perspective-Survey-Briefing-Watch-1200px.jpg 675 1200 NCCS Staff https://canceradvocacy.org/wp-content/uploads/CancerNation_Logo_40Yrs_Stacked_TwoColor-scaled.png NCCS Staff2026-09-16 12:01:452026-09-24 12:28:10Cancer Nation Releases Results from Survey of 600 Clinicians on Survivorship Care

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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