NCCS is now Cancer Nation. Find out more about our next chapter. Join Us
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.

About Ellen L. Stovall
Learn more about Ellen’s decades-long advocacy to elevate patient voices and improve the cancer care system in America.
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 »
Erin Geddis Cummings, MSW, LCSW
Patient Advocate Award
“Few individuals have transformed a field as profoundly as Erin Geddis Cummings transformed Hodgkin lymphoma survivorship.”
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.

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.”
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).

Past Stovall Award Recipients
Find out how Stovall Award winners have impacted the cancer care system and watch short films about their pioneering work.
For questions about the Stovall Award, contact:
Karen Wilson, Development Manager
About Ellen L. Stovall

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.


