• Link to Facebook
  • Link to X
  • Link to Youtube
  • Link to Instagram
  • Link to LinkedIn
  • Link to Rss this site
  • Store
  • Donate
  • About
        • 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.

        • About NCCS

        • Our Mission
        • What is Advocacy?Learn about the different types of cancer advocacy, from personal advocacy to public interest advocacy.
        • Our HistoryRead how Cancer Nation’s leaders coined the term “cancer survivor,” and established the nation’s first survivor-led non-profit organization.
        • Our Team
        • Financial Information
        • Employment
        • Contact Us
        • Support Our Mission

        • Make A GiftSupport our mission of quality cancer care for all with a gift to Cancer Nation.
        • The 1986 ClubMake a monthly commitment to support Cancer Nation, empower cancer survivors, and advance public policy.
        • Ways to GiveLearn about other ways you can contribute to Cancer Nation such as planned giving, employer matches, shopping online, and more.
        • Partnerships
  • News
    • Cancer Nation News
    • Advocate SpotlightEach month, Cancer Nation highlights a cancer survivorship advocate, sharing their story and the work they do in their communities.
    • Policy CommentsRead Cancer Nation’s comments to Congress, HHS, and other federal policymakers in Washington, DC on proposed rules and legislation.
    • Issue StatementsRead Cancer Nation statements on pressing issues and developments in Washington affecting cancer survivors and their families.
  • Policy
        • Policy

        • 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.

        • Our Policy Priorities

        • Quality Cancer CareQuality cancer care is essential for patients. Learn how Cancer Nation and others define quality.
        • Access to CareCancer Nation believes cancer care and clinical trials should be affordable and accessible to everyone.
        • Health EquityThe cancer experience is not the same for everyone. Cancer Nation works on policy efforts to reduce disparities in outcomes.
        • Current Issues

        • 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.
        • Policy CommentsRead Cancer Nation’s comments to Congress, HHS, and other federal policymakers in Washington, DC on proposed rules and legislation.
        • Issue StatementsRead Cancer Nation statements on pressing issues and developments in Washington affecting cancer survivors and their families.
        • Quality Measurement Research
  • Get Involved
        • Get Involved

        • 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.

        • Join Cancer Nation

        • Cancer Nation AdvocatesA program that brings together individuals who care about cancer care to learn how policy shapes our health care system—and how we can improve it together.
        • Cancer Nation Leadership AcademyEmerging leaders improving cancer care in their communities.
        • Cancer Nation Corporate Council
        • Advocacy OpportunitiesThis page provides a list of upcoming events, webinars, conferences, and advocacy campaigns from Cancer Nation and other leading cancer organizations.
        • Connect with Us

        • Subscribe to Cancer Nation Updates
        • Follow Cancer Nation on Social Media
        • Survivor Stories
        • Cancerversary
        • Support Cancer Nation

        • Make A Gift
        • Ways to Give
        • The 1986 Club
  • Survivorship Survey
        • State of Survivorship Survey

        • Cancer Nation conducts an annual State of 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.

        • Reports by Year

        • 2025 Survey Report
        • 2024 Survey Report
        • 2023 Survey ReportThe 2023 Survey explored the caregiver experience for the first time, and features new data on the effect of cancer treatment on employment.
        • 2022 Survey ReportThe 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 Survey ReportThe 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 Survey ReportIn 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.
  • Survivorship Checklist
        • Cancer Survivorship Checklist

        • 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.

        • Start Your Cancer Survivorship Checklist
        • Survivorship Checklist Guide for Clinicians
        • Resources for Cancer Survivors

        • Survivorship ResourcesA collection of resources that provide information about navigating the cancer journey.
        • Cancer RehabilitationA supportive health care service that helps improve a person’s functioning during and after cancer treatment.
        • Integrative OncologyA field that combines traditional cancer treatments with therapies that support a person’s natural healing ability.
        • Palliative CareSpecialized medical care for people living with a serious illness that provides relief from the symptoms and stress to improve their quality of life.
        • Cognitive HealingA resource to support cognitive functioning after cancer treatment. Includes cognitive training strategies and tools for both adults and children.
  • Resources
        • Resources

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

        • Resources for Survivors and Caregivers

        • Health Insurance & Open Enrollment
        • Cancer Survival ToolboxA free, award-winning audio program created by leading cancer organizations to help people better meet & understand the challenges of their illness.
        • Ina® The Intelligent Nutrition Assistant
        • Telehealth
        • Care Planning for Cancer Survivors
        • Remaining Hopeful
        • Self Advocacy
        • Talking With Your Doctor
        • Taking Charge of Your Care
        • Order Our Resources
        • Resources for Health Care Professionals

        • Tools For Care Providers
        • Telehealth Project
        • Survivorship Champions Webinars
        • Survivorship Checklist Guide for Clinicians
  • Events
    • 2026 Cancer Nation Summit
    • Igniting Hope Awards Reception
    • Ellen L. Stovall Award
      • 2025 Winners
      • Awardees
      • Nominations
      • Committees
    • Cancer Nation Webinars
    • Cancer Nation Policy Roundtable
      • Fall 2025
      • Spring 2025
      • Fall 2024
      • Spring 2024
      • Fall 2023
      • Spring 2023
  • 0

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

NCCS Blog Guest Post

A Medical School Perspective: Beyond the Science, We Must Learn to Communicate with Patients

July 16, 2018/in Cancer News, Cancer Policy Blog Doctor-Patient Communication, Palliative Care, Quality Cancer Care, Shared Decision-Making, Survivorship Care Cancer Nation News
Nainika Nanda, MDBy Nainika Nanda, MD
Otolaryngology Resident
University of Wisconsin-Madison

Survivorship. What does this mean? Oncology highlights patients currently battling cancer. However, survivorship encompasses a longer timeline. Cancer requires lifelong care, which is best achieved through proper doctor-patient communication. This relationship is a keystone of medicine. Unfortunately, that focus can be lost in the sea of information medical students must master.

A common analogy for medical education is “drinking from a fire hose.” In having to learn this quantity of information at this pace, curricula are classically centered on textbook knowledge in the earlier years. My first year of medical school required ten hours of physician shadowing. During my second year, the hours of patient contact increased, as we conducted patient interviews every 1 to 2 weeks. They were often during peak exam time and focused on complex patients with medical issues beyond our previous scope of exposure. So, our effort was inevitably directed towards learning the science of medicine—diagnosis and treatment—rather than the art of medicine, puzzle-solving, and empathetic interactions.

Understanding the science and getting the treatment right is crucial, but that’s only part of the equation. We as physicians must also remember the humanity of every patient and loved one. We need to be better equipped to serve as supportive, empathetic, and honest advisors to patients.
In fact, topics vital to oncology—such as end-of-life and palliative care discussions—are frequently cited as subjects that entering residents do not feel adequately prepared to handle. My school focused on these topics with a couple of lectures in a single one-semester course during our four years. With the demands of the training and loss of focus on individual patients, students often lost sense of why they chose to pursue medicine.

I had the honor of participating in the CUPID (Cancer in the Under-Privileged, Indigent, and Disadvantaged) program in the summer after my first year of medical school. This fellowship through Sidney Kimmel Comprehensive Cancer Center and Johns Hopkins Medicine created opportunities to work on research in diagnostic tools for pancreatic cancer, shadow clinicians in the operating rooms and clinics, and be introduced to NCCS.

Having had minimal direct patient interaction in my education hitherto, these experiences were invaluable. I saw firsthand how important the clinician is to the cancer patient and their family. In the following years of medical school, I was able to seek out further exposure to clinicians handling such complex situations, because I had learned of the value of these experiences to my education.

Yet, one of the most influential experiences was at a metastatic breast cancer retreat hosted by Johns Hopkins Hospital for patients and spouses, which I attended during my fourth year of medical school. This weekend-long event created an atmosphere outside of the clinical setting for patients to hear each other’s stories without physician interaction inadvertently directing focus to therapy options. Patients welcomed me, sharing deep, personal stories of how their illnesses were impacting their lives and relationships with their families. They were eager to provide feedback to a budding physician based on interactions they had with physicians during their care, some heart-warming and some devastating.

Clinicians are devoted to their patients’ well-being. Yet so often, the challenges of providing high-quality care often rely on using the limited time available per patient appointment, often 15 to 20 minutes, to discuss complex topics. These concepts—complex therapeutic regimens, the concept of a lifetime illness, and advanced directives and end-of-life care—are not addressed in the early part of our training and take years to learn.

Medical training should incorporate these topics early and routinely, possibly through standardized patient encounters, case scenarios, and shadowing more experienced physicians dealing with these situations. In an educational system with so much to learn in so little time, adding more formal instruction will not be easy, but it is critical.

Understanding the science and getting the treatment right is crucial, but that’s only part of the equation. We as physicians must also remember the humanity of every patient and loved one. We need to be better equipped to serve as supportive, empathetic, and honest advisors to patients. Even when the discussions are challenging, decisions must be made by optimizing the doctor-patient relationship.

# # #

About Nainika Nanda

Dr. Nanda recently graduated from West Virginia University School of Medicine. Experiences throughout her medical school training inspired her to pursue a specialty with vast opportunities in research and patient care related to both benign and malignant tumor biology. Currently, she is a resident physician at University of Wisconsin-Madison in the specialty of Otolaryngology-Head and Neck Surgery, commonly known as ENT.

Note: The views and opinions expressed in any guest post featured on our site are those of the guest author(s) and do not necessarily reflect the opinions and views of the National Coalition for Cancer Survivorship. Read our blog and comment policies here.


Tags: cancer care, Cancer Survivorship, communication, CPAT, Decision-Making, Guest Post, Palliative Care, Patient Navigation
Share this entry
  • Share on Facebook
  • Share on X
  • Share on WhatsApp
  • Share on LinkedIn
https://canceradvocacy.org/wp-content/uploads/2018/07/NCCS-Blog-Guest-Post.jpg 600 1200 actualizedevs https://canceradvocacy.org/wp-content/uploads/CancerNation_Logo_Stacked_TwoColor.svg actualizedevs2018-07-16 16:25:302018-07-16 16:25:30A Medical School Perspective: Beyond the Science, We Must Learn to Communicate with Patients

Latest News

A graphic showing the Medicaid.gov website

Cancer Nation Statement: Medicaid Work Requirements Will Unfairly Burden Cancer Survivors

June 4, 2026
Cancer Nation strongly supports a health care system free of waste, fraud, and abuse. Health care resources must be directed to delivery…
Read more
https://canceradvocacy.org/wp-content/uploads/Stock-Medicaid-website-Adobe-927192378.jpg 675 1200 NCCS Staff https://canceradvocacy.org/wp-content/uploads/CancerNation_Logo_Stacked_TwoColor.svg NCCS Staff2026-06-04 12:56:142026-06-05 13:42:09Cancer Nation Statement: Medicaid Work Requirements Will Unfairly Burden Cancer Survivors
Image with graphics and text that reads Cancer Nation Understanding Blood-Based Testing in Cancer Care | Watch Now | With Support From: Guardant Health Logo

Webinar – Understanding Blood-Based Testing in Cancer Care

May 29, 2026
Cancer Nation's Webinar Series presents a clear, practical conversation about advances in blood-based testing and how they're shaping…
Read more
https://canceradvocacy.org/wp-content/uploads/Blood-Based-Testing-Webinar-post.jpg 675 1200 NCCS Staff https://canceradvocacy.org/wp-content/uploads/CancerNation_Logo_Stacked_TwoColor.svg NCCS Staff2026-05-29 11:28:002026-05-29 11:28:00Webinar – Understanding Blood-Based Testing in Cancer Care
a picture of susie leigh similing wearing a purple top. Words over the photo read In loving memory, Susie Leigh, Cancer Nation Co-founder, 1947-2026

Remembering Susie Leigh: A Founder, a Force, and a Friend

May 28, 2026
Susan (Susie) Leigh, BSN, RN-Retired — one of the founding members of Cancer Nation, a five-time cancer survivor, and one of the…
Read more
https://canceradvocacy.org/wp-content/uploads/Susie-Leigh-In-Memory-blog.jpg 900 1600 NCCS Staff https://canceradvocacy.org/wp-content/uploads/CancerNation_Logo_Stacked_TwoColor.svg NCCS Staff2026-05-28 15:14:382026-06-04 14:32:40Remembering Susie Leigh: A Founder, a Force, and a Friend

Take Action

Link to: Survivorship Champions

Get Involved in Research

Cancer Nation conducts an annual Survivorship Survey to explore how patients and survivors are living with, through, and beyond cancer. 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.

Learn More and Request Data Here »
Link to: Cancer Nation Advocates

Join Cancer Nation Advocates

Cancer Nation Advocates is a a program that brings together individuals who care about cancer care to learn how policy shapes our health care system—and how we can improve it together

Learn More and Join »
Link to: Survivor Stories

Share Your Story

Cancer Nation 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 »
  • About
    • Our Mission
    • What is Advocacy?
    • Our History
    • Our Team
    • Financial Information
    • Employment
    • Contact Us
    • Make A Gift
    • The 1986 Club
    • Ways to Give
    • Partnerships
  • News
    • Cancer Nation News
    • Advocate Spotlight
    • Policy Comments
    • Issue Statements
  • Policy
    • Quality Cancer Care
    • Access to Care
    • Health Equity
    • Protecting Access to Medicaid for Cancer Survivors
    • Comprehensive Cancer Survivorship Act (CCSA)
    • Cancer Care Planning and Communications Act (CCPCA)
    • DIEP Flap Access
    • Policy Comments
    • Issue Statements
    • Quality Measurement Research
  • Get Involved
    • Cancer Nation Advocates
    • Cancer Nation Leadership Academy
    • Cancer Nation Corporate Council
    • Advocacy Opportunities
    • Subscribe to Cancer Nation Updates
    • Follow Cancer Nation on Social Media
    • Survivor Stories
    • Cancerversary
    • Make A Gift
    • The 1986 Club
    • Ways to Give
  • Survivorship Survey
    • 2025 Survey Report
    • 2024 Survey Report
    • 2023 Survey Report
    • 2022 Survey Report
    • 2021 Survey Report
    • 2020 Survey Report
  • Survivorship Checklist
    • Start Your Cancer Survivorship Checklist
    • Survivorship Resources
    • Cancer Rehabilitation
    • Integrative Oncology
    • Palliative Care
    • Cognitive Healing
    • Survivorship Checklist Guide for Clinicians
  • Resources
    • Cancer Survival Toolbox
    • Telehealth
    • Health Insurance & Open Enrollment
    • Care Planning for Cancer Survivors
    • Ina® The Intelligent Nutrition Assistant
    • Remaining Hopeful
    • Self Advocacy
    • Talking With Your Doctor
    • Taking Charge of Your Care
    • Order Our Resources
    • Tools For Care Providers
    • Telehealth Project
    • Survivorship Champions Webinars
    • Survivorship Checklist Guide for Clinicians
  • Events
    • 2026 Cancer Nation Summit
    • Igniting Hope Awards Reception
    • Ellen L. Stovall Award
      • 2025 Winners
      • Awardees
      • Nominations
      • Committees
    • Cancer Nation Webinars
    • Cancer Nation Policy Roundtable
      • Fall 2025
      • Spring 2025
      • Fall 2024
      • Spring 2024
      • Fall 2023
      • Spring 2023
  • Search
  • Cart

Charity Navigator Four-Star Rating

Cancer Nation Logo

Cancer Nation
8455 Colesville Road  |  Suite 1025 | Silver Spring, MD 20910
info@canceradvocacy.org | (877) NCCS-YES
Privacy Policy  |  Terms and Conditions

Copyright © 1995-2026 by Cancer Nation. National Coalition for Cancer Survivorship, NCCS, Cancer Survival Toolbox, Cancerversary, and related Logos are registered in the United States as trademarks of Cancer Nation (formerly the National Coalition for Cancer Survivorship).

Link to: Health Care Roundup: CMS Halts ACA Risk Payments, Slashes Navigator Funding; Long-Term Outcomes for Young Survivors; Drug Pricing; More Link to: Health Care Roundup: CMS Halts ACA Risk Payments, Slashes Navigator Funding; Long-Term Outcomes for Young Survivors; Drug Pricing; More Health Care Roundup: CMS Halts ACA Risk Payments, Slashes Navigator Funding;...NCCS Starburst 250px Link to: NCCS Joins Cancer Leadership Council Comment Letter Regarding the Drug Pricing Blueprint “American Patients First” Link to: NCCS Joins Cancer Leadership Council Comment Letter Regarding the Drug Pricing Blueprint “American Patients First” NCCS Policy Comments HHS bldgNCCS Joins Cancer Leadership Council Comment Letter Regarding the Drug Pricing...
Scroll to top Scroll to top Scroll to top

This website uses cookies to improve user experience. By continuing to use this site, you agree to our Privacy Policy. Learn More.

Get Updates From Cancer Nation

Be the first to hear about cancer policy and survivorship issues! Subscribe and receive the twice-monthly Cancer Nation News, invites to webinars and events, and more.

  • This field is for validation purposes and should be left unchanged.

Connect With Us

Twitter     Facebook     Instagram     LinkedIn     YouTube

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