FMEC_YBCS_Provider Resource Files.xlsx

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1	Resource File Name	Resource Description
2	These resources are being shared in good faith by project participants and are intended for informational purposes only. The FMEC does not necessarily endorse the resources listed. If you have additional resources you would like to add, please email them to rebecca.bouck@fmec.net
3	The American Cancer Society Leadership in Oncology Navigation (ACS LIONTM) - Patient Navigation Training and Credentialing	The American Cancer Society Patient Navigator Training (ACS LION™) is a free, evidence‑based online program designed to build core competencies for non‑clinical oncology navigators across the cancer care continuum. The training aligns with national Professional Oncology Navigation (PONT) standards and meets CMS requirements for Principal Illness Navigation (PIN) reimbursement, making it a practical option for clinics strengthening their navigation infrastructure. Modules cover barrier assessment, communication, care coordination, documentation, and connecting patients to supportive services, with a proctored final assessment to verify competency. This training helps teams deliver consistent, high‑quality navigation support, reduce disparities, and enhance patient experience from screening through survivorship.
4	American Society of Clinical Oncology (ASCO) - Survivorship Care Educational Opportunities	The ASCO Survivorship Care Educational Opportunities page compiles a wide range of trainings, courses, conference libraries, and educational resources designed to strengthen survivorship knowledge for oncology and primary care professionals. It highlights ASCO’s core survivorship curriculum—covering surveillance, late and long‑term effects, health promotion, psychosocial well‑being, special populations, caregivers, and care coordination—along with introductory survivorship course collections, Annual Meeting abstracts, and the Cancer Survivorship Symposium library. The page also links to additional offerings from national and international organizations, including e‑learning modules for primary care providers, childhood cancer survivorship courses, supportive oncology training series, and survivorship courses from institutions such as GW, MSK, Stanford, Peter Mac, and The Ohio State University. It serves as a centralized hub for clinicians seeking to expand their skills in evidence‑based survivorship care across diverse settings.
5	American Society of Clinical Oncology (ASCO) Survivorship Care Guidelines, Care Plans & Resources	The ASCO Survivorship Compendium provides a centralized collection of evidence‑based tools, guidelines, and educational resources designed to help clinicians deliver high‑quality survivorship care. It brings together ASCO’s recommendations on follow‑up care, management of late and long‑term effects, care coordination, and patient education, along with practical materials that support implementation in real‑world settings. The compendium is intended to help oncology and primary care teams strengthen communication, streamline survivorship workflows, and ensure that patients receive comprehensive, coordinated care after treatment.
6	American Society of Clinical Oncology (ASCO) Survivorship Care Plan	The American Cancer Society’s Survivorship Care Plan resource explains what survivorship care plans are, why they matter, and how they support patients after treatment. It outlines the key components of an SCP—such as treatment summaries, follow‑up schedules, symptom monitoring, and information on long‑term and late effects—and emphasizes how these plans help survivors understand what to expect, who is responsible for different aspects of their care, and when to seek support. The page also highlights the role of SCPs in improving communication between oncology and primary care and empowering survivors to navigate their ongoing health needs.
7	Breast Cancer Survivorship Tool: Facilitating breast cancer survivorship care for family physicians and patients	The Canadian Family Physician Breast Cancer Survivorship Tool is a practical, primary‑care–focused resource that outlines key follow‑up needs for breast cancer survivors. It provides clear guidance on surveillance, management of late and long‑term effects, health promotion, and psychosocial support, along with prompts to help clinicians structure survivorship visits. The tool is designed to be quick to use in clinical settings and supports family physicians in delivering coordinated, comprehensive survivorship care. - More information at https://pmc.ncbi.nlm.nih.gov/articles/PMC7219819/
8	Cancer Nation – Tools for Care Providers	A collection of practical resources designed to strengthen communication and shared decision‑making between clinicians and people living with, through, and beyond cancer. Tools include the Cancer Survival Toolbox®, worksheets to help patients prepare for appointments, employment rights guidance, self‑advocacy materials, and communication aids such as “Talking With Your Doctor.” The site also offers Survivorship Champions, a national community for clinicians interested in improving survivorship care, along with guidance on using care plans and supporting patients in early steps of self‑management.
9	CDC - Bring Your Brave	Bring Your Brave is a CDC education campaign that shares real stories of women under age 45 to raise awareness about breast cancer risk, early detection, and the unique challenges younger women face. The campaign provides evidence‑based information on risk factors, genetic predisposition, and early‑onset breast cancer, along with videos, podcasts, and clinician‑focused resources to support risk assessment and patient education. It is designed to help both the public and healthcare providers better understand and address breast cancer in young women.
10	CDC - Cancer Survivors	The CDC’s Cancer Survivors page provides evidence‑based guidance and practical tools to support people living with and beyond cancer. It includes resources on healthy living after treatment, managing side effects, caregiver support, and information specifically for healthcare providers on preparing patients for long‑term effects. The site also features survivor stories, educational videos, and the “Talk to Someone” simulation to help patients understand post‑treatment health needs, making it a useful reference for survivorship education and clinical communication.
11	CDC - Young Breast Cancer Survivors Program	The CDC’s Young Breast Cancer Survivors (YBCS) Program funds organizations nationwide to provide structured support services for young breast cancer survivors and metastatic breast cancer patients. The program focuses on improving quality of life, increasing equitable access to psychosocial and clinical supports, strengthening patient–provider communication, and expanding survivorship education for healthcare professionals. It prioritizes populations disproportionately affected by breast cancer and supports policy, systems, and environmental changes that address long‑term survivorship needs.
12	CDC- Cancer Survivors "Talk to Someone" Simulation	The CDC’s Talk to Someone Simulation is an interactive, virtual conversation tool that helps cancer survivors practice discussing concerns with a supportive, AI‑guided “cancer survivor coach.” The simulation models common questions about life after treatment—such as managing symptoms, navigating follow‑up care, and coping with emotional or practical challenges—and provides tailored, empathetic responses. It is designed to build confidence, normalize survivorship concerns, and help users prepare for real conversations with their care team.
13	EmpowerHER Connections: Psychosocial Resources for Cancer Patients and Their Families	The NACDD Young Breast Cancer Survivors (YBCS) site provides comprehensive resources to support young breast cancer survivors, particularly those facing higher risks and greater barriers to care. It highlights evidence‑based tools, state and community programs, educational materials, and strategies to improve navigation, psychosocial support, and long‑term follow‑up. The site also showcases partnerships and initiatives aimed at reducing disparities—especially for young Black women—and strengthening coordinated survivorship care across public health, oncology, and primary care settings.
14	FMEC -Confidence in Hereditary Cancer Discussion for Primary Care Providers Modules	Free CME Modules - This series is designed to improve family medicine healthcare providers’ skills and confidence in identifying and managing patients who may have a higher risk of hereditary breast cancer (HBC) due to genetic factors . Each module explores a vital aspect of identifying and managing HBC. Of particular interest is the use of narrative medicine, a powerful tool for engaging patients in discussions about HBC risk. Other topics include setting up the primary care office for HBC screening and referral, working with genetic counselors, and addressing patients’ concerns about insurance, disclosure, and communicating with family.
15	FORCE: Facing Our Risk of Cancer Empowered - ABFM PI: Improving Assessment and Management of Hereditary Breast and Gynecologic Cancer in Women	The FORCE ABFM Performance Improvement (PI) activity is a structured quality‑improvement program designed to help family medicine clinicians strengthen care for young breast cancer survivors. It provides a step‑by‑step framework for assessing current practices, identifying gaps, implementing evidence‑based changes, and measuring improvement over time. The activity focuses on enhancing communication, care coordination, risk assessment, and survivorship support, and it offers tools, templates, and educational resources to guide clinicians through the PI process.
16	International Cancer Control Partnership (ICCP): National Cancer Survivorship Resource Center Toolkit: Provider Tools Implementing Clinical Practice Guidelines for Cancer Survivorship Care	The National Cancer Survivorship Resource Center (NCSRC) Provider Toolkit is a comprehensive, evidence‑based guide created by the American Cancer Society and the GW Cancer Institute to help primary care, oncology, public health, and navigation professionals implement survivorship clinical practice guidelines for breast, colorectal, head and neck, and prostate cancers.
17	MSK Survivorship Care Plan	Memorial Sloan Kettering provides a detailed Survivorship Care Plan framework outlining a patient’s cancer history, treatment summary, and individualized follow‑up recommendations. The plan clarifies provider responsibilities across oncology and primary care to support coordinated, long‑term survivorship management. MSK also offers guidance on implementing care plans, including data collection, transition visits, and electronic storage, along with links to national templates and tools such as ASCO, Journey Forward, NCCN, and OncoLink resources.
18	Medscape: NACDD: Talk to Someone: Helping Survivors With Healthy Lifestyles	Activity introducing “Talk to Someone: Meet Linda, a Virtual Cancer Survivor,” an interactive program developed by the CDC, NACDD, and Kognito. The tool includes four separate modules addressing key lifestyle issues and allows cancer survivors to ask questions and have brief, guided conversations with a virtual character named Linda. Her responses are based on real survivor experiences, and each interaction lasts about three to five minutes. The modules are available in both English and Spanish. The goal of this activity is to improve the knowledge of the primary care and oncology teams in identifying and managing lifestyle challenges in patients after cancer treatment, and to improve their ability create personalized treatment plans and direct their patients to appropriate support resources, such as the Talk to Someone conversation simulation modules, where they can interact with Linda, an empathic virtual cancer survivor.
19	National Comprehensive Cancer Network, Survivorship Guidelines -	The NCCN Survivorship Guidelines provide evidence‑based recommendations to support people after cancer treatment, including monitoring for late effects, addressing psychosocial needs, promoting healthy lifestyle behaviors, and coordinating follow‑up care across oncology and primary care. They outline practical approaches for surveillance, symptom management, risk reduction, and referrals, helping clinicians deliver comprehensive, patient‑centered survivorship support.
20	Project Implicit: Implicit Association Test (IAT)	The Harvard Project Implicit “Take a Test” page provides access to a series of Implicit Association Tests (IATs) that measure automatic attitudes and beliefs people may not be aware of. Participants can choose from a range of topics—such as race, gender–career, disability, weight, age, and more—and take the tests anonymously. The site explains the purpose of the IAT, offers background on implicit cognition, and allows users to participate as guests without creating an account. It is widely used in educational and training settings to support reflection on bias and decision‑making.
21	Susan G. Komen’s Patient Navigation Training Program	Navigation Nation Training Program (Komen) — Free national online training for patient navigators covering breast health, oncology navigation basics, cultural humility, MBC navigation, and communication skills. Includes self‑paced courses, live sessions, tailored learning pathways, and a self‑assessment tool. Participants receive documentation of completed training and access to the annual Navigation Nation Summit.
22	The American Cancer Society Resources for Health Care Professionals	The American Cancer Society’s Resources for Health Care Professionals page provides a centralized hub of evidence‑based tools, guidelines, patient‑education materials, research data, and professional development opportunities to support clinical practice across the cancer continuum. It includes patient‑facing education in multiple languages, printable materials, and referral resources for housing, transportation, and practical support. Clinicians can access current cancer statistics, ACS journals, and prevention and screening guidelines—including HPV vaccination tools and implementation guides. The page also highlights collaboration opportunities through ACS roundtables, the ARC Network, and Project ECHO, along with global cancer support initiatives. Additional offerings include navigation training, toolkits, funding opportunities, and ongoing webinars focused on prevention, screening, disparities, and evidence‑based cancer care.
23	Young Adult and Teen Cancer Pocket Guide - Coping with cancer between 15 and 39	The American Cancer Society’s Young Adult and Teen Cancer Pocket Guide is a clinician‑relevant resource designed to help adolescents and young adults (ages 15–39) navigate the medical, psychosocial, and developmental challenges of cancer. It highlights key communication needs, including open‑ended inquiry, validation, and proactive discussion of sensitive topics such as fertility, mental health, body image, and relationships. The guide also outlines common late effects, quality‑of‑life concerns, and supportive resources, making it a useful reference for providers working with young survivors.
24	These resources are being shared in good faith by project participants and are intended for informational purposes only. The FMEC does not necessarily endorse the resources listed.
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