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You are here: Home1 / Events2 / CPAT

CPAT

Join Us

What you have experienced, endured, and learned matters to not just you, but to everyone who has and will be touched by cancer. Your story, and how you tell it, can shape how decision makers provide quality cancer care to millions of cancer survivors. That is why NCCS invites you to the annual Cancer Policy and Advocacy Team Symposium, virtually on June 15-16 and June 22nd-23rd from noon to 3:30 p.m. ET. each day, including a virtual Hill Week June 22nd-26th.

Advocates from around the country will connect to listen and understand your journey. There will be three different tracks so you can choose your own Symposium experience, whether you’re new to advocacy or a seasoned Symposium attendee.

You’ll also:

  • Hear from health care and policy experts about the future of cancer care, managing stress and anxiety, how to “return” to work, and more;
  • Participate in a roundtable on what survivorship means for people with metastatic cancer and help shape the conversation around metastatic survivorship;
  • Hear from Washington insiders about health policy during the COVID-19 pandemic; and
  • Prepare for and attend meetings with Congressional staff through the virtual Hill Week June 22-26.

Thank You for Attending #CPAT2020!

A record-breaking number of attendees joined #CPAT20. Advocates from around the country learned from renowned experts, heard from all-star advocates, and leveraged their personal stories to improve cancer care. Whether it was a brand-new advocate or seasoned Symposium attendee, attendees chose their own adventure to help find their voice, or fine-tune it.

Choose Your Track

NCCS’ virtual CPAT symposium is your opportunity to connect with advocates from across the country while you attend sessions tailored to your level of advocacy. These tracks will help you “choose your own adventure” — whether you want to find your voice, or fine-tune it.

Track 1: If you are new to advocacy, this track is for you. You’ll receive a big picture overview of the economics behind cancer care. You will also hear how to tell your story and prepare for conversations with policy makers.

Track 2: If you are ready to take your advocacy to the next level, choose this track. You’ll learn about the need for expanded diversity in cancer care, how to balance work, and unique engagement opportunities that can help advance your advocacy efforts.

Track 3: If you’re a provider or caregiver and want to learn more about survivorship, this track is right for you.You’ll receive specialized topics, such as what survivorship means to metastatic patients, engaging more men in cancer advocacy, and understanding patients’ perspectives. This track will also include a unique discussion from survivors that you won’t find anywhere else.

Access the Recordings

You can still access the recordings here. Learn more about speakers, too! Thank you again for shaping important conversations and tools for everyone touched by cancer.

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Join CPAT

The NCCS Cancer Policy & Advocacy Team (CPAT) is a program for survivors and caregivers to learn about pressing policy issues that affect quality cancer care in order to be engaged as advocates in public policy around the needs of cancer survivors.

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NCCS represents the millions of Americans who share a common experience – the survivorship experience – living with, through and beyond a cancer diagnosis.

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  • About
    • Our Mission
    • Our History
    • The 1986 Club
    • Our Team
      • Policy Advisors
    • Employment
    • Partnerships
    • Financial Information
  • Policy
    • Quality Cancer Care
    • Access to Care
    • Health Equity
    • Redefining Functional Status (RFS)
    • 2022 State of Cancer Survivorship Survey
    • 2021 State of Cancer Survivorship Survey
    • 2020 State of Cancer Survivorship Survey
    • Cancer Care Planning and Communications Act (CCPCA)
  • Get Involved
    • What is Advocacy?
    • Cancer Policy and Advocacy Team (CPAT)
    • Survivorship Champions
    • Subscribe to NCCS Updates
    • Elevating Survivorship
    • Survivor Stories
    • Cancerversary
    • State-Based Cancer Advocacy
  • Resources
    • COVID-19 Resources for Cancer Survivors
    • Survivorship Checklist
    • Cancer Survival Toolbox
    • Telehealth
    • Publications
      • Talking With Your Doctor
      • Self Advocacy
      • Employment Rights
      • Remaining Hopeful
    • Cancer Convos Podcast
    • Taking Charge of Your Care
    • Care Planning for Cancer Survivors
    • Tools For Care Providers
    • Order Our Resources
  • News
  • Events
    • Ellen L. Stovall Award
      • 2022 Winners
      • Awardees
      • Sponsors
      • Committees
    • Cancer Policy Roundtable (CPR)
      • Fall 2022 CPR
      • Spring 2022 CPR
      • Fall 2021 CPR
      • Spring 2021 CPR
      • Fall 2020 CPR
      • Spring 2020 CPR
    • Cancer Policy and Advocacy Team (CPAT) Virtual Symposium 2022
    • 2022 State of Survivorship Survey Results
    • Webinars
  • Contact Us

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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