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The Role of the PACT Act

Join the NCCS Cancer Policy & Advocacy Team: Empowering Those Touched by Cancer to Change Cancer Care

May 11, 2016/in Cancer Policy Blog, NCCS News NCCS News

CPAT Word CloudIf you have ever wanted to use your cancer journey—either as a survivor or as a caregiver—to make a difference, you are invited to join the NCCS Cancer Policy & Advocacy Team (CPAT)!  Driven by the energy and experiences of the CPAT Steering Committee, CPAT provides cancer survivors and caregivers with tools and training that build upon their personal experiences to become effective advocates to improve cancer care. Through NCCS events and materials, CPAT members gain an in-depth understanding of public policies that impact survivorship: to quote from someone who attended last year’s symposium, “(The) quality of content presented was amazing.”  Another noted, “As a new advocate, this (meeting) was very helpful in understanding the full breadth of issues surrounding cancer survivorship.”

CPAT members have access to a number of resources related to current issues, programs, and policies that affect cancer survivors.

  • Webinars: CPAT members participate in webinars with experts who speak about different issues related to cancer survivorship such as “Strategies for Cancer Survivors to Implement When Choosing Health Insurance” and the upcoming “A Conversation Around Shared Decision-Making and A Patient Revolution—and The Role of the PACT Act.”
  • Symposium: CPAT members are invited to the annual two-day meeting in Washington, DC where they can network with other advocates from around the country and learn from cutting-edge researchers, health care professionals, and policy leaders. Travel scholarships to the conference are available to CPAT members.
  • E-Newsletter: CPAT members receive a periodic e-newsletter with updates on policy issues that affect cancer care and highlights advocates’ efforts in their communities.
  • CPAT Forum: The CPAT Forum on the NCCS website allows CPAT members to interact with others and to access material and resources relevant to their advocacy efforts.

If you are interested in using your personal experience to be a transforming, positive force to affect change through CPAT, simply complete a brief online questionnaire to become a member.  (We will then send you information about registering for this year’s symposium and webinars, and we are always interested in hearing about your ideas for CPAT.)

If you’d like to learn more about CPAT by participating in the upcoming webinar “A Conversation Around Shared Decision-Making and A Patient Revolution—and The Role of the PACT Act” on Wednesday, May 25 from 3:00 pm to 4:30 pm Eastern time, please complete the registration form as well.

If you have any questions or ideas for CPAT, please contact Christin Engelhardt, Director of Policy and Advocacy or Kelsey Nepote, Consultant, Cancer Policy & Advocacy Team.

Tags: Advocacy, cancer care, CPAT
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Survivorship Champions is a program for all clinicians and researchers, both oncology and primary care, who are interested in improving survivorship care and primary care’s role in caring for cancer survivors.

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Link to: Cancer Policy and Advocacy Team (CPAT)

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.

Link to: Survivor Stories

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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)
    • State of Survivorship Survey
      • 2022 Survey
      • 2021 Survey
      • 2020 Survey
    • Cancer Care Planning and Communications Act (CCPCA)
  • Get Involved
    • What is Advocacy?
    • Cancer Policy and Advocacy Team (CPAT)
    • Advocate Engagement Opportunities
    • 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
    • Cancer Rehabilitation
    • Integrative Oncology
    • Publications
      • Talking With Your Doctor
      • Self Advocacy
      • Employment Rights
      • Remaining Hopeful
    • Telehealth
    • Taking Charge of Your Care
    • Care Planning for Cancer Survivors
    • Tools For Care Providers
    • Order Our Resources
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      • Awardees
      • Reception and Sponsorship
      • Committees
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    • 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