Partnership to Improve Patient Care

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  • Home
  • About
    • Mission and Priorities
    • Meet the Chairman
    • Steering Committee
    • PIPC Member List
    • Contact
  • The Issues
    • Action Center
    • Value Our Health
    • International
    • Where We Stand
    • Value Assessment Frameworks
    • Engaging Patients in Value-Based Payment
    • Patient-Centeredness in Research
  • Resources
    • Advocacy
    • Letters and Comments
    • PCORI Meeting Transcripts
    • Polling
    • Roundtables
    • White Papers
  • News
    • Press Releases
    • PIPC in the News
    • PIPC Weekly Update
    • PIPC Patients' Blog
    • Chairman's Corner
    • The Data Mine
  • Events
    • Nevada AB 259
    • QALY Panel
    • QALY Briefing
    • Past Webinars >
      • MFN/IPI Webinar 2025
      • Discrimination & Health Care
      • C & GT Webinar
      • ICER COVID Webinar
      • Value Our Health Briefing
      • ICER SCD Webinar
      • VOH Sickle Cell Webinar
      • Rare Disease Webinar
      • QALY Webinar
      • PCORI Advocacy Webinar
      • APM Webinar
      • Patient Empowerment Webinar
      • Value Assessments Briefing
    • Past PIPC Forums >
      • 2023
      • 2022
      • 2021
      • 2020
      • 2019
      • 2018
      • 2017
      • 2016
      • 2015
      • 2014
      • 2013
      • 2012
      • 2011
      • 2010

State Advocacy: Pennsylvania

Become a Patient Advocate

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Pennsylvania Facts and Figures
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Tell Senator Casey: Don't Let Medicare Get Between Patients and Doctors

PIPC strongly urges patients, people with disabilities, caregivers and providers to write letters to Congress to express concerns with CMS’ newly proposed payment model. We strongly support comparative effectiveness research as a tool for patients to better understand their treatment options and the impact on outcomes they care about so that they can make informed decisions with their providers. However, proposals that set national coverage policies based on bureaucratic determinations of average value pose a grave risk to patients, and especially people with disabilities who are most disadvantaged by average value assessments. 
Write to Sen. Casey

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Op-Ed: Holding Health Systems Accountable for Patient Value

In a recent op-ed published in the Philadelphia Enquirer, John Doe, a cancer survivor and self-advocate, encouraged Senators Bob Casey and Pat Toomey to advocate for giving patients a seat at the table in the development of new payment systems that could impact patient care. "Nowhere in this 'value' discussion do we see an honest consideration of the real-world impact these proposals would have on the individual patient or the person with a disability for whom an innovation may have significant value," he said. "Never has it been more important for our elected officials to stand up and demand that the patient voice be included at the forefront of policy development."
View the Op-Ed

Patient Advocacy Resources in Pennsylvania

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Epilepsy Foundation 

919 Walnut Street, Suite 700
Philadelphia, PA 19107-5237
Main Number: (215) 629-5003
[email protected]

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National Alliance on Mental Illness 

NAMI is currently in the process of rebuilding a NAMI State Organization in Pennsylvania. If you would like to be involved with this process, please contact the national office at [email protected].

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Easter Seals

Easter Seals Southeastern Pennsylvania
3975 Conshohocken Avenue
​Philadelphia, PA 19131
Main Number: 215-879-1000

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