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The Haystack Project
  • Home/
  • About/
    • About Us
    • Participants
    • Partners
    • Board and Advisors
  • Priorities/
  • PROTECT Rare/
  • FDA/
    • Rare Disease Approvals
    • HEART Act
  • Programs/
    • Speaker Series
    • Payer Engagement
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January 12, 2022

Copay Accumulator Fact Sheet→

January 12, 2022/ Michelle Osburn

Read more.

January 12, 2022/ Michelle Osburn/ /Source
Patient Assistance Progra, PatientAssistancePrograms
copay, advocacy, HELP Act

Michelle Osburn

December 28, 2020

Haystack Joins Others in Opposing Copay Accumulators→

December 28, 2020/ Rebecca Balliet

Read more.

December 28, 2020/ Rebecca Balliet/ /Source
Letters, Comment Letters, PatientAssistancePrograms, Patient Assistance Progra
patientAssistancePrograms

Rebecca Balliet

December 23, 2019

Anti-Kickback Statute Comment Letter→

December 23, 2019/ Rebecca Balliet

Read more.

December 23, 2019/ Rebecca Balliet/ /Source
Letters, Comment Letters, Patient Assistance Progra, PatientAssistancePrograms
patientAssistancePrograms

Rebecca Balliet

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The Haystack Project is a 501(c)3 nonprofit that brings together patients organizations representing patients suffering from or caring for patients with extremely rare diseases. Our mission is to educate policymakers and other stakeholders about the need for policies that recognize the unique circumstances of extremely rare conditions and treatments and expand incentives critical to ensuring they can reach patients.