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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
    • Health Equity
    • Rare Cancer
  • Policy/Comments/
    • Inflation Reduction Act
    • Medicare
    • Section 340b
    • Medicaid
    • FDA
    • ICER
  • Patient Stories/
  • Join/
  • Take Action/
May 05, 2023

Haystack's letter to NASEM Requesting a meeting regarding the HEART Act→

May 05, 2023/ Michelle Osburn

Read more.

May 05, 2023/ Michelle Osburn/ /Source
Comment Letters, Letters
HEART Act, GAO, NAM, FDA

Michelle Osburn

May 04, 2023

Haystack requests meeting with GAO leadership and staff→

May 04, 2023/ Michelle Osburn

Read more.

May 04, 2023/ Michelle Osburn/ /Source
Comment Letters, Letters
HEART Act, GAO, NAM, FDA

Michelle Osburn

March 09, 2023

Haystack's Project Letter to FDA on the Implementation of the HEART Act→

March 09, 2023/ Michelle Osburn

Read more.

March 09, 2023/ Michelle Osburn/ /Source
Comment Letters, Letters
HEART Act, GAO, NAM, FDA

Michelle Osburn

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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.