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The Haystack Project
  • Home/
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April 29, 2022

Haystack's AA Pathway "Reforms"

April 29, 2022/ Michelle Osburn

Read more.

April 29, 2022/ Michelle Osburn/ /Source
Position Statements
advocacy, other issues

Michelle Osburn

February 10, 2022

Haystack Project's sign-on letter commenting to CMS' proposed NCA for monoclonal antibodies→

February 10, 2022/ Michelle Osburn

Read more.

February 10, 2022/ Michelle Osburn/ /Source
Letters, Comment Letters, Position Statements
news, medicare, medicaid, other issues

Michelle Osburn

April 12, 2021

Medicaid Network Adequacy (ACE Kids 2019-20)→

April 12, 2021/ Saira Sultan

Read more.

April 12, 2021/ Saira Sultan/ /Source
Position Statements
medicaid, Medicaid

Saira Sultan

April 12, 2021

Bundled Payments and Rare Disease Ombudsman →

April 12, 2021/ Rebecca Balliet

Read more.

April 12, 2021/ Rebecca Balliet/ /Source
Position Statements
medicare

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.