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      <FactsAndCircumstancesTestTxt>Prior Year Facts and Circumstances: The PAP Foundation seeks both a cure and effective treatment for Pulmonary Alveolar Proteinosis (PAP). PAP is a life-threatening lung disorder that affects men, women and children. PAP is very rare. As a consequence, the pool of donors is small as compared to most publicly-supported organizations. The PAP Foundation does not benefit any one individual or any related group; rather, the Foundation is dedicated to finding a cure for all those afflicted with PAP, and as such represents the broad interests of the general public. The Foundation promotes research on PAP and provides information and support for PAP patients, wherever they may be. The Foundation seeks to expand its contribution base through the provision of information to patients, healthcare professionals and the public.In 2019, two large contributions were received from donors who previouly had not made gifts in prior years. Those contributions are included in full in Schedule A. Additionally, substantial contributions were received in 2020, 2021, 2022 and 2023 from relatively few donors, all of which are reported on Schedule A. The Foundation is slowly building its support from the general public. Only relatively small contributions were received in 2016 and 2017. The Foundation anticipates that it will not meet the 33 1/3% test for several years. The public support percentage does continue to rise - from 21.6% in 2022 to 22.6% in 2023. Gifts are currently being made by multiple non-related persons. The board consists of unrelated individuals who represent a broad spectrum of society.</FactsAndCircumstancesTestTxt>
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        <ExplanationTxt>Form 990 is provided to the board president prior to filing, and then posted on the Foundation's website. The board is currently revising its policy so that a full board review will occur prior to filing.</ExplanationTxt>
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