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National Organization for Rare Disorders (WORD), with The APS Type 1 Foundation Inc. AnnouncesResearch Seed Money Grant (up to $100,000)autoimmune Poly glandular Syndrome Type 1 (APS Type 1) also
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National organization for rare is a non-profit organization dedicated to supporting individuals with rare diseases and advocating for research and treatments.
Non-profit organizations that focus on rare diseases or conditions are required to file national organization for rare.
To fill out national organization for rare, organizations must provide detailed information about their mission, funding sources, programs, and impact.
The purpose of national organization for rare is to provide transparency and accountability for non-profit organizations working in the rare disease space.
Information such as financial statements, board members, fundraising activities, and program outcomes must be reported on national organization for rare.
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