Stiftung Lichterzellen is a disease-focused foundation centered on improving research, diagnosis, and treatment for PNH (paroxysmal nocturnal hemoglobinuria) and aplastic syndromes. Its work also emphasizes direct support for patients and families, plus raising awareness among the public and physicians, rather than broad general grantmaking. The foundation appears to operate more like a mission-driven advocacy and fundraising organization, closely connected to medical experts and community fundraising efforts.
Appears to support its mission through fundraising partnerships, benefit events, and donation platforms rather than issuing broad public grant cycles; any support is likely highly program-specific and relationship-based.
No public grant application process is evident from available data. Organizations working in rare hematology, patient support, or awareness should contact the foundation directly and expect a relationship-based, mission-aligned approach rather than an open call for proposals.
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¿Quién puede postularse? Funding is limited to the foundation's statutory purposes and the implementing body must be tax-privileged (steuerbegünstigt) for international requests as well. The foundation states it can fund research projects and scientific events within the scope of AA/PNH and related bone marrow failure disorders.
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