Grants Program
We envision a world where DHX30 is fully understood, treatable with measurable impact, and never a barrier to any child’s potential.
Our Focus
The Rare Remy Foundation supports innovative and collaborative research to expand understanding of DHX30-related neurodevelopmental disorders and advance meaningful progress toward effective therapeutics.
Our research priorities include studies that deepen knowledge of DHX30 function, clarify disease mechanisms, identify therapeutic pathways, and test strategies that could improve outcomes for individuals living with a DHX30 mutation. We strongly value collaboration, transparency, and urgency with our partners.
Check out our Research page to learn about some of our Research Needs.
Eligibility
Eligible applicants can include investigators from academic research institutions, hospitals, non-profit organizations, government research programs, and industry partners. We welcome proposals from early-career researchers to established scientists.
Proposals
Proposals may be submitted at any time and will be reviewed as received, with funding decisions contingent upon resource availability and alignment to our mission.
To inquire or submit a proposal, we invite you to Contact Us.