2026 International HNRNP Gene Family & Research SummitJune 28–30 in Sheffield, UKRegister Now
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Mary, who has HNRNPU-NDD, chatting with Dr. Meena Balasubramanian, a clinical lecturer and geneticist from University of Sheffield, one HNRNP Family Foundation research collaborator

Mary, who has HNRNPU-NDD, chatting with Dr. Meena Balasubramanian, a clinical lecturer and geneticist from University of Sheffield, one HNRNP Family Foundation research collaborator

Issac Soul, who has HNRNPQ-NDD or SYCRIP, multitasking at 2024 conference

Issac Soul, who has HNRNPQ-NDD or SYCRIP, multitasking at 2024 conference

Kathleen Morton (center), who has HNRNPK-NDD or Au-Kline, her sister (left), and father (right) engaged in 2024 foundation conference

Kathleen Morton (center), who has HNRNPK-NDD or Au-Kline, her sister (left), and father (right) engaged in 2024 foundation conference

Families and researchers connecting at the 2024 HNRNP Family Foundation conference

Families and researchers connecting at the 2024 HNRNP Family Foundation conference

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Fund Research

Support groundbreaking studies to better understand HNRNP disorders and develop treatments.

Support Families

Help us provide resources, guidance, and community connections to affected families.

Build Community

Enable conferences, support groups, and educational programs that bring families together.

The HNRNP Family Foundation is a 501(c)(3) nonprofit organization. Your donation is tax-deductible to the extent allowed by law.