Improving the lives of patients impacted by Krabbe disease and Cystic Fibrosis through research funding and disease advocacy.
The grant program aims to support the foundation's mission and vision by considering funding for basic science research, translational research, and clinical research that can lead to or enhance treatments and cures for Krabbe disease and Cystic Fibrosis. Additionally, it supports programs promoting the expansion of Newborn Screening, and education and awareness about Krabbe disease and Cystic Fibrosis. Grants are awarded to projects that address specific scientific questions or specific educational/awareness goals aligned with the foundation's mission. Up to two New Investigator Grants are available, offering up to $60,000 per year for up to two years, with overhead funding capped at 5% of the total award.