Be the Spark for VLCAD Research

Every day, children and families living with VLCAD deficiency and other long-chain fatty acid oxidation disorders (LC-FAOD) face medical uncertainty, hospitalizations, metabolic crises, and the ongoing risk of life-threatening complications. Your donation helps fund rare disease research, support emerging technologies, advance clinical trial readiness, and improve disease management for individuals living with VLCAD and related fatty acid oxidation disorders.

With your support, we can help turn research into real-world solutions for families who cannot afford to wait.