The CACNA1A Foundation is a 501(c)(3) nonprofit that was established by the parents of children with CACNA1A gene variants. In their search for better treatment options, they created a foundation that helps fund CACNA1A research, connects affected families, and encourages collaboration among researchers. A major tool that this website provides is its resources on navigating health, safety, schools, and available state assistance for children with CACNA1A variants.
Dr. Gomez serves on the Scientific & Medical Advisory Board and is also listed as an available physician for CACNA1A disorders.
Visit cacna1a.org to learn more of their mission
Infographic taken from cacna1a.org.
