CACNA1A Foundation

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 to learn more of their mission

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