How One Foundation Is Laying the Groundwork to Advance Treatments for an Ultra-Rare Disease

Pediatrician and mother of a daughter with CACNA1A-related disorder Deborah Ondrasik and CACNA1A Foundation Vice President Sunitha Malepati discuss the ultra-rare neurodegenerative condition, how it progresses, and what the CACNA1A Foundation is doing to advance research to speed the development of treatments and a cure.