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Description ABOUT US The mission of the Hydrocephalus Association is to find a cure for hydrocephalus and improve the lives of those impacted by the condition. Founded in 1983 by the parents of children with hydrocephalus, the Hydrocephalus Association (HA) is the nation’s largest and most widely respected organization dedicated to hydrocephalus. We fund high-impact research, provide support and educational resources for patients and caregivers, and advocate on behalf of the hydrocephalus community on key policies and legislation. Since 2009, HA has invested over $14 million in cutting-edge research, making us the largest non-profit, non-governmental funder of hydrocephalus research in the United States. Our Mission HA's mission is to find a cure for hydrocephalus and improve the lives of those impacted by the condition. Our Vision Our vision is a world without hydrocephalus. Diversity, Equity, and Inclusion Statement At HA, we are committed to fostering an inclusive and equitable environment where all individuals, regardless of their backgrounds, experiences, or identities, feel valued, respected, and empowered.

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