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Hydrocephalus Association
Misión
The mission of the Hydrocephalus Association is to find a cure for hydrocephalus and improve the lives of those impacted by the condition. We will accomplish this by collaborating with patients, caregivers, researchers, and industry, raising awareness, and funding innovative, high-impact research to prevent, treat and ultimately cure hydrocephalus.
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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 $13 million in cutting-edge research, making us the largest non-profit, non-governmental funder of hydrocephalus research in the United States.
Áreas de Impacto incluyen
- Educación
- Salud & Medicina
- Adultos Mayores
- Voluntariado
Información y Contacto
- 2404834543
- 4340 EAST WEST HIGHWAY, SUITE 905, Bethesda, Maryland, US
SUITE 905
Avisos recientes
| Volunteers Needed for HA Connect Conference Indianapolis, IN- Kids Camp | Indianapolis, IN | ... |
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