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Meet The Peters Family
In 2018, the Peters welcomed their first son, Cavan, who was diagnosed with hydrocephalus at just four months old. They were told it wasn't genetic, but when their second son, Breccan, was diagnosed at two months, the family realized they were facing a rare and challenging journey. Now, their youngest child, Teagan, has also been diagnosed with hydrocephalus. Despite these difficulties, the Peters remain resilient, navigating countless brain surgeries and advocating for answers!
OUR RESEARCH IMPACT
The Hydrocephalus Association is focused on funding high-quality, high-impact research and building the hydrocephalus research community. Our impact can be seen far and wide throughout the hydrocephalus research field.
Programs & Services
HA offers specialized programs and services to support anyone impacted by hydrocephalus at every stage of life. We partner with leading experts in the field to provide the most current, relevant information, programs, and events to help you manage the complexities of this condition.
Get Support
HA is here to help. We are eager to guide you to the support you need for your particular situation. Get access to informed and current resources to help you understand and deal with the complexities of hydrocephalus.