HA Conference 2026
HA CONNECT
Mark Your Calendars!

The must-attend event for the hydrocephalus community is back.
July 23-25, 2026 | Indianapolis, IN.

Video HCRN
Transforming Hydrocephalus Care

HA President and CEO Diana Gray connected with new HCRN Chair, Dr. Bill Whitehead, to discuss how this network is changing hydrocephalus care through their research findings.

Research Priorities
We Are Listening to the Hydrocephalus Community!
Recognizing the impact of neuropsychological and cognitive challenges on quality of life, we’ve published our Research Priorities in Fluids and Barriers of the CNS.
2025 Scholarship Cycle
The 2025 Scholarship Cycle is Now Open!
The Hydrocephalus Association’s Scholarship Program is now open for applications.
Apply by April 15, 2025.
Resource Library
Announcing Our New Hydrocephalus Resource Library

Discover everything you need in one place —from toolkits and medical insights to expert tips for thriving at every stage.

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Let’s Navigate this together

Trusted resources to help you on your journey.

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Hydrocephalus Resource Library

Discover everything you need in one place —from toolkits and medical insights to expert tips for thriving at every stage.

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Tools for Daily Life

Learn how to manage the day to day symptoms and challenges you might encounter on your journey with hydrocephalus.

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Get Support

We're here to help! Find the support you need and talk to people who know what you're going through.

Driving Research Forward

Improving lives now and funding the breakthrough research of tomorrow.

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$16 Million

Invested in research
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$91 Million

Additional Federal Grants Awarded
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13

Preclinical Drug Therapies

Make An Impact

We come together in so many ways — all of us driven by a passion to find a cure and improve the lives of those impacted by hydrocephalus. Whether you participate in a WALK to End Hydrocephalus or join our advocacy efforts, you’re making a difference!

Community

Our community of patients and caregivers is there for you so you can connect, share life experiences, and find hope.

Research

Researchers need input from people living with hydrocephalus in order to ask the right questions and develop treatments.

Advocate

The best advocates are patients, family members, medical caregivers, and others who are directly affected by the condition.

Shop

Raise awareness about hydrocephalus and look great doing it!

Connect With Us

When you're ready, let's take the next step together. Stay informed with our monthly newsletter! We'll share inspiring stories, and information about our programs, events, and research.

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