Search results for: Hydrocephalus education and support
Get the Hydrocephalus Scoop on Capitol Hill for March 2024
Things in Washington, DC are both quiet and chaotic at the same time. Apparently, it’s a thing with the political world. Here’s the scoop on what’s happening on hydrocephalus issues.
Read MoreHydrocephalus Association Congressional Briefing on Capitol Hill
The Hydrocephalus Association recently partnered with the Defense Health Research Consortium (DHRC) to host a research-centered Congressional Briefing on Capitol Hill.
Read MoreHydrocephalus Association Highlights Revolutionary Women in Medical Research
Celebrate Influential Leaders during National Women’s History Month. Dr. Robinson & Dr. Jantzie are both revolutionary women making strides for hydrocephalus
Read MoreGet the Hydrocephalus Scoop on Capitol Hill for February 2024
Things in Washington, DC are both quiet and chaotic at the same time. Apparently, it’s a thing with the political world. Here’s the scoop on what’s happening on hydrocephalus issues.
Read MoreThe Hydrocephalus Scoop on Capitol Hill for November 2023
Things in Washington, DC are both quiet and chaotic at the same time. Apparently, it’s a thing with the political world. Here’s the scoop on what’s happening on hydrocephalus issues.
Read MoreWALK to End Hydrocephalus 2023 Season Recap
Thanks to the Hydrocephalus Association’s wonderful volunteers, 40 WALKS were held across the U.S., with nearly 7,000 participants representing over 800 teams.
Read MoreAnnouncing our 2023 Hydrocephalus Association Scholarship Recipients!
The Hydrocephalus Association (HA) is pleased and honored to announce our 2023 Hydrocephalus Association Scholarship Recipients.
Read MoreThe Hydrocephalus Scoop on Capitol Hill for October 2023
Things in Washington, DC are both quiet and chaotic at the same time. Apparently, it’s a thing with the political world. Here’s the scoop on what’s happening on hydrocephalus issues.
Read MoreThe Hydrocephalus Scoop on Capitol Hill for September 2023
Things in Washington, DC are both quiet and chaotic at the same time. Apparently, it’s a thing with the political world. Here’s the scoop on what’s happening on hydrocephalus issues.
Read MoreThe Hydrocephalus Scoop on Capital Hill for August 2023
Things in Washington, DC are both quiet and chaotic at the same time. Apparently, it’s a thing with the political world. Here’s the scoop on what’s happening on hydrocephalus issues.
Read MoreA Conversation with Emily and Russell Fudge – Pioneering Leaders of the Hydrocephalus Association
In honor of the Hydrocephalus Association’s 40th Anniversary, we had the privilege of interviewing with Emily and Russell Fudge, the visionary leaders that were the driving force behind the establishment of HA.
Read MoreCelebrating the 40th Anniversary of the Hydrocephalus Association
The year 2023 marks the 40th Anniversary of the Hydrocephalus Association (HA). Throughout the year, we will honor our legacy with all of our community by celebrating our milestones and exploring what has been accomplished over the past four decades.
Read MoreAnnouncing our 2022 Hydrocephalus Association Scholarship Recipients!
The Hydrocephalus Association (HA) is pleased and honored to announce our 2022 Hydrocephalus Association Scholarship Recipients.
Read MoreWALK to End Hydrocephalus® Participant Privacy Policy
This privacy policy governs your use of the software application WALK to End Hydrocephalus® for mobile devices.
Read MoreStatement by Hydrocephalus Association President and CEO Diana Gray on Washington Post Article About Chloe Kral
The Washington Post recently published a story about Chloe Kral, who suffered for years and was told she had severe mental illness before discovering later that she had hydrocephalus. Here’s a statement from HA’s President & CEO Diana Gray about Chloe’s remarkable story.
Read More2021 WALK to End Hydrocephalus Raises over $1.6 Million
Our WALK to End Hydrocephalus program had a successful year, raising over $1.6 million for HA’s research, support, education and advocacy efforts.
Read MoreAnnouncing our 2021 Hydrocephalus Association Scholarship Recipients!
The Hydrocephalus Association (HA) is pleased and honored to announce our 2021 Hydrocephalus Association Scholarship Recipients.
Read MoreThe Hydrocephalus Scoop on Capital Hill for August 2020
Things in Washington, DC are both quiet and chaotic at the same time. Apparently, it’s a thing with the political world. Here’s the scoop on what’s happening on hydrocephalus issues.
Read MoreNew Ask the Expert Video Series for Adults Living with Hydrocephalus
Check out our latest Ask the Expert Video Series developed specifically for adults living with hydrocephalus. The series answers some of the most common questions we receive to our support line.
Read MoreWALKs to End Hydrocephalus Help Raise Nearly $2 Million
The 2018 WALK to End Hydrocephalus season is in the books! And what a year it was. Thanks to the Hydrocephalus Association’s wonderful volunteers, 43 WALKS were held across the U.S., with more than 14,000 participants representing over 1,200 teams.
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