From the Association
Advancing Hydrocephalus Research and Treatment Options: Non-Invasive Therapy Research Workshop
More than 75 experts in hydrocephalus gathered in Cincinnati, OH for the 2024 Research Workshop focused on finding ways to better treat hydrocephalus, aiming to make treatments safer and less invasive.
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Grey’s Anatomy Airs Episode on Congenital Hydrocephalus Performing Endoscopic Third Ventriculostomy (ETV)
Hydrocephalus in Pop Culture Sierra SPEAKS OUT HA’s Support & Education Program Assistant A Review:…
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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.
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Kim Apurado Awarded Prestigious Mary Decker Mentorship Award
Kim Apurado has been awarded the prestigious Mary Decker Mentorship Award. This accolade, open to all AANN members, celebrates neuroscience nurses who exemplify excellence in mentoring.
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Hydrocephalus 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.
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Revolutionary Women in Hydrocephalus Research – Dr. BlazerYost
Celebrate Influential Leaders during National Women’s History Month. Dr. Robinson & Dr. Jantzie are both revolutionary women making strides for hydrocephalus
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Hydrocephalus 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
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Get 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.
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Hydrocephalus Association Unites Advocates for 2024 Rare Disease Week
Members from the Hydrocephalus Association Action Network came to Washington, DC, to participate in the Everylife Foundation for Rare Disease’s Rare Disease Week, which took place from February 25-28, 2024.
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Get the Hydrocephalus Scoop on Capitol Hill for January 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.
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The Hydrocephalus Scoop on Capitol Hill for December 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.
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Dr. Peter Chiarelli Receives the Hydrocephalus Association Cynthia Solomon Resident’s Prize for Noninvasive Shunt Function Assessment Method
The Resident’s prize is awarded each year to the most promising hydrocephalus-related research paper presented by a neurosurgical resident at the Pediatric Section meeting of the AANS/CNS. The prize is designed to encourage young doctors to focus their research efforts on advancing treatment and care of individuals with hydrocephalus.
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Coast to Coast for Hydrocephalus – An Amazing Family’s Journey
On November 17, 2023, the Touchberry Family embarked on an extraordinary journey, setting out on a cross-country drive in their century-old Model T Ford—a symbolic quest aimed at raising awareness and crucial funding for hydrocephalus.
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The 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.
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WALK 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.
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Announcing our 2023 Hydrocephalus Association Scholarship Recipients!
The Hydrocephalus Association (HA) is pleased and honored to announce our 2023 Hydrocephalus Association Scholarship Recipients.
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Celebrating Milestones and Empowering Hope at our 40th Anniversary Gala
In celebrating this milestone, the Hydrocephalus Association reaffirmed its pledge to persist in driving forward research, support, and advocacy, ensuring that every step brings us closer to a world where hydrocephalus is a thing of the past.
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The 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.
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The 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.
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The Hydrocephalus Association Earns Coveted Four-Star Charity Rating
The Hydrocephalus Association has achieved the pinnacle of recognition by being named a Four-Star charity…
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