Hydrocephalus Blog & Resources

Grey’s Anatomy Airs Episode on Congenital Hydrocephalus Performing Endoscopic Third Ventriculostomy (ETV)

April 9, 2024

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

April 8, 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 Mary Decker Mentorship Award

Kim Apurado Awarded Prestigious Mary Decker Mentorship Award

April 5, 2024

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

April 5, 2024

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

March 31, 2024

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

March 13, 2024

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

March 8, 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 Advocates for Rare Disease Week

Hydrocephalus Association Unites Advocates for 2024 Rare Disease Week

March 5, 2024

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

February 6, 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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Representative Ritchie Torres Joins Pediatric and Adult Hydrocephalus Caucus to Advocate for Affected Families in NY-15

January 8, 2024

Representative Torres will play an integral role in advocating for increased awareness, funding, and support for pediatric and adult hydrocephalus patients. His commitment further amplifies the voice of those impacted by this condition and allows him to support hydrocephalus research at Columbia University.

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The Hydrocephalus Scoop on Capitol Hill for December 2023

January 2, 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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Dr. Peter Chiarelli Receives the Hydrocephalus Association Cynthia Solomon Resident’s Prize for Noninvasive Shunt Function Assessment Method

December 18, 2023

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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