Press Releases
Harnessing the Power of Artificial Intelligence and Machine Learning to Innovate Treatments for Hydrocephalus
[Dallas, TX, October 4, 2023] — The Hydrocephalus Association (HA) and the Rudi Schulte…
Read More
The Hydrocephalus Association Earns a Prestigious Four-Star Rating from Charity Navigator
[Bethesda, MD, September 29, 2023] – The Hydrocephalus Association is proud to announce that our…
Read More
Danny Bonaduce’s “Mystery Illness” Explained
(June 6, 2023) – Danny Bonaduce’s recent battle with a “mystery illness” and lack of…
Read More
Zach Roloff Emergency Brain Surgery
(February 13, 2023) – A few days ago, Zach Roloff, one of the stars of…
Read More
The Phoenix Community Rallies for Hydrocephalus
President and CEO of Anuncia Medical, Inc., will join hundreds of families and medical professionals at the Phoenix WALK to End Hydrocephalus as they rally to raise awareness and critical funds for hydrocephalus.
Read More
The Burlington Community Rallies for Hydrocephalus With the Hydrowarrior Ride
“We are so excited to be hosting this charity ride and benefit for the fifth year,” said Cathi Roberts, local event lead whose 19 year old daughter has hydrocephalus, “The event has been doubling in size each year. Last year we raised approximately $15k for critical hydroecephalus research and awareness.”
Read More
A Father’s Love Knows No Bounds
The Marquez Family, and other families, will be attending the National Conference on Hydrocephalus July 14-16 at the Austin Marriott Downtown and are available for interviews. They are also available for phone interviews at any time before or after conference.
Read More
Statement 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 More
AHCRN Awarded $14 Million NINDS Grant to Study Effectiveness of Shunt Treatment for idiopathic Normal Pressure Hydrocephalus
The AHCRN, one of three research networks HA funds, was awarded a $14 million federal grant to study the effectiveness of shunt treatment for NPH.
Read More
Fighting for Hydrocephalus Funding in Congress. October Update
October has been a busy time for Congress, and the Hydrocephalus Association has been hard at work ensuring that we have a seat at the table. We have an exciting new bill introduced and an update on congressional funding for hydrocephalus research.
Read More
Congressman Mike Levin Joins Congressional Hydrocephalus Caucus
Caucus helps families impacted by a brain condition that has no cure. Rep. Mike Levin (CA-49) has joined…
Read More
Congresswoman Cindy Axne Joins Congressional Hydrocephalus Caucus
Caucus helps find solutions for the leading cause of brain surgery in children. Rep. Cindy Axne (IA-3) has…
Read More
Congressman Lloyd Doggett Recognizes September as Hydrocephalus Awareness Month
Raises awareness of the leading cause of brain surgery in children. There are over 1…
Read More
Local Mom on a Mission to Find a Cure for Son’s Brain Disorder
Will take part in Cincinnati WALK to End Hydrocephalus on Oct. 3rd Chase Parker Lorenzo…
Read More
Massachusetts Governor Names September Hydrocephalus Awareness Month
Hydrocephalus is the leading cause of brain surgery in children. Every 15 minutes, a brain…
Read More
Congressmen Lloyd Doggett and Chris Smith Join Forces to Raise Awareness About Hydrocephalus
Representatives Lloyd Doggett (D-TX) and Chris Smith (R-NJ) have joined forces to champion two critical…
Read More
The Hydrocephalus Scoop on Capitol Hill December 2020
October and November have been a super busy time for all three branches of government (Executive, Legislative and Judicial). Here’s our latest summary of what’s been happening on Capitol Hill.
Read More
Two Sisters, Two Brain Disorders, 36 Brain Surgeries
St. Louis family fights for a cure for leading cause of brain surgery in children…
Read More
The Hydrocephalus Scoop on Capitol Hill for September-October 2020
In addition to celebrating Hydrocephalus Awareness month, the Hydrocephalus Association has been tracking the ins and outs of what’s happening on Capitol Hill. Read our latest advocacy update!
Read MoreLocal Mom Living with Brain Disorder Fights for a Cure
Hopes to raise funds for a cure at the New Orleans WALK to End Hydrocephalus…
Read More