Hydrocephalus Blog & Resources
HA Welcomes New Board Member Deitra Matthews, Columbia, SC
The Hydrocephalus Association (HA) would like to warmly welcome new board member Deitra Matthews, MPA. She is CEO of The Ram Foundation and serves on HA’s Support and Education Committee.
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Welcome New Board Member Deitra Matthews
The Hydrocephalus Association (HA) would like to warmly welcome new board member Deitra Matthews, MPA.…
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‘He’s never alone’: See the tattoo dad got to honor his son’s brain surgery
Carlos Marquez has a tattoo for each of his children, but this one feels extra special as son Luke has already been through five brain surgeries.
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Life-changing Impact at Hydrocephalus Conference
How do you put a life-changing experience into words? The 17th National Conference on Hydrocephalus, is now in the rearview mirror for everyone in attendance from across the country and internationally, but the memories and the connections will leave a lasting impact.
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Medical disorder common to infants found in astronauts; doctors seek solution
Medical disorder common to infants found in astronauts; doctors seek solution Was this article helpful?…
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How science, space travel may help families living with neurological conditions
How science, space travel may help families living with neurological conditions Was this article helpful?…
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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.
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Remembering Dr. Taeun Chang
It is with great sadness that the Hydrocephalus Association announces the passing of our colleague…
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Brainy Camps and Camp Headstrong are Back This Year!
The camp’s mission is to help campers form friendships, become responsible leaders, and develop independence and self-reliance.
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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.
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The Hydrocephalus Scoop on Capitol Hill: Jan/Feb 2022 Update
It’s been a busy time in Congress. Find out what we’ve been up to on Capitol Hill!
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Five Scientists Awarded HA Grants for Their Bold and Innovative Work
Announcing our 2021 Innovator Award recipients! These brilliant scientists are exploring new ideas about why hydrocephalus develops and testing new treatments to improve long term outcomes.
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