Hydrocephalus Blog & Resources
Announcing our 2022 Hydrocephalus Association Scholarship Recipients!
The Hydrocephalus Association (HA) is pleased and honored to announce our 2022 Hydrocephalus Association Scholarship Recipients.
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Diana Gray Honored for Exemplary Service for the National Health Council
Diana Gray, M.A., President and CEO of the Hydrocephalus Association, was honored for her outstanding service for the National Health Council (NHC) at their annual membership meeting.
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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.
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Why one family hopes for a ‘smarter’ device
Dr. Jamie Wright, diagnosed with hydrocephalus as an infant, begins her second year as a UW Medicine neurology resident.
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Hydrocephalus Spotlight on Two Medical Drama TV Series
Hydrocephalus was highlighted with patients on two medical drama TV shows. The Good Doctor and The Resident.
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Oppenheimer Employees WALK To End Hydrocephalus
Oppenheimer’s Seattle and Bellevue offices recently participated in the Seattle WALK to end Hydrocephalus. Oppenheimer Financial Professional, Lou Conyard, and his wife Betsy, have been involved in organizing Team Oppenheimer and participating in this effort for years.
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September is Hydrocephalus Awareness Month. How much do you know about this life-threatening condition?
Dr. Jamie Wright, diagnosed with hydrocephalus as an infant, begins her second year as a UW Medicine neurology resident.
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What I Know Now: Tips to Prepare for Shunt Surgery
If you are an adult with NPH heading into your first shunt surgery or revision Frank Salamone has some tips for you!
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She Once Thought Becoming a Doctor Wasn’t Possible
Dr. Jamie Wright, diagnosed with hydrocephalus as an infant, begins her second year as a UW Medicine neurology resident.
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Detroit Walk to End Hydrocephalus to be held at River Bends Park
Joshua is a twin and a week after he and his brother Jacob were born, Emily and her husband, Jimmy Sajor, were told Joshua has hydrocephalus and would never crawl, walk or speak!
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Hydrocephalus fundraiser aims to support better treatments and a cure
Joshua is a twin and a week after he and his brother Jacob were born, Emily and her husband, Jimmy Sajor, were told Joshua has hydrocephalus and would never crawl, walk or speak!
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Welcome New Board Member Michael Siegel, Ph.D.
The Hydrocephalus Association (HA) would like to warmly welcome new board member Michael (Mike) Siegel, Ph.D. He is the Executive Director of the Pediatric Dermatology Research Alliance (PeDRA) and serves on our Scientific Advisory Board & Research Committee.
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