Celebrating the 40th Anniversary of the Hydrocephalus Association
The year 2023 marks the 40th Anniversary of the Hydrocephalus Association (HA). Throughout the year, we will honor our legacy with all of our community by celebrating our milestones and exploring what has been accomplished over the past four decades.
Read More >Announcing our 2022 Hydrocephalus Association Scholarship Recipients!
The Hydrocephalus Association (HA) is pleased and honored to announce our 2022 Hydrocephalus Association Scholarship Recipients.
Read More >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.
Read More >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.
Read More >Welcome New Board Member Stephanie Vogt
The Hydrocephalus Association (HA) would like to warmly welcome new board member Stephanie (Buffa) Vogt, M.S. She is a Vice President of Supply Chain Strategy with Express Scripts at Cigna and has served as the chair of the St. Louis WALK to end Hydrocephalus since 2008.
Read More >Welcome New Board Member Deitra Matthews
The Hydrocephalus Association (HA) would like to warmly welcome new board member Deitra Matthews, MPA.…
Read More >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.
Read More >Remembering Dr. Taeun Chang
It is with great sadness that the Hydrocephalus Association announces the passing of our colleague…
Read More >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!
Read More >HA’s Medical Advisory Board Issues New Statements Regarding COVID-19
The Hydrocephalus Association (HA)’s Medical Advisory Board (MAB) recently issued two new consensus statements regarding COVID-19 for people living with hydrocephalus.
Read More >Celebrating the Life of Dr. Shirley McBay
The Hydrocephalus Association celebrates the life of Dr. Shirley McBay, who passed away in late November. Dr. McBay was the first Black person to receive a doctorate from the University of Georgia and was a pioneer in advocating for diversity in science and math education. She was diagnosed with diabetes and Normal Pressure Hydrocephalus.
Read More >2021 WALK to End Hydrocephalus Raises over $1.6 Million
Our WALK to End Hydrocephalus program had a successful year, raising over $1.6 million for HA’s research, support, education and advocacy efforts.
Read More >Isabella Advocates for Children in Congress
Like many kids living with hydrocephalus, Isabella is a fighter. This year, she brought her fighting spirit to Congress advocating for better healthcare services for children!
Read More >Announcing our 2021 Hydrocephalus Association Scholarship Recipients!
The Hydrocephalus Association (HA) is pleased and honored to announce our 2021 Hydrocephalus Association Scholarship Recipients.
Read More >The Hydrocephalus Scoop on Capitol Hill – Sept/Oct 2021
The Hydrocephalus Association has been busy protecting hydrocephalus-related research dollars in Congress, and working with members Congress to recognize National Hydrocephalus Awareness Month.
Read More >Make Some Noise for Hydrocephalus Awareness Month!
September is Hydrocephalus Awareness Month (HAM), our chance to shine a light on hydrocephalus and how it impacts our community!
Read More >The Hydrocephalus Scoop on Capitol Hill March 2021
The cherry blossoms are blooming in Washington, DC, which is a sure sign that the new Congressional session is well underway. Let’s get you up to speed on what’s been happening on hydrocephalus policy issues so far.
Read More >Diana Gray Named Chair of National Health Council Board
Diana Gray, HA President and CEO, was named Chairperson of the National Health Council (NHC) Board of Directors for 2021. She was elected to the role at the NHC’s annual membership meeting this week.
Read More >Announcing our 2020 Hydrocephalus Association Scholarship Recipients!
We’re pleased to announce the 2020 Hydrocephalus Association Scholarship Award Recipients. HA’s scholarship program was established in 1994 to provide financial assistance to capable and promising teens, young adults, and adults who live with the ongoing challenges and complexities of hydrocephalus.
Read More >HA Welcomes New National Director of Development
Linda Riley has joined the Hydrocephalus Association as the new National Director of Development. Linda brings more than 20 years of fundraising experience to this position.
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