Welcome New Board Member Michael Siegel, Ph.D.

August 22, 2022
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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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Welcome New Board Member Stephanie Vogt

August 15, 2022
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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.

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Welcome New Board Member Deitra Matthews

August 11, 2022
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The Hydrocephalus Association (HA) would like to warmly welcome new board member Deitra Matthews, MPA.…

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Life-changing Impact at Hydrocephalus Conference

July 25, 2022
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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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Remembering Dr. Taeun Chang

June 24, 2022
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It is with great sadness that the Hydrocephalus Association announces the passing of our colleague…

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The Hydrocephalus Scoop on Capitol Hill: Jan/Feb 2022 Update

February 7, 2022
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It’s been a busy time in Congress. Find out what we’ve been up to on Capitol Hill!

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HA’s Medical Advisory Board Issues New Statements Regarding COVID-19

January 20, 2022
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The Hydrocephalus Association (HA)’s Medical Advisory Board (MAB) recently issued two new consensus statements regarding COVID-19 for people living with hydrocephalus.

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Celebrating the Life of Dr. Shirley McBay

December 16, 2021
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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.

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2021 WALK to End Hydrocephalus Raises over $1.6 Million

December 6, 2021
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Our WALK to End Hydrocephalus program had a successful year, raising over $1.6 million for HA’s research, support, education and advocacy efforts.

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Isabella Advocates for Children in Congress

November 29, 2021
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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!

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scholarship, hydrocephalus

Announcing our 2021 Hydrocephalus Association Scholarship Recipients!

November 29, 2021
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The Hydrocephalus Association (HA) is pleased and honored to announce our 2021 Hydrocephalus Association Scholarship Recipients.

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The Hydrocephalus Scoop on Capitol Hill – Sept/Oct 2021

October 4, 2021
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The Hydrocephalus Association has been busy protecting hydrocephalus-related research dollars in Congress, and working with members Congress to recognize National Hydrocephalus Awareness Month.

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Make Some Noise for Hydrocephalus Awareness Month!

August 13, 2021
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September is Hydrocephalus Awareness Month (HAM), our chance to shine a light on hydrocephalus and how it impacts our community!

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The Hydrocephalus Scoop on Capitol Hill March 2021

April 1, 2021
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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.

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Diana Gray Named Chair of National Health Council Board

December 8, 2020
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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.

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Announcing our 2020 Hydrocephalus Association Scholarship Recipients!

October 12, 2020
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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.

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HA Welcomes New National Director of Development

September 22, 2020
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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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