hydrocephalus research
Get to Know Dr. Joel Geerling: HA 2019 Innovator Award Grantee
In the 3rd installment of our Meet the Innovator Awardees Blog Series, we interviewed Dr. Joel Geerling, one of four scientists who received our 2019 Innovator Award, and Maggie Tish, who works in Dr. Geerling’s lab. They delve deeper into their fascinating research on Normal Pressure Hydrocephalus (NPH).
Four Scientists Awarded HA Grants to Deepen Our Understanding about Hydrocephalus
There is a lot we do not know about how hydrocephalus develops and how to best treat the condition across our many communities. Our 2019 Innovator Award recipients are looking to change that.
St. Louis Event Celebrates 10th Anniversary of HA’s Research Initiative
Families and researchers from across the country came together on Nov. 3 to celebrate the 10th Anniversary of HA’s Research Initiative. The event, held in St. Louis, MO, highlighted the successes of our research investments and honored the trailblazers who started it all.
Three Scientists Awarded HA Grants for Their Bold and Innovative Work
What if you could prevent or stop the development of hydrocephalus after a brain bleed or develop a shunt that doesn’t get clogged? That’s what the 2018 HA Innovator Award grantees are hoping to do through their research projects.
Conference Registration is OPEN!
Registration for our 15th National Conference on Hydrocephalus is OPEN! Join us in Orange County, California, June 28 – 30, 2018.
A Possible Cut in Hydrocephalus Research Funding from Capitol Hill
Congress is currently debating a bill that could have major implications for hydrocephalus research through the Department of Defense CDMRP program.
Meet our Conference Team!
HA is pleased to announce some of the brightest minds in the field who are generously offering their time, expertise and talent in planning the 15th National Conference on Hydrocephalus
Book Your Hotel for Conference!
Housing is open for the National Conference on Hydrocephalus which will take place on June 28-30, 2018 at the Renaissance Newport Beach in Orange County, California. Book your hotel!
2016 Year-In-Review
As we close out yet another banner year, we are grateful for all that we have been able to achieve through the support of our caring community.
Historic #GivingTuesday for Hydrocephalus!
We have the chance to raise $80K in one day to support hydrocephalus research as well as programs and resources to support individuals and their families. #GivingTuesday is BIG this year!
Why Join the Hydrocephalus Professional Member Society?
Professional members enjoy the benefits of the association working on your behalf to ensure greater coordination of research, identify and reach the patient population and provide training and educational opportunities tailored to the needs of the professional community. Join us today.
Families Unite with Scientists to Prevent Leading Cause of Brain Surgery in Children
The Hydrocephalus Association’s annual Vision Dinner will serve as the catalyst for a focused research initiative that aims to prevent or minimize the development of hydrocephalus after a brain bleed.
Hydrocephalus Association Converges on Capitol Hill for Rally for Medical Research Hill Day to Advocate for Increased Funding for the National Institutes of Health (NIH)
The Hydrocephalus Association joins more than 300 organizations to ask Congress to provide robust, sustained, and predictable budget increases for the NIH
September 22 is a National Day of Action!
Thursday is a National Day of Action across the country as advocates converge on Capitol Hill at the Rally for Medical Research.
Team Hydro’s Commitment to Curing Hydrocephalus Receives National Attention
Featured in Forbes, Team Hydro, now in it’s ninth year, has raised $546,335 for hydrocephalus research.
Nonprofit and Government Leaders Unite Around Medical Research
Dr. Jenna Koschnitzky, Hydrocephalus Association Director of Research Programs, speaks at the 2016 NIH NINDS Nonprofit Forum.
Forbes Features Story on Team Hydro
Forbes features a story on the inspiration behind Team Hydro and their mission to fund hydrocephalus research. Pam Finlayson, a Team Hydro founder and a member of the Hydrocephalus Association Board of Directors, in interviewed with her sons, Peter and Sam.
Congressional Action Supports the Hydrocephalus Community
Congress is hearing our message and starting to act on measures that will help our #hydrocephalus community, but we need to keep pushing our priorities.
Hydrocephalus Clinical Research Network Adds Five New Centers
The Hydrocephalus Clinical Research Network (HCRN) adds five new research institutes to the network.
Advocacy Webinar: What You Can Do to Increase Funding for Hydrocephalus Research
Join us for our advocacy webinar covering the Congressional appropriations process and what you can do to help protect medical research program funding.
Conference Registration is OPEN!
Registration for our 14th National Conference on Hydrocephalus is OPEN! Join us in Minneapolis, Minnesota, June 16 – 19, 2016.
10 Reasons to Attend Conference!
Our biennial conference is a cornerstone of our commitment to serving our community. You don’t *need* a reason to attend conference but here are some good ones!
Hydrocephalus Advocate Joins Scientific Peer Review of Research Applications for the Department of Defense Peer Reviewed Medical Research Program
Peer review advocate Barrett O’Connor participated in the evaluation of research applications submitted to the PRMRP sponsored by the Department of Defense.
Countdown to Conference: Tips on making it affordable!
The National Conference on Hydrocephalus takes place June 16 – 19th in Minneapolis, Minnesota. Join us! Here are tips to help make it affordable.
Announcing the 2015 Innovator Award Grantees
2015 Awardees focused on research to better understand why hydrocephalus develops and to identify therapies to prevent or reverse hydrocephalus.
LEARN MORE: National Conference on Hydrocephalus
LEARN MORE: The 14th National Conference on Hydrocephalus will take place in Minneapolis, Minnesota, on June 16-19, 2016!
Next Steps for the Adult Hydrocephalus Clinical Research Network
The Core Data Project of the Adult Hydrocephalus Clinical Research Network (AHCRN) has enrolled nearly 200 patients since in late 2014.
Diana Gray Announced as the New Chief Executive Officer
The Hydrocephalus Association (HA) is pleased to announce the appointment of Diana Gray as the new Chief Executive Officer (CEO).
Hydrocephalus Association Announces New Chief Executive Officer
The largest hydrocephalus patient advocacy organization, the Hydrocephalus Association (HA), selects Diana Gray as the new Chief Executive Officer (CEO) to lead an aggressive growth strategy.
Upcoming Webinar: AHCRN Update
Join us for our next webinar on the Adult Hydrocephalus Clinical Research Network (AHCRN). Tune in to hear about progress after 1 year of patient enrollment.
New Research Initiative to be Launched at HA’s Vision Dinner
The annual Vision Dinner held in New York City will unveil the new Hydrocephalus Association Network for Discovery Science (HANDS).
Identifying Best Candidates For Spina Bifida In-Utero Surgery
A new study found that fetuses with enlarged brain ventricles are more likely to get a second surgery after birth.
Partnering with Government to Shape Disease Research
HA played a key role at the annual NINDS Nonprofit Forum, which provides an opportunity for nonprofit leaders to engage in dialogue with NINDS staff.
UNCP Hopes to Push TBI Research Forward With Help of Recent Grants
University of North Carolina has been awarded a grant to fund a study for neurotoxin action. Lead Scientist Dr. Bahr hopes the recent grants will push forward traumatic brain injury program and Alzheimer’s research.
Seven States Join Congress in Declaring September Hydrocephalus Awareness Month
Local volunteers joined forces with elected state representatives in Connecticut, New York, Tennessee, Virginia, South Carolina, Colorado and Illinois to proclaim September as Hydrocephalus Awareness Month.
Scientific Networks are Changing the Research Landscape
Together the HA-funded HCRN, AHCRN and HANDS are changing how hydrocephalus research is conducted and accelerating research progress.
Research 101: The Importance of Sample Size
Having a large number of participants reduces the risk of accidently having extreme, or biased, groups. Let’s find out why.
MINNEAPOLIS: We are on our way! 2016 Hydrocephalus Conference
SAVE THE DATE: The 14th National Conference on Hydrocephalus will take place in Minneapolis, Minnesota, on June 16-19, 2016! Our patient-centered conferences empower all of us to understand, seek out and put into place the care, programs and services that will meet our needs now and well into the future.
The Patient Voice in Hydrocephalus Research Studies
Our Patient Partner Committees provide the patient perspective throughout the duration of a research study, making sure the patient voice is at the table.
Hydrocephalus Association Announces a New Grant Opportunity
Innovator Awards on understanding disease mechanisms and the identification and preclinical testing of therapies to prevent or reverse hydrocephalus. Apply here!