FEATURES
Endurance Events: Every Mile Matters
The Hydrocephalus Association’s Endurance Program continues to build momentum, offering supporters meaningful opportunities to raise awareness and funds while pursuing personal athletic goals.
In 2025, 15 dedicated runners participated in the 50th Anniversary Marine Corps Marathon in Washington, D.C., collectively raising nearly $30,000 in support of HA’s mission. Their commitment not only generated critical funding, but also helped expand HA’s visibility within the endurance community.
As interest in the program continues to grow, HA is excited to build on this success with new endurance event opportunities planned for Minnesota and San Diego in 2026, creating even more ways for supporters to make an impact while crossing the finish line.
"I'm excited to run with a team of individuals all working toward the same goal: raising awareness for hydrocephalus. My son and countless others have to undergo multiple brain surgeries in their lifetime, so I run one more mile just for them." — Caroline Sekercan, Marine Corps Marathon Participant
A Landmark Trial for iNPH Treatment
For decades, controversy surrounded a deceptively common condition in older adults. Idiopathic normal pressure hydrocephalus (iNPH) affects nearly one million older Americans, yet more than 80% of cases go unrecognized or untreated, often misdiagnosed as Alzheimer's disease, Parkinson's disease, or dismissed as normal aging. The condition is commonly associated with a triad of symptoms consisting of difficulty walking, cognitive impairment, and impaired bladder control, although not everyone experiences all three symptoms. Left untreated, iNPH can lead to falls, loss of independence, and severe disability. The primary treatment has long been shunt surgery, but its effectiveness was disputed for years, leaving many patients without access to the care they needed.
That all changed in 2025. The Placebo-Controlled Efficacy in iNPH Shunting (PENS) Trial has become the first large, double-blind, placebo-controlled study of its kind, definitively demonstrating that shunt surgery improves walking and balance, reduces falls, and restores independence in older adults with iNPH. The results were published in The New England Journal of Medicine, one of the most prestigious peer-reviewed medical journals in the world. The trial was led by Johns Hopkins University School of Medicine and the Adult Hydrocephalus Clinical Research Network (AHCRN), a collaborative network that the Hydrocephalus Association helped establish and has funded since 2012. In total, there were 21 active sites in the United States, Canada, and Sweden in the study, with 17 enrolling patients. The PENS trial will continue to follow participants for 12 months to measure long-term outcomes, including cognition, daily functioning, and quality of life, with early findings already suggesting gains beyond walking.
The recognition this work has received reflects its extraordinary impact. The National Institute of Neurological Disorders and Stroke (NINDS) named the PENS Trial one of its Top 10 Research Advances of 2025, a distinction that spans basic, translational, and clinical research, further highlighting breakthroughs advancing neuroscience and improving care for people with neurological conditions. For the hydrocephalus community, this honor marks a turning point, one that will help ensure more patients are recognized, diagnosed, and treated in time to preserve their independence and quality of life.
“This study is an important step in raising awareness of iNPH among the medical community so that individuals can be referred early in order to get the treatment they need. We are proud to have played a critical role in funding research that directly improves the lives of the community we serve.”
— Diana Gray, President and CEO
Legacy Giving: Creating Impact for Generations to Come

The Fudge Solomon Legacy Society plays a vital role in advancing HA’s mission to eliminate the challenges of hydrocephalus while ensuring the strength and sustainability of our programs for years to come. Through planned gifts and estate commitments, Legacy Society members help build a future where individuals and families affected by hydrocephalus have access to the resources, support, and breakthroughs they need.
By including HA in their will, trust, or estate plans, supporters create a lasting legacy that helps sustain critical research, education, advocacy, and support programs for generations to come. In recognition of their commitment, members of the Fudge Solomon Legacy Society receive special communications and invitations to exclusive HA opportunities.
Longtime community partner and Legacy Society member William Vincent exemplifies this spirit of generosity. Inspired by his dedication to improving understanding and care for people living with hydrocephalus—and informed by his own experiences—Bill chose to include HA in his estate plans. His thoughtful commitment will help advance research, strengthen advocacy efforts, and create lasting impact for future generations.
We are deeply grateful to Bill and all 143 members of the Fudge Solomon Legacy Society, named in honor of HA’s founding members, for their vision, generosity, and enduring belief in our mission.
"Each person's journey with hydrocephalus is unique, and every story is worth sharing."
— William Vincent, Fudge Solomon Legacy Society Member
Ready to Get Started?
Creating a will is one of the most important steps you can take to protect your loved ones and document your wishes.
Through HA's partnership with FreeWill, you can create a legally valid will online—at no cost and in as little as 20 minutes.
Questions?
Contact Linda Riley at linda@hydroassoc.org or (240) 483-4475.
Make Waves for Hydrocephalus – Fundraise Your Way
Want to join the fight against hydrocephalus in a way that's uniquely your own? Our Do-It-Yourself (DIY) Fundraising Program empowers individuals and families to create personal campaigns that support families, advance research, and raise awareness.
From bake sales and poker runs to pickleball tournaments, Mahjong gatherings, endurance challenges, and memorial tributes, each DIY fundraiser reflects the passion and creativity of our community.
We are especially grateful to those who have made these efforts an annual tradition, including:
- The Maynard family, led by daughter Caitlin, for their "Thanks for Running" event
- Cathi Roberts and her annual motorcycle ride
- The Alston family for their larger-than-life backyard BBQ
- Ray Moser and his son, Raymond, who participated in One Lap of America
By starting or joining a fundraiser, you help fuel progress, provide hope, and ensure no one faces hydrocephalus alone. Whether you walk, run, celebrate a milestone, or honor a loved one, your impact matters.
Together, we are creating meaningful change.
HydroAssist
Resource Spotlight: HydroAssist®
Managing hydrocephalus often means keeping track of complex medical information. HydroAssist®, HA's free mobile application, helps individuals and caregivers securely store treatment histories, track symptoms, record shunt and ETV information, upload imaging records, and share important information with members of their medical team.
Designed by hydrocephalus experts and built with input from patients, caregivers, and healthcare professionals, HydroAssist empowers users to access critical information whenever and wherever they need it.



