An Easy Way to Shop on AmazonSmile!

 Your Amazon mobile app is not able to support HA when your purchase from your phone. But we have a great hack for you…

CONTINUE READING

Advocacy Wins for the Hydrocephalus Community

While impeachment still occupies the headlines, it’s not the only thing that happened this past December in Washington, DC. Amidst all the end-of-year chaos, Congress handed the hydrocephalus community a number of big wins!

CONTINUE READING

High School Student Educates Others about Hydrocephalus

Mauryce Thomas organized an event in Mobile, AL to educate his community about hydrocephalus. The event raised awareness and $1,320 to support HA’s mission!

CONTINUE READING

New Ask the Expert Video Series for Adults Living with Hydrocephalus

Check out our latest Ask the Expert Video Series developed specifically for adults living with hydrocephalus. The series answers some of the most common questions we receive to our support line.

CONTINUE READING

Congressman TJ Cox Joins Congressional Hydrocephalus Caucus

Caucus will help families in California’s Central Valley impacted by a brain condition that has no cure This week, Congressman TJ Cox (D-CA) announced that he has joined the bipartisan Congressional Pediatric and Adult Hydrocephalus Caucus. The Hydrocephalus Association applauds Representative Cox’s support for our community. His action reflects a welcome commitment to working with […]

CONTINUE READING

James Forrest Vedder Hydrocephalus Research Challenge

The challenge is made possible through the generosity of Ms. Leslys Vedder, in tribute to her late husband, James Forrest Vedder, PhD, a scholar, archaeologist and physicist.

CONTINUE READING

HA WALKs Help Raise Over $2 Million for Key Programs

Over 15,000 individuals and families participated in a WALK to End Hydrocephalus this year, raising over $2 million to support HA’s mission!

CONTINUE READING

The Hydrocephalus Scoop on Capitol Hill

Believe it or not, the impeachment debate isn’t the only thing happening in Washington, DC! Here’s a quick rundown.

CONTINUE READING

Changing Lives This Giving Tuesday

Giving Tuesday is on December 3rd this year! We hope you’ll stand with us this year and support the Hydrocephalus Association!

CONTINUE READING

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.

CONTINUE READING

NYC Grandmother Fights for a Cure for Leading Cause of Brain Surgery in Children

Will take part in the NYC WALK to End Hydrocephalus on Nov. 9 Dreame Saliyah Monplaisir was just 3 months old when she had her first brain surgery to treat her hydrocephalus, a life-threatening neurological condition that has no cure and can only be treated with brain surgery. As is often the case, Dreame’s family […]

CONTINUE READING

Caucus Briefing Educates Members of Congress About Hydrocephalus

Over 60 people attended the Hydrocephalus Caucus Briefing on 10/17. The briefing, hosted by the Hydrocephalus Association and PHF, explored how hydrocephalus impacts patients & how Congress can help.

CONTINUE READING
Change this in Theme Options
Change this in Theme Options