Hydrocephalus Blog & Resources

Hydrocephalus Association at 30

January 30, 2013

In 1983, a small group of parents of children with hydrocephalus living in the San Francisco Bay area came together seeking community and support. Thirty years ago could this group of determined and committed individuals have imagined that the Hydrocephalus Association would become the nation’s largest and most widely respected advocacy group dedicated to hydrocephalus?

Read More

Teen Voices: Taking on High School with No Regrets

January 22, 2013

Starting high school can be tough, especially when you are dealing with a medical condition such as hydrocephalus. Madeleine shares her advice for taking on high school.

Read More

Is There a Cure for My Dementia?

November 11, 2012

Today’s article in Parade Magazine, What If Grandpa Doesn’t Really Have Alzheimer’s?, plays an important role in our quest to educate the public about the form of hydrocephalus called Normal Pressure Hydrocephalus or NPH. While the condition was identified over 50 years ago, there is little research into the condition, which so far is the only known reversible form of dementia but it is often mistaken for Alzheimer’s or Parkinson’s Disease.

Read More
scholarship, hydrocephalus

Announcing our Hydrocephalus Association TTC Scholarship Recipients!

November 2, 2012

The Hydrocephalus Association Teens Take Charge program trains teenagers and young adults (and their siblings), who are affected by hydrocephalus, to take charge of the condition and become self-advocates with both health professionals and with their legislators. Through a generous grant from the Medtronic Foundation, the Hydrocephalus Association is able to award five scholarships, in the amount of $1,000, to teens and young adults (ages 17 to 25) who are affected by hydrocephalus.

Read More

Making Life Happen: Living Life with Spina Bifida and Hydrocephalus

October 25, 2012

Meet Luke Russell, a freshman at the University of Wisconsin-Whitewater who plans to major in marine biology with either a second major or a minor in psychology. He has spina bifida and hydrocephalus.

Read More

Voices from Our Community: David Walters Shares his Hydrocephalus Story

September 24, 2012

David Walters was diagnosed with hydrocephalus at 2 weeks old and has had one shunt revision. He is an active teenager and member of the Hydrocephalus Association Teens Take Charge program. Read his story.

Read More

Voices from Our Community: Joyce Schwartz Spreads Her Message about Normal Pressure Hydrocephalus

September 14, 2012

Joyce Schwartz shares her 23 year journey of searching for a diagnosis and then treatment for Normal Pressure Hydrocephalus (HA).

Read More

Voices from Our Community: Milton Newman Shares His Story of NPH

September 7, 2012

Fog is Lifted After 15 Years of Confusion and Misdiagnosis Milt Newman’s retirement was not…

Read More

Voices from Our Community: Abby Shares Her Life Experiences With Hydrocephalus!

September 3, 2012

By: Abby Wood Hi!  My name is Abby.  I turned 12 years old at the…

Read More
scholarship, hydrocephalus

Announcing our 2012 Hydrocephalus Association Scholarship Recipients!

August 2, 2012

We are pleased to announce the 2012 Hydrocephalus Association Scholarship Recipients. The scholarship program marks…

Read More

Congress Discusses Hydrocephalus and our Military

July 19, 2012

by Paul Gross, HA Chairman of the Board of Directors Yesterday, hydrocephalus was a hot…

Read More

Hydrocephalus Association’s Resident’s Prize: Dr. Ashley G. Tian

February 16, 2012

One way the Hydrocephalus Association promotes research and leadership in hydrocephalus is through our annual Resident’s Prize.

Read More