My Nonprofit Reviews

When our daughter was diagnosed with hydrocephalus at birth, we were very afraid that she would never live a full and normal life. But luckily my husband is an excellent “Googler” and he found the Hydrocephalus Association right away. HA was there to answer questions and provide hope.

The sense of community we have found has been a godsend to our family. My best friend is a fellow “hydro mom” and someone I never would have met without the HA network.

Even though Ashley has had five revisions in eleven years, she is a happy, upbeat kid with a bright future. And when HA funds a CURE, her path will be even brighter!