Back to Hydrocephalus


My daughter, Kayla, was diagnosed with Hydro when she was 10 years old, in 2005. Her first VP Shunt was inserted and then re-done 11 months later. Today, 7 years later, and thankfully no more operations, this page is for those of you out there who have, or are going thru this awful dis-ease. There is hope. Keep the faith. Looking at my now 17 year old daughter, you would never say she has hydro....... she is one of the lucky ones.........

this is about you, your experience, your thoughts, what you need. The aim is to make this web site a place where people come to chat, ask questions and just be themselves?
What do you need?

For more information - go to..............

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