Hydrocephalus
When you have no where
else to turn, there is always hope !
When you have no where
else to turn, there is always hope !
When you have no where else to turn, there is always Hope!
Welcome to Madison's web site. This site is dedicated to our daughter, Madison, as well as families everywhere who have walked in our shoes, getting ready to, or are in the process of traveling down a very long, long road. Our prayers are with you and your loved ones. We want to give other famlies hope, and let you know you are not alone.
Madison ( one hour old) Madison (18 months)
Madison was born six weeks early with Hydrocephalus. I found out in my 24 th week of pregnancy that she had fluid on the brain (Hydrocephalus). I had never heard of this before, and the doctor was telling me she probably wouldn't make it through the rest of my pregnancy. I went to the Internet, as most of us do. I was scared to death. Everything I read was telling me that she would either die or be brain dead. It didn't matter to me what was wrong with her, I just wanted the miracle God gave me. I want to give other families like ours reliable and correct information about Hydrocephalus. God, Hope, and Faith kept me going through the roughest time of my life. I hope what you read here can give you some hope too.
DISCLAIMER: We are not doctors. Any information contained in this site is no substitute for the advice
of your own physician.
of your own physician.
