I would like to share our journey with you. Please go here and read it from the beginning. If you recently had the diagnosis of hydrocephalus for your baby in utero, please also visit here for tons of valuable information and so many stories of miracles and hope. It is one of the first places we landed when we searched the Internet after Camilla's diagnosis. There is TONS of hope on this site and TONS of information about what hydrocephalus is. This diagnosis can be serious, but its implications are very different for each and every baby. I think you will find throughout your reading that many of us had similar experiences in the ultrasound room, but very different experiences when our babies were born. So many of us heard the word "termination" along with sentences about our baby's diagnosis. For us this was never an option. Please search your own heart about your situation and do some research. There is a huge community of support across the world, many people of which we have come to know and love this last year. If you would like any questions answered about our baby girl's journey, or just someone to lend an ear to your situation, please contact me by commenting on this post with your email address. I will be happy to respond, answer questions, and pray for your baby. There is nothing more true than this: each and every baby is a blessing. So many miracles and so much of God's work is done through these children.
make sure to read Camilla's full story from the link above all the way
to the present. She is such a miracle to us and I thank God every day
for her. I wouldn't change our experience, while difficult at times, we
are so much closer to God and what is truly important because of her
With man this is impossible, but with God all things are possible. Matthew 19:26