camillajoy blogspot.com

The Journey of Camilla Joy

The story of our family39;s and Camilla39;s journey with moderate ventriculomegaly, diagnosed at 20 weeks gestation.
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Our Little Pieces of Heaven

Mark, Jennifer, Ethan, Emily. This blog is about our family, who have dealt with the loss of two sons with Muscular Dystrophy, the adoption of a son diagnosed with Agenesis of Corpus Callosum and the birth our a healthy little girl. Friday, May 27, 2016.

Anything Can Be

Friday, June 19, 2015. This is mostly a good news thing. George in early May for her one year follow up, and I had to snap our traditional picture with him. I think she likes him as much as her mom does! I am in my next to last semester of grad school! Saturday, June 14, 2014.

The World According to Will

Sunday, March 11, 2012. The surgery went quick! Friday, January 13, 2012.

Just The Five Of Us

I spent hours adding borders and doing fun things to the photos. so here is a post of some of the FAVORITES! Posted by Mrs.

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The Journey of Camilla Joy

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The story of our family39;s and Camilla39;s journey with moderate ventriculomegaly, diagnosed at 20 weeks gestation.

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This web page camillajoy.blogspot.com states the following, "Wednesday, November 18, 2015." We saw that the webpage said " I would like to share our journey with you." It also said " And read it from the beginning. If you recently had the diagnosis of hydrocephalus for your baby in utero, please also visit here. So many miracles and so much of Gods work is done through these children. With man this is impossible, but with God all things are possible. Saturday, November 2, 2013."

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