ABOUT

Hello! My name is Christie. In an effort to help those who have a child with this same condition, I wanted to start this blog. I am hoping that someone will be able to find it and be able to learn more and realize they are not alone. Although people will tell you it will all be over soon and not to worry, you still do! And it's still very hard.

This is my family now--beautiful Bailey in the front, standing and holding her Daddy's hand. She is awesome. We have known the hospital well over the last few years. Devon on the right there had his appendix rupture and had a week stay, Bailey with her head at 2 months old, and Ruby Jane (now 21 months old at the time of this update) was born with Tetralogy of Fallot, a congenital heart defect. She had open heart surgery at 6 months old. I can say that I LOVE doctors and nurses, so very much.  How thankful I am for their expertise, kindness, and for the advancements made in the past years to make each of these surgeries so successful.

Please feel free to comment or ask any questions. I know that there are more serious things that can happen with your precious little one, but we were still scared and had many questions!

I also blog over at Lemon Squeezy Home, and Love From Ruby. :)

Contact me by clicking the CONTACT button on the top menu bar.  Thank you!