Matt and I adjusted and are reasearching everything we can about A. Chiari Malformation and Doctors who specialize in it. Well, God must not have been pleased on how well we are adjusting. Then he says, "Let's throw in a little something for Cooper, their 3rd child.
Let's give him something not so dramatic, but that would need surgery to fix." So, God blessed Cooper with a hernia. It's easy to fix, but once again....it's another hurdle for Matt and Cindy to jump over. We will over come this on April 7th at Children's Hospital and Cooper should do well. Well, you would think that God would atleast wait until Cooper's surgery is over to throw something else at us. Nope, he must feel we need one more thing at this point. So, God says," Little Miss Carson, the youngest of the Cole kids - let's give her an issue with her head. Matt and Cindy handled Riley's ACM so well, let's see how they handle this one." So, Carson had a CT scan the other day and the radiologist found that the bones behind her soft spot are starting to fuse together. Not good. Her head looks like it could fit into a toaster. The fuse is not letting her head grow the width way, but only the length way. So, she will be joinging Riley in seeing the Neurosurgeon. 
So, God says, "This should keep Matt and Cindy busy for awhile. In the mean time, I will let Keegan be the healthy child."

Ok, now God....if you are reading this blog.....would you mind taking a few hours to explain WHY you believe that Matt and I can handle all of this??? I am dying to know!



I will never forget that day, and Coopers either. Cooper was well enough to make it home on December 24th, Christmas eve morning. I couldn't have asked for a better Christmas gift....to have all my babies home with me











