Unique

After David being diagnosed with a rare chromosome "genetic" disorder I was referred to a web site called rarechromo.org and I found there facebook page for parents who have children with a rare chromosome disorder. There is approximately 3 families that are registered in the United States and most of the families are registered in the UK. My son was tested by his Metabolic and Genetic doctor for Fragile X Syndrome and even though he had the defect of the "X" chromosome he did not have Fragile X. It's not until 3 years later that he got tested for the deletion of his genetic chromosome and therefore diagnosing him properly. I recommend that ALL parents have their children tested by a genetic doctor, you just never know what you'll find out.

Friday, June 28, 2013

To my surprise

So, we get up earlier than usual and David is in a good mood ( he must of gotten enough sleep ). He looks over to my night stand looking for his toy, he stretches his neck forward and looks down to the floor where he notices his toy, he jumps out of bed and picks it up and begins to play with it. I then get him ready for school, put on his AFO's and make him oatmeal...that kid loves his oatmeal. We wait outside for the bus and its taking long for the bus to show up. So, we wait and wait and I realize its not coming, I called transportation and no answer; I put David in the car and I drive to the school complaining to the Gods as to why the bus didn't show up, I drive up to the school to drop him off, but to my surprise there is no school today...whaaaa??? Gee, thanks for the "heads-up"....I drive up to just see an empty parking lot and the school locked up.


No comments:

Post a Comment

Note: Only a member of this blog may post a comment.