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.

Saturday, July 13, 2013

Neuromuscular Appointment

So about a month ago my son went in to see his Pediatrician and I asked him about David getting checked for scoliosis, he gave David an x-ray and we left it at that. He has been referred to a Neuromuscular Doctor and I am assuming that David might have scoliosis...here is another rock to climb in this already precarious situation, if it isn't one thing its another. Lets pray that he only needs a brace and not surgery, depending on the results I get next month.