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.

Monday, April 11, 2011

Back to School

Well spring break was too long, but I had a chance to take my kids to a museum and Chuck E Cheese. David really enjoys the Telly Tubbies ride, he just smiles and cracks up on his own. So this morning David tried to pretend that he was asleep, but I just had to get him ready so he doesn't miss the bus again. Yawning and whinning off to the bus he goes, yes! I got him on the bus, so now I won't be late for work. Toke my daughter next to school...she forgot her Clarinet and I had to turn back, which just made me late for work. So much for my achievement this morning.

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