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.

Wednesday, April 20, 2011

Sleepy time

Today after school David came home tired and he toke a nap for two hours, well that nap only gave the will to stay up longer. After his bath and brushing his teeth, I put him to bed as usual and when I went in to his room to check on him, he had gotten out of his room and entered mine. He was in the dark playing with his piano and musical light toy, laughing and sitting on the floor. So I gave him 30 minutes more to play and then I put him on my bed and turned off the light. I went back to the living room to watch the Laker game and within 10 minutes he pops out into the living room playing peek a boo, he knows he is suppose to be in bed, so playing peek a boo is a way for him to get us distracted. Well this time his peek a boo will not work with me, so while walking him back to my room for bed he tried the peek a boo one more time, no chance. Good night, my love.

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