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 2, 2011

Non stop eating

David has this thing that he likes to open the fridge and grab for what he wants, if we don't keep him away from the fridge he will keep asking to eat. My son will non stop eat if you let him, so teaching him to control his eating habits was a challenge. We started him with small portions at a time and then got him into a routine of breakfast, lunch, dinner and snacks in between. He use to just put food in his mouth and would stuff his mouth without knowing it, so teaching him about good eating habits was important. Now I am so happy to see him sit at the table and control his eating, we still have to monitor him because if he finds food next to him he will snatch it! So I posted this web page from Fragile X.org and I hope by reading it you will understand how sensory is important to kids with fragile x and how we as parents have to monitor all habits and just go with it and learn from it.

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