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.

Thursday, March 31, 2011

Oh Sunny Day

Today was a beautiful day and I did not plan to stay in doors with my kids, so we drove to the San Bernardino County Museum in Redlands and enjoyed the day there. We got to see live insects and Sinclaire got to touch it, the assistant asked if David would touch the snake, "no...he'll just tap it to hard thinking its a toy", I said, so the assistant just smiled. David really liked being there, he loves the fish and he got to listen to some bird calls. Right after we decided to go get ice cream and as soon as we parked, David had a fit, he just wanted to go home. So, we waited and sang to him and then kind of dragged him out, he was upset but soon after he tasted that yummy yogurt and was watching You Tube video's of Noggin, he calmed down. I was nice day and it was better then sitting at home watching T.V.

No comments:

Post a Comment

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