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, June 4, 2011

Say Cheese

When David was a child it was easier to take photos of him because he seem to be "in the zone" a lot, for example watching T.V. or playing with a toy. Since he has gotten older he is very spastic in his movements, unintentional movements by his hands or just his swagging back and forth. So when we take pictures of David sometimes we get lucky and other times we just get a smudge of his image, it's not easy to be photo ready but it is funny at times. David can care less if the camera is in his face, he thinks its a toy with the red flashing light before the photo, he see's his image in the viewer and thinks its a T.V. David is curious in his own way when it comes to taking pictures and I love that about him.

No comments:

Post a Comment

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