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, June 13, 2011

sick and sad

David has had the sniffles since Saturday at first I thought it was his allergies so I gave him his allergy medicine, well this morning he woke up with a runny nose and slight fever, he was also cranky which tells me that he does not feel well if his cranky mood last all day. So I gave him his medicine for his cold because he loves to take medicine it makes it so much easier to tend to him when his sick. All day he has been whinny and complaining about what is on television and his dvd player. He refused to take a nap and was not as hungry as usual he just wanted to snack a lot. So bed time it is for Mr. cranky pants, put him to bed at 8p.m. instead of his usual time 8:30. So we'll have to wait till tomorrow to see if the Nyquil did its job.

No comments:

Post a Comment

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