Thursday, May 22, 2008

A testing we will go.

So today's visit to the Genetic Neurologist was fairly benign. We were hoping to have Dr. Lipkin's written report from last week's visit to Kennedy Kreiger but alas the mail failed us again. So while Dr. Cohn caught up on the usual topics, and was impressed to know that we are completely off of tube feedings, there really wasn't anything remarkable to report. He did end up ordering the test for Fragile X syndrome, so after the appointment we walked down the hall to the phlebotemist for a blood draw. (I think it is safe to say that was Jackson's least favorite part.) Additionally Dr. Cohn ordered a MRI for sometime in July to check for all the normal structures of the brain and eliminate the possibility of any abnormal structures. After our 60+ minutes with Dr. Cohn we zipped up I-83 back to Towson where I dropped Jack at daycare and then crawled into work. Thus the day began.

1 comment:

MandyT said...

Hey Lauren,
Thanks for letting me in on your blog. So happy to hear that feeding tubes are a thing of the past for Jackson. He has gotten so big and what a cuttie!
God Bless,
Mandy