This blog is dedicated to Gabrielle Jane. Born with a rare Neurological condition called Hydranencephaly, "Gabby" was given no hope after being diagnosed three days after birth. This is "Gabby's" journey of life and my journey of healing after her passing.
Saturday, October 9, 2010
CCHMC Hospital Stay
Well today is day 19 of me being in the hospital. I am really glad that they are taking such good care of me, but boy am I ready for my shunt surgery and ready to go home. Since I have been here they have done many test on me. I have had a cat scan wich has showed only minor differences from my first one. The most rescen one showed that I had a tear in my cotortum. This is the lining in the skull that is between the skull and brain. Having a tear there is very normal for children with my condition or also, Hydrocephalus (water on the brain). There is no treatment for it, but it shouldn't get any worse when I get my shunt. While I was here, they also had me see an Endocrinologist. The Endocrinologist ran all sorts of test on me to see what hormones I was lacking. Amazingly enough I wasn't lacking any of them. Also, I saw a Urologist here and I was diagnosed with having Kidney reflux (stage 1). Stage 1 is just a minor case and luckily it doesn't require any surgery. The Urologist placed me on a daily med called Bactrim and this will help prevent me from getting Urinary Tract Infections. At this point, I am not sure when I will be getting discharged. I am hoping that they will be able to do my surgery on Monday and I will be able to go hom on Tuesday or Wednesday. It has been a long few weeks and I cant wait to go home and sleep in my own bed.
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment