Wednesday, May 11, 2011
going home!
We met with Dr. Levy about an hour ago and he cleared Naysa to go home! The fluid levels on her brain are up and down which is curious but nothing he was too concerned about right now. She will have clinic visits every 2 weeks to keep an eye on her head growth and another CT in a month. He said if she is to develop hydro the fluid will take the path of least resistance, which is in the back of her head where the bone is missing creating a bigger cone. If that's the case she will need a shunt and her little cone will go down and flatten out, so that's good I guess. She is more alert and acting like herself so as long as she isn't super lethargic, irritable, continues to eat well etc..she will be okay until clinic visits. The first one is just in a few days on the 16th since it was already scheduled before this hospital visit. I am so thankful she doesn't need surgery again right now and I just hope and pray it stays that way. Dr. Levy got called to the OR before he got to write discharge orders so we are waiting for him to get out and come back before we can start the going home process. Thank you all for your love and prayers, once again they pulled her through :)
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Yay for going home! Go, Naysa!
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