Didn't see the neurosurgeon today

Kelly & John waited patiently all day to see Dr Burson and he never arrived. Being in the medical profession, I try to give the Dr, therapist, etc the benefit of the doubt. I mean, I work in a hospital, I know he has a lot of patients and things come up. But when you are on the family side of things, you have a totally different view. Of course to us none of his patients are more important than Max. So we still don't know about the shunt. Hopefully Kelly & John will be able to get some answers tomorrow either from one of the neonatologists or from Dr Burson. It is so hard to wait and not know something. Since Max wasn't put on the surgery schedule for tomorrow I came home to Memphis tonight. I am working a 12 hour shift tomorrow so I won't be able to post until tomorrow night. Please pray throughout your day for peace and understanding for Kelly & John as they talk with Dr Burson. And please pray for Dr Burson. Please pray that God will put it on his heart and in his mind to spend some time with Max, Kelly, & John tomorrow. Please pray that he will have wisdom and compassion as he makes decisions for Max's plan of care and as he communicates with Kelly & John. Please continue to pray for Max. His head was 1cm larger today. They went back to nursing every other feeding today because he was pretty tuckered out. He still has his NG tube. Thank you so much for all of your comments and prayers over the past couple of days. I want to specifically thank Kim, Ashley, and Kelly W. It has been so encouraging to hear from other professionals that have training in therapy. It has really meant a lot to Kelly & John to hear what you have had to say as they were pretty discouraged and confused after the PT's evaluation of Max's muscle tone. Also thanks to those of you that have shared experiences and success stories from children that have been given a similar diagnosis. Thank You so much for your continued thought and prayer, We Keep Praying, Karie