We went back to Vanderbilt yesterday to meet with Dr. Bennett, the maternal fetal specialist, as well as Dr. Tulipan, the pediatric neurosurgeon. For once, we actually left the visit with a big smile on our face and feeling more confident than ever. No miracles have happened, the CC is still not there, but we were still given a good report.
The ultrasound showed no new concerns or problems. Other than showing how much Anderson has grown in a month, everything developmentally looked just like it had at our last visit- The doctors and sonographers seemed puzzled however because it appears that the cavum septum is present- which usually isn't the case when the CC is missing. You either get both or none, from what I understand. But the CC is still unable to be seen on ultrasound or in any of the MRI films (which we got to see yesterday and are AMAZING!)
So, we still know that if God wants that piece of Anderson's brain to be there- it will show up, even though the doctors say it won't. We still believe that God works miracles, but at this time we're okay if we don't get that miracle. After talking to the nerologist, our hope for Anderson's future seemed to be affirmed. My first question for the neuro was "What should be expect when he is born? Will there be lots of doctor's visits, tests, blood work, etc?" His reply was simply this..."I would like to get an MRI of him sometime in the first 3 months or so after he is born, but other than that, you will take him home and love him and treat him like you would any other baby. No special circumstances. You will watch him and if something arises, then we will go from there, but until that happens you just enjoy your new baby like you did with your other 2." I did ask him about Early Intervention, and he said "It won't hurt anything, so if you want to do that, go for it." But his tone indicated that it was not absolutely necessary.
This was very refreshing to hear. I had wondered if we would have lots of doctor's appointments, therapy, etc...that would begin like a whirlwind as soon as he is born. The fact that things will be low key like any other normal pregnancy/delivery is wonderful! Knowing that we can come home from the hospital, rest, rock, and relax is like a dream come true.
We have a little less than 2 months before he makes his arrival because we have already been scheduled for a C-Section on Friday, June 11th. So for those of you who have been praying with us, please continue to pray that things will stay like they are for the next 2 months and that no unforeseen problems should arise. If you still want to pray for the miracle, that's good too! :) I know it is my will that everything miraculously be healed and fine, but when I pray I make sure to tell God that I want HIS will to be done- HE is the one who knows what is best, HE is the one that knows what the future holds, and HE is the one who knows the master plan for Anderson. I don't want my selfish desires to get in the way of HIS plans.
1 comment:
Great Post! I will continue to pray for Anderson and his precious family. Those big sisters are just going to love him to pieces.
Connie
Post a Comment