Wednesday, March 29, 2006
Bye Bye Baby Hair
This is Micah's new look. He looks like a big boy now. I held off on his first hair cut as long as I could, but today I put my emotions aside and got his baby hair chopped. I did save some of it. I even have part of the hair that was dyed red at his birthday party.
Friday, March 24, 2006
Step by Step
Wednesday, March 22, 2006
What a Trooper!
He was a little fussy when they brought him back to me, because he woke up and did not know where he was. Once he was in my arms, he slept for the rest of the time we were there. He slept most of the afternoon after we got home. When he woke up, he acted as if nothing ever happened. This was a pretty easy experience for Micah. He has been through much worse. I am very glad that it is over and hopefully we will see a difference in him real soon.
Tuesday, March 21, 2006
Big Day Ahead!
Monday, March 20, 2006
Slumber Party!!!
Saturday, March 18, 2006
New Milestone!
Wednesday, March 15, 2006
Monday's Appointment
There are some great things that came out of the appointment and there are some things that are still uncertain and a bit discouraging for me. First of all, the neurologist said that it is not Muscular Dystrophy. That is a wonderful blessing! There is not to much that could have been worse then that, so although we feel that there is something going on with Micah, it is minor compared to Muscular Dystrophy. Thank you Lord for answering our prayers! Another great thing that came out of the appointment is that the neurologist praised our pediatrician for doing such a wonderful job in getting the proper care for Micah up to this point. That makes me feel more at ease in the situation to know that Micah is in good hands and that she has been and is taking all the steps necessary to get him the best care.
The discouraging part of the entire visit is that I don't feel like we have gotten anywhere else with the whole ordeal. The neurologist read the MRI that he had taken back in December and said that he did have enlarged ventricles. Basically that means that he has extra fluid inside the brain. That was a shock to us, because his neurosurgeon who has been monitoring him for that never mentioned it to us and feels strongly that fluid is not causing Micah's problems. The neurologist has placed him back in the hands of the neurosurgeon, because he gave a 50/50 chance that Hydrocephalus could be causing the problem. He also said that it could be CP, but he would let the therapist further diagnose that after she has worked with him for a longer period of time. He said that most of the time with mild CP you can't really diagnose or know the extent of it until the child is about 2 or 3. I still just wonder about the MRI. Did someone read it wrong or read the wrong one??? I wish I knew. We go back for a CT scan in June and then follow-up with his neurosurgeon, so we will know for sure then. The idea of two different opinions on that makes me uneasy, but for now I will focus more on turning that over to the Lord and enjoying my precious, lovable one-year-old.
Saturday, March 11, 2006
What a Day!!!
Thursday, March 09, 2006
The End is in Sight!!!
He was very cheerful with the doctor and he did not seem like a sick kid, so they had to do a test to confirm that he really did have fluid in the middle ear. I did not have any doubt that it would come up positive for fluid. Bless his sweet little heart, he has been pretty pleasent through this entire ordeal. I, on the other hand, having the same problem, kept my mom up all night and gave her fits! The test showed that he had an excessive amount of fluid behind both ears. The doctor also said that he is experiencing some hearing loss right now. If his ear infections are taken care of soon that should not be a long term issue for him. It will just affect his verbal skills right now, so he will probably not be picking up new words any time soon. That is what I hate the most for him, because he is such a bright child. The doctor also said that he should have his adenoids out as well.
So, the date has been set...the end of weekly trips to the doctor's office is in sight! He goes for pre-op on the April 3rd and will have surgery for tubes and to remove his adenoids on the 4th. I am hopeful that this will help with a lot of the other things that Micah is presently struggling with.
BLONDE MOMENT!
Tuesday, March 07, 2006
Beautiful Two-Year-Olds!!
I teach the two-year-old class. I never realized how interesting two-year-olds can be. There is never a dull moment! The four hours that we have them, there is not a minute of down time. We are always running back and forth to the potty, cleaning up smashed playdough out of the carpet, watching to make sure that they don't eat the glue, and my favorite...dancing to The Wiggles!
As I observe all the different personalities in the room, I often wonder which one of the children Micah will be most like when he is two-years-old. I have my picks on that one!!!
Saturday, March 04, 2006
Beautiful Saturday!
Micah's New Favorite Thing
This is Micah's new favorite toy! Mimi and Pappy gave it to him for his birthday. Whenever he sees it he points and fusses until I take him to it. It is great for Micah to do this, but it wears his mama out! I have to walk around with him everywhere he goes. That is why Charlie attached the rope to it, so that we can guide him around. He has not learned how to get it out of a jam or turn it, so the rope makes it easier on our backs.
Giddy-up Doggie
Thursday, March 02, 2006
Appointment With Neurosurgeon
We had a rather long and busy day yesterday. I left the house at 7:20 to get to Mother's Morning Out. Charlie met us up there at 12:00, we went to
So here is the update from Micah's two month follow-up with his neurosurgeon. He measured Micah's head and checked other things that would indicate that the water around the brain was causing increased cranial pressure. Micah's head has grown some, but not to the extent that it is suspicious of Communicating Hydrocephalus. He does not show other signs of that at this point other then delayed development. He said that there was a huge list of things that could cause developmental delays that would not show up on an MRI. He listened to our concerns and said that he felt an appointment with a neurologist would be appropriate. His pediatrician has already scheduled that, so at this point we are on the right track. That appointment is on the 13th. He felt that the neurologist would do more testing. He has scheduled Micah for a CT scan and a follow-up in three months to make sure that the water around the brain is not increasing. At this point we will take it as good news that he does not have Hydrocephalus, but continue to pray about the unknown. The best news that we received yesterday was that the neurosurgeon said that he thought there was a 50+% chance that Micah may turn out to be a normal child. I know that that is about a half and half chance, but when you go for a while thinking that there is definitely something wrong with your child...that is encouraging news. So we are still waiting and praying, but we cling to the hope that God is in control and He has a very special plan for Micah.
The even better news of the day was received when we got home and listened to our messages. There was a message from Micah's pediatrician’s office, saying that they have gotten an earlier appointment for him to see the ENT for tubes. He is now going on March 9th instead of April 10th. He has had the same double ear infections since December 19th, so hearing that news makes me want to turn cartwheels!! I couldn't do that with a headache last night, so I might have to go do that right now. :)