Luke has been really active over the past couple of days. He has been babbling and moving around like crazy. Last night, he got on his elbows and knees and started almost crawling. It was awesome! I tried to get a picture, but every time I would click the camera, Luke would go flat. I am so thankful that I am seeing progress with Luke. He is such a great little boy! He has been laughing and playing. He has even been interacting with his grandparents. I am proud of my little boy- he is working hard :)
Wednesday, November 26, 2008
Progress
We are in Georgia right now. We have been here for 4 days now. I love Georgia! It is peaceful and beautiful. We are staying with Marty's parents. It is truly wonderful to be here.
Wednesday, November 19, 2008
So Thankful
I am so thankful that I have my family and that I have my God! I am not sure how I would get through life's trials without them.
God knew what He was doing when he gave me a mother who is so strong and has faith like no other woman I know. I strive to be like her. If I could have half the faith and half the strength she has, I would be just fine. I don't think my mother truly understands how much I admire her. Every day she does something for me. She emails me and encourages me. She sees something in a store that she thinks I might like and she buys it for me, hoping that it will make my day. The love she has for me is so unconditional. For that, I am eternally grateful.
My step-father is equal in strength. He is such a good man. I am proud to call him dad. He has been patient and kind. He also loves me unconditionally. I don't know if I deserve the love he has given me, but I am so thankful for it! He is wonderful with my children and so very giving. Having him as an example has made me want to be a better person.
I strive to be a parent like my parents are.
I am also so very thankful for my husband. A little over two years ago, he chose to marry me and be a step father to my children. He is a passionate father. He looks out for the best interest of his children. They are blessed to have him. We are still trying to blend our family... we still have a road ahead of us. I pray that God bring us closer together through our diversity and not further apart.
I am so thankful that I have a merciful and forgiving God. He loves me no matter what I have done. I am proud to bring my family to church and I am hopeful that all of my children will know Jesus at the earliest moment. My oldest daughter, Sydney, asked Jesus into her heart on July 16th this year. I was not sure that she truly understands what she did, but I have found that she does know. She prays every day. She writes about God. She tells me that she loves Jesus. I am a proud Momma because I know that she is building a foundation. God will always be by her side.
I have a wonderful family. Each person is so unique and special. I am a very blessed lady!!!
God knew what He was doing when he gave me a mother who is so strong and has faith like no other woman I know. I strive to be like her. If I could have half the faith and half the strength she has, I would be just fine. I don't think my mother truly understands how much I admire her. Every day she does something for me. She emails me and encourages me. She sees something in a store that she thinks I might like and she buys it for me, hoping that it will make my day. The love she has for me is so unconditional. For that, I am eternally grateful.
My step-father is equal in strength. He is such a good man. I am proud to call him dad. He has been patient and kind. He also loves me unconditionally. I don't know if I deserve the love he has given me, but I am so thankful for it! He is wonderful with my children and so very giving. Having him as an example has made me want to be a better person.
I strive to be a parent like my parents are.
I am also so very thankful for my husband. A little over two years ago, he chose to marry me and be a step father to my children. He is a passionate father. He looks out for the best interest of his children. They are blessed to have him. We are still trying to blend our family... we still have a road ahead of us. I pray that God bring us closer together through our diversity and not further apart.
I am so thankful that I have a merciful and forgiving God. He loves me no matter what I have done. I am proud to bring my family to church and I am hopeful that all of my children will know Jesus at the earliest moment. My oldest daughter, Sydney, asked Jesus into her heart on July 16th this year. I was not sure that she truly understands what she did, but I have found that she does know. She prays every day. She writes about God. She tells me that she loves Jesus. I am a proud Momma because I know that she is building a foundation. God will always be by her side.
I have a wonderful family. Each person is so unique and special. I am a very blessed lady!!!
Saturday, November 15, 2008
A Day in the Life of Luke
This is Luke's usual schedule during the week...
6:15am- wake up
6:30am- be carried out the door into the cold wind by Mommy.
6:50am- arrive at the daycare provider's house and immediately demand food.
6:55am- a nice warm bottle with Kepra (seizure med) in it.
7:05am- bottle is finish, I am ready to play for a little while.
7:30am- breakfast (usually consists of fruit and cereal)
8:00am- ready to play again... put me on the floor!
11:30am- lunch
12:00pm- play or nap
3:00pm- snack time!
4:00pm- Mommy's here to get me!
4:30pm- We are back at my house. I get on the floor and play with my toys.
4:45pm- My sister Sydney brushes my hair. I act like I hate it, but I secretly love it!
6:00pm- Dinner
7:00pm- bath time... I have made a mess of myself :) Mommy takes a bath with me and teaches me how to play in the water.
7:30- 8:30pm- Play time and family time.
9:00pm- bed time (I sleep all through the night)
He has such a good time during the day. He loves to play with his toys. He also loves to listen to music. If I sing or play a cd for him, he will stop everything he is doing and listen. I truly believe that he is going to have a gift for some sort of music. I have the sweetest little boy in the world :)
6:15am- wake up
6:30am- be carried out the door into the cold wind by Mommy.
6:50am- arrive at the daycare provider's house and immediately demand food.
6:55am- a nice warm bottle with Kepra (seizure med) in it.
7:05am- bottle is finish, I am ready to play for a little while.
7:30am- breakfast (usually consists of fruit and cereal)
8:00am- ready to play again... put me on the floor!
11:30am- lunch
12:00pm- play or nap
3:00pm- snack time!
4:00pm- Mommy's here to get me!
4:30pm- We are back at my house. I get on the floor and play with my toys.
4:45pm- My sister Sydney brushes my hair. I act like I hate it, but I secretly love it!
6:00pm- Dinner
7:00pm- bath time... I have made a mess of myself :) Mommy takes a bath with me and teaches me how to play in the water.
7:30- 8:30pm- Play time and family time.
9:00pm- bed time (I sleep all through the night)
He has such a good time during the day. He loves to play with his toys. He also loves to listen to music. If I sing or play a cd for him, he will stop everything he is doing and listen. I truly believe that he is going to have a gift for some sort of music. I have the sweetest little boy in the world :)
Sunday, November 9, 2008
Mixed Emotions
I really feel like I am going through some sort of grieving process. I have gone through all of the same emotions. <> I was, at first, in denial. I did not want to believe that something was wrong. I was seeing "red flags", but I was desperately trying to ignore them. Then, I began to let myself admit what I was seeing. I would only admit it to my mother, though. Admitting it to my mother helped me begin to seek help for what I was seeing. So, testing began. I was like a robot. I did not feel anything. I just knew that testing needed to be done. The EEG came back abnormal and I went into denial again. I thought that if I waited a while, Luke would grow and begin acting normal. All the while, I was feeling sad inside. Then, all of a sudden, I became angry about the situation. This is what led to the last doctor's visit. The anger allowed me to have the strength to be up front with his pediatrician. It also allowed me to be able to hear what she had to say to me. Immediately after the doctor's appointment, I became extremely sad again. Now, I am feeling angry again. At some point, I will accept what is going on and move on. Until I get to that point, I will just continue to walk through each day a small step at a time. Accepting Luke for who he is and what God made him will mean that I will have to let go of some things. It will happen. It is just a matter of time.
Tuesday, November 4, 2008
A Step Closer to Knowing...
I had a meeting with Luke's doctor today. Marty was there and so was Luke. Luke was tired and on his worst behavior. I was actually ok with that because it gave the doctor an opportunity to see the behaviors that worry me. I have a typed document with me to remind me of all the questions I wanted to ask.
Luke is going to have a follow up EEG and is going to have an echocardiogram. This will help us be informed when we go to have the genetic study done at Shands in Gainesville. Luke has had the following tests;
MRI (normal)
Chromosome analysis (normal)
EEG (abnormal)
Vision test (normal)
Hearing test (normal)
Metabolic testing (normal)
Swallow study- showed he needed therapy
Now, he will go through the genetic study at the end of March 2009. I asked what the doctor thinks the genetic test will do. We all know that if he is autistic, the genetic study will be inconclusive. So... here is what the doctor said- She said that, from the documentation I provided and what she has seen in the office, Luke has autistic behaviors. When I asked her what she thought would come back on the genetic study, she said that she thinks he has some sort of syndrome. He has some sort of syndrome with autistic behaviors.
I respect Luke's doctor very much. She has a son, who is now in high school, that is autistic. She has been through the struggles. She told me to not be afraid to allow myself to grieve. She says that she has been there.
When I ask Marty how he feels, he only says that Luke is his son and he is special and loved. He says he is not sad or upset. I feel like a complete idiot for being so torn up inside about this. I want, more than anything in the world, to go through this process with Marty. I just feel like he doesn't want to go through it with me. He gets impatient and snappy when I get emotional. Truthfully, I am hurting. I need something- some support, someone to talk to, someone who will let me cry and let me know that everything is going to be ok. My mother provides that for me... but... I would like it from someone who is not my mother... You know?
Luke is going to have a follow up EEG and is going to have an echocardiogram. This will help us be informed when we go to have the genetic study done at Shands in Gainesville. Luke has had the following tests;
MRI (normal)
Chromosome analysis (normal)
EEG (abnormal)
Vision test (normal)
Hearing test (normal)
Metabolic testing (normal)
Swallow study- showed he needed therapy
Now, he will go through the genetic study at the end of March 2009. I asked what the doctor thinks the genetic test will do. We all know that if he is autistic, the genetic study will be inconclusive. So... here is what the doctor said- She said that, from the documentation I provided and what she has seen in the office, Luke has autistic behaviors. When I asked her what she thought would come back on the genetic study, she said that she thinks he has some sort of syndrome. He has some sort of syndrome with autistic behaviors.
I respect Luke's doctor very much. She has a son, who is now in high school, that is autistic. She has been through the struggles. She told me to not be afraid to allow myself to grieve. She says that she has been there.
When I ask Marty how he feels, he only says that Luke is his son and he is special and loved. He says he is not sad or upset. I feel like a complete idiot for being so torn up inside about this. I want, more than anything in the world, to go through this process with Marty. I just feel like he doesn't want to go through it with me. He gets impatient and snappy when I get emotional. Truthfully, I am hurting. I need something- some support, someone to talk to, someone who will let me cry and let me know that everything is going to be ok. My mother provides that for me... but... I would like it from someone who is not my mother... You know?
Tuesday, October 28, 2008
Perspectives
*Mommy* is concerned about development. She is concerned about how he is viewed by others. She feels like what is going on with him is her fault. She wants her little boy to live a successful life.
*Daddy* wants his little boy to live a good life. He does not want Luke to live life watching it pass him by. He wants his son to be able to participate in his life. Marty has a hard time dealing with the fact that he can't solve Luke's problems.
*Mimi* is concerned, yet has great faith in God, doctors, and therapy. She makes Luke food for when he stays at her house. She has high expectations.
*PapPaw* is a great support for the whole family. Luke goes to PapPaw's house all the time and he loves it there. PapPaw's heart is hurting because he feels that Luke doesn't notice him like the other kids do.
*Grandma and PaPa* are trying to stay informed in Georgia. They have been a great support and want Luke to have the best life possible.
*Sydney, Gracie, and Logan* all notice that Luke is different. They wish that Luke would respond to them more. They try to play with him and interact with him as much as possible. They are really good to look. They all protect him and watch out for him.
Thank God for family. I realize that everyone is affected by what is going on with Luke. I want everyone to know that I am thankful to have the support network that I have.
*Daddy* wants his little boy to live a good life. He does not want Luke to live life watching it pass him by. He wants his son to be able to participate in his life. Marty has a hard time dealing with the fact that he can't solve Luke's problems.
*Mimi* is concerned, yet has great faith in God, doctors, and therapy. She makes Luke food for when he stays at her house. She has high expectations.
*PapPaw* is a great support for the whole family. Luke goes to PapPaw's house all the time and he loves it there. PapPaw's heart is hurting because he feels that Luke doesn't notice him like the other kids do.
*Grandma and PaPa* are trying to stay informed in Georgia. They have been a great support and want Luke to have the best life possible.
*Sydney, Gracie, and Logan* all notice that Luke is different. They wish that Luke would respond to them more. They try to play with him and interact with him as much as possible. They are really good to look. They all protect him and watch out for him.
Thank God for family. I realize that everyone is affected by what is going on with Luke. I want everyone to know that I am thankful to have the support network that I have.
Friday, October 24, 2008
Seizures
I have known for several months that there is strong possibility that Luke is having seizures. In either March or May (I can't remember) of this year, Luke was admitted to the hospital because he was having breathing problems. During his hospital stay someone came an did an EEG. An EEG records brain activity. The results were "abnormal". Of course, they could not say that he was having seizure, but they speculated as a result of all provided data. Luke does not have typical seizures. He does not shake. He does have moments where he appears to completely space out. He doesn't breath. He doesn't even move. After several seconds it passes and he goes back to acting normal. He also has times where he "postures". He is in a sitting position. His arms are bent and stiff. His hands are also stiff. His eye are looking up at different points, so it appears that he has a lazy eye. He does not breath. Sometimes he makes strange noises. These moments also pass quickly.
He is taking a small dose of Kepra two times a day to control the seizures. I will admit that when he misses a dose, his strange behavior is even more strange than when he is taking his meds regularly. Sometimes I am not sure if the strange behavior is seizure activity or if it is just strange behavior. It is hard to tell the difference.
The strange behavior usually appears at a consistent time every day. It usually occurs after he has had a busy day. Around the time I pick him up in the afternoon (4:00pm), he begins to act overstimulated. He continues this pattern well into the evening. Sometimes he takes an early evening nap. The behaviors usually improve after that point. Sometimes, they don't improve. I can't wrap my mind around the reason that he acts certains ways. I guess we will just give it time. Answers will come.
He is taking a small dose of Kepra two times a day to control the seizures. I will admit that when he misses a dose, his strange behavior is even more strange than when he is taking his meds regularly. Sometimes I am not sure if the strange behavior is seizure activity or if it is just strange behavior. It is hard to tell the difference.
The strange behavior usually appears at a consistent time every day. It usually occurs after he has had a busy day. Around the time I pick him up in the afternoon (4:00pm), he begins to act overstimulated. He continues this pattern well into the evening. Sometimes he takes an early evening nap. The behaviors usually improve after that point. Sometimes, they don't improve. I can't wrap my mind around the reason that he acts certains ways. I guess we will just give it time. Answers will come.
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