Friday, February 3, 2012

Becoming...

The Daniel Family Christmas 2011
Marty, Jaime, Logan, Sydney, Gracie, and Luke
Taken at PapPaw and Mimi's House (The Rogers' Christmas Celebration)

The Rogers and their lovely grandchildren - Christmas 2011
PapPaw, Mimi, Logan, Gracie, Luke, and Sydney


Luke's Christmas Experiences

Daddy and Luke bonding time with presents. Pure joy!


My BIG Tampa Family
We took the kids (Logan, Gracie, Sydney, and Luke) to see Grandma A. They all adore her. Luke had a chance to meet some extended family that Mommy hadn't seen in years. It a blessed trip to Tampa

To Grandma and PawPaw's We Go- finally!
Luke truly enjoyed rolling his bus up and down the hardwood floors in their home. He feels perfectly comfortable there :)


Becoming...
We are all truly unique, yet we are becoming a beautiful blended family. 


Saturday, December 17, 2011

The Untitled Holiday One

This would be my facial expression after being told that there are only 7 days until Christmas! Ahhh! I have so much left to do! So, today was my day to accomplish I few things.  My Christmas shopping is completely done. The decorations are all up and the presents are wrapped under our beautifully decorated Christmas tree. I got my first spray tan done last night. I went from pale to waz-am in 20 minutes. I like it and I believe I might do it again. It's helping me out of this "I have four children, a second full time job teaching kids, and no energy" attitude.

So, I am taking a new approach. Everything is great and I will choose to see the humor in the things that aren't so great. So, I am going through another Christmas with children who may or may not be completely happy with what they have been given. One of my four children will find more joy from banging the Christmas toy against the tile than actually playing with the toy. It's all good. We are all so wonderfully unique. God bless Logan for having to go through two separate Christmases and feeling uncomfortable living a split life. God bless Sydney and Gracie for having a father who is choosing not to be involved in their lives. God bless Luke for being disabled. Honestly, God blessed my children through their circumstances. God gave Logan a step-mom who loves him and provides for him. God gave Sydney and Gracie a step-father to help them grow spiritually. God blessed Luke by giving him an entire family who prays for him every day.

So, for all that could frustrate us, we choose to view the blessings. What an awesome life we live and what an awesome God we serve! Merry Christmas all~

Sunday, December 11, 2011

It's Christmas Time Again- Updates

Wow! I just realized how quickly this past year has flown. It seems like yesterday that we had bought our new house and were putting up new Christmas decorations.

So here's for our updates:

Luke's Broken Clavicle
Last Saturday, Luke fell out of our tall chair on to the tile floor. He immediately started fussing and continued fussing for the next couple of hours. So, I took him to Santa Rosa Medical Center. After 3 hours and a CT scan, we were discharged. They said he would be sore for a while. I took that at face value. So the next day, I was getting ready to give Luke a shower and I noticed that his right shoulder was really swollen. Marty and I made the decision to take him to "Dr. Happy" that next day. Long story short, his right clavicle is broken. He is a brave little boy and is now doing great. He is healing quickly.

Christmas Shopping With Luke
Marty and I discovered the greatness of taking your child with autism Christmas shopping for himself. We were able to go through the store and let him try different toys. We found three that he really liked and bought them. We got home and he still wanted to play with the toys, so while I was wrapping other gifts, he kept playing. When he moved away from the toys, I took each one and wrapped them and placed them under the tree. He didn't even realize what had happened. I bet that he will be surprised on Christmas morning!

The Decorating of the Christmas Tree 2011
We take pictures and videos every year of the children decorating our Christmas tree. We listen to Christmas music and drink hot chocolate. This is the picture of our four darling children. It will not be long and we will be looking at teens in this picture! Oh how I want to treasure these memories. They are so precious to me!

The Love Between a Father and His Son
Luke loves his daddy. This picture was taken as Marty and Luke were watching Logan's basketball team, The Hurricanes, play a game. Luke desires closeness with his father. 


Friday, November 4, 2011

Faith: The Replacement Behavior for Fear


Halloween 2011!


I love these pictures!!!

I have been reading a daily devotional written by a lovely woman who has a son with autism. In the devotional, she is very truthful about the joy and pain of raising a child with a disability. Their is a short story, verses from the Bible, and a short prayer for each day. What a blessing this devotional has been! It is amazing to find out that other ladies have gone through what I am going through. I truly believe that God has called parents of children with disabilities to bless each other.

Our Testimony:

I put a picture on Facebook that had the four kids with a grocery cart. I was thinking that Marty and I were kind of brave that day. We took all four kids to Winn-Dixie to get groceries for the next two weeks. There were two comments that changed my perception of our situation;

"Saw you and the girls holding Luke's hands and walking down the sidewalk after church this morning...thanked God for all He is doing in the lives of your family. It was so precious watching Luke walk. Just wanted you to know that God is using you and this journey with Luke as a testimony of God's faithfulness!"

" I was there walking with Amy, it was definitely a God moment. Luke is a walking testimony and so are you and Marty."

Our family has a testimony. Each one of us has a story. God has been with us and has had His hand on all of our lives. Luke has a testimony. He was born to bring Glory to God.

My Ministry:

"Chasing Away"- I was called to bless the lives of other parents who have children with disabilities. The following comment was left on Facebook;

" I'm so happy to see you've made a group for other moms in the area to get together and support each other! That's a ministry need that's so often overlooked. : )"

The person who left this comment helped me realize that what I am already doing is a ministry. It needs to be thought of as a ministry.

An Update:

Luke is now attending a new school. He is doing so well where he is! His teacher is an amazing lady. There is not a day that goes by that I don't thank God for leading us to this class. Luke is walking more and more. we have found a gate trainer that Luke likes. Hopefully we will have one for him soon. He is also finger walking. He will hold on to one person's finger and walk. I am so proud of him. He is making such great gains. I have to give glory to God for Luke. He continues to do better than anyone could have expected!


Monday, September 12, 2011

Beauty




This is Luke at Splash in Panama City, Florida. Splash is a resort with condos. The bottom floor has pools, a lazy river, and something called "The Bucket". Logan, Sydney, and Gracie LOVE this place. It is perfect for them. They don't stop moving until around 9:00pm. My parents take us every year. It is a huge blessing! We arrived on a Friday evening with Luke. He swam with Marty and the older kids at the lazy river. After 45 minutes he was purple because he was cold. Here is a picture of him when he was cold-

He enjoyed himself, though. So, he did not go in the water for the remainder of the trip. 

I am truly amazed by Luke. I just love watching him. He is beautiful. I wish I had the words to describe my love for him. My love for him is truly unique. It is different than my love for my husband or my girls. My girls give love back. I say. "I love you" and they say "I love you" back. Luke has his ways of giving love back to me also. I pick him up and he puts his head on my shoulder and touches my back. He presses into me. 

Luke is a beautiful child inside and out. He is the glory of God revealed in a human being. He is not God, but he proves that God exists. God's hand is on this child. He brings so much blessing into the lives of the people he is around. His teacher says that he is unique. He is unique indeed. 

Thank you God for giving me this beautiful little boy to love and care for. God has changed my life through knowing and loving Luke!



Sunday, August 28, 2011

Time to Update


So much has happened this summer. I have decided that it is time to update. I have avoided it because I really didn't feel like I had the energy to write about it. Now, I am feeling motivated. 

The "A" Word

During the summer I became motivated again to push for a diagnosis for Luke. I knew that one diagnosis would not be the end of our story, but we had gotten to the point that we needed some financial help with testing (medical) bills. I had talked to Luke's doctor about the autism diagnosis, but she was not comfortable with giving that diagnosis. At the beginning of the summer, we got the diagnosis of "an unknown syndrome with autistic features". It turns out that our insurance company would not take that as a diagnosis. So, at the end of the summer we went to the neurologist. I was shocked when we didn't see the doctor. We ended up seeing the nurse practitioner. I was upset at first, but it ended up being a God thing! At the end of the appointment we scheduled another EEG. We also were told that we needed to have a sleep study performed for possible blockage apnea. We were told that no one would take our insurance, so we would need to pay $650 for the study. I am still looking for a place that will cover this. The last thing we were given was a diagnosis! We finally received the autism diagnosis! I was so relieved. Now, we can try to get ABA services covered. That's a whole other issue! Autism is definitely not the end of Luke's story, but I was relieved to have something so I could move forward with pursuing social security disability and get Luke on the Medwaiver waiting list. I am still working on that at this time.


The First Day of School

As you can see from this picture, Luke was quite annoyed that he had to wake up so early. He went on to have a great day at Benny Russell Elementary. This year is going to be an awesome year for him!

EEG's and Doctor Appointments

Luke was scheduled for an EEG this past week. He screamed from the moment he arrived until his Mimi had had enough. She has rescheduled his EEG for a later date when he can be sedated. 

He had his well-child check-up and we found out that he had gained a pound and a half since May. Go Luke!!!


So many reasons to celebrate and so much work ahead! 


Tuesday, August 2, 2011

GI Clinic and Children's Hospital in Birmingham, Al (Trip #1)


We saw a doctor at a GI clinic on Thursday July 14th. Marty, Luke, and I traveled up to Birmingham that 
day. It was a really peaceful trip. We went to see this specific doctor because we had concerns about Luke's digestion or lack-thereof. His stomach just gets so big and hard as a rock. He also passes some pretty obnoxious gas. 

The GI doc suggested that we have a "breath hydrogen test" to test for intolerance of fructose. Long story short, we ended up staying the night in Birmingham and the test was performed the next morning at 8:30. Luke had to fast overnight. Once we arrived, a nurse (really sweet lady) put a mask on Luke's face to collect his breath. She did this twice. Then, she gave Luke a really concentrated amount of fructose in his sippy cup. Every 30 minutes after, she would do the mask thing twice. 

Several days later we found out that he is, indeed, fructose intolerant. He can no longer have corn, foods with fructose (or high fructose corn syrup), corn syrup, tomatoes, peaches, cherries, and a few other fruits that I cannot recall. The number one thing he can't have is sweet potatoes and carrots. These two veggies have been a staple in his diet since he was an infant. 

Over the past two weeks we have adjusted his diet. He is also taking Flagyl (a medicine to rid his intestines of bacteria). The medicine has really helped and I have found out that Luke's body does not tolerate peas well at all. We are still working on the diet. I think we will continue to see improvements. 

Thank God that the doctor was knowledgeable enough to suggest the fructose intolerance test. Now Luke is enjoying gluten and dairy! He loves whole milk :)