Saturday, June 14, 2014
Sunday, May 25, 2014
The Hoover Household@ the Bluebonnets 2014
Tuesday, December 24, 2013
Tuesday, December 10, 2013
Our Big update and more pics
Thursday, December 5, 2013
Halloween pics
Sarah at her last ECI Visit... We passed the skills test at the school district with flying colors and as soon as we get potty trained will be going to a mother's morning out program at a nearby church, and not the school. Hallelujah!
Sarah at Daddy's work at The Family movie night under ste stars... they watched a new movie (to them) which Became their favorite movie... Despicable Me ...Sunday, October 13, 2013
Looking at the trials of the past to see where We've been to see where
Sometimes it's a great thing to look back at something that was so horrible and heartbreaking and to be able to see where God has brought is through.
We've had a lot of challenges recently(not just Daniel) , which would leave me feeling hopeless and depressed, if it were not for the Lord making a way to not feel this way.
Other than finding at least five things to be grateful, another way I often use is to look back at something hugely difficult where God proved his trustworthiness and faithfulness. Also Known as a BUT God....moments.
This video was taken on Jonathan's 6th day of life. He had just been transferred to the Neonatal ICU level 4 at what would become Levine Children's hospital in Charlotte, NC from somewhere locally. At the time this was shot we didn't know whether or not he would continue to be here. This was one of our biggest trials, and to this day I'm so very thankful for the home group we were a part of that walked beside us every step of the way, even when there wasn't a pastor to come pray. This group became the Church.. We we had bad days in the NICU, they cried and prayed, when we had great days they cheered. When Jonathan came home, we praised God for his wonderful work together. Meanwhile another of it's members we were all praying for was in his final months of his life. I was told at his funeral that he was praying for Jonathan and that to this very day still has touched me.
Jonathan has days where it seems he's 7 going on 14, and although he has physical challenges, and learning differences, we keep cheering him on because we Learned that life is a gift. And we share things together on this journey of life.
Here's another video that ministers to me every time I hear it.
Worn by Tenth Avenue North
Be Blessed
Sunday, October 6, 2013
And the result is somehow different than what we expected?
The morning of the third was crazy only because we had to get everybody in the house ready because after we took Jonathan to school, we left for Fort Worth.
It didn't take us very long to get there as it was our third trip collectively. We sat in our car for twenty minutes just listening to the radio and praying.
As soon as we checked in, Daniel heard his name called. After answering a billion questions Daniel's measurements were taken. The little dude is 43 pounds and 43 inches tall.
We were led into a exam room that had some toys in it and a table in it, but not much else.
What seemed like forever ticked by (more like twenty minutes) and the doctor comes in. I answer more questions, and show her the video off of my phone. She then examines him and points out every last flaw.
She talks to me about his IEP and how it was almost stripped out of services he needs at school just so he is stable enough to learn effectively. I told her another meeting has been scheduled later this month on this very issue. She leaves and comes back with her recommendations. Apparently he exhibits symptoms of opposition defiance disorder and a borderline cognitive disability(he probably poorly when he was tested on the spring). She is going to send us to a psychologist to learn how to parent him when he is in full force. She said that he acts out because he may not understand how to process his emotions and he also may be acting out to avoid doing things that he perceives as difficult for him. His people at school and us as his parents need to learn to spot this and shepherd him in how he can deal with a given set of feelings.
The doctor is also sending him to be fully tested through genetics. This is great and we've been praying they'd send him for testing there.
As for the ODD diagnosis, here's my take. We don't really know what that all means, but it doesn't really change who God created him to be. He may face a few extra challenges right now, but eventually something wonderful will come from this sweet little man. Who knows maybe he'll be a doctor or a fireman. He probably can be who he wants to become. I pray every day for him that he would know that we are in his corner cheering for him, and that he learn to work through some of his issues that someday we can laugh about this.
It's really a uncomfortable feeling to understand that some things are really out of your control and ultimately in the hands of God. Ultimately this is always a great thing.
We have already attempted a couple strategies from a love and logic type of approach and have seen some success in the limited situations we have tried it in.
In any case if you feel led please feel free to pray for him. It would bless me if you left comments and I promise to read them to Daniel.
Be blessed.












