I chose the Blog Background!

So Ari gave me free reign on making the blog the way I want! Yes!!

Fall Fun

      Isaac napping when we arrived at the maze.
Miles taking it all in on Daddy's sholders.
Slidding with my boys.
Wild Child Wild Smile!
Duck Races

The boys and I are in major celebration mode as Michael has some time off work right now. We are having family cuddles and "group sugar" all over the place. We really love spending time together as a family I am living it up having a second set of hands to dress, hold, and corral the kiddos. 

Miles is a lover of all things party related and has an incredible memory. Last year in October we went to the Harvest Festival and corn maze close to our home. Miles was in heaven. He didn't really care about the corn maze but the party atmosphere was like caffeine for him. He ran pin-ball style all over the place. For the last year every time we drive by the corn-maze location I hear "hey mom when are we going to corn-bellies again." About 6 months ago I started answering "in October baby." Three year olds don't know their months right so he would just kinda wait for October forever; YEAH RIGHT! He has asked since then "In October I get to go to Corn-bellies OK?" Well Sept 26th he informed me "Mom Corn-bellies is open cause it is almost October." I don't know how he came up with that but he was right. We packed up and went to Corn-bellies for a night of total ecstasy three year old style. Above is visual proof.

If the Army would just give me that bonus!

So, Michael here.  I just called Adoption for All Children and found that if we were able to get our formal application in today, we would be #26 on the list.  The receptionist also told me that from the time the formal application is process the current average wait time would be 15 to 18 months.  THAT IS CRAZY!!! Just really wish the army would give the bonus that I was supposed to receive in June!!  We are trying to pay as much as we can with our money prior to getting any loans!

Michael

FINALLY!!!!!!!

We have been waiting to submit our paperwork to AAC because we wanted to have the cash on hand to pay for the first phase of the paperwork; well today we got the GREAT NEWS that Michael's bonus from the Army is on it's way!!!! We will be submitting our formal application on Monday!!!! When AAC gets this paperwork and puts us on the list, we are officially waiting for ABENI!!! Ok so I am looking at this and I have lots of capitals and exclamation marks. Trying to express by emotions with words is something that I am clearly going to have to work on. I will post tomorrow about an excellent adventure we all just had. Laters all.

Family pics and day trips!

Here are some overdue pictures of us.

WOW III

Ok so it has been a long time since I posted and I need to finish the story. Over the last year we have seen miracle after miracle with our little man. The first being that he is alive. Isaac came home from the hospital and returned two weeks later when he was having pain and no one could identify where it was coming from. No one would listen to us so we brought him home still screaming before he went to sleep. Isaac caught a cold at the end of October and we had to admit him again because he was just unable to fight the virus on his own. We did an MRI to rule out seizure or brain related problems with his sleep. The Dr's didn't find a problem actually they found something they certainly didn't expect; Isaac had no more visible brain damage. We started seeing a Sleep Dr. to help him sleep and found out that he was really struggling to breath at night. He was given oxygen and we waited to see another Dr. to have his tonsils and adenoids removed. After that his sleep improved slowly and surely. Isaac was also diagnosed with GERD and we began treating that which helped with his struggles. We started physical therapy and early intervention. Our little has gone from not being able to turn his head and not smiling or laughing to walking in just over a year. We treasure every goofy little smile that has always been his trademark. We received yet another miracle this last Month. On Aug first Isaac had a cardiac catheterization to get detailed pictures of his heart. The Dr's were shocked and thrilled with what they say blood flow to the damaged part of his heart had returned as had his flow to his left femoral artery. The truly amazing part is that his coronary arteries have shown remarkable progress; beyond what the Dr's had even given us as a hope. Isaac continues to amaze us and inspire us!

Good Night 

Ari

WOW part II

Ok so the flight crew from the children's hospital arrived Isaac was so sick and there were so many people who had come to care for him that there was no room in the helicopter for me. My Aunts Karen and Juli arrived at the hospital, this was a great comfort to me as Juli is a nurse and had helped me through some medical struggles in life; besides Rib and Juli were always a source of comfort to me as a child and even now they calm my center.

Isaac was taken to the helicopter and everyone raced to the hospital. Michael's parents were on their way there already. We arrived at the hospital and the trauma team there was just doing their job but I was so offended when they began to question me about what had happened. I got the feeling they thought I had shaken my baby. They did a CT scan and figured out that that wasn't the case and he was admitted to the PICU. Michael and I followed him up stairs and watched as Dr's and Nurses swirled around him asking us questions and working on his little body. We had to leave as they placed several more permanent lines to access his bloodstream. It the time they assumed that he had Meningitis and they were treating him for it. A spinal tap was never performed and all of his cultures kept coming back negative. Isaac had began over-breathing the ventilator in the helicopter but his muscles were stiff and the neurologists told us that 35 minutes was just to long for the brain to go without sufficient oxygen. We were told to be prepared for a child that was either brain-dead or close to it. The neurology team hooked  him up to an EEG and the lines were just so flat. The attending thought we should get a consult from a geneticist and they tried to find something but again nothing came up. It was a few days later when Isaac was finally able to get a MRI of his brain. The neurology team was shocked with what they saw. They even had to wait an extra day to try and enhance the images, they had expected to see large areas of dead brain matter, but instead saw only  smaller then sxpected patches of dark areas that they had to look hard to see. Also his EEG was beginning to look more normal. They took him of the sedatives and extubated him. It was so good to finally hold him but he was so stiff and like a newborn all over again he couldn't nurse, couldn't smile, couldn't roll over, couldn't laugh had difficulty moving his head and following objects with his eyes. We spent a few more days in the PICU but then we were ready to graduate to the infant floor. Isaac was doing great but the attending still wanted to be able to give us a reason for what had happened. As a last ditch effort she had an ECHO done of his heart. What they saw gave them a reason for what had happened and us a whole new set of worries. Isaac had giant coronary aneurysms, he had suffered a heart attack that night. We were given the diagnosis of probable Atypical Kawasaki Disease. No one knows what causes this disease, it isn't genetic, bacterial, or viral, it responds to IVIG and generally has a whole list of symptoms, none of which Isaac had demonstrated. We were offered the chance to give Isaac and experimental medication that had sometimes helped with the remodeling of the aneurysms, and went ahead with it. We also started him on aspirin and indictable Lovenox, a blood thinner, to prevent future blood clots and heart attacks. We stayed in the hospital a few more days for observation and then we were on our merry way home with a baby whose future was more then uncertain. More later I need to put the boys down for a nap loves Ari