Sunday, December 19, 2010

Random pics and Christmas with the Klaws/Claus!

Getting ready to make Gingerbread Houses with friends.

Adina's Christmas dress. Nope it's not red or green, but poofy and pink like a princess. That was her pick, this way she can wear it for Christmas and Easter. My view? It's only a dress!


Daddy, Cora, and Oli Bear.


Cheese!


Our deck during the last big storm. This was only half way through the storm. More to come!! Gotta love Minnesota!


Adina loves helping her sissy eat.


Cutie in her beautiful dress from Grandma Ruth. Cora is almost 7 months.


Grandma and the girls.


Adina and Grandpa coloring her new castle! Every princess needs a castle =)


Oli checking out his new wardrobe.


Princess all dressed up. Notice the heals.


Cora and Elmo.


Oli loved Elmo too!


Elmo is seriously a big hit.


I have always felt like Oli is saying I love you! He is so wonderful!! Cora makes kissing sounds all day. Of course on video she only does it once!!

Wednesday, December 8, 2010

Catching Up

I realized I have missed some cute pics of kids. Adina got to go to MOA yesterday to go on some rides. It was good for her to do something fun and wild since the last few weeks have been very stressful on her I think. She loves her brother so much and hates when he is gone. The day he was back she played hair cut with him. She covers him with a blanket and pretends to cut his hair. Sometimes he likes it, this time was special, he got beads in his hair as well. Next time I will take a video of it! I just looked back at some older posts and videos of Oliver and got a bit emotional. He has changes so much. The hardest part about not knowing exactly what Oliver has is not knowing the future, but I guess none of us really know our future. Still waiting on the state to hear about more hours. It is a little overwhelming to have so many new nurses coming to interview. Having a nurse a few days a week and soon having one everyday is an adjustment. We love the help but just have to get used to trying to have a "normal" family life with a non-family member in the house. Oliver is doing okay today, pain is a little better and he is tolerating foods.

Adina's favorite ride! She has to do it all by herself!



Making a wish. Her first wish was, "I wish Oliver would feel better." I gave her another penny and said, "make this one all about you!" She said, "I wish for a big dolly house!" We will see what Santa can do about that!


Adina with Curious George

Adina and the frog from the Rain forest Cafe. I think it looks a bit like an alien!


Cora sitting with God mama Vicki mouse. Cora loved George too!


Tutu cute!


Adina and Cora with all the boys on Halloween.


Clowning around with dad. (Cora is the clown!)


Family pic at pumpkin patch.


Three baby Klaws. Adina is such a loving little girl. A few days ago she said she wanted to be a mommy like me when she grows up! Then yesterday she changed her mind and said she wants to be a garbage trucker! I told her what ever makes her heart happy is fine with mommy and daddy.



Oli's first real hair cut. (One by a professional) Jen, his main nurse and second mama is holding him. He did awesome! Poor Jen had a work out this day and was covered in hair! This pic was taken about 3 weeks ago. The tape on his cheek is to hold is oxygen tubing.



Oliver getting a ride to one of his tests at Gillette. He loves the wagon rides!


We wish you a Merry Christmas! You may notice that the second verse of the song is Adina's version!

Sunday, December 5, 2010

home?

Doctors just did rounds. I know they love me! When they stand in the hallway in a big circle I join the circle and give my expert opinion! I have noticed none of the other parents do it. He is doing well today so far. Last night he had about a 5 minute seizure which he has never had before. They will either discharge us home or send us to Gillette. They are not comfortable with his neurological stuff here so it is up to the Gillette neuro team. Update again soon, hopefully we are home today.

Saturday, December 4, 2010

ok

Oliver is having a good day so far. Struggling with some secreations and a little belchy but doing good. I am staying on top of his meds at any sign of discomfort because I know if he starts to feel pain he will have seizures and then we will be headed to Gillette. We need to be home now. I know that this is a great hospital for kids who have cardiac issues and transplants and other issues. When you have a kid with special needs who is a bit of a mystery already the best place to be is Gillette. The charge nurse has checked in with my a lot to makes sure that we are happy. I know I can count on the nurses here. They have been pretty good advocates. I am just looking forward to getting back to our doctors.

Wednesday, December 1, 2010

Surgery

Oliver is having surgery December 3rd at the U of M Amplatz Childrens Hospital. Not my favorite place but they don't do this surgery on little kiddos at Gillette. He is having a Nissen Fundoplication and an ERG (electroretinogram). We will be there for about 2-3 days unless there are complications. Oliver has been feeling really good the last month. He has been throwing up a lot more, that is why he will be having the Nissen. Since he will be sedated I called and ask that they examine his eyes really well. He does not like it when he is awake so he has never really had the best eye exam. The ERG hopefully gives us more information about Olivers eyes. I will be with Oliver during the day and John at night. We kind of have a routine with hospital stays now. We are waiting to hear about more nursing hours. Story of our lives. He was bumped up to 8 hours a day, now that he is on high flow oxygen and having more seizures he qualifies for 16-20 hours. We started having two new nurses alternate Sunday shifts so I could take the girls to church. The first Sunday I received a call at church asking me to come home. She quit after one shift. Oliver was not breathing well, supposedly seizing, and just pissed at the world.
The girls are doing well. Adina is still loving school. Cora has two teeth and loves blowing spit bubbles. Life is good!
The doctors are pretty sure that Oli has a Mitochondrial disorder. They are testing but who knows. He is our Mystery man and he is strong. We have tons to be Thankful for, three awesome kids who love each other and are super loved by us.
Peace~

Kimono cutie. Dressing up at the Childrens Museum.



Two cuties, one not so happy.


Decorating the tree


Cousin time with the greats


JUMP


Adina making her Lefse



Adinas Lefse, rolled out all by her. Cutest little piece of Lefse.