Skip to main content

Day ???

Well I should first start by apologizing for not updating Mason’s site yesterday. We had a big day of visitors so we spent our time enjoying each of them.

I also want to apologize if any of the information that I am going to share with you is repetitive. My days, nights, blogs, and hours just all run together.

We lost a chest tube. Mason has gone from three chest tubes to two chest tubes. HOORAY!
This is great progress and we are excited and thrilled for all positive steps and now comes the dreaded word BUT… He has two chest tubes left that are still draining a significant amount of fluid – specifically the right. We had fair warning about how frustrating this would be and I can now say from experience each person who warned us was correct! It is frustrating knowing that outside of prayer there is nothing anyone can do to slow this down. So we wait!
Today Mason will have an echo to rule out the possibility of any blood clots and to make sure his heart looks strong. I think when the doctor said “blood clot” my blood pressure rose significantly… This Mom and blood clots do not get along. We are confident he does not have any but want to be 100% sure since this has been an issue in the past.

Mason is now peeing like a champ – so we have no concerns with this any more.
However he has not had a bowel movement which could be one of the things causing his nausea. Sunday night after receiving his medication he got sick and then again this morning after receiving his medication he got sick. Again this could be due to no bowel movements or it could be from his medication.
So we are re-evaluating how he gets his medication (form) and the type of medication he receives to get his nausea under control.

Saturday Night (around 9pm) Mason got his appetite back and requested spaghetti... Of course the kitchen was closed and we could not grant his request. So I went by faith and promised him that on Sunday he would have spaghetti for dinner… Praying I could some how figure out how to make this happen. So as Sunday night was approaching it was time for Mom to make spaghetti appear. So I went to the cafeteria prepared to beg the cook to make me a special order but when I arrived I saw the most amazing thing… The cafeteria was featuring a spaghetti buffet. Any type of noodle or sauce a kid could ask for was there.
I couldn’t believe it – and in that moment I was amazed at how God provides for all of our needs (BIG & SMALL).
Proudly I made my way back to Mason’s room with the spaghetti in hand – just in time for his dinner tray to be sent to his room and on the menu Spaghetti… Of course how could it have been anything else… Needless to say we have enough spaghetti now saved for Mason so at any time if he has a craving we are ready!

Yesterday Mason had a big day in terms of activity. He was out of bed a total of five times and we went on four walks. Our goal each day is three times so we reached our daily goal for the first time and I anticipate that today we will be over achievers as well and exceed our goal!



As I write this Mason is lying sideways in bed – laughing at whatever cartoon he is watching on the iPad. It has only been 7 days since I heard him laugh but that is 7 days to long and I have missed that sound.


At times I feel like pinching myself while I am waiting for the “other shoe to fall” – we are blessed beyond belief and I will be forever grateful!

Kelsey

Comments

Esther said…
Yes, Kelsey, no request is too small. Tears of joy for the spaghetti.

Popular posts from this blog

10 Years....

Mason, It is amazing how time passes by in the blink of an eye after you have kids…. It seems like just yesterday, yet this week, 10 years have passed since our life was turned upside down. The day our world took a turn we never saw coming. Each year leading up to the anniversary, I get anxious, emotional, sad, scared, and angry. I WISH 10 years later I felt differently. But I don’t. It almost feels just as raw as the day we were told…. This year. I am consciously recognizing what it is… MONDAY FEBRUARY 11 th ,2008. We sat in a room where a Doctor carefully articulated and explained to us about your special heart. There is one detail about this day I have seemed to forget in time. That is the name of the doctor who told us about our fate…. I could describe to you in details about anything else you might want to know, who was there, what we were wearing, what the Doctor himself looked like and the conversation we had. Yet his name, which used to be

Loaded Diaper?!?!?

Today's post title comes to you from the one and only Greg Garka... Thanks for the idea babe! As far as Mason is concernced today was another good day for our little man! We made our goal and got up and went on a total of three walks. The last walk of the night he spotted the “playroom” and was interested so we stopped and visited with our neighbors while he played. It was the highlight of the day. His appetite decreased today but that is to be expected since he hadn’t yet had a bowel movement (in 6 days)– however about 60 minutes ago things changed in that department and I am happy to report his bowels are working and back in action… During his echo he was again a crowd pleaser and was on his best behavior. The technician said that he was the best 3 year old she has done. It is so funny; he gets upset when something is about to happen and he doesn’t understand what. He tells us he is scared and then after we explain to him what they are going to do and that it won’t hurt –

Our Day at Children's

Hello all, Kelsey and I spent the morning at Children's Hopsital in Seattle today, what a place! They sure do a good job of trying to make the kids feel comfortable...part of me didn't even feel like I was at a hospital. We met with a Cardiologist, Dr. Vernon, and a Paranaetologist, Dr. Holmgren (yes, Mike Holmgren's daughter). Both of them were very nice and extremely informational. Dr. Vernon did confirm that Mason has HLHS and is a candidate for the Fontan Operations, which are the three stage surgeries he will have to go through to get his heart working as normal as possible. Kelsey and I have been talking about where we would want to do the surgeries in case we weren't comfortable with Seattle Children's. We knew going in that Children's in Seattle is one of the premeir hospitals in the country, but weren't sure how they were compared to other hospital's like University of Michigan with this particular heart disease. I'm glad to say that w