Grandma, my mom, is now bed ridden with a disc issue. Her leg has been bothering her for quite some time and apparently got worse when she was out stalking Dr Ghisoli walking Tau a few weeks ago. Last night the pain was so bad that she couldn’t sleep and so she finally went in to see the doctor. She needs to have more tests run, but the doctor thinks it could be a collapsed disk. For now she is flying high and snoring away thanks to some good pain meds. Hopefully dad remembers to check on her to make she is breathing every few hours.
Author Archives: teamfricke
Wrong Direction, But Still Smiling
Early this morning Cutler started to run a fever and was still crying out in pain. He was immediately started on antibiotics as well as given pain meds. By 3 am I was able to lay him back to sleep in his bed where he slept until around 8 am. His fever has gotten as high as 102, but fortunately has stayed pretty low throughout the day. Blood has been drawn and multiple tests are being run to detect any potential infections as well as a chest xray was run. The doctor did say that the fever could be from the inflammation as he continues to receive tons of fluids including more and more blood. I tease the nurses that they should just draw the blood for the tests from the bags that they hang as it seems like they pull out as much as they put in.
For the pain, Cutler has been put back on the constant drip where he receives a dose of fentanyl hourly and the button is always there when I need a sleep/potty break he is showing pain. He is also getting a diuretic to help with the fluid retention. He did spend the majority of the day napping in our arms, but I did get a full hour of play time with him this evening when I relieved Nana. For now he is fast asleep, hopefully for the night and we will just pray and wait for the test results.
Together Again
After a quick road trip and a couple days isolation due to an ear infection, Cutler and I are back together again. I forget where Melanie left off, but things have been going pretty well so far. there was some concern about the area of the line due to some inflamation, but it looks like all is well there now. He is continuing to cough up and sneeze some blood tinged mucus and the mucus is now getting so thick it is causing some choking. Starting today he has had issues coughing up the mucus to the point he turns red and eventually vomits it up. We have also started to use the suction to help him out, but it is quite shocking to see it happen for the first time. I will be sleeping lightly in fear of him choking on it in his sleep. Hope to get better situated with the computer and pictures tomorrow where I can give a more thorough update as well as some stories of Mason from the weekend.
At last…a picture!
This picture was taken on Wednesday, Dec. 9 and as you can see, he was very happy. Cutler had another good day today, however, around 7:00 Grandma noticed the area around his central line was a little swollen. The doctor stopped the TPN (steak & potatoes in a bag) and started more fluids. We’re hopeful the swelling goes away tonight, and that the central line isn’t leaking. The last thing the little guy needs is to have another operation on his central line!! I’m happy to report that he is sleeping soundly.
Mason and I had a special day – I picked him up early from school and we spent about 3.5 hours at NorthPark mall. We saw 2 puppet shows, toured the train display, tried to have our picture taken with Santa (along with thousands of other like-minded families), and shared ice cream. He has been such a good boy lately I felt he deserved some one-on-one time. Poor little guy fell asleep in the car on the ride home! Will post pictures tomorrow.
Aaron is taking the red-eye home from Seattle…which will put him in a fantastic mood, I’m sure. We all look forward to having him home!
Absence makes the heart grow fonder…
If Aaron had left the “thingy” at the hospital, I could have downloaded some great pictures from the camera to the laptop to the blog… I’ll get some up tomorrow or the next day. So far so good this Day +6 (transplant day + 6 days). The doctors and nurses have been telling us that most kids are very sick at this point, with mucisitis or bad diaper rash, but not Cutler! Superbaby has spit up some mucus the last couple of days, but once he does, he’s ready to play some more!
Thank you to the nurses and doctors at Medical City who are taking such wonderful care of Cutler. A sincere thank you to my mom and Aaron’s mom who have been working shifts at the hospital to give me time to rest and time to hang out with Mason while Aaron is out of town. And I can’t forget Aaron’s dad, who is doing me a tremendous favor by keeping the refrigerator uncluttered of leftovers! And of course Mason, who continues to be a sweet and understanding little boy – most of the time 🙂 The biggest praise goes to God, who is keeping a watchful eye over Cutler and laying His healing hand on my precious little baby.
I hope everyone is feeling the blessings of this holiday season!
Great Sendoff
Cutler provided an incredible send off for me today. He woke around 8 am and was in the best mood that I have seen him in for quite some time. He had an incredible amount of energy and just wanted to play all day long. His usual smile was almost constantly on his face. This is the best I have seen him since we started the prep for the transplant and I think if we had the exersaucer there he would have been jumping the entire day. He even drank 2 oz of pedialyte for me. I believe this was his way of reassuring me that it would be alright to leave town for a few days. What an incredibly strong and loving baby we have. We are extremely blessed.
Oh and I have been meaning to reply to a question from the “comment hog”, Aunt Linda, his transplant date is considered to be his new birthday here as well. So going forward we will have two birthdays to celebrate for Cutler. 3/14 and 12/3.
Fresh Picture, Get Em While They’re Hot
Bleeding And Pain Under Control
Looks like, for now, we have the bleeding and the pain under control. Since the last changing of the dressing yesterday morning, we haven’t had to make another change and judging based on the color of the gauze the bleeding has stopped.
It also looks like the fentanyl drip is working. The drip sends the meds to him every hour, but we also have the option to press the magic button every 30 minutes to send more, but so far we haven’t had to press the button. Even better is that despite the constant flow of pain meds, he is not overly tired and sleeping all of the time. He is back to his happy and playful self, just without showing any interest in eating. As the mucasitis continues we may have to start suctioning him a bit to help with the discharge and I can hear it in his nose already, but at least he is comfortable.
Unfortunately I have to fly to Seattle on Tuesday morning and not get back until early Friday morning, so I am going to spend a little extra time with him tomorrow. I keep praying and telling Cutler that if an infection is going to happen, he has to hold off until Friday when I can be here for him. It’s funny, when I was sick I didn’t get to see him for longer than I will be in Seattle, but the thought of being away for so long makes it more difficult to handle. However, I am not going to complain as my company has been ridiculously accomodating and understanding about everything we are going through, so a few days away won’t hurt us.
Below are a few pictures of Cutler playing. I will do my best to show Melanie how to get the photos off the camera so we can keep providing them while I am away.
Exciting Night At The Mavs Game
No Pain Like Your Child’s Pain
Unfortunately Cutler is still in a lot of pain from the mucisitis and cried out several times throughout the night to let me know. On top of that pain, he is also having to endure the pain of having his dressing changed multiple times since yesterday as the blood is still not clotting. They say that his platelets are alright, but he will be receiving more soon and he was also provided with a medicine called amicar that should help in the clotting process. With the most recent dressing change they have applied some more surgiseal and gauze with pressure prior to applying the covering so we are hoping that with the pressure and new gauze it will finally clot.
Just watching him go through the pain he is makes me realize that there is no pain as great as that of your children. It breaks my heart every time to watch him go through the dressing change especially when they clean the area and you can tell the alcohol wipes are burning him. But amazingly enough, Cutler quickly recovers and reminds me that pain is only temporary. Regardless, we are waiting on a pump to have a fentanyl drip set up so that we will have control, with the friendly button, on how often he receives the relief. Below is a picture of Cutler showing his strength not ten minutes after one of his dressing changes.







