Tuesday, August 31, 2010

home again home again...

A friend mentioned that I needed to update the blog, since I hadn't since Kate went back into the hospital.

All is well, Kate came home again last Friday night. It isn't exactly clear what the problem was, but it was likely a virus and unrelated to the surgery. I think she just wanted all the attention again that the nurses give her because she's such a cutie.

So she's home, and healthy. She is suddenly growing like a week, and laughing and giggling all the time. We'll keep the blog occasionally updated with the big news, but otherwise, you can still look for the Daily Kate on facebook.

Much love!
Team Kate

Friday, August 27, 2010

Burnin' for you




Well, evidently Kate was missing all the attention she got from the hospital nurses, so she cooked up a plan to go back.

Last night I cam home from a great first night's class to find Brandi looking pretty exhausted and Kate looking pretty restless. But oh, the night had just begun. A mild fever kept her hot, sweaty, irritable and just generally loud and fussy. All night. Did I say all night? Yep, all night. By 7am, her fever was only going up and it crossed over that threshhold that the nurse had told us when she was discharged. So I called the advice nurse. 30 minutes later, i was checking in with Little Kate at the ER.

Did I mention she was awake all night? Well, y'all also know what that implies...I was too. Just sayin'.

So back to the ER...by 2, she had finished a chest xray, echocardiogram, an array of blood tests, seen 2 pediatricians and her cardiologist. And, nobody could figure anything, except that she was hot. So the admitted her out of an abundance of caution.

I like that they use that abundance of caution. She is blessed to get this kind of care. So now, she pretty much just being watched. Her fever is up and down and up and down and up and down. But the good news is that she did finally rest...but not until about 7 pm. (Which of course means taht now that it is midnight and I am ready to collapse from being tired that she will now be wide awake! But alas! There is a wonderful nurse here tonight to help answer those midnight cries who is a bit more used to the night shift than I am.

She won't go home until the fever subsides. We are hoping that it goes away with the same manner that it came...quickly. I'd sure like to be back home tomorrow.

We'll keep you posted. Much love,
Team Kate

Thursday, August 19, 2010

HOOOOOOOOOOOOOOOOOME!!!!!!!!!!!!!!!!!!!!!!!



Little Kate came home today!!!!!

What a celebration! And what a journey! Seriously, looking at her today, you would never know that 9 days ago her heart was rebuilt. That 8 days ago she was miserably uncomfortable. That 7 days ago she was nowhere near smiling...Today, you'd look and see a smiling, giggling, cooing, flirting little squirt who is already back to playing with her big brother and tugging on her favorite labrador for kisses. Grandma Diane is finally getting to snuggle her forever and is completely adoring every moment.

Just fyi, Kate chose today's music. The last week, I've tried to thematically match the tunes to the post. Today, I was hunting for a song of celebration. Song after song got no reaction from Kate. But when I chose "Everybody Dance Now" she started to wiggle and groove, and then she started to completely giggle and couldn't stop. Perfect.

Thank you for all of your thoughts, prayers, notes, emails, comments, likes, and most of all, love.

Kate is an incredibly special little girl who I know will fill this world with pure love. I am glad she has touched your heart.

Much love,
Hallie, Brandi, Rhys, and Kate (and of course, Dodger!)

Wednesday, August 18, 2010

Feeling stronger every day


Kate got her chest tubes out yesterday, and as you can see she's pretty happy about it. She flipped right onto her tummy and started back to work on learning to crawl. I am amazed at her strength and determination.

I also got to actually hold her for the first time in a week. I thought she might want to cuddle and snuggle, but after about a minute of that, she pulled right up to a sitting position, where she stayed for the next our. She waved and blew kisses to anyone who went by like she was in a parade. What a sweetheart!

She comes home tomorrow barring any surprises today. I have a suspicion that they will send us home with some oxygen for when she sleeps, but we'll see what happens. We are just happy that she's headed home soon.

Much love!
Team Kate

Monday, August 16, 2010

Almost there!!

Today I walked into Kate's room and she SMILED!!!!! What a treat. I have missed that smile so much. It wasn't her biggest smile, but it was definitely there. And then, as if that wasn't treat enough, she giggled a soft giggle and then spent the next hour touching my face and my faux hawk. I believe she is starting to feel better!

The chest tubes will come out tomorrow, and with that she will get to lose the oxygen tube/mask in her nose. She is going to be SO happy about that. The best part about tomorrow will be getting to finally hold her.

And then....she's comin' home!! Probably Wednesday, if not then Thursday. How about that?? It seems to take forever, and then at the end, the time just flies. I am glad we are in the flying stage now.

Thanks for all the thoughts and prayers. She's got a whole lot of love, this little one.

Much love,
Team Kate

Sunday, August 15, 2010

"I will protect her"


Today as Brandi and I were leaving for the hospital, Rhys said to B, "Mama, I want you to tell Kate something for me. tell her I love her, and I will protect her." Now if that isn't enough to just melt your heart! It is amazing how much love a 4-year-old can feel for his baby sister. He really misses her, and can't wait until he gets to visit, and even more, he can't wait until she comes home.


The good news today was that Kate was doing well enough to move her out of the PICU and into the regular pediatric wing. She still has her own room, which is more comfortable for us visiting, and still has a nurse assigned to only 1 other patient. She also still has the 3 chest tubes in and an oxygen mask with two little tubes that shoot pure oxygen into her nose. She really dislikes all of these!! She can remove the oxygen mask in a fraction of a second, all you have to do is look away for a moment! The chest tubes don't just annoy her, they actually hurt. We are hoping that all the drainage comes to an end so that she can get those taken out. In the meantime...morphine!!


She had a pretty good day. We are still waiting for that smile, but she certainly showed some good ol' Kate spunk. She kept trying to roll onto her tummy like she was going to just crawl away. she played with her feet and kicked, and for a while when I was cuddling her, she put her arm up on my shoulder and gave a little hug. Maybe, just maybe, we've turned that elusive corner.


Thanks again for all the positive thoughts! We enjoyed seeing some good bubble photos, especially from cousin Josephine. (When I showed Kate the picture on my blackberry, she tried to take it from me. I think she wanted to text her cool Seattle cousin!!)


Much love!

Team Kate

Saturday, August 14, 2010

Kate is an icosahedron

An icosahedron is a 20-sided figure. I say Kate is an icosahedron because every time I feel like we have turned the corner, there is another corner. It's fevers, and potassium levels, and extra fluids, and general discomfort, and contact rashes, and and and. And it's all part of recovery. She's doing just fine, it's just that recovery is hard.

Here is a list of other things that are hard:
Hearing her cry and not being able to just pick her up and hold her.
Not being able to make the hurt just go away with a kiss and a bandaid.
Leaving her each night at the hospital.
Leaving her sweet brother each day to go back to the hospital.
Waiting.

I know it's all just time now. She gets a little better each day, even with all the challenges. And in 2 months, she'll likely be right back to her old self working on crawling and getting into all kinds of mischief. But for right now, tonight, this is hard.

So as not to leave anyone on a downer note, she played with bubbles today. She was crying and uncomfortable, but had already had all her medicine for the pain. So the nurse brought in some bubbles, and for the next 30 minutes, as I blew them, you could just see total satisfaction in her eyes. She watched, and tracked, and savored them. And she stopped crying. So, as a little tribute to Kate, go blow some bubbles today and bring some joy into the world. And if you do, take a picture and send it to me. we'll print it out and put it up on her crib so she can see all the fun.

Much love,
Team Kate