Tuesday, August 23, 2016

Update!


I have been bad about updating over the past few days.  Matt is back at work, and I am trying to get the hang of this NICU parenting thing on my own.  Yes, we have nurses eager to help, but I like to try to do it all--it's good practice for when we get out of here (or in nurse code, "going to the zoo"--they say that instead of h.o.m.e. because babies tend to hear that word and then throw a wrench in the plan).   We still aren't really sure where that is on the horizon for us, it just depends on how Quinn continues to progress.

As of today, we have been cleared to "ad-lib" her feeds.  This means that because she had successfully taken 60 ml from a bottle, we could let her eat to her hearts desire every three hours.  This also included me being able to attempt breast feeding.  She's figuring it all out, and getting in between 60-80 ml a feed between bottle & mama.  What a big girl! We are really focused ultimately on Quinn's ability to pack on the pounds.  She had a steady increase but went down a bit as of recently.  Last night she seemed to level out and remained exactly the same.  We are hoping that is a sign she is going to go up tonight! If she can continue to eat, have semi normal bowel habits, and gain, we will officially label her as the cutest, biggest, badass peanut that ever lived (no bias there ;)  But really...we are so so proud of her and so impressed by her each and every day.

So for now, we continue to let Quinn tell us what she needs and let her little body figure things out.  When she is ready to "go to the zoo", her body will let us know.  For now, we will keep snuggling & spoiling her rotten.

Quinn Loves:

  • Eating & Snoozing
  • Having her hands up by her face (or attempting to claw her eyes out--mittens have come in handy, although I find them to be hideous and annoying)
  • Her nurses who always stop by to check in, even when they don't have her: Lindsay, Rachael, Kat, Melanie, & Brooke.
  • Her new book from Emme & Jack "Wherever you are, my love will find you" (try reading it without sobbing--I dare you)

Quinn is not a fan of:
  • Her "care" every four hours (vitals, measurements, temperature probes & diaper changes)
  • Having to wait to eat...you think her mama gets hangry--she takes it to a whole new level
  • Being in the NICU...everyone here has been wonderful, but she wants out!

    

Wednesday, August 17, 2016

25 ML

Let me tell you what I don't like...doctors and nurses who feel the need to rain on your parade or take away every ounce of positivity you are hanging onto.

The goods news, Quinn has continued to up her feeds by 5 ml a day (today she is at 25 ml -- whoop whoop). She hasn't thrown up or shown any signs of discomfort, other than that the girl is starving and about 30 mins before each feed she gets hangry (who could blame her-like mother like daughter). Our girl has also consistently gained weight over the past 5 or so feeds, weighing in at 5 lbs 11 oz!

What are we watching? Her poop--as usual. I have always been particular about my bowel movements, but never did I think my days would revolve around my sweet girls bowels. If things get too "watery" or too frequent, we will have to pull back on feeds and give her belly a chance to adjust. We need to be sure she is absorbing nutrients to grow.

Here is where the "what I don't like" comes in. Yes, I get that doctors and nurse practitioners have to be cautionary, they want to keep us informed of all possible issues, but for once, how about a "wow, Quinn is so strong and doing so well" without following up with "let's talk about 3 possible things that could by chance happen".

In order for me to survive this roller coaster, I've surrendered to positivity only. So far Quinn has surpassed any and all expectations of her as she heals. I don't have room in my life these days to play over in my head all of the "what ifs". Today, she continues to kick butt and I believe in her and her strength to get better more than I've ever believed in anything. She wants to be home where she belongs just as much as Matt & I want that and I know it will happen. She is going to do things in her own time and while she does, the two of us will remain her biggest cheerleaders. We continue to spend as much time snuggling her as possible!

In other news, we finally started to put big girl clothes on her. Poor thing lived swaddled up in a diaper for way too long.  She has also become quite famous around here with lots of her favorite nurses popping in every day to check in on her, or just to visit.

Thanks for buying me clothes that are small enough to fit Grammy, Aunt Julie Alloway & Shari Bland! New polka dot blanky compliments of Grandma Ullmer.  


         

    

Sunday, August 14, 2016

I'm Eating!

This weekend our girl continues to amaze us! Yesterday Quinn started bottle feeding, receiving just 5ml's of mama's milk every three hours.  It took a little practice to start, but by the end of the day she was a pro.  She also had her biggest poop yet...and you know how we feel about poop around here! I took pictures and got teary eyed and was way more enthused than the nurses.  After her successful day yesterday, they have slowly increased her milk by another 5ml's.  She drank round #1 (of her 10 ml's) like a champ this morning--so far so good.  As her milk intake continues to increase they start to back off on her IV nutrition.  It's a balance so ensure she is getting what she needs and starting to grow.   She is back to her birth weight essentially, maybe a touch bigger, and we eagerly await her "weigh in" every evening.  We continue to cross our fingers for regular poo's and continued tolerance of her feedings.  I don't know where this girl gets it from, but she is such a badass (is it bad to say that about your 18 day old daughter?!?!).  She has been faced with more in her first few weeks of life than most people ever endure and she just keeps hurdling over each milestone.  We are the most proud parents and have so much confidence in her strength to keep moving forward.

Since she started her feeds, she has become quite the smiler--everyone's always happier when they're well fed, right?!?!


Friday, August 12, 2016

Friday Progress!!


What do you notice about me today (other than that I am really stinking cute)?!?!?!?

Today we took another step forward.  Quinn got her OG tube removed early this morning.  Surgeons noted that Quinn's x-rays are showing more normal gas patterns within her intestines, and they are hearing "bowel sounds"when they listen to that little belly.  Her OG output was also significantly lower and light in color, therefore, they pulled that annoying tube out today.  We are crossing our fingers that her body tolerates it, hoping for no throwing up and no belly distention.  So far, so good.  

Doctors keep prepping Matt & I with the fact that there are almost always set backs, and that it is not smooth sailing with procedures like this-so we are cautiously optimistic.  With how hungry this little nugget acts, she is ready to start eating, and we just know it.  She tries to eat her hands, her PIIC line, her blankets, and whenever Mama holds her she is fiercely searching for milk.  We continue to be blown away with how strong and tenacious our little peanut is, she makes Matt & I stronger as parents just because of who she is.  We have a feeling that she will give us a run for our money as she grows up--but we wouldn't take her any other way.

As always, thanks to all of you who continue to show your unwavering support of our little family of 3.  As we open up gifts, and cards and eat the meals people drop off, we are consistently teary eyed and so blown away by how many people out there are thinking of our girl.  No words will ever be enough to thank you.

PS- thanks for the cute swaddle blanket aunt Kate & Maddie! It was perfect for our tube free photo shoot!

XOXO

Thursday, August 11, 2016

Hats on Hats






















Today has proven pretty uneventful as far as milestones go.  Quinn's OG tube stayed in today, and it's looking like tomorrow may be the day to remove it--barring any issues tonight.  The girl can't wait for that tube to be out, she tries to pull it out herself any chance she gets.  The surgeons took off her steri strips today from her incision, and it looks really good (I joke with her that we are twins in that department, but her precious little belly has healed way faster than mine).

In the meantime, we have been sporting a wide variety of new headwear compliments of our many friends and visitors.  Since we can't dress her up yet, hats and headbands are our go to, and we enjoy staring at the little peanut in all of her cuteness as she models them. Thanks to her babe aunties, aunt Sara, and to Mary for keeping keeping our girl stylish :)



   

Wednesday, August 10, 2016

Happy Two Weeks

Here are a few of our favorite pictures of our sweet girl on her two week birthday.  It was hard to narrow it down from the 348 pictures of her in our phones.  Clearly she is a fan of having her hands by her face (unless we are holding those sweet little hands - aka our favorite thing to do).


               





G.I. Update: The suction tube was turned off today to help with Quinn's digestive recovery.  If all goes well, the tube should come out tomorrow or the following day.  We are excited for every little step of progress she makes.  Keep those prayers and positive thoughts coming.  They are certainly helping.

Tuesday, August 9, 2016

Thank You


Since the day Quinn was born, and still each day that passes, Matt & I have been so completely overwhelmed with all of the love and support we have received.  From thoughtful calls and texts, to cards in the mail, gift cards, meals, visits, we don't really know how we can ever thank all of Quinn's "fans" enough.  Without a doubt, we couldn't have made it this far without all of you, and we thank you all from the bottom of our hearts for standing by our little family of 3 as we continue on Quinn's journey to recovery.  We talk about all of you with her as we pass the time each day, so know that when she comes home, she will be super excited to meet you all.

Thanks for being on team Quinn (and team Matt & Carly), we are beyond thankful for all of you each and every day!

G.I. Update: Quinn's OG tube output is looking clearer by the day, a lot more "spit" like.  We are waiting for it to lessen in volume.  Her x-ray isn't showing much air passing through her GI tract yet, nor do we hear any true "bowel sounds" when they listen to her belly, BUT, we know it will happen soon.  Just like Quinn entering the world...she will do it in her own time (we just hope that's soon).  Once those things start to happen, we look forward to moving onto the next step in the process--thinking about feeding.  For now...we wait, and we snuggle that little peanut 24/7.

XOXO


Monday, August 8, 2016

POOP

If it wouldn't deter you all from reading on, I would post all of the pictures of Quinn's diapers that we have taken over the past three days.  Pooping is a sign that Quinn's bowels are starting to wake back up post surgery.  She has started to poo lately (although it isn't typical poop, it's something) and Matt & I celebrate it, and document it.  Fingers crossed for this to continue, and for Quinn's bowels to wake back up!

Hi! I'm Quinn


Wednesday, July 27th at 3:30p.m. our sweet Quinn decided to join the world a bit early, 4.5 weeks to be exact.  There was nothing like the moment that the doctor held her up and said "it's a girl" and from that moment on Matt & I have been totally in love.  She was perfect in every way, a tiny little peanut weighing 5 lbs. 6 oz. Popular opinion is that she looks just like her daddy, but has her mom's personality (particularly the sass).  I like to think that she has a little more of me in her than that, but baby girl is going to need that sass to get through the rest of our hospital stay, so I guess that is a good thing.  

Two days after Quinn's birth, she was taken to the NICU because she couldn't seem to keep anything in her belly.  They ran some tests and took x-rays and found some shadowing in her mid section.  We were transported immediately to Children's Hospital, where we have been ever since.  

Quinn was diagnosed with type IIIb jejunal atresia, a very rare type affecting approximately 1 in 60,000.  Her surgery was extremely complicated but our surgeon is one of the best in the country and we feel so fortunate to live in Columbus where Nationwide Children's is so highly acclaimed.  Quinn has already demonstrated her tenacity and strength as she made it through surgery like a champ.  Only two days post surgery our little fighter came off of her pain medication and was extubated.  Two days further and she didn't even need her nasal canula to help with her oxygen intake.  We are proud parents :)

As of today, 8/8/16 Quinn is breathing on her own, and working on getting stronger and stronger by the day.  She receives nutrients via IV since she can't have mama's milk yet (although props to the girl for trying to find it every time we snuggle--she knows what she wants and will be quite the little eater when she is allowed).  At this point, we continue to watch the contents from her OG tube to look for it to turn clear/yellowish and lessen in volume.  This will be out indicator for when we can start instituting feeds. Essentially, it is a waiting game to let Quinn's intestines learn how to work again.  SO....we wait.

One thing remains the same for Matt & I, we love this little peanut more than life itself and finally know what it means to be parents.  We feel so fortunate that Quinn chose us to be her parents, and we wouldn't do a thing to change it.  Although this has been the most challenging thing we have had to endure, we know that our love, the love of all of our family and friends, lots of snuggles, and lots of prayer, and Quinn will be back at home with us where she belongs.