Thursday, August 31, 2017

Inevitable

Today we had an appointment at the Children's Heart Clinic.  
attempt at a family selfie
Not to be too dramatic, but overall things with Margaret's heart aren't really where her cardiologist was hoping they would be this far out from surgery (5 weeks yesterday...1 more week left until we can lift under her arms!).  Her pulmonary arteries have not grown like they hoped they would and the pressures are still needing to be addressed.  We both got a little bit of a pit in our stomach when our wonderful cardiologist told us that he wants to get Margaret back into the cath lab sooner rather than later, as in within the next week or two. 

helping mama hold the transmitter
Margaret has been a little "off" the last week or so and every now and then she gets a dusky look to her.  Last week it became extremely noticeable to me so I threw her pulse ox on to see what her sats were and they were bouncing around in the low 70s.  This is still okay considering her heart is continuing to adjust to it's new anatomy and her type of CHD but that doesn't make it less scary that's for sure.  She's also been getting extremely sweaty randomly which might suggest her heart is working harder.  
she's such a happy girl

We started with getting Margaret's pacemaker checked - she loves these ladies.  Lots of smiles, squeals and babbles came out of her and it's always fun for us to see her being so social.  The pacemaker still is functioning with about 10 years of battery life left which means it isn't needing to pace very often.  The data shows that it has paced 0.2% of the time since May and we suspect that is actually only from the time when it paced her right after her open heart surgery.  Margaret was a great helper and kept her hand on the machine to help hold it steady while the data was being transmitted. 

Next, we headed in for the dreaded echo.  I warned the tech that Margaret really hates these lately and he reassured me that he'd get what they needed and do his best to not upset her.  Of course, Margaret started screaming the second we went into the small dark room because I'm confident that she knows exactly what was to come...We tried having her lay on the table but she really was exercising her strong lungs and I ended up needing to hold her for the entire echo.  Once she got settled, the tech was able to get the pictures and measurements he needed and overall she did okay.  

I promise, the echo doesn't actually hurt
We spent some time talking with the cardiologist and are a little bummed with the lack of progress from surgery to now.  Unfortunately her echo today looked worse than the one they did after surgery so that means they need to do intervention soon.  I just got off the phone with the clinic and Margaret is all set for pre-op on Sept. 11th and the heart cath the next day on Sept. 12th.  

daddy's girl
The goal of the heart cath is to balloon Margaret's pulmonary arteries and maybe place stents if needed.  There is a chance that her arteries won't stay ballooned and the stents won't work.  Her PAs are around 3mm and a normal size is around 10mm.  If that happens, we'd be looking at Margaret having heart surgery at that time.  Bill and I are choosing to be optimistic and believe that the ballooning will work and if she ends up needing surgery, her team will take very great care of her.  We've got this.  Not exactly how we were hoping today's appointment would go, BUT, it is what it is and we shall continue to move forward.  
not thrilled with the news
zonked out




















Thank you for continuing to keep our precious warrior in your thoughts and prayers!  We're doing our best to keep everyone updated but sometimes it's nice to not have anything major to update!  

Wednesday, August 23, 2017

1 month post-op



Can you believe it?  Margaret's open heart surgery was 4 weeks ago already!  It is amazing how fast the weeks have gone by now that we are home and settled back into our routines.  
Thanks Susie for the adorable headband!!!

The emotions we've experienced over the last month have been kind of all over the board.  It's such a relief to see Margaret doing so well, thriving really, at home but it's also a bit terrifying.  You see, it can be easy to forget that Margaret has a fragile heart.  She's spunky, sassy and most of all SO SO happy.  Seeing her in pain was the hardest thing either of us has ever experienced.  When we brought her home after surgery she was still struggling with not feeling quite like herself and we were still working on weaning her off of a pain med -- not because she was in pain, but because she was struggling with withdrawal.  I wasn't sure how much we would be willing to share about our journey as a family impacted directly by a rare CHD but ultimately the goal is to spread awareness and sometimes that's leaving your comfort zone.  Sometimes that means sharing more than you thought you would be comfortable doing and I guess that's kind of how we feel when we update everyone with how Margaret is doing.  We don't want anyone to feel bad for us --- look at this beautiful little girl we have been gifted by such a gracious God!  No matter what we go through, we are together and we will continue to focus on the good while also giving ourselves some time to deal with not so pleasant emotions occasionally because lets be real, we are still human!


Anyways...back to Margaret 😊

She's was able to wean off of the pain med much faster once we were home.  It was AMAZING to see her realize she was home and her adorable smile and goofy personality soon came back a few days after she realized she was here to stay.  We had a post-op appointment a few days after discharge and Margaret's cardiologist was happy with how well she transitioned home.  We did learn that she will unfortunately need a heart cath in mid-September.  We were hoping we would have a few months before going back for another procedure but it is what it is and we just remind ourselves how amazing our team is and that they really and very truly put Margaret's health and well-being as #1.  Have I mentioned how great they are?  They are like family to us even if they don't realize it, we love them!  

Next week, Margaret will have an echo (cue anxiety!).  After the echo Margaret's cardiologist will meet with us and we will discuss the plan for the heart cath.  The heart cath will not be diagnostic this time, it will be for them to do more intervention.  Something about checking on the pulmonary arteries, measuring leakage in a couple of places and measuring the pressures more accurately and deciding from there.  We will be staying overnight.  

For now, we will continue to bask in all of the glory that is our life and remind each other how blessed we are with the life we've been given.  We worked hard to get where we are and are glad we can share our experiences with you all.  

In honor of it being 4 weeks since the big surgery, of course, I snapped some pictures of Margaret in her Heart Warrior onesie --- looks like I'll be needing to order a new one very soon!  It was awfully snug but With Hope & Grace does such a wonderful job and her products are high quality.  Sharon is a heart mom as well and she truly loves what she does and we love supporting a small business like hers.  πŸ’“


OH - those pesky teeth that have been trying to come through have FINALLY popped and they are the cutest!  We're still waiting for them to finish coming all of the way through but Margaret is obviously much more comfortable now that they've popped through the gums.  Success!

Friday, August 11, 2017

Post-Op Update

ready to go!
Today was our post-op appointment at the Heart Clinic.  Overall, things look good and we are happy with the progress she's made since her big surgery.  Can you believe how these heart babies bounce back SO fast??!!  We are in complete awe - seriously!
super irritated with the x-ray
We will go back in 3 weeks to have an echo done and follow-up with the cardiologist again at that time.  The pressures in the left and right sides of Margaret's heart are still a concern as are the size of her pulmonary arteries and the small MAPCAs.  The echo will give the team an opportunity to get an idea as to whether or not her PAs are growing at a sufficient rate or if they need to place a stent.  They will also be able to get estimates of the pressure measurements to see if they have changed at all since surgery.  After the echo we will discuss scheduling a heart cath for mid-September.  We are a little bummed to have to be going down this road already, but the anatomy of Margaret's heart is complex and we knew this all along.  A heart cath is much less invasive than open heart surgery and with the amazing advancements in technology we are extremely thankful that it is even an option.  During the heart cath the surgeon and cardiologist will be able to get precise measurements of the pressures, see the blood flow, place a stent (if needed) and be able to coil the unnecessary MAPCAs.  
trying to distract her while we waited

At this point, Margaret's heart is functioning well but one way to look at it is that it just needs a little more work to be done for a while.  The need for a heart cath does NOT in any way mean that her open heart surgery was not successful.  Actually, her surgery resulted in what the team wanted and we always knew there would be a cath scheduled sometime after surgery.  

Our appointment went smooth and was relatively quick, today.  The x-ray of her lungs looked great and we get to wean off of lasix over the next week and by then we will be done with the last med from the hospital stay as well.  This will leave Margaret only on a small dose of aspirin every 48 hours (so many alarms/reminders set to remember this one...it's kinda important...!) and her reflux medication.  This is remarkable for a kiddo who has a "broken" heart!  Definitely thanking God for her great blood pressure and sats! πŸ™Œ

oops - slept through lunch w/auntie
Margaret is absolutely thriving at home.  She had a couple of tough days and very rough nights but we seem to be getting back into our old routine thankfully.  We haven't gotten out of the house too much as we want to let Margaret's sternum heal and it's hard enough keeping her from being too wild at home let alone out and about where she tends to get extra excited!  We have 3 and a half more weeks of sternal precautions.  Technically she's allowed to do some tummy time now but she hasn't been very happy with it so we aren't pushing it.  

Shout-out to Aunt Jessie for treating us to a delicious lunch after our appointment.  Margaret says she's sorry she slept through most of our time together and promises to be more alert and exciting next time.😘
getting too big for this swing ha!

OH - for those wondering, the teeth that appeared to be ready to pop through while Margaret was in the hospital have NOT popped through yet.  The saga of teething continues...😜

That's all we've got for now!  Thank you for keeping our family in your thoughts and prayers.  




Sunday, August 6, 2017

up, down, backwards, sideways...FORWARD

the many faces of Mighty Margaret
Today we are composing this update with an overflowing amount of excitement!

Our weekend has been anything but boring.  Margaret had a very rough couple of days (again) and the result was a consult with the pain and palliative care team.  It was decided that the oral medication that had been prescribed in order to replace the IV med was not working well enough.  Apparently most kids can't tell the difference between the two meds but there are some who can...no surprise to us that Margaret can totally tell the difference.  She can also tell the difference between certain PPIs that she's been on for her reflux, but thankfully we figured that one out finally with help from her truly amazing pediatrician and team.  I'm hoping somewhere in Margaret's chart it's written in giant red letters the words:  VERY SENSITIVE TO MED CHANGES!  GLACIAL PACED-WEANING ONLY. πŸ˜†


Anyways, back to this weekend.  Yesterday, after consulting with the team, the dosage for the oral medication was increased to more of a moderate level - she was previously on a minimal dose with hopes that it would do the job.  Mom might have had a mini breakdown and finally told the doctors that enough is enough and clearly the current plan was not working.  The new dose seemed to be working MUCH better.  Phew. 

Advocating is hard.  I have a whole new outlook on how the families I work with must feel!

Overnight Margaret was able to get a solid 5 hours of sleep before waking up fussy.  She was able to calm down after a while and actually went back to sleep and woke up around 8:15.  We celebrated by accidentally disconnecting her extension from the feed pump and spilling formula all over me.  Whoops.  We couldn't help but laugh because that's totally something that has happened many times at home and it felt like we finally were able to think about something other than withdrawal.  
finally got some sleep!
our little fam bam

Margaret has been in a great mood and we can tell she's feeling a million times better.  It's absolutely crazy to think that less than 2 weeks ago she had open heart surgery!  It's kind of funny because I used to joke with Bill prior to surgery that this time we would bring her home with the glue still on her incision...guess not this time as the last piece of glue fell off yesterday.  Maybe next time we will be able to skedaddle out of here a little faster.  It's all up to Margaret, that's for sure.  

Overall, we are all feeling refreshed and super excited because discharge orders have been written and now we are just waiting for everything to be done!  We are going to RUN out of this place.  (discharge usually takes a while so we just hope to be home later this afternoon). 
adding more to her Beads of Courage



Friday, August 4, 2017

Breathing easier

Brace yourselves, this is going to be a long one but I promise to include pictures to make it more fun. πŸ˜‰

It's been a week, y'all!!!  
Tuesday/Wednesday this is how she looked...
Margaret had a rough couple of days this week as the IV meds were being weaned off.  At one point she hadn't slept more than a few 10-15 minute restless naps in a 24 time period.  It was awful.  Clearly the snails-paced weaning was not working and we had to switch to more of a glacial pace.  We also ended up adding a new oral medication as the IV med was decreased to help with lessening the discomfort that and it seems to be working well.  Yesterday and today have been so much better and Margaret looks and feels a lot more like herself.  She's still pretty unpredictable and we can tell that she's experiencing some discomfort but not nearly at the same level as she had been.  


loving the swing
On Wednesday the NP and Cardiologist let Margaret try hanging out without the oxygen support.  She was able to keep her sats within an acceptable range AND she made it through the night without needing it!  We were pretty pumped to see her sweet face without the nasal cannula.  Next up was the line in her foot.  Margaret hated having that one in and it randomly started not working so it was able to come out sooner than expected.  The only line left was the neck line and that one came out today!!!  πŸŽ‰

Thursday Margaret was feeling much more peppy and we even got to get her dressed in her jammies.  She insisted on having a bow, too.  Such a girly girl.  πŸ˜œ  We were able to get her into a swing and a high chair and get some actual playing in as well.  Margaret was excited about the change in routine - things can get pretty boring around here...I even was able to get a little giggle out of her while playing in the high chair.  SO fun to start hearing her make noises and facial expressions that she had been making prior to surgery. 
dressed, playing & watching Moana

Today, Friday, was a good day.  Margaret is still a little more irritable than normal but that's to be expected when weaning off of the type of meds she's been on.  We stopped the continuous feeds and have started working on getting her back into her bolus feeds.  She's done okay so far and unfortunately still refluxing pretty bad.  We can handle reflux.  Often we are asked what her baseline is and it's refreshing to be able to say "yep, this is what she was doing before surgery" and then it doesn't become a concern for the team.  We just need her to be at baseline in order to bring her home.  

The age Margaret is at can be hard.  Why?  2 words: stranger danger.  Margaret is typically extremely social and LOVES people -- seriously, I have videos of her trying to reach out to and play with strangers at the grocery stores.  She LOVES people.  It's been a bummer seeing her go through stranger danger here, though, but it's totally understandable.  This place can be scary when you're too young to understand why you hurt and that the nurses and doctors are actually helping you.  When someone takes a bandage off your tummy and it doesn't feel good, wouldn't you scream when you saw them, too?  As a result, Margaret has become even more of a mommy's girl and the poor nurses struggle with keeping her calm when I'm not here.  Thankfully we shouldn't be here too much longer and we are hoping Margaret becomes a social little butterfly again soon.  
more playing

We also discovered that Margaret seems to be teething more and we think her bottom two teeth will pop through soon.  Go figure, her body chose now, right after open heart surgery, to put her through teething!!  

Overall she's had an extremely busy but productive week.  We are very optimistic that we will be able to go home soon.  


helping update the blog

mommy's girl

Tuesday, August 1, 2017

Status Change

Today was a big day!  Margaret got switched off of a couple of IV medications and her pain med is now an oral one.  Of course, for Margaret, this means it goes into her g-tube so she doesn't have to actually take it by mouth - guess that's a "perk" of having it!  She seems to be starting to be more okay with being awake, too, but it's definitely still tough.  Child Life brought us some fun toys to play with and help get her moving a little more.  We've also seen PT and OT this week already and both have some good advice for helping get her movin' and groovin'.  


the look of pure exhaustion and maybe annoyance
This morning we got the go-ahead to have her arterial line that was in her left arm removed. πŸŽ‰Margaret was super cranky about having arm held straight while removing the line and then extra upset about her arm being held while the bleeding slowed.  She's such a champ.  SO tough.  I'm constantly in awe watching how she goes through all that she has to endure and still manages to flash us that adorable little smirk of hers.  I definitely would have put up more of a fight if I were in her place, but it goes without saying that both her daddy and I would switch places with her in a  heartbeat if it was possible.  Seriously though, look at that face!  How can you not feel terrible when she flashes that look at you...if looks could kill...

new room!




The other big news is that we got moved down the hall!  Margaret is no longer ICU status and that means a new room with a new view and a bit more privacy.  Margaret got switched out of the big bed and into a crib when we got to our new room.  She even played with me a little bit today in between trying to sleep.  

Since her art line is out, that means mom and dad finally get to hold her again (with help from the nurses, of course).  She still has a few lines (in her neck and foot) and is on oxygen.  We weren't kidding when we said weaning will be careful and slow for this mighty little warrior.  Overall we're making some great strides forward and home shouldn't be too far away.  

back where she belongs

On our way home last night "mom guilt" hit hard and a million questions raced through my mind as it felt wrong being home without our leading lady.  One highlight of being home, though, was finding the bows that I had impulsively ordered off Amazon were in the mailbox!  Yay!  πŸŽ€ Those of you who know us know that we've been spending our Sunday evenings taking the Dave Ramsey FPU course so it's become a running joke in our house to comment about whether or not Dave would approve of some of our spending...he most definitely would not approve of my ordering of bows but when your infant goes through open heart surgery, you make sacrifices.  πŸ˜œ We'll make up for it in our August budget. ha!

starting to be interested in playing!





OHS #2

Now that our big day yesterday is over and we've been able to get a few hours of sleep, we are feeling rested and ready to give a p...