August 26, 2013

UPDATE (8/26/13)

HOME 2….the sequel

#GoBeckett
#ODAAT

August 25, 2013

UPDATE (8/25/13)

Honestly, not much to update tonight:

Both my parents were here again (came all the way down from Ohio just for the day!), and spent some good quality time with Beckett. We were greeted with the news that Beckett had a fantastic night last night (which is always music to my ears!). He was just laying in his bed…just cooing and playing. Other than him throwing up a few times today (which weren’t devastating), he was such a good boy today! When he was awake, he played, otherwise he slept (mostly in my mother’s arms). My mom kept saying politely and confidently, “I’ve got the touch.” It was funny. My Dad gave him a few trips around the floor in his wagon…and like I said, we mainly just played and slept.

Soooo, we are just holding our breath concerning tomorrow. We truly don’t know much yet, but what I do know is that a lot will need to perfectly fall into place to make tomorrow a complete success (from my finite mind’s standpoint). We’ll see how it unfolds……either way, “To God be the Glory, Great Things He has Done!”

#GoBeckett
#ODAAT

— with Leah ‘Whiteley’ Rupp at Riley Hospital for Children at IU Health.

August 24, 2013

UPDATE (8/24/13)

Not much to report on today:

I pretty much just hung out with Beckett all day. He’s been whimpering a lot, but it wasn’t until later this evening that I remembered they weaned his methadone again yesterday (they really really wanted to), and we might be seeing the first signs of the withdrawal from that wean. But he wasn’t mad all day. We went on numerous wagon rides, hung out in his room, practiced sitting up, we played with his toys, I played guitar for him, played peek-a-boo…..all kinds of stuff. He’s such a smiley/good little boy (most of the time). He usually is only ever mad or upset if there is actually something “wrong”, in which case he obviously deserves to be a little fussy.

As you might have read from yesterday’s post, we’ve been anxious to find out about those goofy little beats Beckett dropped yesterday. Remember, one scenario is bad and the other is acceptable. Well, our nurse told me that the Cardiologist didn’t feel comfortable sharing his thoughts with me about it until he spoke with our Cardiologist. To be frank, that kind of freaked me out. So I tried to text that to Leah (cause she was at work today) in a way that didn’t sound bad or make her worry…but I think I failed because she has been on edge all day about it too. So I decided to just take a deep breath and just wait. So I waited, and waited…and waited some more for the Cardiologist to even come and tell me something. 3:00pm rolled around, and I decided to solicit some clarity. I told one of the nurses at the front desk that I’ve been waiting to hear from the Cardiologist today about an “issue” with my son, and asked if she could page him. She told me she’d try. About 5 minutes later I was told that the Cardiologist had already left for the day and that she was able to get a Resident to come and try to answer any of my questions.
Ooooooo.K.
So up came a Resident in which I proceeded to ask for clarity on their opinion on Beckett’s heart rhythm issue from yesterday, she said she didn’t really know much…and that she thinks they are just gonna wait it out until Monday and talk about it then.
That would have been nice to know.
Again, we are trying to assume that no news is good news…but things like this can be unsettling, and not encouraging to our goal of being discharged on Monday morning at some point. But I guess I’m thankful we are being “better safe than sorry”.

I was also told today that IR (the ones who did his J-Tube), may want to redo his stitches on the J-Tube. The stitches are “loose” and are quite irritable to Beckett. However, IR is off on the weekends, so we have to wait till Monday on that as well.
Oh dear.

So here we are, just kinda sitting on our hands (once again), waiting for Beckett’s withdrawals to start kicking in full-swing (not good times), waiting on answers, making countless laps in a wagon, hoping to go home, yet realizing it could very well be delayed once again. It’s hard not to get frustrated, discouraged, and even angry…..but as I was telling a friend today, perspective really is key. I’m thankful I even have Beckett here with me today to get angry “about” (not at him, the situation). As I continue to say over-n-over, this is clearly not the story for every parent we have met these past 8 months…and we are truly thankful for the struggle, it just reminds me that we still have our son to struggle over……..one step at a time.

Psalm 139:1–4
O Lord, you have searched me and you know me. You know when I sit and when I rise; you perceive my thoughts from afar. You discern my going out and my lying down; you are familiar with all my ways. Before a word is on my tongue you know it completely, O Lord.

#GoBeckett
#ODAAT

— with Leah ‘Whiteley’ Rupp at Riley Hospital for Children at IU Health.

August 23, 2013

UPDATE (8/23/13)

Please excuse my brief update. I usually try to provide details that are both informative and engaging….but today I am feeling a little drained. Not because we had a bad day or anything, but more-so the fact that it’s been a long 8 months (almost), and these updates can sometimes be challenging to compose.

Beckett has had a much better day once again today. We hardly had to give him any meds to settle him; maybe a lil Advil and/or Tylenol. Though he definitely had his moments where he got tired and grumpy, it was nothing a lil orajel and/or a wagon ride couldn’t fix. Thankfully Leah was able to actually hold him today and console him that way (in which I heard her whisper while holding him, “I missed this”. That usually hasn’t been working because of the sensitivity of the newly placed j-tube in his belly. She had to be careful, but he certainly seemed to like it (once again).

Two more things:
1) We are possibly on track to being discharged on Monday…which would be awesome!
2) But, they did find some very unique and potentially very undesired heart rhythms today in the telemetry room that could either be signs of a “bad thing” or signs of an “insignificant thing”. Clearly we are hoping and praying for the “insignificant thing”….but we are now waiting to hear back on the overall consensus from the team. Hopefully we’ll know more by tomorrow.

That’s about it. Love you guys! Goodnight!

#GoBeckett
#ODAAT

— with Leah ‘Whiteley’ Rupp at Riley Hospital for Children at IU Health.

August 23, 2013

“Faces-of-Beckett”
….with a touch of crazy hair!

20130823-175641.jpg

August 22, 2013

UPDATE (8/22/13)

I was at home (in Upland) this morning getting ready to put in a full day at work, and couldn’t shake just how discouraged and tired Leah sounded last night from the exhausting day with Beckett. I decided to call Beckett’s nurse and see how his night went and she blew me away with how many drugs they had to give him throughout the night just to keep him mildly calm. She explained that they gave him some Ativan last night before Leah even left; after she left, however, he received Benadryl, Tylenol, Morphine, his scheduled Methadone, Lortab (Hydrocodone), and even another dose of Ativan this morning. Un.be.liev.able! And yet he was still angry. It literally brought Leah to tears from both physical and emotional exhaustion. No matter what she tried yesterday, nothing worked. And as parent, that can really do something to you; you can easily feel discouraged from the inability to console your child.

So, as I was saying, I was in Upland and decided to meet with my boss/friend and tell him that I just don’t feel right not being there for Leah today. He agreed and said (something along the lines of), “Ten years from now, you will not regret leaving us on this day to spend time with your family.” Wise man….good man.

So, off I went, back down to Indy once again. As I was pulling into the parking garage at the hospital, I saw the most beautiful woman walking from her car into the hospital, naturally I couldn’t help but whistle and say, “hey there, hot stuff” (nice and cheesy). Yeah, yeah…it was Leah. But it was great to watch her handle a car coming from behind her with a dude whistling at her. Ha…perfect timing. Of course she asked what I was doing there, and I simply told her that I’m on “Beckett Holding Duty”, and that we are going to figure this thing out.

As we were walking up to his room, Leah asked me her infamous and impossible question, “Is Beckett ok?” You may think that question is similar to, “Do I look fat?” In which we men have learned to never hesitate, but quickly, confidently, and with an unrehearsed tone simply reply, “No”. Well, I struggle with this question from Leah. Nowhere in scripture am I guaranteed Beckett will pull through this. Just as nowhere in scripture are YOU guaranteed to live to see tomorrow. I believe that Beckett is doing well, and I truly believe my God can heal (continue to heal) my son….but I have never “been told” how this story will end. I prefer to echo a man’s phrase, in whom I greatly respect who is currently battling cancer, in regards to that question, “He can, He will, and even if He doesn’t”. Kind of deep….but kind of simple. In this particular moment I told Leah that they have ran many tests (x-rays, and echo on his heart, they’ve checked his levels), and everything is normal. He isn’t running a fever….he’s appears to be “ok”. We just need to be patient with him and continue to try to figure this out. She couldn’t help but respond with, “but those aren’t answers”, in which I replied, “they sure are, they are answers that everything is ok”.

Well, as we approached his room, he was awake and kind of playing. He actually lit up and we played with him for a little while until he started moaning and grunting a bit. I asked Leah if I should pick him up (which is usually the golden ticket for him when he’s cranky). Though it wasn’t working at all yesterday, we decided for me to give it a shot. Well….long story a little shorter, he flipped out. He went absolutely bonkers. The nurse came in and started to suggest some medications, in which we refused at the time. I asked Leah if she tried a wagon ride yesterday (they have a bunch of little red wagons here, and Beckett seems to enjoy rides in ’em when we can). She said no, so I said, “Well, we could just be carting a screaming baby into the hallways, but I say it’s worth a shot.” So off we go, and almost as soon as we rolled even a foot outside the room, Beckett stopped crying! Amazing! Leah and I made lap-after-lap until it appeared he was finally getting a little tired of it. We came back to the room, in which, Beckett began to cry again. This time we were informed that our previously inquired suggestion of using orajel for his teething (which was shot down from a resident) was unequivocally signed off on by one of the Cardiologists. So we applied a little to his emerging teeth, and within 10 minutes, he was a brand new baby. Amazing (again)!

In conclusion (at least as of today), our best friends were not narcotics, but rather a little red wagon and some over-the-counter orajel. So Awesome! Every time (and I mean EVERY TIME) Beckett began to get mad, I would try one or both of those solutions (we can only give the orajel once every few hours though)…and it worked like a charm.

Sooo, later on Leah left to go to her younger sister’s first collegiate volleyball scrimmage of the school year. I was glad she was able to get away for a bit while I held down the fort here with Beckett (making lap after lap in that silly little wagon). We were also visited by one of Beckett’s favorite old nurses. They just played and played….he’s such a lil flirt, and when he’s not screaming…he really is such a good/cute little boy.

If you’ve been following these posts the past few weeks, you will be aware that we’ve been struggling with Beckett’s reflux and throwing up. I’m happy to announce that today he only spit up twice and only refluxed less than a handful of times. Though that’s not ZERO, it’s way better than before! I just hope that the spit up continues to lessen more-n-more, and that we hopefully get to go back home sometime here soon.

Lastly, I want to attempt to share my gratitude once again to all of you who soooooo consistently follow Beckett’s amazing lil journey. You are such a blessing to us, and I’m amazed, each time we post anything, as to how many of you are still following……nearly 8 months later!!!! Your kind words, prayers, encouragement, and even financial support…..truly astounding. I literally do not know how to arrange words in such an order that could accurately and sufficiently express our gratitude. Sooo, for now: Thank you, Thank you, Thank you!

Hang in there with us. We aren’t done yet, but are still very anxious to introduce each of you someday to our precious little boy!

Isaiah 30:18
Therefore The Lord is waiting to show you mercy, and is rising up to show you compassion, for The Lord is a just God! Happy are all who wait patiently for Him!

#GoBeckett
#ODAAT

— with Leah ‘Whiteley’ Rupp at Riley Hospital for Children at IU Health.

August 21, 2013

UPDATE (8/21/13)

Today has been a very difficult day. I walked in this morning to a nurse bouncing Beckett while another gave him meds. I was told he had been pretty grouchy last night and for most of the morning. So, I took him and bounced him for a while. He settled down rather quickly, so then we rocked in the chair before I laid him down in his mamaroo. He slept for maybe half an hour before he started back up again. This time I couldn’t really calm him down, so the nurse gave him Ativan. He slept for about two hours and then was awake, for the rest of the evening! He was super mad throughout most of the evening, and was only happy right after he woke up from the nap. We tried everything, but he just wouldn’t settle. He would fall asleep for a few minutes in my arms but it was always short lived and then he was mad all over again. I tried for about three hours to get him to calm down enough to actually sleep for a while, but to no avail. At one point the nurse brought in the resident because he was so beside himself. She made a comment that he had just gotten his methadone so surely that would help. I took the opportunity to tell them we don’t think methadone does much anymore in the way of actually taking away his pain, but rather is more of a maintenance since he has been on it so long. With that being discussed they decided to give him a different type of pain medication because they agreed he is probably sore from his tube conversion yesterday, but they had thought the methadone would be helping with that. The new med did seem to help, so now they are able to give that when he needs it.

They didn’t really make any changes today. They wanted to wean his methadone again, but since he had a rough night last night they wanted to hold off. Thank heavens after the day we had. They increased him to his goal volume on his feeds and increased the calories tonight. He has been doing pretty well with it. He did throw up today, but it was just bile, and he handled it pretty well.

So, nothing major today. It was truly exhausting and I can hardly feel my body after having bounced, and swayed, and anything else I could think of to help Beckett. Guess I won’t need a gym for a while since I have him. But seriously, I am beat, and I pray Beckett has a better night tonight and that he can actually sleep. They did give him some medicine to help calm him down right before I left, so I was able to at least leave on the note of him smiling and playing. Not sure how long it lasted, but hopefully it was just the thing to get him over this hump. Please pray for rest for him tonight as I am sure today was stressful on his body. Tomorrow will be better!

— with Jonathan Rupp at Riley Hospital for Children at IU Health.

August 20, 2013

UPDATE (8/20/13)

Beckett has had a very busy day. Beckett was an add on today for his G-tube conversion, so Jonny and I were planning to be there earlier than normal to be safe. Well, I got a call before 8:30 this morning for consent because they were taking Beckett down already. Yeah, we didn’t think he would be that early since he wasn’t actually on the schedule. Turns out there was a cancellation and Beckett’s procedure was finished before we even got there. It went really well, and Beckett behaved like such a good boy. We were told they would probably need an IV to give him sedation, which meant putting one in today, but they gave him some medicine through his g-tube and that was all he needed. He literally played almost the whole way through. Not needing to have and IV put in was a huge plus! However, the conversion didn’t end up exactly how we thought. We were expecting a GJ-tube so he could be fed into his intestine, but still get meds in his stomach. This would also allow us to slowly try introducing foods back into his stomach once he was ready but still have a tube in his intestine should we need it. Long story short, that is not what Beckett ended up getting. He got just a J-tube. So now he has a tube going just into his jejunum without a port into his stomach. We were informed they tried to put the other one in, and it was simply too big. They didn’t want to run the risk of forcing it and potentially perforating his bowel, something the cardiologist said might be the very thing to send him over the edge where he might not recover. So, they went the safe route with the smaller j-tube, which we definitely appreciate. When Beckett gets bigger, and we are ready to try putting food back in his stomach, we will simply come back and they can exchange the tube for a GJ. Beckett has spit up some stomach acid today, but it is nothing compared to the volume of milk he was throwing up before. Beckett also had an Echo today, but we are still waiting for the results. We continue to trust that no news is good news. Of course we always look forward to hearing that his heart function is still doing well, and we believe they will tell us nothing less.

We spent lots of time loving on Beckett and then Jonny had to head home to do some things for school. Jonny leaving afforded me lots of snuggle time with my son. I can never get enough of just holding and rocking him. We also went for a wagon ride around the unit and Beckett absolutely loved it. He just looked all around and was perfectly content. We put him in the bumbo and the exersaucer because we are trying to do as much therapy as we can. He seems to enjoy it for a little bit, but he of course gets tired. He is getting stronger every day, so we continue to work on it.

Finally, it is official…Beckett is getting his first tooth! We could totally see it about to come through tonight. I can’t believe he is old enough to be getting a tooth. Although sometimes the last eight months have seemed like forever, it is times like this it seems as though it is flying by. I will try to get a picture and share it as soon as it comes through. Until then, pray that Beckett has minimal discomfort, as his belly is also probably sore from the procedure. We just never want him to be in pain, even if it is something as simple as a tooth.

I also want to share just how good our God is. Our little friend Henry, whom we met when we had just arrived at Peyton Manning Children’s Hospital, has taken his last big step in his fight against leukemia! He officially has gotten his trach out! What a huge answer to pray. He just has to spend a night or so in the hospital to be watched, but seriously, this is incredible. I can remember days of talking with his mom Kim, and honestly, she only had her faith to cling to because it was unsure if Henry would ever recover. Now, today, he has made a complete recovery! God is so faithful!! May our boys forever bring praise to his name!

— with Jonathan Rupp at Riley Hospital for Children at IU Health.

August 19, 2013

UPDATE (8/19/13)

A day filled with many questions and some answers. In just starting this update, I’m already convinced I will not be able to cover everything that went on today, but I’ll obviously try to hit the highlights.

I had many different conversations today with multiple Cardiologists, a Dietitian, numerous nurses, etc etc….to figure out where we are (with Beckett), where we are going, and how do we get there (sound familiar?). I expressed concern that I didn’t feel like everyone is on the same page. I used the example that our Cardiologist expressed an opinion last Friday to slow down on the volume of Beckett’s feedings, yet the very next day the team decided to increase his feedings! I also feel that since Beckett doesn’t appear to be as “serious” (or critical) as he pretty much has been his entire life, that his care (or at least the planning) is not driven, focused and intentional. Yet another week has gone by, and we feel that we have very little to show for it. It is really frustrating, and it seems like whenever we ask to speak with someone about all this (or even something more specific), we are always speaking to someone new, or (no offense) a student or resident; we’ve learned that we have to be intentional in asking to speak with someone specific (like our Cardiologist). So that is exactly what I did today, and we arrived at some answers.

Long story short (because there are many details), we are officially going to do his GJ-Tube tomorrow! Though he is not officially scheduled (he’s an “add-on”), we are prepared to go down this road. A GJ-Tube will hopefully lessen Beckett’s reflux (sooo, less of a chance of choking or aspirating), it’ll give his stomach a break, but it’ll also put him on “continuous feeds” (24 hours a day….just nice-n-slow). This hasn’t necessarily been presented to us as “THE solution”, but rather a “solution” (emphasis/quotation on solution). We are going to try this and hope it helps…it’s not a guarantee, but it fits what I’ve been begging for: forward progress. I feel like we’ve been sitting on our hands for so long, that at least now we are actively doing something tangible.

Like I said earlier, there were a lot of other details I’m missing (like double checking his digoxin level and even a 12-Lead EKG because of some funny heart rate issues from earlier this morning). But with all that being said, we are taking a step forward tomorrow (a step of faith), and trusting that God will continue to lead us.

On a more fun note, we’ve tried taking his therapy into our own hands a little (since we can’t seem to get that message across to them as well….that we want continual PT, OT , & ST for him). Our nurse suggested an ExerSaucer (I had no idea what that was) and we even tried his Bumbo…..and he did both without us helping to hold him up!!!!!! It was awesome! #GoBeckett! I have a video I may try to post….but I’m not sure it turned out the greatest.

That’s about it. One day at a time (#ODAAT). Please continue to pray for Beckett’s complete healing and our patience. We really do love our care we are receiving here at Riley (and everywhere we’ve been for that matter), but at times we just need some extra grace and understanding while also trying to protect and defend the exceptional care for our son. We may have sounded harsh as of late, but I promise it doesn’t fully/accurately reflect our gratitude for all that has been done (and is being done) for Beckett. Amen.

— with Leah ‘Whiteley’ Rupp at Riley Hospital for Children at IU Health.

August 18, 2013

UPDATE (8/18/13)

Wow….Sunday is (generally acknowledged as) “the day of rest”. Well, ain’t that the truth for Beckett?! He slept soooo much today. My parents and I arrived this morning to the news that our nurse was literally sweating after the workout Beckett just gave him. He said that Beckett was sooo out-of-control, he did everything he could think of to get him to calm down. Unfortunately (for the sake of his heart) / Fortunately (for the sake of his much needed rest), he wore himself out and eventually fell asleep. So the rest of the morning consisted of our “inside voices” while Beckett slept. Thankfully he maintained that “state of rest” until around 1:30pm or so. He woke up for a bit, we played with him, then rocked him back to sleep. He then slept in my mother’s arms for hours this afternoon. She was a champ. Beckett woke up a few times absolutely furious, yet my mother maintained her composure, and just rocked/bounced him back to sleep each time.

We think he could also be teething. We’ve been talking about this for months now, but aren’t seeing any teeth poking through yet. There are soooo many factors right now potentially contributing to his irritability, it’s truly hard to say what the actual culprit is (probably a combination of it all). Beckett had a crazy bad meltdown again this evening in which I didn’t really successfully calm him down from, he just kind of wore himself out and stopped. By that point, he coincidently summoned (by the screech of his scream) a few nurses to his room. As we were talking about what to do, or what all could be wrong, I looked down at Beckett (who was in my arms) and noticed that he was just “sitting there” staring at me while I was talking to the nurses. What a funny lil guy. Now with him just being as calm as he could be, the nurses decided to give him some of his meds a few minutes early….in which he follow up with a lil spit up. Thankfully we do not think he threw up his meds this time (as I think he did last night before we left). Another 20 minutes later, however, he threw up again; it was very little, but he still did it. Poor little guy… Please continue to pray for us as we are trying to figure out what may be best for him during this irritable time. He’s such a little trooper, but throwing up everything has gotta be “the worst”.

Before I conclude with a lil story, I want to ask for some prayer for some friends of mine. I just received word that a family from my school (Taylor University) is in need of prayer. A husband and wife named Chip and Debby are expecting there first child. However, they are only 20 weeks in right now and Debby has begun to dilate. The baby’s name is Sophie. There is obviously more to the story, but they just really need prayer right now. Sophie needs to “hang on” in the womb until at least 24 weeks to even give her a 50/50 chance of surviving, and if she came now she would only survive a maximum of 20 minutes. Please pray for this family.

I want to wrap this update up with a little story I was reminded of today by my mother from Mark 4:35-41 and Matthew 8:23-27 where Jesus calms the storm. As we were discussing the age old story (and “Sunday School” classic), I couldn’t help but think of Jesus simply saying to his disciples “You of little faith, why are you so afraid?”, he then calmed the waves and amazed them. Yes, the same disciples who have already seen countless miracles by Jesus, however, this time he displayed his power over the wind and the waves. I guess I’m feeling obliged to share this because I completely resonate with the disciples. Not in a way where I feel like we are “on the same page”, or something….but more-so in that I feel embarrassingly faithless at times. I’m actually not addressing the issue as to whether or not God will heal Beckett, but rather how foolish I can be in all the amazing miracles I’ve genuinely seen before my very eyes with my son (just like the disciples with Jesus), yet surprisingly lack “faith”. Just like Peter (in Matthew 14)…I can get caught up in the waves and lose sight of my Lord. Guess what, it’s amazing (in a non-awesome way) how I completely (metaphorically) begin to sink! My God is in the business of miracles. My God is in the business of healing. And often times I feel as if the only thing that holds back his miracles is our lack of faith. HOWEVER, take note that this story of Jesus calming the storm ends with Jesus “reprimanding” his disciples, yet used it as another opportunity to teach them by revealing his power over the waves and the wind.

May God unleash his power, that even the wind and the waves obey, on my son. May we have the faith to trust he can heal, and that no matter what may happen….we never lose sight of our Lord.

‪#‎GoBeckett‬
‪#‎ODAAT‬

— with Leah ‘Whiteley’ Rupp at Riley Hospital for Children at IU Health.