Author Archives: Heart Of Beckett

April 17, 2013

UPDATE (4/17/13)

What another great day! Beckett slept peacefully literally almost the entire day. He was awake for about an hour during lunchtime, and then for about another hour this evening. He was so happy when he was awake. He smiles so big and talks to us. Boy does he have a lot of stories to tell. This evening my mom was here while he was awake, so he was able to show off how he reaches and plays with the toys hanging over his bed. He does really well for not having had a lot of true playtime the last three and a half months. Everyone talks about his attentiveness and social skills. They say he makes great eye contact and loves to interact with people. Even the neonatologist had to spend some time playing with him today after her assessment. It is so great to know he is a happy baby despite all he has been through.

On to the logistics. The big news of the day is Beckett’s billirubin came way down today and they were able to pull out his drain. We pray this problem does not creep up again down the road. This morning when the doctors were in his room, they said his Vapotherm was barely in his nose and he was doing just fine, so they turned his flow down to 3 liters. He has been doing great with that. They are continuing to wean his Milrinone which he has been tolerating, and it will be turned off completely tomorrow morning. They also have an echo scheduled for the morning once he is off it altogether, as well as started him on a small dose of Captopril, which will help with his heart function. His last IV med was switched to oral today, so after his antibiotics in the morning he will no longer need the IV in his scalp. I cannot wait for that to come out, which I am actually surprised it has lasted this long. They also plan to begin weaning his fentanyl again tomorrow. So, lots of changes, but all in the right direction. I have told Jonathan for a long time that eventually the drastic set backs will have to stop and Beckett will have to make continual progress. I am praying that he has turned that corner and it is only up from here.

We had some special visitors today. One was a nurse that sat ECMO back when Beckett was first put on. She could not believe how big he is, nor can I half the time. The other was a family we met here whose son also has HLHS. It was so good to see them, especially since it’s not as convenient for them to visit anymore. It is always nice to have people come see how we are doing, or sit and chat, like yesterday, when my lifelong best friend sat with me for hours. It helps to have some positive distraction every now and then.

Each day I get to help a little more with Beckett’s care. Obviously there are things I’m not allowed to do, but each day it feels like I get to be more and more of a mommy, taking care of my baby like normal. It feels so good to be able to do this for him, as well as help me get comfortable with what life at home will be like. I love that I get to be here all day to watch over him and care for him. He truly is such a special boy and is going to do big things in this world. I can’t wait. It is such an honor to be able to watch God’s plan unfold, and he is not done with Beckett yet. We are all privileged to watch him work, and I pray our eyes are open to his power being displayed before us. Thank you Jesus for choosing to use my son to do such a mighty work in this world.

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

April 16, 2013

UPDATE (4/16/13)

My how I love good days. Today has been just that. A calm, quiet, wonderful day. Beckett spent a lot of the day sleeping, which is always good to allow his body to heal. When he wasn’t sleeping he was calm and peaceful in his bed smiling and playing. He also had multiple rounds of snuggle time with mommy. It is so fun to watch him be a normal baby. He is getting his voice back and making lots of baby noises. He also has some rings and rattles hanging over his bed and he played with them for quite some time this evening, just reaching out and grabbing them. It is so precious to see how he is developing. And already they are falling in love with him here. The nurse today told me people come in to visit just so they can look at him, and when the doctors handed off this evening they saw his pictures and literally all said awe! They thought he was adorable, which of course we do too!

The cardiologist came by today and said Beckett is looking really good. They are extremely pleased with how well he is responding to having his coarctation ballooned last Friday. So much so, they are weaning his milrinone and hope to have it off on Thursday. They then plan to do another echo to see if his heart is functioning better. They also decreased his vapotherm to 4 liters today, which is back to where he was before we came to Riley. At this point, all his meds but one are back to oral, which is awesome. His billirubin and liver enzymes have also come down a little more today, so they are hoping to pull the drain out tomorrow. He seems to be making great strides in the right direction, and we pray he continues down this road of progress. So, today was a day of positive and planned changes, and we are grateful for each one. He was even able to have clothes on again tonight. I know I have mentioned this before, but it truly does make a world of difference.

So, Beckett had a good day, and enjoyed all his playing. The nurse sang him songs and told him the story of Noah. Tuesdays are Ariana’s book cart day, where you get to pick a book to keep for you child. I picked a book about a busy helicopter and read it to him this afternoon. It was amazing to see him actually looking at the pages. He is such a good little boy, and I am truly blessed to have him for a son. We continue to pray for his healing, and that we are once again headed toward home.

— with Jonathan Rupp at Riley Children’s Hospital.

April 15, 2013

UPDATE (4/15/13)

Sorry these past few updates are so brief….but that should be translated as a good thing, as there is not much to really update y’all on (in comparison to the past few months).

– Beckett’s direct bili has come down once again! Love it!
– They did his test today and discovered some lingering sludge (yes, “sludge” is the technical term they actually use with me). So they’ve decided to keep the tube in for now and flush it with saline ever so often (on a schedule), but the tube may come out as soon as tomorrow or Wednesday if his numbers continue to improve like they are.
– They will be reevaluating his overall game-plan either tomorrow or Wednesday now (which we are clearly eager to hear).
– They did, and have, adjusted a few of his meds today from IV to oral….which concerns Leah and I. However, we have obviously shared our concerns and have warned them what to be on the lookout for. He can’t stay on these IV meds forever….soooo, here we go again. :-\ They assured us that they will go “slow”….sooo, we’ll just take it a day at a time and see what happens.
– I surprised Leah tonight and had all of Beckett’s decorations hung for when she got back from a long day of work. …..I could tell it made her happy. Just tryin’ to make things a lil homier, ya know?

More miraculous updates are to come….I just know it! #perspective

#ODAAT
#GoBeckett!

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

April 14, 2013

UPDATE (4/14/13)
-“no news is good news”-
Beckett has had a great day again today! No real changes, OTHER THAN…he’s got his crib back! It may not seem like a big deal, but it’s one more seemingly insignificant step towards “normalcy”.
A Reminder:
Please pray for tomorrow as they analyze his gall bladder with some dye. If what they see looks good, they will remove the tube! At that point they will formulate a proposed “game-plan” for what they feel would be the best “course of action” for Beckett. We will know more then.
Additionally, please continue to pray for Leah as she is going back to work all the way up in Fort Wayne. She has decided to work again tomorrow, as front loading her week last week seemed to pay off as a wise plan.
And for me, and to state it clearly, I’m concerned about the remaining work-load for the few weeks left of our semester. A lot needs to get done in a short period of time, with constrained focus and available time. I’m so close, and am currently caught up, I just want to finish strong while properly balancing my beloved responsibilities with my family.
Thanks everyone! #GoBeckett! #ODAAT

— with Leah ‘Whiteley’ Rupp at Riley Children’s Foundation.

April 13, 2013

UPDATE (4/13/13)

Good evening. What an emotional roller coaster, huh? We are now making our new home here at Riley, the 4th Hospital (3rd Network) since Beckett has been born. We have been welcomed with open arms here at Riley, and have really appreciated the care and concern they are already showing towards Beckett. However, we do miss our old friends from St. V’s, but they each know they can visit us at anytime. That offer is open to anyone else as well. Clearly, it may be challenging if a few hundred people show up at the same time, but as long as you are healthy, and you are reading this post, you are welcome to visit! If you think the pictures are cute, you are in for a treat to experience our Beckett face-to-face. He’s got an incredible skill to just draw you in with his eyes and not let go. 😉

Sorry we did not post a second post last night. I actually did not get back home (here in Indy) until about 2:00am. Beckett had such a great day yesterday that as the evening began to wrap itself up, Leah looked at me and said “If you promise to take me home [to Indy] tonight after Beckett’s [2nd] Benefit at Taylor University…I feel comfortable enough to come”. That’s a big deal. Leah rarely leaves Beckett’s side. In fact, as I type this update, she has been holding Beckett for the past few hours, and when I asked her how long she’s been holding him, she seemed to surprise herself when she realized it’s been so long. It just feels like time is an irrelevant continuum when it’s just her and her son…it’s a beautiful thing. I can’t help but laugh, in which she questions why I’m laughing, and I don’t really ever have a good answer other than how endearing it is to simply watch her lose herself through the undeniable love she has for our son.

The Benefit was amazing last night. So many people came out in support for our son…I just wish we had a better word than humbled, because I feel as if that word isn’t quite adequate. If I begin naming names, I’m confident I will accidently leave someone out, buuuuut, I have to mention a few. Sooo, a huge thanks to the MAHE Cohorts, Amy Wilson, Steve Austin, Jake McCurry, Taylor Smythe, Eric Strong, Josh Kiers, Seth Abram, Jason Miller, and all those who donated gifts, time, talent, etc. And then to all those who came…geesh…so cool. So so cool. Thank you.

To fill the gap of my last post from yesterday (late morning) until now…Beckett is rockin’ it! Sorry, I should state it more professional, but “good” just isn’t cutting it anymore. He had that “invasive” procedure in the morning and did really really well. Then, when moving into the afternoon, we realized that the communication began to slow down. Later it was made evident that they were rethinking things throughout the early afternoon (when he was suppose to be having his MRI of his belly). They decided that this wasn’t the appropriate measure (for various reasons) and encouraged us to flush out his gall bladder. They made room to squeeze it in that evening, and after some Q&A time, we said “Lets do it!” So, this is now the second “invasive” procedure of the day. It was a concern, but he had handled the early procedure so well, they truly felt he could and would handle this just fine. After a longer time than we were expecting passed us by, they finally found us and calmly explained how well he did and they were able to clear our a tiny obstruction in his bile duct. They are now just draining any unnecessary sludge with a drain, and we were informed this morning that his bilirubin has already decreased another 2 points! Then, today, he got extubated once again!!! Yay! He’s handling it well, and we are just sooo relieved and at peace with his current care and condition (hence, emotional roller coaster). He currently looks great, and the plan for this weekend is to just chill and recover. Beginning early next week, they will shoot some dye into his drainage tube to confirm that everything has been relieved and “fixed”. If the dye flows well and correctly, they will simply remove the tube and that problem is theoretically solved. We will be waiting to then hear further details to a game plan for Beckett’s recovery and will have more details at that time.

As always, thank you for all of your unwavering support. It is so encouraging and invigorating throughout this journey. Beckett is nearly 4 months old now, the Heart of Beckett website has only been live for about 3 months, and we’ve already had over 50,000 hits! That’s just crazy! Sooo, hang in there with us and with Beckett. We are in another upswing, and it feels sooo good.

#ODAAT
#GoBeckett

— with Leah ‘Whiteley’ Rupp at Riley Children’s Foundation.

April 12, 2013

UPDATE (4/12/13)

As Leah and I sit here in one of Riley’s Family Rooms waiting once again while Beckett undergoes yet another operation, I am reminded of a song, recently brought back to my attention by a friend of ours, titled “Hallelujah”, by Leonard Cohen. It was made famous by many, but particularly to the younger generation through Rufus Wainwright. One of my favorite renditions of it is from an artist I’ve liked for a very long time. His name is Phil Wickham. I’ll provide the link at the bottom of this post and strongly recommend listening to it if/when you get the chance. It’s very genuine and raw, and appears as if it was simply recorded with 1 take in a random hotel room…I love it!

I’ve actually always wrestled with the phrase “cold & broken Hallelujah” in that song. It forces me to wrestle with what it can even look like to sing a “cold & broken Hallelujah”. Now, I’ll clarify that this song is not “gospel truth”, but it is art, and if you allow it, it can make you wrestle with deeper issues like the one I want to present in this post.

As many of you know, I believe in a God. I believe in one God…“the” God. And even those few sentences are a huge turnoff to many of you following Beckett’s journey. But I must plead for those of you who disagree with my beliefs to please hang in there with me and to not take your encouragement and support away from Beckett because of this disagreement. I truly believe Beckett still needs and wants all of our support! I am not so dogmatic to belittle anyone who believes different than I, but I cannot bend in my values and beliefs. With that being said, I believe in the Bible, and I am not deceived to trust in its infallible nature. I do wrestle, however, with scriptures like 2 Corinthians 7:4 “In all our affliction, I am overflowing with joy” or Romans 5:3 “we rejoice in our sufferings” or James 1:2 “Count it all joy, my brothers, when you meet trials of various kinds”. What do we do with passages like this? Are we to just smack a smile on our face as we are beaten, broken and run down? I don’t think so. But I do think we can sing “praise” and “hallelujahs” with a troubled spirit knowing that our “suffering produces endurance, and endurance produces character, and character produces hope, and hope does not put us to shame, because God’s love has been poured into our hearts through the Holy Spirit who has been given to us”. Nowhere in scripture does it say that we can get what we want with enough prayer. I think the key phrase to pull out of that last sentence is “get what we want”. What a selfish phrase that is. People like to use the passage Romans 8:28 “that for those who love God all things work together for good…” But what does “good” mean? What we desire? I don’t believe we aren’t suppose to ask for the desires of our hearts, but I do believe we are to follow it with “but Your will be done” as a sign of our trust in His sovereignty and complete control. Romans 8:28 ends with “for those who are called according to his purpose”. I think that is where we are given a glimpse of the definition of “good”…”according to his purpose”. I am constantly reminded of Job’s story where he lost nearly everything…his wealth, ALL his children, his health…yet he gave God the glory. How is that possible? Job 1:21 says “The Lord gave, and the Lord has taken away; blessed be the name of the Lord.” Take note, he says, “The LORD GAVE, and the LORD has TAKEN AWAY”, not Satan, or evil…God did. I think back often to December, before Beckett officially joined us in this world. I believe that if God would have given us the option to choose a smooth journey as opposed to this challenging one we are currently right in the middle of (even knowing all the good that has truly come from this situation and will continue to come from it) we would still choose the smooth journey. Right? I’m weak. I’m closed minded. And I’m selfish. Even if God is doing greater things through this struggle, my heart bends towards what is easy. I believe this is where “the rubber meets the road”, especially in my prayer life. I beg God daily to preserve Beckett’s life, but I believe my ultimate priority is to know God fully. A close second (a very close second) is Beckett and my family, but again, my priority is to know God and worship him fully. I think we can, in a genuine spirit, cry out “hallelujah”, even in the midst of confusion and heart ache begging God to help us embody a healthy perspective and understanding of his control and purpose through our calamities.

Since this post has taken me so long to type, we’ve actually already now received news that Beckett did GREAT, no glitches, with his cardiac cath!!!! That is awesome!!! We are so thrilled, and now continue to just take another step forward in this journey. Truly One.Day.At.A.Time.

Phil Wickham – Hallelujah
http://www.youtube.com/watch?v=0Q00mWa0_ig

#ODAAT
#GoBeckett!

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

April 11, 2013

UPDATE (4/11/13)

If you recall, I posted a few days ago that I feel as if I’ve been getting sick. This, in addition to all the emotion yesterday as-well-as overall exhaustion, today has been a challenge. Leah has worn herself out as well, yet we are so thankful she has already put in her hours for the week in Fort Wayne as we could not have anticipated what the backend of this week had in store for us.

As soon as we arrived last night at Riley, they began numerous tests on Beckett…and continued to all throughout the night. They were thoroughly assessing him today until they finally reached a conclusion. They need to do a cardiac cath on him tomorrow and not only evaluate his heart function, but also fix a small portion of his heart that they believe should really help his overall cardiac condition.

Additionally, and while they have to unfortunately reintubate him once again for the cardiac cath, the plan is to do an MRI of his liver/gall bladder area to get an extremely accurate view of what all is needed to repair it. What is planned after those results are analyzed is still to-be-determined.

Beckett has had a “good” day and, to none of our surprise, continues to steal hearts right-n-left. Everyone seems to comment on how cute he is, and “those eyes!!!!”. He has been very chill today and behaved very well during his examinations. Leah got to hold him a few times today, and you could tell that he just loved it! I, unfortunately, have been wearing a mask around him, and even though I had gloves and a gown on, I didn’t necessarily feel that comfortable even touching him much with the smallest possibility of him catching anything from me. That’s some torcherous tension that I attempted to “mask” (no pun intended) all day.

So, I guess I conclude that today was a “good” day overall. We are still very concerned for Beckett’s immediate future, but that ideology conflicts with our #ODAAT principle to simply take this journey one-day-at-a-time. Please pray that tomorrow’s cath goes well, and that they find what they need during the MRI. I do have some good news to share though (sorry, I nearly forgot), Beckett’s direct bili has come down!! Now, it is still high, but not as high as it was….which really is great news! Sooo, we press on and continue to love and cheer Beckett on throughout this journey. And please excuse my preface, but as self-medicating and overused as this sounds and is, I truly do want to continue to give God ALL the glory and trust that we are now here at Riley for a reason. We may or may not ever fully know the reason, but Beckett is not “ours”, he’s a gift and a blessing that we lay at the Lord’s feet entrusting him (Beckett) to His care.

I conclude, and was reminded of, a powerful and applicable scripture posted yesterday by a faithful follower of Beckett’s story (thank you Sharon):

Romans 8:26-27
“In the same way, the Spirit helps us in our weakness. We do not know what we ought to pray, but the Spirit himself intercedes for us with groans that words cannot express. And he who searches our hearts knows the mind of the Spirit, because the Spirit intercedes for the Saints in accordance with God’s will.”

#ODAAT
#GoBeckett!

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

April 10, 2013

UPDATE (4/10/13)

I must begin by warning you that this is not a “good” update.

As many of you know, we were prepared to transfer Beckett this morning back to Peyton Manning for a HIDA scan. This was a test to observe Beckett’s Liver, Gall Bladder and Kidneys. Well, they tested his Bilirubin again this morning, and it went up a lot once again. This inspired the decision to skip the HIDA scan and begin the conversations for interventions via procedure/operation.

The first theory seemed quite noninvasive. We heard one technician say it may only take 10 minutes to complete. They were also talking about trying to just do it here rather than being transferred over to Peyton Manning. These conversations were quite encouraging and seemed quite doable.

As the day progressed, we were preparing ourselves with questions for the care conference later in the afternoon at 3:00pm. At around 2:00pm, one of Beckett’s primary physicians came in the room to update us on the current plan for Beckett’s operation (as we had been thinking that this would have been “done-n-over” by now). Plans actually changed multiple times throughout the conversation. By the end, it was determined that Beckett needed to be transported to Riley Hospital for the best care for the particular procedure they are recommending. This was interesting news and definitely evoked further questions.

We then began our care conference with a room full of his primary specialists for his various areas of concern. It began with a conversation about his consistent and continual rise in his bilirubin level. Eventually the cardiologist spoke up and shared her concerns. This is where the vibe of the day takes a sharp turn.

The Cardiologist proceeded to explain her theory that she believes Beckett’s Liver, Gall Bladder, and Kidneys are being affected by his heart. She continued by reexplaining that Beckett’s heart is still enlarged and not functioning as well as he needs it to. She seemed to follow each statement with the words “I’m concerned”. She has always spoken very direct with us. In fact, she was the first person to really explain Beckett’s condition when we first arrived down here in late December. It seemed as if she was concerned enough about Beckett’s condition to reinforce any risks the “operation” may have on Beckett. She said that Riley will evaluate Beckett from scratch to even determine how safe this “procedure” will be, because there is always a chance with how fragile Beckett is on if he can/will even survive it. Additionally, she shared her concern on if Beckett will ever be ready for the phase 2 operation (for his HLHS). She didn’t necessarily seem convinced that he will ever quite develop enough to be ready for it. Furthermore, she discussed with us the very real potential for Beckett to possibly require a heart transplant. She explained the risks involved with that, but mostly focused on the fact that Riley can actually do transplants if we ever get to that stage (and St. Vincent’s/Peyton Manning do not).

After she explained these “concerns”, hardly any of our premeditated questions were even applicable. It was hard to know what to say. One insignificant question came to mind concerning moving out of Beckett’s room (aka: taking down all his pictures, decorations, etc). Other than that, it took all that we had to make it out of the room with a “thank you” without crying. Walking back to Beckett’s room was a blur. Our eyes filled with tears, and Leah and I just held each other for a while and cried.

The Cardiologist met up with us once again in Beckett’s room, to offer us an opportunity to privately ask any questions we could think of. Unfortunately, our questions were so direct, her general response was “I don’t know” or “I’m not sure” “…I’m just concerned”.

After she left Leah and I took a walk outside.
-more crying-
-more hugging-
Our concern is not necessarily just going to Riley, but rather the fact of feeling like we are starting all over again with brand new doctors, surgeons and nurses….but more-so the overwhelming concern that our Cardiologist made evident. I could spin this in “good light” and “good perspective” (like: fresh set of eyes, option for transplant, continual and respected reputation for patient care), but it just currently seems more fitting to just say nothing. I would just look into Leah’s eyes and cry with her. I still trust in God’s control, but mourn in the unknown. We are forced once again to trust in our Savior and his sovereign plan. This is a lousy situation, but we press on one step at a time. There is no reason to get ahead of ourselves. We are yet blessed once again with another day with Beckett, and another day as a family.

So, I conclude with an inadequate attempt to show our sincere gratitude to the St. Vincent / Peyton Manning medical staff. We are so grateful for your talent, care, and love you’ve faithfully and generously demonstrated to both us, and particularly, to our son. We are forever in your debt. Though we know we are in “good hands” once again, it was through your fervent effort and skills (and our God’s control) that we are even at this point in this journey. May God continue to bless each of you as you bless many other families with the level of care you’ve shown us. Please don’t be a stranger, as I’m sure Beckett would enjoy seeing you all as often as possible.

#ODAAT
#GoBeckett!

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

April 9, 2013

UPDATE (4/9/13)

An interesting day…

As soon as I finished my responsibilities at school today, I drove right back down to Indy. After texting Leah a cute pic of Beckett with the caption “Hi Mom! I’m sleeping good. I miss you!”, she was pleasantly surprised at how quick I was back by his side. I knew it would make her feel better if I could manage to get back down to him as-soon-as-possible….and I was right.

I slept horrible last night and remained in a state of limbo between awake and asleep until well after 3:00am. All I could keep thinking was, “this is gonna ‘hurt’ tomorrow”. Sure enough it did. I say that because I think I’m starting to get sick. My nose is runny, I’m sneezing more often then normal, and I keep clearing my throat way too frequently. This made today even more miserable as I could only (for Beckett’s sake) stand by Beckett’s bed and talk to him (often with my hand in front of my mouth). I didn’t realize just how much I enjoyed touching my son and rubbing his head until it was “taken” from me. But all is well as I peer across the room right now and watch my beautiful wife hold my precious son. It just warms my heart.

Some announcements/updates:

We were informed today that the current plan for tomorrow is for Beckett to have a HIDA-Scan. This is in reference to his increasing bilirubin. They need to see if everything is working well in/around his kidneys, gall bladder and pancreas. This involves a trip back over to Peyton Manning Children’s Hospital. Though we are thrilled to possibly see some of our old friends from over there, we aren’t too excited for this transportation.
…for no particular reason…..just uneasy about it.

They weaned his fentanyl again today by .5 (first time in 5 days). So far he is handling it well, so we are very thankful for that. They are also eager to continue to increase his feeding. So far, for the most part, he is handling that well too. This is a really good thing for him, so please pray that this continues to increase at a rapid/healthy rate.

Sooooo, please:
-Pray for the transportation of Beckett.
-Pray for the hida-scan and the results.
-Pray for his bilirubin to go down.
-Pray for him to handle his weaning well.
-Pray for a safe/consistent increase in his feedings.
-Pray for the “care-conference” tomorrow at 3:00pm (that I’ve been talking about for the past week or so).
-Pray for my health
(these are just a few specifics for the day, we always appreciate pray for other-all health, for Leah, our marriage, for safe travels, etc, etc, etc…)

If you haven’t seen the picture I just recently posted, you must check it out. My son is just so darn cute. One day at a time…..Go Beckett, Go!

#ODAAT
#GoBeckett!

— with Leah ‘Whiteley’ Rupp at St. Vincent Women’s Hospital.

April 9, 2013

my son is so darn cute

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