Category Archives: Jonny

September 19, 2015

UPDATE (9/19/15)
You all deserve an update….sorry for the delay. As many of you know, we had a GI and Cardiology Appointment a few weeks ago, and we’ve been meaning to inform you all as to how it went.
General consensus, Beckett is doing great! At one point our Cardiologist looked at us and said, “Let me put it this way….when we first met Beckett, if someone told me that this (pointing at Beckett) was going to be the outcome, I’m not sure I would have believed it.” That’s pretty great news.
For GI, we’ve actually begun weaning some of his meds…which is awesome! I’ve longed for this moment. Just a few weeks ago, Beckett still received a little over 130 syringes of medicine a week. We are now just under 100…..I’d say we’re moving the right direction.
Concerning Cardiology….he’s looking great, but now it’s time to begin having our dreaded conversations of Beckett’s next/last operation. However, first, our Cardiologist would like for Beckett to have a Cardiac Cath. Beckett has had a couple of these….but they aren’t fun. For the first time in a little over 2 years Beckett will undergo another invasive operation where anesthesia is involved. Worst scenario, it is possible for Beckett to code on the table (we have good friends whom this happened to), or, he could go home the same day. I believe it’ll be somewhere in the middle…but either way, we are just hoping and praying for a successful and informative operation. After this Cath, the Cardiologists will have a much better understanding of just how well Beckett is truly doing, and how close he is to being “ready” for his last open heart surgery.
We are very anxious to have these days behind us, but are fighting to cherish the present moments. This is probably the most accurate reason why we haven’t posted updates as much as we’d like/should…..we’re just genuinely enjoying long walks in the evenings together as a family, going to fairs, zoos, etc. We had a wonderful summer vacationing for a few days with my family, with some of Leah’s old college roommates, and you may have seen the pics…Beckett was in a wedding this summer! Life has truly been a blast, and sometimes Leah and I just look at each other in disbelief at our “happy ending.”
His Cardiac Cath is on October 6th at 7:30am. Please pray for us, and certainly for Beckett, the Cardiologist who’s doing the Cath….etc, etc, etc.
This has been quite the story…quite the journey…and quite the testimony of God love, grace, and sovereign care. We are very blest and are trusting in the Lord’s care over our son heading into this last and final chapter. Thank you all for your continual support and love…we are so very grateful!
#GoBeckett

#ODAAT

August 16, 2015

#SuperSlide

July 30, 2015

Oh man….so grateful!  

July 18, 2015

Melts my heart every time….  

July 4, 2015

🇺🇸 #merica 🇺🇸
  

April 29, 2015

Driving his first #Deere. He’s a natural! 

March 16, 2015

UPDATE (3/16/15)
Hey everyone, I know it’s been a long time….a really long time. So, for those of you we’ve heard have been longing for an update, we do apologize. I assure you, however, that our delay has been filled with a lot of love and good times together as a family. With that being said, let’s dive in:
You may have seen in any videos or picture we’ve posted some of the things I am writing about, but hopefully those were helpful. First, Beckett is walking! Well, even better than that…he’s beginning to run now. It’s amazing! He did get fitted for some ankle braces (due to some weak ankles from, most likely, him learning how to walk a little “late in the game”…but that’s ok). He’s getting so strong and confident, it’s amazing to watch him make huge strides (literally) these past few months. If you haven’t seen him in person for a while, he seems like a whole new boy from just a few months ago. He’s doing so good that our physical therapist isn’t certain she needs to meet with him as often anymore. That’s scary, but exciting!
Speaking of therapies…he still does get physical therapy, occupational therapy, developmental therapy, and now…..drum-roll…..speech therapy!! If you’ve been following Beckett’s story for a while, that is something we’ve been praying for for a long time. We finally got one, and she comes to our house weekly. She helps Beckett with his resistance towards eating. This has been a huge struggle of ours ever since we brought Beckett home (1.5 years ago now…crazy, huh?!), but we are finally starting to see some major improvements. In fact, nearly 2 months ago….HE STARTED TO EAT! That is HUGE! When we started this journey, if even a spoon of baby food touched his lips, he’d throw up. He’s slowly getting more and more confident, and we are finally finding some food (and methods) that work! Yay!!
To rewind a little…we had a busy Fall. We went to the Indy Zoo, Leah took Beckett to a Pumpkin Patch, Beckett got dressed up like an Oompa Loompa for Halloween (he was so cute…reference the pic I posted), and we had a fantastic Thanksgiving and Christmas! If we missed ya, I’m so sorry. But thankfully, we were able to get Beckett “out” a lot this Fall. Not only did we do everything I just mentioned, but we had the opportunity to speak in my home church in Archbold over Thanksgiving, we spoke here in Upland as well for a couple services (for the entire service…that was emotionally exhausting), and we’re even able to make it back up to Michigan where we use to live a few years ago (it was GREAT to see you all again!). It was really neat to share Beckett with so many people who have been supporting us, encouraging us, and praying for us all these years! It has brought me to tears many times when I really think about it.
Ok, ok…and now for the nitty-gritty:
We had a Cardiology follow-up appointment a little while back…..and….I think the words used was “Beckett looks amazing!” …..music to our ears! Actually, some of the Cardiologists (who had since left Riley Hospital, and are now back) dropped their jaw at how good he looks to them. I kind of asked, sheepishly, “Do you remember Beckett?” and I believe the response was a respectful yet blunt “how could you forget him?!” I got the unfortunate feeling that Beckett is (or was) that “case” that the numerous Cardiologists who worked with him would reference when they’d think “it could be worse.” However, I think I’m okay with that. I mean, it’s so rewarding, and brings such a huge smile to both Leah and my face when we are reminded (or simply remember and acknowledge) how far our little boy has come. When reading through our original entries from the blog last year, it was a rude-awakening how dark and heavy those many months were. But goodness…..Glory to God, right?! Great things He has done!
Sooo…..for our future. We are still working through a lot of meds. Beckett is currently dependent on over 130 syringes of meds each week. Leah does a wonderful job keeping up on all that…and Thursday night in our house is “Med Night.” Leah’s mom still comes over nearly every Thursday and helps us organize and fill each med for the next 7 days…it’s amazing! We have so many good friends and family who still check in with us from time-to-time…and that is greatly appreciated. All of it can get exhausting, but it isn’t too hard to push through and think “I’d do all of this every day for a million years if it meant I got to keep my son home from the hospital.” Sort of on that note, we were able to adjust one of Beckett’s meds about a month ago from 2:00am to midnight. Soooo, that means no longer needing to stay up until then (or waking up in the middle of the night anymore) to give Beckett that med. It’s amazing how getting those extra two hours of uninterrupted sleep can be (that was getting old and quite tiresome after a while). Oh yeah…back to the future (no pun intended), our Cardiologist loved how Beckett was looking, which certainly prompted the question, “Sooo…..when is his next surgery?” Beckett has only done 2 of the necessary 3 open heart surgeries to fully address his condition. I guess the plan (as of right now) is to do another Cardiac Cath (those can be scary) this Spring to asses just how ready he might be. After that, I guess his next (and final) surgery COULD be this year (2015)….but it could also be sometime next next, or even the year after that. We clearly want to do it when it’ll be best for him, but we are anxious to get it done and over with. The longer we wait, the older he’ll be…the more he’ll remember, and somehow the harder I feel it’ll be to give him back to our surgeon (as much as we do trust him). So, if you would, please just pray for continual guidance there while we figure out that next step.
So, as for now…we’re just trying to enjoy the moment. We have been grateful for the opportunities to share Beckett’s story and just do life. I do apologize again for the lack of communication, but I hope it was/is somewhat understandable. Going forward, we will continue to try to post pictures and videos from time-to-time….but it may be a little while until we get to another update again. However, feel free to message us or simply comment on this post…we still read them all. AND, if you find yourself around Upland….look us up! We’d love to meet you and share our little bundle of joy with you as well.
Until next time, continue to just take it one day at a time!
#GoBeckett
#ODAAT

March 8, 2015

The Boys!



December 24, 2014

Merry Christmas (Eve) from the Rupps!

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September 4, 2014

UPDATE (9/4/14)

Greetings! Let’s dive right in:

First off….we’ve been busy. A good kind of busy though. I do apologize for not posting in a while, but truly, we’ve just been enjoying our summer as a family….and it’s been great!

In early July we went on a family vacation (with my side of the family). It was kind of a big deal because it was the longest we’ve ever been away from home with Beckett. It was genuinely shocking just how many things we had to pack for Beckett to be gone for a measly 3 nights. However, we seemed prepared for everything. We had enough meds, enough milk, supplies, emergency supplies/equipment, etc. It all went very smoothly, and Beckett seemed to thoroughly enjoy his time with his family (and definitely ALL his cousins)!  We got to enjoy so many firsts including: a boat ride, playing in the sand, and swimming in the lake.

Also, we’ve started dropping Beckett off in the nursery (….that’s a big step for us, AND for Beckett). Some Sundays it has gone well, and other Sundays it was not so good. Beckett tends to have a little bit of separation anxiety, but that’s expected, and he truly does well on some days. Anyway, it’s a semi big deal…and we’re glad we’re at this stage.

Here’s a little update on Beckett and his precious little heart. As some of you know (or remember), Beckett has HLHS, which requires 3 stages of surgery. Well, Beckett has only (technically) had 2 of those 3 surgeries. With that being said, it is common to do the final stage surgery when you  are about 2 years old. Beckett will be 2 years old this December, but we were being told that we might not do it until next Spring (of 2015). However, we had a Cardiology appointment this Summer in which we received very interesting and surprising news. The current story we are being told by our Cardiologist is that we might not actually do Beckett’s final surgery until he’s 3 or 4 years old!!! Wow! That news literally made my jaw drop. I wasn’t quite sure how to respond. It’s kind of good news and “bad” news. It’s great news because it’s a good thing our Cardiologist doesn’t feel like we need to be rushing into that last surgery. It’s difficult news because it delays the inevitable, and even gives Beckett a better chance of remembering it (and for me, I think it’ll be way more difficult to hand over my “fully-aware” 4 year old to a surgeon, than a 2 year old. Both are difficult, but I hope you understand what I’m trying to say. Soooooo….anyway, there’s that. Kind of interesting, huh?!

Last weekend was really neat. There was a “fund raiser” for Beckett at a local Harley Dealership that was ran by a few very loving and generous people. They call it the “Jackie Dudding Poker Run,” and it’s a fund raiser in memory of this couple’s daughter (Jackie) who past away (way too early) at the age of 30. This past weekend was the 5th year they’ve done this, and they basically choose a family who lives in Grant County and preferably has a heart condition. Well….we fit the bill. So, they “interviewed” us last spring and decided that Beckett is who they’d like to do this for. It was really really neat, and quite the honor to be chosen for something like this. Thanks again Margorie and Myron! You guys are great!!

Then that weekend ended with Upland’s annual Labor Day parade. We were able to kind of take Beckett last year (as the parade goes right by our house), but this year we actually went back to my in-laws “spot” and enjoyed the bucket-fulls of candy being thrown out….even though Beckett can’t technically eat any. 😉

Which kind of reminds me. The Labor Day parade is really one of the “first things” we did with Beckett last year when we got home. This may really surprise some of you, but Beckett has now officially been home from the hospital for a year (as of August 26th). I’m still reading through last year’s blog entries each day, and it was really neat to read last years entry on August 26, 2013 (and many others). He’s still home, he’s now 20 months old, and…………..he’s just now (finally) beginning to walk!! It is sooo exciting!!! He’s got weak ankles, so we had to fit him for ankle braces (which he’ll be getting in the next few weeks), but it is really neat to see him progress to that level. I think we have our hands full now with him scooting around everywhere….I’m sure I haven’t seen anything yet until he’s actually walking around EVERYWHERE! Oh boy….lots of broken toys of daddy’s, but oh well. It’s just stuff, right?! 😉 Anyway…that’s just some really exciting news too!

I’m actually typing this update in the living room of my parents home in Archbold where we are getting ready to take Beckett to his very first demolition derby at my hometown fair! This will be quite the experience for him….and, I love it! I love watching him react to new things. He’ll just sit there and stare. Sooo, if we bump into you at the fair, don’t feel bad if he just stares at you….he’s just checking you out. He’s a very curious little boy, which I love….but it’s always neat to watch his little mind process something new. He soaks it in like a sponge.

I think that’s it for now. Please don’t hesitate to reach out….but I apologize for the infrequent posts. However, please know that we read every comment….and some of the things you guys say are so incredibly encouraging, I can’t even begin to tell you how much we’ve appreciated all your support! If you’ve made it this far in this fairly lengthy update, you are probably one of the ones who have stuck by our side since day one. Please know just how grateful we are for you and your support/prays. The encouragement is humbling, and something we will never be able to properly share our gratitude for. But I can at least say (or type), “thank you.” Our support system is amazing and off the charts. We only hope to run into you “soon” and share with you the beautiful gift we’ve been given named Beckett Jude Rupp.

Signing off for now (and maybe for a little while), but we’ll certainly try to post a pic or video here-n-there just to keep you all “in-the-loop.” Thanks again and God bless!

#GoBeckett
#ODAAT