Skip to main content

✌🏼 years of Beckett


For a long time now I've been wanting to put a medical binder together of all his paperwork from specialists, testing results, anything that may come in handy for someone else to have but also a great resource for future reference. As I was online printing off all the documents I wanted to put into this file, I came across this list pictured above; his diagnosis list (and not even the most updated one). When you look at this list, and you compare it to who Beckett is today, he is far exceeding anything I could have predicted based on his extensive diagnoses. 

His first trip around the sun, I truly would have thought we would be lucky to get a decade together earth side. He had so many hardships, his EEGs were showing seizure activity, he wasn't progressing much in his physical development, and it was quite taxing on us. One year ago, he couldn't sit independently, and was just barely rolling over. It's interesting because on one hand I'm grateful for all these diagnoses. They have given him access to so many different resources from therapies, to the birth to 3 program, to his countless approvals for medical equipment. On the other hand, I hate that he even has these diagnoses. He will continue to have hardships for the rest of his life when it comes to feeding, communicating, and even movement.

From a devastating diagnosis, to a hopeful heart for the future, year 2 was so bright. While it has brought new challenges, it has also brought so much joy. Regan and I are so thankful for his continued health and development. In fact, when we sit down at the end of the year and share our top moments in the year, we both agreed that the best thing of 2023 was Beckett taking steps. I cannot believe my eyes when I see him walking into the kitchen from the living room. As unstable as he may be, he's taking independent steps and I know he's not stopping here.

He is a mischievous, determined, strong boy, with a sweet, cuddly, loving side he only brings out on his terms. His laugh is by far the greatest sound I have ever heard, and it just puts a smile on all our faces when we hear his belly laugh. Since he was born, I would venture to guess he's had around 500 different appointments over his two years, whether that be a specialist, or a form of therapy. And through it all, he's so happy. He's so happy to be here, and so happy to be taking in the world on his terms. 

Two years ago was not only the day we brought Beckett into this world, but also a day that a huge part of who I am today was born. I have been forever changed since his arrival but couldn't ever dream of another way to complete our family.




Comments

Popular posts from this blog

Year end close out deal

We had the absolute best visit with Erin and Charlie, complete with game nights, Lego building, human playgrounds, ringing in the big 2-8 with my favorite local restaurant (and people), and a Thanksgiving turkey that was less than delicious. Shortly after they left, my mom came and she helped with all the things! She watched the boys so we could finish our Christmas shopping, and forced us out on a date (which I admit its never easy for me to leave Beckett, but we don't have the chance to do it often, so we try to take advantage.) Beckett is so motivated to move. He has taken steps independently from me to Regan across the playroom, can stand on his own for about 30 seconds, and has even gotten himself up to standing from sitting a few times. He has been at this spot developmentally for awhile, but he is clearly driving this ship and has his own path he's forging.  His main choice is to crawl everywhere, so we try to keep our shoes off in the house as much as possible. Since Be

The final countdown

It's been a minute since I shared an update on Beckett. We're finally getting some nice weather here and are able to spend more time outside comfortably,  so that's been a great change in the last couple weeks, as we are spending our last weeks here in Washington.  After initially receiving his hearing aids, we noticed a lot of high pitched noises from the aids, so I brought it to the attention of Beckett's audiologist. After being assured that was not the way they should be, we went back in and got some new molds created, and those came back a few weeks later. Thankfully, they no longer were making any noises. It's amazing the night and day difference he is when he's wearing them. When he's not wearing them, he's very quiet, much more docile, his arms are up higher as he's compensating for his lack of awareness to his surroundings. When he's wearing them he's much more vocal and engaged with his outside world. This change is he most noticeab

Little fall update

He's still doing all the same great things in PT and OT. He's trying so hard to stand independently, loves to hand us toys, loves to climb into our bench seat at the bay window and watch out the window, still walks along the couch holding on, and is even starting to take a few independent steps, but understandably very nervous! His therapists feel like he's sort of plateaued in his physical development for a little bit because he is becoming more cognitively aware. He's starting to understand cause/effect in play and he focuses so much during therapy on those things while being in difficult physical situations to work many things as once. We're continuing to work with his AAC in speech, and he really enjoys touching the screen, mostly for play, nothing for communicating his needs or wants. He does understand what we are saying though, and that's clear. Regan frequently asks for kisses and he will bump his head into Regan's each time he asks for one. He clear