Saturday, January 25, 2014

Happy 8th Birthday, LS!

Lilly Scott turned 8 on January 11. We discuss her birthday party at least twice a month. Every time she attends a party it becomes exactly how she wants to celebrate her own. Finally she decided what she wanted, and I agreed to a slumber party with her closest friends.
 
Carsen and Bailey came to celebrate with us. They were the ring leaders of the party, and LS was excited to have 'cool' girls there with her friends. It's already started, I'm no longer cool.







The next morning LS asked to go skating. We met a couple of her friends there, and they had a blast.


 Cadence, LS and Gracie
 Even Paisley got in on skating. She wanted to skate so badly, but I was solo and had Wells. We will definitely have to go back to let her try it! This time, Ms. Rachael and Cadence walked around with Paisley. She felt like big stuff.

 After skating we met Mimi, Geep and Caitlin at Steak N Shake per Lilly's birthday lunch request.
 Then we came back to the house.
Caitlin brought her rollerblades so she and LS could skate around the cul de sac.
 We ended the birthday celebration with a bubble bath and the jets going full force. The girls loved all the bubbles. It made quite the bubbly mess.

Lilly Scott/ Scotty,

You are such a girl. You love dresses and shoes. You covet your personal time and acknowledge when it is needed. Your imagination is incredible as you can entertain yourself with the most random items. Reading isn't your favorite, but you are learning how important it is. I appreciate what a helper you can be, and I love the heart you possess. You get frustrated with Paisley who wants to be with you every second, but you really are a great big sister. When I hear how you teach her and love her, it touches my heart. Thank you for giving her the attention she craves from you.

You're a smart one! You make great grades, and you have so many friends who adore you. Drama is definitely a part of our world with you, and I hope one day it pays you well ;o)

You love, love cheetah print. Your laughter is contagious, and once the giggle box is turned, laughter fills the room.

I love you, sweet girl. You are a mix of dependent and independent. You struggle with not being good at everything and often give up after the first attempt. One goal we are working on is being involved in a team sport- swimming. We are starting with lessons to strengthen your swim strokes, and hopefully you'll progress to swim team. We'll see!

You are such a homebody. You would stay in your pajamas and at home 24/7 if you could. It's actually an ordeal to go places sometimes because you resist. Stubborn could be a word to describe you, my darling. I'm not sure where you get it ;-)

We love you, LS!

-Mom and Dad

The Last of the Cast

Celebrate good times, come on! After 6 weeks, the cast is off, and we are in full rehabilitation mode.
We went to the doctor January 20 for x-rays. We were hopeful all would be healed, and our prayers were answered 'yes' to get off the cast. Hallelujah!
 
This is how he started every night. We tucked him into bed, and he would scream until we got him. He would lay in our bed until he could fall asleep. We did love the sweet cuddles :o)
 
 
The last few weeks of the cast Mac was REALLY over it all. He was impatient, tired of everything he had been doing and pretty grumpy. It's like the first couple weeks he was adjusting, we hit kind of a plateau for a few days, then it was back downhill as he was completely ready to be independent of the cast. We all were ready for this day to learn what our next step would be.

 
 I took pictures of his cast signatures just in case it would be cut to pieces.
 

 
 The spot on LS' name is where he ventured out the last week of the cast. He started asking to crawl and would pull himself around with his arms. He loved his newfound independence, but it wore him out quickly. We would take turns crawling around with him to motivate his movement. Even Paisley got in on the fun :o)
 
 
 
 
 

 
 Waiting to see the orthopedist!
 
 
 Now waiting to get to business and cut off the cast. It was definitely scary for Mac, but this was so temporary for the long term result.
I was fortunate to be at this appointment because Nana was at home with LS and Paisley.
Thanks, Nana!
 




 
 Let's go home!!
 
 
 First things first... bath time! He had been asking to get in the bath for 2 weeks.
 
 
Back in gingham!
 
 
 After nap we went to a neighbor's playground where Mac could swing.
 
 
I wasn't sure where Mac would be (physically) after getting off the cast. He has been timid and very cautious of any movement. The best thing we did was put him in the bath (twice!) the first couple of days. He would freely move his legs there. Outside of the bath, he often sits like the cast is still on. We were told he would be his own best therapy.
He isn't pushing himself to try new things just yet. He is scooting on the floor. After the first few days he has started pulling himself up, and that lasts a few minutes before his legs start to shake. We are on the mend, my friends.
I have signed him up for aquatic therapy to strengthen his muscles. We start next week! His legs are pretty skinny now from the muscle atrophy. He lost 12 pounds. :o( 
His appetite is still scarce, but we are working on it. This boy can have whatever he wants to eat!
Thank you for following this journey.
We go back to the doctor February 17 and will update as we can.
 
as always,
ashley

Our Christmas 2013

I can't believe Christmas has come and gone. It's one of those things I look forward to all year, and it flew by this year! Thank goodness it comes around every year :) We were able to spend our holiday season with family in Murfreesboro and Chattanooga.
 
The weekend before Christmas we went to Murfreesboro for the Allen family Christmas. It was a LOT bringing 4 kids, but making memories for my kids trumped convenience.


We went to Paxton's hockey game Saturday morning and opened gifts that night. We fellowshipped over delicious foods and fun. I love how much the cousins love one another. In my childhood I was never close to any cousins so I relish the idea of my kids having what I didn't. It's pretty special.


My parents and brother (Uncle Jeff) came for Christmas at our house. The kids woke up to all the goodies of Christmas morning. We held of on some gifts until Mac is able to enjoy them. I didn't want to separate him any more than he already felt segregated from Lilly Scott and Paisley.

Mac had fun playing with his Cars track, LS was pumped about rollerblades, Paisley was excited about all the festivities and wrapping paper and Wells was super stoked about his 4 new pacifiers.








  

My mom made a heap of sausage balls, and we had our traditional hors devours lunch. Over lunch Lilly Scott read the Christmas story from her Bible, and we celebrated the birth of our Savior.

It was another special day with family where we relaxed, napped and enjoyed quality time.


 
 :-)

as always,
ashley
 

Monday, January 6, 2014

Life In the Cast Lane

Please note the title of this post. I am pretty proud of my genius ;o) In all seriousness, here is what our life has been like with the spica cast.

First off, here's what we are dealing with here. This is a picture of the x ray from Mac's last orthopedic appointment. The (spiral) fracture is behind the staples in the cast.

Let me back up a bit... Paisley hadn't seen Mac- other than a quick facetime conversation- since school that day. I took her with me when Mac was being discharged. The first thing she did when she walked in his hospital room was run to the bed and try to climb in as she yelled 'Mac!! Mac!!' In return, Mac said, 'Sissy! I missed you!' She crawled on the bed but stopped at the cast. He was (is) apprehensive anytime someone got near the cast so he puts up a stiff arm and yells to stop. Paisley listened. That was a sweet twin moment. She had her brother back. Those were the first nights they ever spent apart, and Paisley looked in his bed and asked for him every.single.nap and night.
The first night home Mac cried for several hours. We had all gone to bed, and Jordan was with him in the den. My mom stayed in my room to be near the monitor should Paisley wake. We had juggled beds and who to put where so that Mac would be catered to and comfortable. We decided that an air mattress would support him while also molding to his awkward cast position.
We have all adjusted to the cast and it's monstrosity. It's pretty overwhelming. I was overwhelmed by the diaper changes and care of the cast. We were warned it would smell really awful before too long. Fortunately Mac's internet research savvy Mimi hopped on the issue at hand and found us great tips for keeping it sanitary. For one, we sponge bathe him every night. We can't wet the cast, but it's bound to happen so we dry it with the hair dryer on cold. We dry every spot of that cast. Then we use a makeup brush to apply a corn starch and baking soda mix. This method must be working because we are 24 days in without a stench.
Mac and Wells get sponge baths together.
Next we were concerned about his well-being. That's not such an easy fix. We've purchased and borrowed special pillows to support him. He can't sit up all the way, and laying down all the time is terrible. We prop his legs up with pillows and blankets to support the position of the cast. There's also the issue of skin breakdown so we rotate or adjust him at least every 2 hours. Now that we are a few weeks into it he's becoming more secure with laying on other surfaces. We've even managed to sit him up while one of us completely supports him in a chair. He loves it, and even though my arms and hands are asleep, I will hold him so that he can enjoy playdoh with his sisters.
The reality of the cast stinks. Honestly. We are blessed that he has had amazing care. We are grateful, but we are also living this reality. He's temporarily limited. He doesn't understand it. He fights it several times a day. Just last night he had an episode over not being able to get in the bath. He's cried and begged to get in the bath for a week now. It breaks my heart.
For the most part nights are rough... brutal. Mac wakes up screaming several times a night. I think it's pain and insecurity. Plus the fact that he can't move. When I say he screams, he literally belts out a shrill sound that wakes anyone who isn't used to it. He flares his arms and slaps his legs. He screamed so hard (6 hours) one night that he had no voice the next day. Nothing comforts him. In the midst of this, he has huge tears streaming down his face. I can't let him see that I am also crying. I can't do anything for my baby, and he hurts too badly to let me hold him. When I get too close he slaps me or pulls my hair. Nothing can calm him. I can't even accurately describe what these episodes are like. He does them until he exhausts himself and basically passes out.
This is pretty much the only way he will sleep for any length of time. He wants to be held. Mac is such an affectionate person, and the cast is awkward and heavy to hold. He often raises his arms and says 'hold you' to get quality cuddle time
.

If you know Mac, you know this isn't him. He is the sweetest, softest boy I've ever met. Sure, I'm biased, but it's also truth. He is a gentle, cautious spirit. He is so laid back. This child didn't walk until he was 20 months old because of his laid back nature. It's who he is. Seeing this tantrum he has displayed turns my stomach and melts my insides.
Jordan nor I can leave him for any length of time. When I'm able to sneak away for a shower or a quick errand, he asks for me constantly. Sometimes he starts an episode while I'm gone. (I refer to this behavior as an 'episode' because I'm not really sure what else to call it...) He asks for one of us in his presence at all times.
In all the lows, Mac still loves his cars. We love that he still wants to play :)

 When my dad visited recently, he walked outside with Mac for TWO HOURS. He later said his biceps felt like they had run a marathon. What a champion Paw Paw is for Mac's happiness. Because that sweet boy wanted to be outside. Mac was on cloud nine. LOOK at that smile!

We have the wheelchair, but it scares Mac. He isn't a fan, but we want to get him out when possible. Jordan proposed using our Britax stroller, and it actually works pretty well. He can't sit all the way back, but we support his back with blankets and pillows so he can be comfortable.


With a newborn who has to be fed every 3 hours, Mac turned every 2, Paisley who is trying to find her place in this picture, and LS who also has needs, we are pulled a million directions. I can't do the daily stuff by myself. It isn't fair to me or any of the kids. Mac requires constant adjustments as well as his essential needs. One being the duty of making him eat and drink. Because he isn't active he doesn't have an appetite. We are giving him supplements to help with his weight loss. We can put our whole hand down the torso of his cast now, and his rib cage sticks out over it. My chunky monkey has taken a hiatus, but he WILL be back.

This week Uncle Jeff has come to visit. Mac loves his 'Jeff'.


My mom has been here every chance she could. She has taken loads of vacation to be here to help cook, clean and keep the kids. She never hesitates to change a diaper or scrub a toilet. I can't thank her enough. 

Mimi spent a week with us after the incident. She prepared dinners and stayed with the kids so I could run an errand or pick up and drop off Lilly Scott at school. My dad and Uncle Jeff were also huge help with school travel. 

Our friends and family have brought meals for us. We SO appreciate this blessing as eating is the last thing on my mind. It has been so helpful that the kids could be nourished when I am unable to complete a thought.

We go back to the orthopedist January 20.
Hopefully we will have the cast off sooner rather than later.

Thank you for reading. Thank you for caring. Most importantly, thank you for praying.

-ashley