Skip to main content

Christmas Eve Reflections

Tonight is Christmas Eve.  All of the presents are wrapped and put under the tree, Caleb's big presents have been set up, the songs have been sung, the boy is asleep, and I am here taking a quiet moment to write a thoughtful blog post while Matt is stil at church.  All is well....except...

...Except that it could be really easy for my thoughts to revert back to an issue that struggles to consume me at times.  That's not what Christmas is about.  In case you haven't heard, it's supposed to be a celebration of the birth of Christ, who was sent here to save us from our sins!  SO, tonight I am choosing to be thankful for everything I do have instead of lamenting over what I don't.  Here goes:

I am incredibly thankful for the gift God gave me just 2 weeks after Christmas 3 years ago.  That little boy gives me more joy than I could have imagined possible.  I love him with every ounce of my being---as is proven by the tears streaming down my face right now!  His laugh lights up my day and he can make me smile like no one else can.

Naturally, I am also thankful for Matt.  (Without him, I couldn't have had Caleb!)  Just kidding!  :)  Seriously though, he is a wonderful husband and father and is always there when I need him.  Most importantly, he puts up with my moods and always apologizes--sometimes without knowing what he did wrong--sometimes without doing anything wrong at all!  He knows me better than anymore.

My family is amazing.  I have grown to love and appreciate them in a new way since Matt and I became parents.  I realize now how much they must have worried about me and how the way they responded to certain situations (like not letting me go to the mall to sing with the choir in middle school without a chaperone!) were just because they loved me and were concerned about my well-being.  They say a parent's love has no bounds, and I'm glad I can reflect on the truthfulness of that statement in my own life.

I am thankful that we are all relatively healthy.  Caleb gave us a scare a few months ago, but God answered prayers and the tests came back clean.  My cousin's son, Jacob, is battling a brain tumor and is currently undergoing radiation therapy in Boston.  They are celebrating Christmas a long way from home, but things are looking good for "our Jacob," as Caleb refers to him!

Along with that, I'm grateful for good insurance!  Say what you want about our public school system, but they definitely do offer us fantastic benefits.  Caleb's bills from Johns Hopkins would have cost us close to $10,000 without insurance.  We paid a mere $70 total in specialties fees and copays. 

Lastly, in this economy, I am thankful that Matt and I both have stable jobs.  While yes, the system is trying to make cut-backs to the budget, the truth is that I will have a teaching job for as long as I want it!  I know so many children whose parents have lost their jobs or aren't getting much work right now, and I can't imagine the stress that might put on a family.

I hope that you will join me in focusing on the thankfulness of the season instead of the I wants and I don't haves that we are all so prone to.

With that...

Merry Christmas to All, and to All a Good Night!

Comments

Popular posts from this blog

Cerebrocostomandibular Syndrome

If you happen to pick up the latest Reader's Digest, there is an article in there about Piper Breinholt , a four year old with CCMS.  If you've been around here a while, you'll remember wayyyyyy back when we first received Abby's diagnosis that I was able to speak to Piper's mom, Reagan.  The article is more about their story and not as much about the ins and outs of CCMS, but I think it's probably enough to get some people googling it and I'm hoping a few will end up here. Every once in a while, I give a blog post the title of Cerebrocostomandibular Syndrome so that it would show up in Google.  My ever-present hope is that people will stumble across my blog and 1) be encouraged by the hope we have in Christ, 2) feel a connection with someone in a similar situation as them, or 3) get excited over the miracles that have been performed in Abby's life!!  (a combination of all 3 is great too!)  :)   Notice that it's not to get famous and it ...

Bath Time Photos!!

As promised, here are lots of photos of Abby's first bath. Caleb was supposed to be in bed, but the bathroom is right next to his room... "I'm not too sure about this..." Once she learned how to splash, she was all smiles! Her first good hair wash! Gotta protect the trach! She really liked getting water poured on her head.  It was cute! Smiley (and bubbly) for Daddy while he dried her off. All clean!!  (Note the Lysol wipes in that last picture.  They are NEVER far away!)

Imagination Movers Photo Recap

Seriously, The Imagination Movers were so much fun!  They played lots of their own music, with some classic rock mixed in for the adults.  There were also quite a few jokes and references to Baltimore, which was kind of fun.   The whole night centered around this robot named Rock-o-Matic, or "Rocko."   This is Mover Scott, and he wears Wobble Goggles that help him see new ideas.  Caleb and Abby have a pair of goggles too.  :) There are 4 main Movers that are part of the TV show, but they have 2 extra movers to play instruments and do back-up vocals in their live tour. Abby finished up her feed before the show started so that she would be free to dance! My dancing queen did NOT want to sit in my lap.  The row in front of us was empty, and that is where she stood almost the entire show--dancing the night away. My Imagination Movers  Caleb did his share of singing and dancing too.  He knows m...