Skip to main content

A Sad, Sad Tale

We released our butterflies last Thursday evening because we didn't want to become a funeral parlor they were ready to explore the world.  Our first, most fluttery butterfly, Cookie, was released first.  High into the air he flew, the sound of sweet freedom mingling with the cheers of celebration by its young caretakers below.

And then...

A bird swooped in and grabbed it out the air, gobbling it in one foul swoop.  

No joke.  It really happened.  

Matt and I looked at each other in shock, and Caleb was quite confused.

Once he realized what happened, he swore it wasn't Cookie--that one was actually Milk.  (Cookie was one of "his" butterflies!)

So, I will leave you with pictures of happier times with our winged friends...before the fluttery one got eaten by a bird in our backyard.


(Caleb is chewing "therapy gum" here, per the suggestion of our speech therapist.  He is missing a few speech sounds and she thought that this would help to strengthen his tongue and jaw muscles.  He's not arguing about doing "therapy" one bit...)



This is Cookie...right before she flew to her sudden death.


Is it terrible that all through the ordeal, "The Circle of Life" was running through my head?!

Comments

Mary Lou said…
Julie....
I love that picture of Abby!! Her sweet face brought a smile to my face!! ;)
Caleb is not arguing about his "speech therapy"!! Crack. Me. Up!! ;-D
Sorry about Cookie!! :-(
"The Circle of Life" is now in my head, thank-you very much!! Hee, hee, hee.... ;-D
--Raelyn



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...