It's ok, my thumb isn't lonely.

Tonight we were getting ready for dinner and Skyler came running up to me calling "Mommy Jacque!" (which is annoyingly adorable, but that's another post all together!)

I bent down to see what she wanted to show me, and she held her hands out. She said: "Look! I have five fingers!" I replied "Yes, you do!" and then she held out her left hand and said "I don't have any fingers. Just a thumb."

We talked for a few moments about her hand, as a two year old she was content to know that she had pointed this out to me and ran off to play. Fast forward about 20 minutes to eating dinner and she looked at me, very serious and said: "It's ok Mommy Jacque, my thumb isn't lonely. My thumb is special because it doesn't have fingers." And then she smiled and ate her grilled cheese.

I know we'll have another discussion in the future, but this was the first time she really acknowledged out loud that she knows she's different.

Before I even start, let me apologize in case this gets rambly...



When Skyler was first born, I was in a bit of shock that she had been born missing fingers. I wasn't angry, I knew it wasn't my fault. But I was worried about the teasing that was to come. (And the way we hear about bullying on such a huge level, it is still a very real concern for me.)

I knew a boy growing up, from a wonderful family at my childhood church who had a similar limb difference to Skyler's, and I knew that he was a normal adult with a regular life. So my concerns weren't with tying her shoes, I remember he'd worn shoes with laces - and I was pretty sure that he didn't have to go have his Mom tie his shoes for gym class. They weren't with what she'd be able to do; because he was able to do anything any of the other kids were - he was an amazing soccer player.

Aside from the potential teasing; I wasn't worried about much. But I did want to know more and more and more about what she was going to face in life. So I started searching for everything I could about Amniotic Band Syndrome and Limb Differences - I found several great blogs. One was Born Just Right -  She has a fabulous blog, and a beautiful little girl with a limb difference.

Which brings me to my actual topic... *lol*


Today she posted an excellent post "Beauty - How far should you go?" which touched on my big concern - bullying. She talked about a young girl recently in the news who had surgery to have her ears pinned due to teasing.


Reading her post, and the news article and watching the video... I went through a range of emotions. I felt bad for the child for getting teased. I was annoyed with the mother for going for surgery at such a young age. I was jealous, that a simple surgery could "fix" the problem.

I know Skyler is still young; we've only had a small handful of children who have noticed her difference; it's primarily adults who notice and comment. But having been through what we've been through with Skyler so far, and what we are preparing ourselves for in the future? I'm not sure what choice I would make in the situation where a simple cosmetic surgery could repair the "problem" -- My gut instinct is that I would not approve a surgery like that. That I would do all in my power to give my child confidence and self worth, to help her with ways to battle the inevitable teasing.

As we are, Skyler and I have already had a talk about her fingers. We've told her that some kids have red hair, some have blond, some have black. Some kids have blue eyes, some green. And some kids have ten fingers, some only have five. It's just how you're born and there is nothing wrong with it. Of course, she shrugged and ran back to playing with her baby dolls.

I suppose I just wanted to share the information; share my thoughts and just get it all out there :) Next up? A post with some fun photos...


One more photo post...

A few more photos from our Lincoln trip! Since I forgot them...  (If you're on facebook; you've no doubt seen these already!)


The Good Life

While we were in Lincoln this past month, I made the biggest mistake! I'd forgotten to take the charger for my camera! And even worse? When we left Colorado - my battery was already almost dead!! *gasp* So I was virtually without a camera while we were there. Thankfully my Mom let me use her Olympus point and shoot for a few things!

I wanted to share a few photos from our recent trip with you! A little of everything from just relaxing photos, to playing at the park and touring the state capitol! (Skyler really loves "The Capitol"!!)

(Please forgive me - this entry will be VERY graphic intense!! And I know what a pain it is - since I'm on a dial up connection at the house in Pueblo right now! I'm sorry; but I wanted to share!) 

 Skyler at Holmes Lake Park
Skyler and Grandpa Brian at the Capitol 
(looking at former Governors)

The ceiling near the elevator on the observation floor
 The ceiling on the 2nd floor - where you meet for the tour!
The view to the West of the Capitol
From the Observation Deck
Skyler on the Observation Deck
She LOVED it up there, looking out and running across!


I think for the first time in the 14 years that I've known my husband and his family - I didn't have my camera glued to me!! I feel a little bad that all the photos I took were while we were with my family, but never fear! His parents are on their way to Colorado soon, so we will take double the pictures! (And since I know you are reading this, you have been warned -- please see the smiley face below!)


I'm a bad Blogger!

I haven't updated in AGES - (But to be fair? I haven't really taken any photos in ages either...) So I thought I'd give a quick update/rundown of what we've been up to!

We've had a lot of playdates lately! (Skyler had a lot of fun playing "Dress Up" with her friend Taylor! They were the cutest princesses.)

On a trip to the Children's museum, Skyler had her face painted like a Kitty. (Which resulted in her crawling around and meowing for 3 days after!)

And me? I've been reading and writing!