Extra 21: the years...

Wednesday, October 16, 2013

the years...

{10-16}

Here's some pictures of Leighton from the past 2 years.

Can you believe how much she's grown? It has gone way to fast.

Home

Newborn shots at 3 weeks

He first modeling gig for Infantino Everybody plays.

(trip to San Deigo)

meeting Kelle Hampton

Her First Birthday

Up at Primary Children's Hospital just 4 days after her Open Heart Surgery.

Her Trip to Scottsdale, AZ

Her trip to Hawaii

Her trip to Puerto Rico

Being Pretty

That isn't even all the trips this little girl has been on, or exciting things she has done. Going through the pictures on the blog I can't believe all the highlights we have of her life. I would have to say it's been a really good two and a half years!!

-JS

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About This Blog-

This blog is mostly about Leighton, and how she has changed our family. We were blessed with our little Leighton in 2011. We didn't know she had a little something extra before her birth. She was born with an extra 21st chromosome. We didn't know it at the time, but she was going to change our lives as most babies do, for the better. This is just a day to day of what life is like having a daughter, or sibling with Down syndrome. It's truthfully in essence the same, if not better as our life before we had her. We do the same things, but some how she makes us better, and happier people. She has become the center of our family. We heard about a boy in college who also had Trisomy 21 wearing a shirt that said High on Chromosomes, and I decided that's what I want Leighton to feel. So I named her blog after that shirt. I want her to feel an extra chromosome is nothing to be ashamed of (it's something she can't change, and you may not believe it, but I wouldn't want that anyway). It's always going to be a part of her. I want her to be proud of it.