Today is a very special day in our family. Here is our recap from
last year.We had some fun things planned to show Jaymi how we celebrate her and Kaelyn's extra chromosome! (Sadly I forgot to take pictures of most of it, lets just say my hands were definitely full all day) We enjoyed some free ice cream from Cold Stone creamery with our friends Holly, Mia and Lily. Mia is a cutie with Ds and is Jaymi's age, hopefully they will be in the same kindergarten class next year. Ice cream is Jaymi's favorite treat, she knows how to sign it and asks for it pretty much every day. Definitely fits into our family!
Next Kaelyn and Bryn got to go hangout with Grandma Amy while Jaymi and I did a little shopping. She helped me pick out spring outfits for her and her sisters for Easter. She was pretty scared when she saw the mannequins without heads in one of the stores. After showing her they were not real and she could touch them she was okay. She kept tapping their neck, obviously wondering why they didn't have heads. Its funny the things she notices, she is a smart little girl.
Then we got to hangout with Grandma Amy for a bit while Bryn finished up her nap. Jaymi loves Grandmas house and her big piano.
This evening the girls and I went with "friend Sarah" to watch a few of our neighborhood friend's dance performance while Wayne played in his volleyball league. When the lights went down and the music started, all three girls perked up and loved it! Jaymi cheered her little heart out at the end of each performance. Bryn got so excited she started giving Kaelyn, Sarah and I hugs and kisses. Kaelyn's little face light up and she even imitated some of the moves. I know our dance parties are going to have a few new moves next time and I can't wait. It was a great moment sitting in the theater with my three happy girls, seeing the pure joy on their faces.
We had a great day and are excited to celebrate again next year! Wayne and I are so thankful to be parents to children with Ds. When Kaelyn was born our lives were changed for the better. She has taught us more in her 3 1/2 years of life, than we have learned in the many years prior. We say it all the time, having a child with Down syndrome isn't that big of a deal for us. People think that it would be so hard, but its not a lot a whole lot different. For two years it was all we knew and we loved it. Yes it comes with some extra challenges, but it also comes with lots of extra blessings!
This year we are part of the International Down Syndrome's Coalition to show the world who our children are, their beauty and worth. Enjoy the awesome video they made to help advocate for people with Ds.
<iframe width="560" height="315" src="http://www.youtube.com/embed/9VG7dh5W40I" frameborder="0" allowfullscreen></iframe>