Today is World Down Syndrome Day.
We are with William while he competes in the Special Olympic State Basketball Tournament. It’s the perfect place to be on a such a day as this.
I couldn’t go the day, though, without sharing a few words. What better day to share words about something that is so close to my heart. In a form of a list, since that is so close to my heart too.
1. They are a part of me
When William was born in my state of shock and confusion he looked like an alien to me. I had not worked up the courage to tell my parents that my first baby “probably had Down syndrome,” since those were the words everyone was telling us. My parents kept calling to check on us, I’m sure sensing something wasn’t quite right, and in those phone calls were always questions about who he looked like. I didn’t know how to answer. My eyes had not adjusted and all I saw was this alien baby. It sounds sad, now, but it was necessary in my healing, I think.
It didn’t take took long for my eyes to adjust and to see that he was the most beautiful baby in the world. By the time Mary came along I had come to that realization that just because they have extra chromosomes doesn’t change the fact that they still have pieces of me. They still have genes and traits that came straight from me. Straight from us.
2. Different is wonderful
When my children were younger I just wanted others to see how similar they were to every other child. And it’s true, they are. They have definite likes and dislikes. They have moods, high and low. They have humor. They have desires. They play, they resist sleep. The similarities are too many to number.
Now I find myself getting a little uncomfortable, though, when parents are preaching “more alike than different.” The fact of the matter is they are different. They have Down syndrome and that makes them different. That difference is important. That difference has shaped us and pushed us to become better. That difference has changed me.
It’s the differences they have that draw people to them. People notice them. They notice how cute she is and how determined he is. I think with all their extras they also have an extra light in them that those around them can’t help but see. Can’t help but feel. That difference is a very good difference. It’s that difference that is changing people.
3. It’s not a matter of “if” but “when”
As a mom of two children of Down syndrome I quickly learned that getting discouraged because they weren’t doing something yet just wouldn’t do. My thinking changed sometime in William’s first year. I cam to realize that it wasn’t if he’ll walk, it was when. Not if she’ll ever sit up, it’s when. Not if he’ll write his name, but when. Not if she’ll ever be potty trained, but when. Not if he’ll read, but when. Not if they’ll talk clearly, but when.
Making those lists of things they probably won’t do is pretty much useless.
4. Sometimes it can be hard
The older my kids are getting the more I’m coming to find that sometimes I have to acknowledge this to myself. Especially at times when I feel like others in similar situations are only speaking of rainbows and butterflies. But I’m coming to realize that it’s ok if I think it’s hard sometimes. The fact that it’s hard doesn’t change the road we’re on, it doesn’t change our progress. If anything it makes me push harder. I think of one of my favorite movie quotes,
It’s supposed to be hard. If it wasn’t hard, everyone would do it. The hard is what makes it great.
Lately I’ve been trying to shift my thinking. For most of their lives I’ve been thinking about how their diagnosis affects me. And it does. But this isn’t just about me. It’s about them. They have these extra challenges to live with and work through. This is their diagnosis. And it is hard. It’s hard for him to have to work so hard to communicate. It was hard for her to work up those muscles to finally walk on her own. It’s hard work. But it’s that hard work that makes them great.
5. If you’re happy…
A few weeks ago we were at a small basketball tournaments with William. Turning the team event they pass the ball around and then the last person shoots. They each got a couple of turns at the basket but just had one chance to get it in. Sometimes he gets in a hurry and when he does he often misses so I was holding my breath when he was standing under that basket and the ball was passed to him. He put it up and in it went. We cheered. He jumped in the air with excitement and without skipping a beat ran to his dad to share in that excitement. Watching him is the stuff of chills. He was happy for and with himself. And he had to share it.
I could go on and on about how they can find contentment and happiness when I can’t see it, my eyes are still adjusting. But I think the bottom line is, if you’re happy show it.
And when possible, jump in the air.