He is enough

IMG_1195Photo by Sara’s Photography

With the acceptance we’ve experienced, it’s still shocking how little people understand about Down Syndrome. There is a lot of misconception and confusion. And I’ll be the first to admit, we knew nothing initially and we’re still learning. But it’s so incredibly important to know how to discuss Down Syndrome, so I thought I’d share some insight from our journey so far.

I read recently that words – using the proper terms and tense when talking about Down Syndrome – are important. And it’s true. Most comments we’ve encountered from others are innocent and come from a place of little awareness. In fact, I can often sense the hesitation as they try to choose the rights words mid-conversation. There are some comments that immediately strike me hard and my protective nature revs into overdrive. Others, I’m not quite sure how to feel about just yet. Ultimately, my goal is to educate myself so that I can educate others.

First, I’ll level set this by being clear that every single person with Down Syndrome is an individual with different abilities. It’s not okay to say someone “is Down’s,” or to use the term “Down Syndrome baby,” for example. Instead, say someone “has Down Syndrome” or use the term “baby with Down Syndrome.” Semantics, I know – but these statements are not accurate, and making them opens the door for people with Down Syndrome to believe that they are defined by their condition. And they are not. They are NOT Down Syndrome. They HAVE Down Syndrome. We all have our own battles but it is imperative to us that Callan knows – and believes – that our conditions are NOT who we are.

Second, parents (regardless of age) have a 1 in 700 CHANCE – not risk – of having a baby with Down Syndrome. That word risk can be tricky. During my pregnancy, that terminology was used often and it has the innate ability to strike all levels of fear in a parent. RISK. I remember harping on that word while asking the universe how we even became that 1 in 700. The diagnosis didn’t fit what we thought our family would be. But with every accomplishment, full-body smile and giggle, this now-18 pounds of pure joy assures us that he is who he was meant to be, and that THIS – this is what our family should be. Someday we’ll tell Callan just how grateful we are that we weren’t the other 699. But for now, we’re busy showing him each and every day that he is enough.

Questions? Ask away! As I said, we’re still learning but I’m always willing to help spread clarity and understanding.

 

 

12 thoughts on “He is enough

  1. I love this post! Spreading awareness is so important. Thank you for sharing.

    1 in 700, Callan is such a blessing ❤️

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  2. Great job. We kind of went through the same thing with the word “adoption”. Even though it wasn’t a medical condition it sounded like it the way people said it.

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