When I married nearly 16 years ago, I never dreamed I’d be parenting four kids, one with Down syndrome. I had no intention of managing what feels like a circus most days–not that I was opposed to circus life or extra chromosomes–I just wasn’t thinking about motherhood in any form when it chased me down.
After birthing my two oldest and struggling with post-partum depression, I waved the proverbial white towel, calling a truce with my mind and body. I needed mental space and rest to find my sanity (and sleep) with two Littles.
But, dear readers, babies just don’t keep. Eventually, diapers morphed into undies, sleepless nights rolled into sweet dreams, and my once helpless cherubs began to feed and dress themselves. ThankyaJesus.
I shed the zombie look (sort of) and my capacity to form coherent thoughts returned at last (still debatable). This was the season in which I sensed a holy nudge, a gentle Voice asking, “Are you willing to let My dreams become yours? Are you willing to rethink your own ideas about your family and future?”
As many of you know, that nudge led to prayers and conversations and new dreams and eventually, a baby boy with Down syndrome–our Sam.
Prior to Sam’s arrival, I read all I could about Ds, sought advice from experienced parents and professionals, and grew in my awareness of potential issues related to this diagnosis. I researched possible medical complications, physical care, therapies and education, finances, future work, state and federal policies, and our culture as it relates to people with different abilities. Even with all my experience working with people who have Ds, months of personal education, and now 4+ years of parenting Sam, I’m still discovering new truths and learning important lessons.
In a time of divisive politics, hateful rhetoric, and social media outrage, I want to highlight this truth as we celebrate Down Syndrome Awareness Month:
Choosing to believe stereotypes creates distance between ‘us’ and ‘them.’
While Ds is its own culture with a handful of common traits, those with Ds are individuals. Each person brings his own genetics, personality, family, life experiences, needs, preferences, education, and more. Just because we might know a few people with Ds who have sunny dispositions doesn’t mean all people with Ds do. (This is probably the most common stereotype.)
Like any social group, people with Down syndrome cannot be put into a ‘one-size-fits-all’ category. When we do that, we miss the unique gifts found in each person.
This idea goes beyond the community of Ds to other neighbors who don’t typically fit the majority profile, whether immigrants, refugees, Muslims, people of color (POC), folks with disabilities, the incarcerated, those who identify as LGBTQI, or anyone else who might be considered the ‘other.’
Choosing to believe stereotypes can actually prevent us from learning from people who differ from us, who have very different experiences, who look at life through a lens other than our own. We take one conversation or experience or person and craft stories about what we think is true of an entire group and as a result, fail to see the Divine imprint on each human.
In our pride and ignorance, we may write another narrative, one that pens an incomplete, often negative story. Confident we have the whole truth, we often assign motive and value to groups of people we haven’t taken the time to know. Instead of graciously moving toward individuals, we use our limited knowledge and assumptions to determine whether to engage ‘the other.’ I wonder who we miss connecting with when we do this?
I’ve noticed people writing a limited story about Sam. In social settings, I watch as kids and parents determine his physical differences. Most observe that he doesn’t engage like a typical peer, his mannerisms more juvenile, his marked delays perceived as a nuisance. I witness the furrowed brows, rolled eyes, heavy sighs, and the turning away to avoid him–my son, the ‘other.’ With imaginary pen in hand, they hastily make note, “This kid is so annoying. I don’t know how to relate to him. I’m uncomfortable. I’m going to find someone who’s more like me.”
I grieve not only for what this incomplete storytelling means for Sam as he begins to understand his differences but also for what those kids and their parents are missing by choosing to ignore him.
I wonder what we might be missing, too, when we don’t acknowledge the image of God in the ‘other’, when we refuse to find ways to connect with those who differ from us.
Sam’s life reminds me to resist the easy route of stereotyping, to lean in and listen to those whose perspectives and lifestyles don’t mirror my own. Down syndrome spurs me on to move closer to others so I can more clearly see the Imago Dei in each person and love them as I’ve been loved.
Who might you be avoiding because of your assumptions or limited perspective?
What is one step you can take this month to move toward someone (or a particular group) you consider ‘the other?’
Karen Brown says
Well written as always, Katie. Thank you for your thoughts, ideas and passions and challenging “us” to think and reach outside the box and our comfort zone.
Katie says
Thanks, Karen. I hope you were inspired to figure out one action you can take to move beyond your comfort zone right in your own community. What’s worked for us: simply inviting a neighbor over for a simple meal. So many folks are lonely and actually enjoy our chaos :)!
Carol Long says
Reminds me of Peter’s vision of the sheet- He had been taught to have nothing to do with the items on it. God told him to ignore that teaching, that everything on the sheet was OK to touch and eat. So what is on my sheet? Who is on it? What should I do about it?
Katie says
Great way to look at that, Mom! Looking forward to hearing how this translates into action for you. Keep me posted.