Special Needs Parenting

Finding Faith And Friendship On The Special Needs Journey

  • Facebook
  • Pinterest
  • Twitter
  • YouTube
  • Home
  • Our Mission
  • Our Writers
  • Resources
  • Special Needs Parents Appreciation Month

My Kids Teach Me to See

June 24, 2015 by Kara Dedert

We worked as a team, Sophie and I. She brought the plates and scraped them clean and I stood at the sink with hot soapy water. These ordinary places and mundane tasks seem to be the very places where we flip ourselves inside-out to one another. She started the talking tonight. “Mom, how are you going to take care of Calvin when your old? Like, 92?” I laughed, “We will probably both be gone by then sweetie.” “Calvin won’t be, mom, he’s not going to be old then.” she challenged. “If you can’t take care of him I could,” she offered. “He would love that wouldn’t he?” I smiled.

The silence spaced out the clinking dishes in the sink both of us lost in our own thoughts. I was imagining Calvin with eyes that could see, a mouth that could speak, arms that could hug, and little feet that could run to me. She stood holding the next plate. “You know mom, I don’t want Calvin to have a problem with his brain, but I don’t want him to change. I want him to be just the way he is.” It seemed to surprise her, this realization and she let it out slowly. Noah chimed in, “Yeah, and I want him to make the same noises!” “Yeah!” shouted Evie, “and kiss us the same.” They batted a balloon back and forth in the diningroom hardly doing their dinner duties.

Really?!? It seemed like just last week a very indignant Evelyn pronounced, “I wish I had a little brother who didn’t slobber and could walk.” She, his chief adorer and president of his fan club. Maybe it was the fact she needed a “dad” to play house with and Calvin was the only option. I could see how that would be frustrating. But here, today, the tune was different. How are they catching the joy? How are they seeing the beauty? 

It’s not because they don’t see the loss. Noah had just asked me about his little wonder-cousin Quinn (who is beginning the real adventure of walking!), “Did Quinny go to therapy mom?” No.  “Where did he get lessons to walk?” He just learned by himself, his brain told him it was time. Noah was amazed at this revelation.

Maybe they are catching the beauty because they are seeing him. The essence of the little boy who is growing like a weed (and oh how are we going to carry him?!) and making new squeals of delight as the days go by. The days go by and he still can’t walk and play Hotwheels and pretend to be “daddy” for Evie’s games. BUT these inconveniences are shoved under the rug when it comes to him. His person, his essence, his love, their relationship with one another. They love him as he is. They find him endearing as he is. They want him to always be as he is.

I’m not always there, I don’t always get that. I hand him over to Darryl, frustrated with his consuming care, wanting more of a life and feel a complaint deep inside because of the way he is. I get tired of his needs, of holding his pacifier in his mouth for hours so he can go to sleep while the laundry piles and the garbage can overflows and children beg for a story.

Slow down. See him as he is. See him. See him as the kids do.

Have I forgotten this in all my wishing in all my longing for something more? Have I passed over the beauty and forgotten the joy?

Open the eyes of my heart, Lord!

The following two tabs change content below.
  • Bio
  • Latest Posts
My Twitter profileMy Facebook profileMy Instagram profile

Kara Dedert

Kara is mom to 5 kids, including Calvin who was born with a neurological disorder. She's the creator of Live Better With Disability, a positive place for parents of special needs kids to find strategy and perspective. She writes about their journey at www.karadedert.com
My Twitter profileMy Facebook profileMy Instagram profile

Latest posts by Kara Dedert (see all)

  • Frustrated with a lack of milestones? Collect moments instead. - August 24, 2016
  • Using Grief for Good - July 27, 2016
  • Mother’s Day — It’s Complicated - May 6, 2016

Share this post with friends:

  • Share on Facebook (Opens in new window) Facebook
  • Share on X (Opens in new window) X
  • Share on Pinterest (Opens in new window) Pinterest
  • Email a link to a friend (Opens in new window) Email

Like this:

Like Loading…

Filed Under: Joy, Kara Dedert, Living Life Daily, Medically Fragile

Join Us On Facebook!

Join Us On Facebook!

Top Posts & Pages

  • Two things I wish I knew at the time of my child's diagnosis
    Two things I wish I knew at the time of my child's diagnosis
  • What If She Lives With Us Forever?
    What If She Lives With Us Forever?
  • God's Purpose in My Child's Disability
    God's Purpose in My Child's Disability
  • Our Amazon Store
    Our Amazon Store
  • Shannon Pruitt
    Shannon Pruitt
  • The Sacrament of Letting Go
    The Sacrament of Letting Go

Recent Pins

Visit Not Alone's profile on Pinterest.

Copyright © 2026 Not Alone · Built on the Genesis Framework · Site by Design by Insight

Copyright © 2026 · Not Alone on Genesis Framework · WordPress · Log in

%d