As the parent of a child with different abilities, I tend to be hyper aware of the comparison games we play in our culture. I’ve grown weary of the social competition in which our kids become pawns we move around the proverbial chessboard, always looking for a checkmate.
Comparison usually does one of two things: It can pull us toward pride or leave us discouraged.
I understand that exchanging information about our kids can be a helpful way to gauge their progress, to get another perspective. I also understand the desire to share our enthusiasm about our kids’ accomplishments. I want to trade info and celebrate, too, as long as our goal isn’t to one-up others or assign value to ability. To do so can lead to pride or discouragement, depending on where our kids land on the developmental map.
When my two older kiddos were born, I read through the What to Expect series with a big, fat magnifying glass, taking copious mental notes. I did all I could to help them excel in every area. As they grew, I compared them to their peers, hoping to keep them ahead developmentally. I actually wanted them to reach their milestones at record pace. Ridiculous, right? I could feel my competitive nature at work and I didn’t like it.
When Sam came along, I gave away those books. Soul work and parental experience were significant factors in this shift in perspective. I wanted to enjoy our new, sweet bundle without focusing on the speed of his milestones, especially compared to his typically developing peers.
Photo cred: Richelle Gregory Photography
In Sam’s first year of life, every doctor visit reminded me of his slower development. Medical paperwork revealed his progress as literally “off the charts”: at six months of age, he was in the 0.083 percentile for his height. There was no line on the age/height/weight graph. We recently celebrated his third birthday and he remains well below the typical percentiles in height and weight. His IEP indicates deficits in every area, a sobering (though not surprising) reality that tempts me to discouragement.
BUT.
I am learning to compare Sam to himself. While I celebrate his milestones, give thanks for his health, and want him to excel, I understand most importantly that he’s a person. He’s a soul. He’s my son. His abilities and placement on a chart do not determine his worth.
Will he know how to read? I hope so.
Will he know how to catch a ball? Tie his shoes? Jump? Eventually. Maybe.
Will he know how to sing? He’s trying.
Will he know a skill well enough to earn some money? Possibly.
Will he know how to live independently? Maybe.
Will he know how to effectively communicate to others his needs and wants? I pray so.
When I look at Sam, I don’t see stats in black ink on white paper. I witness something more that begs me not to compare him to others. I see a little human learning how to love and relate to his world. I see a cuddly boy who tickles his sisters, wrestles his brother, snatches warm cookies from the table, signs “Jesus”, and grins when he’s been naughty.
Sam is teaching me that he will learn and grow at his own pace. Instead of comparing him to others, I’m praying for wisdom and working to help him achieve his full potential. Seems to be a better use of my time.
Maddie says
I never thought I’d be one to compare…but I fell into it much too easily. Especially with E and the boom of babys she shared a birthday month with. And then we had our boy…my amazing wonderful half hearted boy and everything changed. And I’m so glad it did.
Katie says
Maddie,
Thank you for responding. I didn’t think I’d be one to compare, either–our culture doesn’t help our natural tendencies toward this competition. I’m so glad you’ve grown beyond the drama to a healthier place now with your darling Tin Man.
Sarah says
A beautiful reflection on Sam’s life–his own sacred pathway. <3
Katie says
Thanks, Sarah. Always grateful for your input. Love you!
Jan Hunter says
What a lesson for everyone! Katie, I don’t know how u find time but please never stop writing. What a God given gift!!
Katie says
Jan,
Thank you for taking the time to reply and for your kind words. I hope we can all learn to release our need to “be the best” and focus instead on connecting with each other, regardless of our abilities.
I’m so grateful for you and your sweet family and hope you all are well!
beth willis miller says
What beautiful, anointed, heart-warming words of love. Many blessings to you and your sweet family ❤️
Katie says
Thank you, Beth!
I trust you and your dear ones are well–your delightful grandsons are growing up so quickly, as I’m sure you know. Take care, my friend.
Julie Olszewski says
All that matters is Sam will know love because you and your wonderful family love him. Katie, you are a gifted writer …….please keep sharing. I so admire you and love seeing your posts.
Katie says
Thanks so much, Julie. I appreciate your kind words and support. I marvel at how we connected and remain in touch. Your life inspires me–all the loss that you’ve endured and yet you keep moving forward, doing good & meaningful work, keeping the faith. Love you, my friend!
Joy says
I just want to tell you….I adore you and your family! Sam and Eden have made a difference in my life. I know I have told you that I work with children day in and day out on the school bus. And when I made the switch to the “County” and we solely transport special needs students – well they completely have stolen my heart! anywho… I write a monthly newsletter for all 700 drivers and attendants and the director wanted me to put an article in about Down syndrome. After reading articles, facts, website after website – they are so harsh and cold. I found yours. I do not want to do a disservice to Sam! and would love any input that you would have to offer. Love you all very much!