A Different Life is Not a Less Life

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A Colorado Kindergarten teacher allegedly said the following on social media: I’m so tired of hearing about special needs children…They were re****** before COVID and they’ll still be re****** after…Do you really think they will be any different after staying a year at home with their parents…Sorry, you f***** got pregnant and had a re****** kid. Your problem not mine. And yes, I’m a f****** teacher.

Of course, this is despicable. The school board is moving towards dismissing him.

Still, special needs parents are posting the story. Why? Because it goes deeper than just one man’s words.

You see, most people don’t make outwardly horrendous comments like these about our kids. They are much more subtle.

It’s the in-law’s friend who decides to pull you aside and explain why your views on school inclusion are wrong.

It’s the acquaintance who makes you feel guilty for using tax dollars to get services for your child.

It’s the online commenter who says you did society a disservice by choosing not to abort.

It’s the disapproving stares from the old man at the store.

Do you see what I’m getting at? It’s not just this one man’s words.

It’s that over the years we have received a similar message from strangers and those who are close to us:

Your child is not as worthy as others.
Not worthy of services.
Not worthy of rights.
Not worthy of human dignity.
Not worthy to pursue happiness.
It’s your problem.
It’s their problem.
Not ours.
Deal with it.

I’m not saying these comments are the norm. I can’t speak for the special needs parenting community, but I can tell you that the positive outside encounters with our child have outweighed the negative ones.

But the negative ones are not forgotten.

And when we see something said that’s so egregious like the statement above, those old memories come rushing back. Do you know why so many special needs parents are posting this teacher’s words? Because we know the truth- they are simply a symptom of a collective illness.

Thanks to the tireless work of advocates, society has improved for our children with disabilities. And yet still has so far to go.

Part of the cure is knowing this- a different life is not a less than life.

Our children are worthy.
Of rights.
Of extra support.
Of inclusion.
Of dignity.
Of growth.
Of the pursuit of happiness. Why? Because they are human. Fully human.

Like me. Like you. We know that. We want you to know it too.

Written by, Jillian Benfield

Jillian Benfield is author of the free e-book 5 Spiritual Comforts for Special Needs Parents. You can find her writings at JillianBenfield.com, Facebook and Instagram.

Finding Cooper’s Voice is a safe, humorous, caring and honest place where you can celebrate the unique challenges of parenting a special needs child. Because you’re never alone in the struggles you face. And once you find your people, your allies, your village….all the challenges and struggles will seem just a little bit easier. Welcome to our journey. You can also follow us on Facebook, subscribe for exclusive videos, and subscribe to our newsletter.

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Kate Swenson

Kate Swenson lives in Minnesota with her husband Jamie, and four children, Cooper, Sawyer, Harbor and Wynnie. Kate launched Finding Cooper's Voice from her couch while her now 11-year-old son Cooper was being diagnosed with autism. Back then it was a place to write. Today it is a living, thriving community of people who want to not only advocate for autism, but also make the world a better place for individuals with disabilities and their families. Her first book, Forever Boy, will be released, April 5, 2022.

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