You Were Always Special

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“Hi Mrs. France, we wanted to call and let you know that everything was fine with Jack’s X-rays. There are absolutely no abnormalities.”

As your mother, you would think this would have been a phone call that I was elated to receive. Instead, I hung up in tears.

It’s not that I want anything to be wrong with you, my sweet boy. I was just hoping that what was going on was something that could be “easily fixed.”

I thought that maybe you just couldn’t hear the world around you very well.

What followed were weeks upon weeks of appointments, evaluations and testing. An emotional roller coaster filled with endless questions and worry about what your future may look like.

As I sit here now digesting all that the doctors have told us, I realize…

You were always special.

The way you showed us that our family planning was a little off and that God had bigger plans for what would be our family of 6.

You were always special.

You quickly made your fierce entrance into this world, again showing me that my planning wasn’t always going to be the way. You showed this mama just how incredibly strong and brave I truly could be.

You were always special.

Your overly energetic behavior was your way of showing your excitement for the world around you. Your energy and incredible cuteness had us all wrapped around your little finger from day one.

You were always special.

You didn’t follow the typical charts. You strayed from “normal” behavior, instead you interacted with the world in your own unique way.

You were always special.

You were always so fascinated with anything that had wheels. Studying their movement back and forth for extended periods of time seemed to allow you to enter a separate world that calmed you.

You were always special.

When you turned two, you showed us that we drastically underestimated the “terrible twos.” From the epic public melt-downs to the seemingly stubborn ways you wanted things exactly your way but just didn’t know how to tell us. You truly humbled us as parents.

You were always special.

Now, we have come to realize that you are even more special than we ever really understood. So special, that others in this world want to officially label you with that word; that’s just how very special you are, my boy.

But know this, my sweet Jack, even though you are now labeled “Autistic” and have “Special Needs” and may not fall into the norm of learning and adjusting to the world around you, a label will not define you or limit you. You will thrive. I know this.

You will accomplish anything you set your mind to. We – your family and your community – just need to learn what special help you may need in which to make that happen.

This is all new for your dad and me. We have gotten past the self-blame and doubts, and have arrived at a place of acceptance.

Our focus now is on giving you all the love, support and help that we can.

Please be patient as we try our best to adapt and learn all we can in order to allow you to be all that you are meant to be.

And please always remember, baby, you were and always will be special. Your unique needs are what make you, YOU; and that is such a beautiful thing.

Love always, your mama.

Written by, Vanessa France

Vanessa France is a working mama of 4 children – ages 9, 8, 6 and 3. She’s a self proclaimed hot-mess mom trying her best to raise polite and happy humans all while documenting the beautiful, messy world of motherhood on social media. Vanessa works in Hospice full-time and runs her own skincare business on the side with Rodan + Fields, where she loves to share amazing products and a work from home business opportunity with others looking for more. You can follow Vanessa on Facebook, on Instagram, for her skincare line and on her website.

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 and subscribe to our newsletter.

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This post originally appeared on Her View from Home and was shared with Finding Cooper’s Voice by the author.

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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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