The Girl with The Prosthetic Leg

February 28, 2020 in Disability & Inclusion - 1 Comment

The other day we were at Callie’s ballet studio, and Callie and I were tucked away from some of the kids.  She was tired after a long day at school and was more comfortable leaning up against me while we waited for class to start.  We could hear a few of the girls talking around the corner from us.  They were animatedly talking about who was in their act.

“There’s Sarah and Gia and Samantha and Callie,” said one little girl.

“Who’s Callie?” asked another voice.

“You know, the girl with the prosthetic leg,” she answered.

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I didn’t have to look up.  I already know what the look on Callie’s face would be.  I already know that her shoulders would slump.  I already know that she’d slap a reassuring smile on her face as my eyes met hers.

It’s such a hard place to be.

Yes, she has a prosthetic leg.

Yes, that’s not normal in most of the world.

Yes, that’s something that identifies her quickly.

Yes, that makes her stand out.

Yes, I get that kids use the most literal descriptors that they can.

Yes, that sets her apart from others.

Yes, that makes her unique.

And yes, I want her to embrace the heck out of it.  Rock. That. Leg. Baby. Girl. I want her to be a role model, an advocate, a voice for inclusion.  I want her to feel as if her prosthetic IS her leg and is an extension of herself.  I want her to be so proud and secure in herself that she can confidently OWN that piece of herself.

Because that’s what it is.

A piece.  But only a piece.

Not all of her.

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It’s not the only thing that makes her special or unique.

There’s so many other terms you could use to describe her.

The girl with blue eyes and long blonde hair.

The girl with glasses.

The girl who likes horses and reading.

The girl who gives great hugs.

The girl who has a quiet laugh.

The girl that loves animals.

The girl that just started ballet dancing.

The girl that is strong and brave.  Friendly and kind.

It’s a difficult balance at times.  How do we balance wanting her to be so secure with her differences but not letting her be defined by them?  How do we make sure that she’s comfortable in the skin she’s in but not only valued for the things that set her apart?  How can we make sure that she knows how unique she truly is but also how she is just like everyone else?

I think it’s in teaching her that no one can do Callie better than Callie can.  It’s always having conversations centered around comparison and the pitfalls of it.  It’s reminding her that you can admire someone else’s beauty without questioning your own.  It’s reminding her that flowers are beautiful.  But so are sunsets…and those two are nothing alike. It’s teaching her that self confidence it a super power and one that she should embrace daily. It’s teaching her that the magic, the joy, and the light she sees shining in others is shining in her too.  The world needs HER magic.  It’s something that only she can share.  Some of that magic is based on her hardships but not all of it.  The light that shines through the mosaic that is composed of all of the breaks, battles, and scars she’s endured?  That light?  It’s all hers.  Every last bit of it.  And we’re trying to figure out how to let all of it shine.

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Jaime

Jaime is a writer, editor, and lifestyle storyteller focused on modern womanhood, slow living, and life after survival mode. As the founder of The Wildflower Edit, she creates thoughtful, beautifully honest content at the intersection of motherhood, disability, emotional healing, and intentional living. Her work invites women to edit their lives with care — keeping what feels true and releasing the rest — for anyone learning to bloom in their own way.

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1 Comment

  • Judith Dill March 1, 2020 at 12:29 am

    Beautifully written. Beautiful momma and beautiful little girl

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    For the women blooming in unexpected places…..

    For the women blooming in unexpected places…..

    Hi Y'all

    Hi, I’m Jaime — writer, mother, storyteller, and the heart behind The Wildflower Edit. For nearly a decade, I wrote online as The Princess and the Prosthetic, sharing my daughter’s journey with disability and the lessons our family learned along the way. It was a beautiful season — full of advocacy, connection, and community — but as my daughter grew older, I felt a shift. She deserved more autonomy. More privacy. More room to decide how she shows up in the world. And I realized something else: My own story was expanding too. Motherhood was still here. Disability was still here. But so were grief, healing, womanhood, nervous system care, feminine energy, homemaking, identity, softness… the fuller, deeper pieces of life that were ready to be spoken aloud. Whether you come for the cozy routines, the motherhood reflections, the disability advocacy, or the soft life inspiration — thank you for choosing to share this space with me. Pour a warm drink. Settle in. Let’s grow a life that feels like you again.

    Jaime

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