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The Princess and The Prosthetic

I’m Sorry

February 1, 2021 in Warrior Princess - No Comments

“I’m so sorry.”

That usually is what we hear when we share the complexity of Callie’s medical situation.

When she was first born, those were some of the first words we heard from doctors, nurses, specialists, and counselors.

“I’m sorry.”

But doesn’t saying “I’m sorry” in response to a new mother (or parent) of a child who’s differently abled lay a tragic foundation for their life?

Speaking the words over a new baby and in within a few hours of the miracle of their birth?  Doesn’t that cast a shadow of the event?  Doesn’t that take away those first few hours of joy, bliss, empowerment, love, accomplishment, and togetherness that a new family should feel?

Those should be the sweetest moments not the ones that a parent looks back on in pain.

Let’s not start the conversation of a differently abled child’s diagnosis with “I’m sorry”.

Looking back, I can see that they meant well but it also brings up  a lot of questions.

Did they think that because of her diagnosis Callie would not amount to “as much” as an able bodied person would?

Doesn’t saying “I’m sorry” convey that her diagnosis was bad?

Did they think her life was less valuable now?

Doesn’t that set a very low bar for her?  Would that continue through her life?

Was that really how society saw differently abled people?

Did they think that with this diagnosis she would be considered with less worth?

And how did they know that she would lead a lesser life simply because she was different?

What exactly were they sorry for?

The thing is…….

Nothing positive ever follows the phrase “I’m sorry.”

“I’m sorry” is a phrase followed only by something negative.  In addition to mourning the loss of our plans and expectations, now we were had to brace ourselves for more bad news.  As time went on, we realized the diagnosis wasn’t bad but I wish we would have had that insight and opportunity from the beginning.

In those early moments of life, we don’t know what lays ahead for our little ones.  And who are we to project a life of “tragedy and hopelessness” onto someone for being born different? Can we shift the perspective to the infinite possibilities instead of the loss?  Can we try to look at all the ways they are perfectly and beautifully made instead?  Can we assume competence and achievement? Can we treat this as a gift with endless amazing opportunities?  Can we revel in the miracle?

I think we can.









Hi everyone! Thanks so much for stopping by! My name is Jaime! Wife to my better half, James, who is my moon and all of my stars. We are parents to our little warrior princess, Callie Grace. We started this blog to share our journey as we navigate through our crazy beautiful life. Callie is a lower limb amputee and I am a Type One Diabetic. We are hoping to change the face of beauty one step at a time! We hope by sharing our story, you leave with a little bit more inspiration and hope! Thank you so much for stopping by and joining our tribe!

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About Me

About Me


Hi Y'all! I’m Jaime, a proud working mama, author, girl boss and wifey to an ultra-adorable husband. I am a huge book nerd, I drink coffee like my life depends on it, and run on dry shampoo and Amazon Prime. Leopard print is my favorite color. I am a story teller at heart and this blog is a virtual scrapbook of our crazy beautiful life. I'm a Type One Diabetic and our little warrior princess Callie is a lower limb amputee. By sharing how we’ve chosen to flourish in the garden we’ve been planted in, we hope you can take some small nuggets of hope, inspiration, and laughter. We are so grateful that you’ve found us—welcome to the fam. We embrace our perfectly imperfect lives and don’t let the doctor’s appointments, spreadsheets, speaking engagements, 10th birthday parties to plan, housework or date nights overwhelm us. Those things are just the beautiful reminders of all the blessings in our lives. Read More




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