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The Princess and The Prosthetic

The Loneliness of Disability Parenting

I have tremendous friends.

I do.

They are generous, encouraging, and life giving.

They are willing to overlook how many times I have to do a rain check for dinner plans. They send me memes on the daily, make me laugh til I pee my pants and absolutely are the difference between me completely losing it, and me just kinda losing it.

Related: 6 Easy Ways to Support Your Friend with a Disabled Child

They love me well.

But the truth is, they have absolutely no idea what it’s like to raise a child with a disability.

 

My daughter was born with a chronic heart condition that has required three heart surgeries (two of which were open heart).  She also has several skeletal abnormalities along with being a lower limb amputee.  She walks with the assistance of a very snazzy rainbow leopard print prosthetic running blade.

As my daughter gets older, the more I realize I have been clinging to the idea that I will still have a “normal” experience of motherhood. I have been reassuring myself for years that no matter how tough things are, I still will have the chance to experience motherhood the way my friends do.

That I will have a child who no one stares at when she walks into a room.

That I will have a child who doesn’t get tired more easily than other kids.

That I will have a child who doesn’t have to have things modified, adapted or adjusted for her just to be able to participate.

But I’ve learned more and more, this is just simply not my reality. I still to this day, am mourning the loss of motherhood as I hoped it might be.

Please know I 100% realize this sounds a bit self-absorbed.

I realize it’s horrible to be whining about my lack of a normal motherhood when my baby girl struggles just to make it through the day sometimes.

But in all honesty, sometimes I see my friends’ children and feel a pang of envy.

I leave every function a little sad that they all are going home to children that are able to move freely around the world.  That don’t have mobility issues.  That aren’t living in a world that’s not built for them.

I feel a deep, almost visceral sense of loneliness when I hear other mamas talking about their children — their struggles, their classes at school, their crushes, their vacation activities, their hobbies, their sports, their birthday parties, their lives.

It makes the differences between us feel more apparent.

The world tells you that grief gets less over time, but I think grief is a lifelong process.  It’s layers and layers of love, pain, disappointments, heartaches, dreams, hopes, and sadness.

On my worst days, my grief stricken heart feels so broken I can barely breathe.

On my best days, my grief stricken heart feels so broken I can barely breathe.

The only difference between the two, my best and my worst day, is mindset.  It’s how I respond to the loneliness that inherently comes with the circumstances our family is facing.

At my worst, I am focused on all the differences, on all the seemingly unfair, on all of the heartaches, on all the things I might be able to do to “fix” our lives.  The grief can drown me….

 

At my best, I am encouraged by all of you. I am aware that no matter what my motherhood journey looks like, I am not alone in this. I am aware that so many of us tell the same tales, feel the same feelings, hurt the same hurt, and pray the same prayers. The grief could drown me……

Or I can remind myself I taught myself how to swim. I can remind myself that I’ve gotten stronger.  I have gotten better equipped at carrying the weight of the grief.  I’ve learned new skills to adjust my balance so I can somewhat function in life as I carry the weight of this substantial loss. Balancing, adjusting, and navigating life with it.

Being a mother of a child with a disability is lonely work, for sure.

But it is also the most inspiring work. It is work that matters. This work allows me to celebrate progress with absolute abandon because every single victory matters. It gracefully brings me closer to mamas that I will never get the opportunity to meet in person but make connections with every day online.

Motherhood brings out the absolute worst in me.

Motherhood also brings out the best in me.

It’s true for all of us I think. We are more alike than we are different, us mamas.

And this is the balm, antidote, and cure to my loneliness — because we all hurt when our babies hurt. We all dream of a bright future for our children. We all hope. We all struggle.  We all grieve.  We all rejoice. We all triumph.

We all want to throw in the towel sometimes. We all love with every golden fiber of our being.

Disability or not, a mama is a mama.

I am forever grateful to be in such good company.

Jaime

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

Jaime

Hi Y'all! My name is Jaime and it's so nice to meet you! Welcome to The Princess & The Prosthetic! This brand is inspired by my daughter Callie who is a lower limb amputee. We're dedicated to inspiring others to embrace their own perfectly imperfect fairytale. We advocate for people with disabilities and hope to inspire everyone--regardless of ability--to love and accept themselves just they way they are! I am a story teller at heart and this blog is a virtual scrapbook of our crazy beautiful life. You're in the right place if you are a huge book nerd, drink coffee like your life depends on it, and run on dry shampoo and Amazon Prime. We live a semi-crunchy lifestyle but still love a good Texas BBQ. Inclusion is our love language. You can find us either on the archery range, at the stables, on a hiking trail, or walking our rescue dog, Jack! We are so grateful that you’ve found us—welcome to the fam. Read More

Jaime

All of these things can look like rest 🌙✌️✨️

I'm learning all I can about how important rest is for me (#hashiwarrior ) and I'm discovering.....it's not just about sleep. 

Taking time for me, prioritizing things that are truly important, and getting rid of pesky perfection are some of the things I'm implementing! 

#hashimotosdisease #autoimmunedisease #restday #perfectionism #timeforme
If I do anything as a mother........
It will be to make sure she knows that she is loved beyond measure ✨️✨️✨️

#ksmomsday
Slice of life.....

Spring Potting

New Workout Space

Grounding + morning coffee + vitamin D

Puzzles + Coffee

Farming co-op pick up day

Life After Gluten 

25lb draw + 50 meters

ERG Mixer

Board of Directors meeting

Walks on walks
Sharing all the beautiful things that happen when you set (and hold!) a boundary!

#boundaries #boundariesarehealthy #toxicfamilymembers #toxicfamily ##toxicrelationship #toxicrelationshipsurvivor #relationshipadviceforwomen
SIXTEEN YEARS......

It's a lot of showing me what a mature love is...
Laughing so hard at your jokes, I pee my pants.
Making me feel gorgeous when I roll out of bed in your oversized academy tee and a messy bun. 

It's a lot of pushing me to be 1% better every day....
Believing in me when I have nothing left in the tank.
Couch dates, the space in-between my fingers that your hands always seem to be, and pulling me back to bed pleading for just five more minutes. 

It's a lot of when I doubt myself, you walking side by side with me through the darkness....and quietly pointing out the places I shine the brightest. 

It's a lot of choices, promises, commitment, and loyalty. It's a lot of stolen kisses, inside jokes, and catching your eyes on me from across the room. 

It's a lot of work. Long walks with the dog on Sunday. "I'll be late. I love you." texts. 

It's a lot of five page love letters in a world full of status updates, dream come trues, and waking up next to you. 

It's a lot of falling in love with each other's chaos. Conquering our demons and wearing our scars like wings. Unpacking childhood wounds, setting boundaries, and seeing each other for the perfectly imperfect humans that we are. 

It's a lot of sighs, eye rolls, heartaches, and comebacks. Wiping away tears and promising to try again.  Wanting to be close instead of wanting to be right. It's a lot of grace and forgiveness.  Healing and inner work.

It's a lot of figuring out if we're wild wrapped in fragile or fragile wrapped in wild when it comes to our love. Because in some ways, this feels so incredibly strong--unbreakable. In other ways, I want to fiercely protect this beautiful, delicate, amazing once in a lifetime thing at all costs from the world. You and me, baby. Always. 

And as we go to sleep tonight, my head tucked neatly into your shoulder....
Every thump.
Every drum.
Every pump of your strong steady heartbeat....
Reminds me of one thing. 

Home.
Home.
Home.

Happy Anniversary ❤️

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