Subscribe to our Mailing List

Get the news right in your inbox!

The Princess and The Prosthetic

Victim or Warrior?

December 18, 2019 in Family, Warrior Princess - 1 Comment

Sometimes I feel like it’s very easy to fall into the “victim” mentality.

Especially with our situation.  I mean how could I not?  How could I honestly not look at all of the challenges we’ve overcome, all of the hurdles we’ve crossed, all of the doors slammed in our face and not felt the teensiest bit victimized?

Type One Diabetes.

Amputee.

Chronic heart condition.

Cancer.

It’s a beautifully brutal list.

I think it’s because we’ve always asked ourselves “Do you want to be a victim or do you want to be a warrior?”

Instead of asking “Why is this happening to us?” we’ve focused on “What is this trying to teach us?” Or even more so……”How is this situation happening FOR us?”

Because we want to look at all of the things that we’ve been through and be able to shout from the roof tops “We are STILL here!  It did NOT break us!”

Because we want to be proud of our ability to recover, achieve, and rebuild.

Shouldn’t we want to be able to say that those hard things did not decimate us, they did not destroy us, they did not beat us?

We refuse to play the victim.  We refuse to quit, we refuse to be fueled by fear or pessimism.  Or negativity……especially negativity.

IMG_1871

“Do you want to be a victim or do you want to be a warrior?”

We are not victims.  We are warriors and survivors, setting the world a blaze with our truths.  Sharing our light, our warmth, and our fierce courage.

We want to say that despite the hellfire.  Despite the soul crushing.  Despite the grief.  Despite the pain…..WE ARE STILL HERE.  That we did not give up.  That we have a history of victory because no matter what we have not given up.

Life comes at you.  No matter the circumstances.  Some people chose to play the victim.  Some people chose to merely survive.  Others, like my family, chose to pick up the sword and fight like a warrior.  Our family, with fire in our veins and courageous hearts, will fight.  Because we see the sunset, even on the darkest days.  We see the opportunity in every difficulty.  We see the quiet moments of beauty that others take for granted.  We see the crazy blessing that is our life.

I don’t know how our story will end.  What I do know is, that absolutely nowhere, in any of the chapters…..will it say we quit.

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!

All posts

1 Comment

  • Judith Dill December 19, 2019 at 3:09 am

    Beautifully written and very inspiring!! FIGHT ON WARRIORS you will be rewarded

  • Leave a Reply

    This site uses Akismet to reduce spam. Learn how your comment data is processed.

    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

    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 ❤️
    I started to feel off in the fall of 2022. I couldn’t sleep, was so tired during the day that I could barely finish my work, and felt hungover every morning even though I wasn’t drinking alcohol at the time.

I was also experiencing strange heart flutters, anxiety, brain fog, difficulty concentrating, cold intolerance, headaches, joint pain, weight gain, and many other vague symptoms.

Over the last almost two years, I've visited a number of doctors, including a cardiologist, an endocrinologist, and my OBGYN. Every test came back "within" normal ranges.

It was gently suggested that I was "getting older." 
And that maybe it was just "stress." 
And that maybe if I "ate less and worked out" more, I could lose the weight.

Several of the doctors were very dismissive and tried to tell me this was just a part of getting older. 

And frankly, I felt like I was going a little crazy. Was I over-reacting? Was I imagining it? I started to question myself.

But I wasn't over-reacting. I know my body better than anyone else. I've lived in it for 42 years. I know when something is wrong. I know how I was feeling, and as a last-ditch effort, I made an appointment at a hormone clinic.

This week, I finally got an answer.

I was diagnosed with an autoimmune disorder called Hashimoto's disease. It's a disease that damages the thyroid, a gland that releases hormones that control metabolism, growth, and a number of other bodily functions.

Needless to say.....I'm glad that I never gave up advocating for myself. I'm glad that I didn't take the first doctor's response at face value. I'm glad that I continued to ask questions, get blood draws, and ask for clinic recommendations. I've glad that I have an answer, a path to take, and a treatment plan.

Am I heartbroken? Yes. On one hand, I want to ask the universe why it continues to give these health challenges to me. When is enough....enough?  Cancer?
Type One Diabetes AND Hashimoto's Disease? One is hard enough, and right now, two feels insurmountable.

On the other hand, I know why.

It's because I'm strong enough to handle it.

#hashimotosdisease
#hashimotosthyroiditis
#hashimotoswarrior #autoimmunedisease #autoimmuneprotocol
    I'm super excited to announce that I've joined the board of directors at @opentrailranch !

O.P.E.N Trail is an amazing organization that provides equine assisted services to children and adults with physical, cognitive, and emotional challenges in South Texas.

We have been part of the OTR family since Callie was five years old so I could not be more proud to be stepping into this position.  I believe in the importance of the work that they do and, more importantly, have had a front row seat to witness the impact of the work they do in the lives of their participants ✨️🐴🐎✨️

#equinetherapy #equinetherapist #therapyhorse #horsedoftexas

    Latest Posts

    Let’s Hang Out

    Subscribe to our Mailing List

    Get the news right in your inbox!

    The Princess and The Prosthetic

    Popular topics

    Archives

    ×

    Discover more from The Princess & The Prosthetic

    Subscribe now to keep reading and get access to the full archive.

    Continue reading