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The Princess and The Prosthetic

No Options

April 24, 2020 in Family, Motherhood - No Comments

I’ve never had the option to give up.

I’ve never had the option to “mail it in.”

I’ve never had the option to kick back and let up off the gas.

I never had the option to quit.

If you have people counting on you, you can’t stay down.

I chose to be a mama.  I took on that responsibility and made that decision.  That means I have to show up every day for her.  I have to show up as a role model, a guide, and a North Star.  I have to carry myself knowing that she is always looking to me and watching how I respond.  How I respond to the homeless person on the side of the road, how I respond to people being disrespectful,  how I respond to someone posting something rude and ignorant online, how I respond to stress, and how I respond to challenges.  She is watching me and subconsciously creating her own foundation for how she will handle adversity, trauma, and hardship.

I have to take care of myself physically for her.  I had to fight cancer for her.  I have to take care of my diabetes each day for her.  I have to fuel my body with healthy foods and give it the exercise it needs for her.  I have to show her how to love her body and all of it’s imperfections.  I have to show her how to set boundaries, how to fall in love with herself first, and how to find a partner that respects and adores her.  I have to teach her how to be strong, brave, kind, courageous, smart, feisty, fierce, giving, and generous.

I can’t mail it in because she’s watching me.

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I chose to be a leader in my career.  I signed up to lead people, work long hours, do the unglamorous stuff, and be a catalyst for change.  I chose that.  I chose to light some hearts on fire in my direct reports, to help them grow and develop, and to take on the pressure of leading a large team.  I took on the challenge of building a legacy.  I took on the challenge of being a working mother AND being a leader at one of the biggest medical device companies in the world. I chose to go into a career where I can impact someone’s life in a profound, life changing way.  My team, my colleagues, and my patients need me to show up on fire every day.  They need me to bring my A Game every day.  They need my courage, my compassion, my hustle, my out of the box thinking, and my never say die mentality.  Give up on my team?  Absolutely not.  Give up on being a provider for my family??  Never.

Because I don’t have that option.

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I chose to be a wife.  I chose to spend the rest of my life with this man.  I chose to love him when it’s hard to like him.  I chose to start a family with him.  I chose to build a life with him.  I chose to ignore other’s definitions of a “perfect marriage” and focus on what makes our marriage perfect.  He needs me to show up as my best self every day.  He needs me to be his safe place to land.  He needs me to be his cheering squad, his sounding board, and his teammate.  He needs to know that I have his back in everything.  He needs me to protect us, protect our daughter, and protect our peace.  He needs me to make him laugh, dance in the kitchen with him, and chase away the darkness that tries to follow him home from his job.  Quit on him?  Mail it in with our relationship?  Lean back and coast?  I don’t have that option.

Working three jobs in college?  Beating cancer?  Managing my Type One?  Working since I was 11 years old?  Fighting for coverage with insurance companies?  Cutting out toxic relationships?  Losing my job?  Overcoming my anxiety and depression? Having a heart condition? Advocating for our little girl?  Managing being a first responder’s wife?

I’ve never had the option to give up on any of those things.  I couldn’t coast, I couldn’t have someone save me, I couldn’t rely on handouts or goodwill.  I could’t mail it in.  I couldn’t quit.

When people ask me, “What’s your plan?”  my response has always been the same.

“Whatever it takes.”

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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

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

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