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The Princess and The Prosthetic

The World Kept Spinning

We were slammed by grief….but it was another family’s Tuesday.

We were wrestling with the diagnosis of a chronic heart condition and pending open heart surgery…..and others were standing in line at Starbucks.

We were spending the nights in a rocking chair in the NICU…..and others were complaining about traffic jams on their morning commute.

We were learning how to walk with a prosthetic leg….and others were cheering on their favorite sports teams on Sundays.

We were going on a Disney cruise in the event our daughter didn’t make it through her upcoming open heart surgery–desperately trying to squeeze in as many memories as we could….and others were going grocery shopping.

We were drowning in millions of dollars of medical debt….and others were worried about not being able to get their nails done that week.

We were going through cancer treatments……and others were trying to figure out what movie they were going to see that weekend.

We were kissing our daughter goodbye as they wheeled her back to her second open heart surgery…..and others were on going to work that day.

I would battle with myself wondering how we could be grieving or going through so many hard things……and others were just going about their day.  Untouched.  Unphased.  It would make me want to scream.  How could they just be living their lives….when ours was falling apart?  How could they be worried about something so trivial when my daughter was battling for her life?  How could they be worried about such small insignificant things when we were trying to find our footing?  Could they not see that the small sad spot in their day was a huge gaping hole in our lives?  Our life had been repeatedly turned on it’s axis….and the rest of the world just kept on turning.

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It took me a very long time to not be angry about that.  In fact, if I’m being completely honest, I still have to work through this.  It’s a work in progress.  I still find myself mentally thinking “Really????” when someone shares a concern with me.  I have to actively work through reminding myself that I can’t compare our struggles.  That each of us are on a different journey.  Something completely manageable to our family that we wouldn’t skip a beat over–might be a huge mountain for someone to climb. Something that we’ve done many times before might be a first step for another family.  It’s the reminder that the comparison game goes both ways–the good stuff in life and the challenges.

It’s the acknowledgement that personal grief is like living a double life.  One where you just go about your day like everything is fine….while your heart is silently breaking into a million pieces. We don’t know what others are experiencing and its a reminder to always respond with kindness.  Its the reminder that although I am try to be transparent with our struggles, other people might be quietly sitting in sadness.  It’s a reminder that when you deal with loss, a tragedy so large you aren’t sure how you will ever recover, that the world keeps going.  The seconds pass, the days change, and the month still progresses.

Grief doesn’t have any rules or time lines.  It can last forever–just like the hope or the love you experienced.  It might come in giant waves–and you might have days where you are drowning.  Or it might quietly lap at your feet, a quiet reminder of the things that you have been through.  But you have to keep your head above the water.  You have to wave to the shore when you need someone to come tow you in.  You have to look for the undercurrents and know how to avoid those.  You have to use a life vest when it gets too deep and your toes can’t touch the sand any longer.  You have to learn……….. to swim.

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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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4 Comments

  • Jessy Munch February 2, 2020 at 6:39 pm

    You both are so strong, amazing and inspiring. I hear you and see you and can do relate to your strength in many ways 💜

    • Jaime February 2, 2020 at 6:46 pm

      Thank you sweet friend. Thanks for being here and the support ❤

  • Betty February 2, 2020 at 10:35 pm

    Very well written, thanks for sharing this.

    • Jaime February 3, 2020 at 1:15 am

      Thank you so much for being here! We appreciate your support!

    Leave a Reply to Jessy MunchCancel reply

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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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