Type 1 Diabetes Looks Like Me

April 3, 2019 in Diabetic Diva - No Comments

 

T1D looks like teamwork.  It’s not just me in this fight, it’s my husband, my daughter, my family, my friends, and my coworkers.  They all contribute and help me in their own ways.

T1D looks like strength.

T1D looks like friendship.

T1D looks like insulin in the butter compartment of the refrigerator.

T1D looks like a juice box that has saved my life before.

T1D looks like thousands of blood sugar checks, injections, and infusion set changes.

T1D looks like courage.

T1D looks like the Medic Alert bracelet that I’ve worn since I was 3.

T1D looks like always having a plan.  Even if that plan is to fly by the seat of my pants sometimes.

T1D looks like perserverance.

T1D looks like a delicate life support system that I have to manage every single minute of every single day.  No days off, no sick days, no vacation days.

T1D looks like the callouses on my finger tips.

T1D looks like crumpled up Starburst wrappers on my nightstand when I wake up…..a reminder of the low I had the night before.

T1D looks like defying the odds.  Pushing yourself to excel.  Shattering glass ceilings.

T1D looks like the extra carry-on bag that I have when we travel just for my pump supplies and insulin.

T1D looks like my daughter who knows how to get Mama’s bg meter, glucose tabs, and call Daddy if Mama passes out.

T1D looks like the miles I run every day.  Despite the fact that I have diabetes.  Despite the fact that my oncologist said I wouldn’t be able to run again.

T1D looks like the bottom of my purse that is littered with test strips, candy wrappers, and random infusion sets.

T1D looks like the look of concern on my husband’s face when I tell him I don’t feel well.

T1D looks like me testing my bg at a restaurant and the waitress notices and shares with me that they have “Sugar Free” Syrup for my pancakes.

T1D looks like hope.

T1D looks like……me.

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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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A softer life starts here….

A softer life starts here….

Hi Y'all

Hi, I’m Jaime — writer, mother, storyteller, and the heart behind the blog. For nearly a decade, I wrote online as The Princess and the Prosthetic, sharing my daughter’s journey with disability and the lessons our family learned along the way. It was a beautiful season — full of advocacy, connection, and community — but as my daughter grew older, I felt a shift. She deserved more autonomy. More privacy. More room to decide how she shows up in the world. And I realized something else: My own story was expanding too. Motherhood was still here. Disability was still here. But so were grief, healing, womanhood, nervous system care, feminine energy, homemaking, identity, softness… the fuller, deeper pieces of life that were ready to be spoken aloud. Whether you come for the cozy routines, the motherhood reflections, the disability advocacy, or the soft life inspiration — thank you for choosing to share this space with me. Pour a warm drink. Settle in. Let’s grow a life that feels like you again.

Jaime

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