We have started to celebrate every tiny little victory. And I truly hope that no one ever takes our joy, pride, and happiness for bragging. I won’t though ever downplay what we’ve achieved because it makes someone uncomfortable. Our family…
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We are asked all the time “How Can We Help?” Our daughter Callie is a lower limb amputee that walks with the help of a mermaid print prosthetic running blade. She also has a chronic heart condition called Tetrology of…
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I don’t think I have the right words to describe how I felt last night. Last night was Callie’s first dance recital with CBSA’s production of The Nutcracker. I pretty much cried through the whole thing. Seeing our baby girl…
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I had to politely explain the difference between diversity and inclusion to someone the other day who ignorantly told me… “All dance studios are inclusive.” Um no. We had one studio that flat out told us Callie was not welcome. …
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I thought it would be kinda neat to share our “Goal List” with everyone. We are HUGE on goals in our family. Normally, we have smaller measurable goals that we are working towards and then bigger, more audacious, game changer…
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We’ve had a few questions recently about Callie’s amputation surgery so I wanted to share a little more about it…… We made the decision to do her amputation at 18 months. By then, she had recovered substantially from her heart…
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My sweet girl….. I can not believe that you are 11 today!! It literally seems like just yesterday that I was pregnant with you and now here we are! Callie Bear–you are an amazing miracle of a child. One of…
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I thought it would be fun to share Callie’s Halloween costumes through the years! We LOVE Halloween because it just so happens to be our little pumpkin’s BIRTHDAY too! So we celebrate BIG in our house!!! Here are some of…
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In honor of Throwback Thursday, here is a look back at some of my favorite pumpkin patch pics of our little pumpkin. Oh my gourd look at how little she is!!! Our little Hallow-queen! Pumpkin Spice and…
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The other day at Callie’s orthopedic appointment, we had an X-Ray done of her back. Callie, in addition to her other health issues, also has scoliosis. We have to do yearly X-Rays, especially as she starts rapidly growing, just to…
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Hi, I’m Jaime — writer, mother, storyteller, and the heart behind The Wildflower Edit. 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
