Before I had Callie, I thought I was strong. I managed my own chronic illness, worked two jobs, and went to school. I was out spoken and lively. I did a lot, gave a lot, and was a lot for…
As a mama, I knew there’d be days like this. Days where I’m so tired. Days where everything tests my very last nerve. Days where I literally am so all over the place its a miracle I’m standing up right…
Read More »
I get asked that question a lot. And it’s understandable. Short of my husband and maybe our immediate family, not many people can understand or have insight into what our life consists of….. I’m a Type One Diabetic. I am…
Read More »
We had to do Callie’s IEP for next school year a few weeks ago. For those of you that don’t know what an IEP is, its an individualized education plan that we fill out for the school. It details what…
Read More »
I went for a workout yesterday. Not because I hate my body. Not because I “ate” bad things. Not because I “need” to lose weight. Not because I felt “fat” and “ugly.” Not because I was worried about the calories…
Read More »
You know what’s hard? Motherhood. You know brings me more joy than anything else? Motherhood. You know what makes me feel like I can’t do a damn thing right? Motherhood. You know what makes me feel like Wonder Woman? Motherhood….
Read More »
When Callie had her amputation, we vowed that we would never let her prosthetic leg limit her in any capacity. Anything that she wanted to do, any activity she wanted to try, any trip she wanted to take we would…
Read More »
Mom Guilt. For me, this takes on an entirely different connotation. For years, I blamed myself for Callie’s health issues. One hundred percent blamed myself for every single health issue that she had. We spent three months in the NICU…
Read More »
How’s Callie doing? We get asked that a lot. Thankfully because we have a huge tribe and a lot of people that care about our little warrior. It seems like a simple enough question….but sometimes it’s not. I never know…
Read More »
“She’s your only one?” “You didn’t want anymore kids?” I never know what to respond to those questions. We both wanted a large family–we both grew up with siblings. I’d always imagined a loud, rambunctious, crazy household full of babies….
Read More »
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
