You Don’t See….
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 »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 »Someone reached out on social media the other day and asked why Callie had a prosthetic leg. First, I love the way they asked. It came from a place of curiosity and acceptance. I wish more people would feel comfortable…
Read More »This piece is based on a love letter that James wrote to me when we first started dating. We took pieces of the letter and created this piece. For most of my life, my diabetes was a…
Read More »Callie and I were in the checkout line at Target the other day and I looked behind me. I haven’t seen him in 10 years. He looked the same as he did that day in the hospital. I wondered how…
Read More »We had the honor of going to Camp No Limits Texas this past weekend. Their mission is to educate, empower, and support individuals with limb differences. We were so lucky to receive a scholarship for our whole family from Hanger…
Read More »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…
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