It’s been just over two months since Kay was diagnosed with Type 1 diabetes, and although that might seem like enough time to adjust, everything still feels very new to us. There’s so much to learn and figure out, and each day brings its own set of challenges.
Kay seems to be fluctuating in and out of the honeymoon phase, where her pancreas sometimes decides to work, meaning some days she needs more insulin than others. There are moments when I give her insulin, and it works so quickly that her blood sugar drops rapidly, forcing me to give her a sugary snack or drink to stabilize her. But too much sugar can cause her levels to spike too high.
In my efforts to better support Kay, I’ve signed up for a Type 1 Diabetes summit hosted by Breakthrough T1D (formerly known as JDRF) in September. I’m constantly searching for resources that can help me understand diabetes more deeply so I can care for Kay as best as possible.
I’ve also joined a few Facebook groups, one of which offers a podcast filled with helpful information that I’m eager to explore. I won’t lie—diabetes is scarier and more overwhelming than I ever imagined. But I trust that with time, I’ll gain the knowledge and confidence needed to care for Kay and ensure her health stays on track.