By Kay Jacoby
Both Alese and I have been busy and we haven’t written much. There have been lots of changes for both of us and it feels like life is moving at light speed. The speed of life. Life speed, full ahead.
I had a moment to slow down a bit after one of Grasshopper’s routine appointments at Children’s Hospital of Alabama. We loved getting to see Heather Jordan to talk about how to better tackle some of the issues we face like helping Grasshopper through the annual blood draws he has to have. The last one was… intense.
After our appointment we were waiting for traffic to ease so we spent some time in Children’s Harbor. I have heard various reactions when we share that we are headed back to Children’s. Fairly often others react with sadness or say some form of, “Oh, that is such a sad place.” Granted, my view of it is due to Grasshopper’s successful diagnosis and treatment there. There certainly are many possible outcomes. For our family Children’s has been and continues to be a place of hope.
I thought I would take some photos to share why Grasshopper is always so excited to go to Children’s Hospital. Continue reading →
In the space of about 20 minutes on Tuesday evening, the following happened:
- I dosed Grasshopper for a 40 gram weight piece of cinnamon roll for dessert. That is a sliver of a roll, not a whole one. It was a 20 gram carb treat. I sent him to put on his pjs so the insulin could have a little time to work.
- He walked out a few minutes later holding his insulin infusion site… that was supposed to be attached to his body. I tried to hide my instant anxiety. When did it come off? Did it come off before his 24 gram carb dinner? Did he get any insulin for dinner? Did it come off after dinner but before I dosed for the cinnamon roll slice? Did he get any insulin for that??? Continue reading →
Sunday was not as much of a fun day as promised. I have been using expired Dexcom sensors because you know I’m cheap. It turns out they expire for reason. My numbers last night were 150 points higher than my readings.
So this morning I feel like I slept on a bar room floor. Continue reading →
Back in the fall of 2017, I saw a familiar name on one of the T1D Facebook pages I follow. Scott Benner, T1D dad, blogger at Arden’s Day and podcaster at Juice Box Podcast, asked what other parents might want to hear on upcoming podcasts. I posted asking for more discussion about parenting a young child with diabetes, and offered to talk with him about it.
Continue reading →
Fear is a terrible thing. It blocks, prevents, withholds. Strangely, it simultaneously drains my energy. For too long I have let my fear take charge.
When Grasshopper was born I had great plans of getting him into swimming lessons very early. Continue reading →
I’m staring into the pantry with a deer in the headlights look. Wide eyed, slack jawed… it can’t be THIS hard to come up with two snacks and a lunch for my kindergartner. Continue reading →
A few months ago Grasshopper’s school nurse, Amber, told me she had been contacted by some folks from the Pike Road Lions Club. Continue reading →