Blue November Prep

While I am still getting ready for Halloween, I’m also looking forward to our diabetes awareness efforts for November. We participate in Project Blue November by wearing blue on Fridays and posting on social media. Last year I painted a craft pumpkin with the international symbol for diabetes, a blue circle. We collected all of Grasshopper’s used diabetes supplies and empty packets of Annie’s Fruit Snacks in the pumpkin to show all of the supplies and low blood sugar treatments he used. Continue reading →

Life Speed

By Kay Jacoby

By Erin

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 →

20 Minute Poop Storm

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 →

T1D is a Beach: 7 Tips for Your Summer With Type 1 Diabetes

by Erin

Summer is almost over (officially) for us, and I have been taking notes and pictures all season long. But let’s get real. We live in Alabama and it will be hot through October! So these tips and products are relevant for us most of the year. Continue reading →

Podcrastinate

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by Alese

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 →

Camp Seale Harris

by Erin

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 →

Choose Kind

by Erin

I recently watched “Wonder” on Amazon Prime Video. It is the story of a family whose son is born with Treacher-Collins syndrome, a condition which alters the development of the bones and tissue in the face. I know I am late to the conversation as the book was published in 2012 and the movie came out in 2018, but I have had a couple of kids and some crazy years recently. Reference: all of my posts on this blog. Continue reading →