By Erin Schovel Turnham
Tuesday, June 11, 2019
Mr. Mister and I woke up late. I wanted to try breakfast at a place new to us and he obliged. We made our way to Gypsea Crepes just before they stopped serving breakfast. I loved everything about it!! Continue reading →
I shared with my blog partner, Alese, what I am about to share with you. She started sending me Chuck Norris memes and called me a type 1 diabetes black belt. I think I am still a white belt, but I’m adding stripes!
Thanks to resources like the books Think Like a Pancreas by Gary Scheiner, and Sugar Surfing by Dr. Stephen Ponder, I’m figuring out the timing for my 7 year old Grasshopper’s insulin. I’ve been trying this stuff for maybe a year and a half now and I think I’m finally starting to get it. Continue reading →
What music moves you? What songs resonate with you?
When you are having a difficult day… or week… or year… with type 1 diabetes, or just with life, what do you listen to that helps you get through?
Leading up to the spring of 2017 I was having a rough time. I felt like a failure, like everything I was doing as a T1D mom and in life was not good enough. It turns out that depression tells a person those kinds of lies. Continue reading →
Friday is car wash day. I vacuumed up at least 20 test strips and ALL the raisins. Dealing with a chronic condition like T1D means the highs and lows happen anywhere, anytime. It doesn’t stop for car washes. Thanks to the noise of the water and then the vacuum I couldn’t hear the Dexcom low alert and for some reason it didn’t show up on my watch. Grasshopper said he felt low. Yep. 55 on the meter, 50 on Dexcom. 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 →
If I were to choose an icon of motherhood right now while my children are six and two, it would be an emblem of a little hand giving me a Kleenex tissue. And you know what? I accept that tissue. Continue reading →
Gabbing with Grasshopper
Him: What did you say those big kids in white clothes were doing at school today? Typeonediabetesdo? Continue reading →
After dealing with diabetes as a family for four years and four months, I think of it as if I am holding a pencil in my outstretched hand. I am relatively confident now in the daily decisions that need to be made. Thanks to Sugar Surfing techniques I am usually able to run Grasshopper’s blood sugar control as a background program in my mind instead of as the main focus of my day. But of course it is always there. Continue reading →
That’s what the mom right before me in line to check in late to school had written in the “reason” column. Continue reading →
We are HUUUUGE fans of the Dexcom continuous glucose monitor (CGM) here at Sugar Rush Survivors. It has helped our lives in so many big and small ways. So when there is news about new developments in Dexcom technology, like the FDA approving the release of the Dexcom G6, we get excited! Exhibit A: an evening of text messages between me and Alese. Continue reading →