By Erin Schovel Turnham
Wednesday, June 12, 2109
Mr. Mister had to work on our last day at the beach but thankfully he is able to work remotely. We had another day near the beach if not physically on it. I walked to get breakfast from Gypsea Crepes again and this time I remembered to take a photo before gobbling it up. Continue reading →
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 →
By Erin Schovel Turnham
Monday, June 10, 2019
Then an avalanche of guilt because I feel relieved. Alarm free sleep. Anxiety free sleep. Uninterrupted sleep. Just sleep. 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 →
Now that Grasshopper is playing baseball we have some evenings when we have to grab dinner and head to the field early and stay late. Here’s our Tuesday evening in photos, from dinner in the car on the way to the ball field for pictures, to batting practice, the game, with Dexcom G6 graph screenshots throughout. Thanks to Sugar Surfing and Arden’s Day/Juicebox Podcast, we had a smooth night of blood sugars! We bumped it up with carbs when needed, reduced his pump a bit, and he had a ton of fun out there. The icing on the cupcake is that his team won, 14-3! Continue reading →
I like to share the positives. The triumphs. The laughs. I like the sunshine and light.
Those things are easy to tell. Easy to share and pass along.
This day earlier in January was a triumph of fun even though we had to treat several lows.
It is important, however, to also share our struggles. That is when I hear from others, “I am so glad to know I am not alone.” 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 →
I’ve taken some time off from writing and posting so I can focus on my family. I’m trying not to feel guilty about the fact that my time off has coincided with November, Diabetes Awareness Month, and the feeling that I need to be posting MORE right now. But wow, I am DRAINED. The Pike Road Lions Club Strides Walk was a great event and I am excited to help again next year. I have a post coming with pictures of the event and a big thank you to all who made it a success. Continue reading →
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 →
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 →