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, Sugar Surfing by Dr. Stephen Ponder, the Juicebox Podcast by Scott Benner, and online support groups like SHIFT: Proactive CGM Management, 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 →
“Why did you forget your diabetes supplies??”
“You should check your blood sugar more often.”
“It is SO important for you to take your insulin on time because if you don’t you could go into a coma!”
I spent my Saturday morning as a participant in a research study conducted by Dr. Jan Kavookjian at the Harrison School of Pharmacy, Auburn University. The purpose of the study, per Dr. Kavookjian’s materials, is to “gather parent perceptions about what it is like to communicate with a child or teen who has type 1 or 2 diabetes.”
As parents and caregivers we want to FIX IT. Both the big things we know we can’t fix (our kids are stuck with T1D until there is a cure) and the smaller things (my kid won’t bring along the needed supplies). Continue reading →