If you can name it, you can tame it! In this episode, Qiana Drew clears up some misconceptions and shares how, when it came to her diabetes, she would often do things to try and keep up with her thin peers. Eventually, she realized this mindset was not a healthy way to live and decided to share her journey with Type 1 diabetes and diabulimia to help others live their best life.
At the JDRF Summit last January in Oklahoma City, we struck up a conversation with the father of Lily, an adorable, youngster who lives with T1D. She had on this awesome-looking watch with her blood sugar. So did her Dad. We had to explore further. In this episode, Clayton shares his family’s philosophies on parenting and empowering the T1D life. While not a “techie guy”, he managed to discover and use Night Scout… while continuing to develop an artificial pancreas in his basement. There’s some wisdom in this one folks. Continue reading →
It’s one thing to be the person receiving a type 1 diabetes diagnosis. It’s yours. It’s pretty straight forward for you. Take shots, count carbs, and survive. To be on the other side of the glass, as the parents, is another challenge in itself. Parenting can set the foundation for a successful life of type 1 diabetes management. The Fightmasters have an endless collection of diabetes experience, including crazy low blood sugars, insulin mix-ups, little league sports, and sending a kid to college. Their perspective is one of autonomy, flexibility, forgiveness, and empowerment. We joked, debated, and even came close to shedding a tear, although it was right in the middle of Oklahoma’s allergy season. Continue reading →