In May, I was invited to be part of an adults with type 1 diabetes panel at a local JDRF event. I wasn’t the youngest person on the panel, but I’d had type 1 the shortest amount of time as I was the only one diagnosed as an adult. I was asked to share about the adjustment to life with type 1 as an adult, so I gave my abbreviated diagnosis story.
I talked about the time five years ago as a recent college grad and new wife. I listed out the symptoms I was experiencing: unquenchable thirst, peeing all the time, tired, blurry vision, weight loss, vomiting… “My husband finally convinced me to go to the doctor,” I told the audience. “And they gave me a pregnancy test.” The audience had a visible physical reaction to that statement. Everyone present knew those symptoms, knew what they meant and expected me to say that when I went to the doctor they diagnosed me with diabetes right away, the pregnancy test was a surprise to them.
As I sit here in the middle of my season of 5th year milestones, I have trouble believing that five whole years have passed. And in the next minute, it’s hard to believe that only five years have passed because it feels like a life time. There’s a lot that I’m thinking about on my 5th diaversary. Continue reading →
I’m still wearing the first insulin pump I ever got… sort of. Since I started pumping with OmniPod in December of 2011, I’ve had two generations of pods and at least 5 PDMs, but as far as Insulet and my insurance are concerned, I’ve been out of warranty since December.
I think I’m going to stay that way for awhile too.
I like my OmniPod and don’t really want to switch off of it. I could choose to re-up on OmniPod and get myself a new PDM and keep the old one as a back up, but to do so would essentially lock me into OmniPod for another four years. I feel like we have finally reached a point in technology and development that there are actually new and significantly better things around the corner. Continue reading →
Hello dear readers, I’m back from vacation! I’ll share pictures soon.
Over the weekend I had the opportunity to attend my local JDRF Type One Nation Summit. It’s the first time I’ve been able to go to one and I’m so glad that I did. About a week before the summit, I got an email from my local Dexcom rep asking if I’d be willing to participate on a panel of Super Stars with T1D, which was a huge honor.
The day started with a research update from Kady Helme of JDRF. She talked about the artificial pancreas study that she’s a part of, Beta cell replacement and other research efforts that the JDRF supports. The current research gives me hope for improved treatment options for type 1 diabetes. Continue reading →