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 →
Today’s the 5th and final day of Diabetes Blog Week, some may continue posting over the weekend for the wildcard topics, but I think I’ll wrap it up today. To be honest, with how infrequently I’ve been blogging lately, I’m surprised I’ve made it this whole week. Kudos to Karen for selecting topics that I could write about! Today’s topic is tips and tricks.
Let’s round out the week by sharing our best diabetes tips and diabetes tricks. From how you organize supplies to how you manage gear on the go/vacation (beach, or skiing, or whatever). From how you keep track of prescription numbers to how you remember to get your orders refilled. How about any “unconventional” diabetes practices, or ways to make diabetes work for YOU (not necessarily how the doctors say to do it!). There’s always something we can learn from each other. (Remember though, please no medical advice or dangerous suggestions.)
I love it when people share really helpful, actionable tips for dealing with diabetes in real life. Two years ago, we “hacked” diabetes and I shared a list of things that I do to make living with diabetes easier.
Most people who live with a chronic illness end up with a lot of experience when it comes to dealing with healthcare. How would you improve or change your healthcare experience? What would you like to see happening during medical visits with your healthcare team? How about when dealing with your health insurance companies? What’s your Healthcare Wish List or Biggest Frustration? Today is the day to share it all!
I have to acknowledge that I’m in an excellent place when it comes to healthcare. I truly have access to world class medical care living in Cleveland. Overall I have a good team and I can’t relate to all of the horror stories that I hear from others, but my care is not perfect.
There are always areas to improve. In U.S. healthcare, the first area to improve is insurance. Somehow in our twisted system, the insurance companies started determining care, not doctors. Pharmacies will literally fill prescriptions differently than written if the insurance company pushes back. Even doctors will bow to the demands of insurance. Continue reading →
There is an old saying that states “Sticks and stones may break my bones, but words will never hurt me”. I’m willing to bet we’ve all disagreed with this at some point, and especially when it comes to diabetes. Many advocate for the importance of using non-stigmatizing, inclusive and non-judgmental language when speaking about or to people with diabetes. For some, they don’t care, others care passionately. Where do you stand when it comes to “person with diabetes” versus “diabetic”, or “checking” blood sugar versus “testing”, or any of the tons of other examples? Let’s explore the power of words, but please remember to keep things respectful.
I love that it’s a prompt about words that needs to ask people to be respectful. Words get folks all riled up sometimes. I work in PR/marketing communications, let me tell you, we have debates about single commas in come of the things that we develop, so of course word choice is important. I’m one of the folks that the above prompt refers to when saying, “May advocate for the importance of using non-stigmatizing, inclusive and non-judgmental language when speaking about or to people with diabetes.”
We think a lot about the physical component of diabetes, but the mental component is just as significant. How does diabetes affect you or your loved one mentally or emotionally? How have you learned to deal with the mental aspect of the condition? Any tips, positive phrases, mantras, or ideas to share on getting out of a diabetes funk?
When people see my life with type 1 diabetes, the then to fixate on the food, the needles, the gadgets and overall physical aspects of my life with diabetes and assume that is all there is. “Just do X and you’ll be fine, right?” I’ve been asked.
I can do everything that I need to do the be physically “fine” but that doesn’t necessarily make me fine. I’m approaching my 5th year with diabetes (my diabetes is younger that #DBlogWeek!) and I can tell you that there’s a whole lot more to being fine with this disease than meets the eye. Continue reading →