I have a history of very vivid and weird dreams. I’ve heard of others with diabetes having strange diabetes dreams and even stranger dreams when a low blood sugar is involved. In more than 6 years with type 1 diabetes, I hadn’t experienced a diabetes dream… until the other night.
I woke around 2:00 a.m. to my Dexcom alarming low, so I checked my blood sugar and it was 66 mg/dL. A little low, so I treated with a marshmallow from the bag on my nightstand (don’t judge what you don’t understand) and ended up slipping back into sleep. I can’t remember everything about the dream I had next, but here’s what I do remember… Continue reading →
There’s a heroin epidemic in my home state. Drug addiction is a sad and serious problem in our country that is getting a lot of media attention. This crisis has had an unexpected impact on people who live with diabetes.
via Type 1 Diabetes Memes
Because after insulin, laughter can be the best medicine, those of us with diabetes make jokes about it, specifically type 1s like me who have to inject either regularly or occasionally. We joke about being high, we joke about shooting up to keep from getting high and we joke about being insulin addicts. All of which are true but out of context could sound bad.
However some of the actual realities of this disease have lead to mistaken identity in some cases.
Three things happened in the course of one week over the summer that prompted me to write this post.
I’m excited to introduce a new diabetes blog series and the awesome organization making it happen. Op4G is a market research panel company which stands for Opinions for Good. When someone joins an Op4G panel, they have the option to select a nonprofit that they want to support from a list of 300+ non-profits) and when they complete a survey, a portion of the incentive goes directly to the nonprofit. So far, Op4G has donated over $447,000 to non-profits.
Op4G is open to the general population, however they are working to form niche health communities… starting with diabetes. Op4G partners with organizations with research needs that focus on diabetes, while also giving you a way to contribute your voice to research on products and services that could impact you in the future. They’ve teamed up with me to produce a series of diabetes-related blog posts so this is a win, win, win, win kind of series (4 wins there). Continue reading →
Insulin and other diabetes medications and supplies can be costly. Here in the US, insurance status and age (as in Medicare eligibility) can impact both the cost and coverage. So today, let’s discuss how cost impacts our diabetes care. Do you have advice to share? For those outside the US, is cost a concern? Are there other factors such as accessibility or education that cause barriers to your diabetes care?
As I thought about this post, I felt the urge to start with a disclaimer or an apology. But I’ll start with thankfulness. I may complain about having been forced into an insulin that doesn’t work as well for me or having to wait on hold to get a real person to talk to about my supplies, my medicine or my next appointment. But at the end of the day, I’m very lucky when it comes to diabetes costs.
And I don’t use “lucky” in a flippant manner. I generally refuse to refer to myself as being lucky, blessed (or in some other way gifted what I need) to be where I am in my life when it comes to career, home and relationship. I work hard and make choices to get to where I am. But when it comes to the access to what I need to not only stay alive but be healthy, I’m really lucky. I have insurance, I have an HSA, I have the means to pay my high deductible and I have the best medical care in the world right in my back yard. That, my friends, feels a lot like luck.