Category Archives: Being Diabetic

Can You See Me Now?

When I saw this diagram, it reminded me of the iceberg that destroyed the Titanic.  Then I read it.

Wow. That’s me. And like the Titanic, it was the below the surface crap that crippled and nearly sunk me. However – this post is not about me. “What?!” you say.  Yeah yeah.

I was compelled to share this with you, my dear readers, to hopefully educate you about people with chronic (invisible) illnesses. Maybe, you deal with one, but certainly someone you know has a chronic illness, whether you are aware of it or not.

I know about it now. Way too much, to be honest.

If you have read any of my posts under “Being Diabetic” or my “Insulin Pump Saga”, I talk not only about my disease, but how I try to cope with everyday life.  Just telling y’all is cathartic, so I benefit, but I also have my BFF, God, my diary and a dog I can talk to, so these posts are more for those newly diagnosed with a chronic illness, or the people who care about them.

It’s a walk in my shoes to look at how things go, from a person living with one (chronic illness). Live information, instead of all the books, pamphlets and videos thrown at you to absorb. Don’t even think about getting rid of those, BTW!  Mine are filed away in the black-hole under my office files, but they are there when I need to refer to them. Yes, even after being diagnosed 10 years ago, I still need them occasionally.  You can’t know everything!  Not at the same time.

Some days I may seem a little “off”, or not myself.  OK, so most days I seem like that – Ha!  I don’t usually mention it because words of explanation are tough to come by without sounding like a complainer. [Y’all know I’m a complainer, but it’s usually about politics, law, football or stupid people – not all about me.]

Well, it’s time to check my sugars and have a snack (or not) and put my ass in bed – that’s a big job these days…


If you have Diabetes (Type I or II) and would like to comment, ask questions, or relay information – PLEASE do so!!



My Little Friend & I


The Pod

A few weeks ago I introduced ‘my little friend‘ to the world.

It was my fault that we got off to a dodgy start. Between my ignorance and nervousness, our relationship was strained. Today I’m happy to report that the ‘bugs’ in our friendship seem to be worked out. After all, practice does make perfect, or at least comfortable.

For my beloved readers who are following the “Insulin Pump Series”, I will post about this journey now and then, to keep you in the loop about my new ‘remote controlled’ life.  Or however you think of it. Lord knows my family has their own way of referring to this change: The Pod person. The adventures of Robo-Grandma.  My youngest granddaughter has trouble remembering the word “Pod”. She calls it a “boob”. And she likes to pat it, as if it’s a pet, instead of a medical device. (She’s so sweet, I can hardly stand it! But I digress…)

Today’s report is short and sweet. 🙂

It used to take me 30-minutes to do the Pod change because I would verify everything in the User Guide, before doing it. Since I change Pods every 3-days, I have done it 7 times now, twice without the Guide! The “remote” (its official name is “Personal Diabetes Manager” or “PDM”, but that’s boring), takes you step-by-step through the process. Although there are a lot of steps, they become easier every time I do them. I don’t dread Pod change day like I did at first.

Y’all have a fabulous week & thanks for listening!