hell yea
Posted by: typeofl1fe on: June 30, 2009
This is freaking awesome. It’s incredibly inspirational, and I’m not going to lie, I teared up a little bit when I read it. Not that it’s an emotional article; it just tugged at my heartstrings, personally. I think these people are so, so kick-ass. They deserve a huge amount of admiration for this accomplishment, although I think it’s difficult for people without diabetes to really conceptualize and understand the level of dedication it requires, at any level. But I’m digressing. Just wanted to share this bright spot in my day.
ugh.
Posted by: typeofl1fe on: June 15, 2009
Searching for stuff to watch on the comedy channel of hulu, I came across the pilot episode of a show titled, “glee” and decided to check it out. It seemed like an okay show, albeit chock-full of stereotypes (another “ugh”), but it was somewhat entertaining, and I was enjoying the understated humor – until, about 12 minutes in, the protagonist goes to visit his wife at work (she’s a manager at “Sheets ‘n’ Things”), and brings her a sandwich. “It’s roast beef and pumpernickel. Your favorite.” And she’s all “oh thanks, honey!” Then she gets this look on her face and says, “Wait. Does it have mayo?” Yes… “Honey, if my diabetes comes back, we can’t get pregnant!”
WTF. asjdfweiounjkval;jse;fa. SO MANY MISCONCEPTIONS. One of them being that mayo causes diabetes. Um, seriously? Or that it will “bring it back.” Guess what, folks. Once you’re diabetic, type 1 OR type 2, you are diabetic for life, no matter how much weight you lose, how healthy you eat, how frequently you exercise, or how much medication you don’t have to take.** The ADA website states that “diabetes is a lifelong, chronic illness,” and the Joslin Diabetes Center provides a more thorough and satisfactory explanation of that statement here.
Here’s a tip. Don’t start talking about stuff you don’t know about, unless you are asking questions and looking to educate yourself. Certainly don’t pretend to know what you are talking about if you don’t. Because you will inevitably run into someone who does know what they are talking about, and you will look like a fool.
Sorry for the rant. But I was inspired, and, as evidenced by the lack of posts, I haven’t been for a while.
**Gestational diabetes is a kind-of exception: yes, it “goes away” after pregnancy, but chances are high that it will “return” in subsequent pregnancies, and those who have had gestational diabetes are much more likely to develop type 2 later on.
This Is Reality
Posted by: typeofl1fe on: February 28, 2009
green-eyed monster?
Posted by: typeofl1fe on: November 30, 2008
I went out with a friend from high school tonight – someone I knew in my pre-diabetes days, who didn’t know yet that I’d been diagnosed. This presented a small dilemma that I’ve wrestled with for a little bit: In the first few months of being diagnosed, I kind of struggled with how to tell people in my life that I had diabetes. For a while, I ended up hiding it when I could. It’s not exactly an easy thing to bring up in daily conversation:
“Hey! How was your weekend?!”
“Oh, I just spent the weekend in the hospital – diagnosed with diabetes! What were you up to?”
Hmmm, no. I realize now that concealing it was not at all conducive to my mental health. (One might say it was “detri-mental,” ha ha. sorry.) Anyways, that’s one of the reasons that going to Paris was so liberating for me: I only knew one person prior to the trip, so I just went about my business out in the open, and my new acquaintances could take it or leave it as they wished, and I was more than pleased to field questions. It was different and refreshing to be up-front and open about it from the get-go instead of figuring out a minimally awkward way of bringing it up. “Coming out” played a big part in my self-acceptance of this disease. So I’ve decided it’s in my best interest to adopt this policy in virtually all cases, but especially with those that I’ve known since before I was diagnosed. I think it’s a whole lot easier and healthier that way.
But I digress (WOW I digress. haha) The point of this post was supposed to be that while I was talking to my friend about diabetes, he mentioned (as most people seem to) that he should get his blood levels tested. Depending on the situation, I’ll sometimes offer to test for them right then and there, which was the case tonight. At this point, most people seem to get nervous for a variety of reasons: they’re afraid it will hurt, or they’re afraid of what the result will be. I just have to laugh, because in all likelihood, they have nothing to worry about. And sure enough tonight, the number was a perfect 96 (and this was after a small popcorn at the movies). Whenever I’ve let my friends test their blood sugar before, I always get a little pang when I see that peachy-keen number on the screen of my blood glucose meter. And I could never put my finger on what that feeling was, but tonight I realized that it’s jealousy. Don’t mistake me, I am undoubtedly happy that my friends don’t have worrisome test results. But it struck me tonight that that number has such a different meaning for me than it does for them. When I get a number like that, I feel damn proud of the hard work it took to achieve that number. Because more often than not, that’s what it takes. But for them, that number is just the way things are, not the way they should be. They don’t realize all the effort it can take a diabetic to get a lovely little number like that. Which is a little frustrating. 
World Diabetes Day
Posted by: typeofl1fe on: November 14, 2008
So today is World Diabetes Day, and I figured I should probably do something, even though (or especially because) I haven’t written here for weeks… oops.
In a lucky stroke of impeccable timing, I serendipitously happened upon this video on the New York Times Health page. It’s snippets from a day in the life of a normal 16-year-old girl, recently diagnosed with Type 1 diabetes. It gives a pretty good overview of things, albeit at a very basic level. The one thing that was weird to me was that she used blood samples from her forearm to test her BG – not her fingertips, which I can’t say I’ve ever heard of anyone using anything other than their fingertips. I think I may have come across a booklet or two that mention using one’s palm or forearm, but by and large, the common practice is to use one’s fingertip.
Anyways, it was interesting to see, and kind of touching. Seeing another young, newly diagnosed diabetic hit home a little bit.
Back to WDD: this year’s theme is “Diabetes in Children and Adolescents,” addressing the growing numbers of youth with diabetes. Check out the website for more information about the campaign and need-to-know facts about this disease.
Fun Fact: According to the WDD website, November 14 is designated as World Diabetes Day to commemorate the “birthday of Frederick Banting who, along with Charles Best, first conceived the idea which led to the discovery of insulin in 1922.” And how very grateful I am for that. It absolutely dumbfounds me that this discovery took place less than one hundred years ago. Sometimes I wonder how close to death I really came, because I know that I was not in a good state when I was diagnosed. And because of the serendipitous (love that word!) nature of the circumstances leading to my diagnosis, I wonder if and/or when something else would have happened to send me to the hospital. It’s scary to think that I might not be alive today if things hadn’t fallen into place the way they did (although I might rather argue that it was more of a disruption), because as hard as that is to believe, it could have happened. It speaks a lot to the fact that there remains a lot to be done in the realm of diabetes awareness and education, even (and especially) today. So do your part, and spread the word. And if you don’t know much about diabetes, investigate a little! Satisfy your curiousity. Even just a little bit of knowledge helps. 
Key Information
Posted by: typeofl1fe on: October 14, 2008
This post from a blog on the NYT is kind of brilliant – it’s a compendium of super-useful keyboard shortcuts for those small-but-essential computer tasks that you never realized were inconvenient until you discovered an easier way to do them. ; )
I already knew the majority of these, but I definitely had a few “a-ha!” moments (who knew that the “Shift” key reverses just about any other command key?). And as someone who uses a laptop, they’re especially handy. Enjoy!
http://pogue.blogs.nytimes.com/2008/10/02/tech-tips-for-the-basic-computer-user/
“I get by with a little help from my friends…”
Posted by: typeofl1fe on: October 3, 2008
Today, I am happy. I am in a good place. My life is full and vibrant, and I know that I am lucky. I am working through my issues, and because of that I am (becoming) a better, stronger person. I believe that everything happens for a reason, and although life isn’t always easy, one should always make the most of it.
Even though the week started out on a rough note, thanks to some fantastic friends that I am quite lucky to have, I’ve made an about-face in my perspective and my outlook. They were there for me when I needed it, and I can only hope that I can do the same for them. It’s amazing how some people can brighten your day simply with their presence. It makes me realize even more how true it is that very often, the little things are what matter most in life.
This is my life, take it or leave it, and I wouldn’t have it any other way.
One Year
Posted by: typeofl1fe on: September 29, 2008
- In: diabetes
- 3 Comments
The anniversary of my diagnosis with diabetes is fast approaching, and I don’t like it. In fact, it kind of scares me. I know it doesn’t really mean anything, but it signifies something to me. It signifies permanence, that this isn’t going away. All these things that I already know, but that this date forces me to acknowledge once again. It’s a different kind of reality check. It brings fresh memories of my life before and without diabetes, and dredges up a whole host of associated emotions, and I’m really having trouble dealing with that right now. I don’t want to have lived with diabetes for a year. I don’t want to have this degree of familiarity and comfort with it. I don’t want to be used to it. And I don’t want to deal with it, but I have to. And right now, it seems like the hardest thing in the world. So much in my life has changed after and as a result of my diagnosis, and in so many respects, I just want it to go back to the way it was before. I don’t know what else to say.
Think Before You Bolus
Posted by: typeofl1fe on: September 26, 2008
So I’ve gotten into this bad habit of bolusing for my meal the morning after a night of drinking (the trend seems to be Friday mornings), without taking into account my alcohol intake of the previous evening. And as a result, I start to get a headache and feel crappy in class, and I attribute these to a hangover, wishing I’d thought to take an Advil. Only when I start to get really uncomfortable (read: symptoms other than a headache) do I think that Oh, maybe I should check my blood sugar. And oh hey, that happened this morning, and what number did I see? 47. And two weeks ago? 43. Not fun stuff. It doesn’t help that for both of these occurrences, I haven’t had any food on me to treat a low with. That’s happened on a couple other occasions, too – not good. So I had to leave class once (which I don’t like doing in the first place because it draws attention) to go to the vending machine for a snack, and today, since I didn’t check my BG until I was out of the building, I had to wait about 10 minutes while I walked across campus to the next building I had class in. ughhhh.
The part that frustrates me most is the fact that it totally could have been avoided, if I had just thought about it – although it is decidedly more difficult to SWAG a bolus after drinking because it throws a whole new bunch of variables into the already populous mix.
Sounds like Sci-Fi…
Posted by: typeofl1fe on: September 11, 2008
I feel like every time I read science news like this, it seems like reality is getting closer and closer to that science-fiction world that it used to be difficult to imagine.
