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November 21st, 2009
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Okay, I will warn you up front that this post is a total rant and has no other substance besides the fact that I need to let off some steam. I am also looking for some of you who have dealt with this annoying stereotype.
As I was minding my own business here at my desk the janitor comes up to me and asks me if I have to take shots everyday. I realize that he was listening to a conversation I was having with a co-worker about insulin and so on. A total eavesdropping moment right? So I answer, "nope." And totally leave it at that.
He says, "Oh you got off of insulin. That's good. Just a diet now or pills?"
"No I have an insulin pump."
"There is a gal in another office I clean that has to shoot up every day." Then he does it. He does this sort of motion with his right hand towards his left upturned arm. As if he is shooting up heroin or something right into his vein! (READ MORE)


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When to tell?

 

I have accepted a new job. It's in a new city (half way across the country!!). It's with new people. New people who don't know that I have diabetes.

 

It was during my four-year tenure at my current job that I was diagnosed. I had no problem telling just about everyone in my very small office about diabetes. I already knew them and their personalities.

 

It's different now. I have a problem with going in to the boss on my first day and saying, "Hey, guess what..." I also have a problem with waiting three months until my benefits kick in, or even longer when someone sees me checking my sugar (or doesn't know what to do if I pass out) to say, "Oh, yeah, maybe I should have told you sooner."

 

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The letter C brings us to cannula, by request.
I found an interesting photograph of an insulin pump cannula that said much of what I'd decided to write when I was thinking through this post. Essentially, the photo verbalizes for me the sentiment that my life - the lives of all of us who use an insulin pump - turn (quite literally) on a dime. The cannula that delivers the medicine that keeps us alive is smaller than a coin that, this day and age, won't even pay for a gum ball. (READ MORE)


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In the beginning, there is orange and black foil.  That foil is joined by yellow and red, with the black fading away.  In what seems like an instant, the yellow and orange are things of the past and the red takes hold alongside glittering green and silver.  All of these beautifully colored foils, they signify the enemy.   They are the harbingers of what is, quite possibly, the most difficult time of year for me; the dreaded days between Halloween and Christmas. 

 

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The fact that I have diabetes is not the first thing most people learn about me.  In reality, it's often one of the last things I reveal about myself.  An exception to this rule is disclosure in the workplace. 

 

Because I am hypoglycemic unaware, and because I don't think it's fair for a person to find out about my diabetes because I've either lost consciousness or behaved aggressively, I typically let the people I work with know what they might be up against.   It's never really "comfortable" to disclose - as I'm never sure how people might react - but I find that it's absolutely necessary.  

 

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By the end of the day I was almost regretting that I had been drinking so much water throughout the day. I was in the bathroom about every 20 minutes or so.
It started yesterday when I got a twinge and a sort of seize when I used the bathroom. It was different from the feeling I had gotten (or seemed to remember) when I had a urinary tract infection in the past. But I knew something was still definitely wrong. Especially when I got up at 4 a.m. last night to go potty, and then again 20 minutes later, and still getting this seizing twinge of a pain in my very low abdomen.
I decided I'd load up on water today and even--gulp--drink some cranberry juice even though I really can't stand cranberry juice (I found some cran-grape at the gas station, which may not have the same effect as cranberry, but it was all I was willing to tolerate, especially since it wasn't sugar free). (READ MORE)


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Olivia is planning on going trick-or-treating tonight. She's 13, so a bit old to be doing it, but she's using her little sister as an excuse. Who am I to knock that? I did the same thing all the way thru high school - hey, someone had to take my sister out. My parents were more than happy to let me do it.
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In the last several weeks at work I've gotten two "Is that your phone?" comments about Dex, one "Is that your pager?" comment about Toohey and one "I think we just violated HIPPA" comment. Oh, and two very long, in-depth conversations about diabetes, pumps and continuous glucose monitors. It's interesting how much of this information had become visceral to me... I found myself explaining things I hadn't thought I would need to but realized that basic diabetes knowledge is not so common.

 

Actually, I take that back. Some people know enough about diabetes to be dangerous, but what they have no clue about is pumps and CGM. Which is fine. In fact, today I told a co-worker after a lengthy conversation about how the pump and the CGM work that I don’t mind talking about it. I clarified by saying as long as I wasn’t being judged and people who were asking questions were willing to accept that I am the expert.

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A week ago I was all prepared to write a post about how I was ready to lose weight. I was tired of my muffin top and of my clothes being too tight. And I fear this summer's trip to the beach in a bathing suit.
That was a week ago. A week ago, when I was ready to dig my workout clothes out from their hiding places. A week ago, when I was ready to shun fast food and treats. It's amazing what a week can do. (READ MORE)


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Last week I wrote about my fattest night ever and how I was going to begin the road of weight loss.

 

That was dumb idea to start on the Friday before a holiday weekend.

 

But I did anyway and honestly, couldn't we always find an excuse as to why we should wait to start losing weight? I can always think of something it seems.

 

Over the weekend I did everything in my power to stay off the couch and get out of the house. This stops me from snacking and sitting and watching cooking shows that just make me want more snacks!

 

The other thing I am doing is making some better choices when it comes to food. I have to be honest with myself. I am not going to eat salads everyday, or bun-less burgers. That is not me.

 

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Scott Marvel
Scott MarvelScott lives an active life with type 1 diabetes. Aiming to stay on top of his unexpected diagnosis, he puts a strong foot forward to stay in control.
Living life in the sun and fulfilling his dreams, Scott tries to educate himself, and others, on the unquestionable possibilities of a life with type 1 diabetes.
(Read More)
Carey Potash
Carey PotashCarey is a full-time hater of diabetes. The benefits stink. His 7-year-old son, Charlie, has been giving he and his wife the finger since November of 2003. Carey's parenting humor has appeared in various websites and print magazines. He resides in the suburbs of Philadelphia with his wife and three children. (Read More)
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