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February 9th, 2012
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I’m not afraid of needles, but I must admit that I’m a little fearful of the bloodwork I’m scheduled to have in a few weeks.
 

Since I finally found an endo practice that I enjoy (yes, I know I still haven’t blogged about it yet!), they naturally want their own bloodwork. Which is great. And fine with me. It’s just the type of bloodwork that’s being done that’s leaving me a little uneasy.
 

I know it shouldn’t. And, really, I’m not uneasy I’m just kind of … I don’t know… just nervous? anxious? curious?
 

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I did an insulin pump infusion set site change this morning, by the ubiquitous lamp light on the dresser. My fiance (seven weeks until the wedding!) and I were talking about thresholds for pain and how I don't have much tolerance for emotional pain but my threshold for physical pain is high.
"I know. You can stick yourself with needles all day long but you freak out if you see a spider." He grinned at me.
"I know that needles aren't going to try and crawl on my head at night, that's for sure." (READ MORE)


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In the life of a diabetic, blood draws are fairly common. I can remember being a little girl in my pediatric endo's office waiting for the inevitable butterfly needle after the appointment. My mom and I claimed that the nurses in the hospital were always rougher than the ones in my normal physician's office. It seemed like those quarterly blood draws hurt more and more every time.

 

But I was always used to them. Needles never have been my problem. Maybe it's because before I even begin to remember things, I can remember diabetes. Needles and those blood draws are so common to me that I know no other way. But even though I'm not scared of needles or opposed to the routine draw, I still hate the way it all happens now.

 

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Fear of needles. Fear of blood. Fear of hospitals or doctors. These are all normal phobias in the world. People commonly relate to one or all of these fears, whether from bad experiences, horror stories or movies/TV shows.

 

But for a diabetic, what are our fears? Of course, many diabetics deal with the fear of needles, blood or hospitals/doctors. I'm fine with the needles and the blood, but I have a strong dislike towards doctors. I wouldn't say I'm afraid of them, but I don't particularly like to hear what they have to say (this stems from every doctor's appointment in my past that I would leave crying from because my control just wasn't good enough).

 

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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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I've been on Lantus for about ten years now. I tried different insulins over the years (NPH, Ultralente, and the like) plus that almost two year stint on the pump. Lantus seems the best for me, although I'd still like to try Levemir. Lantus keeps me stable without giving me constant lows.

 

The drops are predictable. With split doses, I get fairly steady blood sugars. Overall, I've been happy with Lantus for years. But lately, I've noticed a change that I've very rarely experience but often heard about.

 

With every injection lately, I'm experiencing a lot of pain. It isn't happening with Humalog, just my Lantus. I'm not sure if it's the location or just the insulin. I generally give my morning and evening Lantus injections in my bottom. Both my doses are too big for what's comfortable for me elsewhere.

 

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I remember posters of dull needles from the pediatric endo's office. The difference between a new needle and the old was always quite disgusting. The old was frayed, with shards of metal sticking out abnormally. It was definitely a good way to scare a teenager into changing lancets and syringes on a regular basis.

 

The bad thing was that I never remembered that poster after I left the doctor's office. I'd go back to my usual routine. I wouldn't change the lancet until someone reminded me. I'd use a syringe repeatedly, until the numbers wore down or the needle bent. It could be days before I'd even think about switching it out...after multiple uses per day.

 

It's a bad diabetes habit that I'm in. I try to be better...I put extra lancets and syringes in my meter kit. I try to make schedules, changing them on Sundays or once a night or on the 1st of the month. Anything to make the habit more often than it is.

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Dear Diabetes Supply Bag,
It is with regret that I write to inform you that your services are no longer needed. Though your time with me was short, you have provided me with dependability, style and functionality that I will forever appreciate.
I remember when I found you. My family and I were leaving on our first airplane trip. For the sake of airline carryone rules, I needed something I could pile all my diabetes supplies and regular purse supplies in. I searched the purses and handbags area at my supercenter rather quickly. Some bags were too big, some were too small. Some were just plain ugly. Not only did I need something for that trip, but I needed the bag to be functional after the trip, as well. (READ MORE)


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I went to the movies with a girl friend last night. We've only met one other time and I didn't feel that instant "best friend" vibe but Marvin was busy and I was dressed cute. So I decided to venture outside my shy self. We ended up seeing Next Three Days at Studio Movie Grill. Dinner and a movie all in one. Expensive, but good.

 

Next Three Days hasn't really been advertised here but the few times I'd seen it come up I thought it looked good. It seemed like my type of movie. I had no idea if it'd be hers, but her pick was sold out. We ordered dinner. I had a glass of wine. The movie started.

 

**Notice: some spoilers here...a big part of the movie will be given away if you continue to read. Just for those of you planning to see it (which I do recommend!)!**

 

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After making those Christmas lights the other day, I got to thinking about what else you could do with the flotsam and jetsam of life with diabetes. A few ideas were:

1. Test strip bottle garland - using fishing line, thread thru where the cap joins the bottle. 100 bottles should make a manageable garland.
2. If you really want to drive yourself mental, make garland out of used test strips. You could either thread them on fishing wire using an upholstery needle or you could glue them together. I have doubts as to whether the glue would hold up for very long, though.
3. Syringe icicles. Snip the needles off (obviously), put fishing line or ribbon around the plunger end and hang on the tree.
4. Syringe icicle lights - using the same Tiny Lights that I used for the insulin bottle lights, string the syringes (again, snip the needles) onto the lights. (READ MORE)


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Michelle Kowalski
Michelle KowalskiMichelle Kowalski, a writer, editor and photography hobbiest living in Phoenix, was diagnosed with Type 2 diabetes in February 2005. In January 2008, as part of her quest to start on an insulin pump, Michelle learned that she actually has type 1 diabetes. (Read More)
Lindsey Guerin
Lindsey GuerinLindsey is a typical, yet unique, Texas girl who loves shopping, movies and reading. She loves to travel and take risks. She dreams of diabetes cures, never-ending cheesecake and her own airplane. The rest you can discover in her blog! (Read More)
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