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February 10th, 2012
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Just the other day I was speaking with a group of co-workers about different life changing events in the life of someone with diabetes. As we sat there and talked about it I began to reflect on my own. I thought about the different times in my life such as diagnosis time, school, relationships, complications, and work. All things that every person living with diabetes can relate to, or will eventually deal with.

Where were you when you were diagnosed? What were you doing that day or at that particular time in your life? Were you at work? Were you at school? Did you go into a coma or diabetic ketoacidosis? Was your vision so blurry, that like me, you realized you couldn't see the picture on the t.v.?
(READ MORE)


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(Continued From Previous Post)
I am dependent on insulin. But I am otherwise an incredibly independent person. I like taking risks - on my own. I enjoy the feeling of having accomplished something by my own will and my own action. I am more outgoing and more confident than I think I would have been if I'd not been diagnosed. A combination of wanting to be able to handle my disease on my own, without pity or judgment AND the experiences I had as a young woman - through the Clara Barton Camp and the ADA's Youth Congress - transformed me from a shy, albeit precocious kid, to a person who stands on her own. A person who keeps her head up and battles mightily - in the face of whatever wrong she sees and whatever challenges she faces. But would I trade my independence for a life without diabetes? I would - though again, who's to tell if something else might have brought me to this same place. (READ MORE)


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Fifteen years. A decade and a half. Thousands of days. Millions of minutes. Over half my life.
It doesn't seem real that I've lived with diabetes for fifteen years. It doesn't seem fathomable that this is only the first fifteen years of many more. I can't imagine how the rest of my life will daily involve diabetes despite the daily involvement of the last fifteen years. I just can't picture more infusion sets, more doctors appointments, more worries. (READ MORE)


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Today is the sixteenth anniversary of my diabetes diagnosis. And I'm not sure that I know what I feel, or if I'm feeling anything at all. Should I celebrate? Should I reflect? Should I move on and never recognize the day at all?

 

I definitely believe that it's a day worth recognizing. Sixteen years with this disease is a lifetime, a major feat, a true achievement. But I guess I just don't know how to feel on the actual anniversary.

 

For me, diabetes is a daily walk. It's a constant celebration. I'm always cursing it. Not a second of my life goes by without considering the consequences of diabetes, both in the present and in the future.

 

(READ MORE)


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I recently "celebrated" my fourteenth anniversary with type 1 diabetes. I wasn't really sure how to celebrate it though. I actually didn't even tell anybody about it. It's not like I was trying to hide it from anyone or the opposite, make a big deal about it, I just didn't give it much thought. Now that I look back at it though, this anniversary actually marks my, "half of life" with diabetes day. I have had diabetes for 14 years now and it is hard to imagine. I look back and reflect on those years, and it blows me away that is has been that long. Time really does seem to fly by. What I find funny is that I really only consider my diabetic years as the ones that really count. In a way, my life got started the day I got the diagnosis.
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It dawned on my recently that I completely missed my diagnosis anniversary. It is not like I throw a glucose filled party or anything but I like to recognize "another year, still here" kind of mentality.
But I missed it! I was kind of upset about this since it makes for a good blog post (LOL) but maybe it is not what I was supposed to be thinking about. Diabetes is on my mind constantly and forgetting something like my anniversary is really not that big of a deal.
Not only that but I always feel like it is and it isn't something to shout about. Sure I have made it another year but when I give diabetes all this power and attention it seems like it is getting the best of me in a way. I know some of you will disagree and I would love to hear how your diagnosis anniversaries go for you. (READ MORE)


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Today, I have had diabetes for twenty five years. And I'm not sure exactly how I feel.
I guess, lucky - my body is free, so far, of complications.
I also feel somewhat happy and strong - I mean, I started this journey as a scared, angry little girl and I'm here now - a somewhat accomplished, otherwise healthy, happy woman.
And I feel a little sad - for the weight of diabetes is surely heavy on some days. I don't let myself think of what life might have been like if I'd never been diagnosed - because - really, what would be the point? I think more of the constant juggle and the often unavoidable failures and the sheer relentlessness of diabetes management. And yeah, that makes me sad. (READ MORE)


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Charlie has been on the pump for one year. What do you get a person with diabetes and their pump for their first year anniversary? Is it something made of wood? Paper? I can never remember.
Charlie never wanted to name his pump like so many others do. He turned down many of my recommendations such as Pumpy, Bluey, PumpBot, Slumpy the Pumpy, Mr. Beeps, Insulindiana Jones, Pumpio, Alan Pumpstein and Cheryl.
Maybe he's right not to name it. He doesn't name his sneakers or his ears. It's not a pet. Though he does keep it on a leash of sorts. He has been known to name his poop, but let's not go there, uh, girlfriend. Anyway, everyone names their poop.
Right? (READ MORE)


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Recently, I was searching thru some paperwork that Olivia needed for school (OK, truth be told, I was desperately hunting down her immunization record for the first day of school - yeah, I'm just a little unorganized. Just a little.) and I came across her discharge papers from when she was diagnosed.
For the last, oh, 8 or 9 years, I've said that Olivia's diagnosis date was 9/14/97. Well, I was wrong. It was 9/10/97. So we missed it. Totally blew it. I'm kind of OK with that, though.
We've never really marked the occasion with anything more than a "Hey, it's been X years since you were diagnosed," and a bit of a discussion about how far she's come, how her care regimen has changed and then we move on with our day. I thought the ten year mark would be a bigger deal, though. But even when I thought it was on the 14th, that day came and went, and while I knew what day it was (or, rather, what day my confused brain thought it was), I never said anything to Olivia. (READ MORE)


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March 3, 1993. I was 4 and a half years old. My parents were worried. I'd been sick for too long and continually got worse. Vomiting, thirst, excessive urination, extreme weight loss. I was wasting away.

 

March 3, 2010. I'm 21 and a half years old. I'm still diabetic, but I'm not wasting away. I have no major complications. I have to say that seventeen years ago, as a tiny four year old, I had no idea what diabetes meant. I certainly didn't foresee seventeen years with a chronic illness that takes up every moment of my life.

 

It's strange to know that seventeen years have gone by now. Yesterday doesn't feel much different than today. It's more the accomplished feeling that runs through me when each D anniversary passes by.

 

(READ MORE)


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Kim Doty
Kim DotyKim is a computer systems administrator for a major food manufacturer and lives in Colorado with her husband, Steve, and their children. She currently battles the bulge and tries to develop an exercise habit to better manage her blood sugars. (Read More)
Julia
JuliaJulia lives behind the Tofu Curtain, in the Pioneer Valley, in Western Massachusetts. It's a nice place. She likes it there. Her eldest daughter, Olivia, has type 1 diabetes. She's also 13. It's a real toss-up as to which is more difficult -- the diabetes or the teen-age drama. (Read More)
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