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May 25th, 2012
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Diabetes is a unique disease in many ways.

 

One way that I never really realized until recently is the guilt it places on the patient.

 

With other diseases, your doctor is in control of everything. Your medicine, how often you take it, and how much. But with Diabetes, the patient is the one who has to manage it. So when there is a problem, the patient gets blamed.

 

But is that fair? Sure, I know that I decide if I am going to take my insulin on time, or bolus correctly. I am the one who either chooses to exercise or not and eat healthy foods or not. Those are up to me.

 

But, tell me this, who is to blame when I take my insulin correctly, exercise, do everything right, and for no reason my blood sugar is 270?

 

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Sometimes I am shocked at how invisible diabetes can be. I was having practice at church the other night for the contemporary band when my Bass player asked us to pray for him.
"Of course! What is going on?"
He explains to me that he is having surgery on his eye to drain fluid in it and would just like us to keep him in our prayers. He started telling us about how he had this same surgery on his other eye and that it worked really well so he his hopeful that this surgery will be another success. I asked him what causes the problem he is having.
"Diabetes." (READ MORE)


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Back on November 14th was World Diabetes Day. I really wanted to do something special to mark the day this year. I decided I would write a song and record myself playing it to try and raise some awareness.


On my drive home from work on Thursday the 13th I started humming a tune that I thought would work. I knew I wanted the song to be my personal feelings about my disease and I wanted it to be empowering.

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One thing I have learned over my years with this disease is that many people know nothing about it. All of those typical stereotypes are still running rampant and sometimes its up to us to educate these people.
At times I feel like my shoes are soapboxes when I talk about diabetes to my family and friends. I never used to be this way but more and more I see how diabetes is misunderstood and instead of complaining about that I hope I can make a difference. I'll tell you, it is worth. (READ MORE)


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"I don't care."
That has been a familiar phrase from my lips lately. My wife asks me how many Weight Watchers points a particular meal is when we go out to dinner and I will respond with "I don't care." That probably explains why I have gained two pounds over the past two weeks. I just do not care.
And with that I have not really calculated my carbs. I have been loosely guessing and then making major corrections 2 hours later. I am still checking my BG. I am not guessing on that. But I just feel so uninterested in my life right now. I know that makes no sense especially since I am writing about it now.
I guess I am looking for advice although I do not feel I am in a place to accept or follow any of it. Maybe I want to hear, "I've been there and its okay." Maybe that will make me feel better. I don't know. (READ MORE)


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ADM logoSince November is National Diabetes Awareness month I have been trying to think of ways to raise awareness about this disease so I, too can do my part.
 

Now one thing you should know about me is that, although I am a pretty outgoing guy, I am not one to just walk up to people and strike up a conversation about diabetes. The thought of doing that actually makes me a little light headed. I cannot imagine every doing that.
 

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and it's not about me.

 

I'm not even sure it's about medical insurance -- but it's sure about the D.

 

I've recently learned that a recent infection has cost a close real-life friend (and fellow PWD) another one of his toes, and a sizeable chunk of uncovered medical expenses. Until this weekend, a number of his close friends (including me) had known he'd been hospitalized, and that there was talk about a skin graft after everything healed -- but we didn't know the extent of the damage (both physical and fiscal).

 

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Last week, Kelly at Diabetesaliciousness blogged and tweeted about diabetes misconceptions she'd like the folk at Mythbusters to debunk. This past Tuesday, the theme for the sixth annual D-Blog Day was "Six things you'd like people to know about diabetes". Around the blogosphere we saw everything from "Don't tell me I can/can't eat that" to "don't pity me" and, most of all, "Don't assume that my diabetes is the same as your [cat's, aunt's, grandmother's, BFF's ex-lover's second-cousin's mother-in-law's] diabetes". (READ MORE)


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When I think about a cure I get excited. There are so many people out in the world that struggle with this disease day in and day out and for them to be free from all that would be amazing.


I imagine all the candy shops would have to order more stock because I know I would be eating candy and cakes and drinking lots and lots of orange juice.


A cure would change my life, but for the better? I am not sure. Would I eat food that is bad for me? Probably. I have to be honest, I am sure I would put on a lot of weight at first. But I know at least the likelihood of going blind or losing a limb would be gone. So in that way it would be better.

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In observance of D-Blog Day, diabetes bloggers all over the world have been asked to identify six things they'd like people to know about diabetes. The following are mine:

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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)
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)
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