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March 22nd, 2010
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Congratulations to Halle Berry on the birth of her healthy baby girl on Sunday! The height and weight were not divulged, so let's all hope the baby doesn't suffer from macrosomia, a common complication for women with diabetes. Regardless of Halle's ignorance about her diabetes, the healthy arrival of a baby is ALWAYS news to celebrate!
A conference this week in Washington is focusing on the subtypes of both type 1 and type 2 diabetes. At least 16 different genes can impact type 2 cases, and 14 genes can be involved in type 1. One of the goals of the conference is to increase awareness of the many possible forms of the disease beyond type 1 and type 2. (READ MORE)


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In February and March we sought the guidance of diabetes author and coach Gary Scheiner to see if we too could "Think Like a Pancreas." Our few meetings energized us briefly, but soon enough, we were back to feeling lost and utterly confused. After about five months, the pump wasn't working out as we hoped it would.
In April we decided to throw out all carb ratios and basal levels and begin with a clean slate, following more pump frustrations and a disappointing A1c of 9.6. We felt we hit rock bottom. We worked daily with the pump educator, tweaking and tweaking and tweaking and scratching our heads until we could tweak and scratch no more. (READ MORE)


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A presidential promise. A statement to advance us into a more lucrative future of healthcare. A hope that technology in healthcare can further help fulfill patient’s needs.

"We will restore science to its rightful place, and wield technology's wonders to raise health care's quality and lower its cost….. All this we can do. And all this we will do."


This quote came from President Barack Obama's Inaugural Address on January 20, 2009. It is a bold statement on his desire to make improvements in todays healthcare system and expand on the successes of technology for everyone.

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When I look back at the first pediatrician we had for No. 1 there's really one thing that stands out: Had she been a parent when she was treating us I think the care would have been different. Not better, mind you, just different.

 

Of course, I didn't realize this until after we had more kids and moved and had to find another pediatrician. Someone who had her own kids. The connection between me and her was different, as was the one between the kids and her. Yes, in a way, that connection was better, not just different.

 

Now, don't get your panties in a bunch because I'm not saying being a parent is a prerequisite for being a good pediatrician. What I'm saying is that I'm wondering if having an endo who has diabetes -- particularly type 1 -- will make a difference for me or not. See where I went with that?

 

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Many of us have wondered "Why me?" when confronting this disease. It’s easy to get caught up in pity when you’re diagnosed with a chronic illness. We want a reason for our diabetes. Not a medical cause, but a legitimate human reason. What did we do to bring this on ourselves? Is it some sort of punishment? Is it a test? Is it God’s/god’s/the universe’s doing?

 

The "Why me?" question seems to be a necessary phase in order to fully cope with diabetes. Granted, we may never find a true answer to why this happens to us, but processing the information and coming to terms with it helps us deal.

 

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The start of every semester is difficult. Getting back into the groove of school can be daunting. Some are worse than others though. And this semester is on that list of worst semesters.

 

I'm behind in every class. I've missed weeks of some of my classes. The lab that I'm supposed to be taking...I've never been to. Assignments are beginning to pile up. Tests are starting next week. There's just too much to handle.

 

I know that I could have pushed myself harder. I know that this is a big chunk of my own fault. Yes, the fatigue has been incredibly rotten. My blood sugars have been bouncing up and down. I've had migraines for days on end. And just the general malaise and lack of motivation are enough to make me crawl into bed forever.

 

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This is not the post I intended to write this morning.
Today, I woke up to a fasting of 151, which is pretty darn good considering where I've been lately. I dressed for my morning walk, sat on the couch and ate what I'm now referring to as a snack--a small cup of yogurt, just 15 grams of carbs. It was all I needed to sustain me through my walk. I used to eat half of a peanut butter sandwich, but it's really hard to choke down that much dryness before the sun even comes up. But I digress.
I decided that with a fairly decent fasting, so few carbs and a 30-minute walk upon me that I didn't need to take any insulin. I mean, 15 grams of carbs! C'mon! (READ MORE)


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I get frustrated every day. Diabetes is making me feel like I am semi-losing my mind. I literally have to ask myself everyday, "Am I losing it"? To be honest with you it is scaring me a little. My sugars are all over place. Is this blood sugar roller coaster "normal" for those people out there who are doing "good" with diabetes?

I would like to pose a question to you if you're reading this right now and you are a person with type 1 diabetes and take daily insulin injections. If you have an A1C of 6 or lower, how often are your sugars in the 200's... if ever?
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I don't expect everyone I've ever met to remember that I'm diabetic. There was a period that I barely told anyone about it, unless I was absolutely forced to. So how could they remember if they never knew?

 

I do expect my close friends, family and important people (i.e. my coworkers, my professors, etc) to remember that I'm diabetic. After all, most of them see the daily battle that diabetes is. How can you forget that?

 

But so often, my friends forget. Sometimes I feel like my own family forgets. They get involved in their own lives, their own problems and forget about this portion of my life. Yet, I can't excuse them.

 

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Waiting.

 

Waiting for his blood sugar to come down.

 

Waiting for his blood sugar to come up.

 

Waiting for the school to call with his numbers.

 

Waiting for him to come out of hiding so we can get this damn thing over with.

 

Waiting for the bruises to heal.

 

Waiting for science.

 

Waiting for his A1c result.

 

Waiting for good news.

 

Waiting for ketones to go away.

 

Waiting for his test strips to be delivered.

 

Waiting for technology to improve.

 

Waiting for restrictions to be lifted.

 

Waiting for people to understand.

 

Waiting for him to get older.

(READ MORE)


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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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