6 things for 6 years

9 11 2010

Happy D-blog Day!

To celebrate the 6th annual d-blog day, here are 6 things I think people should know about diabetes.

  1. Yes I can eat that! With the advent of insulin pumps and CGMS, there is no real reason I can’t eat whatever I want.  Not to mention that sugar-free stuff just plan tastes nasty.  If I’m going to eat the carbs anyway, it might as well be something delicious.
  2. Taking insulin is not “bad”. I do not have it “really bad” because I have to take insulin. My body simply doesn’t make insulin anymore, so I need to replace it manually.
  3. I’ve got it, but sometimes I need help. Most of the time, I am super aware of all the intricacies of what’s going on in diabetes-land.  I know that my blood sugar is going up, but it’s okay because I just ate and I know I bolused accurately, etc.  Or that I may be dropping, but that’s good because I was high before.  However! Sometimes I am low and I don’t know why and I need someone to cut me some slack and get me some Starburst.
  4. My CGMS is amazing. This thing catches everything.  It tells me when I’m high; it tells me when I’m low; it tells me when I’m going up or down too fast; it will remind me later if things haven’t improved.  Because of this device, I have kept my A1c at 6.2% or lower (below 6.0% is NORMAL) for 2 years.
  5. Diabetes is expensive. 4 endo visits, regular doctor, OB/GYN, eye doctor, dentist.  6 test strips per day x 365 days = over 2000 strips per year.  New infusion site, pump cartridge, and tubing every 3 days.  A CGMS sensor is $135 before insurance, which is only supposed to last 7 days.  The pump itself is over $6000.  I just started with new insurance, and next year I will EASILY hit the out of pocket maximum of $2500.  Probably by May.
  6. The D-OC is awesome. George, Kerri, Scott, Bernard, LeeAnn, and Allison are all household names.  You are all my friends.  And not qualified with “diabetes online friends”.  Just “friends”.  ❤
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Maybe I’m just lucky

16 11 2007

I got a few negative comments about my pump post earlier this week.  Saying that it was dangerous to start without training, or that people can be super sensitive to insulin, or whatnot.

I’ve also read a lot of diagnosis stories where people have to go to the hospital and spend a week in ICU or whatever.  I have to say, that I had none of those things.  When we tested my blood sugar and it said “HI”, we didn’t rush to the hospital or anything.

I guess I’m just lucky when it comes to diabetes.  I’ve never had to be hospitalized, I’m not super sensitive to insulin,  etc.  I suppose I should just count my blessings.





Alzheimer’s could be related to diabetes

2 10 2007

GiR pointed me to this article, which claims that Alzheimer’s could be another type of diabetes.  They are calling it “Type 3.”  From the article:

In the brain, insulin and insulin receptors are vital to learning and memory. When insulin binds to a receptor at a synapse, it turns on a mechanism necessary for nerve cells to survive and memories to form. That Alzheimer’s disease may in part be caused by insulin resistance in the brain has scientists asking how that process gets initiated.

Of course, they also mention (way at the bottom) that Alzheimer’s would be more related to Type 2 diabetes, rather than Type 1:

“With proper research and development the drug arsenal for type 2 diabetes, in which individuals become insulin resistant, may be translated to Alzheimer’s treatment,” said Klein. “I think such drugs could supercede currently available Alzheimer’s drugs.”

I love hearing about this research; it’s baby steps closer to figuring this stuff out.