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The politically anticipated Iowa caucuses offer a strong foreshadow on who will take lead towards being the next United States president. The two current party front-runners in this race were decided tonight, giving Democrat Barack Obama and Republican Mike Huckabee a head start. Without doubt- health care reform is a hot topic for presidential candidates. This is the look on what Barack Obama and, type-2 diabetic, Mike Huckabee promise in their health care platforms. (READ MORE)

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I don't know a lot about the Canadian universal health care. What I have learned has been in dribs and drabs, culled from friends and from the few Canadian posters to the Children With Diabetes parents email list. I knew it varied from province to province but assumed that most diabetes supplies were covered.

 

And then I read this post by Andrea, over at A Garden of Na Mmoy. She has type 1 diabetes, although she doesn't post about it very often. She has a few other posts about diabetes and she's an eloquent writer no matter what the subject - you should check her out regardless. But that post really opened my eyes to the limits that any insurance, universal or private, puts on our health.

 

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One of the ways I break up my day is to frequently check in with my sisters at Diabetic Mommy. This morning I posted a question on the message board that has gotten me thinking lately.
I wanted to know how much everyone spends on groceries on a weekly basis. For our family of five, I spend an average of $200 a week on food, toiletries and other incidentals. Basically, anything I can pick up at WalMart. Our budget, though, needs some tweaking and there are few things left to adjust besides our grocery bill. (READ MORE)

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I am lucky. I have insurance. Sure I pay a lot out of pocket each month but the coverage is decent. Especially for my prescriptions. My co-payment is not too bad which I am thankful for since I have not only my insulin and strips for my BG machine to buy but also 4 pills for other ailments. But each January I get shocked by the same surprise.
My $200 deductible. Now I am not fortunate enough to be able to drop 2 "C-notes" here and there. I live pretty much check to check and unless I get an extra $200 for "passing Go" then I am gonna have a problem. Luckily the pharmacy I use is awesome. They gave me one bottle of insulin and are letting me come back on my next payday to pick up and pay for the rest of my order. What life savers, literally. (READ MORE)

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As a member of the media, you might think that I would get riled up about news stories all the time. Strangely, though, I don't find that to be true. So I guess it's no surprise that when I do get moved by a story, I get really moved.
There's not often much information in the e-newsletter from Diabetes Health magazine that pertains to me, but I look forward to reading it nonetheless. I usually scan the headlines and teasers, and maybe read a story or two. I sometimes forward it on to my mom and two aunts who help their 90-year-old type 2 mom with her diabetes management.
Today's newsletter, though, had a story that I read several times. The headline, Psychologically Dependent Type 2s Use Too Many Test Strips?, intrigued me; the story, on the other hand, made the fire rage. (READ MORE)

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Last week I wrote about my experience with my new endo. Today marks a week from that first visit and the day I am supposed to fax over a weeks worth of BG readings and boluses from my pump.

 

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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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My job will be ending sometime this summer. Consequently, I am investigating our health insurance options. Since hubby is self-employed, we have always covered the family under my work policy.

 

Now, I know that "health care in this country is in crisis"!  I know this is a huge touchpoint for political candidates.  Yes, I know all this intellectually. 

 

Now it's PERSONAL.  COBRA, offered by my employer by federal mandate, is more than a house note EVERY month.  Private insurance is still pricey - more than what we paid on 2 car notes.  And it carries a $2000 deductible per person.  Some sloppy math later and it could be $15,000 a year before they pay any expenses for us.

 

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I've been doing some reading on diabulimia. It's not a recognized eating disorder, but it certainly sounds like it should be.

Diabulimia is a means of weight loss, primarily suffered by young women. In order to lose weight, they use far less, sometimes even no insulin and let their blood sugars run very high. It means they can eat whatever they want without it having any repercussions on their weight. I remember how skinny Olivia was when she was diagnosed, just before her 3rd birthday. She only weighed 24 lbs. Her body was eating itself.
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I just finished reading this post over on Momocrats. To say that my blood is boiling would be an understatement.

It's no surprise to people with diabetes (or those who carry insurance for said people) that insurance companies make you jump thru hoops for test strips and doctor's visits. My daughter's endocrinologist is no longer covered by either of the health plans we will have at my husband's new job. I'm not sure what we're going to do about that. I certainly can't afford to pay out of pocket for that. Do we switch and only go to Joslin once a year? Olivia loves her endocrinologist. She does not want to switch, but she's not the one footing the bill - my husband and I are and we can't afford the out-of-pocket cost.
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