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We found 10 result(s) that match your search "diabetes care":

I've always been blessed with fairly amazing insurance. My dad worked for the city of Houston for several decades, so our family has always had the group policy with a large subscriber base and it's stayed the same since I was born.

 

After he retired, we kept the same insurance as part of his pension plan. Our co-pays rarely change for either doctors or prescriptions. They pay roughly eighty percent of most procedures and devices. And since I was blessed with a stable income family, I'm able to afford the $45 copays and twenty percent of the pump.

 

But in the last few years and with the new health issues, my health bills seem to be piling up. And with the economy the way it is, I'm starting to stress about how to pay for some of the necessary (and probably not so necessary) items.

 

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I have voted in every presidential election I've been eligible for. Even casting an absentee ballot my senior year of college, which I believe was my first presidential election. All of which seemed rather obligatory to me. I voted because I was supposed to and because it was my right and privilege to do so.

 

Until this year. I waited in line for about an hour this morning to cast my vote. I've never waited more than several minutes to vote in an election. This is my first presidential election since being diagnosed with diabetes. The first presidential election that I was actually interested in, paid attention to and in some ways looked forward to. The first election where I really looked into the issues to base my vote on how the person in the Oval Office would affect my life.

 

Selfish? Yes. But I have reason to be selfish this year.

 

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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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Do you consider yourself to be selfish? That's the topic I've been pondering over today and for many years since becoming diabetic. Sometimes I can't help but feel like because of diabetes I am forced to think of myself, or my diabetic needs, before the needs of others. Maybe selfishness is a characteristic that is inherited in people who develop life threatening illnesses or diseases. Perhaps because we live with the constant reminder of the thin line between life and death, we are more in tune to our needs.

Is it true that selfishness and diabetes go hand in hand?

What do you think? Have you, like me, thought about this before? Do you think of yourself as a selfish person?
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The last time I saw Dr. R (my new endo's office), the lady who checked me in noticed that I had just been in the week before. She joked, "Has anything changed since the last time you were here?"

 

We said something about how often I'm at the office and she said (strangely since it is an endo's office), "Well hopefully you'll get the issue figured out."

 

"Nope," I said. "I'm a lifer."

 

They always ask if I have a primary care doctor. I had thought about asking Dr. R if she could be my PCP, but even without asking it seems clear that my internal medicine issues would be better served with an internist.

 

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Yesterday was Earth Day and, as usual, I'm late to the party.

Diabetes care does generate a lot of waste. Olivia's on a pump, so she has tubing, cartridges, insulin vials and test strips that all wind up in the trash. For the last couple of years, I've been trying to figure out how, or even if, I could recycle any part of that waste.

For a year, we saved insulin vials. Last December, I popped out the rubber seals on 50 of them and strung them on some tiny, battery-operated Christmas tree lights. I'm thinking of doing that again this year and giving them out as presents to people - it would definitely be making a statement.
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One of the issues that crops up with the Mulligan's Stew of insurance benefits that come courtesy of our employers and the States in which we live is the order and manner in which those benefits are applied to the charges incurred by our use of the services covered in those plans. In insurance-company parlance, this is called "Coordination of Care". Back in the days of traditional indemnity plans, medical insurance didn't kick in until after one met an annual deductible, and even then, it was split into two separate policies: normal medical (aka "Blue Cross/Blue Shield") and "Major Medical" (single-incident costs of, in today's money, probably $4000 or more). (READ MORE)

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I was in my truck today picking up some fast food from Mickey D's. I typically don't eat fast food. Actually, I never do- but today I was in a hurry and I just wanted to get something fast and not have to put to much thought into it. As I was ordering, I realized that with diabetes there is no such thing as just a "quick little meal". Any time I eat something, I have to put some serious thought and effort into it. Everyday, I put serious energy and brain power towards calculating things in my head.

My life revolves around eating and calculating.
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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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Sometimes I really want my friends to know about my diabetes. Other times, I really hate that they know anything about it at all.
My mom always told me to be open about being diabetic so that my friends would know how to treat lows and what to do in case of emergencies. She's right (why are mothers always right?!?). My friends need to know where my glucagon is in my house. They need to know the symptoms of low blood sugars. My friends need to be prepared for the emergency situations that come about when you're diabetic. (READ MORE)

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