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If you experience pain as a result of your diabetes, what have you found to be the best way to alleviate it?

May 25th, 2012
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I've swallowed my pride and decided to apply for disability services here at school. They can offer me a few resources that I do not have access to otherwise. Most importantly, they give me the ability to register early for class and to notify my professor's that there is a legitimate health issue that I deal with.

 

The past two semesters, I've considered doing it, but I've also thought it was too embarrassing. But finally, things have gotten to the point where I'm realizing that it's not embarrassing, it's reality. So I've taken the initial steps to go through with it.

 

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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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Every day with diabetes is a little different from the last. There are ups and downs. There are good days, bad days, and something in between. I never know what diabetes will toss my way. I never know when it will knock me to the ground or give me the strength to rise above the ashes.

 

Today was a fairly normal day, with a few diabetes kinks. So I decided to track a day with my diabetes...to show the world what it's really like inside these walls.

 

11:25am: Oversleeping is the enemy right now. And my blood sugar starts out high at 160. I'll take that over another low like last night though (a sneaky 57 that left me with no symptoms at all).

 

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Well, as you may have read in one of my earlier posts, I had my appointment yesterday with my endocronologist. I had also told you I was hoping for a good A1c and I knew if my test wasn't good, I could expect to have the "you're a great candidate for the pump" talk. Well, I got my test results back and I can honestly say that I had one of the highest A1c's that I have had in years. I was very dissapointed. I am actually so ashamed, embarrassed, and frustrated that I don't even want to share my number with you. Maybe, if you're reading this and you are diabetic like me, then you can relate to this feeling of not wanting anyone else to see your score. I even go out of my way to hide my blood glucose reading every time I test. I'll be the first one to admit that this fear comes from being insecure about what other people might think of me. Or fear that someone might make a judgement of either my health or my diabetes management based on the number. (READ MORE)


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There has been much heat in the diabetes online community concerning the new Medicaid/Medicare restrictions on paying for blood glucose testing supplies for people with diabetes, including the belief that these limitations will quickly replace current private-insurance coverage policies. We're seeing some of those repercussions here as The Other Half has just been informed that instead of covering testing supplies ad libitum (as many as his doctor writes for, for whichever brand she writes for), they will only cover OneTouch or Accu-Chek strips, to a maximum of 51 strips per month for people with diabetes who do not require injectable insulin, and 204 strips per month for those who do require it. (READ MORE)


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Thirty-three years ago this semester, the frequent repetition of those words (or others to that effect) by high school classmates led me to take an extra semester of English in the spring term of my senior year. Anyone stepping onto my school bus and smelling the pungent odor of marijuana burning would have easily understood the reasons behind their lack of preparedness to study.

 

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I've been somewhat ambivalent about today's rally surrounding the United Nations Summit on Non-Communicable Diseases. The libertarian "party line" is that the United Nations does little more than abrogate nation-states' sovereignty and forcibly redistribute income from the wealthier nations to the less-wealthy, dampening incentives for innovation and destroying private charity efforts which would otherwise improve the lives of those in need. On the other hand, the prospect of spending time with friends I seldom see in-person is an opportunity not to be missed.

 

It's a dilemma I'd been wrestling with for a couple of months, and friendship was winning over politics. However, neither friendship nor politics had the choice to decide.

 

The deciding factor was money.

 

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On Tuesday, Brian Bosh (@bosh) tweeted, "Do you (as a #diabetic) avoid publicly announcing extreme blood sugars for fear of discrimination regarding future coverage? #bgnow private."

 

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Nicole Purcell
Nicole PurcellNicole Purcell lists having type 1 diabetes last when she's asked to provide information about herself - because that's where it belongs.

(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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