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January 9th, 2009
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It was mid-afternoon as I strolled into the local pharmacy. I needed more Novolog insulin pens and today's trip would prove itself as unsmooth as usual. The diabetic smack in the face did not come for me, however, but for the slightly unsorted diabetic fellow ahead of me.
This day's pharmaceutical quest was not stunted by the feared insurance decline, or the "too early" for a refill drama. Not even the "out of stock" song from the pharmacy tech, or wrong sized needles being slid over the counter. It was simply an, "I'm sorry, I can't help you" interaction.
Unsorted Diabetic: What do you mean I can't refill my syringes here?
Pharmacy Tech: I'm sorry. I have no record of you as an approved customer.
Unsorted Diabetic: I don't usually get my refills here. I was just in the area.
Pharmacy Tech: Some muffled explanation and seemingly helpful recourse. (READ MORE)


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I don't have to take a ton of medicines to maintain my health, but there are a number of bottles from several pharmacies in my bathroom cabinet and by the kitchen sink. It's easy for me to know when I need to renew these meds because, well, when I look in the bottle and see only two pills left I know it's time to call the pharmacy!
But with insulin, there are no pills to count, no obvious visual reminder (unless you run out, of course!) that it's time to renew. It's only supposed to be good for about 28 days, but I never count the days. When I think it's about time to renew, I may look at the date on the prescription label to see when I last renewed it. If it's around the same time frame a month later, I know it's time to renew. However, it's usually more than 28 days; often it's more like 30 or 32 days. But what's a couple of days, right? (READ MORE)


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It sounded like the ideal situation. One phone call and all my diabeetus testing supplies and medicine would be delivered straight to my door. No last minute trips the the pharmacy. No paying out of pocket to be reimbursed later. Everything would be taken care of with one quick phone call.


I fell for it in September. Like most relationships, it started out nicely. Three or four "quick" phone calls and they promptly delivered a three month supply of test strips and an equal number of lancets. And for a girl who only changes her lancets when we change the clocks (and only if I remember to that week), I now have a 600 year supply of lancets in my closet.


At the time, they were also supposed to send a three month supply of insulin. It still has not arrived. Five or six phone calls later, they tell me they are still waiting on my doctor to return their call.

(READ MORE)


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I was busy. I thought it'd be here sooner. I just didn't take the time to think about it. The insurance company shouldn't be so slow. I have too many other things to handle. I'm still new to pumping so I haven't realized the increased needs. I couldn't really judge how much was left. (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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I don't find it common place when I get excited about diabetes, but yesterday, oh boy. I had my first appointment with a new P.A. and I think I gave him a hand cramp!
This visit marked my first day with a new bout of medical pros. I signed up with a new primary doctor, new endocrinologist, new P.A., and even new crabby dr.'s office receptionists that somehow came with the package. (They are another story though). (READ MORE)


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Olivia told me the other day that she was nearly out of test strips. I dutifully called in the refill and went to pick them up today.

When I got to the pharmacy, I gave him Olivia's insurance card. O is on her father's soon-to-be-ex-wife's insurance.

I know, it's confusing, but I don't really want to get into all of that garbage on here. Suffice it to say, her dad's not really, uh, involved in Olivia's life. It's been a year and a half since he's seen her. He lives an hour away. Somehow, there's always something more important. It's beyond infuriating. But I digress.
(READ MORE)


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Yeah, I know. Duh, right?

I was just reading a post over at Diabetes Daily by Bernard Farrell. He was discussing the astronomical cost of test strips. It is ridiculous that they cost $1 a piece. On an average day, Olivia tests 8 - 10 times. When she's sick, it's even more frequent. That's $10 a day, just in test strips.

The insurance company's answer to this, usually, is "Well, test less frequently." Yeah, you know where you can shove that statement, bucko. Get lost.

But why aren't the insurance companies pushing back on this? Why are they content to let manufacturers charge so freakin' much for test strips? I don't understand it.

I've done this before, but I think it's time to break down what diabetes costs us every month.

-- Approximately $750 for health insurance. Per month. Yeah. Ouch.
(READ MORE)


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My husband just switched jobs, which is always a headache when it comes to health insurance. If you are lucky enough to be allowed to start right away, with no waiting period, there's still that period of limbo when the old insurance has been cancelled (and man, they don't waste any time doing that) and when your new insurance is in the system.

 

Of course, Olivia needed insulin while we were in limbo. I went to CVS to pick it up and it was going to cost $335.99 for three bottles of insulin. Needless to say, we can't afford that.

 

(READ MORE)


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The pharmacy technician said it when I bought the "real" Sudafed (not that fake PE crap you can get over the counter that they reformulated so the stupid methamphetamine manufacturers have to work harder to find their main ingredient). The nurse at the doctor's office said it when I went in for a steroid shot.
It's bad around here. Really bad. Allergies, that is.
I'd say roughly six years ago I developed seasonal allergies. I was able to handle it with over the counter antihistamines, usually. But each summer seemed to get progressively worse. And this year has been by far my worst ever. Claritin and Sudafed weren't coming close to touching my itchiness, sneezing and extremely congested head. (I was like three of the Seven Dwarfs: Itchy, Sneezy and Why Won't My Ears Pop?) (READ MORE)


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Kerri Sparling
Kerri Sparling, diagnosed with type 1 diabetes when she was six years old, doesn't let diabetes define her. It just helps explain some things.
Creator of the diabetes blog Six Until Me and an editor for dLife, Kerri is an awareness advocate and an active member of the diabetes community. She'd also like a kitten. (Read More)


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