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8:09 AM Jul. 1, 2008 - 0 comments
Filed under: Diabetes Life
As I mentioned in my last post, Gina has had the wonderful idea that we all raise our voices today and let the insurance companies know how much we need them to approve requests for CGMs.

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I've been on my pump for about 2 1/2 months. Before I took the plunge, I couldn't see how the "new" pump technology could really help me any more than taking injections. After all, both have the same end result - getting insulin into my body. Now, as a pumper, I can attest to how much better this little piece of technology is. My blood sugars have never been better (although I hate to say that for fear of jinxing myself and ending up with a boat-load of highs - I think it will take a while before I get more confident that control this good can last). Pumping has also made my life much easier in ways I never could have imagined.

So what does that have to do with Continuous Glucose Monitors? Well, like the pump, in the not so distant past I had no desire to try a CGMS. I figured why mess with what I know - finger sticks? How could a CGMS be any better, especially since the technology is new and all the kinks have not been worked out yet?

Well, my views on CGM have changed in the last 2 1/2 months as well. I can see how, even if right now they are not always 100% accurate, a CGM can help control immensely. They help spot trends and pinpoint times of the day when a basal tweak may be necessary. They work hard in the over-night hours, when I'd be asleep and less likely to catch a low - ready to sound the alarm if my blood sugar starts to crash. I am sure a CGMS would make my life easier in ways I could never have imagined - just like my pump. So I am very upset to know that if my doctor agrees with me that I am ready to start on one, chances are good the the insurance company will jinx it.

I have had an important point ingrained into me over and over - the most important thing a diabetic can do to stay healthy is to check blood sugar often and keep it under control. This is the best way to fend off complications and live a long and healthy life. Yes, the cost of a CGMS is not small - but the insurance companies need to understand that the costs are much smaller than the cost of managing and treating diabetes complications. And on a personal level. the costs are nothing compared to the improved quality of life a CGMS can bring me.

I did not ask for this disease. It's something I was dealt, and I live with it every day and work constantly to manage it the best I can.

I did not ask for this disease. But you can bet I'm ready to ask for anything that will help me manage it. Don't deny me that right.
1:51 PM Jun. 21, 2008 - 0 comments
Filed under: Diabetes Type 1
Gina over at Diabetes Talkfest has declared July 1st as Continuous Glucose Monitor System Denial Day. I personally have not been denied the CGMS . . . . but that is partly because I haven't tried to get coverage for one yet. The way things seem to be going, once my doctor and I decide I am ready to use one, chances are very good the insurance company will say it's a no go.
This is completely unacceptable! Let's raise our voices against the frustration of being denied this new technology which can be crucial in helping us avoid complications! Join us on July 1st when we send a message to the insurance companies!

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To learn how to get your voice heard, go here.
7:31 AM Feb. 10, 2008 - 6 comments
Filed under: Other
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You helped cheer me up when I was sad, you helped keep me positive when things got tough, and you helped me take better care of myself while taking care of you.  I wish you could have stayed with us longer.  I will always love you, and I miss you more than you could know.
12:45 PM Feb. 6, 2008 - 1 comments
Filed under: Diabetes Life
As a diabetic, we are all very used to needles.  Blood draws, finger sticks, and for some, insulin injections.  How many times a year do we deal with needles?  Too many.

I've never really thought much about it, and never found anything good in the fact that I jab myself all the time.  Until this week.
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This is Charlie, a sweet little 16+ year old kitty we adapted four months ago.  In the past two weeks, he has suddenly become very sick.  He had feline renal failure (and isn't kidney failure something we all fear as diabetics as well?).  He is also severely dehydrated.  If we can get him strong again, we may be able to manage his kidneys with medication.  So how do we get him strong again?  Well, every day I have to hook him up to an I.V. for 5 - 10 minutes.  When the vet asked if I would be comfortable handling the needles, I was happy to be able to say yes.

Mind you, I was surprised to find out it is much harder to stick someone else than it is to stick yourself.  The pain I feel every time I insert the needle into my poor little guy is much sharper than any pain from a needle I've given myself.  But it's making him better, and that's the best news ever!  So today, I am very thankful for needles and for my familiarity with them.
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