Monday, April 20, 2009


I just sent off a 30 day blood sugar log to Dave, the Mini Med rep I've been working with on the continuous glucose monitor. He called on Friday to tell me some interesting news with my insurance company. Last Wednesday my insurance company decided to change their policy. They now cover continuous glucose monitors for patients!!!! Wahoo! I was required to send in 30 days worth of blood sugar readings with at least 4 tests a day. Easy. I had to look at my graphs for 2 days while I was on the trial CGM to find some readings since I wasn't pricking my finger as often. Dave will talk with my endo about a good day for me to go in to have another trial CGM. This one will be a professional model so I won't be able to see any readings on my pump. I test and go about my business for a few days and then have all the info downloaded when I have the device removed. Hopefully, my 30 day log and the info from the new CGM trial will be enough for my insurance company to approve me. I really hope. I had several readings in the 50's but only one below 50. It happened early Friday morning, hours before Dave called.

It's somewhat depressing to me to write down my blood sugar readings. I never do. My endo downloads info from my pump every time I go in. Anyway, I can't believe how bad my readings actually are. Hubby said that hopefully the insurance company decides I need the CGM because of my roller coaster blood sugars. We'll see I guess. The graphs I got when I had the sensor taken off aren't as pretty as I thought they would be. But for a weekend, I was in pretty good control.

Yesterday Hubby was watching some show on the History channel about the top 7 ways the world will end. It was interesting to listen to while I was primping for church. At one point they were talking about how dependent people have become to computers and machines. They were talking about an incident in space where the computers could have killed the astronauts if the astronauts weren't able to override the computer systems.

I recently had a conversation with my mom about the CGM I used. She was saying that she was surprised it worked the way it did. She thought it would let my pump know what my blood sugar was and my pump would automatically give insulin as needed. I could see where she was coming from and that would be cool. But I told her that I love being the final say in what happens to my body. I can override my pump anytime I want. With my pump tracking the active insulin in my body and me knowing how my body reacts to different things at different times of the day, I know whether or not I should override my pump's suggestions. Or shut off my basal rates for a while. I do that at church a lot especially when I sub in Primary. I don't see how I can leave my class to eat if I need to and I certainly don't want to eat in front of them. So I anticipate lows and try to avoid them.

Hubby told me that scientists are working on something interesting for diabetics. He said they have created these tiny computers that can be injected into a diabetic maybe once a year or so. The computers will regulate the body's blood sugars the way the pancreas did before it stopped working. So the computers will act as insulin when needed and other computers are designed to be glucose when needed. That is amazing to me. I know that some people have had stem cells implanted and their Type 1 diabetes is completely cured. I want that! I am happy that stem cell research is moving away from embryonic stem cells. Scientists are learning now that you can get stem cells from just about anywhere. I could have a small hole cut into my arm and they could get stem cells from that! I saw that on TV a while ago. I could use my own stem cells to cure all of my autoimmune disorders. Now that would be awesome!

It's incredible to think that it wasn't that long ago that diabetes started being managed with animal insulin and now they have cloned human insulin (what I use). Blood sugar monitoring has gone from peeing on a stick to being able to poke your own finger and see accurate results in 5 seconds. The first year I went to diabetic camp, the counselors were talking about when they were younger and they had to pee on a stick several times a day to monitor their blood sugar. There was no other way. These were people maybe 10-20 years older than me!!!! Now we have pump therapy and continuous glucose monitors to better monitor diabetes. Diabetics can afford these things while surgery is still a little risky and definitely not affordable to everyone. What else will they come up with to increase diabetic control and comfort?

I was certainly not a pioneer as a diabetic bearing her own children but I will never forget being a teenager and hearing horror story after horror story of women who did try to have their own children. As soon as someone knew I was diabetic they immediately said I couldn't have my own kids. This was in the late 80's to mid 90's! I am astounded at the medical miracles that keep me alive and brought my children here.

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