Blog

  • What’s it like to pump?

    The more I talk to people, the more I realize they haven’t got a clue — and these are very educated people, very technology minded and sometimes even medical people.

    First, the pump only pumps insulin. It’s only a pump.

    The pump holds a given amount of insulin. Some cartridges hold 200 units, some hold 300 units.

    It pushes the insulin down the tubing and into a cannula — a small piece of plastic tubing that is inserted into the skin with a needle. It’s slightly worse than a regular insulin injection and loads better than a cortizone injection in the foot.

    The pump doesn’t do anything “automatically”. You program it to deliver a basal dose. Mine is around 1 unit an hour, and the pump divides that into how every many times it delivers insulin an hour. So you get a fraction of that insulin every few minutes. This replaces the long acting insulins, which use chemical to slowly release the insulin.

    You also have to enter a bolus for whenever you eat depending on your insulin to carb ratio. Thus, if I want to eat 40 carbs, I divide by 8, and program the pump to give me 5 units of insulin. Rapid acting insulin works about the same speed as metabolisming the average meal.

    My goal, throughout the day, is to keep my blood sugars as stable as possible. If the basal amount is programmed correctly, my blood sugar will stay within 20 points, provided I don’t eat.

    If I calculate my meal correctly — and there are variables on that — my blood sugar should be in the 140 range two hours after a meal.

    Therefore, what I do, is throughout the day, check my blood sugar with a normal, over the counter blood sugar device, and make sure that my blood sugars are in the right range.

    There are several factors that can through it off ….

    First, hormones, an being female, hormones especially can cause blood sugars to be erratic. Both internally produced and externally delivered hormones can change blood sugar.

    Stress — which causes hormone and adrenal production (isn’t that a hormone), can also change blood sugar.

    The make up of food — high fat foods tend to slow absortion down, cause the insulin curve to be faster than the food curve — though that can be fixed with an extended bolus. The pump has an extended bolus feature that lets the delivery of insulin be divided by a time period. Works great for pizza and mexican food.

    Pure sugar has the opposite effect. I still get a short sugar buzz off of things like Lifesavers or Gummi Bears. In that case the food gives off sugar faster than the insulin works.

    Just being off on the calculation. Let’s say I go to Wendy’s. Well, if the person serving the fries gives me 3 fries less than what has been measured and recorded in the FDA database, or 3 fries more, I’m going to be off on my carb to insulin ratio.

    And sometimes the database is wrong, or the food doesn’t have the same ingredients.

    Yeah, it isn’t fun, but better than the alternatives.

  • Pumping isn’t a no brainer …

    … but it’s still better than the alternatives.

    Last night I started going to bed, did my nightly blood sugar test and was 234. Yeah, I’d had a headache and didn’t feel well, but I ttributed it to the week from hell and being in two different school buildings. I am really allergic to dust and different buildings really get to me.

    So site change time. Had to check periodically through the nice, but it was dropping nicely and was at 105 when I woke up.

    I love my pump.

    It took a LOT longer for my blood sugar to go down when I had a shot failure. However, those were usually from eating the wrong thing, not taking a shot, or just some weird system stuff.

    And of course, medication didn’t budge the blood sugar at all.

    So yep, I still love my pump.

  • Yep, the new insurance is working!

    They have a nice website where you can track what is going on. The podraist has been paid, Animas has been paid — I do own them some money but haven’t gotten a bill yet and no problems.

    Even the pharmacy isn’t too bad, but I haven’t had them process an allergy script yet.

    One of my coworkers had problems as it has to be precertified with additional paperwork.

  • Type 2’s on Insulin

    Just read an article in Diabetes Forecast about Type 2’s being resistant to going on insulin.

    Well, DON’T BE!

    The most frustrating time in my life was the few months I was on diabetes medication. I swear to GOD, that the blood sugar was run by a random number generator … nothing I did seemed to affect my blood sugar, it just was what it wanted to be.

    Insulin is a pain, and the pump makes it more complicated, BUT I feel better. Plus, I’m in control, not some silly little pill.

  • Something COOL!

    Thanks to MedicMom, I went to http://www.htmlkit.com/services/favicon/ and made a Favicon, SO if you bookmark my site, you’ll get a tiny little picture of my insulin pump with my listing in the favorites.

    Yeah, I’m such a geek!

  • Navigator Granted Expedited Review Status by FDA!

    TheraSense | Investor Relations

    Here’s the important quote:

    We are also pleased to announce that the pre-market approval application for Navigator, our continuous glucose monitoring system, has been granted expedited review status by the FDA,” said Mark Lortz, President and CEO of TheraSense.

  • Texas Department of Insurance

    Good Site!

    Agent, Consumer, Industry News from the Texas Department of Insurance

    They have an online compliant form, which I’ve filed out and I’ve requested an Independent Review of the Pump Rejection.

    I’d LOVE to have the pump covered — the policy covered up to $3500 in durable equipment expenses, and I’ve spent less than $200. Especially since I’ve found out that the humidifer is a rental, not a purchase. Weird.

    So the max I can get back on the pump is probably $3250 or so. It’s still over half the cost of the pump.

    I’ll of course, be happy for the supplies alone, but I should get at least one of them.

    And it’s diffently been worth the full cost.

  • New Insurance seems to be working out!

    So far, so good. I’ve been to my primary care physician twice. Once for update on scripts and blood tests, and once because I was having a crisis with my GERD and needed doctor’s advice.

    I’ve been to my podrist for a cortisone shot for heel spurs.

    I’ve ordered 3 months of supplies from my pump company.

    I’ve filled 3 prescriptions — one on the way, two delivered.

    So far, everything’s been smooth, and no problems.

    Blue Cross/Blue Shield of Texas PPO, through the State of Texas teacher’s insurance program.

  • This is one of those “duh” things.

    Head To Head Study: Pumps Versus Glargine and Fast Acting Insulin

    Actually it isn’t because they went further than just finding out whether or not the patient perferred the pump. What they found out was that the patients had at least the same numbers, if not slightly better with the pump.

  • Managing Supplies — Test Strips and the like

    Be VERY careful on how you get your doctor to write your supplies. I swear my prescription says to test 8-10 times a day.

    Medco has choosen to interpret this as test as many as 8 times a day and is sending me 7 boxes of 100 test strips. Instead of 9.

    At least so far, they have not tried to get me or the doctor to change brands.

    I check — between January 1 and January 15, I had 129 entries in my log. That means I have been testing 8.6 times a day.

    Typically I check when I wake up. Two hours after meal. If I am driving without eating or checking. Before and after exercise, and sometimes during if things aren’t right — I tend to go low exercising.

    Yep, that’s a lot of holes. Bring on the continuous blood sugar monitor device. PLEASE!