Today and tomorrow I’m going to leave settings alone since this is a "weird" day. We’re doing staff development all day, which means sitting still and maybe even getting stressed by the information.
I don’t know how I did yesterday, either, because I had my pump off for about half an hour. Today was a full site change, both infusion set and sensor. I tend to be very slow this mornings.
Had a "normal" morning, both breakfast and activity level, and went high, so I tweaked down my morning Insulin to Carb ration — going from 8 to 7. I’m focusing on that number right now, and trying not to worry about the others, though I’m still thinking my corrections are too low.
So I download my data again today. I’m looking at two important numbers — my blood sugar from this morning and from yesterday morning. Yesterday morning my blood sugar was 156 and today I was at 146, so I am probaboly doing in the right direction.
Breakfast was looking okay — my blood sugar at breakfast was at 141, and two hours after my blood sugar was 156. I am suspecting that the problem is with corrections, but I’m not sure about that yet.
Someone on the IR2020 list was asking about whether or not boluses were working and I realized that mine weren’t. Not surprising as I have not been exercising as much and have been eating more. So I decided to document the process of updating everything while I was doing it.
My next steps will happen over the next few days. I will be watching breakfast first. If I am within target at breakfast, then I’ll start watching lunch, etc. After I’ve fixed all the meals, then I will focus on the corrections.
By the way, this is easier to do as you go. What I usually do on a normal basis, is down load easy manager, and again, watch breakfast, then lunch, and then dinner and I’ll document that process as I do, mainly to keep myself back on track.
My gastro doctor called last night and said she had not received the coverage review paperwork for me, but had for other patients. She also wondered if there was another medication we could use that wouldn’t cause so many problems. So I called Medco last night, they told me I had to call the coverage hotline to get the paperwork sent and that all other medications that could be used instead also had to have coverage review under our policy. Also called the coverage hotline and they are supposed to send in the paperwork. She also said that she’d have her people call the 1-800 number.
On my part, I’m experimenting with going with 1 tablet a day instead of 2, and see if there is a difference in my sleep. Scary, but I am going to give it a try.
The best part though, is the samples from the endo’s office, because now I can relax a bit and don’t have to have the protonix TODAY.
And the gastro doctor did call in an emergency supply but the insurance doesn’t want to pay for it. (According to Alberton’s pharmacy).
At least, I assume that giving patients samples are no big deal to most doctor’s office. I have had a few, especially primary care physicians, that always made sure you had enough medication samples that you’d "covered" the copay.
However, for me it’s a BIG deal. My prescription bottle of Protonix is going to run out the middle of next week. Right now, Medco is still showing that the gastric doctor hasn’t asked for the coverage review — though it could be that she has, and they haven’t done it yet. At any rate, it isn’t shipping.
I’d emailed my endo’s office at the beginning of this saga (on Monday, December 24, when this all started on December 22), and asked for Prontonix samples. They’ve actually been able to hook me up before, so I was hoping. I’d even called the Primary care physician but they were out.
Well, the endo’s assistant was back in this week — he’s still out — and she gave me a huge bag of Prontoix samples. Enough to last me over a MONTH! I didn’t realize just how much at the time, I always think it’s rude to look in the horse’s mouth when it’s handed to you — so I didn’t look until I got back home. So I can relax a bit now.
Stopped by the pharmacy at my endos office and their wholesaler shows the pens are in the system as a new product but not available for shipping.
This is scary until you read the explaination and then it makes sense. And yes, I have documented restless leg syndrome from two sleep studies. I wasn’t a believer in it until they put me on Requip. It seems that some patients respond to it and not to the other medication (which I was on and saw no difference in sleep). Luckly, I still find gambling boring (a side affect of these medications). And a good pun, now that I think about it.
Restless legs and heart… – Blogs – Revolution Health
artery disease. Over 3000 men and women were evaluated in the Sleep Heart Health study, a large ongoing group of patients being evaluated for various sleep disorders. About 7 % of the women and 3.3 % of the men had RLS.These people were then compared to the people without RLS for the likelihood of having either ccronary artery disease (heart attack) or stroke. People with RLS were about 2 times more likely to have one of these conditions.
Check the URL of the website — this content is currently being stolen. For legimate content, see http://www.kweaver.org
I know I was! I still miss my local gym — I worked out there for years and really enjoyed them. Used their personal trainers, etc. Since they closed I built a home gym. I’ve never really been happy at any of the chain gyms, even those that specialized in women.
The gyms at Texas Instruments was great too. A benefit I really miss.
Quoted from http://well.blogs.nytimes.com/2008/01/02/local-gyms-outpace-the-national-chains/:
Local Gyms Outpace the National Chains – Well – Tara Parker-Pope – Health – New York Times Blog
If your New Year’s resolution includes going back to the gym, you may be happier at a local club than a national chain, according to a new survey by Consumer Reports.
Actually a combination of a couple of these items happened during my first period class. My Dexcom reciever kept going during my first period class — I teach computer science so random beeping always disturbs the class.
I pulled out the receiver and said, "whoops, I’m high". My kids said that was the first time a teacher ever said that to them, and it was the first time that they realized it probably wasn’t a good thing.
Quoted from http://www.diabetesmine.com/2008/01/you-know-youre.html:
Diabetes Mine: You Know You’re Diabetic When…
You say that you feel “high” in public and then wonder why people around you give you weird looks.