I’m no longer afraid of milk!
We arrived home last night after Cole’s baseball practice around 9 pm. I was answering an email when I heard Arden say the following, “Dad can I have this”. Arden had been complaining about being thirsty before we left baseball so I expected to see a can of diet iced tea or a diet soda in her hand but when I turned around I saw what can only be described as a horror.
She was holding milk and
“Trust the pump” is my mini-mantra this week.
Things have changed in regards to how insulin is measured and delivered so I have to trust the numbers that we’ve entered into the pump and the math that it’s doing based on them. So I trusted the pump, mixed a tablespoon of pink liquid sugar into a glass of milk and gave Arden the insulin that the pump indicated was proper. I would have never, let me repeat never have felt comfortable giving Arden that much insulin before bed in the past and I would have stayed up all night checking and rechecking her blood glucose if I did. My expectation would have been that I’d either have to wake her up to eat (if I gave her too much insulin) or administer more insulin and sit up all night checking her BG (if I gave her too little). That however seems happily to be a thing of the past!
This morning when I checked Arden’s BG at 8 am she was 108! You may have no idea why so I’ll tell you but typing that last sentence makes me so happy that I could cry. Arden got to drink milk like a normal kid, I got to wake up this morning not exhausted like a normal person and the hours that fell in between those two seemingly innocuous events didn’t hurt my little girl’s body. There was no sugar in her blood last night hurling her towards kidney failure, heart disease, amputation, blindness or early death.
Today because of the OmniPod milk is just milk, yesterday it may as well have been rat poison.
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The following are archived comments from this post. You can post new comments below.
AmyK
Oh, how I can relate! My daughter's insulin start on the OmniPod was just a week ago today, and this weekend, after nine months of my waking her to eat breakfast at 6:00am, she slept until almost 9:00am...and her BG was in range! - Tuesday, October 12, 2010 - 02:07 AM
Tandy
Reading this made me tear up! My son has been pumping for over a year now and I remember the moment he got to eat without worry even more emotionally than I remember 9/11. What an amazing moment! - Friday, November 5, 2010 - 10:33 PM
Scott
Thank you both for reading and for commenting! - Monday, November 8, 2010 - 07:22 PM
No, not that basil
Day one was really like day .5 because by the time we got home from the insulin start appointment it was 4pm. The real work began that evening when I did Arden’s first basal test.
Basal refers to a minimal level that is necessary for health or life. As used by diabetics and health care professionals, it describes a low, continuous dosage of insulin (either as a basal rate from an insulin pump or a slow-acting insulin injection) intended to "cover" the glucose output of the liver. This works together with a bolus of insulin, which is a dosage of insulin intended to "cover" a meal or to make a large glucose level correction.
When we were injecting insulin Arden would get a dose of a slow acting insulin called Levemer. It was a time release medication that acted as her basal insulin. It was decent but sometimes unpredictable, would last an indeterminate length of time and caused a lot of lows. So I’m glad it’s gone from our lives. In it’s place Arden’s fast acting insulin (Novolog) is now automatically administered by the pump in tiny increments every hour. To fine tune those increments I had to test her BG every two hours all night long that first night. When Friday morning came I was a bit tired but I had a lot of good data that helped us make adjustments to Arden’s basal rates.
Now truth be told, the rest of that first day I was a bit of a wreck. Not so much because of the pump but because it felt like I was starting over - which I was. I had Arden’s routine down to my own little science and it worked most days very well. Now I’m counting every carbohydrate that she eats and trusting this little piece of plastic to do what I have been doing for the last two and a half years. Most of the day I felt exactly the way I did in the hospital when Arden was diagnosed - heart in my throat and looking for a window to leap from. By the time Kelly got home from work I was fried, unsure of myself and emotional to say the least.
Arden’s BG had been high all day. I realized around 1 pm that her basal rate needed to be increased during the day to a higher dose. I called Kelly at work to run my theory by her. I wanted to run my thoughts past Kelly first to make sure I didn’t sound like a moron when I called CHOP and so I could get my crying done with Kelly so the poor nurse wouldn’t have to suffer through my weepiness. In the end I think I was right, I called Cathy at CHOP made the changes - so far I seem to have made the right choice.
On day two (today) I focused on Arden’s insulin to carb ratio (IC). That number represents how much insulin it takes to combat a certain number of carbs. We initially had it set to 1 unit per 50g... I moved it this morning to 1 unit per 45g. Again, so far so good with that change.
Right now it’s just before midnight and Arden’s BG was 208 about 45 minutes ago. I gave her .2 units with the hopes of getting her into her range (100-150) for overnight. If the new overnight basal rate we programed is correct, she should wake up in the morning still in that range - which would be nothing short of magical for us. I’m less stressed today then I was yesterday but still no where near comfortable. I’m anticipating that by this time next week I’ll have most of the kinks ironed out and I can go back to my baseline, which is being frightened all the time that Arden has type I (but at a much lower intensity level).
I am feeling a little nervous
I’m not the type of person that gets nervous about things. I’m more of a see it, do it kinda guy. That said, Arden is eating some cereal and then we are getting in the car to go to CHOP. In less then two hours I’ll be managing Arden’s diabetes in a completely alien way and well there is no other way to say it... I’m beginning to get scared.
More later if I don’t have a stroke ;)
**
The following are archived comments from this post. You can post new comments below.
Here we go!
On Thursday February 12th at 1 pm Arden will officially begin using the OmniPod insulin pump! If all goes as planned... tomorrow will mark the end of Arden suffering through seven or more needle sticks a day. Yes she will still have to test her BG with a finger stick but eliminating needles will bring her some much deserved relief. I estimate that Arden has received 7,000 injections since her diagnosis. Her injection sites have taken about as much as they can.
I’m anticipating that the next three weeks will be very intensive as I work with the pump team at CHOP to fine tune the pump and it’s insulin delivery. Keep checking back for updates, I’ll be using the site as a diary to help myself keep track of this transition.
Send a thank you to Obama
President Obama recently said that he, “guarantees” that he will sign an executive order overturning President Bush’s policy on stem cell research. I guess that it goes without saying that our family is thrilled that diabetes research will soon have the full support of the US government. If you are similarly minded please take a moment to thank President Obama for his his full-throated support by using the links provided in the letter from the JDRF (below).
The following is from the JDRF:
Greetings Fellow Advocates--
Below you will find a link to an action alert in support of an executive order withdrawing limitations on federal funding for stem cell research. For those of you who are new to our advocacy base, the ban that will be lifted will allow scientists to receive federal funding for what is considered to be our best hope for a cure for Type 1 diabetes and a host of other diseases.
Thank the President for His Stem Cell Research Support!
As this is our first contact with the Obama administration, it is vital that we have our voices heard in support of his signing this executive order. Please respond to this alert by clicking here. The entire process will take less than 60 seconds to complete and send. It will also help our cause if you pass this along to your contacts. And always remember that all communication with the White House and your legislators are counted and are vital in our quest to find a cure.
You can read what the President had to say about stem cell research and his executive order by clicking here. Please send your message TODAY and encourage others to join you in thanking the President!
Warmest Regards,
Fred Sacks, New Jersey State Chair (and the father of a son with Juvenile Diabetes)
JDRF Int'l Government Relations