You won't be disappointed by the opportunities the pump will give your daughter! My 4 yo daughter has been pumping since Oct 2010 and she LOVES it! She gets timid with every infusion site change but she'll just hug a teddy bear or Daddy and grin and bear it because she knows it is only once every three days now.
We are pumping with the Medtronic Minimed Paradigm as well as using their CGM. We use the Lidocaine cream for the sensor installs on CGM but she doesn't need it for the infusion sets. We use the Mio infusion sets with a 23" line at 90 degree angle. I can't install in her belly or it kinks at a 90 degree angle, likely because of what another poster just mentioned about it the muscle getting in the way. Instead, we use the top of the thigh, the top of her bottom, and the back of her arms.
I have an entire list of pro's and con's I send to local parents that ask me about it but more recently, my FAVORITE part, is the reduced lows while active during the summer months. When they are disconnect, they are completely free of insulin. So, when I disconnect for her to swim, we get to go an hour without it and then reconnect, test and correct. Lately, there are many times that we don't even have to test and correct because it is staying so stable. In fact, after two hours of swimming this week, my daughter went from 157 after first hour, to 120 at the second hour. I was so happy! She felt great and she got to be a kid!
Here's my list!
Pros:
It has helped me feel like I can feed her like a normal toddler again and not have to wait until mealtime for a good snack. They still ask that you stick to the three hour rule so snacks would be about three hours from a meal but I’ve gotten a little less strict with that over time as I get used to how the active insulin affects her. Because I have her on the CGM as well, I just feel like I can relax knowing that I can keep up with what her sugar is at all times, and adjust easily with the pump (suspending it if she’s low, and bolus when she’s high) without an extra shot.
Also, sometimes with a toddler you don’t know how much they’ll eat in one meal so a lot of times I start her off on 25g carbs and then if she eats more than I anticipated, then I just bolus a little more to cover the entire meal. Before the pump, I would have had to do two shots to do something like that, or calculate and hope that she eats all of her food.
I used to carry around a calculator, carb book, and notebook to make sure I had all of the carbs and calculations done correctly. But the pump does the bolus wizard so that allows me to just enter the blood sugar, then carbs, and it automatically calculates the insulin for the meal. It is so helpful!! By the way, if you have a smartphone, I use the “GoMeals” app to look up carbs for restaurants or grocery or generic food.
Also, if she’s really active like jumping on the trampoline or playing at the playground, I just take it off when I think she might get low. So, her body can go without any insulin at all and it prevents a lot of unnecessary lows.
I’ve also bought her a whole set of pump belts and she doesn’t even notice wearing it. It isn’t an inconvenience for her and no one even sees it under her shirts.
www.toosweetboutique.net. I think most of the patterns are girly but she has some options for the boys.
I also really like the nighttime basal rates. I rarely have to wake her up for a snack. Before the pump, I had to get her up at least once a night to eat something so she would make it through the night. Now, if she is starting on a trend downward, I can do a temporary basal change (like for 1.5 hours only give 0.05 insulin rather than 0.20) and we make it through without getting up for a snack.
Overall, it just seems to match the insulin to her carbs better.
Cons:
It stinks to have to do the pump change every three days, but it is still way better than 4 shots a day. Look on youtube to get an idea of what it is like to do a pump change.
She’s on a tether with tubing that is 23”. For some kids this is super inconvenient, but again, the pump belt has helped eliminate that problem. She wears her infusion set on her arm.
Some kids look at her funny for having something attached to her arm but my daughter doesn't really care about that too much.
I’ve heard you can get infections at the site but that hasn’t happened to us yet. Just with her CGM site.
I’ve also heard you can get scar tissue at the site areas but that hasn’t been a problem for us yet either.