This patient support community is for questions related to juvenile diabetes including
Celiac disease,
depression, diabetic complications, hyperglycemia /
diabetic keto-acidosis,
hypoglycemia, islet cell transplantation,
nutrition, parenting a diabetic child, pregnancy, pump therapy, school issues, and teens with
diabetes.
First of all 7.5 sounds like you are achieving very good control without the pump. I don't know how much that would improve with the pump.
Beginning on the pump takes a lot of learning and adjusting. So it would be a big investment of time or energy so your family has to be sure that they are ready for it. The doctor might be waiting for you to ask for it, because I do not think that it is a good idea to force it.
I am an adult and I can deal with the inconveniences of the pump, but for a child it can be more difficult. You can read about all the benefits of the pump on the websites (and it really is great), but here are the downsides:
(1) You need to wear it 24 hours a day (which can be annoying, but the most annoying thing for me is to have to wear a visible sign of my diabetes)
(2) Some people have skin problems related to the infusion set (the tube that you insert into your skin)
(3) Someone who knows how to operate the pump would need to be with your child (someone at school as well) until she learns to use it. It is very good about informing you if there is some problem, but someone would need to know how to react
(4) You need to check your blood sugar even more often. If there is any problem with the pump, you need to know right away cause within a few hours you don't have insulin, so blood sugars can increase dramatically in a short period of time (this is rare but does happen).
So the pump is an AMAZING device that gives greater flexibility and control to type 1 diabetics. But you need to know when it is right for you and be ready to put time and energy into learning to use it properly. All the best!
What I am wondernig is, since she does not watch anything, do you think that one day the pump will not work for her anymore because of all her neglect? I try to explain things to her about diabetes and what happens but all I get in return is "I know," I am a t-1 for 49 yrs but not on the pump. She knows that I test myself 4-5 times a day and she cannot believe it.
She also forgets that she runs low with insulin in the pump yet it beeps for her to tell her she is low and will need to put a new cartridge in. She knows this and yet still goes out shopping and wonders why she doesn't feel good. Even taking a walk with her husband, she takes no little snack just in case.
This may not sound nice but I do not feel sorry for her. She is causing things to happen and not in a good way. Would you still call this "in denial?" She is on another board and lies her way through everything. She didn't in the beginning on this other board and caught hell from everyone about how she goes about being a diabetic. It has also been about 16 yrs since her diagnosis.
Thank you for any imput.