My youngest son, Tyler, has been using his Continuous Glucose Monitor (CGM) for about a month now. I have stated before that I love it. I still love it, but some times not so much.
I love the fact that I can “peak in” on his blood sugar levels without having him poke his finger.
I love that it lets him know he should check his blood sugar because his levels are either too high or too low.
I love that I can keep the receiver in my room at night and it will alert me for the same reasons. This way he can stay a sleep and not be bothered by it.
I love that it will keep alerting me until I do something about his sugar levels.
I ultimately love the peace of mind it affords and the tighter control we have on Tyler’s glucose levels.
But some times it makes me no so happy…..
I don’t like it when it alerts that his blood sugar is low/high when in fact it is the opposite.
I don’t like it when it alerts me all night long, even though I know it is only doing its job and the real problem is I can’t get Tyler’s glucose in range for whatever reason.
I don’t like that he has to have another device stuck on him and the he has to carry around another electronic device. He already has to carry his pump and meter with him all the time.
I know that in the grand scheme of things, this new tool will keep his numbers under better control. I know that this tool is helping him with his “Duh – I’m a teenager” moments, and me with my “diabetic care team blues”. It is just too much info at times.
Don’t let my little rant discourage you from trying out this new tool. It really has changed our lives for the better. I do sleep better at night, when it isn’t alarming. The alarming is a good thing. It is letting you know there is an issue that needs to be resolved.
Any advice on raising a teenage boy with T1 diabetes? Or experiences with CGMs that you would like to share?