saffie547 said:I'm after some advice. My son is 7yrs old and was diagnosed last December, his DN has asked about him going on to an insulin pump, I personally think its too soon.
any thoughts?
saffie547 said:He was only diagnosed in December last year and is only 7. Although I do think it would make a difference while at school. His school are not dealing with his correction rates properly.
iHs said:7 is not a great age for going on a pump. In my opinion 11yr old should be the minimum and will be better because child is more grown up and is able to deliver the insulin themselves using the buttons.
A pump can demand an awful lot of attention especially establishing correct carb ratios and getting all the basal rates correct. On top of all this, a pump is connected to the body by a tube and infusion set (cannula). If the pump works all ok then everything is hunky but if something goes wrong and the set gets knocked causing blood to clog the cannula or a bubble gets in the tube or the tube somehow comes undone from the pump... then all hell can break out and you will find the pump will start bleeping loudly and then that will make teachers at school get worried that something is not right. Top it all with bg levels that are sky high because insulin has not been delivered and panick stations start to happen and parent gets phone call from school asking them to get there pronto to sort everything out. So parent at work is always on edge waiting to get the phone call.......
kt78 said:Pumps are great. Period. However I don't know why they don't give all toddlers the omnipod - it doesn't have any tubing and is really robust. They auto-insert the cannula to, via the remote - just feels like a pinch.
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