Thanks for this link it's been helpful I'm goin to mayb leave it in the iPad "accidentally opened at the page c if the hint works lolhttp://www.advancedtherapeuticsuk.com/dana-diabecare-r-insulin-pump
Try this link and click on the 'virtual pump' link.
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I totali forget bout the more actuate insulin dosage to cause I do find myself tidy in her food r increasing it to match the insulin which sumtimes is annoyinNo I would say push for a pump now. Will give you both so much more freedom with giving insulin (down to 0.1 of a U) how often you give it, over what length of time and 1 injection every 3 days vs 12 :-/ if I had a d child I wouldn't even consider injections.
Type 1 diagnosed 1990
HBa1c current 8.3
Pump and CGM used (animas vibe)
Why do u hav more to carry? Jesus I can't imagine hav more stuff lol we hav her rucksack and it goes everywur it has sharps bin finger pricker pouch insulin pouch needles diary lucozade carbs and cals book gels extra needles strips omg I'm insane already lol the list goes on!
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Hi i no exactly how you are feeling my little girl was diagnosed a year ago and started on injection 4x a day then more corrections it could be 8x a day .she hated it was embarrased in school full of bruises and cried a lot .we were offered the pump a 2 months ago and i had my concerns as did she but ....we would never look back ,it takes a lot of hard work on your part getting it right to start with but chloe wouldnt give it back for anything in the world she still hates the injection/cannula but its every 3 days so she is very happy about that .she takes up off at swimming /gymnastics and never found it uncomfortable at night as there is lots of ways to wear it . Keeping her bloods more accurate is whats pleased me the most but the change in chloe is amazing .i felt chloe was getting depressed at 9 !!! She just was not herself most days and always crying re the injections now she has the pump she has changed immensely she i a much more happier child.
Its really down to choice chloe was very very scared at the thought of the pump to start with especially because she had to inject it into her tummy but she wouldnt give it back now for anything
Hope this help you make a informed decision ask as much as you need to x
A lot of wat ur sayin sounds very familiar to me ! I just no if we decide to ever go wit a pump the hardest ting will b for her to say yes to it she is such a creature of habit and I guess if I wana push ESP if she drags her heels I need to b sure it's rite for her! I might b safer waiting for her to make the decision herself ? It's so hard to no! Can't do rite for doin rong but tanks so much very helpful
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Well I guess that makes sense and I'm definateli the type of person I'm prepared for every occasion to a fault mayb a little OCD even :s.I need to carry extra cannulas in case there is a problem and an extra syringe (part that goes in the pump), the cannula inserter (although I could do it just with my hands but choose to carry this) and my insulin pen incase of a pump fail (it has never failed me but it is recommended you carry a pen with insulin in just incase).
Diabetics definitely need big bags!!
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Well I no I'm ott already but of I'm honest I do use majority of the stuff in her bag everyday to b fair! But I'm glad u travel so light it must b greatThe stuff you - or worse, your daughter - is encouraged to cart around is mostly completely unnecessary.
I need only some testing strips (a tube of visually read strips, with a lancet within), some jelly beans, insulin and syringes - that's it.
No meter (or not necessarily), no spring-loaded gadget for getting blood samples, no pen-injector.
No flaming 'purses' full of junk!
I certainly don't need a pump. But I've no doubt that some do.
Is it the way forward! And is it a choice I should leave to her for wen she knows ?!
Yeh I guess ur riteBest to discuss your daughters options with her diabetes care team, most of the feedback from pump users is positive but whether a child so young can adapt to the change is anyone's guess.
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