With Glucopen, do you mean an insulin pen or something to treat hypos?We haven't been given anything to treat hypo other than the Glucopen and the more I read I should have something like Glucogen.
If she has been going low in the past two days, have her insulin doses been adjusted to that? Are you receiving any guidance on doses at th moment? This soon after diagnosis, needed doses can change quickly, and it'll take time to find the right doses in the best of circumstances.but I'm anxious as she has dropped in last two days about what I would give a sleepy baby at night who won't eat.
Have you asked the hospital if this is available for you?the more I read I should have something like Glucogen.
Hi @Kirsty87 , welcome to the forum.
I'm sorry to hear your 2 year old has just been diagnosed, that's a lot going on suddenly.
With Glucopen, do you mean an insulin pen or something to treat hypos?
If she has been going low in the past two days, have her insulin doses been adjusted to that? Are you receiving any guidance on doses at th moment? This soon after diagnosis, needed doses can change quickly, and it'll take time to find the right doses in the best of circumstances.
With nighttime lows, I'd urgently seek advice on dosing, you'd rather run a tad high at this stage than seeing lows.
Would she be willing to sip on some orange juice or coke while half asleep?
Have you asked the hospital if this is available for you?
Glucagon is usually only used with hypos where the patient is unconscious, which thankfully is a rare event. If it's used, you'll still need ambulance or hospital care afterwards as far as I understand (never needed it myself, thankfully), so it's not something to use just because your toddler is being stubborn about eating.
If ambulance/hospital care is quick where you are, calling them will be fine in case of emergency. If you're at a remote spot, I second trying to get emergency medication if possible.
If BG is below 70 you'll need to treat the hypo, but definitely NOT with the glucagon kit! I'm very happy you have the kit in case of emergency, but I wouldn't expect to need it.Sorry reading this again this morning I’ve not been very clear. We have been given an orange hypo kit Glucagen for emergencies but we were told to use it when BS is below 70.
Having read a bit more this doesn’t appear to be the case? Please correct me if I’m wrong
Don't worry, just use an empty water bottle for now.we can’t even get hold of a sharps box.
Being around 100 through the night is pretty much perfect in my book.My little girl dropped to 64 yesterday afternoon and my anxiety is just building around it dropping, she sat around 100-110 through the night. Is that too low?
Do you have a GP in the UK? Can you contact them from where you are now?We move back to the UK in 2 weeks
Hi Marikev, I do hope you're getting on ok on your own, it's a lot to take in but I can imagine Norway is beautiful place to live too and hopefully a little more advanced than here in Cyprus to look after you.Hei Kirsty, this must all be very scary for you. I’m a British granny living in Norway, diagnosed T1 2 years ago and I can empathize with some of what you are going through, language barrier etc. I don't know of any parents of young children on here who can offer better advise, hoping there are some…
I am prescribed a product called Baqsimi, which is glucagon, and is inserted up my nose, should I ever pass out from a hypo. But seeing as I am the one looking after me it would be down to whoever was around at the time to know about it and find it and use it! Mine is a one time use product, so no way to open it up to see how it works. When the old one expired I did open it up to see how it works.
Thank you for the tips on the baby food and yoghurt pouches she will definitely enjoy those but I expect she'll have the same reaction to the savoury ones too. It's a lot to learn in a short space of time but I'm told and I've read so much on here already about everyone who battles this daily and it is normal! My little girl is taking it all in her stride luckily. Take care xxYou are using different units for measuring blood glucose to what I work with. Need to multiply the units I am used to by 18 to get to yours. Pretty sure the UK uses mmol/L, so my target range is 4-10.
So your little girl’s figure of 100/110 during the night would be just fine. I don’t know enough about the management of T1 in little children , the hospital staff should have given you some basic information.
I buy pouches of baby food, fruit yoghurt mixtures that I use for hypos, ie going below 4. Some need to be refrigerated, but here we can buy ones that seem to be OK kept at room temperature. I tried the savoury ones and found them to be disgusting, so stick with the fruity ones.
Things will settle down, but there is a lot to learn and take in.
best wishes from stormy Norway.
Thank you, I did think this was the case but there was still some blurred lines.If BG is below 70 you'll need to treat the hypo, but definitely NOT with the glucagon kit! I'm very happy you have the kit in case of emergency, but I wouldn't expect to need it.
I will definitely try buying a few different things to try her with, this is a good idea and I can see how we can mix it up if we need to.A hypo can be treated with anything sugary, like the glucogel. But also with things like juice, sweets, sultanas, coke, full sugar ice tea, dextro tabs, cake icing, honey, etc.
With your worries about what she'll have, what about going to the store and simply buy lots of different things, especially things she likes so you can try if needed?
That said, most children will sip a juicebox if they're half asleep and someone puts the straw/sippy cup in their mouth with the instruction to drink.
I like using a spoonful of honey if I'm hypo but not wanting to eat.
This is a relief! I'm glad she's sitting where she needs to be and hopefully I can relax about it a bit now too.Don't worry, just use an empty water bottle for now.
Being around 100 through the night is pretty much perfect in my book.
Our current GP done a referral on Thursday so hoping we can get her an appointment pretty quickly when we get back. Thank you for the chart too, I'll have to study this a bit to get my head around the different numbers.Do you have a GP in the UK? Can you contact them from where you are now?
Once you're in the UK, you'll need a referral to an endo to set up her diabetes management.
Thank you, I think I'll be here a lot asking questions and researching. I hope your T1D journey has gone well so far, I know it's a bumpy ride were about to get on but hearing from people like yourself is really reassuring that her life doesn't have to be different going forward.Hello @Kirsty87 and welcome to the forum.
I'm so sorry your daughter has been diagnosed with diabetes. That will have been so difficult for you to hear, and a massive learning curve.
I was diagnosed at the same age, many decades ago. Thankfully treatment has vastly improved since then, and as has already been said your daughter will be under the care of a hospital team, once you're back in the uk. They will be able to help you with all aspects of caring for your daughter, and also give you support.
My mum and dad used honey to treat low blood sugar, because it can be massaged into the gums of an unresponsive child. I also loved it as a toddler.
Take care, and ask any questions you have (there will be many). We're a friendly bunch, and there's a wealth of knowledge on this forum from people living with diabetes.
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