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Had a right battle today

I've read up on them and they seem ideal. I mentioned it last month but it was before the big announcement with the nhs funding it. Im ringing my nurse up on Thursday for my hba1c results, I'll ask then. My first one since my diagnosis, which was 110.
 
Good luck on Thursday, good or bad let us know, we can celebrate or commiserate with you! Don't bank on getting one on prescription just yet, may be next financial year (April) the CCGs may budget for it but most are cash strapped at the moment. And the governing bodies like CCGs etc completely miss the complete and utter difference the libre makes.
 
When diagnosed, my brother a 35 year veteran turned up on my doorstep with a bunch of flowers and a box of Weetabix. Your new best friend he said.
Wow, best present ever!
 
John are you a young person? The space raiders crisps made me laugh...remind me of my younger days.
 
John are you a young person? The space raiders crisps made me laugh...remind me of my younger days.
Well im 43 but im still not ready for the knackers yard yet. Spaces raiders only have 7g of carbs per bag. But the bags are tiny these days.
 
Well im 43 but im still not ready for the knackers yard yet. Spaces raiders only have 7g of carbs per bag. But the bags are tiny these days.

Everything seems to get smaller the older we get!
 
I've just had my hba1c result from the nurse. Back in June it was 103. This is the first one I've had since insulin and diet change and it was 44. The nurse said it was excellent as long as im not experiencing a lot of hypos.
 
well done great result! Did she quantify 'lots of hypos'?!?
 
well done great result! Did she quantify 'lots of hypos'?!?
To be honest bar last Friday's I've only had a couple and I've managed to stop them. And after that the blood sugars been ok, apart from last Friday when I posted this topic.

Im probs having multiple hypos at night to bring my levels down
 
love the space raider crisps (pickled onion my little treat grandkids dont get a look in )
 

Hi. This answer to someone else question rings true with what just happened to us today. Any advice or friendly words would be seriously welcome.

Our 21 month old boy was diagnosed 3 weeks ago. Its a roller coaster and to be honest, some days it feels like a living nightmare that we just cannot sustain.

The past week or two he has had a pattern. Fairly mid range most of the day ( between 5 and up to 11) then at night he would go to sleep and by 1am (we test him then) he is in the mid to high teens so we give him an injection.. by morning he's normal. Today I went to work, our little one was with mum. By mid morning he dropped to 3.7 so she gave him a couple of jelly babies and tested 20 mins later. He was still only 4.0 so she gave him 2 more. Soon after he was in the 5's and it was lunch time so My wife did the usual thing of giving him lunch with his usual dose for carbs.. next test he is in the high teens (18). After a correction he was hypo again.. its been like that all day. It's now nearly 8pm and he's in bed but refusing his milk which we have accounted for.. arghhh!!! its so tough with a little one.

Im terrified of hypo's.. he had a seizure a year ago which was terrifying and the thought of that happening again is my worst nightmare (a febrile seizure apparently but now I'm wondering if it was related to diabetes).

Help help help.
 
I hope someone can can give you the advice you need. Being an adult and dealing with that sort of thing is hard but you make the decision how to counteract the lows/highs yourself. Having to do this for your little lad must be so stressful, but it proves you are good parents and want to help your lad get off to a good start.

I've found out it's all trial and error in the beginning and even long term diabetics don't always get it right.

Good luck, John.
 

Un medicated diabetes doesn't cause febrile seizures. Nor does undiagnosed type 1 diabetes hang around in a toddler for 12 months, it's an acute onset condition.

It sounds like the correction dose might be a little over generous. And having had one hypo makes you more vulnerable to a repeated hypo that day, so exercise caution if you are correcting highs caused by hypo treatment. I mean really the strict advice is don't correct highs caused by treating a hypo.

That is if you treat the hypo in the strict advice way, which is 15g of carbs wait 10 minutes and check again, if under 4 repeat, if 4 or over top up with complex carbs (milk, a plain biscuit, something like that).

At lunch time you son had got over 4 and had more fast acting carbs, so the hypo was over treated and he was on the isle when he had lunch causing a further rise. As he had just had a hypo it might be you would want to consider reducing the lunch time bolus to take account of the increased vulnerability for more hypos.

I think a lot of parents of kids with type 1 don't bolus until they've eaten, especially if they are fussy eaters a likely to leave half the plate. In an ideal world you would bolus before eating but if you can't explain he has to eat because it's been covered all that's going to do is cause hypos so it doesn't seem worth it.

Sounds like you might want to test his night time basal rate to avoid the 1am correction, it would be worth discussing this with your DSN.
 
Don't bolus until you've seen what he's eaten. You don't need to do it before he eats (I don't). Years ago I did when I used Humulin insulin for bolus. Can you use a CGM on a kid that young? Like a Dexcom that puts the sugars on your cellphone and alerts you if he heads low?
 
I'm afraid I've been like this for decades and that's without any medication, blood glucose hitting 17 mmolL-1 then very low hypos often below 2.1mmo-1. I therefore avoid carbohydrate so it is difficult for the blood sugar to go high in the first place. It's worth realising that your reaction to hyper/hypoglycemia can depend on the speed and relative change of blood sugar level. For example if you peak at 17mmol then fall to 6mmol in say 20mins then your hypo at 6mmol will feel like a hypo of less than 3.4mmol. Conversely if you have slipped slowly to 2mmol or less you may not have any symptoms or they are atypical, i.e. illogical behaviour rather then sweaty shaky etc. Exercise will also effect this axis. You can have symptoms of hypoglycemia and when you measure you find it's 14mmol hyperglycemia! Again this is when its gone from 4mmol to 14mmol very fast i.e 20mins. The worst foods for this are fast carbohydrate i.e. processed white rice, natural fruit juice, white bread etc.
 
Actually an acute rise or fall in blood glucose can give you seizures particularly if it has gone high followed by a rapid fall. This is known by medical professionals and can happen during an OGTT. And that's without insulin being given. The reason i know this is that it has happened to me in hospital during an OGTT several times. It can also happen with high carb food and exercise.
 

Ok, I'll clarify, unmediated type 1 diabetes doesn't cause febrile seizures.

What your talking about is reactive hypoglycaemia, which can anecdoteally be noted in the lead up to a type 2 because the pancreas works too hard to deal with spikes and can produce too much insulin. In type 1 there is no insulin being produced.

So undiagnosed type 1 only causes high blood sugar. There are no rapid falls.

Acute hyperglycaemia can cause seizures. If that were the case that would be how the diabetes was diagnosed. It would not remain undiagnosed for 12 months.
 
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