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Insulin

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Hiya

Just popping in and out again I'm afraid but I think that I helped contribute to your original post above about mixed insulins being rubbish. I would like to say that I don't think I would have said rubbish and I hope my previous emails have not upset you, I only try and explain and help. Out of approximately 300 children that I am aware of on an email group, only one child is still on mixed insulins because it works for him, which is highly unusual.

I'm not sure anyone has said about the different insulins so I'll explain it quickly, as easily to understand as I can which is what I needed to hear when my daughter was little.

The Mixtard insulins and Novomix insulins are a mixture of long acting insulin and shorter acting insulin. There are different degrees (some have now been stopped) but for example Mixtard 20, 30, 40 and 50 (they are not all available anymore). I can never remember which way around it is but your Mixtard 30 contains 30 % of either long or short and 70 % of the other all mixed together.

The long acting in theory will last in the body for approx 12 hours ish and the quick acting is approx 6 to 8 hours maximum which is not that quick. The quick acting part of it is supposed to cover what is eaten at breakfast and lunchtime and tea time especially if the injections are say at 7 am and 7 pm, for a child 7 pm is normally way to late for tea on mixed injections.

This is a hit and miss regime as the insulins work at differents speeds, there are definite peaks and troughs in both the insulins and you find you are doing what is called 'chasing the insulin' or 'feeding the insulin' because you HAVE to eat at a certain time to avoid hypos, which happen on a frequent basis on mixes.

MDI (basal/bolus or multiple daily injections) is the same sort of idea but the two insulins are not mixed and are better insulins, they are newer. The long acting insulin will either be Lantus Glargene or Levemir (same sort of thing, different companies). They are supposed to last in you for 24 hours. In reality they last less but only a few hours less and there are ways around that. So the long acting insulin is called the basal insulin (or you may hear people call it the background insulin as it is always there in the background). It is injected and it sits beneath the skin and releases itself slowly throughout the 24 hour period (or slightly less). There are still peaks and troughs but small ones, nothing like the mixed insulin peaks and troughs. This is one injection daily at the same time or in some people if it really only lasts 14 to 18 hours then it is split to two smaller injections 12 hours apart (generally Levemir - most people don't have to split the Lantus).

The other insulin in MDI is a very quick one, normally Novorapid but in some instances Humalog (different company). They peak quickly ie between 2 to 3 hours and by about 4 to 6 hours are out of the body. This insulin is given purely when you eat carbohydrates. This is why it is so important to learn carb counting on MDI and really really helps to get some sort of control of blood sugar levels. For example if for breakfast you have two weetabix and a measured amount of semi skimmed milk I know from experience that that is 32 carbs. You will be given a ratio of insulin units to carbs so you can work out how much quick acting insulin you need to cover those 32 carbs. To make it easy lets say your ratio is 1 : 16 which means for every 16 carbs you eat you need 1 unit of novorapid. So if you eat the 32 carbs you will need 2 units of novorapid to cover that food, so that is what you inject.

If on the other hand you have just bacon and eggs ie no carbs then in theory you will not need insulin. Some people get to know that they need some carbs so would add a piece of toast to the bacon and eggs and you would then need to bolus for the bread which the carbs are generally on the packet.

I hope that is all ok and that I have made it easy to take it. I know how much information thrown at you in the early days makes it so hard to get to grips with everything. I am 10 years down the line and I still learn new things all the time. So ask any question and it will be answered for you.

Take care and good luck on Thursday.
 
Thank You that really has helped.
Im just not sure about his insulin now the past few days his bloods have been really up or really down.
Do you need to eat at set times still and have snacks at set times. becuase i no he struggles eating alot of the time.
And how would i do his insulin at school.
 
With MDI you can be much more flexible with meal times. Katie does still have a mid morning and afternoon snack, though I know not all people on MDI do. She also has a snack before bed. If she didn't have her snacks in the day then I guess I would give less insulin. She likes to have her snacks, esp in the morning as all her classmates have mid morning fruit. Also,if she's not very hungry at meal time then she can have a small meal - we just work out the carb content and give insulin accordingly. We we fortunate in that Katie started doing her own injections just before she moved to MDI and the staff at school just have to supervise (and also work out the correction dose if there is one and add it to the dose needed to cover her lunch). There are many children on MDI who don't inject themselves. The school will hopefully provide a volunteer to do it. If no one volunteers I think that they do have to find someone else who will do it - other people will know more about this than me !!
 
Thank You that really has helped.
Im just not sure about his insulin now the past few days his bloods have been really up or really down.
Do you need to eat at set times still and have snacks at set times. becuase i no he struggles eating alot of the time.
And how would i do his insulin at school.

No problem.

In theory you shouldn't have to eat at all as the basal should keep your levels on an even keel but we all know things don't go according to plan with diabetes.

So yes your son will need to eat. With mixed insulins you have to eat at set times, on MDI there is a much bigger window with each meal. For example what we did was made sure we ate between 7.30 and 9 am and for lunch between 11.30 am and 1.30 pm and for tea between 4.30 am and 6 pm
so you see the windows are much bigger.

My daughter also still needed snacks at about 10.30 am and 3 pm ish (or just after school) but lots of children don't.

As for the injections at school never volunteer for anything, once they have you, they will use you. None of the staff are obligated to give injections or do finger tests, however the school have a duty of care and under the Disability Discrimination Act they have to make reasonable adjustments so they have to ask for volunteers and if none come forward they will have to find someone and employ someone to give them. Where schools are concerned you you have to be friendly but firm and work with them, it gets you a lot further that way.

Hope that helps.🙂
 
Today hasnt been any better all night he was HI and woke up at 4.3 then at 11.30 he was down to 1.7

Cant see it being what he was eating because he had a tin of spagetti for breakfast and a rich tea plus some milk and for his snack at 9.30 he had 1 chocolate cookie and a rich tea.
 
Today hasnt been any better all night he was HI and woke up at 4.3 then at 11.30 he was down to 1.7

Cant see it being what he was eating because he had a tin of spagetti for breakfast and a rich tea plus some milk and for his snack at 9.30 he had 1 chocolate cookie and a rich tea.

Spaghetti for breakfast! Aren't kids wonderful? :D I think a good discussion with the consultant is in order. Most meters only show HI over 33, and to go from that to 1.7 is a heck of a change. I do hope that something can be sorted out, it must be awful for you all :(
 
When Jessica was on mixed insulins before Lantus came out, she once went from HI to 2.3 in 30 minutes. Now I know her bit of pancreas that is left is well dodgy (even dodgier back then) but this is a bit drastic even so and was purely due to the mixed insulin. We had washed hands and checked each time as it was so unbelievable.
 
Im so glad Adrienne has come in to explain things shes very good and helped me and others and are very greatful. I hope you get things sorted with the nurse on Tuesday becca.

Are you up and running on the email list now? x
 
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