INSULIN What is insulin & how does it work? When you have type 1 diabetes, the pancreas stops making insulin. When this happens, there are no keys to unlock the doors to your cells, so they can’t get the glucose they need. You can’t take insulin as a pill, the only way to give insulin is by injection or an insulin pump. Read more info on diabetes and how insulin works. Giving your insulin A syringe for giving insulin comes with a small needle on the end. You use the syringe and needle to draw up your insulin from a bottle. Syringes come in different sizes and have numbers written on the side so you can check your insulin dose. To give your insulin using a syringe, you have to pinch up the skin on your tummy, put the needle just under the skin and push the plunger at the end of the syringe to get the insulin into your body. You can use syringes for mixing different types of insulin. You should only use a syringe once. A pen looks more like a texta that you fill with insulin from a penfill. You have to put a needle on the end of the pen and change the needle every time you give your insulin injection. With an insulin pen, you dial up your dose and press a button to give your insulin. Many kids like to use pens because they don’t look like a syringe, are easy to carry and easy to use. Pens can't be used for mixing different insulins. If you use a pen, it’s a good idea to know how to use syringes to give your insulin in case your pen doesn’t work properly. An insulin pump is another way to give insulin. It is like a small computer that you load with insulin and program to give you small amounts all the time, and extra doses when you eat which is what your pancreas would do if you didn’t have diabetes. The pump is set to give the body insulin through thin plastic tubing connected to a small plastic tube (cannula) or a small needle. This tube or needle is placed just below the skin of the tummy or in your lower back where it stays for about three days. The pump is worn outside the body, in a pouch or on your belt (like a pager). If you use an insulin pump, you have to wear it all the time and change the tubing and cannula or needle every three days. It is important to also know how to use pens and syringes to give insulin in case your pump doesn’t work properly. Some things to help you with your injections (needles) Sometimes kids with diabetes can be nervous about giving needles. Here are some special things to help you – it’s a good idea to talk to your diabetes team if you’re worried. Mum, Dad or someone at home will help you! Inject Ease® PenMate® Insuflon® Jet Injection Devices Where to inject You can also inject insulin into other parts of the body. Have a look at the picture. Some people also use the top of their legs to inject their insulin just before bed so the insulin works slowly overnight. Don’t inject into your legs when you are going to be active (like walking, running or playing sport) because this makes the insulin work really quickly and you might have a hypo. It is important to inject into the fat just under the skin, this is why other parts of the body that have less fat (like the arms) are not usually used. Talk to your doctor or diabetes educator about where to inject. Where to keep your insulin Bottles and penfills of insulin that you are not using should be stored in the fridge until the use by date. They shouldn’t be frozen and if they are, they have to be thrown away. The insulin bottle or penfill you are using can be kept at out of the fridge somewhere safe that’s not too hot or cold. There are special packs you can buy to protect your insulin when you are in hot or cold places. It is best to take your insulin out of the fridge before you use it because cold insulin can sting when you inject it. You should throw insulin away if it has been opened for more than 3-4 weeks. Remember don’t shake up your insulin too much because this can damage it and it won't work properly. Make sure you have spare bottles or penfills in case you break one. TestingTesting blood glucose levels (BGLs) is really important to help you and your family manage your diabetes. You doctor and diabetes educator will tell you how often to test and when to test. Most kids test before meals, at bedtime, when they are playing sport, feeling low or not feeling well. Not all kids with diabetes do all of these tests, it depends on you, and how your diabetes is managed. Meters Click here for info on current meters. It is important to look after your meter so that it works properly. Keep it clean, try not to drop it and make sure it doesn’t get too hot or cold. There are special packs you can buy to protect your meter when you are in hot or cold places. Finger Prickers / Lancets Testing Strips Ketone test strips Blood – There is a meter you can get to test your blood for ketones. You can use the same drop of blood to test your BGL and test for ketones, so you only need to prick your finger once. There are different strips to test your BGL and for testing ketones. Urine – If you don’t have a meter that tests for ketones, you need to test your urine (wee) for ketones. There are special strips for this. To do this test, hold the strip and wee on to it when you go to the toilet. It might sound yucky, but it is really important. Testing Diary / Record Book Hypos Everyone is different, you need to know how you feel when you have a hypo. Hypos can be caused by lots of different things, like: Common times for hypos are just before recess or lunch, during and after sport, but remember they can happen at any time. When you have a hypo you need to quickly eat or drink something sweet straight away like: Then eat something else to stop the hypo from coming back, like: Don’t forget to always carry hypo foods with you and always tell an adult when you have a hypo. Make sure you don’t ignore a hypo even if you are worried about making a fuss or having everyone look at you. No one likes to be embarrassed, but ignoring a hypo can make you feel worse and can be more embarrassing if you don’t treat it. Highs & Sick Days If your BGL is above 15mmol/L and you are feeling OK, you can enjoy all of the fun things that your friends are doing, but don’t play really active sports like football until your BGL comes down. Drink plenty of water and do another test if you are not feeling well. If your BGL is above 15mmol/L and you are feeling sick, you might have ketones. High BGLs and ketones can make you really unwell and give you a tummy ache, make you feel thirsty and want to go to the toilet a lot. This means that things are out of balance in your body. When you feel like this, you need to tell mum, dad or someone at home how you feel, test your BGL more often, drink plenty of water and have some quiet time. When your BGLs are high and you have ketones, you need extra insulin – mum or dad will help you with this. It's really important that you and your family talk to your diabetes educator about what to do for sick days. ID
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