Try and get yourself onto a DAFNE course ASAP. You will learn much more that the carb counting course you've just been on. When you do activities etc, alter the meal ratio before the activity so that you inject less insulin. It seems that you are very resistant to insulin....like me. Any activity which uses arm like DIY, even mowing the lawn with an electric mower would cause my BSs to drop rapidly. Normally I use a ratio of 1 unit quick acting insulin for 5 grams carbs 1:5 or 2:1CP for DAFNE trained folk. I prefer to use the 1:5 method as I just have to divide the amount of carbs by 5. I alter my ratio all the time depending on what's happening. I also take 2 X 500mg metformin SR tablets with my meals as I very insulin resistant. OK, you want to gain weight so don't bother too much about low carbs..have a good size meal and carb count correctly. Test before the meal and 4 hours after. Don't do any corrections if you prefer to test after 2 hours and find that you're high. It can take up to 4 hours for the novorapid to work.. I use Apidra as novorapid stopped working for me. Sorry don't know anything about STOMA. If you have a snack still carb count and allow insulin for the carbs eaten. Be aware of overlapping (stacking) insulin as it depends on when your next meal will be. If you're planning a good amount of DIY say in the next few hours you can half the insulin at the previous meal. Sometimes you can even have the meal without injecting novorapid but it all depends on how activities work on your BSs. I hope you are keeping a blood glucose monitoring diary, then you can see what is happening to your BSs with what you eat and how activities react to your body. Eating healthy can be misleading, as any carbs eaten will raise BSs. Sorry for running on so long.Can others share what they do? I am a type 1.5 female and have been for about 2 yrs. I am now on lantus twice a day (on advice from hospital as once a day didn't work for me) and novorapid and having done a carb counting course have a carb insulin ratio. It was also confirmed a few months ago by blood tests that at long last my pancreas had stopped which was good as suddenly I started to get some stability. Before, despite weighing everything my bgs were v unpredictable. However that stability hasn't lasted and once again I am all over the place. Slight adjustments suggested by the hospital with my long acting help for a few days then its back to being all over the place. I am very sensitive to any physical activity and underweight. I do eat healthily but not low carb as such as I cannot lose more weight and would prefer to adjust insulin to what I eat. I also have a stoma so that affects what I can eat as well. What I am really struggling with is snacking for pleasure and to help weight gain. Eg last night having done decorating during the day, I had my evening meal, underdosed my quick acting insulin by about .7 as usually the affect of physical activity on my bgs continues for a few hrs after and I wanted to have a few doritos as an evening snack. Yet my BG was 13 at bedtime and 19 this morning. It is really getting me down. I don't want to snack all the time nor am I wanting to eat rubbish but I do want to feel I don't just have to eat at meal times and also I get hungry and need to gain weight. The hospital are supportive but even they say I am complex. We have no idea how much my stoma, affects my digestion and bgs and whether this adds to the unpredictability. I can still go from 2.6 to 19 and yet we weigh out everything we poss can and I am diligent with working out my insulin. Can I /should I in inject separately for snacks? Not being able to live and eat normally, bgs being so up and down despite all I do to stop this and my weight is really getting me down. Even the diabetes centre I am under are wary of me doing any exercise as my bgs are so sensitive to physical stuff so I can't even feel I can get fit. Sorry for the long post but I am so fed up. Any thoughts would be appreciated.
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