Hi, Just joined this site as a wife of a type1 for 38 years and thank you for your welcome messages. Hubby has been using a pump for 3 years now. Knows it inside out and could probably pass a degree course in pump using!! The problem we have are unexplained hypos which are at times severe. After each one we try to work out why it happened but sometimes just can't. These are usually the severe ones which require me to force glucose down him in order to bring him back to normality and as other carers will know can be very difficult when the diabetic refuses to cooperate and open his mouth!!
The last one was this week when he was so confused he did not know who I was and was imagining hundreds of people " panicking and trying to feed him sugar and they had to stop." The only way I could get him back to normal was to tell him that he could make them stop by eating these special tablets in my hand (dextrosol ) which thankfully he did. This was the worst one I have ever seen and was quite scary.
As usual when it was over we looked at what could have gone wrong but prior to his tea his blood sugar levels were fine at 6.5 and he pumped in the right amount of insulin for the carb value of his food so why a couple of hours later he should have such a bad hypo is unexplainable.
He is now wearing a sensor alongside the pump to see if we can get a pattern over the next week.
Two things I'd like to ask. Does anyone have any tips/advice to make it easier to get glucose down my hubby at these times that they have tried. Also does anyone know if the blood glucose sensors are available on the NHS yet as they cost us ?50 a time and only last for a week. I always feel much happier when he is wearing one but the cost is just too much to use one all the time.
Sorry to have gone on a bit but thank you to anyone who has read this and I feel much better for getting it off my chest!! I sometimes feel quite isolated as a wife of a diabetic as the emphasis is usually on the patient and not on the person looking out for him.
The last one was this week when he was so confused he did not know who I was and was imagining hundreds of people " panicking and trying to feed him sugar and they had to stop." The only way I could get him back to normal was to tell him that he could make them stop by eating these special tablets in my hand (dextrosol ) which thankfully he did. This was the worst one I have ever seen and was quite scary.
As usual when it was over we looked at what could have gone wrong but prior to his tea his blood sugar levels were fine at 6.5 and he pumped in the right amount of insulin for the carb value of his food so why a couple of hours later he should have such a bad hypo is unexplainable.
He is now wearing a sensor alongside the pump to see if we can get a pattern over the next week.
Two things I'd like to ask. Does anyone have any tips/advice to make it easier to get glucose down my hubby at these times that they have tried. Also does anyone know if the blood glucose sensors are available on the NHS yet as they cost us ?50 a time and only last for a week. I always feel much happier when he is wearing one but the cost is just too much to use one all the time.
Sorry to have gone on a bit but thank you to anyone who has read this and I feel much better for getting it off my chest!! I sometimes feel quite isolated as a wife of a diabetic as the emphasis is usually on the patient and not on the person looking out for him.