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Irene Stratton's avatar

I've been working in diabetes research since 1988 - when the kit to record the data was the size of a house brick! Great to see how things have changed. With better control of their diabetes young people diagnosed now with T1DM are less likely to develop complications - which is starting to be seen.

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Caspar Aremi's avatar

I absolutely love this for her. I've been T1D for over 30 years now, diagnosed just as I started secondary school. Back then the insulin was a mix of fast and slow for some reason, so you couldn't dose as you ate. After about ten years I got changed to seperate insulins, meaning I took a slow release background and a fast one corresponding to the number of carbs I ate.

I've only recently been given a CGM system to monitor my sugars and get rid of the finger prick blood tests, but every time I ask about pumps I'm told 'maybe...' and it's forgotten about. This has been at four different clinics.

Newly diagnosed patients get the newest tech immediately these days, but those who have been injecting for years have to keep doing it. I take eight or more injections some days... I can't wait to able to be eligible for a pump.

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