Hi all,
I have been T1 diabetic for over 30 years, so pretty used to it all now!
Over the last couple of years, I have been experiencing reactions when injecting. It doesn’t happen every time but it is quite regular. Red, warm, painful.
I rotate my injection sites, and will avoid areas where I have recently had a reaction. But as it’s happening more often I’m running out of places to inject!
I mentioned it to my consultant at my last review - which was phone-based. It was brushed under the carpet and they sent me a “helpful” leaflet about rotating my injection sites (which I do anyway)
Anyway, just wondered whether this happens with anyone else? And any tips on managing it? Other than the usual rotate, new needle each time etc.
Thanks,
Em
Hi all,
I have been T1 diabetic for over 30 years, so pretty used to it all now!
Over the last couple of years, I have been experiencing reactions when injecting. It doesn’t happen every time but it is quite regular. Red, warm, painful.
I rotate my injection sites, and will avoid areas where I have recently had a reaction. But as it’s happening more often I’m running out of places to inject!
I mentioned it to my consultant at my last review - which was phone-based. It was brushed under the carpet and they sent me a “helpful” leaflet about rotating my injection sites (which I do anyway)
Anyway, just wondered whether this happens with anyone else? And any tips on managing it? Other than the usual rotate, new needle each time etc.
Thanks,
Em
Anyway, just wondered whether this happens with anyone else? And any tips on managing it? Other than the usual rotate, new needle each time etc.
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