Hi everyone.
My daughter is 25 and has t1 diabetes (diagnosed at 21)
Every time she takes her short acting insulin she gets pain at the injection site and feels very sick. She is fed up with telling her doctors about this, as she feels she is not believed. Her nurse once told her that this can sometimes happen about a year after diagnosis but will settle. It did settle but has returned. She has no trouble with her long acting insulin. It has got to the point where she is avoiding taking it (or at least, taking very little). Has anyone had, or heard of anything like this?
My daughter is 25 and has t1 diabetes (diagnosed at 21)
Every time she takes her short acting insulin she gets pain at the injection site and feels very sick. She is fed up with telling her doctors about this, as she feels she is not believed. Her nurse once told her that this can sometimes happen about a year after diagnosis but will settle. It did settle but has returned. She has no trouble with her long acting insulin. It has got to the point where she is avoiding taking it (or at least, taking very little). Has anyone had, or heard of anything like this?