Hi I posted earlier today about my 20 year old daughter and a very recent experience of DKA - i received some great advice and am really grateful.
She has been on the pump for 8 months, diabetic for 10 years. she went on the pump becaise she was having lots of night time hypo's on multiple daily injections. My daughter has moderate learning difficulties and certainly until she went on the pump i was very much a part of her daily control - i.e. reminders, thinking for her sometimes. however, since the pump she has taken more control. i realised at the weekend that she does have a limited understanding of some of the more complex issues surrounding pump use...ie what to do when she is ill and although she was reminded about the actions she needs to take at these times (earlier this week) she did not think to put this advice into practice today when she was unwell again. i suppose im wondering if this dka experience has made me realise that her limitations in relation to her pump use can have a very very serious outcome. i really feel awful thinking that she may be safer returning to her mdi than remaining on the pump. she has wonderful diabetic support at our clinic but they can't be with her all the time either. it seems unfair - what do others think?
She has been on the pump for 8 months, diabetic for 10 years. she went on the pump becaise she was having lots of night time hypo's on multiple daily injections. My daughter has moderate learning difficulties and certainly until she went on the pump i was very much a part of her daily control - i.e. reminders, thinking for her sometimes. however, since the pump she has taken more control. i realised at the weekend that she does have a limited understanding of some of the more complex issues surrounding pump use...ie what to do when she is ill and although she was reminded about the actions she needs to take at these times (earlier this week) she did not think to put this advice into practice today when she was unwell again. i suppose im wondering if this dka experience has made me realise that her limitations in relation to her pump use can have a very very serious outcome. i really feel awful thinking that she may be safer returning to her mdi than remaining on the pump. she has wonderful diabetic support at our clinic but they can't be with her all the time either. it seems unfair - what do others think?