Eng, I'm not on cgm, but might ask DSN due to issues I have and you've said about. But when I see her I say my bloods aren't what I would like. She puts me in my place(hubby, likes this point) and tells me that we all have blips as we don't have a working pancreas, so we won't get perfect results as injections/pump only play catch up, On our results. And my DSN REPORTS TO PROFESSOR AMIEL, first to help in an islet cell transplant at Kings, she harvested the cells. Take a deep breath and start again, mine have spiked over the last week, but told above 15 start to be concerned. Last night 16.9, after set set change then 18.9 half an hour later, with blood in the whole set, pump didn't alarm, but changed set. As hubby gripped at me to test 30 mins later rather than. 60. Glad he did ( can be a pain, but first time I fitted, scared the life out of him, now love him to bits, as been through a lot, but have given him 2 kids, which he loves, despite my diabetes). Take care and chin up. As hubby has just said diabetes effects all of us in different ways, pump incl( sometimes he speaks ****, but last sentence so true) all new users need help, but we don't need to be told we shouldn't have a pump. Those that have had a pump long term, think back(if you can). Did you have the information that we can get or ask for??? As newbies like Eng, Lucie and myself need are we all going to get the same response I've had great help from Eng and iHs and noblehead, on when my fingers and ears are sore for bg's, so now trying toes. But that info only came from members. And surely we should be helping and offering support, not make the person asking the question like they shouldn't have asked,this or hurt them, in a response?? They are just asking for advice and reasurance??
