Hello, I am writing to introduce myself, my daughter having been diagnosed with T1 in December 2015, two days before her 7th birthday. We are on a multiple insulin injection regime and while we are beginning to grow accustomed to the testing and injecting and carb counting, the high levels of anxiety and rage experienced by our T1 daughter are harder to deal with and do not appear to be reducing. Our older daughters find to difficult to deal with the amount of attention that our T1 daughter requires and sibling relationships are suffering! I am finding it helpful to read all your posts and realise that we are not alone with this life changing condition! I would like to consider the pump this year to help normalise our lives, but my T1 daughter is adamant that she will never consider it. Should I put her on the waiting list anyway, given that in our area it apparently can take up to a year to get it? What seems to be really beneficial are these continuous monitoring devices that I keep reading about, particularly if part of the same pump system. Has anyone obtained one of these for a child on the NHS? Thanks for any advice.