Hannahli
New Member
- Relationship to Diabetes
- Type 1
My 4yr old was diagnosed about a week ago with T1. She's been very very poorly since the age of 2and hasn't had much of a normal
Childhood, due to how ill
She has been. This diagnosis has hit even harder now because it takes even more normality away from her. I'm struggling to come to terms with it all, my daughter is struggling to understand that we have to have a new "normal" and I'm just overwhelmed with all the information and things I am going to have to learn. My daughter had a hypo in the middle of the night but didn't wake up from it, it's only because I did her nightly blood sugar check that I saw she was very low. I'm so scared and now I stay awake all night watching over her and making sure she is ok. The community nurses have told me that it will get easier in time but is this really true!? I'm still finding it hard to let it sink in that this is life changing and it's even worse to see my daughter struggling to come to terms with it, scared of every finger prick she has and refuses to eat because she thinks she won't have to have her insulin! Still hoping that it's all a bad dream really. Does anyone have any tricks on how to make injections/finger pricks more "child friendly" and good 10g snack ideas? Any help/ideas/information/experiences are all appreciated xx
Childhood, due to how ill
She has been. This diagnosis has hit even harder now because it takes even more normality away from her. I'm struggling to come to terms with it all, my daughter is struggling to understand that we have to have a new "normal" and I'm just overwhelmed with all the information and things I am going to have to learn. My daughter had a hypo in the middle of the night but didn't wake up from it, it's only because I did her nightly blood sugar check that I saw she was very low. I'm so scared and now I stay awake all night watching over her and making sure she is ok. The community nurses have told me that it will get easier in time but is this really true!? I'm still finding it hard to let it sink in that this is life changing and it's even worse to see my daughter struggling to come to terms with it, scared of every finger prick she has and refuses to eat because she thinks she won't have to have her insulin! Still hoping that it's all a bad dream really. Does anyone have any tricks on how to make injections/finger pricks more "child friendly" and good 10g snack ideas? Any help/ideas/information/experiences are all appreciated xx