Hi
I'm new to posting on here although I've been reading a few posts here and there since my daughter's diagnoses in March (type 1). She turned 4 a week after her diagnoses and is due to start school next Tuesday. We did have a meeting with the school and her DSN in July but I personally came out of the meeting feeling we had achieved nothing. The secretary of the school has overseen an 11 year old diabetic who basically tested and injected themselves with the secretary double checking his insulin dose first.
Being 4 obviously she doesn't always eat all of any meal she is given and so the current plan is to give extra insulin at breakfast to allow for the fruit snack they have at morning playtime. Then I am to go in at lunchtime to test her and then (I assume) wait around for her to finish her lunch so that I can then work out her insulin and inject her with a view to training her class teachers on testing, injecting and looking out for hypos. I might add that the teacher's looked extremely worried and daunted by this prospect and seemed to be relieved I'd be coming in.
Basically I'm worried sick about it all!! She hardly ever knows she's in a hypo, she is quite good at explaining to people how to do her blood test but we've already had bad experiences at her nursery (they weren't changing to a new needle on her finger pricker each time!) and I can't even begin to explain how nervous it makes me feel the thought of letting someone at the school calculate and inject her insulin!! The DSN is all for the school doing all of it asap as I "shouldn't have to be going into school every day" and whilst I can see what she means to a point this is my baby girl and I feel so uneasy about letting someone else control her health. I'd really appreciate advice from anyone more experienced of having a young child with diabetes.
I'm new to posting on here although I've been reading a few posts here and there since my daughter's diagnoses in March (type 1). She turned 4 a week after her diagnoses and is due to start school next Tuesday. We did have a meeting with the school and her DSN in July but I personally came out of the meeting feeling we had achieved nothing. The secretary of the school has overseen an 11 year old diabetic who basically tested and injected themselves with the secretary double checking his insulin dose first.
Being 4 obviously she doesn't always eat all of any meal she is given and so the current plan is to give extra insulin at breakfast to allow for the fruit snack they have at morning playtime. Then I am to go in at lunchtime to test her and then (I assume) wait around for her to finish her lunch so that I can then work out her insulin and inject her with a view to training her class teachers on testing, injecting and looking out for hypos. I might add that the teacher's looked extremely worried and daunted by this prospect and seemed to be relieved I'd be coming in.
Basically I'm worried sick about it all!! She hardly ever knows she's in a hypo, she is quite good at explaining to people how to do her blood test but we've already had bad experiences at her nursery (they weren't changing to a new needle on her finger pricker each time!) and I can't even begin to explain how nervous it makes me feel the thought of letting someone at the school calculate and inject her insulin!! The DSN is all for the school doing all of it asap as I "shouldn't have to be going into school every day" and whilst I can see what she means to a point this is my baby girl and I feel so uneasy about letting someone else control her health. I'd really appreciate advice from anyone more experienced of having a young child with diabetes.