Sally71
Well-Known Member
- Relationship to Diabetes
- Parent of person with diabetes
Warning - rant coming!
And here we go again. Daughter has just dropped it on me that some people at school are being silly, whispering about her when she's having a hypo (she can hear her name being mentioned but nothing else), asking her if they can have some of her jelly babies or glucose tablets, and declaring it not fair when they can't. They say things like "well if you're allowed to eat in class then I'm going to as well, can't have one rule for you and another for everyone else," and they think she's teachers pet because she's the only one allowed to eat in the classroom. If she tries to explain, they say "oh yes, the life-saving jelly babies" in a mocking tone. They have a "worry box" in the classroom, daughter did put a message in it yesterday about this but I doubt the teacher will have had time to do anything about it yet. I'm going to speak to her tonight.
This all came out yesterday whilst we were having a meeting with the counsellor at the hospital (she's part of the paeds diabetes team so also has a much better understanding of diabetes than most people!). She was horrified, took all the school contact details off me and declared that she and the DSN will go into the school and sort it out. Which creates quite an amusing image, I can imagine that these two ladies are a fairly formidable team when dealing with know-alls and doubters, she said they had to have a meeting at a school last week where a child was having trouble, and she "really enjoyed it"
Of course I'm grateful for all help we can get, but we've already had the DSN doing a special assembly to the whole junior school, and the teacher doing a bit of a reminder lesson to their class only last year, how many more times do these idiots need to be told?! I'm beginning to think that because my daughter looks so "normal", that some people think that there isn't really much wrong with her and that it's all a fuss about nothing, and that unless she sparks out right in front of them they will never believe anything else. (And of course we don't want that.) She says they do understand but think it's funny. So how do you get the message across then, why should they take any more notice this time than they did last time?
Of course we have to try and do something, but it makes me sad that my daughter will have to deal with cr*p like this throughout most if not all of her life. I think we were extremely lucky for the first three years and hardly had any of these problems at all, but we're certainly getting a few now! And next year she will transfer to secondary school and we'll have to start all over again
At least she seems to be able to tell me about these problems a bit more easily now, rather than suffering in silence for weeks, so that's a slight improvement at least. Let's hope that something will get done - although it might take time to organise for the DSN and counsellor to go in. Fingers crossed...
Thank you for reading, rant over now! It does help to have a bit of a rant and get it all out, I'd probably brood about it all day if I didn't, and that's not helpful either. This forum is brilliant 🙂
And here we go again. Daughter has just dropped it on me that some people at school are being silly, whispering about her when she's having a hypo (she can hear her name being mentioned but nothing else), asking her if they can have some of her jelly babies or glucose tablets, and declaring it not fair when they can't. They say things like "well if you're allowed to eat in class then I'm going to as well, can't have one rule for you and another for everyone else," and they think she's teachers pet because she's the only one allowed to eat in the classroom. If she tries to explain, they say "oh yes, the life-saving jelly babies" in a mocking tone. They have a "worry box" in the classroom, daughter did put a message in it yesterday about this but I doubt the teacher will have had time to do anything about it yet. I'm going to speak to her tonight.
This all came out yesterday whilst we were having a meeting with the counsellor at the hospital (she's part of the paeds diabetes team so also has a much better understanding of diabetes than most people!). She was horrified, took all the school contact details off me and declared that she and the DSN will go into the school and sort it out. Which creates quite an amusing image, I can imagine that these two ladies are a fairly formidable team when dealing with know-alls and doubters, she said they had to have a meeting at a school last week where a child was having trouble, and she "really enjoyed it"
Of course we have to try and do something, but it makes me sad that my daughter will have to deal with cr*p like this throughout most if not all of her life. I think we were extremely lucky for the first three years and hardly had any of these problems at all, but we're certainly getting a few now! And next year she will transfer to secondary school and we'll have to start all over again
At least she seems to be able to tell me about these problems a bit more easily now, rather than suffering in silence for weeks, so that's a slight improvement at least. Let's hope that something will get done - although it might take time to organise for the DSN and counsellor to go in. Fingers crossed...
Thank you for reading, rant over now! It does help to have a bit of a rant and get it all out, I'd probably brood about it all day if I didn't, and that's not helpful either. This forum is brilliant 🙂