It depends on what symptoms are being seen and how they affect the child.So sorry to read this
Could your team not have a stern few words with them pointing out that it is in no way easy to flick a switch and have perfect control all of the time?
xx
Why are they sending her home? How is her diabetes team reacting to this?they smile, nod and keep on sending her home.
Our team last time said oh, it’s understandable, they feel nervous... but they make us so nervous too! I’ll talk to our team soon again, we will see... because I have a feeling that our school is up to something. If they don’t want our child - why not saying it, why smiling and complaining?So sorry to read this
Could your team not have a stern few words with them pointing out that it is in no way easy to flick a switch and have perfect control all of the time?
xx
I'm sorry you are having a tough time. My GP doesn't want to manage my type 1 diabetes and I am under the care of a specialist team at the hospital, so it's not surprising teaching staff, without any medical training, can't manage it.
Can you monitor your child's blood sugars remotely with technology? Does your child have a pump that you can programme in advance of the school day?
Why are they sending her home? How is her diabetes team reacting to this?
I know I've recently read something informative on diabetes in school, I'll see if I can find it again.
What does her diabetes team think about this? If her doctor says it's up to her, and not the school, wouldn't this be the case?Honestly, they could leave everything to her, she is a smart child, she can manage.
It depends on what symptoms are being seen and how they affect the child.
I'm sorry to hear that she appears to have been sent home wrongly. They are reacting to the numbers they are seeing on her finger pricks which are perfectly normal if you eat carbohydrates. Insulin follows a fixed curve so does not match the foods you eat. It's normal to spike. As long as you are returning to the same as before you are eating five hours later then ignore the spikes. You will have to have a meeting with the school.They always say the same - she looks pale and shaky. I come to collect her and she looks scared and surprised like - mum, I’m fine, why are they sending me home? They look so terribly worried, always, that I’m afraid she will begin copying them. When she has same high sugar at home, she just doesn’t insulin and feels and looks fine. Yes, she can be grumpy though.
She should be allowed to deal with her condition herself, & make her own decision if/when well enough to continue the day at school.
What does her diabetes team think about this? If her doctor says it's up to her, and not the school, wouldn't this be the case?
Mind, I don't have children and I don't live in the UK, so I may well be wrong because there are different rules in different countries.
I'm sorry to hear that she appears to have been sent home wrongly. They are reacting to the numbers they are seeing on her finger pricks which are perfectly normal if you eat carbohydrates. Insulin follows a fixed curve so does not match the foods you eat. It's normal to spike. As long as you are returning to the same as before you are eating five hours later then ignore the spikes. You will have to have a meeting with the school.
My heart goes out to her for her managing at school. Hopefully, in time, it will fade into the background and managing is something she will just do automatically without it being a big deal.
Hi @FelicityG ,
Welcome to the forum.
Highs can be corrected. Lows can be treated too.. All can be dealt with in situ.
In the real world we deal with this stuff in the workplace too. Blimey i can have myself up & running again in 20 minutes?
I was once a pale child with the school "care package" in his own bag.
As much as i understand that the staff at your daughter's school are covering their backs..
It sounds to me your kid is on the ball at a tricky time for her bloods whilst things get relatively stabilised?
She should be allowed to deal with her condition herself, & make her own decision if/when well enough to continue the day at school.
There needs to be allowed "reasonable adjustments" for your child's education.
There is an equalities act in the workplace. I'm pretty sure it covers education too.
Here are some links that may help you determine how best to tackle the teaching staff.
Here.https://www.diabetes.co.uk/diabetes-at-school.html
Here. https://jdrf.org.uk/for-professionals/school-pack/schools-e-learning-module/
Here. https://www.diabetes.org.uk/resources-s3/2018-11/Make The Grade Schools Pack.pdf
& Here? https://www.diabetes.org.uk/guide-to-diabetes/your-child-and-diabetes/schools
Best wishes.
This times 1000. Sounds like you need your diabetic team to have a word with the school. She's not going to fall down dead through having an occasional blood sugar of 16 and the school should be able to help if she gets into trouble with a low. Is she competent to apply her own correction doses as necessary?
Teen years are stressful for diabetics and non diabetics alike, your school's attitude needs modification so that they support your daughter rather than stress her. Sometimes I am glad that I was a teenager before glucometers were invented. I am sure that my levels were sky high at times but I didn't have to worry about them and though my school knew about my diabetes they didn't have to make any special arrangements for me (or at least none that I was aware of). Virtual hugs for you and your daughter. Consider phoning the diabetes.org helpline for advice about the school.
Why are your daughters school becoming so involved in her situation? It sounds like they are wanting to sit down with her and check her BG then complain it’s high/low. Personally I don’t think it’s got anything to do with them unless your daughter decided to go to a teacher and say she felt unwell. I’d be arranging a meeting with the headteacher to discuss how to move forward.
I was 13/14 when diagnosed, I’m 26 now so not too long since I was in school. I honestly can’t remember a day when a teacher asked how I felt, what my levels where etc etc. I was given a card saying I was diabetic & could go to the toilet whenever I needed and that was it. None of the teachers knew how to control my diabetes, didn’t understand carb ratios etc & I’m guessing your daughters don’t either.
She should be allowed to take care of it herself without them interfering!
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