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sooooooo angry

Secondary teachers - No training at all
It is worrying that so many teachers have such little information about diabetes

I had been teaching in a secondary school for nearly thirty years when I was diagnosed with Type 1 diabetes. It is only since then that I realise how little I knew about it all. I had had no training at all and had picked up very little information from one pupil in my form who was diabetic, because she managed her diabetes so well. I am horrified now at my lack of knowledge in the past.

Once I was back in school after my diagnosis I got together with the small group of students who had diabetes to discuss any difficulties that they had had, so that we could address these and develop a school policy. (These students were also brilliant at helping me understand it all and helped when I was not sure what to do at the start of it all)

Issue raised - Exams
Exams were a big issue, especially for those recently diagnosed. Some were too embarassed to ask to take their test kit into exams as well as a hypo treatment. We made sure that teachers and invigilators were aware that they needed to allow them to test for and treat hypos in their exams.
For external exams they should be allowed rest breaks so that they can treat a hypo without losing exam time. I also encouraged them to make sure that they gave themselves enough time to recover properly from a hypo rather than rush back into doing their paper. They need to be at their best.

I am no longer teaching and I hope that the training has improved in schools, but I think that it is difficult to understand it all until you are directly involved. Think how many doctors and consultants in other specialisms have so little understanding of it all!!!!
 
Hi Anne – Marie,

Sorry been away from this discussion for a while…

I am very pleased to hear that the Lantus is improving the situation: he does eat breakfast I presume?


An aside: I am not as young as your son having had this condition (T1, which I’m sure from your description is the issue), for ~20 years. I can handle 3mmol/l (but realise something is upset, if I do realise!) and have been as low as 0.2 - 0.9mmol/l on reception by the ambulance. No ongoing effects seem to obtain from this after treatment (sugar!). Sometimes I may start fitting at low levels of blood sugar but always come around after treatment (glucagon administration etc.). So, I hope no long lasting damage will have come out of your son’s low blood sugar. In future life he’ll experience it (hopefully not so often). However, I appreciate your concern, because these effects may be different in younger children…

I agree that handwashing is important because he may have had some sugar on he’s hands from earlier (is he taking sweets from school mates, you certainly don’t want to feel left out?). Are the school staff performing the tests correctly?

You need to keep an eye on the Lantus, because failure to eat will eventually cause problems.

I know this (the above) is not quite on the point of what you express in your original posting but I appreciate the other postings from phoenix and annettekp and of yourself of course– this situation really needs addressing in primary schools.

Keep an eye on Dylan… :)

All the best…

Marc Dominic.
 
Hi Anne Marie,

How did you get on? I'm afraid I've been away from this forum due to other duties. Did you have a word with the deputy head? What were there suggestions?

Marc Dominic.
 
hiya marc
things are moving but slowly, the nurse went into school to talk to as many teachers and teaching assistants as possible and ended up with only 6 there she was not happy and neither was i but what can u do. on the plus side dylan has been put on a cgm for the last days and its been lovely peace of mind for me and it means we can look into things furthur he has also had some bloods taken and given samples to have tests done so hopefully we will get to the bottom of his ups and downs
anna marie
 
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