swing of things - you obviously know everything about bringing up a type 1 diabetic child and your tone is condescending and arrogant in the extreme.
DS2 now aged 6.75yrs, got diagnosed with type 1 DM aged 4 yrs, he was on the 50th centile for height so just average, over the next 18 months he plummeted as he simply did not grow. All put down to the trauma of diagnosis and body adapting - not unreasonable. I accept an unusual year but feel free to check the bills, read his medical records etc!
He started the academic year in size 9 shoes and they were big - he ended the year in Size 1. Now I could be a completely useless mother and just increase the size of his school shoes and ignore the trainers and football boots, let him get sores on his feet and thus teach, or not teach him that diabetics must look after their feet. Or just be such a cow like was for the first two months of the year and tell him to stop whinging about his feet hurting and then die of embarrassment when I get him measured and he is now a 10.5. He ruined one pair of trainers on a very muddy field - allowable. With that increase in foot size, there was an associated increase in overall size - we are cheering, in our house and v happy that his body is settling and rebooting.
And as the diabetic expert round here you will obviously know, pumps are not all wonderful,when they stop working, get blocked, still need to check blood sugars, change kit, remind DC to wear it and no taking it off is not an option, finding it stuffed in his school bag for the day, not going hypo in the night. The cgm sensor is not funded so it costs more monies, hospital visits, illness currently wipes him out - he got norovirus from school - it was chaos for a week getting everything undercontrol again. I get called up to the school if the pump stops working/ gets switched off.
There is no doubt I buy much healthier foods because of DS, so the other 2 benefit and treats are more creative as we try to emphasise the lack of need for sugar for all of them. this is not a bad thing just life in a house with a diabetic child.
Also what the Mum gets in benefits is irrelevant to what the father should be paying for his 3 DCs. He had them with his EX, so obviously thought he could afford their upkeep. That has not changed.
So swingforthings, after 40 yrs of being a type 1 diabetic, I know the odd thing or two and yes it does take more time, more effort and in some cases more monies. I come from a position of knowledge for my DS and I now fully understand how scary it must have been for my parents when I was small. It ahs taken me a long time to not go in and check he is not hypo in his sleep.....