Hey, i got diagnosed when i was 16. It was a shock to me although it ran in the family, but still, i'm sure your children will be sensible about it
. I was mainly scared about my friends thinking things, treating me different and people acting as if it was my fault? Almost embarassed? But i went straight to a specialist nurse who gave me all the up-to-date equipment which was good. I see other children on TV with really large testing kits, and i feel that like me, they would benefit from the small one i have, which allows them to test on their arms, palms, and legs so their fingers do not hurt and become hard etc? its Freestyle lite (really small) and it has special freestyle lite testing strips. Also, i take a long lasting Levemir before bed which gives me a base and a novorapid instant? so this actually helped me feel in control as i could gage myself what i needed. I think this, unlike my nan who used to have a large amount and have to catch up with food all of the type and exprience hypos, really helped me come to terms with it all. If you let them know that other kids have it, and there are ways to make it easier it should be fine. Boys probably are a little less worrying about what they eat as they getolder but that's just growing up? theyll be closely monitored with 6monthly health checks anyway
i had an amazing family who really helped me. It was annoying at first as they kept checking up on me! but i have led a normal life, going out, drinking, off to uni soon! just don't let it get you down because they are extremely brave, it will make them much stronger people. and remmeber they rely on you
they can always talk to me on here if they want to, thats the first thing i wantd to do. I found boys living up my road with it who are 19, 17 who had it since they were babies.
All the best