Hi all, my daughter was diagnosed 3 weeks ago, I feel like my life has been turned upside down. I wish I could take it all away from her. She had been feeling unwell a week prior but I never knew the signs. All that keeps sticking in my mind is when they kept saying you did the right thing and got her checked today instead of leaving it till the Monday, her BG was 32, she looked so poorly, each day she is getting better and stronger and I am so proud of how she is handling things. There is so much to take in and lots to learn I just want to get it all right for her so she don’t suffer. I think it will be good for her to talk to others Is there a kids chat group on here?
Thank you for reading my post x
Hi
@Moo moos Mum, welcome to the forum
🙂 Very sorry to hear about your daughter's diagnosis

Well done for getting things checked out, and now that she is receiving the insulin her body needs she will fell SOOO much better, I know I did
🙂 We don't have a specific kid's chat section here, but you can certainly learn a lot from our members who have a great depth on knowledge and experience, so will be able to help with any questions you may have
🙂 If you want to communicate with other parents of Type 1 children and you are on Facebook, then have a look at the
Parents of Children with Type 1 Diabetes in the UK which is full of lovely people, some of whom are also members here
🙂
What insulin is she on, and how old is she? I would highly recommend getting a copy of
Type 1 Diabetes in Children Adolescents and Young People by Ragnar Hanas - it covers everything to do with living with Type 1 and is written in a very positive way. I'd recommend getting the latest edition, as things can change quite quickly, with new treatments and technology appearing frequently over the years
🙂 She may also be interested in getting a
Rufus Bear from JDRF, the Type 1 charity which can help younger children with fingerpricks and injections, making them less scary. For your information, the needles are really small and don't hurt, although sometimes the insulin might sting a bit.
You might also like to read
Adrienne's essential guide for parents of newly-diagnosed children, written by one of our members to help parents understand what has happened and how to come to terms with it.
Please let us know if you have ANY questions at all and we will be more than happy to help
🙂