Hi everyone, I stumbled across this website yesterday and have decided to join in. My name is Catherine and my 13 year old son is T1, he was diagnosed April 2008. Even though it has been 3 years I still don't feel as though we are 100% on top of it, my son is a typical teenage boy and I feel as though I am having to constantly nag and remind him to test and inject.
He is currently on novorapid before meals and lantus morning and night.
3 monthly hospital check up is due on Thursday and as usual I am dreading it, the staff are all lovely but can never shake the feelings of guilt that his results are not as good as they should be!!
Anyway this opening message has ended up longer than I first thought it was going to be, I look forward to chatting soon
Cat
He is currently on novorapid before meals and lantus morning and night.
3 monthly hospital check up is due on Thursday and as usual I am dreading it, the staff are all lovely but can never shake the feelings of guilt that his results are not as good as they should be!!
Anyway this opening message has ended up longer than I first thought it was going to be, I look forward to chatting soon
Cat