Hi,
I've posted before about my dd's severe excema and the problems she has at school, esp. as the teachers are not allowed to apply cream to her.
So I have made an appointment to see the SENCO / INCO and I think what I'm going to say is that dd needs a written care plan / IEP, and ideally two key workers (so that if one is away there is still one there) to be aware of her ercema needs and at the very least, to watch her apply the cream and give advice ("You've missed a bit!")
I am very new to all this and I don't want to come across as a pushy parent (I don't want to alienate myself from the school staff) but I do want to do my absolute best to get dd looked after.
Any suggestions / advice? Any relevant legislation that you know of that miight help me fight my (dd's) corner?
TIA, you wonderful lot (mwah mwah!)