I have argued passionately for total transparency about an SEND register. But once the child has a label, what do you do with it? Are we advocating a need-to-know basis or ensuring total awareness of a diagnosis? Likewise, when a child is placed on an SEND register, how much should we be sharing that information and in what way? In my last blogpost, I discussed lengthy waiting times for SEND assessment and the implications for children, families and SENDCOs.
