Unfortunately, we do need written confirmation though. We can't just take parents word for it that a child is not fit to attend school long term. We have had a case of fabricated illness (what they used to call Munchausen's by proxy) as well as numerous cases where parents have claimed that their child is too anxious to come to school but they were actually working for the family business or out burgling houses or caring for an adult family member or caring for younger children whilst parents work etc etc. Non attendance is a big red flag for lots of issues so that's why we need evidence- it's to safeguard the children involved.
I accept all that. But can I ask why, when you have evidence from 3 specialist paeds, one of whom is on the NICE clinical guidelines panel, and they all insist an ed psych is needed, which you, the school, are blocking, and the child is formally diagnosed with ASD, SPD, and anxiety... how the hell is it right to threaten the Inclusion Team when the parent is asking for an all agencies meeting (also refused) to work out a way forward? And my son achieved the top possible scores in KS1 SATS so his attendance record hardly seemed to be damaging his learning, did it?
I am NOT doubting how it works in your school, or how it's supposed to work. I've had amazing support from the NHS, from the Advisory Teaching Service, from a local ed psych, and from individual teachers. But the head's approach was such that in two (two!) school placements, we were advised by the paed to involve solicitors to force the right provision, or to move him. There was no third option.
I want my child in school. There are all sorts of things schools offer that home ed can't. But he was clinically diagnosed with anxiety, and there was talk of medication at 7 and 8 to address that. SSRIs, which can't be tested on kids for obvious reasons. Psychoactive drugs on a developing brain with no long term studies on outcomes. And now, at home after a year, he no longer has mental health problems other than mild OCD. How is that good practice? How? And yet it is common. I've met too many parents with ASD kids to doubt that. The paed said it was the norm - she can name more schools who don't care properly for ASD kids, than those who do.
It just is not good enough. We are currently spending money we really don't have to home ed to the right level. We pay for private medical support no longer available on the NHS. And we will borrow to send him privately to secondary, because what choice is there? And that's not right not because we resent doing that - we now rent, as I can't work, when we used to own - but because not all families with ASD kids can even afford to do it at all, even by their fingernails as we are. So many kids are lost to this. It's not right. And the fix is relatively simple, is the worst part.