My ds is 5 and on SA+ and under SaLT (nothing too major, sound production issues mainly).
His school are meant to be providing 4 x 15 min sessions of SaLT therapy to him with his TA however it seems that more often than not it's only 3 x a week.
They changed his IEP just before Easter and sent it home for me to sign and i have noticed they have now 'officially' reduced his sessions to 3 times a week. My concern is now it's at 3 they might think oh well it doesn't matter if we only do it twice instead!
I have a meeting with the Senco later this week but have no idea where i stand with them not providing what was in the IEP in the first place (as they have no legal obligation to do so?) and if i can prevent them reducing his support?
SaLT advise a minimum of 3 x 10 min sessions a week so i'm guessing as long as the school offer at least this i can't do much about them reducing his current support?
TIA