Sorry if this is long. NC for this.
My DS6 goes to a school that has a policy that they are not allowed to bring in a lunch. They have to have a school one. Despite watching him struggle with food for over a year, and
Despite me telling them he has ARFID (diagnosed, lots of food aversions and numerous sensory issues), they wouldn't allow me to send him with food he would eat, which means he eats maybe one lunch a week at school. He came out so many times with slips saying he hadn't eaten any lunch that they just stopped giving them. He came out recently in tears saying his tummy hurt because he was so hungry, all he'd had to eat was a little bowl of custard. They deemed that enough food for him as he had "every opportunity to visit the salad bar." He has ARFID! I told them that if I sent him in with a lunch and gave him as little as he eats of theirs, they'd call social services on me. I've been taking him food when I pick him up as he's often starving and tearful. I have tried so many ways to get them to understand! The head teacher was totally unsympathetic, bleating on about healthy schools awards and how proud they are of their salad bar, her utter disbelief that I would be able to offer him food that was more acceptable to him than what they had available and said I needed to get a GP to write her a letter to say he needed to bring food in. Literally needed a doctor to tell her that a child needs to eat. 🙄. Telling me they can give him a marmite sandwich or some plain pasta, totally disregarding me saying he will not eat that. And how is that better than something from home?? My doctor was disgusted and did write and did say that he can't see any value in her pursuing a policy that means a child is going hungry and confirmed that DS has ARFID owing to sensory issues which means he should be allowed to bring in food that he will eat
Today was the first day. I did my best to adhere to a healthy lunch but with a restricted diet there's only a small group of foods to pick from. At the school they provide a dessert, which is normally a bit of cake. So he had jam sandwiches, a rice cake, a brownie I made with sweet potato (he has no idea it's in there) a peach smoothie and some cheese, and I put a packet of wotsits in because he eats them and I wanted him to have a decent amount of food in his belly for once. I just knew his head teacher would find fault somewhere and yep, she had an issue with the wotsits, emailing to tell me they would be taking them off him, there was nothing good in them and children having packed lunches aren't allowed crisps. Wotsits are baked corn puffs but also, how can she reference a guideline of what's allowed in a packed lunch when they don't allow packed lunches? DS has now come home saying wotsits are bad food and won't eat them, so that's now something she's effectively removed from his very small list of foods he will eat! It wasn't about giving him "healthier" food than school were providing, it was about giving him food he would actually eat!
Also, this head raised a concern that DS shows signs of ADHD and dyspraxia after I queried why he was getting hurt so often in school but no member of staff could explain the circumstance or how he came by his teeth almost being knocked out or his cheek being cut or eye bruised, lip split etc. Definitely they were not watching the children properly (open plan school) because injuries to my DS and a few other kids have tailed off since I expressed my belief that adults weren't supervising playtime. There are a couple of kids who have 1-1 supervision who obviously weren't getting it and who were hurting other children when they weren't being guided to appropriate play or supported properly in their work. Once is understandable if you just turned your back for a second. Twice is questionable and requires a sharpening up of procedure. Three times or more is an unacceptable pattern of failure to safeguard the children, in mind opinion.
So, basically she said she has these concerns about ADHD and co-ordination and asked me to raise it with the doctor. The doctor asked that the school sent their evidence in- she sent nothing but a "I've noticed this" sort of letter. They needed an early help record, possible Ed psych observations etc. I asked her ages ago for her attention on this and she said she would chase it all up and get back to me. I reminded her today and have finally had contact from the Sendco who can only say they've been so busy since identifying that my DS needs support that they've not got round to doing anything at all about it.
Is this fair enough on their part as a smallish village school or is this absolutely shit? Genuinely asking because I think it's ridiculous and that the headteacher has no care whatsoever for the individual needs of the children, but someone I spoke to about it said all primary schools are the same!