It makes me sad every time I see someone write this kind of comment up.
My eldest was noted as having some extra needs but there was born support with assessments to get correct diagnoses.
They overlooked (now diagnosed) adhd, autism, sensory processing disorder, and some physical disabilities (invisible kind).
The adhd and sensory processing disorder plus messed up digestive system and bowels caused daily soiling after severe constipation led to needing movicol.
I swear the movicol was useless and once a kid is on it, they're better off in nappies for the sake of their clothes, furniture, dignity and those who have to clean them.
The constipation and attention issues meant he wasn't even staying on the toilet - you'd put him on and he'd almost straight away get back off again, no concept of time, timers didn't work, he didn't have the coordination to eliminate properly.
The accidents didn't stop til the start of year 9 I think it was. Though by then they had tapered off to damp pants and skid marks.
Youngest was dairy intolerant but the GP refused to write a letter for the school, who therefore refused to stop giving her milk to drink during the day. So I'd be called in frequently to change her soiled clothes. It distressed her so much she began wetting herself as well - the primary was absolutely horrid and blamed me for every single thing.
Had they known how much extra effort I had to constantly put in, and as a single parent with their own disabilities to manage too, and had they bothered to help us with accessing assessments etc instead of saying I was making excuses, perhaps they wouldn't have led me to my nervous breakdown.
And my poor kids.
I'm sure there's some lazy parents out there who haven't put the effort in but it often takes until secondary or later for girls and afab kids to get an assessment for SEN conditions.
I'll get off my soapbox now.