Hi. Unusual post here! I deal with special needs at my primary school. I'm not an expert on ASD, but I have taught for many years so I'm fairly familiar. I appreciate how vast the spectrum is: "Show me a child with autism and I'll show you a child with autism" . I have autism in my family so I know about it on a personal level.
We have a very high number of children assessed by one particular doctor as ASD. He ALWAYS diagnoses borderline ASD and if the parent persists, he gives a full diagnosis. If I look back on 5 years worth of parent referrals, he has never not diagnosed. Many of these children exhibit no traits at school and I know that can happen, but really- these are chatty, engaging, quick and sociable children. One parent had applied for Disability Living Allowance before she had the diagnosis and is convinced her child will have an EHCP - I've told her that's unlikely even with a diagnosis, but she says she will get one however it comes about. I believe you can't apply for DLA without an EHCP.
I'm not here to upset parents with experience of ASD, I know autism is challenging- I've been/am there. But I believe these children are being labelled for no genuine reason. There's also the more practical consideration of SEN funding and children in genuine need of support who are missing out. Who can I voice my concerns to?
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9 replies
SNN2017 · 08/02/2017 22:50
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