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AIBU?

Share your dilemmas and get honest opinions from other Mumsnetters.

Child with SEN so violent

28 replies

SomethingInnocuousForNow · 30/07/2025 20:43

I have two autistic DC late junior school age and they both have learning disabilities. My youngest is non verbal with severe learning disabilities and has always been a bit violent to us over the years but recently it's been absolutely relentless.

He's still quite small but (despite professional experience in the area) I've very rarely come across violence this extreme and random- slapping, punching, biting, kicking, eye gouging, scratching, hair pulling, throwing objects at me and he also tried to stab me with a pair of scissors. He's particularly targeting me and it is constant. He's badly hurting me and I'm frightened of him. I keep trying to spend nice quality time with him but he just smiles then attacks me. Tonight, I went downstairs to be with him because I've barely spent any time with him (DH looks after him because DS can't push DH over etc) and sat on the sofa, he came over smiling like he wanted a cuddle then grabbed my head and clawed my face and pulled my hair. Normally I try not to react too much (because I think he enjoys my reaction) but I started screaming and then broke down in tears. I've just had enough.

I don't know what we've done wrong, but clearly we haven't got it right.

AIBU just to stop trying? This is breaking my heart, I love him but I don't want to be anywhere near him.

OP posts:
SomethingInnocuousForNow · 30/07/2025 21:03

We do get 4 hours respite a week, but we're on a waiting list for overnight respite (have been for 2 years) and I think the wait is another 3 years.

I see other families with non verbal children who are so loving. In fact, my other child would never purposefully hurt me. I feel like my youngest hates me and likes it when I'm hurt.

OP posts:
PansyPotter84 · 30/07/2025 21:03

Such children used to be kept in specialist homes. My Great-Auntie used to be a nurse in one in the 1970s. They used to get lots of medication to keep
them docile.

Not suggesting that’s the right way forward but it seems that children with autism have always been around (the ones with milder autism were just seen as “odd” or “disruptive”) it’s just we don’t lock them away out of sight any more.

Far more support is needed, though.

It might be worth contacting a charity or (if you can afford it) paying for some respite care so you can decompress.

Liliwen · 30/07/2025 20:59

OP i dont think you’ve anything wrong at all. He is autistic and non verbal. It’s not anything you have done or haven’t done. It sounds exhausting. You need respite- is that possible at all? Where I live, parents of children with significant SEN can access overnight respite- is that available where you are as I know it isn’t always accessible. It sounds impossibly hard.