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Can we give up one of our children?

570 replies

pinkstargaze · 16/03/2026 18:35

I don’t know where else to turn, this is about my 8 year old.
We have 3 Children the eldest and youngest are lovely but the middle child is making life so hard with her violence towards us.

She comes home from school and shouts and screams and hits me and her siblings, she calls me names, swears at me and won’t listen to a word I say just says shut up and covers her ears if I speak to her.
Her siblings are frightened of her, I’m frightened of her I know as soon as I say anything I will be hurt, she hits me in the back and it takes my breath away, she kicks me and tells me to kill myself, slams doors throws things, screams at the top of her voice by which time the other children are crying and I just can’t do this anymore.

I don’t want this for my other children who are so well behaved, we don’t swear or raise voices, we are just a nice family who all get along and respect each other apart from her, she makes everyone miserable, destroys our home and everyone’s belongings.
It is embarrassing, friends won’t have her around their children and even our own family don’t want her near her cousins because it always ends in tears.
I don’t want to live in a home where I’m scared to tell my child off because she’ll hit me, I don’t want to share my home with someone who laughs and points at me with delight when anything goes wrong, or revels in her siblings misfortune and I don’t want to be called names and be sworn at in my own home or have my things ruined by someone who doesn’t care about me or my things.
I don’t want this to be my life and I definitely don’t want it for her siblings.
I feel strongly that for sake of the family’s safety she needs to go into care but I don’t want to lose all my children.
Is it even a thing to put one child into foster care and not the others?

She is waiting to be assessed but the waiting time is long, the school doesn’t see this as she’s masking all day until she gets home but it’s every day.
I have a lovely family, a lovely husband and we have 2 other children who are lovely but she is making our lives hell and our home uncomfortable and I know I just don’t have what it takes to live with her, I am burnt out and feel so guilty to the other children.
Dh does his best when he’s home but we are all so worn down and miserable, we just can’t carry on like this.
It has broken us both and the others are suffering. I genuinely can’t do this but I so love being a mum to the others who I carry on for.

OP posts:
Thread gallery
7
TheSunjustcameout · 17/03/2026 00:01

RoseField1 · 16/03/2026 19:33

It's true. Removal from the family of origin causes serious harm and is often not better than remaining in the neglectful family home.

I can concur.
My siblings and I were put into a children's home for one week when I was 3 and it was traumatizing.

Yabbadabbadooooooo · 17/03/2026 00:04

If it is PANS / PANDAS then a first step is a two week protocol of round the clock nurofen and antihistamine. If you see an improvement it’s evidence that it is P/P. Also antibiotics if she tests positive for strep. There are only two specialists that treat P/P, both private. Or there is equal success with homeopathic treatment. I see Brainstorm Health mentioned a lot.

BlackeyedSusan · 17/03/2026 00:25

Ha, ha,ha, fuck no. Not a fucking chance. You won't get respite either.

Strategies that help?
ADHD, a fuck ton of caffeine. (Ask other people for more ideas)

School are not meeting her needs. Meet with the Sendco and try and get some accommodations in place. (Quiet space, time out, movement breaks,) They will blame you for shit parenting. This is normal. Do a parenting course. It will either help, or provide evidence for assessment.

Autism strategies:

As soon as she is out the school door, feed her something sugary, and something with complex carbs. Heavy back pack, tight hug. Rock her side to.side. do OT calming activities every day. Try sunglasses or ear defenders big hoody,

No demands, (no questions, no chat, no shopping , no changes of routine) keep her separate from the others. They go in the car while you rock and calm. Or she goes in the car to calm while you three play outside. If you walk she goes one side, held, the others go the other side. You need to be responsible for her emotional regulation until she is capable herself.

You need to keep them separate at home. Strictly supervised.

Learn her triggers. Prevent them. (Great fun if one's autism stims trigger the other's meltdowns)

If she is in meltdown she will not respond to words or discipline. She may not remember what she has done. Safe space on her own or tight hug or rocking may help. Prevention better than cure. You need to be responsible for this, though it will mostly be school who wind her right up.

Lots of decompression time. Lots.

Daily OT will help. Ask for a referral. It might be quicker.

Ask if they have pre diagnosis parent information sessions.

Try to reframe your thinking that this child is overwhelmed and scared. It helps most of the time. Yes I've typed this before, then had to bloody work hard to put into practice and probably will again.

Get sensory toys. Try the works or Amazon. Beware of price hikes for the label sensory toy.

Check uniform for labels and general discomfort.

If school are shit, move her. Find a better one.

Rednorth · 17/03/2026 00:28

My narcissist of a mother could have written exactly the same kind of post about me a few decades ago (she too rarely cried).

Even to this day, with my diagnosis, treatment and well functioning neurodivergent family of my own, she will never accept that she was the problem. I was just a devil child who for all my childhood, 'love' was conditional and I was never deserving.

This level of behaviour doesn't happen in a vaccum.

pinkpeta · 17/03/2026 00:29

pinkstargaze · 16/03/2026 18:47

We have tried but the school don’t see any of this and I don’t think anyone believes it’s as bad as it is because it’s only at home, she’s on her best behaviour at school so there’s no evidence of this behaviour.

Have you ever recorded any of her outbursts? Sorry you’re going through this

GardeningMummy · 17/03/2026 00:30

GrandmasCat · 16/03/2026 18:58

Early help from who??? If we had not gone private 12 years ago we would still be waiting for an assessment…

Nonsense! My DD joined the waiting list in 2017 and was assessed & diagnosed 2019!

LetMeSwinInMiniEggs · 17/03/2026 00:36

monkina · 16/03/2026 19:03

Social Worker here. If you contact Children's Services for support they will complete an assessment and can offer you some parenting support. They will not put any child into foster care in your situation- foster care is an absolute last resort for children at risk of harm & is only considered when all possible other avenues such as other family members have been exhausted.

I wish my social worker got me support when I reached out for help. Instead she came to the house twice to speak to me about my concerns then lied on the end report about visiting me fortnightly. I hadn't seen or heard from her for 3 months! I raised it with her manager who declared the case was closed and that was the end of it

DreamTheMoors · 17/03/2026 00:44

My older sister was the middle child.
She was 5 years older and at least 75 pounds heavier than I was.
I was aware she hated me, but never so much as the night she jumped from her bed onto mine and put her hands around my tiny little neck and tried to strangle me.
She kept up the pressure until just before I passed out - everything was swimming in front of me and I couldn’t calll out.
I asked her about it not too long ago and she acted like she was deaf.
Because to admit to trying to murder your little sister is pretty dark, I guess.
And she sure enough remembers doing it. That’s not something you really forget.

myles2608 · 17/03/2026 00:49

Have you tried the PEGS group on FB. It's specific for CPA. ( Child to parent abuse). Very helpful forum with huge amounts of support and strategies. Your local women's aid should have some support around this too. It's really hard. Not your fault at all.

LancashireButterPie · 17/03/2026 00:59

Forgot to mention, having a dog (the right dog) is very calming for some kids with PDA.

Octaviathethird · 17/03/2026 01:03

ForFluentLimeFatball · 16/03/2026 21:02

What consequences have you introduced? If she behaves at school, she can behave at home as she clearly knows how to be have

She doesn't know how to behave at school, she's too frightened to be herself at school so doesn't interact and keeps her head down. When she gets home, to her safe place, everything she's been holding in bursts out.

SweetnsourNZ · 17/03/2026 01:09

Happyjoe · 16/03/2026 18:58

Sounds strange, can you video her?

Actually perfectly typical with ND children. Sometimes it is the other way around too.

Ivyy · 17/03/2026 01:13

LancashireButterPie · 16/03/2026 19:39

There's a state funded residential school near me that accepts children when families just can't cope any more. I think the bar is quite high though.
Please contact social services, school and your GP and explain all this to them. Don't hide it.
It isn't your fault and you are not to blame.

In the short term you could try a few low demand parenting strategies to help when she immediately comes out of school. Our PDA DD benefitted from being met at the school pick up with a snack that she had chosen in the morning. She would eat this on the way home.
Keep verbal interaction to a minimum.
Use signs, PECS, or even what's app/text when she's old enough to have a phone.
Give her noise cancelling headphones.
As soon as she's home, let her have quiet time by herself to decompress.
Maybe put the softest pyjamas on.
Our DD liked to go to her room to just stroke the dog, others like to snuggle under a weighted blanket, or go outside and do "sensory" activities.
Does she do any "heavy" work, that involves pushing, pulling, squashing etc? If not, that's something to consider. Our DD loved the physicality and discipline of ju jitsu.

There is a wonderful psychologist on Facebook called Dr Naomi Fisher, she is an amazing advocate for families like yours (and mine) and I've learned so much from her.
Also a private autism specialist OT might be able to help.

Once these kids learn coping strategies, things can quickly turn for the better. You are not alone and please don't give up hope.

Not sure I’d recommend Naomi Fisher anymore after the recent controversy! Plus she doesn’t support the PDA “label” anymore apparently (not my words btw)

Todayismyfavouriteday · 17/03/2026 01:16

Kissmystarfish · 16/03/2026 19:12

My family are criminal psychologists and there are studies that show that children even taken away for 24 hours from their parents does such damage that can never be recovered

I remember a study saying that if you had a mother who was a drug addict but was still able to look after their child that it was better to do that then to put them into care for Temp for a short time

How very true, and sad. It has made me so sad to read that anyone would consider getting rid of their own child, regardless of behaviour. Your poor child definitely has terrible issues, and needs help. I really hope you'll get support soon, OP, an assistant who can train you to deal with this behaviour, or whatever help is available for cases like this. Very sorry for you and all your three children.

Ivyy · 17/03/2026 01:38

Wonderingaboutthing · 16/03/2026 21:22

I am so surprised you say this. My kid’s in a special autism school and us parents are constantly comparing notes about meds. Many of us would lie down and beg for things like SSRIs if it would get our kids to behave. I have never, ever heard of such a thing and our psychiatrist told us a child would never be prescribed such things in the UK. They don’t even like prescribing adhd meds to autistic kids. Only for severely disabled / non verbal kids who are doing severely self-injurious behaviour like head banging would the anti-psychotics be prescribed???

It might depend on their age, I know several teens with ASD, AUDHD and ADHD taking ssri’s, sertraline, plus melatonin for sleep, some prescribed privately and some nhs but way harder to get through nhs

Beenwhereyouareagain · 17/03/2026 02:20

pinkstargaze · 16/03/2026 18:47

We have tried but the school don’t see any of this and I don’t think anyone believes it’s as bad as it is because it’s only at home, she’s on her best behaviour at school so there’s no evidence of this behaviour.

I'm so sorry for all of you. ❤ Please get this documented quickly and then share it with the school and HCPs or Social Services. Audio, video, diary- keep track of everything without mentioning any of it to your children. For a true picture they should have no idea you're recording and filming. It would be eye-opening for others and might get you some help much sooner.

angelfacecuti75 · 17/03/2026 02:39

Sounds like autism or Oppositional defiant disorder /adhd (O. D.D ) / Sensory processing disorder. Maybe speak to the disability team.

aster10 · 17/03/2026 03:22

Psychotherapist here. Difficult to get therapy on the NHS. Try to find a good child psychotherapist privately. That will help. We had a number of CPD (continuing professional development) seminars on neurodiversity. If you PM me, I can give you contact details of the psychotherapist who was leading them, she is herself a mother of an ND child.

MyTrivia · 17/03/2026 05:26

This sounds really tough for you as a family but if you send her into foster care, that will be extremely traumatic for her.

I feel as though I’m qualified to say that as difficult as parenting a child with PDA autism can be, we’re not a victim in this situation because our children feel even worse. That is why they behave this way.

Two of my children have PDA. One, in particular has very complex needs. Before she moved into a specialist, residential school at 13, I had 2 long years of her attacking me out of nowhere and trying to escape from the house. It was a very difficult time but I think it probably was even more difficult for her.

I also have a 6 year old with PDA and she is very well behaved, and has limited behaviours. But I figured out she had it when she was 2 and I’ve tried to adapt her environment as much as possible and also I don’t use an authoritarian parenting style with her. This has really helped.

The main problem for your dd is probably school. I expect she’s extremely stressed out in a school environment that isn’t suitable for her. She holds it all in during the day and then takes it out on you, her family when she gets home.

At this point, her anxiety levels may be so high that a specialist residential school for autistic children might be the best way forward - it turned my daughters life around. You will need an EHCP for this.

Seahorsesplendour · 17/03/2026 05:35

@pinkstargaze apologies as haven’t read whole thread sorry if this has been suggested already.

  1. it is incredibly hard you are normal to feel that
  2. there are charities that can help with assessment pm me if you want more info
  3. you can ask for ehcp assessment she needs support in school asap push & push
  4. read up on NVR - it isn’t a magic bullet but it really does help
  5. gather evidence - make a document every day write down behaviour & triggers eg went to school , once home we saw …. Etc
  6. dont be fobbed off by she’s fine in school
  7. read some Naomi fisher online or books
  8. be kind to yourself & talk to your dp
Oaktree1952 · 17/03/2026 06:05

You are not alone. I am a SENCo in a primary school and we have seen many children who are lovely in school and yet parents tell us about such awful behaviour at home.

Have you called sendiass? They should be able to point you in the direction of help.

Personally my middle daughter is also like this. We have put in unbeatable consequences for the very extreme behaviour eg hitting siblings. I take her into her room. She does trash her room but it’s not her siblings. We also read her some books portraying ASD. The one that resonated with her was I’m an Aspie girl. She recognised herself in it. We talk a lot about regulating and different strategies she can use. We are very definite with her that being cross and upset is fine but hurting and being rude is not. Her self esteem is rock bottom. So we try and big that up at every opportunity. It is a slow process and will take time.

FairKoala · 17/03/2026 06:22

Happyjoe · 16/03/2026 18:58

Sounds strange, can you video her?

Sounds normal if child is masking all day and then explodes at home

Legssses · 17/03/2026 06:32

She sounds very like my child at that age, who is autistic but was undiagnosed at the time.

A diagnosis will provide clarity it isn't a magic wand solution, what will help is changing how you view and treat the behaviour.

I could not advocate enough for the book "The Explosive Child" by Ross Greene. Please, please read it. It's filled with case studies of children like our children, and provides clear and useful advice in supporting them.

Behaviour is communication, especially in young children. She is telling you school is too much. What specifically does she struggle with in school?

Are big rooms full of people and assemblies overwhelming, is she anxious about a teacher asking her a question she doesn't know the answer to, is there a specific child or group of children picking on her? They are just some ideas, but i would be asking open questions to see what you can understand.

Our school has been fantastic in adapting to remove or reduce the overwhelm for our child. Often it's little changes (a written promise that they won't be asked to answer a question unless they have their hand up, some low sensory time with the SENCo, reduced homework) that make a big difference in taking down anxiety levels.

What's home life like after school? Is it very busy with after school clubs and people rushing here there and everywhere? What does she enjoy doing? Is there something she could do to regulate when she comes home? Or maybe just having some low demand free time is what she needs (like ours) rather than more pressure to "do".

It's all a bit trial and error, but our family today looks do different and life is so much better since we changed our view of our child to align with one who is significantly struggling and who needs support.

ProudCat · 17/03/2026 06:44

MazJ85 · 16/03/2026 23:48

She probably means group b streptococcus infection - commonest cause of neonatal sepsis/meningitis

It's in the same wheelhouse, look at the article.

Peonyperfection · 17/03/2026 06:50

Stop thinking of yourself and think of your daughter. Show her love and try to work out the stressors in her life. Learn to understand her and help her. This will teach your other daughters compassion.