Need advice on violence and talk of suicide

My son is 7 years old. He's recieved a diagnosis of high dependency autism. He will be starting a resource based school in September because his mainstream school couldn't cope.

What worries me is the fact he self harms, alot. He talks about killing himself alot. He lashes out and is violent alot. It's heartbreaking. As a mother watching my child punch himself in the face or scratch himself deep enough to leave marks down his face or bite himself so hard he leaves bruising is gut wrenchling heartbreaking. But at the same time I do not have a clue what to do. I don't yell at him for it or tell him off because he's never responded well to discipline. In fact it's a trigger to him. If I tell him off because he's having a meltdown all it does is further fuel the meltdown and causes more harm to him in the long run. I try to be kind and positive and loving in all my interactions with him but then I catch crap from my parents for "being too soft".

Recently at my nephews 1st birthday party I tried more than anything to get my son to join in, he hit himself and when I tried talking to him he punched me so hard and with such force I had a bruise on my eyebrow the very next day, but what destroyed me the most was the hate and anger in his face. He's hit me before but it's always been accidental as a consequence of him just flapping... But this was deliberate and with all his strength. The very next day however he woke up and was extremely distressed by the fact he'd hurt me and kept apologising.

2 days later my daughter told me my son was "trying to kill himself in the bathroom" I ran to the bathroom to find him trying to stab himself in the neck with a blunt cut off of the shower shield. He told me he wanted to die because his sister was cheating at a game they were playing. This is something I hear alot - minor things set him off into wanting to die.

It worries me because he doesn't understand how final that is, but I live in a constant state of hypervigalance at home, I cannot go out because he get so anxious whenever he's away from home he has a meltdown. I feel trapped and exhausted and more so than anything else worried about my son's self harming, self hating behaviour.

I know he is a good boy and a very sweet, intelligent person with a lot of potential to do something great in life with the right guidance but how do I get us there without it being the death of one of us?

This is amplified by the fact my daughter has aspergers so my efforts on him seem to result in her being neglected. On top of that I also has aspergers and have battled clinical depression most my life. I feel trapped and then I feel selfish for feeling that way. I just want to help both my babies and not kill myself doing it.

Parents
  • Hi all thanks for the posts.

    He is obsessed with the computer or anything technological. He is incredibly clever using a PC. I like online gaming and have gamed for 13 years but what my son can do blows me away. He's even constructed and fully rendered a 3D model. But his obsession with technology can have a detrimental affect on us. For instance if we leave the house at any point I must take the ipad with me because when he has a meltdown it's the one thing that calms him (or well an APP called living aquarium calms him) - He has a bag we take with us everywhere full of visual and fidget toys, ear defenders and a book on Minecraft (which is another obsession of his).

    His sight reading was measured in the 85% percentile whereas his maths and written English were unable to be assessed due to him not cooperating with the test and not writting at all respectively.

    He barely speaks and the best time to talk to him is when he has something technological in his hands because he will talk about that, you can then manipulate the conversation to get him to talk about whatever is upsetting him, hurting him, distressing him as long as you keep it loosely related to technology or minecraft he'll talk about it.

    CAHMS made the diagnosis and then discharged him. His OT claims he's tried a weighted jacket, blanket etc etc with Henry but that he disliked them. However hugging him is one great way to bring him down during his high stress times, which is probably because it supresses his central nervous system (Temple Grandin - Cow hugging machine and all that!)

    His seperation anxiety from me and his distress and anxiety in general is something I feel he needs help with. His new teacher at his new school (who I've met) informed me that CAHMS shouldn't have discharged him based on this fact so I've asked my doctor for a re-referal.

    I guess I found the whole thing over-whelming. I've spent a small fortune on my kids. Buying memory foam mattresses for their beds, sensory lights for their rooms, liquid timers and fiddle/fidget toys for my son, chewlery for my daughter. I have heard of the family fund but I am still on a waiting list for a 3 bed house becuase my children need their own space and I'd rather wait until they have their own rooms to spring for a grant to help me do something sensory with their rooms. I have looked online to see if their are support groups near me (Stockport) but I've not had the best luck over the summer holiday.

    I would also find it difficult to attend these groups myself because I am litterally terrified of new social situations and strangers and the anxiety it causes me can litterally make me wanna crawl inside a shell and stay there. Which you could probably put down to my aspergers.

    I'm prone to panic initially as a knee jerk reaction but reading your words has helped me feel a little calmer. I must continue to fight for my kids and seek help when things get rough.

    Thanks ^_^ x

Reply
  • Hi all thanks for the posts.

    He is obsessed with the computer or anything technological. He is incredibly clever using a PC. I like online gaming and have gamed for 13 years but what my son can do blows me away. He's even constructed and fully rendered a 3D model. But his obsession with technology can have a detrimental affect on us. For instance if we leave the house at any point I must take the ipad with me because when he has a meltdown it's the one thing that calms him (or well an APP called living aquarium calms him) - He has a bag we take with us everywhere full of visual and fidget toys, ear defenders and a book on Minecraft (which is another obsession of his).

    His sight reading was measured in the 85% percentile whereas his maths and written English were unable to be assessed due to him not cooperating with the test and not writting at all respectively.

    He barely speaks and the best time to talk to him is when he has something technological in his hands because he will talk about that, you can then manipulate the conversation to get him to talk about whatever is upsetting him, hurting him, distressing him as long as you keep it loosely related to technology or minecraft he'll talk about it.

    CAHMS made the diagnosis and then discharged him. His OT claims he's tried a weighted jacket, blanket etc etc with Henry but that he disliked them. However hugging him is one great way to bring him down during his high stress times, which is probably because it supresses his central nervous system (Temple Grandin - Cow hugging machine and all that!)

    His seperation anxiety from me and his distress and anxiety in general is something I feel he needs help with. His new teacher at his new school (who I've met) informed me that CAHMS shouldn't have discharged him based on this fact so I've asked my doctor for a re-referal.

    I guess I found the whole thing over-whelming. I've spent a small fortune on my kids. Buying memory foam mattresses for their beds, sensory lights for their rooms, liquid timers and fiddle/fidget toys for my son, chewlery for my daughter. I have heard of the family fund but I am still on a waiting list for a 3 bed house becuase my children need their own space and I'd rather wait until they have their own rooms to spring for a grant to help me do something sensory with their rooms. I have looked online to see if their are support groups near me (Stockport) but I've not had the best luck over the summer holiday.

    I would also find it difficult to attend these groups myself because I am litterally terrified of new social situations and strangers and the anxiety it causes me can litterally make me wanna crawl inside a shell and stay there. Which you could probably put down to my aspergers.

    I'm prone to panic initially as a knee jerk reaction but reading your words has helped me feel a little calmer. I must continue to fight for my kids and seek help when things get rough.

    Thanks ^_^ x

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