Here some suggested organisations that offer expert advice on SN.
I cant do this anymore(43 Posts)
I am waiting on a final decision on Ds 4.5 on what he has ( they are just waiting for nursery report) .
We saw the specialist last month & he said he was pretty certain that he has Asd/Adhd & Ocd but can not confirm until he has spoken to nursery & will then confirm at his next appointment in September & take the necessary steps to helping me & Ds .
Ds does not sleep he can manage on 2 hours & it doesn't bother him , he often does all nighters & can not be left to fend for or amuse himself as he is uncontrollable so im also doing all nighters with him at least 3 times a week , he doesn't sleep through the day either .
I just can't do this anymore , im so tired & his behaviour is beyond a joke , constantly punching me & swearing at me
Its not that he is distracted by anything in his room etc that is keeping him awake , he just isn't tired , he even does 4 days full time nursery 8.30-3.45 & even this doesn't tire him out , nor does running round in circles persistently for 2 hours I just can't tire him out .
The specialist said that if he was still having sleep problems then he will prescribe him some Melatonin.
I can't do this til September though I can barely manage another minute of it , surely their is something I can do , I need sleep
Where in the country are you op? In some areas there are amazing charities that arrange (well staffed) activity sessions where ds would get well looked after and you could get a rest!
I'm in Lancashire on the Fylde Coast
It's good your mum is coming . I think the hardest thing to do at the very beginning of having a challenging child is admitting you can't cope. It's sort of embarrassing, so we all cling on desperately trying to keep all the balls in the air and pretending it's all ok. Once you admit you can't manage and start asking for assistance that's half the battle.
Of course admitting it brings along another whole raft of emotions - guilt, regret, feelings of uselessness etc, but these are wasted emotions. You are coping well with a difficult child. Which makes you a very good mum. It's easy to cope well with an easy child and you have probably forgotten that.
You really should start a thread in SN - it doesn't matter whether your son has or ever gets a diagnosis, what matters is his behaviour and how it affects your family. There are many who have been there and know the system, so can at least point you in the right direction for help.
I'm not in the UK, so I don't know what to advise you, but they would know.
This is the safe space website I referred to above (obviously this would be a last resort). It is entirely likely that your son will become much easier to manage as he gets older - either through medication if he has ADHD, or through developing interests, or simply by growing through the terrible twos (terrible twos plus ASD = disaster ime), in which case you won't need anything so extreme. But they do exist, so you mustn't think you are going to spend the rest of your life watching him 24/7, things will get better.
Hi - we're about to move this over to the Special Needs section where more people should see it and be able to respond.
Hi crazy. I hope you'll get some more good advice here. Maryz is pretty fantastic, though.
My DS2 has ASD but wasn't anything like as challenging as your DS. He needed little sleep but always slept for at least 6 hours, so I'm not going to be much help on that score.
One thing to remember is that if he does get an ASD DX, his emotional age (not his cognitive age) will be roughly 2/3rds his actual age, so at 4.5 he's more like a just turned 3yo. So yo could easily still be in the midst of terrible twos.
What's his communication like? Is some of his behaviour due to frustration at not getting his needs/wants across? Is his nursery a SN one?
A good piece of advice I have heard is that it won't do your DC any harm to assume they do have ASD and/or ADHD and to start treating them as if they did. Parenting a DC with challenging SN is much harder (obviously) than a NT DC and there's no shame in asking for help with respite or strategies.
A DLA application sounds like a good idea. The cerebra guide to filling it out is excellent. Your DC needing close supervision for much of the night should help you get a reasonable rate. Don't be surprised if you get turned down at first or given a lower rate, it almost seems to be a hurdle you have to jump.
As MaryZ says, things will change, it won't be like this forever, there is light at the end of the tunnel.
Ellen he can talk very well though he does stammer when he is stressed which the speach specialist didnt pick up on as he wasn't stressed .
At first he was in a state nursery & although they were a fantastic nursery , they didnt have a set timetable so he wasn't coping with it so last October I enrolled him in the local preparatory nursery for 4 full days a week as its more like reception with a set timetable & he has settled extremely well & loves it their though it does leave me struggling due to the fees but their is no other choice , luckily they are a free school from September so he doesn't have to go to a different school
School don't notice anything wrong with him apart from how his behaviour changes immediately when he gets collected from school so he goes from quiet to jumping up & down screaming while running off & also he washes his hands alot & runs & hides when spoken to directly
Sorry for rambling
Interesting that he can hold it together at school. That seems to be fairly common with ASD (but not in my personal experience!) but does mean that school don't always appreciate the problem. I guess the fact that he can be calmer at school means that he has some level of control, which may mean the ADHD is a less likely DX? Not sure about that, though. It may also be that the strain of behaving at school means that he's been bottling it all up and has to release it at home, making home life even harder?
The free school, that's one of the new ones, an independent state school? What is their admissions process like, are you guaranteed a place? You may need to be thinking about requesting statutory assessment for a statement if his ability to access the curriculum will be affected.
He has already been accepted for a place as he was enrolled at the nursery it guaranteed him a place .
They have made sure that he was placed in a class with all his friends & a teacher he knows really well .
I did explain to his teacher everything & she did agree with me so hopefully what she says to the consultant will help
That's great that the school seems to be on board. Do you think he'll need any extra support at school?
I'm not sure tbh its not even something I have even thought about
Perhaps you could meet with the school's SENCo (special educational needs coordinator, every state school has one) discuss your DS's probable DX and find out if they have any plans to support him?
Maybe have a read up about statutory assessments? www.mumsnet.com/special-needs/education/statutory-assessments
I will look in to it thanks Ellen
Hi, I don't think I can offer much advice, as others have done this well. my son (now a teenager) has ASD with ADHD (and also LD) and I can empathise with the issues you are living with. However there are many things I did not know when ds was 4 that would have made life much easier had I known. One of them was seeing ds as having additional needs rather than thinking I was a useless parent who could not run fast enough!!
I do think it helps to see yourself as a parent who has to have super parenting skills in order to meet the needs of your child. To have super skills you need to be well - well rested and cared for yourself. The need to be on high alert all the time is exhausting, especially with minimal sleep. I too used a pushchair with multiple harnesses till past age five and a car for everything I could (Dh was often away so I had the car).
A local store gave me a child and family car badge (past age 5) which was really helpful, but I don't know if they do that now, and I frequented a further away branch just because there was a corner family parking space which if I parked a certain way round, made it tricky for Ds to get away until he was secured. If the pram is getting too small but you still need it, a pushchair style wheelchair may help, so you will need to approach the disabled children team to get a wheelchair/ mobility assessment. Others will know how to do this. I did not, and cobbled together my own!!
As others have said apply for disabled living allowance. If you have a child that runs off or refuses to walk where you need him to go (ds used to just sit sack of potato like- in the middle of the road if he fancied it, he had a way of making himself extra heavy and unpickupable I swear) he may get the mobility element as well although you have to wait till 5 for the lower rate. You may want to apply for a blue badge if you have a car although that can be tricky with a child. It is however automatic to grant a blue badge if the child gets high rate mobility DLA - again children who can walk but who have no ability to do as asked (and follow instructions) should in theory get HRmob but rarely do so its a bit hit and miss. There are people who can help you with the forms which are complex - here we have the money advice unit. DLA is not income dependant. It is to help with the extra costs incurred. Ds was 9 before I applied for it, but the extra money was helpful for all those extra things. Special needs harness (crelling), sensory fiddle toys etc)
Finding a safe place to play (our local park had a well fenced play area) so ds could run and I relax just a tiny bit was helpful.
The other thing I would say is that Ds starting nursery and school were some of the hardest times of my and ds life, due to the difficulties of adapting to school, poor sleep and the speed of his impulses. It has got easier. He just saw the world and society differently. Ds got separated from us at 10 and actually noticed and stood somewhere he thought we could find him!! At 13 he no longer runs away ( except in panic if very distraught).
Hi I'm really sorry, I just replied on your other thread but reading this one, I can see how difficult it is for you. I didn't have the sleep probs when my won was younger though he's not so great now. Get all the help you can, buy it in if you have to. I could have made life easier for myself a few years ago but I was in. Too much of a fog to see it.
waiting if I only I could afford to pay for help , hoping to be able to get a cleaner once a week when Ds starts school so that should help
I would contact Social services for assessment and also ask for them to refer you to the OT to make the bedroom safe / sort out some harnesses for car etc. They should provide equipment for free. You can apply for a disabled facilities grant to adapt the house / for safe space etc but they will try various things before they offer anything expensive eg we were advised to clear everything out the room except the bed and put a gate on. My friend paid herself to line the walls with soft play foam. But really this sort of thing should be provided.
Thanks Agnes I will try & make contact with them this week
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