New here

Good luck with that. Make it clear you are all suffering and you need to get him the support to help all of you and to ensure he has an education. You are not alone. us nice people do still exist in this selfish planet of ours. 

Fingers crossed, im going to look into the assessment now. And see what i can find. Then hopefully can send to gp and say look this is what I've found... now how are you going to help. 

As thats all I want for him someone to say yes I'll help you. Rather than send us in a totally different direction. 

He’s the most important person obviously but you need to think of yourself too as burning yourself out isn’t gonna help either of you. You seem very nice and an obviously caring parent trying to do her best by her boy. From what you have said you have grounds for an assessment and if u can find the assessment online that you can do on his behalf it would strengthen your position. Sometimes you have to be blunt and you need ur gp to pursue a diagnosis. Could be adhd or something but you will know and be able to help him accordingly.

Yes I've found that out. 

If i want my boy back into a school which would help him, I need the diagnosis. 

Everything seems to revolve around it. Not the fact you still struggle until you get to that stage.

I must admit talking to you seems to put a few things into prospective. And I will be saying more to the gp Tomorrow. I need the help with him. I get no time to even relax as he's on the go from early dawn until like midnight sometimes later. 

Sounds like you have had a rough run of it. And I think that support is lacking for autistic people. I got told it’s up to me if I feel like I need help. No offers of support in my local area just finding my way as I have always done. Chats like these can make a difference and sometimes it is all that is needed to calm me down. When I lash out it’s either at myself or whatever I’m stood by.   And maybe a diagnosis might be the way forward as these days it seems to be you are normal until that official diagnosis is offered And the help isn’t offered until you get diagnosed. 

Oh rite, will have to look into that. That be nice just having someone to talk to who relates to what im saying. 

He is going to private lessons once a week 1 to 1 and seems to be getting on well. But everything isn't cheap these days. 

Trying to find groups where there are children like him,so he can socialise and be himself without me having to tell him to stop biting, kicking etc. Just so the parents know he has conditions to. Would make it a little easier  for him to have a friend who can relate. 

I’ll support you Too even if only in spirit. Maybe tell gp the home schooling is not going so well and you are worried about his education to give them a prod in the right direction. Or get a second opinion? I did the 50 questions assessment I found online and took it into my gp which seemed to help. I know they do ones that adults can do for their kids as well . 

Hes 7 and in my area the age limit for diagnosis has just gone up to 8. Been fighting since he was 5. Just dont feel like im getting anywhere for him. Im not after a Diagnosis... just the help would be nice. 

I'm a single parent with only my mum for support 

I have suspicions about my daughter as she shows a lot of signs too and we clash big time sometimes. It’s so difficult as u know u r doing the right thing but people judge. One thing I will say is I’ve always been true to myself and who I am however much I was bullied. And feel proud I’ve achieved that. Sounds like you are doing your best for your son and that’s all that matters. I know some areas don’t like assessing kids under a certain age and will monitor them but sounds like there’s no communication from them To you on that front. 

Its nice to see someone else's prospective of it. As for my son he can't tell me whats going on inside his head. Which must be hard. 

I want to protect him but all I get from others is dirty looks coz im shouting at him. He has no danger level. 

I’ve only been diagnosed recently and get told I seem normal.. my assessment score was over double the threshold and met every criteria.. some days I act and feel like a kid as my mind can’t grasp I’m a grown up and it’s a constant battle in my head which unfortunately bubbles over into angry meltdowns and all people can do is laugh at my “overreaction “ which fuels my meltdown. So I can’t win and feel cut off from society. Sounds silly but This conversation is meaning a lot.  Someone is listening...

To be fair its just nice to speak to someone who can kinda relate. 

My boy is under 11 so dosent have to wear a mask. But my mum doesn't also as she has lung disease and some oap was banging on bus window yesterday saying she had to wear it. So frustrating.

Why can't people just keep their opinions to their self. They don't know whats going on behind the scene's. 

No they shouldn’t. I can’t wear a mask so I use a loop scarf and the comments I get are incredible. It’s wrong they are not prioritising ur son. Wish I could help you 

Very true. I dont even have it and it gets me down fighting for what my son needs. 

People shouldn't have to struggle like this just for a bit of extra help 

I would help if I could but the important people need to help. Life has been a constant battle for me esp undiagnosed as was classed as odd and bullied a lot esp at school but was Always true to myself. I struggle to find people to talk to and not always is everyone On line here. 

I have gp phoning tomorrow, so gonna ask if they can help in any other way. I have a 2 year old girl also and can't leave them in same room together. 

I have no life as receptionist said on phone your kids deal with it basically. No help at all. 

I feel like im fighting a losing battle for him and no one wants to help 

• Yeah people are very judgemental when it comes to this. And cruel. Finding it quite isolated in a way as have so much I wanna talk bout but nobody seems interested. I’m relearning my whole life and it’s a lot to do. Surprised gp not doing more esp for a young child. 

Yes, gp is one who referred him. Have done this 4 times since aug 18. 

Since then ive had local LA come out for home schooling and asked about EHCP and they havent even put me in touch with them. 

I'm based in Wiltshire, I know different areas get seen a lot quicker but here its like 3 year wait. 

Yeah since my son has been showing signs of adhd and autism friends dont really want to know anymore. 

Hi. I got referred may last year and got given a choice after a year waiting of either continuing to wait for nhs or accept referral to healios. It does seem to depend on ur location as to how efficiently u get dealt with. Friends are few and far between these days. Have you been to ur gp?