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World Autism Awareness Day

World Autism Awareness Day

You're probably right. Don't forget also with twins, the quicker developer often does things first and the 'slower' developer then doesn't see the urgency to do so. For example, the quicker one might learn to ask for a drink or a biscuit and the slower one then doesn't see the need as you will give them both whatever the quicker one wanted! Conversely, she might also cry and bite out of nothing more than a bit of frustration that the quicker one can do something she can't.
You could be right, me and Mrs could be working ourselves up over nothing. Have to see if/when she’s diagnosed.

Just looking into it all now, I honestly know nothing about condition. I just googled what she kept doing and every article that comes up is autism.
 
You're probably right. Don't forget also with twins, the quicker developer often does things first and the 'slower' developer then doesn't see the urgency to do so. For example, the quicker one might learn to ask for a drink or a biscuit and the slower one then doesn't see the need as you will give them both whatever the quicker one wanted! Conversely, she might also cry and bite out of nothing more than a bit of frustration that the quicker one can do something she can't.


Was going to say this too, by all means see the other traits as potential signs but different development is quite common, partners twins had one walking and talking by 18 months and the other was almost 3 before she did anything because her sister basically talked, fetched, fed , asked for everything on her behalf. It's probably only in the last 3 or 4 years that they've evened out as they've got towards the end of Primary school
 
You could be right, me and Mrs could be working ourselves up over nothing. Have to see if/when she’s diagnosed.

Just looking into it all now, I honestly know nothing about condition. I just googled what she kept doing and every article that comes up is autism.
I know we are all tempted, but Google isn't always the best place to go for this kind of thing or medical stuff as the stuff you find will often serve to just freak you out. I think we should all whenever possible just let our kids be kids as they are a long time grown up!
 
Also as others have said, prepare for some potential poor journey as they are reluctant to really diagnose it with it being a spectrum anyway and then even if you get that far the support and money just isn't there in many schools. Another failing of the system in lots of areas it seems. Often comes down to the schools and the teachers to try and fill in those gaps and give you what support they can
 
I know we are all tempted, but Google isn't always the best place to go for this kind of thing or medical stuff as the stuff you find will often serve to just freak you out. I think we should all whenever possible just let our kids be kids as they are a long time grown up!
Yeah, to be fair, the DSM-5, the manual they use for diagnosing people with Autism and mental health conditions, it's frightening some of the ways the doctors compiling it came to agreements on what certain diagnoses were. When they couldn't agree on the specifics of a diagnosis they would do a show of hands, which to me sounds strange for something so serious.

Much like most scientific things, mental health, neurodevelopmental health, they're constantly reviewed, theories changed.

I do however think it's important to get kids support as early as possible if they are in need of it. It's much harder to rectify later on otherwise.
 
@Double J My mum is a Higher Level Teaching Assistant and Special Educational Needs Coordinator also my younger brother, now an adult, has learning difficulties (not autism) so, as a family we have a lot of experience re funding.

Very early days for you and your family at this stage without even a diagnosis, but should you ever need any advice in terms of educational support and funding, please give me a shout.
 
@Double J My mum is a Higher Level Teaching Assistant and Special Educational Needs Coordinator also my younger brother, now an adult, has learning difficulties (not autism) so, as a family we have a lot of experience re funding.

Very early days for you and your family at this stage without even a diagnosis, but should you ever need any advice in terms of educational support and funding, please give me a shout.
Thank you, hopefully this thread will still be around in time, can always come back to it.

I honestly know nothing about autism but been looking into it today, hopefully, if she is, its not a severe case. Shes a happy little girl though so hopefully just us over thinking things.

Thanks all.
 
Yeah, to be fair, the DSM-5, the manual they use for diagnosing people with Autism and mental health conditions, it's frightening some of the ways the doctors compiling it came to agreements on what certain diagnoses were. When they couldn't agree on the specifics of a diagnosis they would do a show of hands, which to me sounds strange for something so serious.

Much like most scientific things, mental health, neurodevelopmental health, they're constantly reviewed, theories changed.

I do however think it's important to get kids support as early as possible if they are in need of it. It's much harder to rectify later on otherwise.
It's a very deep sea. As it says on the tin it's a spectrum and thus can become conflated with so many other conditions, including those of mental health. What was once diagnosed as AS is now being reassessed as issues such as trauma and PTSD are the cause of similar traits. Same with ADHD, so many kids have been misdiagnosed and wrongly medicated. Big pharma is partly to blame but not wholly. It's just as bewildering for medical/psychiatric professionals.
Add onto that there is also a huge waiting list for educational psychologists who are mostly very good and highly informed of all the nuances of the tangle of various diagnoses.
 
T
Thank you, hopefully this thread will still be around in time, can always come back to it.

I honestly know nothing about autism but been looking into it today, hopefully, if she is, its not a severe case. Shes a happy little girl though so hopefully just us over thinking things.

Thanks all.
That happy bit is all that matters.
 
Thank you, hopefully this thread will still be around in time, can always come back to it.

I honestly know nothing about autism but been looking into it today, hopefully, if she is, its not a severe case. Shes a happy little girl though so hopefully just us over thinking things.

Thanks all.
Even as a severe case, which of course we all hope is not so, there is very little to stop her enjoying a completely happy and fulfilled life.

A person with Autism just has different needs to those of us without it, meet those needs and she'll be just fine. Not to say there won't be challenges along the way but you just meet those head on as a family.

I'm sure whatever the outcome she will be supported and loved, in essence, that is all that any of us need.
 
Even as a severe case, which of course we all hope is not so, there is very little to stop her enjoying a completely happy and fulfilled life.

A person with Autism just has different needs to those of us without it, meet those needs and she'll be just fine. Not to say there won't be challenges along the way but you just meet those head on as a family.

I'm sure whatever the outcome she will be supported and loved, in essence, that is all that any of us need.
Thank you. It’s reassuring to know when you could be faced with the unexpected. Happiness is the most important thing, everything else is secondary.

When you see other stories with children, like the Azaylia story recently, makes you realise how lucky you are.
 
Thank you. It’s reassuring to know when you could be faced with the unexpected. Happiness is the most important thing, everything else is secondary.

When you see other stories with children, like the Azaylia story recently, makes you realise how lucky you are.
There was a documentary about couple of years back with Sally Phillips the actress who's daughter is downs. They were discussing the technology which will be able to pick up the gene thus illiminating downs altogether. She was totally against it because her daughter and her family are just happy as they are and the idea of her not existing was unthinkable.
 
Hey.

Hopefully this is an appropriate thread.

Im absolutely convinced my daughter has autism, as is my Mrs. Shes 16 month old so hard to tell atm.

She does the ‘hand flapping’ and is consistently throwing herself backwards on the sofa or in her high chair. These are both early signs.

From what Ive read online they won’t diagnose it properly till later in life, but we have somebody ringing on Wednesday to go through some questions.

Genuinely not sure what to expect, is there different levels to autism etc? I will be asking the doctor, but you usually get a load of spiel from their training sheets.
Just seeing if anyone has any experience and what signs gave it away for them.

Cheers
My son was diagnosed at 3 but we had strong suspicions from as early as 13 months. Our GP tried his level best to fob us off as overreacting new parents but we persisted until we got appointments with a paediatrician. Glad we did as they agreed with us and we started down the long road to formal diagnosis. He's now 7 and attends a specialist autism school in Longridge (only one of its kind in Lancashire). The key is persistence and trusting your instincts.
 
What's that school like? We'll probably be sending our son to Acorns because of proximity.
It's called Hillside. It's honestly superb. We fought tooth and nail to get a place there. We were basically adamant from the get-go and kept pushing until the council probably just got sick of us in truth and relented!

As mentioned It's autism spectrum specific so really focused on his needs. Only 8 per class maximum. They have things like sensory rooms on site and loads of outdoor space which is perfect. He can also stay there his entire school career as its reception up to A-Levels so gives us that peace of mind that he's there for the long haul. I really couldn't reccommend it any higher.
 
My son was diagnosed at 3 but we had strong suspicions from as early as 13 months. Our GP tried his level best to fob us off as overreacting new parents but we persisted until we got appointments with a paediatrician. Glad we did as they agreed with us and we started down the long road to formal diagnosis. He's now 7 and attends a specialist autism school in Longridge (only one of its kind in Lancashire). The key is persistence and trusting your instincts.
We’ve got a paediatric appointment next week for something unrelated but we’ll be mentioning it there as well.
I get the feeling we’re getting fobbed off an all, but age seems to be a massive factor for those we need to tell. See what happens in time, thanks for the reply though.
 
We’ve got a paediatric appointment next week for something unrelated but we’ll be mentioning it there as well.
I get the feeling we’re getting fobbed off an all, but age seems to be a massive factor for those we need to tell. See what happens in time, thanks for the reply though.
No worries. Anything beyond 12 months and you have every right to see a specialist if you have concerns. You know your child better than anyone so never let a GP talk you out of something or make you question your judgement. It's a slow and arduous process in getting a diagnosis and the sooner you can start the ball rolling to finding out whether you need one the better.
 
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