However, if ND people are all under the umbrella of ND then it’s an issue. You conflate general stress for ND.
For my son ND is not a sense of general stress / unhappiness.
As I have said for my son there were extreme physical issues before he was diagnosed ASD.
NT people don’t have hypotonia muscle tone, swallowing disorders at birth, extreme blue ear ( 2 lots of grommets and adenoids removed resulting in scarred ear drums) bowel disorder and faecal incontinence until aged 10 ,severe motor coordination disorder,prolonged fits lasting over an hour until aged 7. Ongoing,the motor issues and severe receptive language impairment remain.
This constant trivialising of ASD / ND is hugely upsetting be it people who might have more marginal symptoms and want a diagnosis or those who are skeptics because of that I suppose.
For my son,the outside world is hugely problematic. Even a meeting with his ASD support worker at university turned into a whole load of misunderstanding as he did not at that moment have a PA to re navigate the meeting for him and explain the intentions. When semantic pragmatic language are below the 1 percentile the World is really confusing,
The amount of times that teachers, support workers have to intervene to explain what people intended by what they said, the constant upset. This interferes in all communications eg simple task ‘Take a page …’ what does that mean to someone with severe pragmatic language? There were times he came home from school petrified / scared witless because of an innocuous statement made.
As for SPD - at its extreme for my son it means falling asleep on a bus as he cant cope with the journey ( identified as a form of shut down). Literally 2 minutes on the bus and he zones out.
The door at our home is open to him but his further solitary journey is 5 minutes to the local shop. Anything else would be too traumatic for him. He practiced making a shirt bus journey from one site to another with life skills college and would call his dad and then me for reassurance. This was in a quiet town, as fro the city,he bus refuses even with a PA on occasions if the bus is too busy.
The accompanying executive dysfunction is horrible. He has no agency for his own life and without prompts would function in a twilight zone when mornings are nights and breakfast is dinner, when days would blur.
As a carer, it is exhausting having to be in control of everything he does, what he wears where he goes, last week I woke him up in the morning for university and he thought it was the evening and explained to me that he did not have to shower as he already had his pyjamas on! He has no sense of day or night!
Yesterday, I was despairing with the usual thoughts about what would happen when I die. Could he live in a little annex where his sister one day might love? But she wants to live in the country and he would be just left to vegetate. Would he be in the city alone with PA support? He would be so vulnerable and maybe miserable. The fear of leaving him to the care of social services has destroyed a lot of happiness in my life. I try not to think of it but it’s an intrusive and upsetting thought.
It would make me so angry if people do exaggerate to get PIP or whatever, I hope that they don’t as for my DS he has no choice. He is so away with the fairies that he has little inkling into PIP or universal credit, He has a spiky profile where he knows his subject matter for his studies but little idea about the rest of the World.
I don’t understand any of it. I don’t understand how his brain is as it is but is there something wrong? Yes he had a VEP evoke potential test done when young and that showed demylination of white matter,
There is a suggestion by some experts that they might need to separate early physical signs accompanying ASD diagnosis from other diagnosed ASD with no physical signs eg no hypotonia, no significant eczema / asthma /significant motor issues / fits / bowel issues / language impairments etc