Yes, I am afraid you're right about that.
Damn......I am not male, I am a person suffering from maleness (But, I'm not as manly as Gareth :razz: )
I am not a father, I am a person with parenthood. (Amber laughs at my pseudo-maniacal laugh.....
And yes, I am a person with sarcasm! :groupjump: :razz:
Ack, 1 out of three, I'm doomed.......TGIF, Oh well, time to have a shot of the birthday whiskey (I just turned 50 and am a certified "old fart) :twisted: ok, I'll shut up now!! :roll:
Peace
This irritates me. I don't think it's true. Even as a child, I understood a far greater vocabulary, including the terminology of the subjects I perseverated on, that was far greater than what I actually used. I definitely understood the content. It's just that if I am put on the spot and asked to express myself, I will stutter and stammer and have a hard time finding the words, especially if they don't have a visual context to relate to. It isn't the same as having a limited vocabulary, at all....
I believe this mainly relates to very small children, i.e. toddlers who appear so precocious due to echolalia (like, 2 year olds repeating whole films word for word), and are put under a lot of pressure because the parents see their difficulties as much worse than they actually are, since they take the echolalia as 'proof' that their child is a genius and treat it like a precocious NT instead of an autistic child.
You yourself may not have had this level of echolalia, but many autistic children do at first, and rather than encouraging the use of echolalia to help the child communicate, parents often seem to take this level of 'language' as an indicator of what they expect from the child.
Sadly, when the child doesn't 'deliver' (because the level of understanding is lower than that assumed by the parents), it is often put down to laziness, obstinacy etc. because the parents cannot understand how a child who can recite complex texts can't follow simple directions, control their bladder or bowels or eat by themselves. To understand how echolalia works is a step towards understanding how their child works - echolalia can become a very useful tool for a child, but unless the parents understand its nature, echolalia often leads to a lot of misunderstandings and lack of support for the autistic child.
I never had that kind of level of echolalia, but experienced a similar thing insofar as I parroted words and phrases from an early age on, but the speech I produced spontaneously when trying to communicate was quite far behind that level. So my parents expected me to act and behave like a precocious toddler, while for the most part I was pretty much unable to string together a sentence of more than 2 words until I was about 4.
Chain letters *are* tedious 
I think it would be taken more seriously if it wasn't posted as chain letters - they bug the heck out of me!
I agree 
"10 things an autistic adult wishes you knew"?
and circulate it.
Suggestions?
1. I am autistic, not just an adult with autism. It is part of who I am.
That could be 1a)
1b) "Other people may not feel the same way about this, and prefer to be referred to as 'a person with autism' or something else entirely (perhaps they just want to be 'a person'?). Wherever possible, please consider a person's preference and remember to use whatever term they prefer."
"10 things an autistic adult wishes you knew"?
and circulate it.
Suggestions?
1. I am autistic, not just an adult with autism. It is part of who I am.
I prefer to call myself autistic not "an adult with autism" but for all those who would object how about:
1. Autism is part of who I am.
2. Autism is a neurological variation, not a disease. Autism often includes differences in social behavior and ability.
Thanks, I recently read in a book about how the whole person first language was originally an attempt by people to be "politically correct" and not make a person all about a disability or condition, but look at the person themselves, regardless of whether they may be autistic, paralysed etc.
I think it's always dangerous to generalise statements like that - I particluarly like the original article because for the most parts, it uses the words "may" more often than similar attempts at broadening the public's understanding of autism - I appreciated the wording of things like "I am not defective, but my senses may...", because it describes pretty accurately how these things are for some people, while still making clear that this is not the same for everyone (hence the use of "may", "can" and so forth).
"10 things an autistic adult wishes you knew"?
and circulate it.
Great idea, Amy! You can post it in the Articles section of AFF when it's finished, and we can all link to it from our websites.
1. I am autistic, not just an adult with autism. It is part of who I am.
We should also add some explanatory paragraphs under each statement, like the original article does.
How's this for # 1:
Acknowledging my autism as a part of me is entirely compatible with respecting me as a person with thoughts, feelings, and talents. In using words such as overweight or myopic, one would not typically resort to awkward sentence constructions such as "a person with obesity" or "a person with myopia" in an effort to draw attention away from these characteristics. Please do not use language that suggests autism is an unmentionable misfortune.
"9. I do have emotions, autistics are not emotionless like some stereotypes suggest. But I may express them in a different way.
What may make someone else cry, can be different for me, it doesn't mean that I don't care, or am an uncaring person." My facial expressions might not always reflect my emotions.
That's also true of an autistic person's voice.
This article is starting to look pretty good, Amy! :smile:
