What is it like to be nonverbal/non-speaking?

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kraftiekortie
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07 Jan 2020, 7:36 pm

Some autistic people have what is called "apraxia" or "dyspraxia."

It means they have trouble with the "motor planning" of their speech-related muscles.

People with apraxia can range from having slightly "distorted" speech, to having no speech at all.

Intelligence is frequently not affected in the presence of apraxia.



MrZhdens
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08 Jan 2020, 12:50 pm

Spenser777 wrote:
So everything depends on each person, there are darker people in themselves, they are more open. We cannot judge them because they are more closed in them. They may have had psychological trauma or it is difficult for them to expose their emotions, thoughts. For example, my uncle lost his hearing (not 100%) a few years ago, he now wears a hearing aid but almost no one communicates, it was a trauma for him to lose his hearing. We the family bought from access-market.com even a device that increases the sound waves, to hear better. But he has already formed this habit of not communicating too much, of being closed in himself.
I guess no one communicates with you also, because of your bad English. I feel sad for your uncle, I'm sure he is a brave man and a wonderful person, but we cannot fight against God's willing.



dragonsanddemons
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08 Jan 2020, 2:53 pm

I'm not completely nonverbal, but I do have selective mutism and go nonverbal when I am experiencing strong emotion, sensory overload, or lots of stress. For me, the two feel different, which is why I've classified them differently.

For my selective mutism, I have the words, but no matter how hard I try I can't force my vocal cords into action, or sometimes I can manage something but can't speak loudly or clearly enough to be understood. It feels more like a physical limitation, and I can use the text-to-speech app on my phone to communicate in these situations.

When I go nonverbal, it feels more like a mental limitation. I can't come up with the words to use in the first place, there's just too much going on in my brain for me to be able to make sense of it all. Because I don't have words to use, I have to rely on things like gestures. My parents are the only ones who understand the ways I try to communicate when I am nonverbal, and they are usually the only ones I will try to communicate with in this state.


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