What are your thoughts about advance directives, informed consents, patient autonomy and the like? Does it seem like deaf people are often less educated on such things than they ought to be?
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Sorry, that sounded awful. I was not implying at all that the Deaf are less educated. I was meaning to pose a question about access to resources.
I ask because in doing a lot research, I'm finding all sorts of articles saying that the Deaf do not have enough access to info about and are not as informed about these things. Is this true? I know that all of my deaf friends are very resourceful and have very educated opinions on advance directives.
I'm truly sorry for my carelessness. I don't mean to be provocative.