You know about "that population"?
Do you mean people who are reaching out for support?
If that is the case you don't know much about that population.
If you don't have a background in medicine, don't pretend to know about the various causes of aphasia.
If you can demonstrate a thorough knowledge of neuro anatomy and neuropathology, then you can maybe discuss this stuff.
I'm not saying I'm an expert but I definitely have more qualifications than "I know someone who has aphasia".
ecp, talk about the pot calling the kettle black. You're simply trying to grasp at straws to "prove" I'm a "bully"
I know quite a bit about the nonverbal but still mentally normal population. This is a very very low incidence population. Many people with my syndrome actually have severe speech failure. (meaning their speech fails to develop normally, not that they're oral failures) Like the type where kids may use ASL or Dynavox communication devices. Not to mention that one of my close friends is an advocate for this population, as her daughter has severe speech failure. She started an organization to give kids in this population an augmentive and alternative communication device. Most of the kids she serves are the typical "has apraxia/autism/severe mental disability" Most of them have additional issues. It's very rare overall to just have spoken language exclusively as an issue. What he said does not match up with the experiences that people with spoken language issues (and no hearing loss) that I know have. If he had done his research and had posted about say "I have spoken language issues (instead of using a very archaic term) and had said " I have this or that due to this or that." I would have GLADLY GLADLY contribuated information and resources....There are a couple of Deaf Schools that strongly support this population (St. Mary's...some of the kids there use dynavoxes, St. Rita's (has the apraxia program for hearing kids with severe speech issues) and Beverely School for the Deaf/Children's Center for Communication.