Hi,

I am writing on behalf of my brother, Joseph. Joe was born with severe
spastic-athetoid cerebral palsy. Joe grew up at home with the rest of my
seven siblings and myself in the severe poverty in inner city in Chicago.
Because my family has always believed in the tenet of least restrictive
environment, Joe attended mainstream schools and eventually graduated with
a Bachelor's degree from Harvard University. He is currently completing his
PhD in Political Science at the University of Chicago.

It has taken a lot of very hard work on Joe's part to get where he is
today. Because Joe is not physically able to write, it will not be possible
for him to seek employment after he finishes his PhD. Over the years Joe
has participated in various studies in an effort to find speech recognition
software that can adjust to his significant fluctuations in muscle tone.
Here is the reason I am writing, in Joe's own words:

"I have dysarthria -- it matters that I have spastic - athetoid cerebral
palsy. The researcher in Boston said that this is ideal because the
researcher needs persons with spasticity for muscle tone and with athetosis
for intelligence level. I tried the different versions of Dragon. I tried
one of them for an extended period of time -- they didn't work at all. In
Boston I participated in a study of speech but they didn't actually try to
design a program. The head of the study wanted to try to find someone at
MIT but that did not work out. Then I participated in a study at University
of Illinois Champaign in which they were actively trying to design
individualized software for people with dysarthria. The software didn't
work and then I think they moved on to other things. I might be able to get
my speech samples from at least the U of I and / or to figure out how to
give new samples. I know that U of I had some strange video component to
their grant / research -- I think they videotaped me, but I don't remember
for certain. All these people stressed that any software would have to be
designed for me particularly -- for any person with dysarthria,
individually, actually -- at least for now."

Joe is wondering if anyone knows of a FLOSS project that is producing
software that could be adapted for his needs, or of research that is being
done in this area. We would appreciate any and all information in this
regard.

Thanks very much for your time and patience.
Sincerely,
Meg Ford
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