[misc.handicap] More Thoughts!

Linda.Iverson@f10.n130.z1.fidonet.org (Linda Iverson) (11/28/90)

Index Number: 12004

[This is from the Silent Talk Conference]

Hi, James!
 
I know you have said, but aren't you a principal or teacher?  What 
school do you work at?  How many students are in the school?  I always 
attended public school, so don't know much about residential schools, 
but I've heard some people say that when a state combines the schools 
for the deaf and blind sometimes one group gets the short end of the 
stick.  What do you think?  You know, I have learned so much from this 
board, and as I said becauze both blindness and deafness are sensory 
disabilities, I believe there are similarities as how people see us. 
 I met a girl in college whose husband had worked at a school for the 
deaf, and she was telling me that often deaf people are afraid of blind 
people--perhaps because, like the sighted in general, that sight is 
so important and the main link to the world.  I don't believe that 
because I went to junior high with a couple of deaf girls, and I got 
to be fairly good friends with one of them.  I don't believe blindness 
gives you better hearing, but I think you know how to listen.  Anyway, 
one day this girl came to the teacher's desk and asked her a question 
and she couldn't understand her.  My desk was next to the teacher's 
and I just told her what the girl had asked.  Our teacher was really 
surprised.  Well, since this girl had speech-reading skills we started 
to talk to each other.  Our English class was broken into a gifted 
group and we were part of that.  Every day we went to another room 
with a student teacher, and this girl used to walk with me to the other 
class and help carry all my paraphernalia--braille books, typewriter, 
braille writer, etc.  That's why I brought up some of the parental 
attitudes that I mentioned to Karen because we'd talked about it.  
Occasionally we couldn't understand each other, but we both wanted 
to cultivaate the friendship, so I'd either write her a note and she'd 
repeat something until we got it together.  Anyway, the nice thing 
about this board is that we can get to know each other, and should 
the occasion arise where we might meet we'd already have something 
to base a friendship on.
Take care!
Linda
 

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Karen.Keil@f809.n104.z1.fidonet.org (Karen Keil) (12/04/90)

Index Number: 12163

[This is from the Silent Talk Conference]

        You are right about having a disability to really appreciate 
something (like reading books) that other people take for granted.  I 
realize how fortunate I am to be able to pick up anything I choose to 
read without having to have any special helps or procedures to do so.
        One of my friends (also hearing impaired herself) says that 
whenever people ask her what it's like to be deaf, she asks, "What have 
you lost?  It can be comparable to that."
        My friend is losing her hearing, too, but not as fast as in my 
case, but as one of the other people remarked previously, hearing aids 
are basically amplifiers, bombarding the ears with sounds.  I used to 
be able to hear some environmental sounds WITHOUT my hearing aids 
although they were very muffled--e.g. a low-flying jet flying overhead, 
a lawnmower running, but that's not true anymore.
        I used to listen to music, but it's not the same anymore--it 
sounds like noise with much of the tones missing.
        Undoubtedly, your hearing is sharper because you are using it 
to compensate for your lack of eyesight.  I use my eyes a lot and 
believe it or not, also kinetic senses (to sense vibrations.)
        More later....
Karen

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Linda.Iverson@f10.n130.z1.fidonet.org (Linda Iverson) (12/21/90)

Index Number: 12536

[This is from the Silent Talk Conference]

Hi, Karen!
 
Tell your friend I like what she said about describing her loss.  Everyone 
can relate to having lost something.  You know, I still think people 
like us are luckier than people with multiple disabilities, or people 
with autism or mental retardation.  At least with proper training we 
can make our own decisions and control our lives.  I guess my parents 
were protective in some ways, but I've known other kids whose parents 
were worse, so I feel fortunate.
 
You are lucky to be able to read anything you want, and as I told you, 
I love books and miss that, but it's getting better with reading machines 
and computers.  Karen, you wouldn't believe how many bulletin boards 
there are here!  I have found so much information.  We are really living 
in an exciting age.
 
Take care, and keep those thoughts coming.  By the way, I attended 
the National Federation of the Blind convention this summer and met 
a deaf-blind lady who had recently had a cochlear impoant.  She couldn't 
hear conversation, but she could hear a faucet dripping if she were 
close to the sink, leaves and paper rustling, and those kinds of things. 
 I guess it's as much the frequency of the noise as the loudness.
 
I'm not surprised about your use of kinetic senses.  I do that to some 
degree, but probably not as much as you.  I have, and many blind people 
do, what is called "object perception" or "facial vision".  I can tell 
before my cane touches it when I'm approaching a large object--tree, 
truck, those kinds of things--walls and other objects that often block 
a path.  I've tried to cultivate that ability, and of course it is 
caused by the air current being different around those kinds of objects 
which makes the outdoors sound different.  One final thought.  I wouldn't 
worry about music--you're right, some of it does sound like noise! 
 
 
Linda
 

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Mitch.Turbin@f71.n343.z1.fidonet.org (Mitch Turbin) (01/17/91)

Index Number: 13020

[This is from the Silent Talk Conference]

Hi Karen,

I was interested to read your note. Nice to see a person opening up to 
different disabilities. So here's a new one for you to consider--deaf-
blindness. Of course, like all sensory impairments, this one runs along a long 
continuum of "severity". I for instance, have usable hearing and vision, tho 
significant problems in both (as well as significant coping strategies for 
each, and both!) And the interesting thing, that is, the most interesting 
thing for me about this disability, is the way that the two impairments 
interract. It's often said that here is not a case where hearing loss is added 
to vision loss--it's more multiplicative in it's increase in problems. Well, 
I'm not sure about the specific quantification, but one thing is sure--it can 
drive you crazy to realize that the coping strategies that help other HI 
people won't work for me any more, cuz I don't have the vision. And vice versa-
-the ways in which hearing helps most blind people don't work for those of us 
who also have hearing impairments. 

Quite a challenge. I thank God I wasn't born a few hundred years ago, before 
hearing aids, flexible canes and infrared/ultraviolet blocking lenses, and 
computers! Wow, I'd probably been in some kind of institution, if not just 
plain dead!!!
'nuff said
Mitch

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rudy@mtqua.att.com (Rudy Vener) (01/23/91)

Index Number: 13095

Hi Mitch,
 Nice to see you here!  It's been ages.  How've you been?
 
>
  [ some stuff deleted ]
>drive you crazy to realize that the coping strategies that help other HI 
>people won't work for me any more, cuz I don't have the vision. And vice versa-
>-the ways in which hearing helps most blind people don't work for those of us 
>who also have hearing impairments. 
>
   And how!  Such as crossing busy streets.  I still have SOME useful vision
and SOME hearing.  Problem is the hearing is not directional, the vision is
(let us say) unreliable.  I really hate those nasty little cards with the
quiet engines that can make snappy right hand turns faster than you can
say 'run over the blink'.  One interesting thing I found out is that I feel
much more secure crossing in the MIDDLE of the block because a) I usually
cannot spot the traffic light anyway and b) I only have to check two directions
instead of four.   
  
>Quite a challenge. I thank God I wasn't born a few hundred years ago, before 
>hearing aids, flexible canes and infrared/ultraviolet blocking lenses, and 
>computers! Wow, I'd probably been in some kind of institution, if not just 
>plain dead!!!
>'nuff said
    Same here.   The recent events in the Persian Gulf have given me some
cause for reflection and I have come to the (rather obvious) conclusion that
handicapped people can only thrive during times of great peace and prosperity.
Let's face it, accomodating handicapped individuals is a LUXURY that only a
fairly wealthy society can afford.  Let's not kid ourselves that we have some
sort of inalienable RiGHT to equal access and special accomodations.  We may 
have these rights NOW but they are far from inalienable and they could disappear
at the first major, world threatening catastrophe.
   How did I get off on this subject anyway?  I better stop before everyone 
falls asleep.

Rudy Vener  AT&T BTL ...!att!mtqua!rudy