WROCC@WOU Home | WSRD Conference | WSRD Proceedings List
The objectives of this paper are to define and exemplify some possible solutions to the multifaceted problems involved in improving VR and campus services to students who are hard of hearing. Barriers to delivering these services, rooted in attitudes and behaviors of persons who are hard of hearing or hearing, are examined. Case histories are presented to demonstrate how hard of hearing students succeed in college with the assistance of specialized staff. Exemplary ideas are discussed to enhance how to: (1) identify changes needed in VR or Disabled Student Services (DSS) programs, (2) recruit students and facilitate their transition into college, (3) help students overcome resisting acceptance of their hearing loss, and (4) promote college persistence. Extensive comments made by session participants are presented and summarized.
John: An important first step is
to estimate the number of deaf and hard of hearing students attending the nation's
5,000 colleges and universities. This is essential because a director of any
program needs an accurate assessment of its target population for budgeting,
staffing, and services. During the past ten years four national surveys of college
administrators, including those experienced with students with disabilities,
reported between 20,000 and 28,000 such students on their campuses. However,
a very different number results when students with hearing loss are asked directly.
In 1990, a national survey of college students about federal financial aid led
to an estimate of 258,000 deaf and hard of hearing college students. This is
a surprising figure from a group of people who usually do not reveal their hearing
loss. The Research and Training Center at the University of Arkansas estimated
468,000 college students with a hearing loss were enrolled during 2000 (Schroedel,
Watson, & Ashmore, 2003). Among these 468,000, 345,000 were hard of hearing,
115,000 deafened after age 19, and 8,000 deafened before age 19 including 2,500
at Gallaudet University and NTID at RIT. This estimate of 468,000 students was
projected from prevalence rates derived from the most reliable national demographic
study available (Ries, 1994). It is important to clearly define estimated groups.
This report defined deaf people as those who cannot hear and understand speech
and hard of hearing people as those who have difficulty hearing and understanding
speech.
Audience: Was that with or without
a hearing aid?
John: Without use of hearing aids.
Audience: I do not feel good about
that.
John: The 1994 demographic report
was based upon scales developed during the 1960s to assess hearing loss during
household interviews. That history does not take into account the rapid development
of the sophisticated technology in present hearing aids. So maybe the scales
need to be revised, however, the definition of the two groups with hearing loss
makes sense. Note that these demographic-based definitions are dissimilar to
those used by vocational rehabilitation and special education professionals.
One may think that 468,000 is a big
figure, however, this is only 3% of 15 million students attending 5,000 colleges.
A key question is: why the large discrepancy between the estimated 28,000 students
from a survey of college administrators and the estimated population of 468,000?
The most likely answer is that most hard of hearing students are not requesting
campus and VR services. That is the best explanation available for this massive
discrepancy.
Furthermore, other surveys show that
most college-aged hard of hearing persons have a mild loss. From a VR perspective
it would be presumptuous to say such a person does not have a disability and
is ineligible for services. By contrast, consider that a person with a slight
hearing loss may have emotional-psychological difficulties or other functional
limitations interfering with doing well in life. Part of the problem is that
the field lacks accurate assessment measures of the actual functional capacities
of people who are hard of hearing. Furthermore, among college-aged persons (18-34)
only 5% use hearing aids, whereas the other 95% could benefit from hearing instruments
(Schroedel, Kelley, & Conway, 2002). The fact that only 5% use hearing aids
suggests many are not accepting their hearing loss.
There is a need to address some of the social-psychological issues faced by hard of hearing people. In the attached Figure the black boxes refer to hearing persons and the white boxes refer to hard of hearing persons. This Figure represents a model of the attitudes and behaviors many persons who are hard of hearing or hearing display in response to hearing loss. Stigmatizing means assigning a negative attitude to hearing loss and the Figure includes a self-fulfilling prophecy. A step-by-step explanation of the model follows. When a hard of hearing person hears incorrectly, misunderstanding can occur, and this person acts inappropriately. Then hearing persons may say, "That's stupid." This ridicule reduces the hard of hearing person's self-esteem, may lead to social withdrawal, and, in turn, to potential underachievement. Then hearing persons may say, "See, I told you he couldn't do it." This viscous cycle ends in this self-fulfilling prophecy. The question remains: how frequently do these attitudes and behaviors take place? It is important to add that some hard of hearing individuals act as shown in the Figure and others do not. We do not want to create stereotypes.

Individuals who are hard of hearing use different styles to cope with these attitudes and behaviors. Some proactive coping styles include being assertive and working harder than others (overcompensating). More frequently, however, the professional literature reports reactive coping styles characterized by varying degrees of denial, pretense, bluffing, deception, limited interaction, and withdrawal. As a hard of hearing person I behave like this. You can find other hard of hearing people whom have behaved similarly. By contrast, there are hard of hearing people who react positively to negative circumstances by assertiveness or overcompensating. Support for this model comes from interview and focus group research studies with hard of hearing and late-deafened workers. However, other research has ascertained negative attitudes toward some attributes of hearing loss among college students who hear. Therefore, the psychosocial adjustment experiences of hard of hearing workers and hard of hearing college students can be generally similar.
These conditions converge to form
barriers to accessing and enhancing VR and DDS services.
To place these issues in more personalized perspectives, case histories of four hard of hearing college students are presented.
Gina: High school staff encouraged her to use various communication devices. But even with a moderate to severe hearing loss she did not use her hearing aids because of auditory feedback and the ear molds made her uncomfortable. As a high school senior, she wanted to go to a small private college. She told her VR counselor that she often misunderstood conversations on the phone and in groups. She tried an assistive listening device (ALD) and did not like it. She was diagnosed with a learning disability and lower academic skills. Even though she disliked behind-the-ear (BTE) aids, the audiologist put a BTE aid in one ear and an in-the-ear aid in the other. Professionals realize that most BTE aids have more auditory power than smaller in-the-ear aids. Regardless, Gina missed much in class discussions, replied inappropriately, and sometimes bluffed. She did well in remedial classes and hoped to go to a four-year college to become a mental health counselor for people with hearing loss.
Debbie: As a college freshman Deb
was referred to DVR by the Disabled Student Services unit. She has a profound
loss in one ear and a mild loss in the other ear, which exemplifies the unique
problems of uneven hearing loss in each ear. Debbie did not use hearing aids.
During her communication assessment given by VR staff she could not identify
many problems related to her hearing loss. The VR counselor worked with her
to try new hearing aids with telecoils (for a phone attachment). She was instructed
about ALDs and reconnecting with the DSS unit. At first she used an ALD in lecture
classes, but not in discussion classes. One professor used the ALD, but did
not turn it on, and gave Debbie a D. Debbie now uses hearing aids, various devices,
oral interpreters, and has a 2.0 GPA Her career goal was to become a meteorologist
Carol: The names linked with all
presented case histories are fictitious The first two cases emphasized more
about VR services. I will approach the next two cases more from the perspective
of postsecondary support services. These students attended a community college
with a special program for students who are deaf or hard of hearing. This may
differ from your professional situation, but we hope that you will gain some
helpful ideas and suggest to us on how to improve the solutions to problems
we will offer later in this paper.
Dale: Dale has a moderate hearing
loss and his dad is also hard of hearing. He was referred to DSS by vocational
rehabilitation. He had to take an adult basic education test in order to enter
college. Dale was very unhappy about being scheduled to do this with a group
of signing deaf students. VR personnel were aware of his denying his hearing
loss and referred him to a summer transition program. At first he was very uncomfortable
with the signing between deaf and hard of hearing students. He soon warmed up
after he met some hard of hearing students who did not sign, but still did not
feel very comfortable. In the fall he selected a non-signing hard of hearing
student as a roommate. During the orientation program, he was disinterested
in ALDs and oral interpreting. All he wanted was a note taker. Moreover, he
did not want anyone in the classroom knowing whom that note taker was assisting.
Not surprisingly, by midterm he was not doing very well and he went to see the
DSS counselor. Dale decided to try an oral interpreter because he wanted to
be successful. That helped some in the beginning courses. He also stated, "I
missed a lot when I was in high school and I am upset because I was not then
provided these services." This was probably the first step he took toward
resolving his denial. He still is not there yet, but he has progressed. He had
a counselor who was positive, patient, reassuring, and did not push him. VR
approved his request to change his major. However, this new major was more academically
demanding and at midterm again he was having problems. The DSS counselor asked
if he would try C-Print. He did, liked it very much, and requested it until
he graduated. He is still uncomfortable with other people knowing he is hard
of hearing, but I think he has come a long way. He worked with his VR and DSS
counselors to transfer to a four-year university to major in electronics.
Phil: Phil had a moderate to severe hearing loss and attended public elementary
and middle schools. Then his parents moved to a city that has a school for deaf
students where he completed high school. He learned to sign, but was never integrated
fully into the Deaf culture. Later he attended a college with limited accommodations
and withdrew. After working on several dead-end jobs he went back to his vocational
rehabilitation counselor who referred him to an out-of-state college with a
special program for students with hearing loss. This led to some problems. Being
more mature and older, he felt that he did not fit in very well with younger
students just entering college. Subsequently, he did not have many friends and
was very lonely. The counselor got him involved in intramural sports and computers
that became his niches. His interpersonal skills were enhanced by working in
the DSS office, being a big brother to a hard of hearing student, working with
new hard of hearing students in the summer transition program, and developing
friendships with some students who hear.
When he began college, he was placed in remedial classes in English, reading,
and math. He also took one computer course. He did excellently in his reading,
math, and computer courses, but English was another story. He had to take second
level English three times before he could enter English composition, which delayed
his graduation. This made him very frustrated, but the counselor helped him
learn how to deal with his feelings. Because of his determination, his persistence,
and help from his instructors, tutors, and counselors, he completed an associate
of science degree in microcomputer information processing.
Audience: Did he use hearing aids or other technology?
Carol: He had hearing aids and tried a FM system. In college VR usually takes care of those matters, so unless they ask us, we do not get involved with hearing aids. It is really difficult to get hard of hearing college students to try different accommodations. At that time we did not have C-Print operators, but Phil did get through.
Audience: Why is it hard? When my
students at the University of New Mexico get their hands on a FM system, they
love them.
Carol: Does anybody else have problems
with their students using such accommodations?
Audience: It depends on the student. I have two hard of hearing students who
do not acknowledge their hearing loss and would never use a FM device.
Audience (clarification): She has three students. One will use the FM system.
The other two will not. They are still in denial and do not want to use the
FM system.
Carol: Phil really wanted to be hearing.
He did not want to use visible accommodations. We do not push the students about
those issues, because it is their choice whether they want to use ALDs. We make
them available, but if they do not want them, we do not pursue the matter. However,
Phil achieved his goal and VR helped to place him on a job working with computers
in a state Division of Motor Vehicles where he is working still today. I visited
him once and he is doing really well.
There were some observations we noted when we looked at these four students.
Carol: VR and DSS professionals
acted to help these students to effectively deal with these problems. What
were some of the ways VR and DSS personnel helped them? Anyone remember
anything?
Audience: Offered accommodations.
Carol: Yes, they offered the accommodations. DSS staff did not force accommodations
and some students accepted them and others did not. They accepted hearing
aids through the assistance of either VR or DSS or both.
They accepted assessments. Remember Debbie went through the communication assessment to learn what problems she was having. She was not really aware of those problems, but after the assessment she was able to identify them better.
Audience: On your last overhead where
you observed about the students. Would not the last two items, coping with the
reaction to being hard of hearing and developing social activities, come before
accepting hearing aids? It would seem to me that it would be really difficult
for a person to be aware of hearing aids unless you first dealt with the psychological
side. You talked a bit about the student who was having trouble with his English
writing. As a counselor it seems to me you have to deal with the emotional and
acceptance sides before you can move onto the technological side.
Carol: You are very correct. However,
we did not put these observations in any type of order. We just listed some
identified problems. You are very right that until they start working through
denial and becoming active and involved, you cannot really make other progress.
Audience: I wonder how did the DSS
professionals accomplish that?
Carol: How did the DSS professionals
accomplish these changes? These students became successful cases. We excluded,
for example, the ones that withdrew after they twice failed English. It has
to be students that wanted to succeed, then you can work with them. We also
wanted to demonstrate effective professional interventions.
Audience: I was wondering about the
methods that you used such as one-on-one mentoring?
Carol: She was wondering about the
methods that DSS personnel used in getting students to accept the various changes
that we have on the overhead. We shortly will describe more solutions to the
problems. Here we simply presented examples of assisting some students who had
problems.
John: Thank you, Carol. We would
be the first to admit that we do not have all the answers. We want to keep our
part of this presentation brief to give you more time to say what you want to
say because we want to hear from you. We are going to take notes of what you
say. We appreciate your perspectives because we believe many service professionals
are not getting all the training they should be getting. Furthermore, hard of
hearing consumers have meaningful experiences with these issues. Thus, your
ideas are very important.
We have four subject areas with a total of about 20 ideas that may benefit some of these different types of hard of hearing students. We emphasize VR and DSS staff working together. When we mention VR and DSS, sometimes it applies more to VR and at other times more to DSS.
Program Preparation and Changes:
John: Resistance is one way of describing a group of hard of hearing people. There are other categories, but this is one we wanted to address. Signs of resistance include preoccupation with being a person who hears as exhibited by denial, pretense, and withdrawal. This is done by applying much negative energy to maintain a quasi-self-concept, "I'm hearing, I'm hearing, I'm hearing," that does not really fit the person.
Carol: We know that three out of
every four deaf students quit college without completing a degree, but lack
similar information on hard of hearing students. If you have a student who is
informed, involved, and receives appropriate accommodations from well-trained
counselors, teachers, and staff she or he will more likely persist through college.
John: There were many holes in what we said today. We certainly want your ideas as front-line service providers or as hard of hearing consumers. Please come up, tell us whom you are, about your experiences, reactions to some of these issues, and your suggestions to make them better.
Audience: Thank you for a very well
presented program. My name is George Kosovich and for 13 years I have worked
in the Rehabilitation Services Administration (RSA) Deafness and Communicative
Disorders Branch with the goal of improving and increasing rehabilitation services
to individuals who are hard of hearing or late-deafened. I have seen this thing
from all angles. I was a student that flunked out of college because I did not
know what was happening and I was in denial. I was a former VR counselor for
persons with all disabilities and people with hearing loss specifically.
I saw myself in different ways in
all four presented case histories: for example, flunking out. I had a hearing
loss growing up and in retrospect I can understand why I disbelieved I could
graduate from college. I entered college because my high school buddies wanted
me on the football team. I played football, flunked out several times, then
went back and got my grades up. After high school I was not referred to VR and
had a sudden hearing loss in my better ear when I was 25 years old. I had been
doing unskilled work. Then I went to VR and after a complete evaluation my counselor
said I had the ability to go to college and graduate. I never heard that before
and it made a big difference in my life by motivating me. Furthermore, I finally
wore a hearing aid for the first time and that also made a difference, but not
completely. I got a large ALD with a headset then went into the classroom. Talk
about facing denial. I wore the ALD with the headset and some of my football
colleagues would say, "Hey ready to take off?" Joking like that helped
because it was funny. However, by using that device I could hear the teacher
and actually participate in the class for the first time. I could see what denial
is about, but I do not know how to cure it.
On another matter, I think colleges
and universities should adopt a program for screening hearing ability. It does
not have to be sophisticated audiology. You can train someone to use an audiometer.
Advertise the hearing screening on posters with the idea that, "Do not
let a hearing loss sneak up on you because it can affect your grades."
After the screening students can indicate they have a hearing loss, get a more
complete evaluation from VR, then the agency can get involved. But I think the
VR office will not follow-up unless there are more than four students with a
significant hearing loss at a college.
It is essential to have a VR counselor
who knows something about hearing loss. Unfortunately that is not the case in
a lot of places. I know that Kentucky has 40 personnel trained to work with
hard of hearing people. I also think these specialists should be certified.
We have been depending on rehabilitation counselors for deaf consumers, but
there are not enough of them. Furthermore, the master's degree training for
RCDs requires learning sign language and about deafness, but that knowledge
is not primarily useful in dealing with hard of hearing or late-deafened people.
I think Kentucky is the perfect model for a professional VR approach to serving
hard of hearing people.
I am pushing for a new kind of professional.
Joanne Wilson, the new Commissioner of RSA, is advocating for consumer participation
in training professionals. There are some grants coming out now to get consumers
who have successfully adapted to their disability involved in showing other
people they can get by their disability and focus on their abilities. Similarly,
I think there is a role for SHHH members to effectively help individuals who
are newly hard of hearing or just coming to grips with their hearing loss. SHHH
has affiliates all around the country with many longtime members, but these
chapters face the problem that relatively few people join a self-help group.
Therefore, there is a need for knowledgeable professionals and paraprofessionals
to help hard of hearing persons and their family members cope with the hearing
loss. SHHH has been listening to various people and I think that the organization
is willing to get involved in the training.
In summary, we have a long way to
go. Some of the topics discussed today are the same we have been talking about
for 40 years. The stigma and denial still exist and I do not know when they
will go away. We are on the right track as far as VR is concerned and the Kentucky
program is an ideal prototype we should be adopting across the country.
John: Thank you, George. I have encountered
many of the things George has experienced. I withdrew from two universities.
This is your time, not my time. Someone else please come up. Tell us whom you
are and what ideas you have.
Audience: My name is Bonnie Smith
and I am the program services manager for deaf and hard of hearing students
at the University of New Mexico. I have been in this field for 20 years and
I began as an interpreter. However, I soon was working with many hard of hearing
people and started a support group. My basic job when we had group meetings
was to ensure that everyone understood each other. When there was a misunderstanding
I asked them to repeat what was said to help clarify the flow of the conversation.
They shared a lot and I learned a lot.
One key point I learned was that
you have to deal with the emotional aspects before you try giving students equipment.
When a hard of hearing student first comes into my office, I spend at least
60 to 90 minutes just letting them talk. After hearing their story, I would
tell them, "Oh, that is very normal." That often shocks them because
many never have been told they were normal. Afterwards I would say, "Do
you want to try something that we have?" They were amazed by the FM systems.
All this might explain why I have 13 FM systems signed out and have people waiting
for five more I ordered. I had one woman hear her child cry for the first time
in my office when she put on a FM system. At first she was shy and did not think
she could make it through college. She graduated as a special education teacher
who was very excited and confident. I have many stories like that. I agree that
it is worthwhile to take time with them as well as give them a sense of what
is and what is not normal. Another helpful step is to introduce hard of hearing
students to each other on campus. The SHHH group in our town tends to be for
older people, so the young college students are not as interested. But I like
the idea of starting an SHHH chapter on campus.
Working with the faculty ahead of
time is helpful. At the beginning of each semester I inform professors who will
have hard of hearing students in their classes of the names of the interpreter
or note taker and what are their roles. My letter also explains how to use an
interpreter and make audiovisual presentations accessible to students with hearing
loss. I usually get responses from some inexperienced teachers who flip out
before they even get started. We talk and get them ready to handle the situation
when it comes.
Our outreach approach to hard of
hearing students may be unique. We have a welcome back week for all students
which centers around a cultural day, an employment day, and just a regular department
day, including ours. We have different tables for these topics. I find most
of the hard of hearing students come to our department table because they do
not look for disability services. Not considering themselves disabled, most
do not go to the DSS program, but will come to our service unit for students
with hearing loss. At that point I say, "Yes, you are qualified because
you do not have to be deaf to get services." I think many hard of hearing
students feel their hearing loss is insufficient to request services. I do not
have any criteria, such as a cutoff point on an audiogram, but if a student
identifies a problem in the classroom, we will work with them.
John: Thank you very much, Bonnie.
Come on up. More ideas, comments, please.
Audience: Thank you. My name is Mitch
Turbin and I recently started working with the Department of Veteran's Affairs
National Research Center in Portland, Oregon. I have a lifelong progressive
hearing and vision loss. I began using hearing aids when I was in college. I
clearly remember in high school and college I became aware of the hearing problem.
Because it was tremendously scary, I pushed it back, not wanting to acknowledge
it. That represents denial and fear.
One approach I used when counseling
people with disabilities was to encourage them to form a positive self-concept.
This is particularly important to young college students developing their self-identity.
It is stigmatizing when someone says you have a severe hearing loss or you see
your audiogram. These experiences imply that you are defective and people want
to avoid that idea. I have seen some well-intentioned professionals introduce
young hard of hearing students to a deaf person or students with hearing and
vision impairments to a deaf-blind person. When these professionals hear that
the young students run away they say, "Oh, they are in denial." In
my opinion, the professionals are really in denial by denying normal human reactions.
I have seen hard of hearing kids in tears after they encounter deaf people.
That is a normal healthy reaction. The problem is the professionals who insist
that hard of hearing persons are in denial because they do not want to be associated
with deafness.
Conversely, as you know, deaf people
can be frightened to meet a deaf-blind person because they fear loss of their
vision. We need to really take a look at the healthiness of being afraid of
losing a primary sense. Frankly, do not resist the resistance because that is
a very healthy, positive life energy that indicates a person is preserving their
best possible self-concept. One technique in my "tool box" as a counselor
was never use the term hearing loss if avoidable. When I had to talk about the
hearing loss, I would say things like. "Well, you do not have the greatest
ears." It is scary, upsetting, and annoying when people say that you have
a hearing problem you would prefer not to think about the rest of your life.
But you can deal with that if you use the right frame of thinking.
I also advocate support groups for
same-aged peers with disabilities. Several years after I obtained my first hearing
aid, I joined a young adult support group in New York City that shifted my perspective
on life. Such groups provide opportunities so we could talk about problems,
then more important, go out and have fun afterwards.
John: Thanks Mitch. Just one point:
President Franklin D Roosevelt said, "The only thing we have to fear is
fear itself." Think about that. Come on up.
Audience: As an older hard of hearing
student going to a community college I learned some very important lessons.
My instructor assigned us to work in groups, but to my mortification the three
other women in my group refused to work with me. Then I would sit with CART
and it is extremely difficult for people to come over to my side of the classroom
and sit beside me. Would a young hard of hearing student tell you something
like that? Who is going to tell you about an extremely embarrassing social moment?
Young students in denial would avoid admitting an experience almost unimaginable
to face. These are aspects where counselors need to be aware. DSS staff members
need to have mandatory training about the social discrimination and ignorance
about disabilities that especially happens in classrooms. These are completely
foreign ideas to many college instructors.
John: Thank you. We have time for
more.
Audience: I work at a new campus
that lacks a critical mass of students with hearing loss. I have one late-deafened
student in her early 20s desperately seeking other peers for a support group.
She went to the SHHH group, an example Bonnie had mentioned, and found those
people were not her peers. Is there a listserv, network, or other resource where
I can connect my student? She even put up signs in all of the classrooms saying,
"Did you hear dot, dot, dot? Neither did I. Contact me via e-mail."
No one has contacted her.
John: Have you heard of the Association
of Late-Deafened Adults?
Audience: Sure.
John: That is a resource. Contact
me and I can give you more information. Do others here have any answers for
her?
Audience: ALDA has a web site at
www.alda.org. Furthermore, it is difficult for the older and the younger folks
to come together, but it may be helpful if some younger folks realized that
these older folks were young too at one point and had to deal with the same
issues. They might consider them as mentors because we have a lot of older folks
with very germane experiences.
I urge you to look again at the mentor
concept. I favor the mentor approach over the self-help group because the latter
has problems. Whereas 28 million Americans have a hearing loss, SHHH nationally
has between 10,000 and 15,000 members. The chapters fluctuate in their memberships.
Sometimes between 5 and 30 people attend a meeting. If you contact the SHHH
office in Bethesda, Maryland (301-657-2248) they can probably identify somebody
as a mentor helpful to a student.
John: One other positive idea. If
we can persuade one hard of hearing person to accept their hearing loss and
become an advocate for other hard of hearing people then over a period of time
10 to 15 more hard of hearing people will accept their hearing loss, creating
a ripple effect. We have more time. Come on.
Audience: This presentation released
many of my sentiments. My name is Ben and I am a hard of hearing graduate student
at Western Oregon University. I was born this way and many of these topics have
touched my emotions and make me think about many encounters as a hard of hearing
individual. What stands out are the dynamics when I interact with groups of
hearing individuals and these are often stigmatizing. On the soccer team I tried
to be involved in social situations, but did not really understand what everybody
was saying. This led to bluffing and a constant loss of self-esteem. But this
process carries on throughout life. Even now at 29 years old I still unfortunately
repeat past behaviors. I am afraid to ask people to clarify what they said.
I play on a flag football team in Salem and the dynamics are the same as when
I was a teenager.
Even with adults it does not change.
These issues need to be confronted. For example, learning social skills. How
do we deal with the dynamics so as hard of hearing individuals we can be on
the same page as our hearing peers? Furthermore, we have a lot of fears generated
from having been put down, teased, or picked upon because we are perceived as
different due to our hearing loss. It is important to understand that we have
a lot of fears and so do many persons who hear. These issues need to be examined,
for example, during counseling because feelings run deep and we want to be seen
as normal, not different. The dilemma is we cannot change the fact that we are
different. These sentiments are deeply rooted and go on for a very long time.
Consequently, it takes much willingness and courage to accept that we are hard
of hearing and we cannot change the fact that we will always be different.
John: Thank you. I experienced a
lot of that myself. Any other wrap-up comments? Anyone want to say a closing
word? Thank you very much. We appreciate your feedback, listening, and sharing.
Audience: You have handouts?
John: The handouts include a communication
assessment used by Kentucky DVR, a list of references with web sites where you
can get information about hard of hearing people, and a handout from our Research
and Training Center. We have an article about hard of hearing college students.
If you want that or other related articles, contact me at the University of
Arkansas (jschroed@uark.edu).
Session participants made numerous comments that reinforced points from the presentation and broke new ground by providing original insights. Key themes from these comments and related issues are listed below:
Ries, P. W. (1994). Prevalence and
characteristics of persons with hearing loss: United States, 1990-91.
Vital and Health Statistics,10(188). Hyattsville, MD: National Center
for Health Statistics.
Schroedel. J., Kelley, C. & Conway, P. (2002). Where are all the hard of hearing students? Some tips for enhancing services by postsecondary and rehabilitation professionals. In K.B. Jursik (Ed.), PEPNet 2002: Diverse voices, one goal, 105-111.
Schroedel, J. G., Watson, D., &Ashmore, D.H. (2003). A National Research Agenda for the postsecondary education of deaf and hard of hearing students: A road map for the future. American Annals of the Deaf, 148(2),67-73
WROCC@WOU Home | WSRD Conference | WSRD Proceedings List