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The Invisible Disabilities Advocate® |
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Excerpts of this article appear in: Visible? Invisible? What's the Difference?
DISABLED? You Don't LOOK Disabled!
Unmasking Society's Depiction of People with Disabilities.
Copyright © 2004 The Invisible Disabilities Advocate
See Copyright Regulations Below.
IDA is NOT a legal authority, this article may NOT be used in ANY legal situations.
The Survival of the Fittest In a
generation of microwaves, fast food and fax machines, we are a society on the
run. We fill our days with 200 things to do, even though we only have time for
100. From the time we get up to the time we go to bed, we are running around at
work, at home and all over town. Between the stresses of our jobs, our family
and trying to fit in the pleasures we enjoy, we simply do not have time to sit
around. When we feel
a cold coming on, we cringe and yell, "I don't have TIME to get sick!"
After all, we are way to busy to even think about missing a moment lying in bed,
miserable. So, we call the doctor, begging for a prescription that will make it
all go away and fast! We may only be down for a few hours or maybe even a few
days, but we hate every moment of it! We whine and cry to those around us, moan
in pain and panic as we watch the clock wasting away our precious time. Soon, we are
back on our feet and back on track, forgetting how horrible it was to have to
put things aside, feel terrible and not able to do what we want to do. Yes, we
are a world that is accustomed to popping some pills or vitamins and we are back
in the race, feeling like our determination could defeat any viral army. After
all, we did not stay sick for long because we acted, had a positive attitude and
by gosh "we were not going to let any illness keep us down!" So, when we
are confronted with a person who has been sick for months or even years, we
naturally think, "hmmm... they must be lazy and unmotivated. They must not want
to work. They must not be doing what their doctor is telling them to
do." Otherwise, wouldn't they just take some medicine like you did and get
better, just like you did? What an
unpleasant person to be around! Who wants to spend time with someone who enjoys
being sick? Who wants to rub elbows with a person who does not have any goals or
aspirations? Who wants to be with someone who complains or just wants pity?
And, who wants to catch it? No! We want
to be in the company of people who have made something out of their lives;
people who have furthered their education, careers and families; people who are
involved in volunteer work, successful business owners, doctors and parents of
great kids. Not people who are limited, sick or do not fit the mold of what we
should all look like and make the money that we should all be making! Dr. Jeffrey
Boyd wrote: If
you turn on TV or open most popular magazines, you are confronted with healthy
and beautiful bodies of models under the age of thirty. That is what life is
supposed to be about, or so we are told. We are all supposed to enjoy our
bodies, exercise aerobically, be sexy and drive glamorous new cars and remain
under the age of thirty without showing any effects of age, gravity or disease.
Or at least that is the "hype" (Boyd, Tribute to an American Heroine,
2001). Society
tells us that we can measure a person's character by what they drive, the size
of the house they live in and the labels on their clothing. Many people often
talk about their friends as being "successful" or a “prominent
figure," as if their worth as a human is elevated when they have conquered
the latter to financial status. American society puts extreme value on image. How you look, what's your job title, who you know. In many ways life becomes a charade and the essence of who you are stays hidden from loved ones and yourself. In an interview with Lisa Lorden, Gregg Piburn noted: Often people are described by their profession; like in game or talk shows, people are introduced as, "this is Joe, a teacher from California." We are obsessed with what people “do” for a living. Sure it is interesting to find out what careers people are in; but it is sad when we define ourselves by our careers and not by our character (Lorden, 2000). We get so
wrapped up in "who we are" being defined by "what we do"
that it is no wonder why so many who become disabled also become insecure and
feel like their lives no longer have importance. Laura, a woman with
Interstitial Cystitis wrote, "I was a RN, but now am nothing, worthless and
useless, homebound and on Social Security" (IDA Guestbook, August, 2000).
How sad that our very beings, character and purpose in life are supposedly
depicted by what kind of work we are in and how successful we are at it! Now, not all
people with disabilities are unable to work; contrary to popular belief,
"more than three- quarters (77.4%) of Americans age 22 to 64 with
[non-severe] disabilities do not receive public assistance" (U.S.
Department of Commerce, Disabilities Affect One-Fifth of All Americans, 1997). For some,
their illness or impairment may mild, allowing them to continue their careers
and life goals; for many, with some limitations, medications and/or assistive
devices, they are able to continue their professions; for others, they may be
very ill or have great limitations, so it is all they can do to get through the
day, but they push themselves with great effort to stay employed. On the other
hand, only 26% of those who have severe disabilities are still able to work
(U.S. Department of Commerce, Disabilities Affect One-Fifth of All Americans,
1997). Yet, most of them are not quitting or giving up, because they want to!
Instead, they mourn their inability to fulfill their lifelong goals and careers. Frequently,
at a funeral you will hear of people describing their loved one as a
"productive member of society." But what if the person were not very
productive? What if the person were bedridden or physically disabled? How then
would we measure their character and worth as a human who takes up space on this
planet? Would their life be as important or impacting on others? Could they have
had a meaning or purpose, even though they were unable to work? There seems
to be no room here for people who cannot pull their own weight. People work hard
and they get angry to think that others are drawing taxpayers’ money for doing
nothing. They feel that, "if I have to work, so should you." But, they
do not realize that their being able to work is a privilege and
a blessing, not a curse. In fact, most people with disabilities
are not lazy;
they want to! People with
severe disabilities, who can no longer work, grieve the loss of being able to
excel at their talents and utilize their gifts. I do not know anyone who would choose
to be in pain, unable to do what gives them joy and have to fight for a measly
check that is about 10%-20% of what they would be making if they could work! Let us not
be like the general population of this ruthless world. We all need to realize
that every person is valuable, despite the fact they may not be physically able
to function normally, look like everyone else or be a prominent figure. What
kind of people are we if we are judging someone by their outward appearances,
ability to contribute and what they can "do", in order to measure
their value? Everyone has a gift, a purpose and the ability to impact other lives
despite their physical condition. Of course, if a person is healthy and able bodied, there is nothing wrong with expecting them to contribute, work, be a parent or even volunteer. Sitting around, doing nothing, expecting handouts and taking advantage of others when they are perfectly able to function is not upright, responsible, moral nor Biblical. Yes,
there are people in this world who try to cheat the system. Because they do not want
to work, they jump through a lot of hoops to get free money, free food and free
housing, all based on the lies of a lazy man. This lifestyle and attitude is
appalling and abhorrent. Let us be careful not to treat everyone with an
illness, injury or disability like they belong in this group of unethical,
indolent frauds! What is a Disability? When most people think of a disability, they picture in their minds a person with a visible, obvious impairment. Yet, Lisa Lorden, the Director of Communications for The National Fibromyalgia Awareness Campaign wrote, The word disability is defined in the dictionary as a disadvantage or deficiency, especially a physical or mental impairment that prevents or restricts normal achievement" or "something that hinders or incapacitates." However, our visually oriented society may not take the time to look beyond appearances. People tend to believe what they see; and if it can't be seen, it simply doesn't exist (Lorden, 2000, p.1). In
1991, it was determined that, "due to a variety of physical, mental, and
emotional conditions, an estimated 49 million non-institutionalized Americans
(about 1 in 5) have a disability. Of these persons, 24 million have a 'severe'
disability." (U.S. Dept. of Commerce, Americans With Disabilities, 1994). When we see
someone getting out of a car that is parked in the handicapped zone, we usually
look to make sure that person is actually disabled? Sometimes we even wait in
our cars to see if the person getting out is actually handicapped. After all,
those spaces are saved for someone who has a legitimate need to park there! And,
it is a good and noble thing to make sure nobody is cheating! Consequently,
when we see someone stepping out who is not using a cane or a chair, don't we
get angry! Sometimes we even get so upset that we go out of our way to give them
a dirty look or yell something at them! Hey, we do not want to see those spots
abused, because we know they are for people who actually need them! So, what if
someone who looked fine on the outside tried to tell us they needed to park
there? Wouldn’t we think they were lying or just lazy? What if they had a
handicapped placard or license plate? Wouldn't we assume they must have stolen
the card or borrowed the car? For goodness sakes, we can all tell who is
handicapped and who is not, it is OBVIOUS! ... Or, is it? The truth is, there are millions of people in this world who suffer from what I call, "invisible disabilities.” They may have a ruptured disk in their back, a spinal injury, brain injury or a disease that is attacking their cells, muscles and/or nervous system. They may have heart problems, lung problems, neurological disorders, severe pain and/or weakness. In other words, their debilitation is just as real, even though the damage lies under the skin. There
are many reasons why a person with an illness or injury must use a handicapped
parking space: they must stay out of the heat and/or cold; they may use an
electric cart once they get inside; walking through the lot, plus walking
through the store is just too much; it may be all they can do to pick up a few
items at the grocery store once in a great while and without that space they
could not make it; some cannot remember where they parked unless their car is
visible from the store; and others wear themselves out in the store so much that
they need their car to be close when they leave. In fact, without those spaces, thousands of people are not able to simply drop by the grocery store to pick up a few items. Lorden added, “When doing an errand or two would be an insurmountable task if not for the ability to park close-by, the blue tag I hang from my rear-view mirror allows me to function in ways I otherwise could not (Lorden, 2000, p. 1).” Sadly, many who suffer from disabling illnesses and injury are often harassed when they try to park in a space that is legally reserved for people in their condition. In fact, many with legitimate disabilities are so intimidated by onlookers, that they often have to give up even trying to run an errand, because they are afraid someone might yell at them. Lorden wrote about an experience she had when she parked in disabled spot: As I got out of the car, a woman approached me. "I hope you feel good about parking there," she said sarcastically. I was caught off guard, and responded dumbly, "What?" and looked at her, not sure if I had heard her correctly. "I hope you're happy," she said, "taking a space that's for the handicapped." My heart was beating furiously. "I do have a permit," I stammered. “Well," she said, disdain all over her face, "you look like you can walk fine to me—you're about as handicapped as I am! (Lorden, 2000, p. 1)." It
can be quite humiliating and frustrating to be a person who has a physical need
and legal right to park in handicapped when others stare, yell and even become
confrontational. Sara, a woman with Multiple Sclerosis added, "I had a
person chase me down in the parking lot of a grocery store telling me that I
should be ashamed for using a handicap parking space (I have a placard)..."
(IDA Guestbook, 2/2000). Unfortunately, this kind of reaction is all too common. These spaces are reserved for those who have many types of disabilities, whether they are visible or not to the onlooker. The fact of the matter is, if the person has a handicapped license plate or placard, it is not for you to judge if they have a need to be there, simply by they way they look on the outside. Therefore, let us be sensitive to those who are living with illnesses, injury and debilitating pain. On
the other hand, if you know for a fact that this person is abusing the spot, by
stealing or borrowing someone else's placard you can call the local sheriff's
department; they can be ticketed and the placard can be removed. If they do not
display a plate or placard at all and are just boldly misusing the parking
place, you can tell the store manager or security officer. There are
millions of people who suffer from illnesses, injury and pain that make us feel
like we are trying to climb a giant mountain with every step. To the average
person, some of us may not look like we have a disability, because society
thinks that "disabled" = a visibly noticeable impairment or visibly
noticeable need for a wheelchair, cane, crutches or walker. Nonetheless, we
often collapse in stores, parking lots and restrooms, just trying to get out and
pick up a few things that we need. In
1994-1995, the Survey of Income and Program Participation (SIPP) found that: ...20.6
percent of the population, about 54 million people, had some level of
disability; 9.9 percent or 26 million people had a severe disability….1.8
million used a wheelchair….5.2 million used a cane, crutches, or a walker…
(McNeil, Americans With Disabilities: 1994-95, 1997). Notably, 26
million persons were considered to have a severe disability; yet, only 7.0
million persons used a visible device for mobility; thus, 19 million people who
were defined as severely disabled, did not use a wheelchair, cane, crutches or
walkers. In other words, 74% of Americans with severe disabilities do not use
such devices. Therefore, a disability cannot be determined solely on whether or
not a person uses assistive equipment. Many experts
conclude the amount of people suffering from chronic illness is increasing,
because of the improvements in medicine in the past 2 centuries. The reason
being, with past medical care many people with various illnesses and injuries
would not have survived. Today, they are kept alive with drugs, surgeries and
treatments; yet, the improvements have not been sufficient to cure them or make
them well enough to live without symptoms. Jeffrey Boyd
expressed: The fundamental issue is that
contemporary medicine is often able to delay death but not restore health, so
that the more "breakthroughs of modern medicine" we have, the more
sick people we have. I say this without sarcasm and without cynicism (Boyd, Tribute to an American Heroine, 2001). Therefore, the amount of people suffering from debilitating illness and injury that is debilitating, is actually rising. This leaves millions of people disabled, even though they may not appear to have any visible restrictions at all. Who is Disabled? So what does
"disabled" mean? Let us be honest. The label, "disabled" is
quite confusing! We see special interest stories all of the time on television
about a disabled person who just finished a marathon or is on a ski team. They
are labeled as disabled, because they are no longer able to run on their own
legs. Yet, they do not like to be called DIS-abled, because they are still ABLE,
active and vital to do many things. They feel that even though they may
have a limitation or obstacle, they are certainly not unable or DIS-abled. Work
Disabled: The Social
Security Administration defines being disabled in regards to being unable to
work for at least one year, thus qualifying for disability benefits: Disability
under Social Security is based on your inability to work. We consider you
disabled under Social Security rules if you cannot do work that you did before
and we decide that you cannot adjust to other work because of your medical
condition(s) (Social Security, Disability Benefits, 2000 ). Because
Social Security makes payments to those who are work-disabled, their definition
falls under the guidelines of no longer being able to work. Thus, they do not
decide if someone has a disability, instead, if they are disabled or unable to
work. Having a
Disability (in the workplace): The Supreme
Court recently redefined the definition of having a disability in its
relationship to limitations in the workplace for the American Disabilities Act
and the Equal Employment Opportunity Commission: This
year, the Supreme Court held... that the determination of whether a person has
an ADA "disability" must take into consideration whether the person is
substantially limited in a major life activity when using a mitigating measure,
such as medication, a prosthesis, or a hearing aid. A person who experiences no
substantial limitation in any major life activity when using a mitigating
measure does not meet the ADA's first definition of "disability" (a
physical or mental impairment that substantially limits a major life activity) (EEOC,
Instructions..., 1999). One example
might be of a person who is legally blind without glasses, but not with glasses.
They would not be considered as having a disability under these regulations,
because the eyesight is no longer limiting with glasses. But, if even with
glasses, their eyesight substantially limits them, then they would be considered
to have a disability. Having a
Disability (in life, daily living and work): What
constitutes having a disability or a severe disability under the regulations of
SIPP, according to the Census Bureau: A
person is considered to have a disability if he or she has difficulty performing
certain functions (seeing, hearing, talking, walking, climbing stairs and
lifting and carrying), or has difficulty performing activities of daily living,
or has difficulty with certain social roles (doing school work for children,
working at a job and around the house for adults) (U.S. Department of Commerce,
Disabilities Affect One-Fifth of All Americans, 1997). Adults
aged 15 and over were classified as having a severe disability if they used a
wheelchair or had used another special aid for...were unable to perform one or
more functional activities or needed assistance with an ADL [Activities of Daily
Living] or IADL [Instrumental ADL], were prevented from working at a job or
doing housework, or had a selected condition including autism, cerebral palsy,
Alzheimer's disease, senility or dementia, or mental retardation (U.S.
Department of Commerce, Americans With Disabilities, 1994). Generally, if a person has a physical limitation that limits major life activities they have a disability (or impairment). Now, that disability may not keep them from being able to work or participate in various activities with equipment to help them, some limitations or accommodations. In
fact, according to the U.S. Department of Commerce,
"In the prime employable years of 21 to 64, for example, 82 percent of
people without a disability had a job or business compared with 77% of those
with a non-severe disability..." (U.S. Department of Commerce, Disabilities
Affect One-Fifth of All Americans, 1997). In other words, almost the same
percentages of people with mild to moderate disabilities are working as people
without disabilities. On
the other hand, only “26% of those with a severe disability” (U.S.
Department of Commerce, Disabilities Affect One-Fifth of All Americans, 1997)
are able to work, because their disability
impairs them to the point of not being able to work, even with helpful devices.
In all, a person can have a disability or difficulty performing certain
functions; but when their disability becomes so limiting that they are unable to
perform daily activities and/or work, then they are considered to be “disabled.” What are Visible and Invisible Disabilities? When most
people think of a disability, they picture in their minds a person with a
visible, obvious limitation. However, as there are many levels of disabilities,
there are also many types of disabilities. What most people do not realize is
that a person can have a hindrance that comes from the inside and may not even
be visible from the outside. This person
could have debilitating pain, fatigue, weakness and/or cognitive impairments
from a diseased spine, organs, nervous system and/or cells that keep them from
being able to function at a normal level. They may have an injury to their back,
head, legs or spine that limits their ability to work or even complete daily
tasks. Nonetheless, their bodies will not cooperate with their desires whether
or not others can see the damage on the outside. Visible
Disabilities: People with outward limitations like missing limbs,
paralysis or blindness often face the challenge of overcoming society's
assumptions about their disabilities. They are put into a category of being
disabled, but many times they are still able to work, raise children and
even participate in sports with a little assistance. Many become frustrated when
others assume they are helpless and cannot be productive. And, they are hurt
when they are treated like they are not just as valuable to others. Mostly, they
do not want to be defined by their DIS-abilities, but respected for their
dis-ABILITIES. Invisible
Disabilities: Limitations that are not so obvious from the
outside. These invisible limitations can stem from back, brain and spinal
injuries. They can also be the result of diseases, disorders, chronic infections
and birth defects. These injuries and illnesses manifest themselves with pain,
fatigue, dizziness, cognitive impairments, weakness and nausea ranging from mild
to severe to unbearable. People often assume that because someone with
invisible disabilities may look fine on the outside, that they must just be over
exaggerating, making excuses or lying about their situation. Sadly, this leaves
millions of people feeling isolated and alone in their suffering, as their loved
ones question the validity of their limitations. Visible
& Invisible Disabilities:
Some people fall under both categories; they have both obvious, visible
limitations that are mild to severe and invisible damage inside that
causes such debilitating symptoms. They may need to use an assistive device, but
it is not the chair, walker or cane keeping them from being as active as they
would like to be, it is the disabling symptoms.
In essence, for some it is the visible disabilities that hinder them, for
others it is the invisible ones and for some it is both. Below, is a chart of some *general similarities and dis-similarities between having a disability that is visible on the outside, versus one that is not visible from the outside. The purpose is to create a better understanding of the frustrations, concerns and desires of people living with a disability that is visible and/or invisible.
*This chart is a "generalization" and not meant to be a description of all cases and situations! The irony is
that it is not the visible impairments that are usually the culprit in someone
being disabled or unable to work. Yet, when our visible limitations do not seem
that bad, people cannot understand why we are impeded; but, it is the invisible
symptoms they cannot see that are keeping us from being able to function.
Therefore, throughout this book, when I refer to those with "invisible
disabilities," I am speaking of people who have debilitating symptoms,
whether or not they also have "visible" ones." When a
person has a visible limitation, we can see that they have impairments on the
outside thus, we believe them when they tell us they cannot perform a task. For
example, if a friend is in a cast, we do not question them when they tell us
they cannot go water-skiing. But, when a person is debilitated by symptoms that
are not visible, their integrity and intentions are often questioned when they
declare they cannot participate. People with
invisible disabilities are thankful and grateful for the invisibility of their
impairment; yet, it can also be a great burden to bear, with its unique set of
challenges. Because people cannot see
the limitations for themselves, they often show their disbelief with a hurtful
statement. This causes the person with the illness or injury to feel as if their
character and honesty is being judged. Sadly, this cuts deeply, straight to the
heart, when our virtue is being torn to shreds. Debbie, a
woman with APS pointed out: The
greatest barrier I run into every day is people who think I am trying to rob the
system or faking or whatever. I feel guilty when I have a rare good day and get
to go out and act like a normal person, cuz then I know folds are going,
‘See!! I told ya! She is fine!!’ I am seriously ill, but to look at me, you
would think I was young, healthy with everything going for me. I have often told
my husband, at least if I had something visible…folks would not seem to treat
me with such scorn and doubt (IDA E-Mail, 2001). Lisa Copen,
the founder of Rest Ministries, reasoned: He
or she may be young, and no one really believes that there are young ill people
in our country...The invisibility of most chronic conditions makes it even more
difficult to convince others that you really are in pain (Copen, Why Don't
Churches Understand Chronic Illness? pg 8). In all,
please do not make the mistake of making a visual judgment of what a person can
and cannot do and do. We should not judge one another by
outward appearance. Instead we should value each person
individually. Simply talk with them and find out what their talents and needs
are! Refusing to believe what you cannot see will only make others feel isolated
in their struggles and as if you think they are not honorable, respectable and
valuable to you. All too
often, a person with a visible impairment is presumed to be unable to complete a
task or participate in an activity; this is quite aggravating and hurtful to
that person, when they are perfectly able to contribute and partake in the deed. And,
it is just as insidious when a person explains their debilitating illness, yet
people refuse to believe them, because they look fine on the outside; the
disease may have eaten away at the brain, bones, spine, muscles, nerves, cells
and joints, but because others cannot see the damage for themselves, they reject
the validity of their limitations.
So, do not
assume that someone using a wheelchair cannot do something or that someone not
using a wheelchair can. Most of the time, it is not the wheelchair that keeps
people from working and enjoying activities; it is the pain, extreme fatigue,
neurological symptoms and cognitive impairment. Donna
Herrell, a patient’s advocate with Lyme Disease explained: What
most people do not understand is that most appearances are deceiving and do not
reflect the disability caused by symptoms or disease. If someone is overly thin
and looks under the weather, people may jump to the conclusion of AIDS. The
person could be naturally thin with a recent case of flu. Conversely, you can
look good and have cancer. We teach our kids not to judge people by their looks,
but as adults, we do so every day (Herrell, Don't Judge a Disability by Its
Cover, pg 1). In general, neither type of disabilities is
worse than the other, because each person's degree of limitations is varied,
despite their outer appearance. Some have visible disabilities, some have
invisible ones and others fall under both categories. For some it is the visible
disabilities that hinder them, for others it is the invisible ones and for
others it is mutual. Some people's symptoms/limitations are mild,
some are moderate and others are severe. Some are able to work full-time, some
part-time, some not at all and for others it is all they can do to make it to
doctors’ appointments, shower and/or come to church once a week. The key is to
listen, do not assume and take them at their word, despite
what you see on the outside. Be mindful to value each person individually, because they are of great value to God. Whether we have a visible or an invisible disability, we are all striving for respect, understanding, accessibility and most of all... belief. We do not want others to prejudge us and be unwilling to hear the truth; we want people to listen and treat us like valuable, contributing people with integrity, courage and strength. *****NOTE TO EDITORS AND SEMINAR LEADERS: You may use excerpts of this article if it is too long. Do not change content. Please send your edited copy for approval to IDA. You must include the below paragraph.
REFERENCES: Boyd, Dr. Jeffrey (2001, January). A Tribute to an American Heroine: Foreword (2002) to "But You LOOK Good: A Guide to Understanding and Encouraging People with Chronic, Debilitating Illness and Pain!" Copen, Lisa (1999, January). Why Don't Churches Understand Chronic Illness? ...And He Will Give You Rest Newsletter, Volume III, Issue 1, 7-9. Rest Ministries: www.restministries.org. EEOC, "Instructions for Field Offices: Analyzing ADA Charges After Supreme Court Decisions Addressing "Disability" and "Qualified," issued to the Equal Employment Opportunity Commission's field offices on July 26, 1999, www.eeoc.gov Herrell, Donna (2000, October). Don't Judge a Disability by its Cover. Self Published Article. Editor of Lyme Disease Information Resource: www.x-l.net/Lyme/health.html. Lorden, Lisa (2000, October). Privilege and Prejudice: Disabled Parking with an Invisible Illness. Self Published Article. Editor of Fibromyalgia Aware magazine and the National Fibromyalgia Awareness Campaign: http://Fmaware.org Lorden,
Lisa (2000, October). Living
with a Loved One with Chronic Illness: An Interview with Gregg Piburn. Self Published
Article. Lorden
is the
Editor
of Fibromyalgia Aware magazine and the National Fibromyalgia Awareness
Campaign: http://Fmaware.org.
Piburn
is the author of Beyond Chaos: One Man’s Journey Alongside His
Chronically Ill Wife. You may contact Gregg at: gpiburn@msn.com
or through his website: www.LeadersEdgeConsulting.com.
You may order Beyond Chaos from the Arthritis Foundation: 1-800-207-8633. IDA Guestbook: Comments made by readers of the IDA Website in a public format of a guestbook, 1998-2001. NIV, The NIV Study Bible, Zondervan Corporation, 1985. Social Security Administration (2000). Disability Benefits, Part 1- Introduction to Disability and Social Security. (Publication #05-10029). Washington, DC: U.S. Government Printing Office. U.S. Department of Commerce (1994). Bureau of the Census, Statistical Brief: Americans With Disabilities. (Publication SB/94-1). U.S. Department of Commerce (1997). Census Bureau: Current Population Reports. (Publication P70-61). Author: John McNeill U.S. Department of Commerce (1997). Bureau of the Census, Census Brief: Disabilities Affect One-Fifth of All Americans. (Publication CENBR/97-5). Copyright © 2004 The Invisible Disabilities Advocate
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