[Brl-monitor] The Braille Monitor, May 2016
Brian Buhrow
buhrow at lothlorien.nfbcal.org
Mon May 2 22:55:09 PDT 2016
BRAILLE MONITOR
Vol. 59, No. 5 May 2016
Gary Wunder, Editor
Distributed by email, in inkprint, in Braille, and on USB flash
drive, with the audio version being available in both Spanish and English
(see reverse side) by the
NATIONAL FEDERATION OF THE BLIND
Mark Riccobono, President
telephone: (410) 659-9314
email address: nfb at nfb.org
website address: http://www.nfb.org
NFBnet.org: http://www.nfbnet.org
NFB-NEWSLINE® information: (866) 504-7300
Like us on Facebook: Facebook.com/nationalfederationoftheblind
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Watch and share our videos: YouTube.com/NationsBlind
Letters to the President, address changes, subscription requests, and
orders for NFB literature should be sent to the national office. Articles
for the Monitor and letters to the editor may also be sent to the national
office or may be emailed to gwunder at nfb.org.
Monitor subscriptions cost the Federation about forty dollars per year.
Members are invited, and nonmembers are requested, to cover the
subscription cost. Donations should be made payable to National Federation
of the Blind and sent to:
National Federation of the Blind
200 East Wells Street at Jernigan Place
Baltimore, Maryland 21230-4998
THE NATIONAL FEDERATION OF THE BLIND KNOWS THAT BLINDNESS IS NOT THE
CHARACTERISTIC THAT DEFINES YOU OR YOUR FUTURE. EVERY DAY WE RAISE THE
EXPECTATIONS OF BLIND PEOPLE, BECAUSE LOW EXPECTATIONS CREATE OBSTACLES
BETWEEN BLIND PEOPLE AND OUR DREAMS. YOU CAN LIVE THE LIFE YOU WANT;
BLINDNESS IS NOT WHAT HOLDS YOU BACK. THE NATIONAL FEDERATION OF THE BLIND
IS NOT AN ORGANIZATION SPEAKING FOR THE BLIND-IT IS THE BLIND SPEAKING FOR
OURSELVES.
ISSN 0006-8829
© 2016 by the National Federation of the Blind
Each issue is recorded on a thumb drive (also called a memory stick
or USB flash drive). You can read this audio edition using a computer or a
National Library Service digital player. The NLS machine has two slots-the
familiar book-cartridge slot just above the retractable carrying handle and
a second slot located on the right side near the headphone jack. This
smaller slot is used to play thumb drives. Remove the protective rubber pad
covering this slot and insert the thumb drive. It will insert only in one
position. If you encounter resistance, flip the drive over and try again.
(Note: If the cartridge slot is not empty when you insert the thumb drive,
the digital player will ignore the thumb drive.) Once the thumb drive is
inserted, the player buttons will function as usual for reading digital
materials. If you remove the thumb drive to use the player for cartridges,
when you insert it again, reading should resume at the point you stopped.
You can transfer the recording of each issue from the thumb drive to
your computer or preserve it on the thumb drive. However, because thumb
drives can be used hundreds of times, we would appreciate their return in
order to stretch our funding. Please use the return envelope enclosed with
the drive when you return the device.
[PHOTO CAPTION: Palm-lined drive leading to front entrance to Rosen Shingle
Creek Resort]
Orlando Site of 2016 NFB Convention
The 2016 convention of the National Federation of the Blind will take
place in Orlando, Florida, June 30 to July 5, at the Rosen Shingle Creek
Resort, 9939 Universal Boulevard, Orlando, Florida 32819-9357. Make your
room reservation as soon as possible with the Shingle Creek staff only.
Call (866) 996-6338.
The 2016 room rates are singles and doubles, $83; and for triples and
quads, $89. In addition to the room rates there will be a tax, which at
present is 13.5 percent. No charge will be made for children under
seventeen in the room with parents as long as no extra bed is requested.
The hotel is accepting reservations now. A $95-per-room deposit is required
to make a reservation. Fifty percent of the deposit will be refunded if
notice is given to the hotel of a reservation cancellation before May 27,
2016. The other 50 percent is not refundable.
Rooms will be available on a first-come, first-served basis.
Reservations may be made before May 27, 2016, assuming that rooms are still
available. After that time the hotel will not hold our room block for the
convention. In other words, you should get your reservation in soon.
All Rosen Shingle Creek guestrooms feature amenities that include
plush Creek Sleeper beds, 40" flat screen TVs, complimentary high-speed
internet capabilities, in-room safes, coffee makers, mini-fridges, and hair
dryers. Guests can also enjoy a swimming pool, fitness center, and on-site
spa. The Rosen Shingle Creek Resort has a number of dining options,
including two award-winning restaurants, and twenty-four-hour-a-day room
service.
The schedule for the 2016 convention is:
Thursday, June 30 Seminar Day
Friday, July 1 Registration Day
Saturday, July 2 Board Meeting and Division Day
Sunday, July 3 Opening Session
Monday, July 4 Business Session
Tuesday, July 5 Banquet Day and Adjournment
Vol. 59, No. 5 May
2016
Contents
Diversity in the Disability Rights Movement: Working Together to Achieve
the Right to Live in the World
A Hands-On Guy Doing Hands-On Work in the Information Age
by Fred Wurtzel and Gary Wunder
Blinded Driver versus Blind Pedestrians
by Mike May
I Encouraged My Daughter to Be a Cowboy
by Peggy Chong
Transitions: A Conference for Parents and Teachers of Blind Children
by Kim Cunningham
Sharing a Room at Convention and How to Survive It with a Smile
by Grace Warn
If Braille Were Print
by Erin Jepsen
Fake Service Dogs: Problem or Propaganda?
by Marion Gwizdala
How to Pay for Your Hotel Stay in Orlando
by Tony Cobb
Recipes
Monitor Miniatures
[PHOTO CAPTION: President Riccobono welcomes participants to the 2016
Jacobus tenBroek Disability Law Symposium.]
[PHOTO CAPTION: Dr. Maurer moderates panel one of the Building Diversity in
the Disability Rights Movement plenary session with speakers Michelle
Garcia, Access Living of Metropolitan Chicago, and Rabia Belt, Stanford Law
School.]
[PHOTO CAPTION: Jernigan Institute Executive Director Anil Lewis speaks
about his experience as an African-American with a disability during the
Building Diversity in the Disability Rights Movement plenary session.]
[PHOTO CAPTION: Two hundred people from throughout the United States and
Canada attend the 2016 Jacobus tenBroek Disability Law Symposium.]
[PHOTO CAPTION: United States District Judge Myron H. Thompson keynotes the
2016 Jacobus tenBroek Disability Law Symposium.]
[PHOTO CAPTION: Dr. Maurer talks about the right to real work with Ohio
sheltered workshop plaintiffs Joe Magers and Mark Felton on the left, and
Regina Kline, US Department of Justice, and Matthew Dietz, Disability
Independence Group, on the right.]
Diversity in the Disability Rights Movement: Working Together to Achieve
the Right to Live in the World
For the ninth year the National Federation of the Blind demonstrated
its leadership role in the disability rights movement by hosting the
Jacobus tenBroek Disability Law Symposium March 31 to April 1, 2016, at the
National Federation of the Blind Jernigan Institute.
Two hundred disability rights lawyers, advocates, and law students
from throughout the United States and Canada attended. A broad range of
disability rights organizations, government agencies, and law schools were
represented, including: Disability Rights Texas, National Association of
the Deaf, Autistic Self Advocacy Network, US Department of Justice,
Paralyzed Veterans of America, The Arc of the United States, Stanford Law
School, National Black Disability Coalition, Asian and Pacific Islanders
with Disabilities of California, the University of Alabama School of Law,
and Syracuse University School of Law.
With a theme of "Diversity in the Disability Rights Movement: Working
Together to Achieve the Right to Live in the World," the focus of the 2016
tenBroek symposium was to examine the status of diversity in the disability
rights movement and explore ways to increase diversity so that all may
achieve Dr. tenBroek's vision of equality of opportunity. Plenary sessions
were moderated by Dr. Maurer and examined building diversity in the
disability rights movement, arrests and Title II of the ADA, international
progress on improving accessibility, ethical issues in the representation
of persons with disabilities, and the right to real work under Olmstead.
Workshop topics included disability and discrimination in the LGBT
community, how schools are using truancy laws to avoid their
responsibilities under the IDEA, voting rights, and application of the
Americans with Disabilities Act in a school-to-prison pipeline class
action. As the symposium keynote speaker, United States District Judge
Myron H. Thompson provided his thoughts on how the diversity of the
disability rights movement could be increased.
----------
[PHOTO CAPTION: George Wurtzel]
A Hands-On Guy Doing Hands-On Work in the Information Age
by Fred Wurtzel and Gary Wunder
From the Editor: Recently several people suggested that I interview
George Wurtzel whenever I talked about the need to address employment
opportunities for blind folks whose passion is not found in books, letters,
and working at a desk. One of the people who was most enthusiastic about
publicizing the off-the-beaten-path work that George Wurtzel has done is
none other than his brother Fred, known for being a longtime leader in the
National Federation of the Blind. Fred and I have decided to work jointly
to create this article, and it is in his voice that most of it will be
presented. Here is what Fred has to say, with an occasional sentence thrown
in by yours truly:
When I received Gary's notes on my brother, Gary wrote in his email
to me, "I might not want to hire George to work for me, but I would
certainly enjoy watching someone else do it, enjoying both his creativity
and their failed attempts to manage him." I am totally impressed with our
editor's ability to accurately portray the essence of a person in a
sentence. This is why he is the editor, and this is a great way to begin
this story.
What do you say about a broad-shouldered, six-foot-six person with a
huge bushy white beard, a full head of curly dark hair, who wears bib
overalls, has an engaging smile, and an easy infectious laugh? What if that
person was on the first American expedition to cross-country ski across
Lapland? What do you say about a person who has been an auto mechanic, a
bicycle mechanic, a commercial woodworker in three states, was a
partner/baker in a bakery, owned and rode Arabian horses in endurance
rides, makes props for the film industry, has had exhibits in modern art
museums, and teaches blind people to do woodworking? What do you say about
this person when you learn he was born with little eyesight and has been
totally blind since age nineteen? What do you say if the editor of the
Braille Monitor asks you to write about this person, and this person
happens to be your brother?
Dr. Joshua Miele of Smith-Kettlewell Eye Research Institute says, "He
is a bad-ass blind guy."
I feel a need to begin by explaining why I want to tell my brother's
story to the Braille Monitor. Among things I love are my brother and the
National Federation of the Blind. They share a fierce need to be
independent and, some people say, a reluctance to compromise, arguably to
their occasional disadvantage. I do not share the misgivings, but I
certainly observe the fierceness in our common need for independence.
George Wurtzel <http://www.gmwurtzel.com/> has always been an
adventurer, and it hasn't always been easy for him or those around him. The
presence of young George was always accompanied by some kind of sound. It
wasn't a radio or a record player; it was tapping, banging, chiseling,
sawing, scraping, or running feet. Motion is a signature word for George.
When he started riding a bicycle on the street, he could certainly
hear moving vehicles and could detect most of them that were stopped, but
he did have a problem with the postal worker. When we were children the
postman would deliver mail using a push cart with a bag strapped to it. He
and the cart didn't make much noise, and more than once my brother ran into
that cart, spilling its sorted contents on the street and leaving the
postman not only to reload and re-sort, but also to chase his newly freed
letters as they were taken by the wind.
The postman was a fine guy, but George's behavior did not go
unchallenged. The postman confronted my mother, openly questioning the
propriety of a blind kid riding a bike and suggesting that she bolt down
the cycle so George would no longer be a public menace. Mom's reply was
that locking up the bike would do no good since her son would only cut the
bolts. "This is just one of the problems when you have children raised by a
father who loves tools and has a child who is eager to learn to use them,"
George remembers her saying.
Now comes the age-old debate about nature and nurture. Growing up
with George, I know about his innate and irrepressible curiosity. Our
parents were hands-on folks, having grown up in farm families as most
people of their age did. They were skilled at things like cooking,
mechanics, baking, and foraging for wild berries, mushrooms, and asparagus.
One of their favorite pastimes was playing cards with family and friends.
We had an active and social environment in our early years.
We were expected to be outside as long as the sun was up and only
return indoors for food (bathroom breaks were optional, us being boys and
all and living in the countryside most of our childhood). In our earliest
years we lived on three acres in Thomas Township, Michigan. Our father's
excavating business occupied a lot of the three acres with dump trucks,
bulldozers, backhoes, dragline cranes, and innumerable other machines and
fun stuff to play on. Late afternoons were always interesting with the
crews returning, doing machine maintenance like greasing the crawler tracks
on the bulldozers and cranes, loading equipment onto the lowboy trailer to
prepare for the next day's work-and the banter, always the banter among the
crew. I learned lots of words that my teachers were not real impressed
with. During the day we had the run of the area with discarded underground
gasoline storage tanks that were maybe ten feet in diameter. What a
challenge to climb up on them and to hear and feel the really cool, deep
bass sound they make when struck with just the right object. In addition we
played on piles of used tires, catch basins, old abandoned trucks, and so
on. Have you ever seen a fire hydrant out of the ground? It was a paradise
for two curious boys.
Later on, after we moved to northern Michigan, and our father was
selling the kinds of equipment that he had owned as a contractor, we lived
on eighty acres with woods and fields. George and I bought a 1950 Dodge and
a 1953 Chrysler New Yorker for twenty or thirty dollars each. We proceeded
to take the body off the Chrysler and make a dune buggy out of it, and we
amused our friends by driving the Dodge through the fields at high rates of
speed. I had some vision then.
So, was it our genes that made George the adventurous entrepreneur,
or was it our parent's hands-off style of parenting, or was it the teachers
and adults we encountered? If you are a parent and reading this, I hope you
consider these questions. Forget what CNN or Crunchy Moms say; let your
kids run free to go on adventures. Everyone will be better off for it.
Although George appreciates academia, office jobs, and the so-called
information age in which we live, they have never been his cup of tea. He
is what most of us call a hands-on kind of guy, but with George the term is
not figurative but exceedingly literal. "I learn by doing, by touching, by
trying it myself. And, you know, I'm not alone in this. Lots of blind
people are just like me-they aren't suited to a desk job, but they are
ready for some good, honest, physical work."
As I said, our father was a small business owner during our very
young days. He owned an excavating business. Our kitchen was the office
where the workers met in the morning for the day's assignments. Talk of
machines, excavating, leveling, ditches, sewer lines to be installed-all
were part of our morning conversation at the breakfast table.
One time my father found out that one of his employees was taking the
long way home so he could add extra time to his paycheck. This was an
ongoing problem. When this employee came in one morning, George, only about
four years old, said, "My daddy is going to fire you." I guess this
prepared George for his future of managing employees in his various
businesses.
George's story is more than a blue collar versus white collar career
discussion. If one considers George's thought process, it transcends these
artificial definitions. Some people would say that George is eclectic;
others would say he has simple common sense born of his view of life. He is
a synthesizer. He creates new space and concepts out of thought and
creativity through tools, wood, flour, spices, and agriculture, all
contained in his mind and born out of a rich experiential base. What
bothers some people is that George refuses to make overly-simple blanket
assumptions about doctrinal issues. Chair caning, piano tuning, and door-to-
door sales have been stereotypic professions for blind people. Now the
pendulum has swung and many if not most counselors are guiding blind people
away from jobs that have traditionally been good paying. Even the Randolph-
Sheppard program, arguably one of the best employment programs for the
blind, has trouble getting counselors to refer potential businessmen to it
because it is one of those stereotypical blind guy jobs, even though some
blind people are making six-figure incomes. Dogmatism just isn't in
George's personality, unless it concerns the proper care and use of tools.
George does not frown on what some dismissively call the traditional
blind jobs. "If they create real American money, I like them. We should
argue when people say that the traditional blind jobs are the only ones
blind people can do, but we should never argue that, because we have done
them in the past, we shouldn't now see them as good, honorable, and
lucrative jobs."
One of the highest values of the National Federation of the Blind is
developing positive blind role models to demonstrate first-hand that
blindness is not what holds us back. As George says, "In years past schools
for the blind, at least the Michigan School for the Blind, had many blind
teachers. One of these served as a positive blind role model for me. Frank
Rosnoski taught many manual skills, including shoe repair and chair caning.
Another role model was Jesse Manly, who taught piano tuning. Many of us
made good money as students during evenings and weekends pursuing these
occupations. Frank Rosnoski could carve a chain from a single piece of wood
or a ball in a cage. He was an inspiration for me, showing me that a blind
person could not only be skilled at woodworking, but could earn a living
doing so. I had no skill or interest in piano tuning, though it paid very
well."
He continued, "Almost everyone would like to work for what they get.
They may take public money, may believe they deserve it because some
disability has befallen them, may tell themselves they are just getting
back what they or someone else has paid in, but no one feels as good about
taking money as they do about earning it.
"I have argued and fought against sheltered workshops for their
exploitation of the blind. They have long been a thorn in my side. But I am
not opposed to creating environments that pay blind people a real and
meaningful wage," George stated with passion evident in his voice.
When around George there is usually some kind of smell. It is the
fragrance of wood shavings or sawdust, the nose-twitching smell of some
kind of wood finish, the industrial odors of motor oil, WD-40 or gasoline.
If you are lucky enough to get in his kitchen, there will be wonderful
aromas of lovingly made brothy or creamy soups, the homey and delectable
smells of fresh bread baking, or the aromatic vapors of a pot of chili
simmering that promises a welcoming mealtime.
When George operated his countertop business, he provided lunch for
his employees. This was an economic move to keep his employees close by so
they returned on time to work, but it also was a way to share his
hospitality, his creative cooking skills, and his concern for others.
At age nineteen George started his own woodworking shop in Traverse
City, Michigan. "For the first two years I worked a full-time job from
eight to four at a bicycle and ski repair shop, which gave me money to
support my habit-woodworking. In doing that I became a bicycle technician,
fixing and repairing bicycles. This was a great job for me as a blind
person-put the bicycle up on a rack, figure out what was wrong, repair it,
and, sometimes at the peril of other people, I'd go riding to test my
work."
In this job George also learned to repair and mount ski bindings and
was good enough that he was invited to Las Vegas by Salomon, the seller of
running shoes, skis, and snowboarding equipment to work the national ski
show in its booth. "All of the emphasis on the safety of ski binding
equipment was driven by insurance companies who would get sued if an
accident could be traced to mechanical problems with the skis and their
bindings. In order for me to qualify, I had to take a test for
certification. The test involved looking at forty ski bindings and
determining which one of those forty was constructed correctly. In my group
of test takers, I was the only one to find the ski bindings that had no
problem. Lots of us found the thirty-nine that had problems, but I was the
only one to find the pair that was put together correctly. I think the
difference may be that most folks come in looking for problems, but I am an
optimist and tend to assume that things are okay until I find that they
aren't."
But back in Traverse City, having no money to pay rent for his part-
time business, George made a deal with the owner of a commercial office
building to use the unrentable space in the basement for his woodworking
shop. "For the right to use that space, I cleaned his bathrooms, cleaned
his hallways, and shoveled his snow. Because of my job and the building's
business hours, I had to do these office building jobs after five in the
evening. So, after working from eight to four in the bicycle shop and five
until nine or ten at the office building, I could work at making products
in the shop."
In about two years George bought his own building. The business was
open for a little over nine years, but after buying some new machinery and
adding to his original building, he was forced to close in 1982 when the
economy crashed and interest rates were sky-high at 20 percent. This meant
that the building industry came to a screeching halt. Losing the business
took almost everything George had. "You know you are poor when you can move
all of your belongings halfway across the country on a Greyhound bus."
What he left behind in Traverse City was a lot of classic woodwork in
a renovated historic county courthouse, beautifully made store fixtures in
many of Traverse City's gift shops and retail stores, Traverse City's
longest bar in a bowling alley, and beautiful furniture in people's homes
that they will pass on to their children. The city is richer than it was
when he came there and shared some of his passion and creativity to earn
his daily bread.
George moved to Hickory, North Carolina, to get a degree in furniture
production management from Catawba Valley Community College. "The reason
for going back to school was that my failure in Traverse City led to the
recognition that I needed more skills to be a successful business person,"
he said.
While at Catawba College he was hired for a temporary job assembling
upholstered couches for a furniture sample maker. North Carolina hosts the
headquarters of a number of major furniture companies. Companies have
samples made of their new designs to develop manufacturing systems and to
show to their customer buyers. It was a rush job and the owner needed
people who could use tools and knew about upholstered furniture.
"It surprised me that I actually got a job in North Carolina. The
owner hired six people and let five of them go at the end of the job; he
kept me. I was working with guys who were the best of the best. There were
no slackers. I am very good at setting up machines and am not satisfied
until they are perfect. Good enough is not good enough."
After learning his trade George went to work with people who were
creating a kitchen cabinet manufacturing plant. "The reason I was hired to
start a European-style cabinet factory is that there is no room for error
in European cabinet manufacturing. Precision is absolutely mandatory if the
cabinets are to come out right. There is no tolerance for slop. They owned
the building, and I was responsible for purchasing the machinery,
equipment, and tools. I set up the plant, trained the employees, and
started seeing production go out the door." But George does not always play
well with others, so he and his partners separated after a couple of years.
"One of the partners I got along with quite well, but the other partner and
I had a personality conflict, and, in addition, I wanted and thought I
deserved more money."
Soon George started another company of his own: SellAmerica. His
first engagement was with a company selling woodworking routers used for a
variety of woodworking applications, including putting finished edges on
tables, picture frames, and a multitude of other functions (nothing to do
with computers). "The business I contracted with wanted me to do marketing,
but my goal was to become an independent representative and work with
several companies selling other products to different businesses."
George's business morphed into something different when his mother
suggested he make a pretty box for his veteran father's interment flag. The
triangular box was attractive and could be displayed either open or closed.
She showed it to a neighbor who knew someone in the funeral home business.
He in turn showed it to the director of the funeral home, who said, "No one
is doing anything like this. This is a great idea." So George built some
prototypes, did some horse trading with a photographer, created a brochure,
and had about a hundred of them printed up and distributed them by hand and
by mail. His company began selling to local funeral homes. Within two years
he had 2,200 accounts coast to coast and was making about 17 percent on
every box he sold. After seeking and being awarded a contract from both the
army and the air force that he could not fulfill without the capital,
George began looking for an investor. In that search he found someone more
interested in purchasing the company than investing in it. "I won't say how
much I sold it for, but it allowed me to be a bum for a while. I believe it
was Mark Twain who said that 'money doesn't bring you happiness; it just
allows you to purchase the type of misery you most prefer.'" [Our sources
suggests it was actually English comic Spike Millligan.]
In North Carolina George had a lady friend who owned a bakery, so he
spent a couple of days each week working there-baking, making soup, and
building up the dessert business in local resorts. He spent a couple of
days working in his shop, and spent the rest of his time buying, raising,
training, and selling Arabian horses. Horses were a passion he had from
early childhood. In summers during high school he worked shoveling manure
for a local horse raiser in Traverse City, Michigan, in order to earn a
little money and mostly to be around horses. All of these part-time jobs he
did for three or four years before he decided he needed to go back to work.
George moved back to Lansing, Michigan, and started a business in an
abandoned storefront which he and some partners renovated. Its purpose was
designing, building, and selling kitchen cabinets. The business also
included a unit dedicated to countertop fabrication. "In true George
Wurtzel style, as my business grew, I decided I liked working by myself
more than I did with others, so we split the cabinet sales business off
from the countertop business, it being the one I took."
When anyone spends even a short amount of time with George, they will
come to associate him with flavors. It might be some warm whole wheat or
sourdough bread from the oven. He might offer a newly discovered craft
beer, a particular love of his. He has a signature Key lime pie. Simple
things like oatmeal and pancakes are always something special. Quality
fresh ingredients skillfully and creatively prepared with George's
attention to detail are hallmarks of his culinary presentations.
In the early 2000's when the economy, including the building and
remodeling sector, started to fall apart, George closed this business and
went to work as the executive director for Opportunities Unlimited for the
Blind, where he had been serving as a board member. His job was to run a
camp for blind children, and this he did for about five years, something of
a record for George.
During this time George brought the camp program to a new level of
excellence and learned that he liked teaching, and especially teaching
young blind people. In 2009 the camp won the prestigious Dr. Jacob Bolotin
Award for outstanding programs serving blind people. George acted on his
idea to combine art and cooking by designing and having the campers build
an outdoor clay oven for baking pizzas and bread. He hired Steve Handschu,
a nationally known blind artist, to oversee the design and construction of
a dragon-shaped oven later named Smorge. The campers were the primary
designers and builders under Steve's and George's oversight.
After working there George moved to Minneapolis, where he worked for
BLIND Incorporated. "I told my brother in an email that if I made it a
year, I'd be surprised, and I actually worked there for about two-and-a-
half years. I was really proud of myself, and besides, I really needed the
money. ... I'm a really creative person, and I really don't like being
pinned in. I can be a difficult employee because I'm really strong in my
opinions, and eventually those opinions have caused me or my employers to
say that it is time for me to move on. ... I've always wanted to have
complete control over my life and what I did, and I believe that everybody
should have that.
"My rub with much of rehab is that too often you have this thirty-
year-old person telling a forty-year-old that we're going to make you a
desk jockey, when that forty-year-old's skills, talents, and abilities are
in his hands and not in his academic ability. Luckily for me, when I was a
young person in rehab, we had two or three people known as job developers
whose jobs were industry-based. They didn't have fancy degrees, but they
knew how to go out to a factory, look at those jobs, show the factory how a
blind person could do them, and then teach the blind person what they
needed to know to get and hold a position there. Now you have
rehabilitation agencies in the country that are so focused on getting
people degrees that they know nothing about blue collar work. I meet too
many rehab workers who are just dumbfounded at what I do, and they say,
'How do you do what you do?' And I find myself asking, 'How can you do what
you do without knowing this?'
"When I started at the Michigan School for the Blind, they had just
quit raising chickens and teaching people how to take care of them and to
do some animal husbandry. I don't know when the last time was that you
priced free-range eggs, but they are $5 a dozen where I live, and it costs
about three cents per egg to feed a chicken. There's really good money in
that, but when I talk with people about this, they say, 'Do you really want
blind people to go back to raising chickens?' And I say, 'Yes! If the blind
person wants a career in agriculture and there is a likelihood there is
money to be made. Nearly everyone eats eggs in some form or other every
day.'
"Except for those times when I didn't want to work, I've had a job
since I was thirteen years old, either working for myself or working for
someone else. This is because I've developed a skillset that suits me well,
and I've learned how to sell my skillset to people. When you run your own
business, it's like having a job interview every week because you have to
go out and sell yourself, whether it's to a company or a potential
customer. You get a guy who wants to build five or six confectionary
stores, and you want to build all of his cabinetry for him. You have to go
out and convince him that you can build the product the way he wants it,
give him the quality that he wants, and do it in the timeframe that he
wants. You know, he looks at you as a blind person and says, 'I don't know
how the guy gets across the street, so can he do all this stuff for me?'"
This is something George has faced over and over again, but if you do
the job long enough in a city like Traverse City, Michigan, people start to
know you, your business starts to have a reputation, and then the company
becomes the symbol of what you do rather than the blind man who leaves
people with the question of whether or not he can do it. "It is hardest
when starting out and actually gets easier as you get bigger."
When we Americans wonder what the newest trend is, we look to
California. George is currently working for the San Francisco Lighthouse.
In an interview for this article Executive Director Bryan Bashin
<http://lighthouse-sf.org/blog/lighthouse-names-bryan-bashin-as-new-
executive-directorceo/> had a lot to say about the approach that
organization has with respect to rehabilitation of blind people. "There is
a need for outside-the-classroom informal learning, informal mentoring . .
. one of the great opportunities is what comes in nature. When I took the
job at the lighthouse, one of the reasons I did it was because the
lighthouse has owned for sixty-five years this amazing camp on 311 acres in
Napa with every fun thing and bit of infrastructure you can think of. So it
was my dream to bring a critical group of blindness-positive people
together and build that camp. That's what George is really at the center of-
-literally building that camp."
As George sees it, "My current job is the best retirement work one
could have expected. Bryan Bashin engaged in some rather unfair recruiting
practices. He called me on a day when it was minus eighteen in Minnesota
and seventy-two degrees in San Francisco. The line that clinched the offer
was, 'You could be living here.' Before my interview, I had met Bryan a
couple of times at NFB conventions, but he says that when he considered
what he wanted done, I was the only person on his radar. He has a grape-
crushing building that was built in the 1920s. It is a two-story building
with about 3,600 square feet, and he wants to convert it into a place where
we can teach blind people fine arts. The entire top floor has become a
woodworking shop, which contains all my tools, and the main floor of the
building is going to become a pottery studio, a general sculpture area, a
leather-working shop, and then we'll have a small gallery space for people
to display and sell their stuff if they so desire."
Once the building is done, the San Francisco Society for the Blind
will start teaching classes. "I can do some cursory instruction in pottery
and in leather working, but we will find people whose professions are to do
these things, and we will hire them as instructors. We have a stream of
people going through here; some of them want to be good craftsmen for their
own enjoyment, and others want to be good enough at the work to do it at a
professional level and make a living as an artist or an artisan."
One of the things George hopes to have is big gardens and to raise
the produce to feed the people who come during the summer. "We will teach
people to be gardeners because, here again, look at the price of organic
food in the stores. I've never met a vegetable yet that I couldn't
recognize by touch, so why aren't we doing more of this? It's crazy not to
be teaching these skills. Community-based farms make big money for the
people running them. People subscribe to your garden service, and you give
them the vegetables they want either by having them delivered or by having
them come to pick up their order. You don't even have to leave the farm,
and people will just bring you money."
Bashin commented about the Lighthouse, "I think as an organization
that is concerned about employment of the blind, we have to look at the
complete spectrum. We can't just be an organization that helps blind law
students. We can't be an organization to cream-off-the-top people from the
top universities. We have to provide different paths for people who want
different things. So, yes, we do help blind attorneys, but we also have
something we call employment emersion. There we work with individuals in a
very intense multi-month process to learn all the techniques that blind
people use to find jobs, secure jobs. Each job in employment emersion is
one-on-one, so a person who has a desire to work, let's say in radio
station advertising sales--we work with him or her to determine: how do you
find these jobs? What are they called? How do you approach this? What if
you have no experience? How do you disclose your disability? How do you
build a network of people? This is far more than just the regular processes
involved in pursuing job postings . . . There's a lot of work that goes
into getting people to feel that they deserve a place at the table: the
sense of teaching folks about our history and our collective mission and
the legitimacy and the normality of being blind."
George observes that, "Other fields cry out for blind people to
explore them. While at the bicycle store, I also learned to string tennis
rackets. What benefit is that? Well a man who works for one of the
William's sisters makes $300,000 stringing her rackets. Now you may not
make that much, but you can string a racket in twenty minutes."
We asked George an uncomfortable question. "So how did you avoid
falling into the trap of doing nothing and getting paid for it?"
"Well, for one thing I suffer from what the Germans and the Americans
call ants in your pants. I can't sit still-I just can't. The second part is
that I needed to have the money to do what my adventuresome side wanted to
do-bicycling, backpacking, canoeing. All of these are things that require
money. In 1974 I had a custom-made tandem bicycle built just for me. At the
time it cost me $1,000. That's at least a $7,000 purchase today and maybe
as much as $10,000 depending on what you want. Social Security does not
supply enough jingle in one's pockets for those kinds of things."
[PHOTO CAPTION: George teaches a student how to use a lathe.]
George did not set out to become a teacher. He said, "It wasn't until
I was the director at Camp Tuhsmeheta that I realized that I had a talent
and most important, a love of teaching woodworking. I work with every
student as an individual. I begin with teaching measuring using a click
rule and begin to form a picture of the student's skill set. My goal is to
help every student get to the level they want, whether it is a simple hobby
with simple tools or a full-blown shop making commercially marketable
goods. This is their choice, not mine. My role is to help them to fulfill
their dreams and needs."
I interviewed Dr. Joshua Miele (pronounced meelee)
<http://www.ski.org/users/joshua-miele> for this article. Miele is a blind
researcher at the Smith-Kettlewell Institute. The Smith-Kettlewell Eye
Research Institute is a non-profit, independent research institute
affiliated with and located adjacent to the California Pacific Medical
Center in San Francisco. Dr. Miele does work with systems for blind people
to gain access to complex data such as digital maps, tables, and other
digital images, and uses touch and speech to simplify access to complex
information so that blind people can do research, work, and learn in fields
dependent on mathematical and graphical information.
Dr. Miele recently participated in a workshop conducted at the newly
completed woodshop at the Enchanted Hills Camp facility. George has
personally done a lot of the work to renovate the old building, and he also
supervised the work of volunteers and tradespeople on the project. Miele's
view on careers for the blind is, "If you're not going to do it, it should
be because you don't want to do it, not because you can't. I can't stand
the idea of a brilliant physicist being forced to make brooms because
that's his only option, but I also can't stand the idea of somebody who
wants to work with her hands being forced into the knowledge market because
some rehab counselor says that's her only choice."
But Miele didn't just learn about woodworking at that event. He
learned much more from George, and, from the moment they met, as Miele puts
it, "Just as much as learning about the tools and the wood, I feel like I
learned about teaching from George. When I met him and we started talking,
I had this immediate sense that I was dealing with somebody who was at the
top of his game."
Jason "JJ" Meddaugh <http://www.atguys.com/store/> is a blind
entrepreneur who runs a company known as atguys.com. He attended the same
woodworking class as Dr. Miele. He has known George for many years, since
Jason was very young and a camper at Camp Tuhsmeheta. Jason is not likely
to have any inflated opinions of George, having seen him in action in many
settings and circumstances. "George's expectation for me was that, with
enough practice and attention to detail, I could certainly become as good
as him if I put my mind to it. And he has that expectation of all the
students. He doesn't dumb anything down. He'll certainly break down complex
concepts in a way that beginners understand if he needs to. The way he
taught things, he would help you figure out a way to do it.
"Whether it's when he's teaching a woodworking class or sitting
around a campfire telling stories about his travels or his life
experiences, you get the feeling that nothing can get in his way.
"As an entrepreneur who has started my own business, George was one
of the people I looked to, realizing I don't have to do things the way
other people tell me to do them. I can make up my own rules if I want, and
I will live and die by my own rules. George was one of the main people who
encouraged me and gave me the mindset that I could create my own business,
as opposed to just going to college and taking a job offered by someone
else."
George is kinesthetic. George is all about textures and shapes. The
way things feel in the hand or under the foot is an important factor in
George's work. Many of his artistic objects have unusual shapes, and most
include some highly finished surfaces. He often chooses woods that have
unusual grains and grain patterns which can be felt. Other times he chooses
very fine-grained woods with a satin finish. Curves are sensual and
evocative in his decorative objects. Whether it is a utilitarian piece of
furniture or a whimsical wine stopper, the tactile experience will always
exquisitely fit the application.
I remember going with my father to the hospital in June of 1954 to
pick up our mom and my new brother. I remember little trinkets mom brought
from the hospital. Since then, I have known my brother's propensities, his
quirks, and the unique person he is. He has an artistic streak. I am sure
there are books about what compels someone to do art. Art is not as
concrete as most of George's other endeavors. Not all his art pieces are
functional, though all his functional pieces are certainly artistic.
One student of George's was an artist named Emilie Gossiaux
<http://www.emiliegossiaux.com/>. Emilie has a hearing loss and was struck
by a truck while cycling. She lost all her eyesight in the accident. She
chose to attend BLIND Inc. to learn to live as a blind person while George
was teaching there.
Emilee's artistic skills were well-developed before her accident. Now
she needed to learn how to express herself in new ways or express herself
in her former ways using alternative skills of blindness. It was up to
George, along with the BLIND Inc. staff, to help Emilee figure out that she
could do art as a blind person and then help her develop new techniques.
Here is what Emilee said in a speech about George's teaching, "This
man has given me a priceless gift and showed me a valuable lesson: That
sight has nothing to do with making art. It's the vision within that
matters."
In an interview for this article, Emilie said, "When I went blind in
2010, I was very uncertain whether or not I could still be an artist or
continue going to the art college, Cooper Union. Even though everyone I
knew--my family, friends, and my doctors--were all very supportive and
believed that I could still be an artist, I didn't believe in myself. So, I
started to consider doing other things and dropping out of art school
because I was very overwhelmed by everything and too scared to go back to
school.
"When I met George in Minneapolis at BLIND Inc., I was so amazed and
inspired by him and the work he does. We instantly became friends because I
felt like we had a lot in common, and I appreciated everything I learned
from him. He really believed in me, and knowing a person like George exists
in the world gave me the courage to keep going to art school and making
art. He showed me the skills to make objects and sculptures with my hands
again, using chisels and a mallet for woodcarving. He also challenged me to
think creatively and helped me make my visions for art in my head become
physical and real. For that I am eternally grateful for George and his
continued support. Thanks to George, I went back to Cooper Union and
graduated with a bachelor of fine arts, and now I have a studio in New York
City where I make sculptures and have shows. I hope one day I can do the
same for another person, what George did for me."
Professionals, laypersons, and a lot of us blind folks often talk
about careers that are good for blind people. From chair caning and piano
tuning to psychology and social work, all perfectly wonderful professions
in and of themselves, blind people have been herded into them because they
are a simple fix, lots of blind people do them, and this makes work easy
for teachers, guidance counselors, and for blind people who are unsure of
themselves.
Many people associate the roots of the NFB with Iowa. This is for
good reason: Dr. Jernigan put into practice Federation philosophy there and
proved that our ideas could produce superior results. Our deep roots go to
California and even the Bay Area where Smith-Kettlewell and the San
Francisco Lighthouse are. Dr. tenBroek and before him, a STEM person, math
Professor Newel Perry, studied and developed the positive philosophy of
blindness that is now one of the core principles of the National Federation
of the Blind. The Bay Area seems to be a place for upstarts and sages to
mix, mingle, and create change. Given the seventy-five years of our
organization and the forty years preceding it, the Bay Area has certainly
led a revolution in the field of rehabilitation for blind people. It hasn't
stopped. With Bryan Bashin, Dr. Joshua Miele, George, and a lot of other
rule breakers and entrepreneurs, the future is very bright indeed. George
is living the life he wants and showing us all a path of our own. Whether
high tech or primitive crafts, we can all see that it is not blindness that
holds us back.
----------
[PHOTO CAPTION: Mike May]
Blinded Driver versus Blind Pedestrians
by Mike May
From the Editor: One of the most significant freedoms blind people
have gained since the development of techniques to use the long white cane
and legislation allowing the use of guide dogs in public places is the
ability to travel where we want, when we want, with some assurance of
safety. Good training is always essential, but environmental issues are
also important, and so too is a recognition on the part of the driving
public that they command machines that weigh much more than the pedestrians
who share the streets.
Mike May and his wife Gena are no strangers to travel. Mike is the founder
and chief executive officer of Sendero Group, a company that develops and
markets global positioning systems used by the blind. He also works with
the National Federation of the Blind on our project to coordinate indoor
navigational activities. Here is what he has to say about a recent accident
involving him and his wife:
On February 23, at 7:45 a.m., my wife Gena Harper and I, both blind,
were clipped by a vehicle while we were walking in the crosswalk north on E
Street. The Toyota Highlander was heading south on E Street. It stopped at
the stop sign and then made a left turn heading east on Fourth Street. The
driver turned behind us, running over my back heel and knocking Gena's
Seeing Eye dog, Yulie, forward. My dog, Tank, was guiding well in front and
suffered no physical injury, nor did Gen. I doubt it would have made a
difference even if we could see unless we might have been able to dive out
of the way at the last second.
The driver pulled over as did a passer-by who saw the incident. The
driver explained that the sun was in her eyes, and she never saw us as
evidenced by the fact she did not put on her brakes. Gena and I were
halfway across the intersection when we were struck. The first part of that
intersection was shaded by a building. We were in that shaded area when she
started her turn and then hit us.
It would take about three seconds from the driver's stopped position
to complete the ninety-degree turn. It is astounding that in that three
seconds she never saw two people and two dogs in clear view. The obvious
question arises, if you are totally blinded by the sun, why would you take
the gamble to hurdle a 5,600 pound vehicle at ten to fifteen miles per hour
through the intersection?
I suffered a bruised and scraped heel. Yulie was not physically hurt
but was quite scared. Everyone was shaken including the driver. Hopefully
she learned a frightening lesson not to drive when blinded by the sun.
Another lesson came out of this incident; don't expect 911 to know
your exact location when you call from a cell phone. 911 calls from a cell
phone may be routed to one of three entities when you are calling from
Davis, and they cannot identify your address the way they would if you
called from a landline. Thinking the operator would know I was in Davis, I
said I was at Fourth and E. The CHP [California Highway Patrol] operator
who got the call transferred me to the Sacramento Police Department. I gave
my location again and included Davis in the address at which point I was
transferred to the Davis PD and gave my address and story for a third time.
It took four minutes before this round-about emergency call was finished.
Good thing the situation wasn't life threatening.
The 911 system was set up in the '70s based on landline communication
with one carrier. Seventy percent of 911 calls today are from cell phones
from multiple carriers. 911 operators do not get your GPS position, nor can
they receive texts. The FCC reports that 10,000 people lose their lives
each year related to poor 911 cell phone positioning.
In retrospect I should have used the BlueLight emergency app instead
of calling 911 directly on my phone. This would have alerted my emergency
contacts by text of my location while also calling 911.
In some communities like Oakland your BlueLight call is routed to
local emergency services based on your exact position. Perhaps enhanced
BlueLight service will come to Davis sooner than later as a lifesaving
emergency app. For now I have programmed the Davis PD direct emergency
number into my iPhone.
Gena and I and our guide dogs missed being seriously injured by
inches. There are so many pedestrians and cyclists in Davis that this
incident should serve as a reminder for everyone to exercise more cautious
judgement when driving, especially when the sun is in your eyes. Remember
too if you are driving a hybrid or electric vehicle that they are very
quiet at slow speeds, like starting up at an intersection or in a parking
lot. Blind and sighted people alike have been struck by these quiet cars.
The driver who hit us was not driving a quiet car, but she was at a full
stop when we stepped off the curb. Our Seeing Eye dogs were doing their
jobs, and we clearly had the right of way. I don't believe that being
blinded by the sun or any other excuse justifies hitting pedestrians in a
crosswalk.
----------
[PHOTO CAPTION: Peggy Chong with her daughter Tina (left)]
I Encouraged My Daughter to Be a Cowboy
by Peggy Chong
From the Editor: The following article is reprinted with gratitude
from the Winter 2016 edition of Future Reflections. Here is how it was
introduced by Editor Deborah Kent Stein:
Peggy Chong is a longtime Federationist who has developed a deep
interest in the lives of everyday blind people from the past. She says she
draws renewed energy for her Federation activities by looking back at the
struggles and triumphs of blind people who came before us:
When my daughter was six, she told me that when she grew up she
wanted to be a cowboy, a nun, and a mommy. As most moms would, I told her
that was great!
My daughter is sighted. The adults around her assumed that, when she
reached the age to think seriously about her career options, she would
realize on her own that being a cowboy, a nun, and a mommy all at once
might present some problems. As it turned out, I did not have to explain
why her career could not be all of the above. She is now a successful
computer guru, like her dad.
Something different tends to happen when a blind child announces her
future occupation. If a blind girl says to her parents, "I want to be a bus
driver when I grow up," Mom or Dad is likely to say, "That sounds nice,
dear. But you know, you can't get a driver's license. You're blind."
How is a parent to talk with a blind child about careers? What jobs
have blind people chosen throughout history? In what careers can a blind
person succeed today?
Over the past several years, I have researched the lives of blind men
and women in the United States from the 1700s through the early years of
the twentieth century. I have gathered some surprising information.
Newspaper Reporters and Editors
"But newspaper work is all print oriented!" you might say.
Francis O. Edgecomb was born in 1864 to a well-to-do family, and he
obtained a college education. He and his family had great hopes for his
future. In 1890 Edgecomb became a banker in Rulo, Nebraska. He rose
quickly, not only in his local bank, but in the financial community in
general. Then, in 1892, Francis Edgecomb was injured while he was out
hunting prairie chickens. A friend shot him accidentally, and as a result
he lost his sight.
Not knowing any other blind people, Edgecomb assumed that he could no
longer run the bank. Because he had a wife and small children to support,
he determined to find another line of work. The bank owned and operated the
local newspaper. Edgecomb decided that he would become a newspaper editor.
At first Edgecomb performed all the tasks necessary to run the paper.
Through the bank he had easy access to the news of the town. He also had a
network of connections with businesses that would take out ads. He was so
successful that he and his friends began to buy up other newspapers in the
area. Soon Edgecomb was operating his own paper, the Geneva Signal.
Francis Edgecomb did not have training in the skills of blindness.
However, he had a supportive family and the drive to succeed. If one
strategy did not work, he tried another. He had a thirst to learn. Though
he could not read print himself, he found people who could read to him.
When he could not travel to the news, he found creative ways to make the
news come to him. Today his great-grandson runs the Geneva Signal and all
the other papers that Edgecomb purchased.
Was Francis Edgecomb an exception? Well, then there was William
Cramer, who was deaf as well as blind. For seventy years he owned and
operated a newspaper that is now the Wisconsin Journal. Robert Gust and his
wife, who was also blind, ran one of the local newspapers in the new and
growing town of Cyrus, Minnesota, for about ten years in the 1920s. Max
Frost edited and ran the Santa Fe New Mexican for more than ten years,
until his retirement in 1908. B. F. Ervine edited The Oregon Journal for
many years and was a powerful political figure. Franklyn Bruce Smith worked
for more than fifty years in the Saginaw, Michigan, area as a salesman,
reporter, editor, and finally as the owner of a newspaper.
Thomas Muir of Plainfield, New Jersey, became blind as a young man
while working as a reporter for a New York paper. He did not think that
blindness would interfere with his career. In fact, he went on to become
the editor of the Plainfield Record in New Jersey. He was elected to the
state house of representatives and served for twenty-six years.
We do not have space to look at the lives and accomplishments of the
many other blind newspapermen and women I have found. Here is a brief list:
Siver Serumgard, North Dakota; Raymond Blackmer, Minnesota; Edwin Frost,
Wisconsin; and Henry Belk, North Carolina. The list goes on.
Electrician
Not so shocking!
Thomas Nicholson was the first blind electrician I ran across. Born
in 1877, he lived in San Francisco. By the time he was fourteen, he and his
sister were on their own. Nicholson became a messenger for the local phone
company, where his sister also worked. He asked a lot of questions, wanting
to learn all he could about the new invention, the telephone. At the age of
seventeen he was blinded when a piece of copper wire broke off and struck
him in the eye.
After he healed from his injury, Nicholson received blindness
training, probably at the Home for the Adult Blind in Oakland. He learned
to be a piano tuner, but he went back to the phone company and asked to
become an electrician. It took a bit of convincing, but the company finally
hired Nicholson to build telephones. The job required considerable
knowledge of wiring and other electrical work.
Years later, also in California, a man named Jack Polston received
wide publicity. Polston was established as an electrician when he was
blinded in an explosion. He attended the blindness orientation center in
Oakland, where he studied under Kenneth Jernigan and regained his
confidence. After completing the program, he returned to his work as an
electrician. Polston later testified before the US Congress, demonstrating
that blind people can work successfully in the skilled trades.
Due to the labor shortage during World War II, many blind people
obtained good jobs. They proved their ability and did well. Nevertheless,
most of these blind workers were laid off when the sighted veterans came
home. Irwin Herschkowitz was one of the fortunate exceptions. He got his
first job as a radio mechanic during the war, and he kept his job with the
air force for many years. He also worked as a telephone repairman.
Other blind electricians include Pat Knowles of New Jersey, Mike
Mineweaser of Pennsylvania, and Joseph Remington of Michigan. I am sure
there are even more that I haven't found yet.
Barbers
Edward Max is the best documented blind barber I have discovered.
Born in New York, he moved to Michigan and established a successful
barbershop. When he was thirty-seven years old, he began to lose his sight
very rapidly. At first he tried to ignore his vision loss, but soon he
began to explore new ways to cut his clients' hair. His skills as a barber
had long been sought after by clients in Detroit. Now he modified those
skills so he could keep on shaving clients and cutting hair. He trained
himself to listen to the many different sounds in his shop. As the boss, he
managed the till. He could accurately charge a client for the services
rendered by the barbers who worked under him. I have found references to at
least four other blind barbers.
Medical Doctors
Yes, they made house calls.
We have all heard of Dr. Jacob Bolotin, who practiced medicine in
Chicago from 1912 until his death in 1924. Well, there was yet another
blind doctor in the Chicago area, Dr. Robert H. Babcock. Babcock became a
renowned heart specialist. Born in 1851 and blinded at age thirteen, he set
out to get a good education, beginning at a school for the blind in
Philadelphia. He found out that several blind people had become lawyers, so
for a time he studied law. However, his true love was medicine. He took the
necessary courses and then, with his strong personality, he got to know the
right people. He volunteered to serve in many capacities in medical
associations, doing all that needed to be done. He wrote many papers and
articles, and he addressed medical conferences around the United States.
Babcock kept in touch with blind people around the country, including
other blind doctors. He promoted opportunities for blind people and served
on the board of Outlook for the Blind, a publication of the American
Foundation for the Blind. His intimate knowledge of the workings of the
heart made him a sought-after consultant for other doctors.
Several blind people have worked in the field of chiropractic
medicine. Henry Schluntz, a blind chiropractor from Iowa, hired a driver
and visited all of the farms in the area. He provided home treatments to
anyone who was interested, sometimes offering his services free of charge.
In this way he built a loyal clientele, and eventually he became a
millionaire.
Traditional Fields
In the past, traditional fields for blind people included piano
tuning, chair caning, and weaving. Like Henry Schluntz, blind piano tuners
found creative ways to recruit and keep clients. Several blind piano tuners
in Minneapolis and St. Paul, Minnesota, rode bicycles around town to
transport their equipment, moving as fast as their sighted counterparts.
Following the wagon ruts, they rode straight down the streets.
This is only a short summary of the inventive, enterprising blind
workers whose stories I have uncovered in my research. I hope these
accounts show that the choice of a career for a blind person is wide open.
What matters is the person's drive and determination to do whatever the job
requires and to do it well. The individuals I have described built
successful and meaningful lives for themselves and their families. Some had
blindness training, and others did not. None of them had the gadgets that
make our lives so much easier today.
Back to the blind child who wants to be a bus driver, or an Uber
driver, or an airplane pilot: why not? The self-driving Google car is now
on the streets. Technology is advancing so fast that things we think are
impossible today may be taken for granted next month. Still, technology
doesn't have all the answers. Ingenuity is where it all begins.
----------
Leave a Legacy
For more than seventy-five years the National Federation of the Blind
has worked to transform the dreams of hundreds of thousands of blind people
into reality, and with your support we will continue to do so for decades
to come. We sincerely hope you will plan to be a part of our enduring
movement by adding the National Federation of the Blind as a partial
beneficiary in your will. A gift to the National Federation of the Blind in
your will is more than just a charitable, tax-deductible donation. It is a
way to join in the work to help blind people live the lives they want that
leaves a lasting imprint on the lives of thousands of blind children and
adults.
With your help, the NFB will continue to:
. Give blind children the gift of literacy through Braille;
. Promote the independent travel of the blind by providing free, long
white canes to blind people in need;
. Develop dynamic educational projects and programs that show blind
youth that science and math are within their reach;
. Deliver hundreds of accessible newspapers and magazines to provide
blind people the essential information necessary to be actively
involved in their communities;
. Offer aids and appliances that help seniors losing vision maintain
their independence; and
. Fund scholarship programs so that blind people can achieve their
dreams.
Plan to Leave a Legacy
Creating a will gives you the final say in what happens to your
possessions and is the only way to be sure that your remaining assets are
distributed according to your passions and beliefs. Many people fear
creating a will or believe it's not necessary until they are much older.
Others think that it's expensive and confusing. However, it is one of the
most important things you will do, and with new online legal programs it is
easier and cheaper than ever before. If you do decide to create or revise
your will, consider the National Federation of the Blind as a partial
beneficiary. Visit <www.nfb.org/planned-giving> or call (410) 659-9314,
extension 2371, for more information. Together with love, hope,
determination, and your support, we will continue to transform dreams into
reality.
----------
[PHOTO CAPTION: Kim Cunningham]
Transitions: A Conference for Parents and Teachers of Blind Children
by Kim Cunningham
From the Editor: At the annual convention of the National Federation
of the Blind, one division has so many programs and activities that one
could confidently say there is a convention within a convention for parents
of blind children. The agenda produced by the National Organization of
Parents of Blind Children sometimes runs to twenty pages in print, and the
breadth and depth of the activities is impressive. Here is what Kim
Cunningham, the president of the National Organization of Parents of Blind
Children, has to say:
I would like to invite all families, friends, and teachers of blind
and low-vision children to join us at the NFB National Convention from
Thursday, June 30, 2016, through Tuesday, July 5, 2016, in beautiful, sunny
Orlando, Florida. Every year the NOPBC holds our annual national conference
during the NFB National Convention. Our board has been working hard to
bring relevant, informative sessions and activities for families and
teachers of blind and low-vision children. We welcome all families of
children who are blind, low vision, with or without additional disabilities
to come together for a week full of fun and educational workshops. We
believe that all children can learn with the right support and training.
Please help us to share the news that blindness is not what holds our
children back! Together we can work to change what it means to be blind!
Ten years ago my daughter and I attended our first NFB National
Convention. Because my daughter was considered low vision by our school
district, I didn't think the NFB was for us. After all, no one ever called
her blind. But we were at a loss about my daughter's future and how she
would grow into an independent person. We were concerned about how she
would take her science classes in school. We were concerned about the
length of time it took to complete her work. We were concerned about her
identity and feeling like a broken person. We were concerned about her
struggle to read. We had no one to answer our questions and give us
direction.
This all changed when we attended the NFB National Convention along
with 2,000 other blind and low-vision people. Everyone was tapping their
canes and living their lives just like all the sighted people I knew. It
was an energizing atmosphere that I have never felt before. The Federation
embraced us and welcomed us into their family! I learned that low-vision
kids would benefit from all the tools "blind" kids used. The magic wand
ending up being a cane, and the secret word was Braille. I attended
workshops while my daughter learned about accessible science from a blind
scientist. She also learned about the benefits of the long white cane. The
exhibit hall was filled with technology, books, and independent living
items to choose from. If I had a question, someone was there to answer it.
This year our theme for the NOPBC Conference is "Transitions." As
parents we are constantly transitioning from one area to another. When our
children were born, we transitioned to becoming parents of blind and low-
vision babies. Our children transition from toddlers to elementary school,
to junior high, and then high school. Some kids transition from reading
print to reading Braille. And with each new transition, we find we are at a
crossroad of which way to turn. We hope that our workshops will give you
the tools to make educated decisions about the road you want to take.
This is what I want for all families to experience. I want you to
feel hopeful for a bright future for your child. I want you to learn the
skills that blind and low-vision children need to live their lives to the
fullest. I want you to know that we all have the same goal - a bright
future for our children.
Schedule at a Glance:
Thursday, June 30: Seminar Day, Opening Day of NOPBC National
Conference
Our day begins early-registration starts at 7:30 a.m., and our
opening general session is from 9:00 a.m. to 10:45 a.m. Please make sure
you arrive early enough to take advantage of this entire day of learning.
The highlights of our morning general session include a talk for kids
and parents by NFB President Mark Riccobono, a report from NOPBC President
Kim Cunningham, an address given by a mother who has raised two successful
blind daughters, and much more!
Throughout the rest of the morning and afternoon, parents will get to
choose to attend three workshops from a list of fifteen offered. Workshop
highlights include a look inside a model classroom for students from
elementary school through high school, a workshop especially for first-time
convention attendees, a session for parents of children with low vision,
and much more!
In the evening, relax with other parents of blind children at our
annual hospitality event. Great food, great friends, great fun.
Friday, July 1: NFB Registration Day, Meetings of Divisions and Committees
Morning NOPBC Cane Walks (two sessions)
Wondering if your child should use a cane? Curious about how a cane
works? Learn and experience the Structured Discovery
Method of travel at these special workshops. Parents,
teachers, blind/VI children, and siblings are
welcome.
Afternoon NOPBC Style Show
Watch our young blind and low-vision models strut their stuff on the
runway. Come enjoy the fashions and music and support
NOPBC. Tickets are $5 at the door.
Evening "Laps for Literacy" NOPBC Fundraiser
Swim and walk laps for literacy! Everyone is invited to attend and
help raise money and expectations at the same time!
Tickets are $5 individual, $10 for family, or raise
money at home for free entry!
Saturday, July 2: NFB Board Meeting, Meetings of Divisions and
Committees
Afternoon NOPBC Annual Meeting
Be sure to attend this important meeting featuring the 2016
Distinguished Educator of Blind Children; NFB
Writer's Division Youth Contest Winners, Parent
Power, Kid Power; NOPBC business, elections. Special
bonus: meeting attendees receive a priority entrance
ticket to the Braille Book Fair!
Early Evening NOPBC Braille Book Fair
A book lover's dream! Browse tables of Braille and print/Braille
books. Volunteers will box your books and deliver
them to the post office for Free Matter shipment to
your home. Books are free; donations
are encouraged to support our Braille programs.
Sunday, July 3: NFB Opening Day Session
Evening NOPBC Workshops and Children's Activities
Join the NOPBC for our popular IEP workshop. Learn how to adapt
mainstream board games for family fun. Children from
five to eighteen will be kept busy with various game
and craft activities.
Monday, July 4: NFB Business Session
NOPBC Brainstorming Session
Please come to share your knowledge and ideas with us. What did you
like at this convention? What resources would help
you stay connected throughout the year? What
workshops might you like to see us offer next year?
Be a part of this valuable conversation.
Tuesday, July 5: NFB Banquet Day and Adjournment
What about the Kids?
While parents are busy learning, so are children. NFB Camp offers
childcare for children six weeks through twelve years of age. Children will
engage in a variety of activities while in NFB Camp, many of which are run
by blind adults. Children must be preregistered for childcare. For more
information and to register, visit <https://nfb.org/nfb-camp-registration-
form>.
Children ages eleven to eighteen are invited to participate in Youth
Track activities throughout convention. These activities will include
advice on looking great and feeling great, hands-on science activities (led
by blind scientists), and more. Sighted siblings are welcome to attend
Youth Track.
Conference Registration Fees:
Preregister by June 21, 2016:
$30 for an individual adult
$50 for two or more related adults
Children and youth
After June 21, 2016:
$40 per individual adult
$70 for two or more adults
Children and youth
To register, and for a more detailed schedule of events, please visit:
<http://nopbc.org/2016convention>.
In addition to registering for the NOPBC annual conference, you will
also need to register for the National Federation of the Blind National
Convention in order to take advantage of our excellent room rates.
Registration information, as well as a variety of other convention
information, can be found at <https://nfb.org/convention>.
We hope to see many families of blind children in Orlando this year!
----------
Sharing a Room at Convention and How to Survive It with a Smile
by Grace Warn
From the Editor: Grace Warn lives in Missouri, and one of her
passions is visiting Disney World. She believes if there is a good business
model in the country, Disney is it, and that if a good proposal for
providing customer service arrives on the scene, Disney will probably be
the company bringing it.
This kind of loyalty translates into annual visits, and to cut down
on the expenses, she rooms with folks. She thought her advice about
roommates might translate well for those of us going to the 2016 national
convention. Here is what she says:
Going to convention, whether national or state, is an amazing
experience. But it often comes with another experience that isn't always so
amazing: sharing a hotel room. Whether to save money or because you're
traveling with children too young to be on their own, you're sharing a room
with more than just your significant other. And, no matter how much you
love your Federation friends or how well-behaved your children are in close
quarters for a few days, little frustrations can build up and drain some of
the joy from your time at convention. With a minimum of pre-trip planning
and almost no effort while there, you can keep the positive energy and
enthusiasm flowing during your time at convention.
The first step in this process is figuring out who's rooming with
whom. Identify a few simple characteristics of each roommate: who snores?
Who prefers to shower in the morning versus in the evening? Who are the
early birds, and who are the night owls? Who wakes up if a mouse sneezes,
and who can sleep through brass bands? Now take a look at the roommate list
again. Do you have a light sleeper in with three who snore like chainsaw
jugglers riding Harleys? Is there a lone night owl in a flock of early
birds? You may want to see if there's a way to juggle people to keep those
of similar tendencies together. But, if you can't, there are ways to keep
friction from these differences to a minimum:
. If you're a light sleeper, consider packing foam ear plugs or sleep
wearing in-ear headphones. Either of these will block a lot of the
sounds that might keep you awake. If you are more sensitive to light
than sound, think about a sleep mask so that others can turn on
bathroom lights without waking you.
. If you snore, think about ways to lower the volume of it. If allergies
make you snore more, make sure you are taking antihistamines and/or
decongestants. From personal experience I say try BreatheRight strips;
they can make a difference. Be aware of what sleep positions you may
want to avoid if you can.
. Early birds, lay out your clothes for the day the night before. That
way, you avoid making a lot of noise rummaging around in
drawers/suitcases, without feeling trapped by the need for quiet. If
you're the lone early riser, consider starting the coffee maker to
sweeten the inevitable wake-up for the rest of the room.
. Night owls, if you plan to stay out late socializing, be considerate
coming in. Keep your voice lower, and make sure to kick off your shoes
where no one will trip over them. Leave your pajamas in an easy-to-
find spot in the suitcase or drawer. Basically, try not to wake
everyone up, because everyone needs their sleep to make the most of
the short time you'll have at convention.
. Discuss amongst yourselves who prefers to shower when and for how
long. If everyone takes quick showers, it's no problem if each of you
in the room prefers to shower in the morning. Try to work out the
rotation for showering, and keep in mind the number of sinks, outlets,
and their accessibility while someone else showers so that everyone
has a chance to shave, style, and prep for the day without feeling
unduly rushed.
When you first get into the room, take a quick minute for one simple
discussion and define territory. You will be coexisting in a smaller amount
of space than you're used to, possibly with people you don't usually live
with. Setting up whose stuff goes where and then abiding by what is decided
can go a long way toward maintaining harmony. Decide as a group that Joe
will get the bottom drawer in the dresser, Sally and Eric each get half of
the next drawer up, etc. Try to base the division of territory on practical
considerations such as mobility--don't make the person with a bad back bend
to use the bottom drawer. Once each of you has staked out your claim,
respect the boundaries. Throwing something where you please is fine at
home, but it's not fine when it ends up being in a place allotted to one of
your roommates.
Each of you will have a place for your things, and it's a good idea
to have at least one area designated for communal use, such as one place
for all technology to sit safely as it recharges, etc. Remember that
bathroom counter space can be a scarce commodity and a great cause of
irritation before everyone has had their morning coffee. Taking along a
hanging shoe organizer designed to either hang in a closet or over the back
of a door can give you more places to sort your toiletries and leave a
clearer path to the sinks. If you have a guide dog, make sure roommates
know where the water bowl will be and decide whether it will be deployed
only at feeding time or at any time the dog might wish a drink.
Tuck the suitcases in the bottom of the closet or in a corner as out
of the way as possible, and make sure the main walkways remain clear.
Because a tiny little frustration like tripping over someone's suitcase
every time you try to go to the bathroom can become a major annoyance
faster than you would expect, it can poison the rest of the experience.
Depending on who you're rooming with and how long you're staying, a pop-up
mesh laundry basket can be pretty handy for that. It doesn't take up much
space in a suitcase, can be found in many dollar stores, and it can be
endlessly useful. It can be a place to corral dirty clothes, an easy-to-
carry transport for flyers or other merchandise for chapters/divisions, or
can be used as the designated location for the day's haul of souvenirs.
Speaking of things to bring along from home, in this day and age one
of the best items to pack on your trip is at least one power strip. These
days everyone has at least a cell phone. But there's also iPads, handheld
gaming consoles, notetakers, and many other electronics that require
regular recharging. Hotel rooms never have very many outlets, and sometimes
the outlet is in a less-than-accessible place, such as a corner behind a
small table and chair. The longer cord will bring the power strip up so
that everyone can reach to plug in items easily and give you that many more
outlets for everyone to share.
Sit down and consider exactly what your daily routine will involve,
and make sure everyone understands it. You may never have considered that
you have to decide which bed you're sleeping on based on the distance from
an outlet and availability of a flat surface for a CPAP machine, but what's
routine for you may not be for your roommate. That doesn't mean you can't
share a room, but it does mean that you need to make sure they're aware of
the requirements that are important and perhaps even critical for you.
Maybe you're a guide dog user; your roommate doesn't mind dogs--no problem,
right? Except when you were considering who snores in the room, you only
considered the humans, and your dog snores louder than you do. You and your
spouse are used to it; it's white noise that actually helps you sleep
better in unfamiliar places. To your roommate, that could be a week spent
wishing they'd packed earplugs and praying for a decent night's sleep. Or
maybe one roommate has a mild allergy to dog dander. For a couple of hours
during a chapter meeting or dinner with a friend, no problem; but sharing a
room for a week or so might mean they will need an antihistamine.
When you take just a few minutes to prevent the small disagreements
and frustrations, you prevent the larger arguments that can happen when the
little things add up with exhaustion and excitement to fuel them. While it
only takes a few quick minutes of discussion before you leave home, all of
these things become a lot harder to do once you're away at convention. What
you can tolerate for a day or two is a lot less tolerable on day five of a
convention, when you're tired and almost ready to head home.
----------
[PHOTO CAPTION: Abi Jepsen uses a BrailleNote Apex.]
If Braille Were Print
by Erin Jepsen
From the Editor: This article first appeared in Future Reflections,
Winter 2016. Following is the way it was introduced by Editor Deborah Kent
Stein:
Erin Jepsen is a low-vision homeschooling mother of four elementary-
age children, one blind, one low vision, and two sighted. She is passionate
about education for all kids and about teaching Braille. She and her family
live in Idaho.
Chatting with a friend today about a refreshable Braille display got
me thinking again about the absurdities that I've seen firsthand in my
daughter's classes. I've seen a silly attitude about Braille in both a
local public school and in a state virtual academy. I've also heard about
it from friends around the country who support one another online.
This problem comes, I think, from society's general perception that
Braille is complicated, difficult, and specialized. My daughter's TVIs work
endlessly to provide peer enrichment, to normalize Braille, to minimize
errors, and to add Braille in spaces within the school. I have tried to do
the same at home. Still, in spite of our best efforts, misperceptions
remain in attitudes about Braille and print.
To address some of these misperceptions for the non-Braille-reading
public, I want to try an experiment. I want to reframe some of the things
that students commonly hear when they are being taught Braille by imagining
that they are being said to a sighted print reader. I'd like to say these
things about the reading method that nearly everyone in my area uses:
English print.
The Challenges of Print
Imagine a typical first or second grader of average intelligence who
is learning to read. Keep in mind the material this learner will need to
read in eighth grade, in twelfth grade, in college, on the job, running a
household.
1. It makes sense that you're having a hard time with this. It is hard to
learn print.
As your hypothetical classroom teacher, I don't actually read this
print stuff. Your aide took a two-week training course, and we have a
reference chart here, but I really don't know how print works. It just
looks like a bunch of squiggles on the paper. It uses a round symbol for
both a zero and the letter o, and I'm not sure how to tell you which one is
which. There is also special shorthand stuff, like spelling with as w/, and
I don't know how to teach you all that.
Reading a book with writing on both sides of the page is hard for me.
It doesn't matter that it's normal for you; I say it's hard, because for
me, it is.
You have a special print teacher, and you'll see her for an hour or
two per week. Surely that's all the extra help you'll need.
2. I'm not aware of any techniques for reading print at a usable speed.
As far as I know, print readers only read one letter at a time. I
don't know any adults who read printed books. I saw someone do it once on
TV, and it looked like magic. I've heard that people who read print well
are either geniuses or flukes.
3. I'm sorry, but your book is loaded with typos.
The books we're giving you were transcribed by unqualified
volunteers, so there are at least two typos or misprints or misspelled
words for every thirty words. Just remember you're lucky to have print
books at all.
Every other kid in your class gets information from illustrations,
but we're going to skip those for you. They're cute, but probably they're
not important.
4. Technology, schmechnology!
First of all, nobody like you uses computers or knows how to type at
your age. You have plenty of time to learn that stuff later. Your job
someday probably won't require a computer. If it does, someone can give you
a quick training course. For now, we're going to print your books using a
dot-matrix printer. The school bought it in 1989 for our last print reader,
and they don't want to buy anything new.
We're going to get you a special display screen, though. It hooks up
to an iPad. It displays three words per screen. To get to the next screen,
you just press this little button over here. Cool, right?
5. Reading is overrated.
Nobody these days needs to read print or write with a pencil anyway.
You can just listen to audiobooks. It's a lot less work than reading, and
you can dictate anything you want to write. Technology is amazing these
days for people like you.
6. Nobody else reads the way you read.
In your school, no one besides you reads print. The teachers don't
read it. Your friends don't read it. There is no print displayed around the
halls, on the classroom walls, or in the lunchroom. Everybody reads, but
nobody reads English print. Nobody here can read what you write, and nobody
can write to you. Well, one of your friends learned to write to you. He
thinks print is a cool secret code.
There's a sign in print by the bathroom. You say it actually says
"Aathroox?"
We keep reminding you to be grateful for your printed books. The
other students have thousands of books in whatever they read, and no one
tells them to be grateful. But you should be grateful for the twelve books
that you have. Don't forget, people went to a lot of trouble to get them
for you.
You didn't do very well on the reading test last week. Your special
print teacher says it was written like this: %Bgoat %Bpig %Bhorse %Bduck. I
don't read print, so I don't know how it looks to you. I just grade your
test the best I can.
7. You will get your books late-always.
The school ordered the wrong reading book from the supplier, so your
book is the first-grade version, not the second-grade version. It's double-
spaced and uses easy vocabulary, but that's okay for you. Your life is
challenging enough already just learning to read print. You have to learn
all those curves and squiggles. The capital letters are different shapes,
and there are different fonts, too. You have to learn five different shapes
just for the letter A. That's hard! You don't need challenging vocabulary,
too.
You're falling behind your class? Don't worry. You have a lot on your
plate.
Your math book is still at the translator's shop. They say it will be
here in seven months. Everyone else is going to use a math book during the
next seven months, but I'll just read your math out loud to you.
Don't worry about learning to read numbers! When you get your math
book, you can read the numbers all you want! Be grateful you're getting a
math book in print.
8. Of course you're behind.
Kids like you, print readers of average intelligence, are always
behind-always.
In fact, you'll likely graduate from high school with about a fourth-
grade reading level. It can't be helped. It's okay, though, because kids
like you don't usually want to have a career. People who read print usually
get jobs sorting stuff at places like Goodwill. They pay you about $2 an
hour, but you won't notice that because of the math thing.
9. Print is just so cool!
Print looks cool! I see it here and there, like on elevators, and
it's just so neat. It's all swoopy and round, and I like to look at it.
People like you must be really special to read it. I can't believe you can
just walk up to a sign with words printed on it and-boom-read what it says.
Kids who read print are so beautiful and special. They open their
printed books and just go for it. Unbelievable!
10. I love the way you write print, too.
I've watched you write print. You make these marks on paper, and you
actually know what they say. That special tool you use, what's it called? A
pencil? It's so neat! It writes print, just like that!
I've seen you type on a special keyboard. It makes print, too, but it
disturbs the class with the clicking noise, so I wish you wouldn't use it.
You can use it someday when you're grown up, but not in class, okay? Just
tell one of the adults what you want to write, and we'll do it for you.
We'll even spell it right for you. You can practice spelling words on your
special spelling tests in your special writing room on Fridays.
The Print Reader's Experience
Dear Reader, what do you think? Do you think a kid is going to learn
to read in that atmosphere with those expectations and that sort of
encouragement? With that amount of support and practice?
Any TVI or homeschool mom who has tried to even things out for a
Braille reader knows exactly what I'm talking about.
What do print-reading kids typically experience in school? Let's take
a look.
1. Your teacher knows English.
If you are an English speaker, your teacher knows the language in
which you're reading and writing. She or he may even know Spanish or
Chinese or Dutch. She can use all the tools you are expected to use. If she
can't, she is not deemed qualified to teach.
2. Your teacher has books.
Books in print arrive in the classroom on time before the school year
begins. In nearly every school in the country, there are books for every
kid in the class. The books don't come late. The teacher reads them and
shows you how to read them. You have your own copy of each book you need.
The teacher sends books home with you for practice. If your parents know
English, they can read with you.
If there is a quote you want to read at the school assembly, you
don't have to write it out for yourself first because nobody else knows
how.
Your mom can read the story you wrote.
There might be one typo in your whole book-maybe-and everyone
complains about that one.
3. Everyone around you reads.
Your parents read. Your teacher reads. Your lunch lady reads. Your
big sister reads. They read the same way you read.
You are expected to learn to read.
You're told that it's normal to learn to read.
4. You get help when you need it.
If you're having trouble reading, adults act as if this is a problem.
You are expected to take extra classes, to practice, and to get help until
you can read well.
If you can't read, you are called illiterate. You are not given
audiobooks. You are taught to read (one hopes). If you don't know how to
write, you are expected to practice and learn to write correctly.
To get a good job that pays a decent wage, you have to be able to
read well, write well, and use computers. None of that is considered weird.
5. You learn current technology.
Your school has computers, and you learn to use them. You are taught
to type, and you are taught to read on a screen that displays thousands of
words at a time. You learn to scan for information, because your class
moves quickly.
6. You don't get a pass.
You are expected to keep up with the class. You don't get a free pass
not to keep up. You don't get to be lazy just because you're a print
reader. After all, reading print is normal. Everyone knows it's completely
doable, so why should you get to slough off?
You have all the materials you need and all the tools you need. You
can't make excuses, because you have the book you need for the assignment
and the pencil or the keyboard you need for your work. The teacher loaded
and set up the software your class uses, and he knows how to use it.
7. You know you'll use print all your life.
You fully expect that you will grow up, get a job, pay bills, and
become a contributing member of society. You know you will read and write
print as you do all of these things.
8. You read math.
If your teachers did not teach you to read and write the language of
printed math in school, your parents would throw a holy, hell-raising, fire-
breathing, sue-the-school-for-a-zillion-dollars tantrum. And the community
would support them. The school would be put up for review by the state.
If the teachers did not write math code, they would be fired. Period,
the end.
And no one would be surprised.
9. Nobody gushes over your reading ability.
Nobody tells you they saw some print on a box of BAND-AIDs and how
cool that is. Nobody tells you that you literally deserve a medal for
learning how to read-because everybody reads!
You don't give yourself pats on the back for using a computer at the
age of seventeen-everyone uses a computer at age seventeen!
Technology is normal for you.
10. You get all the information in class if you bother to pay attention.
A print reader of typical ability and average intelligence can get
all the information presented in the classroom. All the stuff on the
overhead; all the stuff in every book; all the stuff on the wall; all the
lunch menus; all the recess schedules; all the toy names.
And for all that, nobody thinks to be grateful.
A Few Last Comments about Braille
1. Reading Braille is normal for blind kids.
For blind and low-vision kids, Braille is the normal way to read. The
tools they use are normal. Reading is normal.
Having Braille on the elevator is normal.
2. Reading Braille is not hard.
Reading Braille by touch is not hard.
Many Braille readers are slow because of all the things listed above
that happened when they were learning it.
BRAILLE IS NOT HARD.
3. You can read Braille fast.
Good Braille readers can match print readers for speed. (Not many do
... see above.)
A good Braille reader can read ten thousand pages in a couple of
weeks. (Not many do ... see above.)
4. Braille is not becoming obsolete.
There are Braille displays for computers. There are Braille
embossers. There are Braille transcribers looking for work. There are more
Braille books than ever before. There are computers that transcribe books
more accurately than ever before.
There are blind people who need to be able to read.
There are people who need to read pill bottles and bills and recipes
and blog posts and books and textbooks and math books and elevator signs
and hallway signs and foreign languages and CD covers, and they need to see
how names are spelled.
There are deaf-blind people who use Braille to communicate
everything!
Since the early 1800s when Louis Braille brought the idea of a quick,
dot-based tactile method of reading and writing to his school in France,
there have been naysayers. In the beginning people said that Braille
wouldn't work. A separate code that sighted people couldn't read would
never be widely used.
Blind people used Braille anyway, because for the first time they
could write for themselves. Braille gave them voices. They could read what
they wrote.
When Braille came to America, it had naysayers. People said it was
too expensive to produce. They said there would never be enough books.
Blind people used Braille anyway. They made their own books. They
hired people to learn Braille and transcribe it. They raised funds.
As Braille enters the modern century, it has its naysayers. They say
it's becoming obsolete because of technology. They say it's clunky and
outdated.
Blind people keep using it anyway. We use Braille with technology. We
use it to learn to spell, and we use it to jot notes. We delight in the
thrill of opening a real, paper book and feeling the magical constellations
under our fingers as words and stories come to life.
5. Then what is the problem?
See if you can figure it out.
I can hear what you're thinking: "But Braille is different from
print."
Obviously Braille and print aren't the same, but they're not as
different as they seem to non-Braille readers. I read both. I read Braille
by touch. I read print (sometimes, under the right conditions).
"But I'm a blind person, and I don't read Braille well. I hardly read
it at all."
Why not? Is it lack of desire, lack of support, lack of
encouragement? (I'm not talking about people with multiple disabilities,
cognitive impairments, or nerve damage in their fingers.) If it's lack of
desire, I accept that. You may prefer to use audio, magnification, or other
reading methods. But if you dig deep into your reasons, and it's due only
to shame or lack of good instruction, I feel that those reasons should not
exist. We shouldn't be ashamed to read! We should not be left unsupported
when the rest of our peers have a way to read that fits their needs and
frees them for a life full of options.
"But I teach Braille, and what you describe is impossible."
Is it? See if you can do something about it. Please.
Because if blind and low-vision kids got the support their average
sighted counterparts get in learning to read, they would not face a 70
percent unemployment rate. There might still be workplace discrimination,
but I'd be willing to bet there would be more employed blind folks than
there are today!
I wanted to write "That would be amazing," but I realized that isn't
quite accurate. Amazing implies something above and beyond the norm. It
implies something unexpected. It implies something to be marveled at.
Reading isn't something to be marveled at; it's something that should be
expected, that should be normal. It's basic, like adequate clothing or
nutrition. It's the foundation of every other form of education.
So, instead of "amazing," I write: "It would finally be what kids
deserve. It would be just. It wouldn't level the playing field, but it
would be a start."
----------
[PHOTO CAPTION: Marion Gwizdala]
Fake Service Dogs: Problem or Propaganda?
by Marion Gwizdala
From the Editor: Marion Gwizdala is the president of the National
Association of Guide Dog Users (NAGDU). In this article he begins to
address the question of what constitutes a legitimate service dog and asks
whether greater regulation and standardization is warranted. Here is what
he says:
When I was younger and sighted, I enjoyed an activity called "connect
the dots." This involved a nondescript picture along with a set of numbered
dots. In this activity, one began with a dot numbered one, drew a line to
dot number two, and continued drawing lines between the consecutive
numbered dots as a picture evolved. I want to invite our readers to play a
little connect the dots with me as we examine what some refer to as "the
problem of fake service dogs."
Before we begin connecting the dots, I would like to say that the
labeling of this issue as one of fake service dogs is a misnomer. The dogs
are not the fakers, the people are. They are feigning a disability in order
to attempt to take advantage of the laws that permit disabled individuals
to be accompanied by a service dog. Secondly, I believe that calling this
issue a problem elevates it to the level of needing a solution. It is my
opinion that the real problem is not being created by those who
misrepresent themselves as disabled accompanied by a service dog; rather,
the issue is being presented as a problem by those who would benefit from
the solution. Now, let us connect the dots.
In the field of psychology there is a disorder once known as
Munchausen Syndrome by Proxy, now called, Fabricated or Induced Illness by
Carers (FIIC). This disorder refers to the deliberate production or
fabrication of physical or psychological symptoms in a child by a parent or
caregiver. The theory is that the caregiver gains attention from others
because of their child's illness or is acclaimed for their actions to
rescue the child from harm. In the business arena there is another term for
this known as "evil marketing." This latter term refers to a scheme in
which a company fabricates a problem that does not actually exist or
exaggerates a minor issue for which the company has a product or service to
solve the problem.
Over the past few years there have been numerous articles in the
media about the issue of fake service dogs. Though I know there are those
who mistakenly believe they can call their pet a service animal because
they feel better when their pet is with them, their intention is not
malicious. They may be misguided or misinformed, but they are not
malicious. Then there are those whose intent is less than honorable,
willfully misrepresenting their pet as a service animal in order to take
advantage of the civil rights provisions that allow disabled individuals to
be accompanied by a service dog. I believe these are the exceptions rather
than the rule. As we connect the dots, though, I am confident you will see
a very interesting picture beginning to evolve.
Upon a review of these articles, the one common denominator we find
is that nearly every piece has as its subject a service-animal user who has
experienced an out-of-control dog whose owner has asserted their dog was a
service dog in a place where pets are generally not allowed. Most of these
subjects have another common denominator-they are usually consumers of a
training program called Canine Companions for Independence (CCI). Now let's
connect the next dot.
CCI has created an online petition calling upon the United States
Department of Justice to ban the sale of service-animal gear such as vests,
harnesses, and signs from the internet. Some contend this is not an
unreasonable proposal since service animal training programs issue the
necessary gear, and those willing to take unfair advantage of the
protections afforded us should not be given easy access to it. The
challenge is that many of us have a need or desire for additional gear for
specific reasons, not to mention that gear is not what makes a dog a
service dog. For instance, my wife and I have guide dog harnesses made of
nylon and PVC, which are much lighter than the leather and metal versions
issued by our training programs, will not set off metal detectors in
airports and courthouses, and are more appropriate for beach visits. These
items were purchased online from a NAGDU member who makes these harnesses.
A number of other reputable companies make harnesses and other gear for
service dogs available on the internet, and these companies should not be
prohibited from selling their products in the marketplace of the World Wide
Web. It would be rather naïve to believe that prohibiting the sale of
service-animal gear on the internet will solve the issue of those who
misrepresent their pets as service dogs.
Canine Companions for Independence is also engaging in fearmongering.
Their contention is that those who misrepresent their pets as service dogs
threaten the legal rights of those of us who have legitimate service dogs
by causing businesses to question everyone who enters their business with a
dog. I believe this is actually a good thing. As more businesses learn what
questions they can ask and how to identify a legitimate service dog from a
pet, those who are misguided or malevolent will be deterred from this
behavior. It is also important to share that when someone signs the CCI
petition, they are asked to give their email address and they are advised
they will receive additional information. When I visited CCI's petition
site, they claimed they had more than 17,000 signers, so they have amassed
a very sizeable contact list from this propaganda. I believe we need to
connect a few more dots to really get a clearer picture of the true
motives. Let's take a look at another player in the service dog industry.
Assistance Dogs International (ADI) is the only accrediting body of
service-animal programs in the world. ADI has created an ethical standard
to which all their members, candidates, and program consumers must adhere
as a condition of accreditation. Here is a brief sample of these so-called
ethical standards as they apply to service dog training programs and those
they train:
. The assistance dog program must document monthly follow ups with
clients for the first six months following placement. Personal contact
will be done by qualified staff or program volunteers within twelve
months of graduation and annually thereafter.
. The program will provide a laminated ID card with a photo of the
client and dog and names of both. In public the guide dog will wear
the program's appropriate guide harness.
As it pertains to other service dogs ADI has the following standard:
. Identification of the service dog will be accomplished with the
laminated ID card with a photo(s) and names of the dog and partner. In
public the dog must wear a cape, harness, backpack, or other similar
piece of equipment or clothing with a logo that is clear and easy to
read and identifiable as assistance dogs. [sic]
. The client must abide by the ADI Minimum Standards of Assistance Dog
Partners.
The term "client" used in these standards refers to the service dog
user. The logical follow-up question is, "What would be the consequences if
we, as consumers, refused to comply with these standards?" As it pertains
to the issuance of identification cards and the mandate that the service
dog wear any specific gear, such requirements as a condition of access are
incongruent with the implementing regulations of the Americans with
Disabilities Act and should not be imposed upon a consumer and purported as
ethical.
Throughout its standards and another document published by ADI
entitled "Public Access Test," ADI uses the term "certified by ADI," as if
this certification carries some particular benefit. It appears to me as if
ADI is attempting to position itself as the certifying body for all things
service-animal related. To the best of my knowledge, no guide dog training
program is accredited by ADI, and such accreditation is not required as a
condition of legal access. So, if Assistance Dogs International is so
irrelevant in the guide dog training industry, why even bring them up?
Well, let's connect a few more dots.
On its website, CCI proudly proclaims that it was the very first
service dog training program to be accredited by ADI. Remember that most of
the articles concerning the issue of the misrepresentation of service dogs
featured consumers of Canine Companions for Independence and CCI has a
petition to ban the sale of service dog gear on the internet. Add to this
that a number of states have attempted to introduce legislation that would
require a service dog user to present documentation that a dog is a service
dog, wear specific gear, issue identification tags, and create service dog
registries-all of which are incongruent with the implementing regulations
of the Americans with Disabilities Act-in an effort to combat the false
perception promulgated by the media that there is a problem needing a
solution. Over the past two years Bob Kresmer and our Arizona affiliate
have spent too many hours opposing this sort of legislation, and several
states have such provisions in their law that have been problematic for
guide dog users attempting to protect their civil rights. So far the
National Association of Guide Dog Users and the National Federation of the
Blind have been successful in getting such legislation withdrawn or
amended, but it has created unnecessary work for us. We see a real problem
unfolding, and it is not being created by those misrepresenting their pets
as service dogs. Let's continue connecting the dots and watch this picture
evolve.
Until 2014 the executive director of CCI was a man named Corey
Hudson. Corey Hudson is also a past president of ADI North America. Equally
interesting is that the current president of ADI North America is Paul
Mundell, who also serves as the national director of canine programs at
Canine Companions for Independence. So, if there is a problem with those
misrepresenting their pets as service dogs, if the federal government bans
or regulates the sale of service dog gear on the internet, if those of us
who use service dogs are required to undergo regular recertification, or if
we are required to obtain identification cards for our service dogs, what
organization do you think would benefit from these regulations but the self-
elevated organization that certifies all things service dog?
Long before the fabrication of the nonproblem of fake service dogs by
manipulating the media to shore up the need for a solution, there was an
attempt to convince the United States Department of Justice that a problem
could exist if the regulations did not require the wearing of special gear
and other identification provisions. As early as 1991 Mr. Hudson expressed
his concerns over what he believed would be the abuse of the ADA by those
wishing to pass their pets off as service dogs. Under date of October 23,
1991, Mr. Hudson wrote to the United States Department of Justice, "While
Canine Companions for Independence and other members of Assistance Dogs
International are pleased that the ADA recognizes service animals, we are
also concerned that the law not be abused by others." Mr. Hudson went on to
write, "In April 1991, Robin Dickson, President of Assistance Dogs
International, Canine Companions for Independence, and I believe several
other Assistance Dog Schools/Centers submitted suggestions that ADA regs.
provide for some ID for properly trained assistance dogs. I am again making
this request." [sic]
<https://www.justice.gov/sites/default/files/crt/legacy/2010/12/15/tal207.tx
t>
Fortunately the DOJ did not heed the requests of CCI, ADI, and the
"several other Assistance Dog Schools/Centers" to which Mr. Hudson alluded,
refusing to impose requirements for specific gear or other identification
as a condition of our civil right to be accompanied by a service dog.
Though NAGDU and the NFB have not created an official policy statement on
this question, we have a long history of opposing requirements for special
gear or documentation and supporting the rights of owner-trainers-
individuals who have trained their own guide dogs. During our 2015 annual
meeting, we had about one hundred guide dog teams in the room and about
fifteen of them were owner-trainers. The provisions of special gear and
identification cards advocated by those who would benefit from such
requirements and the prohibition of the sale of service-animal gear on the
internet would have an adverse effect on owner-trainers and anyone else
wishing to purchase service-animal gear for legitimate purposes.
Since the current DOJ regulations do not require a service animal be
trained by a training program to be recognized as a service dog, it is
possible to train one's own dog to perform tasks or do work that meets the
definition of a service animal under the implementing regulations. Training
a dog to pick up dropped items, open doors, or alert to sounds are not
tasks only a professional trainer can teach. In fact, all of the owner-
trained guide dog teams I have encountered have been more highly trained
and consistently better behaved than some of the program-trained dogs I
have come across. Even if such regulations were to be adopted-and I highly
doubt they will-what is to prevent someone who really wants to beat the
system from doing so? Should we ban the sale of lamination equipment from
office supply stores so fake identification cards cannot be produced?
Should we regulate those who make leather products so they cannot produce
harnesses and seamstresses so they cannot sew service-animal vests? There
is a far better solution to this issue, and each of us can be a part of
that solution.
One of my favorite adages when conducting service animal training
seminars is, "It is better to educate than to litigate." Most of us have
faced violations of our civil rights, but few of us have needed to seek
legal remedies. Usually a bit of education is all that is needed.
We want businesses to know the rights of an individual accompanied by
a service dog are not absolute, and businesses have the right to deny
access to dogs that pose a direct threat, are out-of-control and the
handler does not take action to correct the behavior, or if the dog is not
housebroken. I will submit an article in the future discussing the
responsibilities of service dog users and the rights of businesses as they
pertain to access to individuals accompanied by service animals. In the
meantime, if you would like more information about the rights and the
responsibilities of service-animal users, we have the tools and information
to offer guidance. This will go much further than restricting our rights
the way CCI and ADI wish.
In order to be good advocates, we need a few tools and sound skills.
The National Federation of the Blind's National Association of Guide Dog
Users sponsors The NAGDU Information & Advocacy Hotline. This nationwide
toll-free telephone service offers general information about service
animals under the Americans with Disabilities Act (ADA), as well as
specific guidance concerning restaurants, taxicabs, and healthcare
facilities. Callers needing immediate assistance can connect directly to a
live, trained advocate.
Now there's an app for that. The National Association of Guide Dog
Users is proud to sponsor the NAGDU Service Animal Information & Advocacy
mobile app. This innovative app provides general information about the
state and federal laws that protect the civil rights of disabled
individuals who use service dogs. The app contains the full texts of the
implementing regulations of the Americans with Disabilities Act (ADA) as
they pertain to service animals and each of the state statutes that affirm
the rights of those who use service dogs, as well as general guidance
concerning access to specific types of establishments, such as hotels,
restaurants, taxicabs, healthcare facilities, and more. In addition, this
app provides the ability to directly connect with a live advocate who has
been specially trained to resolve access issues as they occur or send an
email for more specific guidance. This app is provided by the National
Association of Guide Dog Users at no charge as a public service. To
download the app, simply type the term "NAGDU" into the app store's search
field.
In an effort to better train our members about the rights and
responsibilities of guide and other service dog users and learn how to
initiate a dialogue with businesses, we are offering a special advocacy-
training seminar, so plan to join us on Tuesday, May 17, at 8:00 p.m.
eastern time for a dynamic training program conducted by the staff of our
hotline. During this training, we will offer you some new tools to help
start the conversation and share the skills of advocacy. To join the
teleseminar, please call the NAGDU boardroom at (641) 715-3300 and enter
participant code 560908#. We look forward to mobilizing our membership to
remove the obstacles we face as we live the lives we want in our
communities and make a meaningful impact on the rights of guide and other
service dog users in the United States.
----------
How to Pay for Your Hotel Stay in Orlando
by Tony Cobb
From the Editor: For a long time Tony Cobb was a fixture in our
national convention hotel lobby, and his kindness, wisdom, and experience
helped to make the convention better for all of us. Here is a reminder we
try to run each year to prevent the heartache that comes from an overdrawn
checking account when one is not familiar with the practices of major hotel
chains. The words below come from the wisdom of those years of service, and
it is with gratitude that we reprint them:
Here is some advice about paying for your hotel stay: every year at
our national convention we have serious trouble with use of debit cards or
cash payments at hotel check-in, and, having worked to solve these problems
for years, I can tell you they can nearly ruin the convention week for
those experiencing them. Planning to attend our national convention should
therefore include thinking seriously about how to pay the hotel, and I
cannot urge you strongly enough to avoid using cash or a debit card as your
payment method. Doing so may seem convenient, but you should not do so. If
you do not have a credit card of your own to use, prevail upon a close
friend or family member to let you use one just for convention. Here's why:
If you are paying in actual currency, most hotels will want enough
cash up front at check-in to cover your room and tax charges for the entire
stay, plus a one-time advance incidentals deposit to cover meals, telephone
calls, internet service, and other things you may charge to your room. The
unused portion of the incidentals deposit may be returned at check-out or
by mail after departure. Understand, however, that, if your incidentals
charges exceed the incidentals deposit credited, you are responsible for
payment of the full balance at checkout. The total can end up being a very
large sum indeed.
If you use a debit card, however, you are really at a potentially
painful disadvantage. The hotel will put a hold on money in your bank
account linked to the debit card to cover the estimated balance of your
stay-that is, for the entire week's room and tax charges plus a one-time
incidentals deposit to cover meals, movies, and so on charged to your room.
You should be aware that the hold can therefore be a considerable amount of
money and that you will not have access to that amount for any other
purchases or payments with your card. (Hotels sometimes also put
authorizations on credit cards, by the way, but those are not often a
problem unless they exceed your card's credit limit.)
Holds can remain in effect for three to five days or even a week
after you check out. If you have pre-authorized payments from your bank
account, for example your monthly mortgage payment, or if you try to make a
purchase with your debit card and it's refused, the hold from the hotel can
cause you trouble or result in very large overdraft fees for payments you
thought you had money in your account to cover. I have seen this hit some
of our members in the form of hundreds of dollars in overdraft fees.
This means that, if you use a debit card, you would have to be
certain you have a high enough balance in your checking account when you
come to convention to cover any debit card holds. This is a perilous
practice since charges may exceed your estimate by a considerable amount.
(Some frequent travelers even open a separate checking account used only
for debits like these.) Remember, a hold is going to be placed on your
debit card regardless of how you end up paying the bill, and the hold is
not necessarily released right away, even if you pay with a credit card or
cash when you check out of the hotel.
Planning ahead in this area can ensure an untroubled week at
convention, leaving you free to enjoy fully the world's largest and most
exciting meeting of the blind-using a credit card, I hope.
----------
Recipes
This month's recipes are from the National Federation of the Blind of
Alaska.
Tortellini Tomato Soup with Italian Sausage and Spinach
by Juanita Webb
Juanita is a member of the Alaska affiliate, who believes strongly in
the power of an individual to make a difference.
Ingredients:
1 tablespoon vegetable oil
1 pound Italian sausage
1/2 cup diced onion (about 1/2 medium onion)
1 tablespoon minced garlic
1 28-ounce can crushed tomatoes
1 32-ounce box of vegetable broth (chicken works as well)
2 tablespoons fresh chopped basil
1 teaspoon salt
1/2 teaspoon pepper
1 package tortellini
1 cup packed fresh spinach
Fresh grated parmesan cheese to taste
Method: Heat a large, heavy-bottomed pan over medium-high heat. Heat
vegetable oil and add diced onion. Sauté until onions are soft. Crumble
Italian sausage and garlic with the onion. Cook until sausage is no longer
pink. Stir in crushed tomatoes, broth, basil, salt, and pepper. Bring to a
boil, reduce heat to low, and cover. Let soup simmer for twenty to thirty
minutes. Add tortellini and spinach and simmer for about ten minutes, until
pasta is tender. Serve with shredded parmesan.
----------
Ranch Chicken Salad
by Shanley Kerls-Brown
Patrick and Shanley Brown, both members of the NFB of Alaska, have
recently made some major healthy lifestyle changes. Shanley went in for a
simple eye exam to renew her driver's license in December of 2015. The eye
doctor informed her that she had signs of diabetic damage to her eyes. She
had bloodwork done which confirmed that she had type 2 diabetes, and her
numbers were off the scale. She and her husband Patrick, who is the first
vice president of the National Federation of the Blind of Alaska, began
making healthy lifestyle changes. Along with exercising they began eating a
healthy low-carb diabetic diet. In three months they had both lost thirty
pounds and both had excellent bloodwork results, with Shanley's within .50
from being under the diabetic window. These are a few healthy recipes they
enjoy.
Ingredients:
3 to 3 1/2 cups chopped or shredded cooked chicken breast
1 cup celery, chopped
1 sweet bell pepper (any color), chopped
1/4 sweet yellow onion, chopped
1/2 cup mayonnaise
1 tablespoon dry ranch seasoning
Method: Mix the chicken, mayonnaise, and seasoning together in a
medium bowl until well blended. Stir in the celery, peppers, and onion
until mixed evenly. Chill one hour to let flavors meld.
----------
Cabbage Creole
by Shanley Kerls-Brown
Ingredients:
1 to 2 pounds ground beef
1 small onion, chopped
1 medium head of cabbage, chopped
1 10-ounce can Ro-Tel tomatoes
1/2 pound Velveeta, cubed
1 teaspoon salt
1 teaspoon black pepper
1 teaspoon garlic powder
Method: In a large skillet, brown beef with chopped onion. Drain if
necessary. Return meat mixture to pan. Add chopped cabbage (this may have
to be done in batches depending on how big of a pan you use). Cook until
cabbage is somewhat wilted. Add Ro-Tel and continue to cook until cabbage
is tender. Add cubed Velveeta and seasonings to taste. Cook until cheese is
melted. Serve hot.
----------
Hearty Hungarian Goulash
by Bonnie Lucas
Bonnie is the president of the Anchorage chapter and loves to cook.
She does her best to share the NFB philosophy of the Federation with the
blind of Alaska as an employee of the Alaska Center for the Blind and
Visually Impaired.
Ingredients:
2 pounds chuck roast, cubed
4 whole carrots, cut into large chunks
18-ounce canned plum tomatoes, crushed by hand
1 onion, chopped
2 tablespoon paprika
1 tablespoon cumin
1 tablespoon dijon mustard
2 tablespoons minced garlic
2 teaspoons cinnamon
2 cups bone broth or organic beef broth
Salt and pepper to taste
Coconut oil to brown meat
Method: Coat large pan with enough coconut oil to line the bottom.
Brown cubes of chuck steak over high heat in batches, about two minutes per
side. Chop carrots and onion. Hand crush tomatoes. Add carrots, onion, and
tomato to slow cooker. Add meat, seasonings, garlic, mustard, and bone
broth to slow cooker. Stir to combine. Cook on high for four to six hours
or low for eight to ten hours. Can serve over brown rice or quinoa. Makes
four servings.
----------
Grandma Jo's Pizza Burgers
by Bill Packee
Bill says of himself: I am a former Alaska state president of the
NFB, assistant manager at Walmart, and a student at the University of
Maryland working towards a bachelor's degree in forensic psychology. In my
"off time" I enjoy my children, grandchildren, our dogs, and maybe some
sleep. This recipe was one of our kids' favorite meals while growing up.
Ingredients:
1 1/2 pounds of hamburger
1 10-ounce can of pizza sauce
1 small onion, chopped
1 can mushrooms
8 ounces mozzarella cheese, grated
1 teaspoon oregano
1/2 teaspoon garlic salt
1/2 teaspoon pepper
8 hamburger buns
Method: Preheat oven to 350 degrees. Brown hamburger and onion
together. Add remaining ingredients except cheese. After adding ingredients
cool mixture, then add cheese and bake at 350 degrees for ten to fifteen
minutes, then spoon unto buns. Yields eight servings.
----------
Flourless Chocolate Cake
by Bonnie Lucas
Ingredients:
12 ounces bittersweet chocolate chips or bittersweet chocolate, roughly
chopped
1 cup (2 sticks) plus 3 tablespoons butter, cut into chunks
1 1/4 cups sugar
6 eggs
1 cup unsweetened cocoa powder
1 tablespoon milk
1 tablespoon honey
1/4 teaspoon gluten-free vanilla extract
Method: Preheat oven to 375 degrees. Spray a nine-inch springform pan
with nonstick cooking spray, then line the bottom with a circle of
parchment paper. Spray the paper with cooking spray, too, then set the pan
aside.
Place two-thirds (eight ounces) of the chocolate and one cup (two
sticks) of the butter in a medium saucepan over medium-low heat. Stirring
often, melt chocolate with butter until completely blended. Remove from
heat, and transfer to a large bowl. (Alternatively, you may use your
microwave to melt the butter with the chocolate, if desired). Add sugar and
mix well. Add eggs one at a time, whisking well after each addition. Sift
cocoa into bowl and stir until just blended.
Pour batter into prepared pan and bake for thirty-five to forty
minutes, or until cake has risen and top has formed a thin crust. The cake
should be just firm in the center when done. Cool for ten minutes, then
invert onto a plate, removing sides of springform pan. Remove and discard
parchment paper and set cake aside to cool completely.
Meanwhile, make the chocolate glaze. Melt remaining four ounces
chocolate and three tablespoons butter in a small saucepan over medium low
heat, stirring until smooth. Remove from heat, then stir in milk, honey,
and vanilla. Set aside to cool slightly.
When cake has cooled, pour glaze onto the center. Using a spatula or
the back of a spoon, very gently smooth glaze along the top and sides of
the cake. Chill cake, uncovered, for thirty to sixty minutes before serving
to set the glaze and make the cake easier to slice.
----------
Mini Cheesecakes
by Tracey Packee
Tracey says about herself: I am a mother of six kids, four boys and
two girls. I also have two grandsons and two more grandsons due in August.
My husband Bill and I consider ourselves to be newlyweds even though we
have been married for seventeen years, four months and three days. I live
in Alaska, where I have been residing for the last nineteen years.
In 2009 I spent nine months at the Helen Keller National Center
learning the skills necessary to adjust to this condition. In 2010-2012 I
attended the University of Alaska Fairbanks and graduated magna cum laude
with a degree in paralegal studies. I am currently the Alaska state
president for the National Federation of the Blind.
Ingredients:
12 vanilla wafer cookies
2 8-ounce packages cream cheese, softened
1/2 cup sugar
1 teaspoon vanilla
1 teaspoon lemon juice
2 eggs
1 can cherry pie filling (or any fruit pie filling of your choice)
Cupcake liners
Regular-size cupcake pan
Method: Preheat oven to 325 degrees. Line cupcake pan with liners.
Add 1 vanilla wafer to each liner. In a large bowl mix cheese, vanilla,
lemon juice, and sugar on medium speed until blended. Add eggs; mix well.
Pour mixture into each cupcake liner until about 3/4 full. Bake twenty-five
minutes at 325 degrees. Cool cakes, then add cherry pie filling or any
fruit pie filling of your choice. Chill before serving. Yields two dozen.
----------
Monitor Miniatures
News from the Federation Family
National Federation of the Blind Praises Secretary Clinton's Remarks on
Employment of People with Disabilities:
The National Federation of the Blind commented on recent remarks by
Hillary Clinton in which she called for ending "the tiered minimum wages
for ... people with disabilities."
Mark A. Riccobono, President of the National Federation of the Blind,
said: "The National Federation of the Blind applauds Secretary Clinton for
stating boldly and unequivocally that she rejects the discriminatory
practice of paying workers with disabilities subminimum wages. We call upon
the other presidential candidates to join with us and over seventy-five
other organizations of people with disabilities in supporting the repeal of
Section 14(c) of the Fair Labor Standards Act and to reject the
misconceptions and low expectations that have for too long kept people with
disabilities from achieving our dreams."
A provision of the Fair Labor Standards Act dating from the law's
enactment in 1938, known as Section 14(c), allows facilities to apply for
special wage certificates that permit them to pay workers with disabilities
subminimum wages. About three thousand entities pay more than 250,000
workers with disabilities wages as low as pennies per hour, according to
2016 statistics from the US Department of Labor Wage and Hour Division.
Health and Wellness Experts Wanted:
The NFB Sports and Recreation Division and WE Fit Wellness are
seeking health and wellness experts for the 2016 NF-BE Healthy Fair.
On June 30, 2016, the NFB Sports and Recreation Division will help
kick off the seventy-sixth National Convention of the National Federation
of the Blind with the first ever NF-BE Healthy Fair. The NF-BE Healthy Fair
is a health fair designed with the blind in mind. Instead of walking from
table to table gathering print information, attendees will have the
opportunity to receive a health assessment, nutrition information, put
their hands on talking health- and wellness-related gadgets, try out
accessible mechanisms for reading nutrition information, check out
accessible activity trackers, and more. In order to make the NF-BE Healthy
Fair a huge success, we are seeking health and wellness professionals who
are willing to show off their skills, sell their products, and help
convention attendees find solutions, tools, and motivation to NF-BE
Healthy!
We are looking for personal trainers, fitness instructors, people who
sell health- and wellness-related products, life coaches, massage
therapists, chiropractors, representatives from sports- and recreation-
related community-based organizations, recreational therapists, nutrition
experts, exercise enthusiasts, and others who may add an exciting dimension
to our 2016 NF-BE Healthy Fair. For more information on how you can become
a sponsor or exhibitor, please contact Jessica Beecham at (866) 543-6808,
extension 105, or email <jessica at wefitwellness.com>.
Convention Announcements from the Assistive Listening Project:
At the 2016 national convention, we will again offer special
arrangements for severely hearing-impaired people attending convention
sessions and the banquet. This will consist of transmission of the public
address system signal over a special short-range radio transmitter for the
severely hearing-impaired. Spanish-language translation of convention
proceedings in general sessions and the banquet will also be provided using
a similar arrangement. The special receivers required for these services
will also be provided.
In cooperation with several state affiliates (notably Colorado, Utah,
and Virginia), the NFB will provide special receivers for these
transmissions to those needing them. The receiver-lending will be managed
by the Amateur Radio Division and will be operated from a table just
outside the meeting room. A deposit of $40, cash only, will be required of
anyone wishing to check out one of the Federation's receivers. The deposit
will be returned if the receiver is checked in at the checkout table in
good condition by the end of the banquet or within thirty minutes of
adjournment of the last convention session that the borrower plans to
attend. Batteries for the receiver will be provided. Anyone checking out a
Federation receiver will be given upon request a miniature earbud-type
earphone to use with the receiver.
Along with explaining what will be available, it is important that we
explain what will not be available. The miniature earbud loudspeaker-type
earphone will be the only kind of earphone offered. If you would like to
use your own earphone(s), silhouette, neckloop, or other device or adapter
cable to get the signal from the receiver we provide to your ear, you must
ensure that the cable connection between your device and our receiver is
one that will fit the audio jack found on electronic devices such as
talking book and MP3 players, laptops, or mobile devices like iPhones and
notetakers. In technical terms, this is referred to as a 3.5 mm (formerly
called 1/8-inch) earphone plug. You are advised to arrange for such things
well ahead of arriving at the convention. Other than the earphone jack on
the receiver, no means of connection to a hearing aid will be available
from the checkout table. The receiver does not have a built-in loudspeaker.
While earphones, and even neckloops, are sometimes available in the exhibit
hall, you cannot be certain of getting one there.
Many severely hearing-impaired people already use radio systems that
employ FM radio signals to carry the voice from a transmitter held by the
person speaking to a receiver in the hearing aid. Some of these hearing aid
systems can be tuned to receive the Federation's special transmitters. In
this case the hearing-impaired person may simply tune his or her own
receiver to receive the Federation's transmitter and will not need to check
out a Federation receiver.
Some audiologists and rehabilitation agencies are now buying digital
and other FM hearing aids that cannot be tuned to the Federation's
frequency. If you have one of these or if you have any other type of
hearing aid, you should obtain from your audiologist an adapter cable to
connect from your hearing aid to a monaural 3.5 mm earphone jack. This will
allow you to plug the cable from your hearing aid directly into a receiver
you check out from our table. This will allow you to hear as well as anyone
else using one of our receivers.
The transmitter for the hearing impaired will be connected to the
public address system so that the signals from the head table and the aisle
microphones will be transmitted on channel thirty-six (74.775 MHz narrow
band FM). People must not operate their personal transmitters on channel
thirty-six or on channel thirty-eight because that would interfere with the
reception for others. This means that folks wishing to use their own
receivers (rather than checking out one of the Federation's receivers) need
to have their personal receivers arranged so that they can switch between
their personal channels and channel thirty-six. Some people may need to
purchase replacement or additional receivers. Caution your audiologist that
there is more than one channel thirty-six, and he or she must also verify
that your frequency matches our frequency.
This announcement is published now to allow as much time as possible
for those interested to make the necessary arrangements before convention.
It contains this amount of detail so that any audiologist who works with
this type of equipment should be able to know by reading this article
exactly what capabilities a person's hearing system must have to work with
the Federation's system at convention.
Even if your hearing aid is not of the FM type, you may be able to
purchase a silhouette, a neckloop, or an adapter cable to couple the signal
from a Federation receiver directly to your hearing aid. Your audiologist
should also be able to help you with this. The NFB Deaf-Blind Division has
offered to provide feedback on their members' experiences with these types
of devices to interested convention attendees. Contact Joe Naulty, 3924
South Wind Drive, West Melbourne, Florida 32904, (321) 768-9500 or
<jnaulty at cfl.rr.com> for inquiries. Please always remember to consult your
audiologist when considering any additions to your hearing aid setup.
The service for Spanish speakers will be similar, except that a live
Spanish translator will speak over a separate transmitter on channel thirty-
eight (75.275 MHz narrow band FM). We do not expect that people will bring
their own receivers for the Spanish-translation service, unless they are
also hearing impaired and use an FM hearing aid system. Spanish speakers
may, however, wish to bring their own earphones. See above for a
description of the type of plug needed.
Conchita Hernandez from Washington, DC, will be coordinating the
Spanish language interpreters, and she would appreciate hearing from anyone
willing to volunteer to interpret. Please call her before convention at
(530) 908-3547, or send her email at <hernandezlegorreta at gmail.com>.
If other state affiliates or chapters are interested in purchasing
this type of equipment for use in state and local meetings, they are
encouraged to purchase equipment that is compatible with that which we are
using and to allow it to be used in the pool of equipment that the Amateur
Radio Division administers at national convention. I (Rachel Olivero) would
like to help you choose equipment that is compatible with that which the
NFB is using. You may contact me at (765) 977-1683 or at
<rachel at olivero.us>. The Federation is pleased to offer these services to
our severely hearing-impaired and Spanish-speaking colleagues, and we hope
and believe that it will again significantly improve their convention
experience.
New Opportunities for Careers in Rehabilitation of the Blind, Scholarships
are Now Available:
Structured Discovery Cane Travel (SDCT) and Structured Discovery
Rehabilitation have been demonstrated to be among the most innovative and
effective forms of rehabilitation training for individuals who are blind or
visually impaired. Louisiana Tech University has operated its Orientation
and Mobility program on this model successfully for eighteen years, with
upwards of 90 percent successful employment and employer satisfaction
rates.
Louisiana Tech is excited to announce that, along with its O&M
program, it has expanded its training and is launching a brand new
concentration in rehabilitation teaching for the blind.
Scholarships are now available for qualified individuals seeking one
of the following degree paths: master of arts in industrial/organizational
psychology with concentration in orientation and mobility, master of arts
in counseling and guidance with concentration in rehabilitation teaching
for the blind, or orientation and mobility graduate certification.
Why me?
. The field of educating and rehabilitating children and adults who
are blind is deeply rewarding and life-changing.
. The job market is wide open; currently we receive four times the
number of employer requests than we have graduates to provide.
. Training occurs on campus in Ruston, Louisiana, and can be
completed in as little as one year.
. No prior background or experience in blindness is necessary-we'll
teach you everything you need to know.
. Scholarships are provided on a competitive basis to qualified
applicants and can cover costs for attending the university.
. Scholarships also support travel to conferences, trainings, and
field-based experiences at Structured Discovery training programs.
Who can Apply?
Individuals must already possess a bachelor's degree from an
accredited university, have a grade point average of 2.5, and obtain a
minimum of 287 (verbal and quantitative) on the Graduate Records
Examination. Individuals must also be willing to attend courses on campus
in Ruston, Louisiana, on a full-time basis.
What's the Catch?
. Payback through service is required. Agreement to receive
scholarship funding requires commitment for you to work in the
field of rehabilitation for two years for each year of scholarship
support you obtain.
. Scholarships cover at least tuition and fees but may cover living
and travel costs as well.
. You have to move to Ruston, work hard, study harder, and have the
heart to be an O&M or rehabilitation teacher of blind people.
Where do I get started?
For program details, visit: <www.pdrib.com>, send an email for more
information to: <dreed at latech.edu>, or call Edward Bell to discuss your
application at (318) 257-4554.
Registration Open for Rehabilitation and Orientation and Mobility
Conference:
Contemporary Issues in Rehabilitation and Education for the Blind
Fifteenth Annual Rehabilitation and Orientation and Mobility Conference
will be held at Rosen Shingle Creek Resort, Thursday, June 30, 2016, 8:30
a.m. to 7:30 p.m. Come and join us! Once again, this year's conference
will be action-packed with a variety of new speakers, topics, and hands-on
events.
Schedule:
7:30 - 8:30 AM Registration
8:30 AM Conference Begins
2:00 - 5:00 PM Interactive Breakout Sessions
5:00 - 7:00 PM NBPCB Awards Reception
Registration fee includes the NBPCB awards reception. The cost before
June 15 is $85 for professionals, $75 for students. After June 15, the cost
is $100 for both students and professionals. To register, go to
<https://nbpcb.org/members/login.php?r=/members/er.php?eid=284>. Those
certified through the NBPCB may register using their username and password.
All other participants should register as a guest.
For questions or special arrangements, contact Dianne Reed at (318)
257-4554, or <dreed at latech.edu>.
Conference sponsored by: National Blindness Professional
Certification Board (NBPCB), Professional Development & Research Institute
on Blindness (PDRIB), Louisiana Tech University, and the National
Association of Professionals in Blindness Education.
Assistance Needed at Convention:
Pauline Murphy is looking for assistance in getting from her room to
convention sessions, restaurants, the exhibit hall, and other convention
activities. She is willing to pay some for this service. If interested in
helping her, call (317) 403-7000, or write her at <paulinemm at att.net>.
A History of Blind People Available:
The Blind History Lady Presents is a growing series of articles and
historical biographies of blind people who lived in the 1800s through the
early 1900s. These blind men and women created their own opportunities,
becoming electricians, boat builders, insurance salesmen, chemists,
chiropractors, and so much more. Peggy Chong is the Blind History Lady. Her
articles have appeared in the Braille Monitor and many other publications.
Now she takes her almost three decades of research on blind people,
compiling them into in-depth short stories and is sharing it with everyone,
blind and sighted. Check out The Blind History Lady Presents at your
favorite ebook store or at <www.smashwords.com>.
Conference Calls for Those with Cerebral Palsy:
Come one and all, blind and visually impaired Federationists who have
cerebral palsy, to create an active and vibrant group of blind and visually
impaired Americans with cerebral palsy. The purpose of this group will be
to provide the following: positive role modeling techniques, leadership,
networking, mentoring, information, referral to agencies, education,
socialization, rehabilitation training methodology ideas, advice about self-
representation, and systemic legal advocacy assistance. This group will
discuss the management of social issues faced by blind and visually
impaired people with cerebral palsy and the management of the
rehabilitation training issues faced by this group. Our goal is to provide
mutual support from those who understand.
Meetings will be held by conference call on the first Sunday of the
month from 8:00 p.m. until 10:00 p.m. eastern time starting on Sunday, June
5, 2016. The conference phone number is (218) 339-3814; enter pin 999999#.
To assist in developing this group contact Alexander Scott Kaiser by
Braille snailmail, by phone, and by email. His postal address is Alexander
Scott Kaiser, 52 Meadowbrook Road, Brick Township, New Jersey 08723-7850;
his email address is <AKaiser999 at gmx.us>, and he can be reached by phone at
(848) 205-0208.
In Brief
Notices and information in this section may be of interest to Monitor
readers. We are not responsible for the accuracy of the information; we
have edited only for space and clarity.
Delta Air Lines Offers a Discount to National Federation of the Blind
National Convention:
Members of the National Federation of the Blind and all individuals
planning their travel to attend our annual national convention are being
offered discounted airfare from Delta Air Lines through their Delta Meeting
Network. Those interested should go to <www.delta.com/booking> to book
their flight and enter the meeting event code: NMNBW. The discount will be
calculated based on your specific travel arrangements and could range from
2 percent to 10 percent. If you have any questions, call the Delta Meeting
Network at (800) 328-1111 from 7:00 a.m. to 7:30 p.m. central time, Monday
through Friday.
SENSEsational Alphabet Books Back at Seedlings:
The ever-popular SENSEsational Alphabet books are back at Seedlings!
And, we are still offering them at our deeply discounted price of $20 each!
The interactive ABC picture books allow blind and sighted family members to
learn the alphabet and beginning words in sign language and uncontracted
Braille together! The book incorporates visual stimuli, movement, touch,
smell, and sound. Feel the different textures of the horse and lizard,
smell the distinctive aromas of apples and roses, move the hands of the
watch, pull the zipper, and much more! To order, go to
<http://www.seedlings.org/browse.php?search=SENSEsational+Alphabet&field=Ite
m_name>. You can also check out our webpage at <www.seedlings.org>, or
follow us on Facebook or Twitter (@SeedlingsBrlBks).
DOJ Reaches Settlement with Greyhound and Disabled Passengers May Be Due
Compensation:
The US Department of Justice ("DOJ") recently entered into a
settlement with the Greyhound bus lines company on behalf of disabled
travelers. The settlement consent decree creates a fund of $300,000 for
"select individuals identified by the United States" and a separate
uncapped claims filing process to compensate "individuals who assert ADA
claims meeting established criteria." The following information is meant
to help clarify some confusion about the significance and scope of this
settlement among members of the National Federation of the Blind. The
information is compiled from the publicly available settlement documents,
court filings, and consultations with the DOJ attorneys responsible for
enforcing the settlement.
Who is generally eligible?
As for the $300,000, that fund is likely set aside for the specific
individuals that the DOJ was already working with during its investigation.
If you weren't already talking with DOJ attorneys or staff about access
problems prior to February 8, 2016, then it is unlikely that this fund
applies to you. If you were talking with the DOJ about your access
problems prior to February 8, 2016, then you should contact them to verify
your status.
As for the claims filing process, you must meet each of the following
four requirements to even be considered for compensation:
. have a disability;
. have traveled or attempted to travel on Greyhound between Feb. 8, 2013,
and Feb. 8, 2016;
. have experienced a disability-related incident during your travel or
attempt to travel (for example, lack of accessible transportation or
transportation-related services, Greyhound's failure to make disability-
related accommodations, etc.); and
. submit a claim form by mail, email, or online to the claims administrator
by no later than Nov. 10, 2016.
The above qualifications are vague and could arguably include quite a
few access problems that members of the National Federation of the Blind
have experienced. Based on conversations with the Department of Justice
attorneys responsible for enforcing the settlement, it appears that the
"criteria" that might be used to award compensable claims is not as broad
as the above language might suggest. Further, the policy fixes outlined in
the settlement also seem to target a broader set of ADA violations than the
monetary claims. Because this settlement is not a class action, the DOJ
and Greyhound retain discretion on the claims that will eventually receive
monetary compensation.
What claims are likely covered?
According to the DOJ attorneys responsible for enforcing the
settlement, blind individuals whose experiences are similar to the types of
access problems illustrated in the complaint should consider filing a
claim. Eligible blind individuals who experienced the following types of
problems should consider filing a claim:
. personnel failing to provide assistance to you in navigating to a bus
from the bus station or boarding and de-boarding buses;
. personnel failing to allow you to leave and return to the bus at rest
stops;
. personnel failing to provide you sufficient time to board or disembark
buses;
. personnel failing to permit your service animal to accompany you in
vehicles and facilities;
. personnel failing to facilitate the availability of seating designated
for use by individuals with disabilities when such priority seating is
occupied by luggage or passengers without disabilities;
. personnel failing to let you sit in seats other than the designated
seating area for people with disabilities;
. other similar issues relating to physical access to the bus and
facilities.
Much of the settlement focuses on access for people who use
wheelchairs or have mobility impairments. Blind travelers who use
wheelchairs or have mobility impairments should consider submitting claims
if they experienced inoperable lifts, inadequate wheelchair securement
straps, or problems related to the operation of the "kneeling" function of
a bus, which lowers the height of the access point to the bus for those who
would otherwise have difficulty navigating the distance between the ground
and the bus's first step. In addition, blind individuals with wheelchairs
who were unable to book wheelchair-accessible travel online or were charged
extra to book wheelchair-accessible travel over the telephone should also
consider submitting a claim.
How do I submit a claim?
The claim administrator website has relevant case documents, contact
information, and instructions for filing a claim at
<www.dojvgreyhoundsettlement.com/>. You may also call the settlement
administrator at (844) 502-5953.
What about other issues not mentioned above?
The National Federation of the Blind is aware of other access issues
that are not clearly addressed by this settlement. The Federation continues
to raise and monitor these issues with Greyhound and the DOJ to ensure that
all of the concerns of the blind community are addressed in the context of
this settlement or other independent action. Individuals with questions or
concerns may contact attorney Timothy Elder at <telder at trelegal.com> or
(410) 415-3493, or contact Valerie Yingling with the NFB's legal team in
Baltimore at <vyingling at nfb.org> or (410) 659-9314.
----------
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Federation of the Blind to achieve equality, opportunity, and security for
the blind; to support the policies and programs of the Federation; and to
abide by its constitution.
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