[il-talk] Illinois Independent, Fall 2016
William Balis
billbalis at sbcglobal.net
Mon Oct 17 22:51:52 UTC 2016
Thanks for the information! When is the convention? Is there a cost to come I do not need overnight accomodations? Thanks! Bill
--------------------------------------------
On Mon, 10/17/16, Deborah Kent Stein via IL-Talk <il-talk at nfbnet.org> wrote:
Subject: [il-talk] Illinois Independent, Fall 2016
To: "'NFB of Illinois Mailing List'" <il-talk at nfbnet.org>
Cc: "Deborah Kent Stein" <dkent5817 at att.net>
Date: Monday, October 17, 2016, 4:28 PM
ILLINOIS INDEPENDENT
Fall 2016
National Federation of the Blind of Illinois
President: Denise R. Avant, (773) 991-8050
davant1958 at gmail.com
Editor: Deborah Kent Stein, (773) 203-1394
dkent5817 at att.net
Coeditor: Robert Gardner, (309) 236-6606
rgardner4 at gmail.com
Formatting: Glenn Moore and Janna Harvey
NFB Newsline Edition: David Meyer, (708) 209-1767
datemeyer at sbcglobal.net
Print and Braille Editions: Bill Reif, (217) 801-2996
billreif at ameritech.net
TABLE OF CONTENTS
From the President's Desk, by Denise R. Avant
The Chicago Marriott Naperville Hotel, Convention
Information, by Patti
Gregory-Chang
Come Spin with Me, by Cathy Randall
Skiing with the Vikings, by Denise R. Avant
Playing with Clay, by Deborah Kent Stein
In Memoriam: LeAnne Mayne
FROM THE PRESIDENT's DESK
by Denise R. Avant
The fall convention season is now underway. But before I
talk about the
excitement surrounding our NFBI state convention, I want to
bring an
important matter to your attention. The National Federation
of the Blind
does many things well. We educate and advocate across the
country on behalf
of blind people. And as I write this article, we the blind
once again need
to advocate for ourselves and educate the public. To raise
money for medical
research, the Foundation Fighting Blindness has launched the
HOWEYESEEIT
campaign. The campaign asks sighted people to put on
blindfolds and try to
do everyday tasks such as cooking, shopping, and caring for
children.
The NFB does not oppose medical research to find treatments
and cures for
eye conditions that may cause blindness. However, this
campaign is misguided
and dangerous. We in the Federation know that if blind
people are properly
trained in mobility and daily living skills, we can perform
the same
everyday tasks that are done by our sighted peers. The
Foundation Fighting
Blindness campaign fails to tell the whole story. Instead,
it plays on the
public's fears and misconceptions about blindness. If not
confronted and
addressed, the campaign will perpetuate these misconceptions
and foster a
culture of discrimination.
One of our greatest concerns with the HOWEYESEEIT campaign
is the way it
portrays blind people's ability to care for children. We in
the Federation
see many cases in which the ability of a blind parent to
care for his or her
children is questioned, and we have seen cases in which
parents lose custody
of their children based on blindness alone. Several states
have introduced
parental rights bills that say children cannot be removed
from the home due
to the parents' blindness. The Foundation Fighting Blindness
campaign serves
to undermine our efforts to protect blind parents and their
children.
As Federationists we know the truth about blindness. We
work, we play, and
we take care of children. The list goes on and on. Please
help educate the
public by taking a video of yourself doing some everyday
task. Upload it to
social media with the hashtag HOWEYESEEIT. Be sure to say
that you are a
proud member of the National Federation of the Blind.
Once again at our convention we will show that blind people
are able to live
the lives we want. Everyone in the Illinois affiliate of the
NFB has been
busy choosing topics, inviting speakers, making arrangements
with the hotel,
and preparing convention materials. This year's convention
will be held on
the weekend of October 28-30 at the Chicago Naperville
Marriott in
Naperville, Illinois. For more information about convention
activities, go
to www.nfbofillinois.org. Following this letter you will
find an article
describing the layout of the hotel.
Our national representative and keynote speaker at this
year's convention
will be Joe Ruffalo, Jr., president of the New Jersey
affiliate and board
member of the NFB. Other speakers include John Olson of 3d
PhotoWorks, Peter
Tucic from HumanWare Inc., makers of the BrailleNote Touch
and other
blindness and low vision products; John Gordon, chief of the
Illinois Bureau
of Blind Services; Karen Woodfork, director of student
education at the
Hadley Institute for the Blind and Visually Impaired; and
Camille
Caffirelli, executive director of Horizons for the Blind.
In addition to hearing from our speakers on various program
topics, you will
meet the NFBI scholarship class of 2016: Ashley Eisenmenger,
Adnana Saric,
Gabe Stanforth, and Aziz Zeidieh. One of the highlights of
2016 for the NFBI
was that all four scholarship winners from 2015 attended our
NFB national
convention in Orlando, Florida. This has never happened in
Illinois before.
We hope that the 2016 class will fully participate in our
organization and
join us in Orlando in 2017.
We have expanded the Braille Readers Are Leaders contest,
which began in
Illinois in 2013. In 2015-2016 the contest was open to
students from
Illinois and Minnesota. The 2016-17 contest will be
regional. Children in
grades K-12 from most of the Great Lakes states can now
participate. On
November 1, 2016, children in these states can begin to
submit their
registration forms. From December 1, 2016 to January 20,
2017, children
compete for cash prizes by reading as many Braille pages as
they can. The
NFB knows that strong Braille reading skills help to ensure
that blind
children will live productive lives.
Do you want to represent Illinois at the 2017 Washington
Seminar? The dates
for the next Washington Seminar are January 30-February 2,
2017.
Applications can be found on our website, and must be
submitted to the state
president by December 1, 2016. Meanwhile, please call
Senators Richard
Durbin and Mark Kirk and ask them to support the Marrakech
Treaty. The
treaty allows books for the blind to be made available to
blind people all
over the world. Also please call your senators and
representatives and ask
them to support the Space Available Bill, (HR 2264 and S
2596) and the
Accessibility in Instructional Materials and Higher
Education Act, AIM HI
(HR 6122).
I look forward to seeing all of you at convention. I thank
you for your
support over the past two years. I could not do it without
your help!
THE CHICAGO NAPERVILLE MARRIOTT HOTEL, Convention
Information
By Patti Gregory-Chang
This quick article explains the layout of the Chicago
Marriott Naperville,
our hotel for the 2016 NFBI convention. It also gives you
basic information
about the facilities and amenities.
Address and Phone: The hotel is located at 1801 N. Naper
Blvd, Naperville,
IL 60563. The phone is: (630) 505-4900.
Sleeping Room Types: There are two types of rooms, suites
and standard
rooms. The suites have a parlor with a sleeper sofa, two
easychairs, and a
coffee table. The room rate for standards is $104. The rate
for suites is
$129. All rooms have hair dryers and coffee makers.
Connecting rooms can be
reserved upon request.
Keycards and Electrical Power: This hotel is modernized. You
need to insert
your keycard in a slot inside your room to the side of the
door to turn your
power on. Leave it in the slot until you exit your room.
When you remove it,
the power goes off again.
Check-in/out: Check-in time is three p.m. Check-out time is
12:00 p.m.
Wi Fi: There is free Wi Fi in all lobby and common areas.
This includes our
meeting rooms.
Facilities: The hotel offers an indoor pool, fitness room,
and Jacuzzi.
There is lots of parking, especially by the side door.
Shuttles: The hotel runs free shuttles within a five-mile
radius. Trains are
scheduled to leave for downtown Chicago at 12:30, 2:30, and
4:30 PM. The
hotel has a contract with a limo company that provides
discounted service to
and from each airport. The cost is under forty dollars,
which compares
favorably to a cab, which would cost approximately
sixty-five dollars.
Layout: If you enter the hotel through the main doors, the
layout is as
follows:
The Starbucks is to the left. You should walk ahead to where
the tiled
flooring forms a cross. If you turn left at the "lobby
cross," with the
doors at your back, you can enter Starbucks by taking the
first left. If you
take a right, you can go to the elevator bank. If you pass
the elevators,
you head toward the meeting rooms.
From the front door, if you simply bypass the crossing of
the tiled portions
of the lobby and keep going straight, you will find our
information desk on
your left and the hotel desk on your right. If you pass
both, there is a
restaurant directly ahead. You can find the bar, which also
serves food from
the restaurant, by turning left after passing the hotel
desk. The bar will
be on your right, although people can also sit on the left
side at this
point in the lobby.
If you stand facing the hotel front desk, the elevator bank
is down the
tiled hall to the right. There are three elevators on your
left side down
that hall a short way. They are fast.
Our meeting rooms are laid out past the elevator bank. Right
after the
elevators there is a cash machine on your left, and there
are restrooms on
your right. Past those, first you come to a hallway where
conference rooms
A, B, and C are on your left heading away from the lobby.
Conference rooms
D, E, and F are on your right.
Past that hall the hall divides at a Y. There is another set
of restrooms
down by the other conference rooms near Bailey. If you go
left, you come to
Bailey-Hobson and if you go right you will get to the Naper
room, which is
where our general sessions will be held. Outside of the
Naper room we will
have exhibits, and we will have our registration.
There is a dog relief area outside of the Naper room. Exit
and walk a short
way, then make a forty-five-degree left turn. There is a
cement patio area
on the left about thirty feet up. At the end of the patio,
you will find a
grassy area with trees; it will work well for dog relief.
There is even a
hydrant!
Both breakfasts and our lunch are scheduled to be held in
Conference Room A.
Hospitality before and after the banquet will be offered in
the banquet
room, Bailey-Hobson. The parents' meeting will be held in
Conference Room C.
Kids Camp is planned for Conference Room F. The scholarship
dinner will be
held in Conference Room E. IABS Idol and General Sessions
for Friday and
Saturday will be in Naper 2 and 3. The banquet and the
Sunday General
Sessions are in Bailey-Hobson. Registration is outside of
the Naper room.
Set-up for Naper Room: When you enter the Naper Room it is
wider from left
to right and shorter going ahead from the doors. You enter
at the back of
the room. We will have information and IABS tables in the
back of the room,
and the head table will be furthest from the doors by the
windows. If you
face the head table, audio will be on your right and door
prizes on the
left.
COME SPIN WITH ME
by Cathy Randall
Exercise has been an important part of my busy life for over
forty years.
Dr. Kenneth Jernigan, my dear NFB mentor, advised me to lead
a balanced
life--and I have always tried to do that. Too much of any
one activity can
make a person one-dimensional and possibly less interesting
to herself and
to others.
Over the years, I have enjoyed various forms of exercise,
including running
and fast walking with guides, floor exercise classes,
swimming laps, and
water aerobics. I have taken part in all these activities as
a totally blind
person.
Now, let me introduce you to spinning. To take part in this
exercise, you
ride a modified bicycle without wheels in a gym with a
number of other
people who are doing the same thing. First you stand beside
the bike and
learn to adjust the seat to the height of your hip. Next you
sit on the bike
seat, lean over, and put one foot in the stirrup, which is
attached to the
pedal. Then you tighten the stirrup as you are shown by the
teacher and
repeat the process for your other foot. It is very important
to have the
stirrups tight, because you either stand or sit for all
spinning exercises.
Once you have adjusted the stirrups, you increase or release
tension on the
pedals by turning a knob between your knees. The tension
knob is where the
bar would be on a standard boy's bike. The more you increase
the tension on
the pedals, the harder you will need to work! When your
instructor asks you
to "put on more road," he or she is asking you to add more
tension.
Spinning class is very verbal, and you don't have to learn
many commands. It
is important that you pace yourself as you learn this
exercise. You have to
work through either a thirty- or forty-five-minute class,
and you want to
work steadily throughout that period. As your conditioning
improves, you
will be able to put more tension on your pedals.
When you go to a spin class, take at least a thirty-ounce
bottle of water
with you. Learn to stretch your water supply so it lasts to
the end of
class. Your water bottle is probably the most important part
of your
spinning equipment.
For class I wear comfortable shorts, a T-shirt, good
athletic socks, and
tennis shoes. I tuck a bandana loosely around my neck inside
the T-shirt to
absorb sweat. I also wear a terrycloth headband, which is
another good sweat
absorber. It is handy to wear a fannypack holding your keys
and phone. Bring
a towel and several sets of earplugs. Without earplugs I
find that the music
can be uncomfortably loud. I can hear the instructor's
commands easily
through the plugs. During late fall and winter, you may want
to wear
loose-fitting yoga pants and a long-sleeved T-shirt.
Year round you will really get hot from spinning, so dress
for your own
comfort. Personally, I don't like real biking shorts because
of the tight
band around the thigh.
I have been spinning for over nine years with friends, and
they are now very
dear friends indeed. Have fun and get fit!
SKIING WITH THE VIKINGS
by Denise R. Avant
I was deep in preparations for the 2015 NFBI convention when
I received an
unexpected call from Miriam Omquist, one of the US
coordinators of Ski for
Light. She told me I had been selected as one of two US
crosscountry skiers
to take part in a week-long skiing event in Norway, all
expenses paid!
I had never traveled outside the United States before, and I
was thrilled to
be offered this amazing opportunity. Immediately I began to
prepare for the
trip, which would take place in early April of 2016. I
thought carefully
about my NFBI commitments, knowing that I would have very
little email or
telephone communication for the ten days while I was away.
The toughest part
was that I was sworn to secrecy until my selection was
announced publicly,
and that wouldn't happen until the end of January. I was
totally excited
about my trip, but for months I couldn't say a word to
anyone.
Ski for Light (SFL) is a nonprofit organization that was
founded in Norway
in 1964. It came to the United States in 1975, but has
always had very
strong Norwegian connections. The mission of SKI for Light
is to give blind,
visually impaired, and orthopedically impaired persons the
opportunity to
enjoy crosscountry skiing. Each skier is paired with a guide
throughout
every Ski for Light event. Skiers and guides tend to form
close bonds,
developing rapport as they ski together, and joining the
other participants
and guides at the lodge for fun in the evenings.
I had been taking part in SFL events in the United States
for five years
before I was invited to go to Norway. As one of only two US
participants at
the Norwegian event, I felt I had a certain responsibility
as an ambassador.
I hoped to repay the generous hospitality of my hosts and to
make a positive
impression, both as an American and as a blind American.
People from
fourteen countries took part in the event, and it was
exciting to get to
know them.
When I arrived in Oslo I was surrounded by people speaking
Norwegian and
other languages. It was unsettling to hear a barrage of
words that I could
not understand. As a blind person, I could not pick up on
the cues of body
language that would have given me at least some rudimentary
information
about what was going on. I was almost wholly dependent upon
people who could
speak to me in English.
Hotel buffets posed another challenge. Even when foods were
described to me,
most of them were unfamiliar. I had no idea what I should
put on my plate.
In the end I took my chances and sampled nearly everything.
Stretching
myself in this way was part of the adventure of travel
abroad.
Many of the street crossings in Oslo are equipped with
audible traffic
signals. However, hotel rooms do not have Braille numbers on
their doors. I
was shocked when the hotel staff refused to clean our room
because of my
roommate's guide dog.
Although Norway is in many ways a highly advanced country, I
discovered that
very few blind people are employed. Blind people
automatically receive a
government stipend. I only met one blind Norwegian who had a
job; she worked
at a university.
After a night in Oslo we went north to the snow fields. We
skied every day
from Monday through Saturday. When we returned to Oslo to
catch our flights,
I had time for a bit of sightseeing. I visited the
Resistance Museum, which
documented Norway's history during World War II. I also went
to the Skiing
Museum.
Crosscountry skiing is a wonderful experience. It's great to
be outdoors,
having fun and getting healthy exercise. You can learn more
about Ski for
Light by visiting their website, www.skiforlight.org.
PLAYING WITH CLAY
by Deborah Kent Stein
When I was four years old, my mother set up a child-sized
table in the
corner of the kitchen. On the table she put some plastic
forks and knives, a
few alluminum dishes, and a box of Plasticene, a brand of
modeling clay
commonly sold in toy stores. She explained that while she
was cooking dinner
I could make believe I was preparing a meal, too.
I was the oldest of three children, with two noisy,
rambunctious little
brothers. My mother hoped the clay would keep me occupied
while she juggled
between cooking and caring for the younger children. As far
as keeping me
busy, the plan exceeded her expectations.
I didn't care about pretending to cook, but I loved playing
with clay. I
rolled long coils between my hands and twisted them into
snakes. I learned
to make a ball by rolling the clay between my palms. If I
pressed a smaller
ball onto a big one, I had the basis for a variety of
animals. I could add
long ears and a tiny tail to make a rabbit, or I could stick
on short ears
and a snake of a tail to create a cat.
Plasticene came in sticks, each one a different color. I was
totally blind,
and at first I didn't care whether I made a green dog or a
red banana. My
mother used my interest in clay to help me understand the
role of color in
the world. When I unwrapped a new package of Plasticene, she
showed me which
stick was blue, which was red, which was green, and which
was brown. "Brown
is a good color for a dog," she told me. "You can use green
and blue and red
for birds." Soon I was interrupting her dinner preparations
to ask, "What
color is a rhinoceros?" and "What color is a sea monster?"
Over the years I acquired more clay, more tools, and more
space, with my own
table in the basement. I made towns with cardboard houses
and clay people. I
made clay forests filled with multicolored birds. I made a
castle with clay
walls, a drawbridge of Popsicle sticks, and tall clay
watchtowers.
One summer day my family visited the boardwalk at Asbury
Park on the New
Jersey shore. We kids stuffed ourselves with saltwater
taffy, shrieked our
way through the fun-house, and visited the Ripley's
Believe-It-or-Not
Museum. My cousin gave me lurid descriptions of the
two-headed calf, the
tentacle of the giant squid, and the baby with transparent
skin, all out of
my reach in glass jars.
At last we came upon an object that was out in the open,
something I could
experience for myself. It was a life-sized, sculpted head. I
studied the
regular features, the thick, curly hair, and the intricate
whorls of the
ears. What was this head doing here, among the oddities of
nature?
My cousin read the printed caption. "This head was fashioned
by a man who
was totally blind," it stated. "He made this likeness using
only his sense
of touch. Believe it or not!"
I wondered how the nameless blind man felt about having his
piece on exhibit
in the Ripley's Museum. Did people really think a blind
artist was as
bizarre as a two-headed calf?
On my thirteenth birthday my grandfather gave me six big
blocks of clay--not
from a toy store, but from a store that sold real art
supplies. He explained
that this was an oil-based clay that never dried out and
could be used over
and over again. If I took care of it, he promised, it would
last as long as
I lived.
A few months later my mother and I visited a local art
gallery. Without
hesitation, the proprietor allowed me to touch all of the
pieces on display.
I studied life-sized ceramic heads, bronze nudes, and an
assortment of
animal figures. I discovered that art was not confined to
realistic forms,
and I found that artists worked in media as varied as balsa
wood, papier
maché, plaster, brass wire, and welded steel.
Inspired by a series of animal sculptures I'd seen at the
gallery, I went
home to my blocks of birthday clay. Night after night I
rushed through my
homework, eager to get back to my work in progress. It was
the detailed
figure of a lion, its head lifted above its outstretched
front paws. When it
was finished, my mother set it on a shelf in the living room
and showed it
proudly to any friends who dropped in.
One of the family friends who saw the lion was a
professional artist named
Don Miller. To my amazement he offered to buy the lion from
me for five
dollars. A few weeks later he returned with a plaster cast
of the original
clay figure. It resided on top of the television for the
next twenty years.
Don Miller's interest transformed the way my family and I
thought about my
hobby. No longer did I play with clay. From that time
forward, I did
sculpture!
At college I majored in English, but for one of my electives
I signed up to
take a studio sculpture course. I looked forward to
exploring fresh
possibilities and learning new techniques. When I arrived at
the first
class, however, the instructor, Mr. D., announced that I
would have to drop
the course. "Sculpture is very visual," he explained. "You
won't be able to
participate. It would be a waste of your time and mine for
you to enroll in
this class."
I was shocked by Mr. D.'s narrow perspective. He utterly
dismissed the idea
that anyone could create or appreciate sculpture without
eyesight. Even when
I showed him some of my previous work, he insisted that
there was no place
for me in his class.
I was so angry that I refused to give up. I was determined
to take the
class, even if Mr. D. made me hate every moment of it. I
went to the head of
the art department, who sent me up the ladder to the dean.
The dean ruled
that I could take Mr. D.'s class, with the condition that I
would have an
assistant with me at all times--essentially a classroom
aide. According to
the dean, the assistant would help me find the art supplies
in the
classroom. In reality, he was there as a buffer between me
and Mr. D. The
instructor and I barely spoke to each other all semester.
Despite this unpromising arrangement, I learned a great deal
in Mr. D.'s
class. I experimented with wood carving and made mobiles
with dangling wire
figures. Most important of all, I gained an invaluable
lesson in
self-advocacy. I learned not to give up when a person in
authority told me
no. I discovered that I could fight my way past barriers to
education and
experience.
My interest in sculpture has never flagged, though I've
encountered plenty
of believe-it-or-not reactions along the way. I create
three-dimensional
works with my hands, yet vision-oriented friends and
strangers often find it
amazing and inexplicable. I strive to be judged not as a
blind sculptor, but
as a sculptor.
In my study of sculpture I always felt that blindness posed
one
insurmountable obstacle. My fellow students worked by
looking at live human
models. The only way I could use a model was through touch,
and I couldn't
conceive of touching someone's nude body in order to make a
clay figure. I
worked from imagination or used plastic models that I found
in art supply
stores. I studied a human skeleton to learn about structure
and proportion.
Nevertheless, I knew I was missing an aspect of training
that is critical to
most serious students of art.
In 2011 I enrolled in a sculpture class at the Palette and
Chisel, a
long-established art school in Chicago. Ralph Cossentino,
the instructor,
had taught other blind students, and he welcomed me into his
class. I began
by sculpting the head of Michaelangelo, basing my piece on a
large plastic
model that belonged to the school. From there I moved on to
a self-portrait,
exploring my own face and using myself as a model. But Ralph
was determined
that I should have the same opportunities as his sighted
students. He asked
me if I would like to work with a live model.
I was stunned by the question. On one hand I was thrilled to
find an
instructor so eager to broaden my learning opportunities. On
the other hand,
I felt apprehensive and uncertain. Society has strong
prohibitions against
touching other people. Artists' models are very comfortable
with being
observed visually, but touch would cross a boundary that,
under most
circumstances, is strictly forbidden. I worried about how
both the model and
I would feel, no matter how professionally we treated the
situation.
In spite of my reservations, I knew this was a chance that
might never come
to me again. Ralph talked with the model, a young woman
named Jessica. He
suggested that I begin by doing a hand study, and Jessica
said that would be
fine with her. As I worked with the clay, I paused
frequently to examine
Jessica's outstretched hand. Step by step I worked to
replicate the complex
mechanics of muscle and bone. Yet a precise reproduction
wasn't enough. The
idea was to convey some form of emotional expression, the
subtle difference
between anatomy and art.
I sculpted another hand piece, followed by a foot study.
Then I did a
sculpture of Jessica's head, complete with her magnificent
braid. At last
Ralph suggested that I was ready to attempt a full, seated
figure. By that
time Jessica and I were very comfortable working together,
and we both said
we were ready to give it a try.
As it turned out, Ralph was more nervous than Jessica and I.
He confessed
later that he was worried about the administrators of the
Palette and
Chisel. What would they say when they found out that a
student was touching
the nude model in one of the sculpture classes? To his
relief and mine, the
director of the school had no objections. In fact, he
commended Ralph for
his flexibility and spirit of innovation.
I have now worked with several models, both female and male.
Each has been
generously receptive to working with me. The models have
always approached
our work together as experienced professionals, and I owe
them my deepest
appreciation.
I have met many blind people who are convinced that they do
not understand
sculpture or raised-line drawings. They are intimidated by
the thought of
working with clay or other art materials. To my delight, a
growing number of
people in the National Federation of the Blind are working
to break down the
notion that art is out of bounds for us as blind people.
Some have even
suggested that we expand our efforts in the STEM fields to
include art. STEM
could become STEAM--science, technology, engineering, art,
and math. Few
people, blind or sighted, ever become professional artists,
but art can
enrich life for us all.
When my mother set up that little table in the kitchen, she
couldn't have
imagined where my love of clay would lead me. And my
grandfather was right
about that oil-based clay he gave me for my thirteenth
birthday. I still
have a three-pound package of it, carefully wrapped, and it
is as moist and
moldable as ever. It looks as though it will last for as
long as I live.
IN MEMORIAM: LEANNE MAYNE
Federationists were saddened to learn of the passing of
LeAnne M. Mayne on
June 28, 2016. She died at the Leonard Memorial Home in Glen
Ellyn,
Illinois, after a long illness. She was sixty-two years
old.
LeAnne was born in New York City on December 4, 1953. When
she was only
three days old her father brought her to Illinois, where she
was raised by
aunts in the Chicago area. She attended the Illinois School
for the Blind
(now the Illinois School for the Visually Impaired) in
Jacksonville.
Diagnosed with juvenile diabetes as a small child, she was
not expected to
live beyond her thirties. LeAnne defied the expectations of
the doctors and
lived a full and active life for as long as she could.
After she finished school LeAnne operated the Mayneway
Vending Company,
which had multiple locations. For a time she and her
husband, Jeff, ran a
pizza parlor in Rockville, Illinois.
LeAnne Mayne was a dedicated member of the NFB of Illinois.
She worked
diligently on many state and national fundraising campaigns.
At chapter
meetings and conventions she was always ready to pitch in
wherever a pair of
hands was needed.
LeAnne was predeceased by her brother, Michael Cramer, who
was also a
dedicated Illinois Federationist. She is survived by her
stepmother,
Patricia Mayne; and by her boyfriend of sixteen years, Blair
Alper.
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