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You never know

In Uncategorized on August 30, 2010 by dtabak

In May of each year, the Guild hosts an exhibition of  works by artists with vision loss.  Shortly before the opening this year, I received an email from a woman who volunteers teaching art to underprivileged children in the Chicago.  She had seen the report on one of the Passionate Focus artists, David Simpson, on WGN-TV (http://www.wgntv.com/community/chicagosveryown/wgntv-chicagos-very-own-david-simpson-artist,0,966096.story).  She was very impressed with David’s art and especially his attitude.  She asked me if I could put her in touch with David so he could inspire her students to pursue art as a way to express themselves.  David immediately accepted.

While I am very proud of our programs and services that help people with vision loss live independently and productively, what impressed me the most about the Guild is our fundamental belief that every person has the ability to overcome adversity and thrive.  This message is applicable to people struggling with other issues.

Simply knowing that some can overcome a disability can be the difference between success and failure.

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Dining with Confidence

In Uncategorized on June 7, 2010 by dtabak

Recently, the Guild hosted three sold-out sessions of our workshop, “Dining with Confidence.” Polly Abbott, our director of rehabilitation services, developed this program to help people with vision loss overcome their fear of dining with friends and families.

People with vision loss, unable to see what is on their plate due to their eye condition or insufficient lighting, commonly experience difficulty when eating. Food falls off the plate, glasses are knocked over, and forks can almost magically lose whatever food was on them before it is consumed. Even trying to cut with a knife and fork can be intimidating. Eating loses all its enjoyment and become a daily ordeal associated with feelings of helplessness and frustration. Ashamed to be unable to eat as neatly as they once did, many people simply decide to eat in private, isolating themselves from the pleasures of the table and the social benefits of sharing a meal with others.

Dining with Confidences addresses issues such as: “How do I tell the salt from the pepper?” “How do I know what is on my plate?” “How do I pick up my water without knocking it over?” “How do I eat without making a mess on the table?” “How do I cut a small bite with a knife and fork?” Eating gracefully without sight requires a few simple strategies and, of course, a sense of humour. Participants practice efficient cutting, scooping, and spearing techniques under the Polly’s guidance and discuss in detail how to handle the most challenging food situations. Participants, armed with new strategies and techniques, leave feeling confident about rejoining their friends and dining in public again.

What has impressed me is the popularity of Dining with Confidence. Sessions quickly fill up and you often hear the sounds of laughter and camaraderie that comes from the room. People are obviously learning and gaining strength from each other. Dining with Confidence truly demonstrates what distinguishes the Guild for the Blind from other agencies. Our goal is not to help our members become more adept visually impaired people; our goal is to help people with vision loss continue to do the things they did before they lost their vision or to be full participants in their communities.

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Who are you?

In Uncategorized on May 25, 2010 by dtabak

“You don’t change when you lose your sight, other people change.” This is what a Guild member, Barry, told me recently. Larry had been a partner in a successful construction firm when he lost most of his sight during a bypass operation. His partner eventually forced Barry out, despite the fact that Barry could still do the job. Another Guild member, Georgiana, told me that when she lost her sight due to macular degeneration, some of her friends abandoned her “as if macular degeneration was catching.”

I have heard this sentiment from many Guild members who have discovered that not only do they have to deal with their own fears after vision loss, but also the perceptions of people around them. People have known each other for years suddenly become strangers after vision loss.

Vision loss is much more than just the loss of a sense. It can also be a true blow to one’s self-image and how people see them. As some one who did not know anyone with vision loss when I came to the Guild eight years ago, this puzzled me. I had no doubt that losing one’s vision is an extremely traumatic occurrence. But fundamentally changing who you are and how people see you? It seemed inconceivable to me.

Over the years, I have come to see vision loss more holistically. It affects your employment opportunities, your ability to do the things you used to do for pleasure and even the most mundane activities like getting dressed or making a snack for yourself. The sheer frustration is exhausting and certainly leads to depression and isolation as others simply do not understand what you are going through.

But Georgiana gave me a new way of looking at it — the popular media. Each day we are bombarded with images of perfect physical specimens. We nearly worship those who have been blessed with seemingly flawless bodies. And soon we come to think of those people as being the norm and we feel all the worse for our less-than-optimal selves. It must be doubly worse for someone with a disability who can never hope to achieve the perfect body.

We give ourselves too little credit if we define perfection as the goal. First, and foremost, it doesn’t exist. Make-up and airbrushing do not constitute true beauty nor does vision loss constitute helplessness.

People are more complex than the application of a single adjective — blind. I have always said we work with people who happen to have vision loss, not blind people. I know lawyers, bankers, teachers, business people and unemployed people who are funny, smart and talented. Some of them have trouble seeing, some of them don’t. Don’t we owe it to ourselves to dig a bit deeper? Treasure rarely lies on the surface.

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In Resources, Uncategorized on May 11, 2010 by dtabak

David Flament, the Guild’s manager of adaptive technology, recently participated in a panel called “What’s in Your Backpack.”  Each panelist was to list the adaptive or assistive technology he or she carries in his or her backpack to make their lives easier.  Below is David’s list:

Thumb drive

For transferring files from one computer to another.  David also carries around an iZoom thumb drive, a screen reading and magnifying program that allows him to use adaptive technology on any computer.  For more information, visit: http://www.issist1.com/

iPhone

Apple’s popular smart phone is now accessible for people with vision loss with either screen reading or screen magnifying capabilities.  To learn more, visit: http://www.apple.com/iphone/iphone-3gs/accessibility.html

Victor Reader Stream

Humanware’s DAISY-MP3/NISO player lets you read and navigate through complex books, such as reference manuals and school books, as well as novels and magazines. You can also use its built in text to speech to read books in text format such as Bookshare. It also has an integrated microphone to record voice notes.  Please follow this link for more information:  http://www.humanware.com/en-usa/products/blindness/dtb_players/compact_models/_details/id_81/victorreader_stream.html.  The Guild is currently offering the Victor Reader Stream for $349, which includes a 4GB SD card.  We also offer free classes on using the Stream.  Please contact the Guild’s Kathy Austin at kathya@guildfortheblind.org for more information on the Stream.

Pocket magnifier and monocular

David also carries a pocket magnifier for magnifying text as well a monocular for seeing distant objects.  The Guild carries a wide variety of magnifiers and monoculars.  Please contact Brian Hollandsworth for an appointment at Brian@guildfortheblind.org.

So that’s what’s in David’s backpack.  What’s in yours?  Please share the adaptive and assistive devices that you carry around with you on a daily basis that makes your life easier.

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What we really want

In Uncategorized on April 26, 2010 by dtabak

Recently I was speaking to a Lion’s Club on the Southside. An older gentleman asked me if there was a cure for his wife’s macular degeneration. She was really struggling with her vision loss and he had heard there were vitamins she could take that would reverse the disease. I have heard this question many times. People have been struck with vision loss and they and their loved ones are grasping at any solution that may provide some hope of regaining their sight.

It is always painful to have to admit there is nothing medically that can be done to help someone regain vision loss. I do mention that there are treatments for the wet variant of macular degeneration including laser and injection procedures. But these only work on the wet variant and only stop more damage from occurring.

This does not mean there is nothing that can be done about macular degeneration, especially for those at risk of developing macular degeneration. The Age-Related Eye Disease Study (AREDS) sponsored by the National Eye Institute found that taking high levels of antioxidants and zinc can reduce the risk of developing advanced age-related macular degeneration by about 25 percent. For more information on the AREDS, please visit: http://www.nei.nih.gov/amd/summary.asp.

But sadly for this man and his wife and the millions of people with irreversible vision loss, once the damage is done there is not much medically that can be done.

But in that moment between question and answer is truly the challenge facing the Guild and all agencies that serve people with vision loss. What we offer is the skills and confidence to live a rich and productive life with vision loss, what people want is to get their sight back. From a promotion standpoint, it is lose-lose. We are offering programs and services that people inherently need but do not want.

I, for one, would never deprive anyone of the hope of a cure for vision loss. In these times of medical advances, it would be foolish to assume that the current situation predicts the future. But, on the other hand, I think one should not simply wait for the cure. There is too much life to living that can be accomplished by receiving visual rehabilitation.

So while the Guild offers a wonderful array of programs and services, our greatest challenge remains convincing people that there is value in visual rehabilitation. While we cannot restore your vision, we can help provide a richer life with vision loss.

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A different language is a different vision of life.

-Federico Fellini

Perhaps I am a little late to the blog game, but I am pleased to welcome you to “A Different Vision,” which offers my personal views on vision loss and rehabilitation.  This blog will have many facets including information on visual impairment, the Guild for the Blind’s programs and services and why we truly believe that the best way to help a person with vision loss is to match the programs and services to their specific goals and needs.

Many organizations that serve people with vision loss state in their mission statements that they exist to help their clients find independence and dignity.  However, true independence depends on self-determination.  For someone who is visually impaired that means finding the tools and skills they need to live the life they wish to live.  If they are seeking employment, true independence requires they have the opportunity to pursue a job that meets their skills and interests.

Since our beginnings in 1947, our goal has been to help our members reach their goals.  Instead of applying a one-size-fits-all approach, we spend time asking our members about their goals.  This does not mean success is guaranteed or that we can provide every program that people want.  But we promise to listen to their hopes and fears.

To that end, “A Different Vision” is about listening and sharing.  Each week, I or a guest blogger will share an opinion, a new adaptive tool or strategy or an idea for a new program and services.  We invite you all to comment on the post or lend tips or tricks or make suggestions for new posts.

So what are the guidelines?  First, the views expressed are of the author and not the Guild for the Blind.  I hope to speak honestly and openly about issues facing people with vision loss.  I hope all participants will adhere to principals of my seven-year-old’s classroom: Is it true?  Is it kind?  Is it necessary?  Follow these guidelines and we will have a meaningful conversation.

So let’s get started.  As always, I welcome feedback, suggestions and criticisms. I also welcome guest bloggers.  Please send me your submissions to david@guildfortheblind.org. I promise to consider all submissions.

A Different Vision

on November 9, 2009 by dtabak

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