Letter to the Editor

 

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Dear Editor,

Several weeks ago I encountered an upsetting incident on our train. I had entered with my Seeing Eye Dog and sat down with her at my feet as usual. An elderly woman next to me suddenly started talking loudly about her neighbour’s grandson being diagnosed as blind, and how terrible that was.

She went on to tell us that there was no future for such a child, what a burden he would be with no prospects in his life. She was very upset for her neighbours who didn’t deserve such a grandchild. Sitting there I felt quite a useless human being. I was not able to interrupt this woman at all and just hoped, in time, she would stop.

As it happens, she suddenly stated that the boy would not even play any sports, would he? I had to concentrate then and replied “Oh, actually he can play cricket, goal ball, or swish; he can go tandem cycling, horse riding, sailing, swimming and play any sports that are part of the Paralympics.” There was finally silence and I realised I had shut her up.

Normally, I can speak quite easily with people, and I can dispel any negative attitudes with my knowledge of how we complete tasks, etc. But this woman did not allow me to say anything, and she had the attitude that she knew all about blindness.

I felt very disappointed and unhappy as I left the train. Her tirade had made me feel less than my usual happy and confident self.

Regards,

Karen, in Perth

* * * * *

Thank you, Karen, for writing about your unpleasant experience. It reminds me of some of my own encounters with people who aren’t well-educated about what living with blindness is really like.

I feel like they’re becoming less frequent over time, but whenever these encounters happen, I, like you, leave them feeling unsettled. They’re disquieting, I think, because we’re left wondering how many people look at us with pity as we pass in the street. How many people like the lady on the train never have their misconceptions challenged?

Your response to her misguided monologue was eloquent and measured. It’s easy to take these things very personally, and react aggressively as a result. I would encourage others in your situation to understand that absence of awareness doesn’t imply the presence of malice. If we correct people clearly, but kindly, I find they often respond very well, and become eager to learn.

I’m very interested in strategies others have used to deal with similar experiences. Tell us how you respond to encounters like the one Karen described, by submitting your own letter to the editor, or getting in touch via phone, Facebook or Twitter.

 

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Editorial

By Jonathan Craig

 

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Communication: The imparting or exchange of information, ideas or feelings.

It’s a theme that arises frequently in this edition of Blind Citizens News. Rikki Chaplin writes about how BCA’s new, fully accessible phone system has made his communication at work much easier. Gisele Mesnage talks about what we can learn from Lainey Feingold, whose innovative “Structured Negotiation” method has led to huge advocacy wins in the US.

Emma Bennison and Joana d’orey Novo both grapple with the way technology doesn’t always have the impacts we would initially expect on our communication. But as we say a fond farewell to SoundAbout, BCA’s quarterly audio magazine, we can also reflect on the innovation and dedication with which leaders overcame the communication challenges of the past to bring us the information we needed.

In my last editorial, I wrote about my belief that communication, through stories and conversations, is the beating heart of our community. But now I want to look outward, to briefly examine the challenges of communicating our unique needs in a society where competing priorities and the constant push for progress make it harder than ever to consider marginal groups.

Since stories seem to be my obsession of late, I should probably tell one of my own. BCA has campaigned tirelessly in 2018 against the increasing adoption of inaccessible EFTPOS terminals. On these terminals, customers input their pin via a touch screen, but customers who are blind or vision impaired have no way of differentiating numbers by touch, and thus can’t input their PIN independently.

Recently, I encountered one of these for the first time, when paying for a doctor’s appointment at a clinic I’d never attended before. The receptionist immediately understood the problem, and seemed more embarrassed than I was by our predicament. Rather than force me to disclose my PIN, she offered to conduct the transaction manually, as if I were paying by credit card over the phone.

This isn’t usually a suitable alternative, because it’s not available to all businesses, carries its own security risks, and takes much longer than an EFTPOS transaction. I agreed in this case, partly because I knew it would be memorably inconvenient for the business.

But mostly, it gave me a chance to talk more with the receptionist and her colleague. I explained that as far as I knew, there weren’t many functional advantages to touch screen terminals, and that they were introduced for aesthetic reasons. They both agreed, and promised to mention it to their manager.

I’m returning to the clinic soon, and will be interested to see whether anything has changed. But I was struck by the genuinely apologetic attitude of the women I spoke to. They seemed to understand how disempowering the situation felt for me, and suggested that the problem had only arisen because no one had thought of it until I arrived at the counter.

I’ve encountered a similar pattern again and again, a confounding combination of good will and bad awareness. I spoke to Martin Stewart for this issue about another advocacy win regarding the high capacity trains to be introduced in Victoria next year. Though I’m very happy to see them resolved, I was shocked that nobody else had thought of the significant issues he raised.

As I’ve said before, I believe the majority of Australians broadly want a more inclusive society, but don’t know where to begin. Maybe this is partly because those who haven’t encountered people who are blind or vision impaired, often don’t have any understanding of what our daily lives are like.

There’s proof of this in this issue’s letter to the editor, which describes some very negative misconceptions about living with blindness. While my personal experience suggests these attitudes are growing less common, I’m reminded, whenever I meet someone who’s utterly fascinated by a screenreader, that a lot of people are still surprised that I can even access the internet.

While I feel there’s a lot of good will at the personal level, I suspect the corporate and policy levels view minorities much more cynically. Businesses are encouraged to be inclusive when they see potential loyal consumers. Politicians are moved by potential votes. Helping minorities, for both, can often generate great, cheap, public relations victories.

But, for example, I believe we don’t have audio description on Australian TV, largely because the Minister for Communications doesn’t feel most Australians know what it is. It isn’t seen as a good investment, because the only votes it will win are ours, and those are not enough.

We often benefit profoundly from social and political progress. But as inaccessible EFTPOS, non-existent audio description, and ill-considered public transport all demonstrate, there are times when progress leaves us behind. As the rate of progress increases, more and more changes will be occurring simultaneously, making it increasingly difficult to catch the harmful ones in time.

This is why I believe raising awareness is so crucial. The more people understand how we overcome our barriers to access, the more support we’ll have for initiatives which help us remove them. The more we can encourage people to consider us as valuable participants in, and contributors to society, the more businesses and governments will be motivated to consider us when designing their products and policies.

This, to me, is the great communication challenge we now face. I think it’s profoundly important that we collectively ask ourselves how we can better inform people, at all levels, about what being a person who is blind or vision impaired is like in the 21st century.

One area where I feel there’s plenty of room for improvement, is our representation in the media. Whenever I see us on screen, I prepare for disappointment and frustration at another wasted opportunity. I enjoyed the “You Can’t Ask That” episode on living with blindness, and I feel we should be fighting for more forums like that where we can be our own ambassadors.

On a personal level, I really encourage readers who encounter something like inaccessible EFTPOS terminals to be careful when you communicate the problem. I know how upsetting and frustrating it can be, and I think it’s valuable to talk about those feelings, as I did.

But the person serving you usually didn’t choose to buy the touch screen terminal, and regardless, they probably feel bad about this situation. Blame is a hard burden to bare, and if you place it directly on their shoulders, they may try to shift or deflect it. Guilt can curdle, and become anger, but it can also turn into action. Which of these will help us more?

Ultimately, I don’t have answers to many of the questions I’ve raised here. My opinions and observations aren’t facts, and I’m happy to be proven wrong, or argued toward different conclusions.

But as an editor, I feel I have two key responsibilities. The first is to be a great listener. I’ll let you judge my success, but to the best of my ability, everything I’ve said here is based on what I’ve heard. The second is to ask great questions, the kind which will inspire readers and writers, and start conversations.

So let me pass these questions on to you. Let’s talk about whether, and if so why, many people still know so little about living with blindness. And let’s talk about the challenge of effectively communicating information about how we live, ideas about how our lives could be better, and how it feels when we aren’t heard. Let’s tackle, together, these big questions about how, through good communication, we can bring about positive change.

 

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Directory of Contact Details

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National Women’s Branch (including Womentalks)
Contact: Janene Sadhu
Email: nwb@bca.org.au

National Women’s Branch (Aspirations Magazine)
Contact: Carmel Jolley
Email: carmeljolley@bigpond.com

National Policy Council
Contact: Fiona Woods
Email: npc@bca.org.au

NSW/ACT State Division
Contact: Joana d’Orey Novo
Email: joanadn76@gmail.com

NSW/ACT State Division (Spring into Action)
Contact: Stephen Belbin
Mobile: 0409 000 100.
Email:  Stephen.belbin@tafensw.edu.au

NDIS / NDIA
To find out when you will be able to access the NDIS, contact the National
Disability Insurance Agency on 1800 800 110.

My Aged Care Contact Centre
Phone:  1800 200 422

Information about co-payments for Home Care Packages
To find out how much you might be required to contribute, contact the
Department of Fees and Charges within the Department of Human
Services (Centrelink) on 1800 227 475.

How to Submit to Blind Citizens News

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The Editor welcomes your submissions for Blind Citizens News. The deadline for contributions for the next edition is Friday, 1 November, 2019. Contributions can be submitted in Braille, print, audio CD or electronic format (in Word in Arial 16-point font).

Send emails to bca@bca.org.au and write “Blind Citizens News Submission” in the subject line. For all other format contributions, please send the document to the BCA Office.

Submissions should be between 500 and 1200 words in length. Submissions cannot be made anonymously, and the Editor must be made aware of any conflict of interest which may be relevant to the author’s work.

Your Advocacy is the Unique You

Martin Stewart

 

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Editor’s Note

Martin Stewart, with support from BCA, was last year instrumental in inspiring Telstra not only to make significant accessibility fixes to all their AFL and NRL apps, but also to hire two world-class app developers with experience writing accessible software.

It seems that by raising awareness of the issue, Martin has helped the telecommunications giant make a new, more sustainable commitment to accessibility. Here, he offers compelling insight into his perspective on advocacy, and an optimistic vision of a more inclusive future.

***

As I mingle and circulate, I often hear it said, “let’s face it, I can’t change this”. “It doesn’t matter what I do or say”. “My opinions do not count”.

These are understandable feelings of alienation and disempowerment. Such feelings are experienced and expressed more often within minority groups. Although this is easily rationalised because of mainstream attitudinal ignorance and therefore outcomes, I say let’s reject such negatives and replace them with the power of our natural, strong and unique character print.

I can hear you asking, “what does this mean”? Here is my explanation, which is based upon my many years of advocacy experience.

Every human being has a unique DNA makeup. This impacts upon how we individually interact. Therefore, each of us possesses what I describe as a unique character print. I strongly suggest that this very individual personality, that each of us has, is actually naturally required to complete society’s jigsaw puzzle. Without you, your opinions, actions and skills, society itself is the loser.

In days gone by, people would refer to sayings such as “the power of the pen” or “the pen is mightier than the sword”. These descriptive sayings were meant to convey the influence that an individual could wield by the simple act of handwriting. Of course for many of us blind or low vision citizens, our words were then primarily produced by writing in brilliant braille.

Thanks to technology, our expression horizons have truly broadened. Now we can express ourselves in so many varying formats, and on social media. For example, I am currently using voice interactive software to produce what you are now reading. This, in the recent past, was simply not possible. This being said, if you choose to make your unique mark by expressing yourself using older technology, such as a pen or landline phone, this is definitely you speaking your own way.

With technology, such as language translators, I believe the cultural gaps are being bridged, and the world is becoming smaller, therefore the opportunity to influence is becoming larger. The use of words, rather than fists, to influence outcomes is increasingly society’s preferred language.

I optimistically believe that this slow but sure global change is the key to true equality and equal opportunity. When this occurs we will no longer be a minority, instead each one of us will be a valued and unique contributor to humanity.

Despite steps back, I believe that this change is happening. Your advocacy is as good as you and your words. You have been born with traits which we need to be influenced by. I hope that we all can respond accordingly when we next face the inevitable advocacy challenge, with self-worth in mind.

 

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