2016 has been a dark year for me. I'm not (just) using 'dark' here for its metaphoric (and ocularcentric) meanings of ''sad' and 'gloomy'. I also mean that my two cataract operations, not to mention the broken leg, obliged me to spend a lot of time lying in the dark. It is no coincidence that 2016 is also the year that I rediscovered the wonder of audio books. When I was a child, commercially produced audio books were hard to find. I had two: The Railway Children and Black Beauty and I listened to them both so many times that I wore them out. But not before I had learnt them off by heart. When my reading glasses were perfected, I abandoned audio books in favour of much more readily available print books. Five years ago I discovered kindle which let me read large-print even as my eyes were failing.
My love affair with audio books began again at Blind Creations when writer and musician Romain Villet introduced me to his electronic reader Victor. The Victor Stream is a pocket-sized machine which reads texts in almost any electronic format (except PDF) out loud using a pretty convincing text-to-speech voice. I find it particularly useful for reading long documents quickly: not only can I accelerate the reading speed, I can also skip material, make notes and highlight important passages. Listening to text will never be as quick as reading it, but I am getting closer. I read Jean Giono's Le chant du monde this way in May and it is perhaps for this reason that I noticed the novel's extraordinary non-visual, multisensory, prose, which I discuss here.
Blind people have listened to stories for as long as blind people have existed. But audio books have only very recently become widely and easily available to the non-blind public.. Libraries now use services like overdrive to deliver audio content electronically, and companies like Audible encourage busy people to multi-task by reading as they run, drive or cook.
I was sceptical about Audible's offering at first. I thought their books were over-priced, especially as the RNIB's talking book service gives me free access to books read by volunteers. Crucially though, it takes the RNIB a while to provide access to recently published books and they do not always have the books I want when I want them; they also have next to nothing in French. Audible, on the other hand, often has books available at the same time as the print versions are published. This means that I can read the same books as my family and friends; now more than ever I feel like I am part of contemporary literary culture.
But for me the main advantage of Audible is the way their books sound. Their narrators are professional performers who deliver their texts in compelling and creative ways. They sound like they have thought about how to read the story; they adopt different voices for different characters, they change the tone, speed and volume of their voice to match the prose and they pay attention to dialects, accents and regional contexts. Chimamanda Ngozi Adichie's wonderful Americanah is an excellent example of the difference a good narrator can make. The novel, which is about a Black woman's experiences in Nigeria and America, is read by Black actress Adjoa Andoh and produced by Whole Story Audiobooks. In what might be the audio equivalent of free indirect speech, I immediately felt a powerful connection with the narrative voice through the narrator's voice. In addition, when Adichie's narrator talks about the different accents she encounters in Nigeria, and how a person's voice does or does not reflect their personality or social situation, Andoh's voice cleverly mimics the different accents that her protagonist is describing. Because of its narrator, I am convinced that listening to Americanah was a more immersive, enriching and fulfilling experience than reading it would have been.
To my great delight, Audible also offers audiobooks in French and I have been devouring Fred Vargas's Commisaire Adamsberg books this year. In the fifth book in the series, Sous les vents de Neptune (Wash this Blood Clean from my Hand), produced by Audiolib, Adamsberg and his colleagues travel to Quebec and spend time encountering, deciphering and discussing the impenetrable Quebecois accents and vocabulary of their Canadian colleagues. The narrator, Francois Berland has a lot of fun putting on Quebecois accents and there is no doubt that his different voices improved my experience of reading this novel.
Audiobooks are a great example of what disability studies would call 'blindness gain': they were first developed for blind people and have now become widely available to everyone. They used to be an assistive technology for a marginalised population; they are now widely and easily available. Non-blind people are now lucky enough to be able to access the wonderful world of audio, a world which was once the closely guarded secret of blind people.
This blog maps my place as a partially-blind academic in a resolutely sighted world. It looks at blindness in history, literature, art, film and society through my out-of-focus gaze.
Friday, 11 November 2016
Saturday, 1 October 2016
Towards a Multisensory Aesthetic: Jean Giono's Non-Visual Sensorium
Next week I am delighted to be travelling to Montreal to speak at the International Visual Literacy Association Annual Conference. Along with my Blind Creations co-organiser Vanessa Warne, and Blind Creations speakers Georgina Kleege, Florian Grond and David Johnson, I am presenting some of the work from my forthcoming book Visions of Blindness in French Fiction in a panel organised by Piet Devos and wonderfully entitled: 'The Distorting Mirror of Blindness: Visual Literacy and Non-Sighted Aesthetics'. Whilst I am in Montreal I am also looking forward to exploring some of the places evoked by Jacques Semelin in his recent blind travel journal Je veux croire au soleil and I will be presenting some of the highlights of the Blind Creations conference at a talk (in French) at the Institut Nazareth et Louis Braille. (Click here for more details about this event and how to watch and listen via videoconference).
Below is a sneak preview of part of my work on Jean Giono which I will be presenting at the IVLA conference:
Passages of this kind are found throughout Giono’s oeuvre. But their relevance only becomes clear when they are read alongside Giono’s depiction of the blind character Clara whom Antonio encounters later in the novel. Antonio and Clara are mutually fascinated by each other’s relationship with the senses. When they talk about blindness and sightedness the usually visually reliant reader is invited to rethink their preconceived notion that blindness is a kind of lack.
When Clara asks Antonio to describe night, day and light to her, Antonio struggles to evoke darkness without recourse to visual language. Like blindness, darkness is here unspeakable because it exists outside the limits of ocularcentric language, a language whose very existence depends on a celebration of sight and thus a negation of sightlessness. Antonio emphasises this link between darkness and blindness by evoking the one in relation to the other, and by paradoxically using a vocabulary of seeing to describe this non-sight. Clara, on the other hand, is not hampered by the constraints of ocularcentric language. Her insistent questioning of Antonio’s language encourages not only Antonio but also the reader to analyse what lies beneath the words non-blind people too often take for granted. She can thus combine sense impressions in creative and liberating ways. In an echo of the description of the river at the novel’s start, she merges two distinct sense impressions, (non)sight and smell, in her assertion that for her, ‘day is smell’.
Later, Clara offers us a more immersive and sustained experience of her impressions of the countryside. Rather than detecting spring through its visual clues, she can tell its arrival by its smells and sounds. As she explains: « Ça sent […] et puis ça parle » («It smells and also it speaks ».). Clara tries to explain how she experiences the world. She recognises flowers but does not give them the same names as everyone else. According to her it is not the names of the flowers which are important, but the multi-sensual way in which she experiences them:
Clara’s relationship with the world is intense, multi-sensorial, corporeal and all-encompassing. She combines sense-impressions to create highly evocative and sensual descriptions of nature in a way which reminds us again of the novel’s opening lines:
These descriptions are striking because they evoke the landscape with no need for visual references. But importantly these descriptions do not alienate the ocularcentric reader. Clara’s evocation of nature is so powerful that we are immediately immersed in it without even noticing her lack of reference to visual elements. It is only because Giono foregrounds her blindness that we notice her non-visual language. By describing her non-visual acquisition of knowledge as ‘seeing’, Clara rids the verb of its associations with eyesight and thus disentangles notions of perception and detection from their persistent association with physical looking. Giono is thus using Clara to destabilise the hierarchy of the senses,
The ease with which Clara discusses her multi-sensual way of not seeing, together with the way in which non-visual descriptions of nature are incorporated into the novel’s prose even when recounted via the consciousness of a sighted character, invite us to read both Clara and Antonio as authorial figures whose discussions function as reflexive comments on Giono’s own non-visual creative processes. In addition, Clara’s non-visual relationship to nature functions to overturn sight’s expected place at the top of the hierarchy of the senses whilst celebrating the creative potential of the non-visual senses. Giono’s prose thus redefines notions of ‘sight’ and ‘seeing’ by detaching them from the physical act of looking, in order to encourage his reader to rethink her own relationship with the visual.
Below is a sneak preview of part of my work on Jean Giono which I will be presenting at the IVLA conference:
La nuit. Le fleuve roulait à coups d’épaules à travers la forêt, Antonio avança jusqu’la pointe de l’île. D’un côté l’eau profonde, souple comme du poil de chat, de l’autre côté les hennissements du gué. Antonio toucha le chêne. Il écouta dans sa main les tremblements de l’arbre. (Night. The river was shouldering its way through the forest, Antonio went as far as the tip of the island. On one side was deep water, as supple as a cat’s fur, on the other side the whinnying of the ford. Antonio touched the oak. He listened with his hand to the quivering tree.)These opening lines from Jean Giono’s 1934 novel Le Chant du Monde, are a characteristic example of the kind of sensuous prose description Giono has become famous for using to describe his beloved Provençal landscapes. Giono’s descriptions have long been celebrated by critics for their power to capture the beauty of southern France. But if we look closely at this passage, we notice that it somewhat unexpectedly rejects the kind of visual description we expect from the realist novel in favour of a sensorium more overtly focused on a powerful combination of touch and sound. This challenge to the usual hierarchy of the senses is in fact announced in Giono’s decision to begin the novel in the dark. The novel’s opening words, ‘la nuit’, tell us that because the sighted protagonist Antonio - through whose consciousness most of the third-person narrative is filtered - does not need sight to navigate, the reader is also asked to imagine the setting without recourse to visual elements. Instead of telling us what the river looks like, Giono evokes it through Antonio’s perception of it, that is, by how it feels (as supple as a cat’s fur) and how it sounds (the whinnying of the ford). The surprising use of words associated with animals to describe a body of water adds to our sensory immersion in the scene by combining different sense impressions in vivid and evocative ways whilst reminding us that we are in a profoundly natural setting. The ford does not really sound like a whinnying horse: through the noise it makes, which is impossible to capture in language, it reminds Antonio of the unpredictable power of a skittish foal. The combination of touch and hearing is continued in Antonio’s relationship with the oak tree. The phrase ‘il écouta dans sa main’ (he listened with his hand) uses a synesthetic combination of the sense impressions of touch and hearing to capture the strength of Antonio’s feeling for the tree.
Passages of this kind are found throughout Giono’s oeuvre. But their relevance only becomes clear when they are read alongside Giono’s depiction of the blind character Clara whom Antonio encounters later in the novel. Antonio and Clara are mutually fascinated by each other’s relationship with the senses. When they talk about blindness and sightedness the usually visually reliant reader is invited to rethink their preconceived notion that blindness is a kind of lack.
When Clara asks Antonio to describe night, day and light to her, Antonio struggles to evoke darkness without recourse to visual language. Like blindness, darkness is here unspeakable because it exists outside the limits of ocularcentric language, a language whose very existence depends on a celebration of sight and thus a negation of sightlessness. Antonio emphasises this link between darkness and blindness by evoking the one in relation to the other, and by paradoxically using a vocabulary of seeing to describe this non-sight. Clara, on the other hand, is not hampered by the constraints of ocularcentric language. Her insistent questioning of Antonio’s language encourages not only Antonio but also the reader to analyse what lies beneath the words non-blind people too often take for granted. She can thus combine sense impressions in creative and liberating ways. In an echo of the description of the river at the novel’s start, she merges two distinct sense impressions, (non)sight and smell, in her assertion that for her, ‘day is smell’.
Later, Clara offers us a more immersive and sustained experience of her impressions of the countryside. Rather than detecting spring through its visual clues, she can tell its arrival by its smells and sounds. As she explains: « Ça sent […] et puis ça parle » («It smells and also it speaks ».). Clara tries to explain how she experiences the world. She recognises flowers but does not give them the same names as everyone else. According to her it is not the names of the flowers which are important, but the multi-sensual way in which she experiences them:
Toutes les choses du monde arrivent à des endroits de mon corps (elle toucha ses cuisses, ses seins, son cou, ses joues, son front, ses cheveux) c’est attaché à moi par des petites ficelles tremblantes. Je suis printemps, moi, maintenant. (Everything in the world comes to a place on my body (she touched her thighs, her breasts, her neck, her cheeks, her forehead, her hair) it is attached to me by tiny trembling threads. I am spring now.)
Clara’s relationship with the world is intense, multi-sensorial, corporeal and all-encompassing. She combines sense-impressions to create highly evocative and sensual descriptions of nature in a way which reminds us again of the novel’s opening lines:
Dans toute la colline il y a des pattes, des ongles, des museaux, des ventres. Entends-les. Des arbres dures, des tendres, des fleurs froides, des fleurs chaudes. Là-bas derrière, un arbre long. On entend son bruit tout droit. Il fait le bruit de l’eau quand elle court. Il a de longues fleurs comme des queues de chats et qui sentent le pain cru. (All over the hill there are feet, claws, muzzles, bellies. Listen to them. Hard trees, soft trees, cold flowers, warm flowers. Over there a long tree. We can hear its noise straight ahead. It sounds like running water. It has long flowers like cats’ tails which smell of uncooked bread.)
These descriptions are striking because they evoke the landscape with no need for visual references. But importantly these descriptions do not alienate the ocularcentric reader. Clara’s evocation of nature is so powerful that we are immediately immersed in it without even noticing her lack of reference to visual elements. It is only because Giono foregrounds her blindness that we notice her non-visual language. By describing her non-visual acquisition of knowledge as ‘seeing’, Clara rids the verb of its associations with eyesight and thus disentangles notions of perception and detection from their persistent association with physical looking. Giono is thus using Clara to destabilise the hierarchy of the senses,
The ease with which Clara discusses her multi-sensual way of not seeing, together with the way in which non-visual descriptions of nature are incorporated into the novel’s prose even when recounted via the consciousness of a sighted character, invite us to read both Clara and Antonio as authorial figures whose discussions function as reflexive comments on Giono’s own non-visual creative processes. In addition, Clara’s non-visual relationship to nature functions to overturn sight’s expected place at the top of the hierarchy of the senses whilst celebrating the creative potential of the non-visual senses. Giono’s prose thus redefines notions of ‘sight’ and ‘seeing’ by detaching them from the physical act of looking, in order to encourage his reader to rethink her own relationship with the visual.
Saturday, 16 July 2016
Shades of Blindness
I think it is fair to say that my cataract operations were successful. For the first time in three years I can read print, the world is so bright and colourful it feels like I am on the set of The Wizard of Oz, and all my friends and colleagues look about twenty years older. But whilst my sight is better than it was when I was an undergraduate student, I am still legally blind. I feel like I can see again but it turns out I still can't read the eye chart, see detail close up or at a distance or recognise people. Navigating in crowded or unfamiliar places is still tricky and stressful and I still need my reading glasses, my telescope and my white cane. And now I also need shades. I used to hate wearing sun glasses. By blocking out what little light made it into my eyes, they made me even blinder than ever. But now I can't go out without them. My new cataract-less eyes are amazingly sensitive to light. Even with my shades, I can see colours more brightly than I could before. But wearing shades has a drawback I hadn't expected. By hiding my eyes, the shades also hide my blindness. And because my eyes look different they work a little bit like my white cane - they tell people that because my eyes do not look the same as theirs, I might not see the same as them. So when I go out with my shades but without my white cane I look completely sighted. And this can cause problems. Last weekend I went to a music festival with my family. We had a lovely time camping, eating bacon sandwiches and drinking wine (not necessarily all at the same time). But when I went down to the front to watch a band (without my white cane), a rather irate lady accused me of pushing in. I honestly had not meant to push in front of her and was genuinely shocked at her anger. I was also upset because I realised that I do not in fact see as well as I thought. I still miss visual cues (and clues) and without my white cane this makes me look at best clumsy, and at worse rude. So even though my cane is heavy and cumbersome, and even though my new sight makes me wonder if I am really as blind as the medics' measurements suggest, I will still be using my cane and still proudly defining myself as 'partially blind'.
Monday, 11 July 2016
Book Review: 'Jules' by Didier van Cauwelaert
Since I discovered his Goncourt-winning Un aller simple in 1995, I have always loved Didier van Cauwelaert's quirky, touching and gently ironic novels. But my heart sank when I learnt that his most recent work Jules (Albin Michel: 2015) tells the story of a blind woman whose sight is miraculously restored. I was worried that this would be a simplistic celebration of the cure whereby Alice's new sightedness would bring her all the happiness and hope denied her by her blindness.
The novel's opening page did nothing to allay my fears. When the sighted narrator Zibal first glimpses still-blind Alice, his lascivious gaze objectifies her by its insistence on her physical appearance:
Hauts talons canari, minishort rouge et top turquoise, elle ne risquait pas de se faire écraser par temps de brume. N’eût été le labrador qui la guidait au bout d’un harnais, ses grandes lunettes noires seraient passées pour un accessoire de star soucieuse qui son incognito se remarque. Les cheveux blond-roux maintenus par un chignon en broussaille, les seins libres sous la soie quasi transparente, un sourire de rendez-vous amoureux allongeant les bavures de son rouge à lèvres, c’était une aveugle particulièrement voyante qui faisait bien davantage envie que pitié. (Jules, Didier Van Cauwelaert (Paris : Albin Michel, 2015, p. 7)Zibal’s emphasis on her physical appearance reduces Alice to nothing more than a collection of sexual attributes without taking any account of her personality, context or even name. She is nothing more than an anonymous ‘aveugle’ who is completely defined in relation not only to how she looks to him but also how she does not look at him. In addition, the form of the text further emphasizes Alice’s objectification. She appears to be defined according to the controlling gaze of a male first-person narrator whose words are motivated by his desire not only to possess her sexually, but also to possess her metaphorically by capturing her in and via his text. This dual act of possession is rendered possible precisely by the very thing which makes Alice attractive to the narrator, namely her blindness. Alice is unaware that she is being looked at in this way and is thus even further objectified by the silence of the controlling gaze and the conspiracy between the sighted gazer and the reader which it establishes.
Happily, this narrator-reader complicity is shattered by the irruption of Alice's voice into the text. As the narrative progresses, Alice and Zibal recount alternating chapters so that a dual first-person perspective is established which destabilizes what the reader thinks he or she knows about both blindness and sightedness. Unlike her friends and colleagues, Alice is not overjoyed when she regains her sight. Far from it. She is horrified by the world she can now see and feels abandoned and lost without her guide dog Jules:
L’enthousiasme autour de moi, l’émerveillement que suscite ma guérison me laissent un sentiment de solitude honteuse que jamais le handicap n’a provoqué. Le devoir de bonheur auquel je m’astreignais, par fierté et instinct de survie, est remplacé desormais par un simple code de décence. Je n’ai plus le droit d’aller mal. (pp. 86-7)
By regaining her sight, Alice has lost one of her defining features; she is no longer herself. It is almost as if she is in mourning for her blindness. She hates the person she has become almost as much as she hates the way her friends celebrate her cure. She sees every congratulation as a betrayal of her blind self, evidence that despite the fact that she was happy being blind, all her sighted acquaintances secretly thought she would be better off sighted.
Van Cauwelaert's sensitive depiction of Alice's reactions to her new state of sightedness is a startling reminder that blindness is not a tragedy. Through a fast-paced (if somewhat far-fetched) tale of love, loss and loyalty we meet a collection of wonderfully eccentric characters who encourage us to abandon our own misconceptions about beauty, happiness and the tyranny of appearances. Without giving too much away, this is a thought-provoking, surprising and engrossing tale about how we see each other and ourselves. Highly recommended.
Monday, 20 June 2016
Bravo for live Audio Descrption at Euro 2016!
When I applied for tickets for the UEFA Euro 2016 football
tournament I did so because I wanted to experience the passion and excitement
of live high quality football and I wanted to do so in my favourite country. I
have attended live football before and know that nothing beats the thrill of
the build-up, the noise of the fans and the atmosphere inside the stadium. I
also (thought) I knew that it would be almost impossible for me to actually
follow what was happening on the pitch. The players would be blurry smears of
contrasting colours and the ball would move far too quickly for me to follow. I
would have to guess the general pattern of the match from the reactions of the
crowd around me and would fill in the gaps later by watching the highlights with
my nose inches from the television screen.
Imagine my excitement when I discovered that a
team of volunteers would be providing live audio description at the match!
Armed with my portable FM radio and headphones I duly tuned in to 91.8 once
settled in the stands. AD can often be fraught with technical problems so it
was a relief to immediately hear a recorded message informing me that the
service was working and that live commentary would start shortly before the
match. Coincidentally, our seats were next to the press stand from where the
audio description would be delivered: as soon as the technical team spotted my
white cane they came over to check that everything was working and they lent me
some special headphones so that the commentary would not be drowned out by the
very noisy Swedish fans sitting round me. When I explained that I have a professional as well as a personal interest in AD they even introduced me to
the two volunteer describers.
Lucas Carcano and Leandra Iacono are studying sports
journalism in Nice and they have been specially trained in live football audio
description. When we met before the match they described the layout of the
stadium to me, gave me an idea of the look and behaviour of the two groups of fans
and told me a little bit about the players’ warm up which was going on below us.
Most importantly, they explained the system of zones they were going to use
during the description. By dividing the pitch into four areas, labelled A-D,
they could accurately give me the position of the ball throughout the game: for
the first time I would be able to get a real sense of where the ball was on the
pitch and follow the players as they moved around it. Like a television camera focusing
in on the part of the pitch in play, Lucas and Leandra’s references to zones would allow
me to focus my attention on the requisite section of the pitch.
Unlike AD tracks on film, which begin at the same time as the
film does (thus rendering ads and trailers inaccessible), Lucas and Leandra started
their description with the pre-match ceremony and described the arrival of the
players, the display of flags, the national anthems and the fans’ reactions to
it all. Without them I would not have known that all the Swedish fans were
jumping up and down in unison whilst unfurling a giant flag with a tribute to
Italy in one corner. By making me feel more involved in the build-up, their
words pulled me into the atmosphere in a way I have never experienced before.
As the game began I
was immediately astonished and delighted by the energy and enthusiasm my
describers put into their work. It was very soon apparent that as well as being
accomplished journalists they were also extremely knowledgeable and passionate football
fans. Without ever seeming to pause for breath they told me who had the ball,
where they were passing it, who was waiting to receive it, who was tackling
whom, when there were fouls and what the referee was dong about them and how
and why the crowd was reacting as it did.
As well as focusing on the detail of the
match, they also managed to give me a sense of the teams’ positions as a whole
and how their tactics varied. I learnt that Sweden prefer long balls which are
not always successfully recuperated, that the Italian goalie takes his time
before every goal kick, that some players get up immediately after falling
whilst others lie there moaning. They told me about near-misses and awkward
turns, substitutions and injuries, yellow cards and free kicks; off-sides and corners. In lulls in the
action they gave their impressions of the game, who was playing well, who
looked tired, who was having fun. They combined detail with knowledge and facts with analysis in a unique and very appealing way: I felt not only that I knew what was happening on the pitch but also that I understood why it was happening and what it might lead to.
I was astonished by how much their audio description
differed from radio commentary. Whilst radio commentators give more of a sense
of the game’s action than television commentators do, they (paradoxically) fall
far short of the detail of AD. Radio commentators tend to do as their name
suggests: they comment on the action, often comparing the current game to
previous performances or listing statistics and interesting facts about the
players. They privilege banter over description and lapse into silence without explaining why the game has paused. On the other hand, Lucas and Leandra worked really hard to provide a rich and enriching aural experience. Whilst they did include some helpful background information, such as which players on
opposing sides were team mates in club football, and how they were dealing
with this on the pitch, they were focused on the flow of
the game. This meant that I felt more immersed in the experience that I have ever
done before. I must have experienced hundreds of match commentaries on
television and radio. But this is the first time that I have felt so involved and
included in the action. It was as if the detail of television close-ups was combined
with the thrill of live action. There is no doubt that I got just as much - and
probably more – out of the game thanks to Lucas and Leandra than the sighted
fans around me.
After the match, and after I’d thanked them both about a
thousand times, my describers asked me how they could make the service even
better. I couldn’t really think of much that they themselves could do to
improve what had been a truly remarkable description. But perhaps live sporting
events could take some inspiration from current practices in accessible
theatre: as well as offering live AD of selected performances, some theatres
also offer pre-show touch tours where blind audience members are able to
familiarise themselves with the set and even the actors. No doubt my experience would
have been even more memorable had I been able to walk the pitch, touch the
goal netting and perhaps even fondle Ibrahimovic’s muscles…
Lucas and Leandra are on duty again tonight for the match
between Russia and Wales and I wish them both 'bon courage'. I also wish I could be there with them. Nothing I experience on TV or radio in the next weeks of the tournament will come close to the intensity and impact of their amazing live audio description.
With thanks to Julie Bertholon from the Federation des aveugles de France for telling me about the service, to my Dad for accompanying me to the match, to all the volunteers who helped me find seats, toilets and transport, and of course to Lucas and Leandra for quite simply transforming my experience of football.
Tuesday, 24 May 2016
Book Review: 'Je veux croire au soleil' by Jacques Semelin
Jacques Semelin, Je veux croire au soleil (Paris: les Arènes, 2016)
Part travel journal, part guide to living creatively with blindness, Jacques Semelin’s humorous description of his stay in Montreal is a charming and honest account of the day-to-day annoyances and joys of life as a blind academic.
Readers familiar with Semelin’s first memoir, J’arrive où je suis étranger (which I write about here) will remember that his gradual journey from sightedness to blindness was not an easy one. Semelin's internalised ableism meant that he spent many years doing his best to 'pass' as a sighted person before finally 'coming out' as blind. In Je veux croire au soleil he celebrates the new creativeness which his blindness has given him and reflects on how to make sense of his non-visual life for a sighted reader:
Je me suis mis en quête d’un autre vocabulaire, de métaphores, de mises en scènes, bref, de tous les moyens de mieux saisir le réel par l’imaginaire.
I found myself identifying particularly strongly with Semelin's description of the 'saut psychologique' (psychological leap) he had to make from independence to dependence. Like him I spent years finding ingenious ways of doing things for myself. And like him I resisted asking for help for as long as I could:
Se faire aider conduit bien plus tôt à reconnaître un effondrement de soi. On ne peut plus faire ceci ou cela. […] Se faire aider revient ici à devoir admettre son infériorité physique en quelque chose, une infirmité en somme.
Whilst the wealthy willingly pay for assistance as a way of asserting their dominance, Semelin recognizes that asking for - and knowing how to graciously accept - help is one of the hardest things a blind person must do. Having to be helped can feel like a loss of personhood and an acknowledgement of inferiority. But knowing when to accept help can feel like a liberation. I recognise in Semelin's references to pride and honour my own (sometimes unhelpfully stubborn) reluctance to ask for help. Perhaps this explains my dislike of taxis and my preference for public transport.
Il faut trouver la force de se pousser dehors. Quand on n’y voit pas il est toujours tentant de rester bien au chaud dans un lieu clos. L’extérieure reste angoissant. Mais la volonté de se prendre en charge et la curiosité de la découverte peuvent aussi vous attirer vers l’inconnu de la rue.
As well as learning how to fight his natural urge not to ask for help, Semelin also describes how he forces himself to leave his cosy flat and explore Montreal. His description of his solitary adventure down the busy rue Saint-Denis is a powerful illustration of the appeal of the sensual world he inhabits. His descriptions of snippets of conversation, cooking smells and the changing feel of the air on his face provide a non-traditional - but equally valuable - visitor's guide to one of Montreal's most famous streets. Semelin's sensual appreciation of Montreal is an evocative celebration not only of non-visual travel but also of the unexpected pleasures of being blind and alone in an unfamiliar environment. Semelin's wanderings are often punctuated by encounters with strangers and these chance meetings, and the stimulating and rewarding conversations which ensue, are a reminder that blindness's enforced dependence on others is a gateway to a shared humanity which is often denied the more self-reliant sighted traveller.
Les personnes qui n’ont pas l’habitude de côtoyer des non-voyants ont souvent tendance à craindre le pire pour leur sécurité à tort.
One of the most appealing aspects of Semelin's memoir is that it is not unremittingly cheerful. He is frustrated and annoyed by his landlady's pessimistic prediction of the problems he will have with dustbins and domestic appliances. Whilst appreciative of the new technologies which make his academic work possible, he is also right to point out that screen readers and talking smart phones are hampered by their reliance on sight-dependent software:
Ce sont les instruments quotidiens d’une dictature qui ne dit pas son nom et qui transcende les régimes politiques, celle de l’image.
In both Montreal and Ottawa Semelin was disappointed that museums - especially those dealing with the persecution of minorities - were largely inaccessible to him. I wonder what he would make of Canada's new human rights museum which recently opened in Winnipeg and which I write about here.
Pourtant une certaine amertume ne m’a pas vraiment quitté. Cette promenade a-t-elle ravivé la mélancolie que je sais toujours au fond de moi comme une nostalgie pour ce monde dont j’ai dû abandonner les rives voici bien longtemps ? Cela fait des années et des années que j’en suis exclu mais quoi que je fasse, une vieille douleur se réveille de tems en autres, comme en ce moment.
Semelin's work made me both smile and cry out in recognition. But it also made me nostalgic. Unlike him, I do not miss the sighted world, but I do miss the time when I too was a lone traveller in a francophone land. Maybe I'll go alone to Montreal one day. And maybe like Semelin I'll do battle with a recalcitrant microwave, relish the sounds and smells of the rue Saint-Denis and explore the wonderfully multisensory Cour des Sens at the Jardin botanique.
Monday, 23 May 2016
Jacques Lusseyran colloquium
I have recently been reading the work of blind academic Jacques Lusseyran in preparation for the one-day colloquium about him which I am honoured to be speaking at along with several friends and colleagues. The day is taking place at the Fondation Singer-Polignac in Paris on 28 June 2016 (coincidentally, and rather wonderfully, the first anniversary of Blind Creations at which Zina Weygand spoke so eloquently about him).
Although I do not necessarily agree with everything he says about blindness, I would argue that Lusseyran's celebration of 'inner vision' paradoxically celebrates the non-visual senses. He also advocates a no-nonsense approach to physical activity for blind people which echoes my adventurous approach to skiing.
Although I do not necessarily agree with everything he says about blindness, I would argue that Lusseyran's celebration of 'inner vision' paradoxically celebrates the non-visual senses. He also advocates a no-nonsense approach to physical activity for blind people which echoes my adventurous approach to skiing.
This image shows the poster for the colloquium
The colloquium is free to attend and is open to all, but pre-registration is required. Click here for more information.
Thursday, 19 May 2016
In Praise of Screen Reading
Ever since I learnt to touch type at age 11, I have preferred writing on keyboards to using a pen. I could not function without my computer and I usually use Microsoft’s accessibility features (such as zoom, magnification and high contrast colour schemes) to help me read what is on the screen. But since my second cataract operation last week, I do not have enough vision in my left eye to read using sighted methods. So I have begun working using a screen reader.
Screen readers are not entirely new to me. Thanks to Blind Creations I have learnt about the practical and creative benefits of using screen readers. Artist David Johnson presented a fascinating screen-reader art installation at Royal Holloway earlier this year, and French writer Romain Villet has produced a playful and clever screen-reader dialogue. Both of these artworks exemplify the creative potential of blind technologies and celebrate blindness for its own sake.
I started using a screen reader myself last week because I knew that after my operation I would have at least a few non-visual weeks. Most blind people I know use JAWS but this software is expensive and complicated to use without training. I decided instead to install the free NVDA software (although I did make a donation to support their excellent work). I had heard that NVDA has less functionality than JAWS but it is working well for me and is more than enough to allow me to comfortably navigate around my laptop and use outlook, word and internet explorer.
As I still have some sight, although not enough to read with, I am using NVDA to read me what appears on the screen and to tell me where to click. As well as speaking the content of dialogue boxes, notifications and documents, it also transforms the cursor into an aural guide whose tone varies in an incredibly intuitive way as I move it around the screen. This is the easiest way for me to navigate around windows but it only works because I am familiar with the visual layout of my screen. If I didn’t know that the file menu was at the top left hand corner of the screen in word, I would never be able to find it with the cursor. I really like the way that NVDA caters for people who are partially blind and want to use a combination of sighted and blind methods.
Another bonus of NVDA, and one which I was not expecting, is that it knows when I am writing in English and when in French and adjusts automatically as word does. This avoids the incomprehensible and frankly hilarious franglais which is produced when VoiceOver reads me French text on my Anglophone iPhone
.
So far I am finding NVDA surprisingly easy to use: I haven’t mastered all its subtleties yet but I know which keyboard commands (usually CAPS LOCK plus one or two keys) will read me letters, words, paragraphs or the whole text. This is the first blog post I have written using NVDA and It is no more effort than my more usual sighted approach. It does take longer because I am still learning, but the advantage of this is that I have more time to think about what I want to say and my prose is more accurate thanks to the built-in typo detector. As has been the case before with other blind technologies such as audio books and my white cane, I am wondering why it has taken me so long to embrace the screen reader. What a relief to be able to use my computer without hurting my eyes. I'm sure too that my posture will be better now that I don't need to sit with my face so close to the screen. I know lots of people who persist in using sighted methods even though screen readers would help them. A lot of people would find some screen reader features would combine well with a sighted approach. But our ocularcentric world dictates that our default technologies are often visual despite the clear practical (and artistic) benefits of blind ways of doing things. I am delighted that I have discovered NVDA and am sure that I will carry on using it even if/when I can use my left eye to read again.
Tuesday, 26 April 2016
Skiing Blind Again
Two years ago I went skiing for the first time. As this post shows, I had a great time and returned from Switzerland feeling confident, empowered and rather pleased with myself.
A couple of weeks ago we had another family ski holiday, this time in the very pretty Monterosa resort in the Italian Alps. This week was both much easier and much harder than my first time. For reasons that will become obvious, it wasn't quite the resounding success of my first ski adventure. But I am still glad I went, and I'll certainly go again.
In 2014 I found the whole pre-ski preparation phrase pretty overwhelming. I hated getting ready every morning and came to loath the hot, smelly boot room and the perilous walk out to the slopes juggling skis, poles, helmet, goggles. This time I was prepared for the hassle and handled it better. Luckily, as soon as people saw my 'blind skier' arm bands they were happy to help me carry things and be patient as I clambered clumsily into cable cars. As in 2014, I had booked a private instructor/guide to ski with me each morning and as soon as I met Chris I felt reassured and relaxed. From our first conversation he was open, honest and confident, which meant that I was too. And as I followed him slowly down the gentle nursery slopes, everything Jolanda had taught me came flooding back. I could still ski! Chris was impressed with my balance and control, and I was delighted that I could still do it.
Chris was so pleased with me after our first session that on day 2 he suggested we leave the nursery slopes and head up the mountain. This was something I had never done with Jolanda. I was nervous of course, but mostly excited: it felt amazing to be up so high, on fresh snow, with just distant sounds of other skiers for company. Chris had picked the easiest blue slope in the resort for my first 'proper' descent, but even so I spent quite a lot of that morning remembering what Jolanda had taught me about getting up after a fall. Luckily, the snow was soft and plentiful so falling didn't hurt.
It turns out that being on a nursery slope doesn't really prepare you for steeper slopes. The only way to learn to ski on steep slopes is to practise skiing on steep slopes. This inevitably leads to tumbles but by the end of day 3 I was feeling much more confident about even the steepest parts of the run. And as I got to know the slope better, I was even able to predict what I might need to do next.
Once I left the nursery slopes, it became clear to me that I would not be able to ski without a guide. Not only did I struggle to see the edges of the pistes, I also found it hard to know accurately which way was uphill and which way was downhill. Mountains are not man-made: they curve and bend at odd angles and slopes go up and down in surprisingly unpredictable ways.
In the afternoons, I really wanted to ski with my family and friends. But they were all (much) better than me by now (although not good enough to guide me). So I reluctantly decided to curb my dare-devil instincts and enjoy some Italian café culture and sunshine whilst they tackled the resort's trickier slopes. This was hard for me, because I don't like to admit defeat, but it also felt good to be making decisions about my safety and confidently explaining my limits to others.
On day 4 the weather changed: it had been much colder than usual overnight and the snow felt brittle and hard under my skis. It sounded different too: when skiers passed me they made a terrifyingly loud rattling noise which made it much harder to hear Chris. I found it more difficult to control my skis on this new, hard snow and needed to quickly learn yet more techniques before reaching the steep bit of the slope.
Sadly I didn't get much chance to practise skiing in these odd conditions. Minutes later I fell and hurt my right knee. Chris called the rescue team who brought a stretcher to take me to the clinic. X-rays revealed a fracture at the top of my tibia.
As I lay in my hotel room with my leg in plaster my disappointment at my curtailed adventure was soon replaced with more worrying thoughts. What if this accident was proof that I should never have been skiing in the first place? What if it showed that blind skiing is a foolhardy, dangerous and irresponsible pastime which is bound to end in tears? I could imagine people discussing my accident: 'Well it serves her right for thinking she can do sighted stuff'; 'This is what happens when blind people try skiing'; 'Look at all the trouble and inconvenience her crazy thrill-seeking has caused.' What if my accident was evidence that there are things that blind people are better off not doing? I couldn't get these doubting, ableist voices out of my head. I was horrified that a little part of me actually believed that I had been wrong to want to learn to ski.
Maybe I was more likely to hurt myself than a fully sighted skier. Maybe not. I know of at least two other people who broke bones on the slopes that day. And the doctors in the clinic told me they see around 600 ski accidents per season. Skiing is a dangerous sport but I was very careful. I always skied with a guide and never tried anything I didn't feel comfortable with. My boys laughed at me for being too slow but I went at a speed that felt right for me.
On the whole I think I agree with blind writer Jacques Lusseyran who urges the parents of blind children to let them take the same risks as their sighted peers. According to him, 'there is a danger far greater than cuts and bruises, scratches and wounds, and that is a blind child's introverted isolation.' Broken legs heal (relatively) quickly and easily. Self-esteem and confidence can take much longer to mend. I am still a little embarrassed that I broke my leg skiing (what a cliché!) but I am proud and glad that I know what skiing feels like and I definitely intend to feel that indescribable rush of adrenaline again.
A couple of weeks ago we had another family ski holiday, this time in the very pretty Monterosa resort in the Italian Alps. This week was both much easier and much harder than my first time. For reasons that will become obvious, it wasn't quite the resounding success of my first ski adventure. But I am still glad I went, and I'll certainly go again.
In 2014 I found the whole pre-ski preparation phrase pretty overwhelming. I hated getting ready every morning and came to loath the hot, smelly boot room and the perilous walk out to the slopes juggling skis, poles, helmet, goggles. This time I was prepared for the hassle and handled it better. Luckily, as soon as people saw my 'blind skier' arm bands they were happy to help me carry things and be patient as I clambered clumsily into cable cars. As in 2014, I had booked a private instructor/guide to ski with me each morning and as soon as I met Chris I felt reassured and relaxed. From our first conversation he was open, honest and confident, which meant that I was too. And as I followed him slowly down the gentle nursery slopes, everything Jolanda had taught me came flooding back. I could still ski! Chris was impressed with my balance and control, and I was delighted that I could still do it.
Chris was so pleased with me after our first session that on day 2 he suggested we leave the nursery slopes and head up the mountain. This was something I had never done with Jolanda. I was nervous of course, but mostly excited: it felt amazing to be up so high, on fresh snow, with just distant sounds of other skiers for company. Chris had picked the easiest blue slope in the resort for my first 'proper' descent, but even so I spent quite a lot of that morning remembering what Jolanda had taught me about getting up after a fall. Luckily, the snow was soft and plentiful so falling didn't hurt.
It turns out that being on a nursery slope doesn't really prepare you for steeper slopes. The only way to learn to ski on steep slopes is to practise skiing on steep slopes. This inevitably leads to tumbles but by the end of day 3 I was feeling much more confident about even the steepest parts of the run. And as I got to know the slope better, I was even able to predict what I might need to do next.
Once I left the nursery slopes, it became clear to me that I would not be able to ski without a guide. Not only did I struggle to see the edges of the pistes, I also found it hard to know accurately which way was uphill and which way was downhill. Mountains are not man-made: they curve and bend at odd angles and slopes go up and down in surprisingly unpredictable ways.
In the afternoons, I really wanted to ski with my family and friends. But they were all (much) better than me by now (although not good enough to guide me). So I reluctantly decided to curb my dare-devil instincts and enjoy some Italian café culture and sunshine whilst they tackled the resort's trickier slopes. This was hard for me, because I don't like to admit defeat, but it also felt good to be making decisions about my safety and confidently explaining my limits to others.
On day 4 the weather changed: it had been much colder than usual overnight and the snow felt brittle and hard under my skis. It sounded different too: when skiers passed me they made a terrifyingly loud rattling noise which made it much harder to hear Chris. I found it more difficult to control my skis on this new, hard snow and needed to quickly learn yet more techniques before reaching the steep bit of the slope.
Sadly I didn't get much chance to practise skiing in these odd conditions. Minutes later I fell and hurt my right knee. Chris called the rescue team who brought a stretcher to take me to the clinic. X-rays revealed a fracture at the top of my tibia.
As I lay in my hotel room with my leg in plaster my disappointment at my curtailed adventure was soon replaced with more worrying thoughts. What if this accident was proof that I should never have been skiing in the first place? What if it showed that blind skiing is a foolhardy, dangerous and irresponsible pastime which is bound to end in tears? I could imagine people discussing my accident: 'Well it serves her right for thinking she can do sighted stuff'; 'This is what happens when blind people try skiing'; 'Look at all the trouble and inconvenience her crazy thrill-seeking has caused.' What if my accident was evidence that there are things that blind people are better off not doing? I couldn't get these doubting, ableist voices out of my head. I was horrified that a little part of me actually believed that I had been wrong to want to learn to ski.
Maybe I was more likely to hurt myself than a fully sighted skier. Maybe not. I know of at least two other people who broke bones on the slopes that day. And the doctors in the clinic told me they see around 600 ski accidents per season. Skiing is a dangerous sport but I was very careful. I always skied with a guide and never tried anything I didn't feel comfortable with. My boys laughed at me for being too slow but I went at a speed that felt right for me.
On the whole I think I agree with blind writer Jacques Lusseyran who urges the parents of blind children to let them take the same risks as their sighted peers. According to him, 'there is a danger far greater than cuts and bruises, scratches and wounds, and that is a blind child's introverted isolation.' Broken legs heal (relatively) quickly and easily. Self-esteem and confidence can take much longer to mend. I am still a little embarrassed that I broke my leg skiing (what a cliché!) but I am proud and glad that I know what skiing feels like and I definitely intend to feel that indescribable rush of adrenaline again.
Wednesday, 13 April 2016
Jacques Semelin
In November 2014 I was pleased to give a keynote lecture at the French Autopathographies conference organised by Dr Steven Wilson at Queen's University, Belfast. As well as discussing Thérèse-Adèle Husson's Reflections
(1825), and Le scaphandre et le papillon by Jean-Dominique Bauby, I talked briefly about Jacques Semelin’s 2007 autopathography, J’arrive où je suis
étranger. Semelin’s account of his gradual acceptance of his own blindness touched me deeply when I read it because it resonated with my own experiences of denial, dissimulation and eventual celebration. To coincide with the publication of his second book about blindness, Je veux croire au soleil (which I review here), I share below some of my thoughts from the Belfast talk.
Unlike
Husson, Semelin did not go blind as a child. He grew up completely unaware of
his degenerative eye disease which was only discovered during some careers
counselling he had in high school. At the age of 16 he was told that his sight
would soon start to weaken and that he would go completely blind at an unknown
and unspecified point in his life. Semelin
is a renowned and well-respected historian and political scientist who is a
researcher at the CNRS and a lecturer at Sciences-Po. His successful career might suggest that his story could be interpreted as a typical ‘triumph over tragedy’ narrative about how he battled to overcome his
disability to lead a ‘normal’ life. But Semelin’s story is far from being the
kind of cloying and self-pitying ‘inspiration porn’ which some non-disabled people
enjoy. Instead he offers a practical, humorous and thoughtful account of how he
has come to appreciate the kingdom of the blind in which he now finds himself:
Maintentant que j’y ai mes repères, je dirai que ce pays a du charme, qu’il est quelque part envoutânt, que vous pouvez y découvrir de nouvelles Muses.
Semelin’s frank descriptions of his early diagnosis
emphasize the dangerous and degrading objectification which is one of the
unpleasant effects of the medicalisation of disability:
Jamais je
n’avais encore eu la sensation d’être considéré comme un cobaye, une variété
exotique d’une espèce pathologique. Désormais c’était fait. En quelques seconds
ils m’avaient transformé en une chose clinique.
Unlike Husson and Bauby, Semelin is at first able to hide his
disability from those around him. His narrative charts his increasingly
unsuccessful attempts to ‘pass’ as non-disabled and his eventual decision to
‘come out’ as partially blind by using a white cane and asking for adjustments
to his working environment. Semelin’s desire to ‘pass’ demonstrates the extent to
which he has internalised the widespread view that disability is a negative,
undesirable state which should be hidden rather than celebrated. As he points
out when describing his years of eco-activism:
C’est bien plus
tard que j’ai pris conscience de la gêne que mon attitude avait suscitée autour
de moi. En fait, j’étais alors engagé dans deux batailles, l’une certes aux
côtés des paysans du Larzac, et l’autre contre moi-même, contre celui que je
redoutais de devenir et que pourtant j’étais déjà.
Alongside Semelin’s recognition of his ableist desire to
deny his own disability, we also find in this quotation a surprising reference
to others’ feelings which he seems to prioritise over his own. Semelin’s desire
not to embarrass his non-disabled friends betrays a concern for ‘normality’
which sits uneasily alongside his celebration of blindness. In the early stages of his journey, Semelin has a somewhat contradictory or conflicted view of his own
disabled subjectivity which reminds us that even the most
proudly ‘out’ disabled people sometimes struggle to reconcile their position
with the ableist views they are continually exposed to by non-disabled society.
For me, one of the most striking things about
Semelin’s story is the honesty with which he interrogates his at times knowingly ‘ableist’
perspective. Shortly after he has become officially registered blind he says:
Je ne parvenais pas à me définir comme handicapé. Le mot handicap
me mettait mal à l’aise. [...] il me
pesait terriblement, comme si on m’avait mis un boulet au pied. D’ailleurs, handicap par rapport à qui ? à
quoi ? Chacun n’est-il pas handicapé quelque part ? Il y a simplement
des handicaps plus ou moins visibles, plus ou moins « handicapants ».
Le mot n’exprime t-il pas avant tout un jugement normatif, pour se mettre à
distance de la différence ?
This quotation illustrates the conflict which characterises Semelin’s work. He seems to agree
with the negative connotations attached to disability whilst at the same time
acknowledging that these connotations are nothing more than
constructs of a resolutely normative society.
Because Semelin is never completely at peace with his
disabled status, his narrative invites us to question are own internalised ableism. And as the book goes on, he does begin to celebrate his blindness for its own sake,
as an positive feature which helps him relate to the world in different and
perhaps better ways:
La perte de la
vue n’est pas une tragédie en soi, elle peut même être une puissante source de
renouvellement et d’enrichissement.
Regular readers of this blog will recognise how Semelin's assertion that blindness is not a tragedy echoes my own approach to blindness.
Thursday, 28 January 2016
Making Space for Accessible Art
Yesterday I was delighted to welcome Blind Creations artist
David Johnson back to Royal Holloway. David’s large-scale outdoor installation ‘Too Big
to Feel’, which was commissioned for the Blind Creations conference held at
Royal Holloway in June 2015, is now part of the College’s Art Collections.
This picture shows 'Too Big to Feel' by David Johnson on the grassy slope below the hockey pitch. The piece is made up of 18 concrete domes, 17 of which are painted white, and 1 of which is red. They look like giant Braille dots and spell out 'Seeing Red' in grade 2 (contracted) Braille.
Yesterday David presented his work in the context of the
College’s ‘Making Space for Art’ lecture series.
This picture shows David during his talk. He is standing in front of a screen on which we are shown an image of 'Too Big to Feel' in its first location in front of the Founder's Building. (Photo by Ruth Hemus)
I particularly like the way that ‘Too Big to Feel’
celebrates the creative potential of Braille whilst at the same time raising
questions about the opacity of language and its meanings more generally. By
making Braille both the subject and the medium of his work, David invites non-blind
people to engage imaginatively with the techniques blind people
use to read and write. Rather than being the reserve of a few, Braille becomes visible to, and
touchable by, everyone. Blindness’s creative potential is thus celebrated and assistive
technologies are consequently transformed into exciting and innovative ways of
questioning our relationship with language and the senses.
This picture shows another of David’s Braille creations, ‘Eggs’. Three casts of egg boxes sit on a table. Inside each nestle concrete eggs. The eggs are arranged to spell out 'egg' in grade 2 Braille. (Photo by Ruth Hemus)
David uses the screen-reading software JAWS to access his
computer. By hooking his laptop up to the seminar room’s projector, we were able
to see images of David’s works whilst at the same time hearing the computer’s
audio prompts to him. This had the unintended consequence of demonstrating to
non-blind members of the audience how screen reading technology works whilst simultaneously
revealing its artistic potential. As he does with Braille, David uses JAWS in
his artistic creations. His work ‘Rosie One’ is an audio installation in which
the screen-reader’s response to a word document reveals both the arbitrary nature
of language and the human brain’s ability to jump between two different
interpretations of the same sounds.
You can listen to the whole of David's talk, including 'Rosie One' by clicking here.
As well as using various kinds of assistive technology in
his work, David also works with friends and assistants in the creation of his
art works. David’s blindness means that
there are times when he has to trust other people to make choices for him,
particularly when he wants to include colour in his work.
This picture shows 'Citrus Corners': several black triangles, which have been made from casts of the inside of plastic bags, sit on a black perspex square on a table. The tips of these 'corners' have been painted yellow. David explained the process of communication involved when his assistant helps him decide which shade of yellow to use. (Photo by Ruth Hemus)
David’s collaborative art practices challenge the received
notions that dependency on others is a sign of weakness, and that disabled
people should strive for independence. During his talk, David asked each member
to the audience to create a human figure out of plasticine. At the end of the talk, he asked us to place
these figures in a circle, facing inwards. The resulting artwork was a
celebration of collaboration: on their own each figure meant nothing, but together
they stood for the creative power of the group.
This picture shows the finished collaborate artwork. Fifteen green plasticine figures of various shapes and sizes stand or sit on a table. They are in a large circle and are all facing inwards, towards each other. (Photo by Ruth Hemus)
I am delighted that as a result of Blind Creations, my
collaboration with David will continue. In February we travel to Boston to take
part in a panel at the 2016 Transcultural Exchange Conference and David has
also secured Arts Council funding to visit Art beyond Sight in New York and to
present a pop-up exhibition in Montreal. We also hope to invite him back to
campus later in the year to run more collaborative art-making workshops with
our students.
Wednesday, 13 January 2016
My cataract operation 2: what I see now
This time last week I was awaiting the first of two cataract operations. On Friday, medics removed a dense cataract from my right eye. Thanks to the magic of general anaesthetic, I was blissfully unaware of the whole procedure. And since I removed the bandages on Saturday morning, I have of course been trying to work out what difference this operation has made to my vision.
For the first 48 hours or so after the op I couldn't see much of anything out of my right eye. It felt very sensitive to light and I kept it closed most of the time. When I did open it for a few moments, everything was very blurry. But I could tell that the colour of the light I could see had changed. Instead of seeing everything through tinges of yellow and brown, I could definitely see white and blue again.
A few days later I am managing to keep my eye open most of the time and I have noticed three interesting things. Firstly, and not unexpectedly, my glasses no longer work. Because the new plastic lens is not exactly the same shape as the one that was destroyed along with the cataract, I'll need to get a new prescription. Apparently this will only happen around 8 weeks after the second operation. So I reckon I'm looking at at least three months of blurry. At the moment this isn't too much of an issue. I got used to life without my glasses when I broke them in November and I do my reading with my left eye so for now if I close my right eye I can more or less see as well (or as badly) as before my operation. This will of course change after the second op.
Secondly, things start getting very weird when I use both eyes for reading. This afternoon I was reading a text (appropriately enough, Kate Tunstall's translation of Diderot's Letter on the Blind) using the kindle app on my iphone:
For the first 48 hours or so after the op I couldn't see much of anything out of my right eye. It felt very sensitive to light and I kept it closed most of the time. When I did open it for a few moments, everything was very blurry. But I could tell that the colour of the light I could see had changed. Instead of seeing everything through tinges of yellow and brown, I could definitely see white and blue again.
A few days later I am managing to keep my eye open most of the time and I have noticed three interesting things. Firstly, and not unexpectedly, my glasses no longer work. Because the new plastic lens is not exactly the same shape as the one that was destroyed along with the cataract, I'll need to get a new prescription. Apparently this will only happen around 8 weeks after the second operation. So I reckon I'm looking at at least three months of blurry. At the moment this isn't too much of an issue. I got used to life without my glasses when I broke them in November and I do my reading with my left eye so for now if I close my right eye I can more or less see as well (or as badly) as before my operation. This will of course change after the second op.
Secondly, things start getting very weird when I use both eyes for reading. This afternoon I was reading a text (appropriately enough, Kate Tunstall's translation of Diderot's Letter on the Blind) using the kindle app on my iphone:
This photo shows some text in the kindle app on my iphone. The text is enlarged so that there are 20 words on the screen. The words are white against a black background and towards the top of the screen a small blue footnote number (52) is visible.
When I look at this screen with my right eye closed, the text is yellow and the footnote number is invisible. But if I use both my new cataract-free eye and my old cataract-obscured one, something very odd happens: two screens appear next to each other. The one on the right is the one I was looking at before. On the one on the left, the text is dazzlingly white and the footnote number is a beautiful, incandescent blue. It is pretty disorienting to see the same thing in two different ways. But it is also a useful way of measuring the difference the cataract operations will eventually make.
When I'm not reading, I've given up using my now redundant glasses. So, thirdly, everything is a lot more blurry than it was. But it is also much more colourful. I've discovered that my favourite grey cardigan is actually a lovely shade of navy blue and that I own a set of very brightly coloured plastic bowls. I'm still getting used to my new psychedelic world. I hope this post will give my friends a sense of how it is that at the moment my vision is both better and worse than it was before.
Wednesday, 6 January 2016
My cataract operation
As Kate Tunstall shows in the Prologue to her important essay 'Blindness and Enlightenment' (2011), the cataract operation, or, more precisely, its triumphant post-operative illumination, is a familiar trope in the narrative of blindness. Three hundred years ago it was the focus of sustained philosophical interest; today it is used by international charities to construct sentimental stories which encourage western generosity. The operation to remove cataracts is a simple one; it takes around 20 minutes and is usually considered low risk, almost always resulting in improved vision. So why do I have such distinctly mixed feelings about this Friday's operation to remove a cataract from my right eye?
Cataracts are the most common cause of vision problems in people over forty. Their removal is a moment of joy and revelation as the world's blurriness is corrected and colours become vibrant once again. 'It is like being a child in a sweet shop' someone once told me. But my case is a little different. Even if my cataract operations go smoothly (something which is far from certain because of the shape and size of my eyes), I will still be registered blind. My underlying condition - retinal coloboma - won't change. What will happen is that I stop seeing the world as I do now. Instead I might see things more clearly, more colourfully, or I might no longer see anything at all.
For most people, the decision to have a cataract operation is a straightforward one driven by the understandable (although ocularnormative) desire to see as well as possible. But my decision to finally allow surgeons to remove the dense disks which cover both my eyes is more complicated. My ophthalmologist first noticed my cataracts 20 years ago and they have been growing, and thickening, ever since. They now prevent me from distinguishing colours and make reading difficult, even with my special glasses and my beloved kindle. I have always used sight where I can but increasingly I am finding that the flawed sight I have is more of a hindrance than a help. Sometimes I think that it would be easier to have no sight at all than to have this unpredictable, fallible sight which I can no longer rely on. And I have noticed that most people feel more comfortable relating to a totally blind person than to one who seems to be able to see some things but not others. Since I started properly exploring my blindness four years ago, I have learnt braille, become a more confident white cane user and discovered the pleasure and potential of the audio book. If the operations don't work, I am confident that I will be happy to live, love and work as a totally blind person.
I know that most of my friends and family are hoping that these forthcoming operations will lead to a marked improvement in my sight. I know that they are hoping for a cure of sorts and I know that they will be upset if I end up blinder than ever. I know that despite my best efforts, most people still think that sight is better than no sight, and that partial blindness is better than total blindness. And on one level they are right. We live in an ocularcentric world in which life is certainly less complicated with sight than without it. Of course I am hoping for some improvement in what I see. Believing that blindness is not a tragedy does not stop me from wanting to be able to read as I could five years ago. The fact that I have had some sight makes it impossible for me not to remember that I used to be able to see much better than I can now. But if the operations lead to total blindness - which is a distinct possibility - I don't think I'll be as upset as those around me.
Any operation performed under general anaesthetic is a little bit scary so whatever the outcome, I am looking forward to several days of enforced bed-rest, accompanied by Radio Four, my new audio book reading machine, regular cups of tea and copious amounts of flowers and chocolates.
Cataracts are the most common cause of vision problems in people over forty. Their removal is a moment of joy and revelation as the world's blurriness is corrected and colours become vibrant once again. 'It is like being a child in a sweet shop' someone once told me. But my case is a little different. Even if my cataract operations go smoothly (something which is far from certain because of the shape and size of my eyes), I will still be registered blind. My underlying condition - retinal coloboma - won't change. What will happen is that I stop seeing the world as I do now. Instead I might see things more clearly, more colourfully, or I might no longer see anything at all.
For most people, the decision to have a cataract operation is a straightforward one driven by the understandable (although ocularnormative) desire to see as well as possible. But my decision to finally allow surgeons to remove the dense disks which cover both my eyes is more complicated. My ophthalmologist first noticed my cataracts 20 years ago and they have been growing, and thickening, ever since. They now prevent me from distinguishing colours and make reading difficult, even with my special glasses and my beloved kindle. I have always used sight where I can but increasingly I am finding that the flawed sight I have is more of a hindrance than a help. Sometimes I think that it would be easier to have no sight at all than to have this unpredictable, fallible sight which I can no longer rely on. And I have noticed that most people feel more comfortable relating to a totally blind person than to one who seems to be able to see some things but not others. Since I started properly exploring my blindness four years ago, I have learnt braille, become a more confident white cane user and discovered the pleasure and potential of the audio book. If the operations don't work, I am confident that I will be happy to live, love and work as a totally blind person.
I know that most of my friends and family are hoping that these forthcoming operations will lead to a marked improvement in my sight. I know that they are hoping for a cure of sorts and I know that they will be upset if I end up blinder than ever. I know that despite my best efforts, most people still think that sight is better than no sight, and that partial blindness is better than total blindness. And on one level they are right. We live in an ocularcentric world in which life is certainly less complicated with sight than without it. Of course I am hoping for some improvement in what I see. Believing that blindness is not a tragedy does not stop me from wanting to be able to read as I could five years ago. The fact that I have had some sight makes it impossible for me not to remember that I used to be able to see much better than I can now. But if the operations lead to total blindness - which is a distinct possibility - I don't think I'll be as upset as those around me.
Any operation performed under general anaesthetic is a little bit scary so whatever the outcome, I am looking forward to several days of enforced bed-rest, accompanied by Radio Four, my new audio book reading machine, regular cups of tea and copious amounts of flowers and chocolates.
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