“The principle of true art is not to portray, but to evoke”: An interview with Daniel Winship

I (may) not agree with what you have to say, but I’ll defend to the death your right to say it.

- Voltaire

An illustration of a child undergoing cochlear implant surgery, created by Daniel Winship and posted on his Facebook page  (warning: explicit) and shared more than 600 times, has generated heated, acrimonious debate among members of the deaf community, including those with implants, and hearing people connected to the community – particularly hearing parents of deaf children with implants. It’s also raised challenging questions about expression through art, how individuals interpret and react to it and each other, what qualifies as propaganda and bullying, and censorship.

Commenters have used a range of words to describe the illustration, including powerful, evocative, propaganda, utter nonsense, crap, an evil depiction, sensationalistic, and patently false. Winship himself has been accused of brainwashing, labeled a sick person, and called a cunt, “closed-minded arrogant twat,” and wacko on the same level as members of the Westboro Baptist Church. Others have made assumptions, including that Winship must be an ex-implantee, that he doesn’t have children – much less any with “a birth defect” – and that his illustration reflects the opinion of the entire deaf community.

After reading the 200+ comments posted on his image, I decided to seek out the man behind the art and find out who he is and why he created the illustration when and how he did. I spoke with Winship and his wife, Darleen Hutchins, via phone. The following is translated from American Sign Language, and I’ve written a commentary below the interview.

Daniel Winship on his art and life: An interview

Tara: So, Daniel, what inspired you to create this illustration? Any particular event?

Daniel: I had been talking with friends about cochlear implants, and these conversations just stuck in my mind. Then someone did a vlog about implants and oppression of the deaf. At the same time, over the past month I’ve focused on making art about deafness. I usually make art for the hearing and don’t share my deaf-related art, just started doing that recently. So one day I just sat down and started drawing this to express myself, looked at what I’d drawn, and just added to it and expanded it. I was thinking, how would I feel if I was that child? And I was exploring the idea of a deaf soul. Children are a symbol of innocence, of an innocent deaf soul.

I like to challenge myself with different ideas, in art, and themes about deafness. I didn’t feel any particular intense emotions when I started this. I was just thinking outside the box, doing a study of sorts.

Tara: So, what was your purpose behind posting this to Facebook?

Daniel: I really just posted it to see what people thought and observe reactions. The reaction I got was very unexpected.

Darleen: We had been discussing art, deaf art, the impact of art on the community, parents, et cetera. It took a LOT of guts for him to post that picture. That’s not something he does. His art tends to be dark, so he doesn’t share it that often. It was just his way of saying, “I am here.”

Tara: Where did you originally post your illustration to? Only a few places, or everywhere?

Daniel: Only to my Facebook page, Deafhood Discussions and De’VIA Art. It was very limited, but people just shared it and it exploded from there.

"I do not support a sick person who thinks this is what a cochlear implant surgery looks like. I'm 100% sure you have never seen the actual surgery. It's a beautiful thing!"

“I do not support a sick person who thinks this is what a cochlear implant surgery looks like. I’m 100% sure you have never seen the actual surgery. It’s a beautiful thing!”

Tara: Were you trying to depict what the surgery actually looks like?

Daniel: No, I wasn’t trying to do that. Just my own envisionment of it. I’ve had surgeries before, and I have some common sense of what a surgery looks like. I wasn’t trying to represent the actuality, just elaborate the idea with my own modifications.

Tara: What was your goal with it? Were you hoping to change people’s minds about the surgery or cochlear implants?

Daniel: Oh, definitely not. No. It absolutely was not my goal to change people’s minds. I only created it for myself and then decided to share it, to share my own thoughts.

Tara: Now, I want to ask … what type of background do you have? What was your experience growing up?

Daniel: I was adopted by a hearing couple. I started out with hearing aids and Total Communication, isolated in the mainstream. Then my parents found out about the deaf school (in Maine) and moved me there when I was about 6 or 7 years old, in 1983. I did a half day there for full access to language and social access, and half day in the mainstream for math, art, gym and to have better education. I still use my hearing aids sometimes to help my hearing in certain situations like movies and music.

Tara: Darleen, what about you?

"How dare you judge someone else, in a situation you know nothing about? If your child were born with a birth defect - which is what deafness is - I guarantee you that you'd explore every option to give them the most whole and complete life possible. That, my dear, is what "love" truly is."

“How dare you judge someone else, in a situation you know nothing about? If your child were born with a birth defect – which is what deafness is – I guarantee you that you’d explore every option to give them the most whole and complete life possible. That, my dear, is what “love” truly is.”

Darleen: I grew up oral. Learned sign at 14, when I transferred to the deaf school in Maine. That was just after Daniel had graduated. Then I went to a very small college.

We have a deaf daughter, you know, and a hearing son.

Tara: Did you two discuss a cochlear implant for your daughter? Did you think about implanting her?

Daniel: No, no. She lost her hearing later, but we decided not to give her one. We felt we didn’t want to get sucked into that cycle, what if her implant broke or didn’t work? We’d have to keep going back and going back and going back to get it tweaked and fixed. We did not want her dependent on that technology. She is just fine as she is.

Tara: Daniel, someone commented on your illustration that you have friends with CIs, some who don’t use them anymore and some who still use them?

Daniel: Yes. Quite a few.

Darleen: You know, one of the first children to get a cochlear implant was from Maine. He doesn’t use it anymore. He actually said, “I’m not using this stupid thing anymore.” And one of my own friends was tricked into getting a CI at 21. Her parents never told her why they were taking her to the hospital, and she woke up with an implant. I was the first deaf person she met in college. She is very angry about the implant now. She has called it her “ball and chain.”

Tara: What about people who are “successful” implantees?

Daniel: I don’t meet a lot of people like that. Just mostly people who don’t use their implants anymore. I met a man whose mother tried to bribe him to get one. She told him she would buy him a car if he would get an implant. So, things like that. Before, I didn’t really care one way or another. I thought it was just normal and went along with my life, not bothering with this debate. But then I started hearing more and more personal accounts and then really just thought about them and turned them over in my mind.

Commentary

The first thing I thought about after seeing Winship’s illustration and the comments on it was, wow … what happened to art literacy and the shared communion of art? You could almost hear the walls of defensiveness slamming up by the minute as people bogged down in the limited framework of their individual and unique experiences with deafness, lashed out in knee-jerk reactions, and made assumptions about Winship without ever meeting or talking with the artist himself. I didn’t get the sense that many people took at least a few moments to reflect and ask whether the picture might be more a deeply personal expression and less a direct condemnation of them as individuals. I didn’t get the sense that they took his labor to heart and wondered … why? Why this? What drove this man to create this? What does the creation of this particular image say about us on a deeper level as a community and as a society?

Instead, many comments indicated that people viewed the image through their own individual frames of reference, took it literally, made assumptions about the artist’s intent, and interpreted it as confirmation of their own views. It resonated with some deaf people who oppose CIs as unnatural and argue for a child’s ability to choose what is done to their bodies, particularly when it’s not an immediately lifesaving procedure. On the other hand, for many deaf people with implants and parents of children with CIs who commented, it solidified their own generalized stereotype that the Deaf community is completely misinformed about and hateful of CIs and people who use them. It has been posted on thedeafcommunity.org‘s Bully File page as an example of anti-oralism, anti-CI bullying (the page, however, includes no examples from the other extreme despite many examples across the Internet).

All this furor raises the question … what is art? What is the value of art? What is the value of the reactions that art produces? Some quotes related to these questions that are very insightful:

No great artist ever sees things as they really are. If he did, he would cease to be an artist.

- Oscar Wilde

Art is the desire of a man to express himself, to record the reactions of his personality to the world he lives in.

- Amy Lowell

When I make art, I think about its ability to connect with others, to bring them into the process.

- Jim Hodges

Precisely because of all the reactions posted on the image and its iterations across the Internet, Winship’s art must NOT be censored, as some demanded, or even labeled as bullying, as the operators of thedeafcommunity.org have done. To do so is to oppress and attempt to intimidate and suppress one person’s truth. That hurts us and our society. Art like this should not be condemned and suppressed, but respected and accepted for the lessons we learn from the ripples it makes. I’ve written against censorship and suppression before - “Why Dirty Signs Should Not Be Banned” – and much of what I wrote then applies here as well.

If art is to nourish the roots of our culture, society must set the artist free to follow his vision wherever it takes him.

- John F. Kennedy

The piece has been labeled and devalued as propaganda, which it is not. Most definitions of propaganda require intent to persuade or manipulate. A site that explores art and propaganda says, “One form of expression lacks the intent to manipulate the viewer (art is the work that is play) and instead is made out of a need to release a sort of creative expression; the other form of art is created with the intention to manipulate the mass audience – propaganda art.” This is why it was so crucial for me to talk to Winship, to discover his intent and the inner source of and motivation behind his art.

Winship took all the personal accounts he had heard from former and current CI users, the discussions he had participated in, and his own musings, and he created in his art a reflection of one small slice of the outcome of that mishmash in his mind. He created a symbolic representation of his own perspectives and feelings.  It is the personal expression by an individual, powerfully and technically very well drawn but which presents

One example of an ugly comment.

One example of an ugly comment.

us with a disturbing image. However, it has elicited equally as disturbing reactions from both extremes of the spectrum. It has exposed to us the degree of ignorance,

Another example of ugliness, from the other end of the spectrum.

Another example of ugliness, from the other end of the spectrum.

misunderstanding, miseducation, anger and even fear that revolves around the issue of cochlear implants, Deaf culture and ASL, and what it is to be deaf or to parent a deaf child. Each and every one of those comments is just as much a part of the artistic experience as Winship’s illustration itself and has as much to teach us as the piece itself.

More ugliness.

More ugliness.

They also force us to ask the question: Which is uglier and more disturbing, the image or the reactions to it?

Art “makes us attentive to the reality of our own life … Picasso and Cezanne help us understand that things can be looked at from several points of view at the same time,” Milton Glaser writes. This is the value of Winship’s drawing. What is not exposed cannot be corrected or confronted. Suppression prevents education, perpetuates closed-minded extremism and insensitivity to others, and aids concealment of those who are deeply entrenched in their prejudices. 

The hope comes in this: Even as it has exposed ugliness, the drawing has spurred quite a few people to reflect and share their own experiences in an effort to inform and correct misinformation and assumptions and attempt to pry open the doors of people’s minds. It has brought out the beauty of the diversity of the deaf community and provided evidence that extremists cannot define the community, even as they seek to outshout and marginalize each other and ignore the bulk of those who sit in no-man’s-land.

"She is and will always be deaf and we will always be members of the deaf community and we will always be learning ASL."

“She is and will always be deaf and we will always be members of the deaf community and we will always be learning ASL.”

Parents of children with CIs have come out of the woodwork to plead for rational, respectful discourse and share their efforts to expose their deaf children to the best of both worlds (despite backlash from both extremes). Deaf parents of deaf children have talked about why they chose to implant their children. Deaf adults with implants have come out to explain what their lives have been like, or why they chose to get a CI as an adult. And deaf people who grew up oral have come out to share their perspectives – not necessarily about CIs, but about what it is like to grow up shielded or restricted from contact with ASL and the deaf community. Deaf people who grew up signing or learned it later have come out to share their deepest emotions about identity and the culture so precious to them – and which they perceive some hearing people would prefer to obliterate much as eugenicists and Nazis murdered people with disabilities in the first half of the 20th century. That fear is real and deserves to be recognized and heard with the heart.

The frustrating part of reading some of these comments, for me, was observing two people on either extreme with the same core belief that they interpreted in diametrically opposite ways. For example, a deaf woman who views implants as unnatural and interference with God’s will that a child be deaf, while a hearing parent talked about implants as a miracle given them by God to help her child overcome a terrible impediment. If their roles were reversed, with their solid belief in God, would their views also reverse? The sooner we understand the common elements we share, the sooner we can achieve understanding. The sooner we recognize that we all look at the same picture very differently, for very different reasons, the sooner, perhaps, we are willing to listen.

People are naturally exposed to different slices of life and different types of people based on where they happen to be in life and who they interact with, and they will hear more stories of a particular slant than others. That’s why it’s so important to talk to and really listen undismissively to those unlike yourself, who interact with groups you don’t and live lives you don’t, so you can see a bigger picture than you would if you stayed within your own sphere of being. All of those perspectives shared by people – whether moderate or extremist – are emotionally and experientially laden and therefore valuable. They should be heard with open minds and hearts and a goal of understanding, rather than condemnation of the art or each other. This means that deaf people should be willing to listen to hearing parents who agonize over their children’s futures, and hearing parents should have the courage to listen to those who most intimately understand what it is to grow up deaf. But this listening did not happen with Winship’s illustration. People even more firmly shut the doors to their minds and hearts. What does that say about all of us?

Winship’s illustration accomplished one job of art: It got people talking. The other component of Winship’s art – the contributions by commenters – has another job to do: to get people to listen.

To conclude:

The aim of art is to represent not the outward appearance of things, but their inward significance.

- Aristotle

9 thoughts on ““The principle of true art is not to portray, but to evoke”: An interview with Daniel Winship

  1. Great discussion of the topic, but left me still wondering how to bring together the extremists. A large part of this is the profit, hype and false encouragement that comes with the CI. If it were just a type of hearing aid no more special than the digital upgrade of HA’s, and received little PR, came with instructions to support it with ASL from the cradle, and had none of the pure oral siren calls, it probably would not be as vehemently opposed. It would also probably be evaluated more neutrally by all concerned.

  2. Wow…. I am so blown away by your article because you make a great many astute, insightful and valuable observations. I am grateful to have read it. It was thought-provoking and I intend to share it with others. Thank you for writing this! The very reaction I am having now, to your writing and your ideas, speaks to the truth of your message.

  3. It is an artwork, not a form of cyberbullying. It is shameful that the so-called administrators of thedeafcommunity.org who claimed to represent Deaf people (when they’re really hearing) branded this talented artist as a bully.

    R-

  4. My lad – born totally deaf – two cochlear implants – signs as well as talks very clearly is on his xbox live now playing on some shoot em’ up with some pretty cool headphones on chatting to his buddies. yeah its not perfect but he wouldn’t be doing that (which is something pretty much taken for granted by every hearing kid over 8 years old on the planet) and he just come back from a bike ride with two hearing kids in our neighbourhood who are his buddies with who wouldn’t be his friend otherwise because there is no way on earth they would be good enough at sign. In fact – there are no kids in bike ride distance who sign for him to play with. So I imagine without them he’d be pretty lonely and probably crying like the kid in that picture when he got low about it. He’s not about to rip his implants out – hes pretty chuffed he’s got them.

    That’s not to say that the picture doesnt have its merits – yeah it shocks and yeah some kids have been implanted and have not found an identity or have no connection to the deaf world which they would normally have been involved in. there are many kids in the middle but dont forget that advances in hearing aid technology and new born hearing screening are keeping kids from the deaf community too and parents force hearing aids into kids ears from birth – but that doesnt have the shock factor, I suppose.

    Still, good artistry but a bit silly and juvenile I suppose is the way I’d put it. There is no way someone with experience on both sides of the debate, who had spoken to a range of families themselves and seen the impact of implants on families would dream of creating something like that – I suppose it reflects an immaturity or inexperience of the issue. Don’t get me wrong, I know there is feeling there and it comes from something but its blinkered – there is a debate to be had about implants on deaf culture and on young people but this drawing doesn’t advance it.

    Cheers!

    Ape

    • Thank you for your comment, but I have to admit I am a little astonished with it. Some parts sound like you’re almost there in understanding … but others illustrate perfectly how assumptions and misinformation go both ways. Naturally, hearing parents of deaf kids think the bulk of misinformation and ignorance is heaped up on the Deaf side, but that’s because they likely haven’t taken a step back to think outside the box or recognize that they canNOT understand the experience of being deaf because they’ve never been deaf themselves. So naturally they don’t recognize how limited their comments appear to those who are deaf, nor how wildly off their assumptions – and consequently thinking – are about deafness from their stance as hearing people (just like they accuse deaf people who haven’t had CIs of being guilty of). Just like white people will never understand the black experience, men will never understand the female experience, and straight people will never get the gay experience. It’s always challenging – sometimes impossible – to think outside the box of your own existence, so often the best people can do is to recognize that … and that goes a long way toward ending assumptions and judgmentality. That isn’t happening on ALL sides, like I said in this blog. But I will freely admit that I can’t understand the hearing experience or the parenting experience (yet!! :D), so please don’t assume I’m trying to speak out of those two boxes :)

      Only going to tackle a tiny part of your comment for now:
      “There are many kids in the middle but dont forget that advances in hearing aid technology and new born hearing screening are keeping kids from the deaf community too and parents force hearing aids into kids ears from birth.”

      And many of them do come over to “The Dark Side” as adults, venting about how they feel growing up like that, force-fit into a mold of normalization, angry that they didn’t have access to sign language or other deaf kids as a child. And some of their parents are even admitting the same thing, that they’re kicking themselves for not also including or learning sign (I recognize that your son signs, and that’s great; but I’m addressing other parts of your comment now). In a ripple effect, these confidences tick off a lot of other deaf people and you get a big angry emotional hot mess as a result from the latter group who haven’t had a lifetime’s practice of putting up and shutting up.

      Are most of the former group of deaf adults (whether they have CIs, HAs, grew up oral, etc.) going to talk to hearing people about their feelings and any experience that’s less than totally positive? Of course not. They’re told overtly or implicitly to put up and shut up, that they need to work harder or something is wrong with them. To not be able to pass as perfectly hearing or to admit that CIs and hearing aids don’t equate normal hearing or don’t work in certain settings/situations is tantamount to admitting failure by hearing people’s definition. When you’ve grown up in a world where hearing people’s words and actions imply or straight-up tell you that anything short of functioning as 100% hearing is a failure, bad, very disappointing, and your parents work SO hard to “help” you function like a hearing person … do you really want to go around telling those same people that it isn’t working out quite that way and deal with disappointment from your parents and everyone who “invested” so much time into you? Nope. It’s other deaf people who hear all of that. Not you. That’s why I said this artwork provides a valuable distillation of Daniel’s mental processing about he heard from other deaf people who have CIs – things that they would most likely never tell a hearing person or a hearing parent precisely because of the defensiveness, denial and judgmentality those admissions often garner in return. It may not reflect the entire spectrum, but it reflects something you and other hearing people rarely have access to. To call this artwork silly and immature reflects back upon you. The sooner you recognize your own blinkers, the better.

      I get the sense from your comment that your son is still young. Kids’ dialogue is still pretty simple and straightforward and a lot of them don’t really sit around shooting the shit. Much less be able to introspect and process what they’re feeling in a mature way that they can express in words, much less to an adult figure. Wait until he gets older, discourse becomes more complex and group situations get involved.

      BUT then you get the problem I mentioned above. Is your son going to tell you everything that happens when you’re not right there seeing it? Is he going to tell you every incident where his CIs didn’t help him function like his peers or when he misses information? Is he even going to whisper a hint of dissatisfaction to his parents or other adults? A lot don’t – especially boys and young men when 1) they’re at the mercy of their hormones and teen angst and 2) the last thing in the world they want to do is to disappoint their fathers. Been there, seen that all the way from 8-year-old boys refusing to admit they can’t understand their teacher up to 25-year-olds tuning out of group conversations in restaurants because they give up on trying to follow.

      Just something to think about, since your son is still young. Would love to hear an update in 10-15 years. In the meantime, I’m going to encourage some adults with CIs I know (who STILL use and love them) to chip in here.

  5. Pingback: Shock cochlear implant picture: Interview with artist | The Limping Chicken

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