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Chuck Close and the Salvation of Work
By Laura Kaminker
This artist doesn't wait for inspiration; he doesn't believe in it. He believes in work. Close paints five days a week, six hours a day (nine in summer), in three-hour intervals. He begins with a camera, chooses a photograph, and then superimposes onto it a precise grid. Next he transcribes the grid onto canvas, then applies paint to the boxes. When he is finished, some four or five months later, the 1,200 squares are filled with dots, daubs and markings, each box a tiny abstract painting unto itself. Together they form a portrait, titled Janet or Stanley or Dorothea. Museum-goers at a Chuck Close exhibit all do the same thing: they walk up to a painting, noses nearly touching the canvas, to examine the colors and textures of the individual squares. Then they slowly walk backwards, stopping when the entire image comes into focus. Then they walk towards the painting. Then they do it again.
In the hospital, Close painted a portrait of artist and friend Alex Katz. When he got out, he moved to an accessible studio, got an electric easel (the painting descends into a slot in the floor), strapped on a wrist brace, popped in a jazz CD, and continued painting. "My process hasn't changed very much," says Close, now 58. "I used to sit in a forklift and I'd move around. Now the painting moves around instead." 1998 seems to be The Year of Chuck Close. In the spring, New York's Museum of Modern Art launched a retrospective of his career, which traveled to Chicago before its current run in Washington D.C., and will appear next in Seattle. There has been a PBS documentary, a children's book and a deluge of press. I spoke with Close in his downtown Manhattan studio, where a portrait of artist Jasper Johns looked on, waiting to be completed. I am happy to report that this art-world celebrity and high-profile quad is a warm, generous, happily outspoken man with plenty to say about art, work, disability and life. LK: Many stories about you still focus on the "overcoming tragedy" angle.
First of all, I'm lucky I already was somebody. There are so many kids in rehab hospitals, because of diving accidents or motorcycle accidents or being shot. They're so young, they don't have anything to return to. I was also lucky that I was self-employed; I didn't have to convince an employer that I was capable of getting back to work, I only had to convince myself. There are two other ways in which I am very lucky. One is that I am by nature an optimistic person, for which I can take no credit; that's just who I am. Other people are by nature pessimistic, for which they should not be blamed; that's just who they are. I think my optimism helped me get back to work. But the last reason I reject the idea that I am any kind of hero is that I could
afford to get back to work. I made a lot of money with my art, so I could build a
wheelchair-accessible studio and hire assistants. I have excellent medical insurance,
for which I pay an arm and a leg. Even so, I have about $50,000 a year in unreimbursed
medical expenses. If I didn't make that $50,000, plus enough to live on, I'd have
to go on Medicaid and become a ward of the state. So another artist, equally committed,
equally determined to return to painting, but without the income, might not have
been able to.
LK: When you have such a distinctive style, how do you keep it from becoming stale and cliched? How do you keep it fresh? CC: I suppose some people would say that I haven't. CC: Actually, that's the indicator that I use. How am I feeling about the
work? Does it feel like I'm getting too good at it? Is it too easy? Ease and facility
are the enemy of the artist. If you do something for too long, you simply display
how well you can do that thing, and it becomes emptier and emptier. So what I've
always tried to do is alter the variables--change the materials, techniques, procedures,
processes, scale, whatever--to keep myself off-balance so that the search is still
on. And to get myself in trouble. It's important to be in trouble. CC: You don't. You can't. Nor should you. If you worried about the whole all the time, you'd be paralyzed--no pun intended. You can refer back--I look up every once in a while to see if what I'm doing here agrees with what I was doing up there--but you can only work where you are. How do you make a sweater? A whole sweater--who knows? But if you knit one and purl two long enough, you get a sweater. And it's in those little movements, those increments, that the sweater gets made. When I was in school, I used to work all over, all at once. But I was never well suited for that, I found it very frustrating, overwhelming. It has a lot to do with my learning disability--I had to break things down into small, bite-sized decisions. And it's actually a great way to work. I think it's very much related to what used to be called "women's work." Women always had so many things to do, they could knit for a while, put it down, go start dinner, come back and knit a little bit more, put it down, go weed the garden. ... It doesn't require that you reinvent the wheel every single day. Each day, you add positively to what you've already done and it just keeps building. When you're done, you might not like that sweater as much as you like other sweaters
you've made. So next time, you change something about the material or the colors.
But you have a belief in the process, and while you're doing it, you give yourself
over to that process. I've found this way of working very liberating.
CC: That's what most people think of first, and obviously there is some connection. But I don't think it's that accurate. I guess the artist I'm most often linked with is Seurat, whom I love. He's a wonderful painter and absolutely one of the great draftsmen of all time. But actually, his pointillist paintings don't really do what we think they do. That is, the majority of the marks in any given area are the generic color of that material. So if it's grass, the lion's share of the marks will be green, if it's sky or water, the lion's share will be blue, and so forth. The other colors in there just sort of modify it. I try to make the skin out of a color--by neutralizing or canceling or combining all kinds of colors--that you're never going to find in anybody's face. The works that I actually feel a closer relationship to are mosaics. Not the Byzantine
mosaics in Ravenna, the glitzy, gold ornate ones, but the really humble floor mosaics
that you get in the South [of Italy]. The [Ravenna] mosaics are so high up, you can't
see the incremental unit very well. But the ones on the floor are clunky, they're
made of big chunks of stone, so you see the face or the animal or whatever is being
depicted, but you also never forget that you're looking at a chunk of stone. It's
that relationship--between the image built and the material used and the incremental
unit itself--that interests me. CC: I've always said that the bigger they are, the longer they take to
walk by, and therefore the harder they are to ignore. That's at least part of it.
I wanted to rip it loose from the context in which we normally see the face--much
bigger and harder to see as a whole, so it forces you to scan it, make it a kind
of Brobdignagian world, like you're traveling across the surface, sometimes at some
distance, not completely aware of what you're looking at. All this information, all
the detail, and you can still get lost in it. CC: When I was lying in the hospital, paralyzed from here [indicates throat]
down, unable to move at all, I thought, what am I going to do? I thought I could
do some kind of conceptual work, and have other people execute it. Since I wouldn't
want anyone else to paint my paintings, I imagined some kind of installation or performance
pieces, and I thought it might be interesting to do work about the hospital, disability,
stuff like that. Then when I got some movement in my neck and head, I thought, I
could paint with a brush in my teeth and make really small paintings. And I thought,
maybe it would be interesting to make paintings about disability. And I didn't think
about that other performance stuff anymore. But once I got enough arm movement that
I realized I was going to be able to paint, I just wanted to make the paintings that
I had always wanted to make. I went back to the method and the subject matter that
I loved and tried to make more paintings that I liked. CC: No, not at all. I do a lot of work with both learning disabled and physically disabled people. I'm not ashamed of my disability, and I don't hide it. I'm out in public all the time, perfectly happy to talk about it and show people how I do things. I just don't want it to be the focus of the stories about me. I'm really glad that there's a disability community. And I'm really glad that
there are militantly active people fighting for access. I work with Hospital Audiences
trying to improve access to cultural institutions. We do assessments of every cultural
institution--every gallery, every museum, every theater--and we publish a book called
"Access For All," which tells you how wide the doors are, how many steps
there are, how you get in. A blind person and a person in a wheelchair go to each
site to do the assessments. CC: No, but I will tell you the most offensive thing people say. Literally,
I don't think a week has gone by that this doesn't happen. I'm in a museum or gallery,
and people are walking around and their legs are tired or their feet ache, and they
come over to me and say, "You're so lucky that you get to sit down." CC: It depends on how they said it and how cranky I am. Either I say, "No,
I'm not, I'd much rather be walking around like you, you asshole." Or else I
just let it go. CC: I don't attach too much importance to it. I probably wouldn't have
kept it, but my wife wouldn't let me sell it. She thought it was too important. But
two interesting things happened with that painting. I'd already taken the photograph
for it before I was in the hospital, and his face looks considerably sadder in the
painting than it does in the photograph. So that probably sneaked in. But on the
other hand, the palette brightened considerably. So I think there's also a sense
of celebration.
LK: Did your disability help you grow as an artist in any way? CC: No. No. In fact, a kind of conspiracy evolves in rehab hospitals. There's a kind of rehab culture, a rehab state of mind. And the conspiracy that both patient and doctor enter into is: You will never work again. I had doctors ask me--or they wouldn't even ask me, while I'm sitting there, they'd look over my head and ask my wife--"What was it that he used to do?" The assumption, of course, was that I'd (a) never want to get back to work and (b) never be capable of it. I went to occupational therapy with the hope that they would help me get back to my occupation. But they wanted to help me do my laundry. I never did my laundry before--why would I want to do it now? In the rehab culture, doctors, shrinks, and some--though not all--therapists unite in a conspiracy with the patient to figure out how they will live, not how they will be productive. You are preparing yourself for a lifetime of watching TV while you're on the dole. I think it's an incredible indictment of the capitalist system that given half
a chance to never work again, most people would choose it. Because their jobs are
so deadeningly boring and meaningless, who would be interested in getting back to
work? But work is salvation. The time you spend working flies by and the time that
you're not working moves at a glacial pace. Not only is it your salvation, but it's
ennobling. You're pulling your own weight and you're contributing to society and
you're doing something important, and those things matter--in terms of self-worth
and not pitying yourself. CC: I was always aware that something was wrong, and so was my mother.
But in the 1940s and 50s the words "learning disability" or "dyslexia"
didn't exist. I was simply dumb and lazy. But my parents knew I was intelligent.
I just couldn't memorize stuff, and I couldn't spit it back on tests. I couldn't
recognize certain things. Luckily my parents helped me feel special and celebrated
my skills, and didn't dwell on my deficits. And my mother fought the system, all
the way through--to the point where it was so annoying, I wanted her to stop. CC: My 25-year-old daughter was 8, so that would have been some time in
the 70s. CC: Oh sure, it put me in very good stead to deal with what happened to
me. CC: I have a survivor mentality. I have a we-shall-overcome sense of resolve. I have a strong questioning nature, which kept me from being a compliant patient, so I took charge of my own rehabilitation. And my learning disabilities, along with the fact that I lost my father at the age of 11, taught me that something terrible can happen to you and you can still be happy again. A lot of people are dreading some disaster, not knowing if it will devastate them or if they will survive. But I already knew. I knew I'd survive, I knew I'd work, and I knew I'd be happy again. Laura Kaminker is a New Mobility contributing editor. peop001 |