Far From the Tree

by Solomon, Andrew

  The spiritual has always been emphasized in Taylor’s life; Carlton is a devout Christian who sings in his church every week and has released an album of inspirational music under the name Carlton David. Carlton said, “I believe there’s a God. I believe God doesn’t make junk. It’s unfortunate that Taylor carries such a heavy burden. But I don’t believe you are given the heavy burdens unless you can handle them.” Taylor explained, “I’ve been going to church since I was born, still do. In the middle of my angry period, I recognized that I don’t fit with Christianity. I don’t think there could be any kind of puppet master that could be both a hundred percent love and power and still allow civilizations to rot and fester, and individuals to be born with this kind of pain.” Over time, though, his anger began to resolve. “You can’t solve what I have, but you can come to accept it. I quit drugs, and after that, in eleventh grade, last year, surrounded by all the coolest people I could ever want, I enrolled in four AP classes.”

  Taylor later said that he always managed to get what he really wanted. “But it requires a step or two more than most people need. It’s pretty painful physically, most intensely in my legs and ankles. I use weights and swim because I care about being healthy and how I look. Going to hike with friends, my back is breaking, my hips are about to fall off. I have to take a break. ‘Taylor, dude, what’s up? Let’s go.’ I’m dying. I don’t think most people realize. I have to purposely laugh if somebody makes a midget joke. I don’t find it funny, but they’re not trying to hurt my feelings, and I’m not going to go on a jihad against Comedy Central. I did the class-clown thing in elementary school, the quiet-in-the-corner thing in middle school, and now I try to balance it. Other people have no idea what it’s like to be me. But then, I have no concept of what it’s like to be normal.”

  Taylor used to want to be alone for the rest of his life, but now he wants to find someone. As he reimagines his future, his grandfather is his inspiration. “Look at what he faced and stood up to,” Taylor said. “So my enlightenment—I kind of like to think of it as my enlightenment—is that I can have dwarfism be a factor in everything I do, but not hate it, not have it limit more than what it limits.”

  • • •

  Dwarfs have created dating sites such as datealittle.com, littlepeople meet.com, lpdate.org, and shortpassions.com. “Much of the dwarf population missed the years the basic ground rules were learned,” one LP said. “We’re naïve. We never leaned over in a movie and gently let a hand fall onto a breast. First, we likely don’t have the date. Second, our arms aren’t long enough.” The challenges may extend beyond those posed by social norms. John Wolin elaborated, “Many of us have trouble coupling. Our limbs may be too short or too rigid to bend around our partner’s. Because of the spinal-cord damage many of us suffer, we may have trouble with erections or may find orgasm a guest with a mind of its own.” Dwarfs must decide how they feel about being involved with average people (APs) rather than LPs. On the LPA website, one woman complained about the difficulty of not being able to kiss an AP or look into his eyes while they were having sex. Harry Wieder said, “For people of equal height, what is mysterious is the lower body, which you have to reach for—that’s what’s sexualized. For me, it’s the opposite. I look at people below the waist all day every day, and my idea of intimacy is the special occasion of looking someone in the face. The feeling when having sex with APs that I needed to relate to the bottom half of the body, and not relate so much to the top half, was problematic.”

  For many little people, the question of whether to partner with another little person or one of average height is political. Some have contended that dwarfs who marry people of average height fail to accept themselves as dwarfs and reduce the available pool of spouses for LPs who seek similar-size partners. Rates of depression seem to be slightly higher among little people in mixed-height marriages. Although almost all dwarfs in LPA who married used to choose other LPs, an increasing number are marrying APs; and while mixed marriages used to be stigmatized at LPA, they are now much more widely accepted. Outside LPA, however, most dwarfs who marry still marry other dwarfs.

  Wolin wrote that before he met his wife, “I feared—and fear doesn’t really do justice to the brutal emotion I felt—that I would never be married.” In researching this chapter, I became friends with the mother of an attractive, short-statured young woman. One day, I suggested that I knew someone who might like to be fixed up with her. The mother, a person of emotional restraint, became tearful. “My daughter is over thirty,” she said, “and in all these years, you are the first person who has ever made such a suggestion. My son, who is average, everyone on the planet wanted to introduce him to their daughter or friend. But no one ever thought of my daughter as a sexual being.”

  Childbearing presents other challenges. The pelvic opening in many short-statured women is not large enough to allow an infant to pass, so virtually all deliveries are performed by cesarean section—which requires anesthesia, a risk for LPs. Carrying a child may be physically stressful to dwarf parents. As part of the overarching theme of dwarfs’ having no privacy at all, dwarf parents are frequently interrogated about their procreative and birthing experiences. “As usual, the most bizarre comments come from the adults,” one such mother described online. “IS THIS BABY YOURS? This is a question I would never think to ask of anyone with a baby but one I am asked several times a week.” Adelson wrote, “For each LP couple that decides to have a child, the decision is an affirmation of their own lives, and a leap of faith about the lives they may expect for their children.” Indeed, for this very reason, many little people, some with biological children and some without, adopt dwarf children given up for adoption by their average-size parents.

  • • •

  Yet many average-size parents do not give up such children, even when strongly advised to do so. When Clinton Brown III was born, his father, Clinton Sr., remembered, “I could see right away his arms were straight out, his legs were straight out, and his body was small. I almost fainted.” A curtain blocked the view for Clinton’s mother, Cheryl, but it did not block her hearing; the baby didn’t cry, and none of the doctors or nurses said anything. When Cheryl cried out, “What’s wrong?” one of the doctors replied in a hushed voice, “We have a problem here.” Although Cheryl wanted to see and hold her baby, he was whisked away. Later, a doctor explained that her son was terribly deformed and likely to die, the result of diastrophic dysplasia. Such profoundly affected children are usually institutionalized, he said, and offered to handle Clinton’s placement without her involvement, since it was sometimes easier for parents to give up a child they’d never seen. Cheryl was indignant. “That’s my baby,” she said. “I want to see my baby.” The doctors were vague about prognosis; only a few thousand people in the world were known to have diastrophic dwarfism. “The information they had on it was two paragraphs,” Cheryl recalled. “Two paragraphs on what the rest of our lives were going to be.”

  Clinton was in an incubator when Cheryl finally saw him, and she was allowed only to touch his toe, but when she did, his eyes opened and she saw that they were blue and beautiful. She also saw everything she would come to know as signposts of diastrophic dwarfism: the unjointed hitchhiker thumb that springs from the bottom of the palm, the flat nose, the cauliflower ears, and the cleft palate. He had scoliosis and clubfeet, and his legs were bunched up under him like airplane landing gear. His head was gigantic. “Some kids have a mild version of this, but he had every symptom possible,” Cheryl said. “I think of it as the deluxe package.” Clinton Sr. said, “We came home without him. I remember pulling into our street, looking at Cheryl, and it was just empty, you know?” Clinton Sr. went back to work as an engineer for a cable TV company, and Cheryl to her job at a call center. Clinton had his first surgery when he was two weeks old to repair an umbilical hernia. When the Browns brought him home a month later, he was so tiny that Clinton Sr. could hold him in one hand.

  Once they had him at home, Cheryl
tried to treat him as she would have treated any baby. “When I was young, I thought life went on a schedule. You go to high school; you find a job; you get married. When you have a child like Clinton, it’s ‘What happened to all that stuff I always counted on?’” When Clinton was eleven months old, Cheryl found Steven Kopits. “From that moment on,” Cheryl said, “he controlled everything that happened to Clinton. Without him, Clinton wouldn’t have walked.” Clinton Sr. said, “You went into his office depressed, and you came out enlightened and with new hope.” Cheryl said, “They weren’t patients to him; they were his children. Nobody else ever comes up to that level. And no one will, because there’ll never again be an angel like that on this earth.”

  Kopits was famous for developing long-term surgical programs for his patients; rather than perform a single operation in the unlikely hope of correcting all of a patient’s problems, he would perform one that promised to reap benefits down the road and facilitate subsequent operations. In the end, he performed twenty-nine surgeries on Clinton Brown Jr. “I had asked my pediatrician what Clinton was going to look like,” Cheryl said. “So he gave me a book on people in the circus. I went to Dr. Kopits. He said, ‘Let me tell you something. That’s gonna be a handsome young man.’” The long waits in Kopits’s waiting room were notorious; a routine visit often became an all-day affair. “No question in my mind I would wait ten hours,” Cheryl said. “He would say, ‘I’m sorry, I have to see this one.’ We knew if our child needed him that he would say the same to another family.”

  When Clinton was almost three, after six months of constant surgery, Dr. Kopits assigned him to one of his staff physiotherapists, and Clinton began to walk. Kopits worked on Clinton’s clubfeet, his tibiae, his fibulae, his knees, his hips. Clinton had eleven back surgeries, cleft palate surgery, surgery to correct an inguinal hernia. He spent six months in a body cast, flat on his back, with a circle of metal with four pins fixed in his skull to immobilize his neck and spine. “I lived in the hospital with him for one month, two months, whatever it took for him to be rehabbed,” Cheryl said. The call center where Cheryl worked gave her extra time off. The Browns needed two parental insurance policies for Clinton’s surgical program; even then, the uncovered expenses were catastrophic. “You’ve heard of the Six Million Dollar Man?” Cheryl said to me, pointing at her son. “This is the Million Dollar Dwarf you’re talking to.”

  Since diastrophic dwarfism is a recessive genetic trait, any other child Cheryl and Clinton Sr. might produce would have a one-in-four chance of inheriting it, so they decided not to have more children. “In the beginning, you live in six-month increments,” Clinton Sr. said. “With our kind of kid, you don’t look long range.” Cheryl said, “The hardest thing was going out in public, that first negative comment or stare. I always had it in the back of my head that it should be a learning experience for everybody that encountered Clinton and me. We made it a little joke: ‘Okay, look at that one, Mom. They’re staring at me!’ Then Clinton would just do a nice little wave and smile.” Clinton Sr. said, “We were in a store once, and this little kid was hovering. So Clinton, who was twelve, ran around the next aisle and, as the kid came by, jumped in front of him and spooked him. The kid freaked out and broke down crying. I said to Clinton, ‘That wasn’t the right thing to do.’ He says, ‘But it felt so good, Dad.’ And I said, ‘Yeah, okay. That one’s for you.’”

  Clinton said, “When I was a kid, I was bitter towards the fact that I was little. Angry that I didn’t have the same opportunities as everybody else. You either face the war, or you falter. It was everyone else’s problem, that they didn’t know how to handle it, and it was my problem that I didn’t know how to teach them how.” Clinton Sr. added, “Once he said, ‘If I was average-size, I’d be great, wouldn’t I?’ He was eleven, in that hospital room. So now I had to leave the room ’cause I was crying, and I felt so helpless. When I came back, he said, ‘That’s okay, Dad. I have the answer.’”

  “I was such a sports fan, and I wanted to be an athlete,” Clinton said. “We used to play hockey in the street, but everybody started getting huge, and running me over, so I couldn’t play. It’s just a big piece of childhood that I missed out on.” During the long periods of immobility and surgery, Clinton was homeschooled. It was his primary distraction, and he worked hard. “I figured I had nothing else to do, so I got ahead of my class on most things. I decided to do really well academically, ’cause I just had to be the best at something.” When he graduated, Clinton was accepted at Hofstra—the first member of his family to enroll in college. He decided to major in banking and finance, volunteered to be a peer counselor, and helped run orientation week for new students. “I wish all life was college. I’m in the big, macho fraternity; I’m friends with all the girls on campus. I’ve dated here and there. I have fun.”

  With his unjointed fingers, Clinton still needed help buttoning a shirt, but he became increasingly independent in other regards, and he got a driver’s license and a specially fitted car. “I remember when he told us he was driving,” Clinton Sr. said. “A friend of mine tells me he saw Clinton on the Long Island Expressway! I go, ‘You saw Clinton in a van, driving on the LIE?!’ So I found his schedule, and I snuck down to school. I didn’t want him to know that I was there, so I parked in the back. I’m thinking the teacher’s drunk or he’s a saint. Because they had a makeshift seat and steering wheel for Clinton. He drove right out. I didn’t say a word because—well, I couldn’t talk. I was amazed.”

  “When he first went to Hofstra, he met this group of guys that he’s been hanging out with for the last four years,” Cheryl said. “They would go out to bars and stuff. I said, ‘Well, how do you get on that bar stool?’ He goes, ‘They lift me up, Ma.’ I said to him, ‘Your body is three feet tall; your friends are six feet tall. If you drink two beers, that’s them drinking four beers.’ I was terrified about his drinking and driving. I went past a bar and I saw his car parked there—it’s very easy to recognize with all those fittings. I didn’t think I could march in there like I wanted, but I left him three messages and sat home by the phone waiting for him to call. So I told this to the mother of a child who had gone to school with Clinton. She said to me, ‘You’re so lucky that he is at a bar.’ I thought, ‘Okay, if you’d told me when he was born that my worry would be that he’d go out driving after drinking with his college buddies, I’d have been overjoyed.’”

  Clinton has learned to set boundaries with a public that takes his size as a waiver of all social rules. “I used to become really upset,” he said. “I would cry. Now I just go right up to the person. My mom’s always, ‘Be nice, be nice.’ But sometimes you can’t be nice. I walked by this guy’s table, and he goes to his friend, ‘Oh, my God, lookit that midget.’ I said, ‘Don’t ever do that,’ and I knocked his beer into his lap. You can’t yell at kids. They don’t know any better. So I go up to the parent: ‘Listen. Why don’t you teach your kid some manners and have some class about you?’ And it’s no better in classy places.” I remembered this conversation when Clinton and I had lunch a year later in a nice restaurant in midtown Manhattan, a place he had chosen near his office. As we walked to our table, every person we passed stopped talking and stared, except a few who looked out of the corners of their eyes. If I had shown up with a ring-tailed lemur or with Madonna, there wouldn’t have been more focused attention. It wasn’t hostile, but it was certainly not relaxing—and it was completely different from the experience I had, for example, pushing a multiply disabled child down a pier in San Diego. Benign pity can wear thin, but it’s still easier than astonished fascination.

  At eighteen, Clinton found his first summer job in finance; five days a week, he made the solo commute by scooter, train, and subway, an hour and a half each way, to the Manhattan offices of Merrill Lynch. “I want to have everything I can in my arsenal of education. My parents worry about me too much, and my way for them to let that go is for me to be financially and physically independent. I was in the ho
spital so much, so my parents were my best friends. Now I have no boundaries; I have no inhibitions; I want to do so much.”

  The great question in Clinton’s life is mobility. For longer distances, he rides his scooter. He is in pain whenever he walks any distance—much sooner than Taylor van Putten, for example. “My hips and knees and joints are real bad. There’s a lack of cartilage between the bones. The cold makes it worse.” Despite this, I was impressed at how gracefully Clinton could swing his body around. He could weave his unbending fingers around the handle of a fork or a knife. “I figured out a lot by myself. I used to pick up pizza or a sandwich and put it on the top of my hand. Writing, I use two fingers. If I could change one thing, I would love to walk like a normal person. But I’m dancing all night; I’m doing everything.” In fact, when I first met Clinton at LPA, he was dancing; he stayed long after I’d gone to bed. The next day, he was hobbled with pain but also on cloud nine, and he teased me about being the only person of average height on the dance floor: “You stuck out like a little person.”

  The summer job Clinton had at Merrill Lynch was in their legal department, filling out forms, and he was determined to secure a promotion. After he graduated, he was hired by Mutual of America Capital Management Corporation, where he prepared income statements and reports for technical analysts, obtained real-time stock quotes, and helped brokers identify trends in certain Internet stocks. During his time there, he had a bad experience with inadequate access on the subway. He obtained permission to address the board of the New York Metropolitan Transportation Authority at their next public meeting. Arriving at the midtown conference room, I found a mob of his friends and relatives who had turned out to support him. “I am standing in front of you as a representative of all disabled citizens of New York,” Clinton said, poised and confident. “My story is of a violation of the Americans with Disabilities Act, a violation of civil rights, and a blatantly dangerous situation presented to all wheelchair-bound citizens who use the MTA’s subways and trains. The purpose of this speech is to illustrate what is going on out there in your transportation system, let you know what it means to the people it is affecting, and drill down to a resolution. I am asking you to be my teammates in a quest for equality, and to work to fix this issue.” At breakfast afterward, Cheryl confided in me that she could never, ever have done such a thing.