Noteworthy News Articles on Mental Health Topics, April 17-27, 2008 A Master’s in Self-Help Jane Gross, New York Times- 4/20/2008 Laurie Duddy thought she was on top of things when her toddlers, Tommy and Alex, were diagnosed with severe autism. She knew that early, intensive therapy was the twins’ best hope of learning simple skills, acquiring language and mastering out-of-control behavior. So at great financial sacrifice, she hired certified therapists to work with them privately for 40 hours a week using applied behavioral analysis (A.B.A.), the therapy of choice for the growing ranks of children with autism. She moved from district to district, seeking the best educational services when they reached school age, and eventually joined a group of parents in starting a private school of their own that would offer state-of-the-art behavioral treatments. Then, more by coincidence than design, she met Sharon Reeve, a consultant for New Jersey school districts who also supervised home programs for families. Dr. Reeve was gearing up to pitch a graduate program in A.B.A. to Caldwell College, and she welcomed an invitation from Ms. Duddy to evaluate her two boys’ therapy. “When she left, I was devastated,” Ms. Duddy said. The twins were not being taught play or social skills, Dr. Reeve had told her; nor was “the science being practiced the way it should be practiced.” Ms. Duddy was recounting her frustration from the student lounge at Caldwell College, where she is working toward an advanced degree in A.B.A. — to “steer the ship better” for her children, now 8. Of the 100 students in Dr. Reeve’s three-year-old program, 17 are parents of children with autism or related disorders. Like Ms. Duddy, they have decided that completing a master’s degree — and investing some $25,500 in tuition — is worth it to help their children. Along the way, most have been inspired to begin new careers. Ms. Duddy hopes to train therapists once her own education is complete. In most states, a generic special education degree is sufficient to treat children with autism and to use the particular techniques of A.B.A., the only therapy for the disorder with proven results in peer-reviewed research. But many colleges and universities now offer specialized degrees in A.B.A. Graduate programs are offered at Northeastern University in Boston, Florida State University in Tallahassee, the University of North Carolina at Wilmington, the University of Maryland in Baltimore County and California State University in Los Angeles, to name a few. Administrators at several of the programs say they, too, have parents of autistic children among their students. Caldwell’s graduate program is the only one of its kind in New Jersey, a state known for pioneering autism education and advocacy. New Jersey is home to the Princeton Child Development Institute and its many offspring, including a host of small private schools founded by parents committed to A.B.A. techniques. The state is thus a magnet for families from out of state looking for the best services for their children. Because of this migration, New Jersey has the highest incidence of autism in the United States: 1 in 94 children versus 1 in 150 nationwide, according to federal studies. The supply of behavioral therapists has not kept up with demand, leading to waiting lists at private schools, an insufficient number of public school programs and desperate families outbidding one another for private instructors. The Caldwell parents, all but one of them mothers, have firsthand experience advocating for services, battling recalcitrant school districts, monitoring what goes on at school and managing home programs to supplement classroom instruction. Many have seen their marriages crumble under the stress; moved multiple times to find a district that can educate their child or pay for an out-of-district placement; and run up staggering debts paying for private school, in-home therapists and lawyers versed in the rights of disabled children to a free and appropriate education. In the classrooms at Caldwell, students study the principles of behavioral learning: to break tasks into their component parts, to reinforce success with tangible rewards like pretzels and intangible ones like praise, to meticulously chart progress, to make course corrections that foster what works and to generalize skills mastered in a controlled classroom for the messier circumstances of everyday life. They study language and social deficits — the hallmarks of autism spectrum disorder — as well as challenging behaviors common to autistic children, like hand flapping, tantrums or self-injury. They also do the equivalent of student teaching in New Jersey’s private schools and in dedicated public-school programs for autistic children. At Garden Academy in West Orange, 8 of 15 therapists and aides are Caldwell students. Among them is Lisa Rader, a 29-year-old single mother who left the Air Force and took a high-paying job with a defense contractor to pay the legal bills incurred in getting her autistic 11-year-old son the services he needed. Now, with the legal battles resolved, she is making another career change. Ms. Rader works at Garden Academy during the week, runs home programs for private clients over the weekend, goes to school at night and does her homework when her son is sleeping. It is an exhausting enterprise. As her son gets older, she hopes to shift her personal and professional focus to adolescents and adults with autism. The Garden Academy, which opened in 2006, has 17 students 3 to 8 years old. They also have a waiting list of 80 — but not enough therapists to expand, says David Sidener, the school’s director. Mr. Sidener’s goal is 24 students. “It’s a seller’s market for A.B.A. therapists,” he says. Sixteen other Caldwell students, including Ms. Duddy, work in the Bernards Township public school district. Carole Deitchman, a former advertising art director and the mother of a 20-year-old with Asperger’s syndrome, teaches social skills to children like her son, who have boundless academic ability but no understanding of interpersonal niceties. One recent afternoon, she instructed a 5-year-old and a 6-year-old, both in mainstream classrooms for the first time, on the rudiments of conversation. Look at the other person when you speak, Ms. Deitchman urged. Then ask a question, wait for an answer, ask another question and say something at the end. The boys’ chitchat, while stiff and halting, fit the formula: “Hi, how are you?” “Fine, how are you?” “What did you do today?” “I played a game.” “What game?” “It’s called Candy Land.” “I don’t have Candy Land yet.” Perfect. Ms. Deitchman beamed and rewarded the boys with high fives and green smiley-face stickers. Most of the parents studying at Caldwell have areas of professional interest related to their own particular tribulations and fears. Martine Torriero, who has a 15-year-old son, hopes to run recreational and cultural programs for autistic teenagers. Delia O’Mahony, whose son is now 22, is interested in adult services, since children like hers “fall off a cliff” when they are past school age. Diana Kelly, who used all her skills as a lawyer to get her two sons properly diagnosed and treated — each has a different variation of autism spectrum disorder — does private consulting for families and schools as she works toward her master’s degree. She hopes Caldwell will add a doctoral program, too. Once a liberal-arts school for “Catholic women of modest means,” Caldwell is now a coeducational institution with 1,032 undergraduates and 625 graduate students, mostly from New Jersey. The college focuses on career preparation, especially in medical and educational specialties. Sharon Reeve, an associate professor of education, started the graduate program with her husband, Kenneth, who is now chairman of the psychology department. They met as doctoral candidates at Queens College, where both were doing basic research in behavioral analysis; she was studying pigeons in a laboratory. One day, a colleague dragged her to a school for autistic children. She knew at once, she says, that the classroom application of applied behavioral analysis was far more compelling than the research she was doing with her pigeons. As final exams approached last semester, a class taught by Kenneth Reeve reviewed how to evaluate treatments based on data, not anecdote. He frequently turned to Ms. Kelly to share her personal experiences. By her own account, Ms. Kelly has tried just about everything, from A.B.A., which many families find harsh and robotic, to kinder and gentler programs with little data to support effectiveness, to special diets and detoxification. Each consumes time and money, Ms. Kelly said, telling her fellow students, as she does the parents she works with, that trying a little bit of everything is tempting but not necessarily wise. “It’s not what looks good, it’s what works,” Ms. Kelly said. “And every hour spent doing X is time lost for Y.” She also laments the imperfect choices available when moving from a home program, usually reserved for toddlers, to a school setting as children get older. Over the years, Ms. Kelly said, she tried a public school classroom for the handicapped, an integrated private school, a mainstream parochial school with a “shadow” for her sons and a school for children with learning disabilities. “Could it be better?” she asked. “Absolutely. Could it be worse? Absolutely. I did a lot of things right and many wrong. I know what was missing for us. And what I’d like to do for other people is help plug the holes.” Stay Stoic or Display Emotions? Barron Lerner, M.D., New York Times- 4/22/2008 A young doctor sat down with a terminal lung cancer patient and her husband to discuss the woman’s gloomy prognosis. The patient began to cry. Then the doctor did, too. The scene was undoubtedly moving. But should physicians display this much emotion at the bedside? For years, medical schools and residency training programs studiously avoided the topic of emotions. Doctors learned the nuts and bolts of cancer and other serious diseases. Yet when it came time to reveal grim diagnoses, they were largely on their own. These days, all medical schools have some type of education in topics like the physician-patient relationship and breaking bad news. But knowing how to respond to a personal wave of stress or sadness remains a major challenge. Is crying O.K.? How about hugging a patient who starts to cry? One physician who cautions against excess emotions is Dr. Hiram S. Cody III, acting chief of the breast cancer service at Memorial Sloan-Kettering Cancer Center. Although Dr. Cody emphasizes the need for doctors “to understand, to sympathize, to empathize and to reassure,” he says his job “is not to be emotional and/or cry with my patients.” There are two reasons for this stance, Dr. Cody tells young physicians on rounds: It is not therapeutic for the patient, and it will cause “emotional burnout” in the doctor. These beliefs are shared by many other physicians, but some new data suggest that crying in a medical setting is common among young doctors. At a recent meeting of the Society of General Internal Medicine, Dr. Anthony D. Sung of Harvard Medical School and colleagues reported that 69 percent of medical students and 74 percent of interns said they had cried at least once. As might be expected, more than twice as many women cried as men. In some instances on the wards, the emotions just flow. For example, in the 1988 PBS documentary “Can We Make a Better Doctor?” a Harvard medical student, Jane Liebschutz, sees her patient unexpectedly die during a cardiac bypass operation. She suddenly bursts into tears and wanders away from her colleagues until the chief surgeon, who has witnessed what happened, assures her that her response was natural. Other physicians may choose to place themselves in emotional situations. Dr. May Hua, an anesthesiology resident at Columbia University Medical Center, recently told me that during her internship, her supervising resident, Dr. Benita Burke, skipped lunch to spend extra time with her cancer patients. They dubbed this time “mental health rounds,” during which they could address issues that were not strictly medical. Many times, Dr. Burke would wind up in tears or giving an embrace. “I think patients adored Benita,” Dr. Hua said, “both as their doctor and as their friend.” But even as she admired her colleague, Dr. Hua realized that such public emotion was not for her. “I knew this was something I couldn’t do, because I needed to have a level of detachment to these people.” I understood exactly what Dr. Hua meant. Whether because of my personality or my being a man, I, too, have never cried in front of a patient. Dr. Burke says she believes that her crying stems from being “very involved” in her cases, which leads her to “take everything to heart.” In the case of the lung cancer patient, Dr. Burke had been the first physician to inform her that further aggressive treatment was unlikely to help. In other words, the patient was dying. Dr. Burke said she realized that this level of involvement was uncommon but believed that she could not be any other kind of doctor. “I’ve always been a very emotional person at baseline,” she said. Dr. Sung’s study concludes with a call for senior doctors to acknowledge and discuss openly the apparent high rates of crying among medical trainees. Yet while health professionals — not only physicians but also nurses and social workers — may debate among themselves the propriety of emotional displays, what probably matters most is what patients think. Just as different doctors respond differently to sad situations, so do patients and their families. While some might appreciate physical contact or tears, others find such displays to be too “touchy-feely.” Cancer patients may encounter such situations more than most. One breast cancer survivor, Sharon Rapoport, of Roanoke, Va., said she greatly admired physicians like Dr. Cody, who may appear reserved but communicate their concern through their actions. But Ms. Rapoport also said she had an extra appreciation for doctors who felt comfortable with outward displays of emotion. “If that means tears,” she said, “bring them on.” Dr. Barron H. Lerner teaches medicine and public health at Columbia University Medical Center. Talking Veterans Down From Despair Patricia Cohen, New York Times- 4/22/2008 CANANDAIGUA, N.Y. — Nancy Nosewicz was busy fielding calls at the new national veterans hot line on a recent afternoon when someone from the Department of Veterans Affairs in Topeka, Kan., phoned. He had a 55-year-old Army veteran from the Northwest on the line who had called to complain about his benefits, but now the guy, drunk and crying, was talking about not wanting to live. Could Ms. Nosewicz pick up? In a slurred voice, heavy from weeping, the veteran, named Robert, told her that he was homeless and wanted to “just lay down in the river and never get up.” Ms. Nosewicz, a social worker, listened. Then in a voice firm and comforting like a big sister, she said: “We don’t want you to either. Today we’re not thinking about the alcohol or the housing, Robert. Today it’s about keeping you safe.” She gave an assistant Robert’s phone number to find his address and alert local police to stand by. The chain of care resembled a relay race, with one runner trying not let go of the baton until the next runner had it in hand. The veterans hot line is part of a specialized effort by the Department of Veterans Affairs to reduce suicide by enabling counselors, for the first time, to instantly check a veteran’s medical records and then combine emergency response with local follow-up services. It comes after years of criticism that the department has been neglecting tens of thousands of wounded service men and women who have returned from war zones in Iraq and Afghanistan. On Monday, a class action suit brought by veterans groups opened in San Francisco charging a “systemwide breakdown,” citing long delays in receiving disability benefits and flaws in the way discharged soldiers at risk for suicide had been treated. Kerri J. Childress, a department spokeswoman, said Monday that there were an average of 18 suicides a day among America’s 25 million veterans and that more than a fifth were committed by men and women being treated by Veterans Affairs. Up and running since August, the hot line tries to respond to at least some of those in crisis. Over eight months, it has received more than 37,200 calls and made more than 720 rescues — sending out, from a narrow office here in upstate New York, emergency responders all over the country to find someone on a bridge, with a gun in his hand, with a stomach full of pills. Paul Sullivan, the director of Veterans for Common Sense, one of the groups involved in the lawsuit, said of the department: “I’m pleased they’re responding. However, much more needs to be done so vets aren’t turned away from health care and don’t have to wait for benefits.” Mr. Sullivan says suicidal patients have not been able to get care promptly; he cited the case of Jonathan Schulze, who was turned away twice from a Veterans Affairs hospital before he killed himself in January 2007. “More than 600,000 veterans are waiting, on average, more than six months for disability benefits,” said Mr. Sullivan, who worked at the department monitoring benefits. Experts agree that veterans are more likely, perhaps twice as much, to commit suicide as people who have never served in the military. Meanwhile, a study released last week by the RAND Corporation estimates that roughly one in five veterans of Iraq and Afghanistan has symptoms of post-traumatic stress disorder, which heightens the risk of suicide. Yet whatever larger failings may exist, the staff of social workers, addiction specialists and nurses who keep the hot line running — 24 hours a day, seven days a week — can count at least some victories by the end of each shift. Unique about this hot line, said Janet Kemp, the national suicide prevention coordinator with the department, is that now the counselors have medical information at their fingertips, which they use to connect vets with counseling near their homes. The model evolved from a new research program on suicide prevention paid for by the department. “For years people thought that asking questions about suicide put the thought in people’s mind, but now we know that’s not true,” said Dr. Kemp, who travels throughout the country training V.A. staff. The department is spending about $3 million to start and operate the hot line during its first year, said a spokesman, Daniel Ryan, and another $2.9 million on a mental health research center at the sprawling red-brick V.A. Medical Center in Canandaigua. Referring to the hot line’s relay model, Kerry Knox, the director of the new research center, said, “You don’t want them to fall through the cracks.” With Robert, for example — whose last name was not provided for confidentiality — Ms. Nosewicz gradually nudged him to agree to be taken to a hospital and to give his name and Social Security number so she could check his file and put him in contact with the department’s suicide prevention coordinator in his area. Meanwhile, Denise Slocum, a health assistant, relayed questions from the local police dispatcher. “The police are asking if you’re near an elementary school,” asked Ms. Nosewicz, who then nodded her head at Ms. Slocum. “No, no, no — no handcuffs,” Ms. Nosewicz reassured Robert. “You’re going to go to the hospital.” “Do you have a tissue to blow your nose? Then use your sleeve.” “When they come in, you put them on the phone with me, and I’ll tell them to treat you with respect.” Twenty minutes later, Ms. Slocum called the police again to confirm that Robert had been taken to a hospital. Ms. Nosewicz alerted the prevention coordinator. One is at each of the department’s 156 health centers. Robert’s name was added to a board near the doorway so that the staff could follow up to ensure a local counselor actually met with him. Of course, sometimes a crack is unavoidable. “He’s going to do it. He’s really going to do it,” said Terri Rose, a counselor who was working the noon-to-midnight shift. She was wiping her red-rimmed eyes. A caller from Texas, who said he was 65 and a helicopter gunner in Vietnam, said he had a suicide pact with his friend, but the friend had gone off and killed himself. Now he, too, was ready to die, saying he had even found a coffin for $150, said Ms. Rose, who is an Air Force veteran herself. The veteran hung up and had stopped answering her calls. Sometimes veterans have a lot of trouble asking for help, said Jacalyn O’Loughlin, a counselor. “They keep saying, ‘I’m sorry, I’m sorry, I’m sorry,’ ” Ms. O’Loughlin said. “Especially marines. They feel they’re weak if they reach out.” Mr. Ryan said about half the calls to the hot line — 1-800-273-TALK (8255) — were from veterans, split fairly evenly between Vietnam and Iraq. Family members and friends also frequently call. About 30 percent of the veterans are women. A couple of months ago, Ms. O’Loughlin said, a distraught woman called from Oregon who was driving to the woods and then threatened to “walk and walk and walk and never come back.” Ms. O’Loughlin rang the tiny silver bell on her desk to signal the health technician. The health tech checked the area code and phoned the closest Veterans Affairs health center. “And lo and behold, that suicide prevention coordinator knew her just by her first name,” Ms. O’Loughlin said. The tech called the police and the coordinator called the woman’s husband, getting the car’s make and model. Ms. O’Loughlin kept her on the line; when she hung up, Ms. O’Loughlin called her back. “This went on for hours,” she said. “I could hear her getting out of the car. I could hear the rustling from the leaves.” Meanwhile, the police and her husband were driving up and down roads. They spotted the car, dashed through the trees and found her. She had a bottle of pills in her hand but had not yet swallowed them. Sometimes, the victories are smaller but no less satisfying. That morning, Ms. Nosewicz spoke to a veteran whose house was destroyed by Hurricane Katrina; he had been relocated to a different state. “He called crying because he can’t find a job, saying ‘my teeth are so rotten and my mouth stinks,’ ” Ms. Nosewicz said. Dental referrals are not exactly part of the job description, but Ms. Nosewicz tried dental schools in his area until she found a school to do the work. “He was crying on the phone,” she recalled, “and said, ‘Thanks so much. Thanks so much.’ ” All in all not a bad day’s work, Ms. Nosewicz said, as she got ready to leave. “Three rescues, four consults and one set of teeth.” Resignation of VA Mental Health Official Sought Matthew Daly, Associated Press- 4/22/2008 WASHINGTON -- Two Democratic senators on Tuesday called for the chief mental health official of the Veterans Affairs Department to resign, saying he tried to cover up the rising number of veteran suicides. Sens. Daniel Akaka of Hawaii and Patty Murray of Washington state said Dr. Ira Katz, the VA's mental health director, withheld crucial information on the true suicide risk among veterans. "Dr. Katz's irresponsible actions have been a disservice to our veterans, and it is time for him to go," said Murray, a member of the Senate Veterans Affairs Committee. "The No. 1 priority of the VA should be caring for our veterans, not covering up the truth." Akaka, the committee's chairman, said in a letter to the VA that Katz's "personal conduct and professional judgment" had been called into question by his response to veteran suicides. Veterans, and the VA itself, "would be best served by his immediate resignation," Akaka said. A number of Democratic senators said they were appalled at e-mails showing Katz and other VA officials apparently trying to conceal the number of suicides by veterans. An e-mail message from Katz disclosed this week as part of a lawsuit that went to trial in San Francisco starts with "Shh!" and claims 12,000 veterans a year attempt suicide while under department treatment. "Is this something we should (carefully) address ourselves in some sort of release before someone stumbles on it?" the e-mail asks. A VA spokesman declined to comment Tuesday. Another e-mail said an average of 18 war veterans kill themselves each day and five of them are under VA care when they commit suicide. "It is completely outrageous that the federal agency charged with helping veterans would instead cover up the hard truth, that more and more Americans coming home after bravely fighting for their country are suffering from mental illnesses and in the most tragic circumstances, committing suicide," said Sen. Tom Harkin, D-Iowa. "Anyone at the VA who is involved in this cover-up should be removed immediately." Harkin, Murray and Sen. Russ Feingold, D-Wis., introduced legislation Tuesday calling on the VA to track how many veterans commit suicide each year. Currently, VA facilities record the number of suicides and attempted suicides in VA facilities _ but do not record how many veterans overall take their own lives. The agency, however, is reluctant to disclose specific numbers, veterans advocates complain. The new bill would require the VA to report to Congress within 180 days the number of veterans who have died by suicide since Jan. 1, 1997, and continue reports annually. Harkin's office said statistics provided earlier this year by the VA showed that 790 veterans under VA care attempted suicide in 2007. That figure is contradicted by the e-mail revealed this week. Two veterans groups last year filed the class-action lawsuit against a sprawling VA system that handled a record 838,000 claims last year. A government lawyer on Monday urged a judge to dismiss the lawsuit, saying the agency runs a "world class" medical care system. The pills worked in a novel way, by blocking pleasure centers in the brain that provide the feel-good response from smoking or eating. Now it seems the drugs may block pleasure too well, possibly raising the risk of depression and suicide. Margaret Bastian of suburban Rochester, N.Y., was among patients who reported problems with Chantix, a highly touted quit-smoking pill from Pfizer Inc. that has been linked to dozens of reports of suicides and hundreds of suicidal behaviors. ''I started to get severely depressed and just going down into that hole ... the one you can't crawl out of,'' said Bastian, whose doctor took her off Chantix after she swallowed too many sleeping pills and other medicines one night. Side effects also plague two other drugs: The makers of the new drugs insist they are safe, although perhaps not for everyone, such as people with a history of depression. Having to restrict the drugs' use would be a big setback because it would deprive the very people who need help the most, since addictions and depression often go hand-in-hand, doctors say. A bigger fear is that the whole approach may be in trouble. Researchers say blocking pleasure, especially the way the obesity drugs do, might take the fun out of many things, not just the harmful substances and behaviors these drugs target. It may be possible to improve the drugs so they act more precisely. Chantix targets a different pathway -- nicotine pleasure switches -- and in a different way than the obesity drugs, which aim at the same pathway that gives pot smokers the munchies. That is one reason many doctors are optimistic that any risks about Chantix will prove manageable. But doctors are no longer talking about so-called ''super pills'' for a host of addictions. ''It certainly diminishes my enthusiasm'' to see these side effects, said Mark Egli, co-leader of medicine development at the National Institute on Alcohol Abuse and Alcoholism. The buzz started four years ago, when studies showed rimonabant helped people shed weight and keep it off longer than previous pills had. It also was being tested for smoking cessation. The Associated Press and other media reported extensively on prospects for a pill that might tackle two big problems at once. Rimonabant won approval in Europe. But advisers to the U.S. Food and Drug Administration opposed it because of depression risks that became clearer with further study. Sanofi withdrew its U.S. application and said it hoped to resubmit after more research. But in a new study last month, 43 percent of people taking rimonabant developed psychiatric issues versus 28 percent of those on dummy pills. One rimonabant patient committed suicide and one in the placebo group tried to. Unlike previous studies, this one did not exclude people who had depression in the past. ''I felt it was important to do an 'all-comers' study'' to see how real-world patients might fare, said Cleveland Clinic's Dr. Steven Nissen, who led the work. Sanofi now tells doctors to avoid giving the drug to people with a history of depression, said a company vice president, Dr. Douglas Greene. ''We are at the cutting edge of being able to manage this risk,'' he said. Meanwhile, Merck had bad news from a study of its obesity drug, taranabant, which showed an increased risk of depression and other side effects among people taking medium and high doses. ''We're doing a lot to define this risk-benefit,'' including adding another year to all studies under way and going forward only with the lowest dose, said a Merck vice president, Dr. John Amatruda. Others were less optimistic. ''The door is closing'' on this approach, said Dr. James Stein, a University of Wisconsin-Madison cardiologist. If another study he is helping lead does not show benefit for rimonabant, ''this drug's already slim chances of approval will be even more jeopardized,'' he said. The situation is murkier with Chantix, which went on sale in the U.S. in 2006 and is sold as Champix in other countries. The drug binds to the same spots in the brain that nicotine does when people smoke, causing release of a ''feel-good'' chemical, dopamine. Taking it is supposed to keep any inhaled nicotine from giving the same buzz. In February, the FDA said a link between Chantix and psychiatric problems appears ''increasingly likely.'' Pfizer added warnings to the drug's label and said that although a link had not been proved, it could not be ruled out. But a Pfizer vice president, Dr. Ponni Subbiah, said nicotine withdrawal and even quitting smoking can cause mood swings and depression. It is hard to know ''what is causing what,'' she said. ''We know that smokers are at higher risk of suicide than non-smokers, and heavy smokers are at higher risk than lighter smokers.'' Some doctors agreed. ''Psychologically, just giving up this 'friend' that they've had many years in their life can be depressing,'' said Dr. Geoffrey Williams, co-director of the Greater Rochester Area Tobacco Cessation Center and a paid speaker for Pfizer. Jeanne Morrison, 63, of suburban of Louisville, Ky., looked forward to giving up cigarettes when she and a friend went on Chantix. The friend did well, but Morrison lasted only 10 days on it. ''I got so depressed, I didn't want to go anywhere. I didn't want to do anything, and I'm a very high-energy person. It was a depression like I've never experienced in my life,'' she said. She also had ''major, major nightmares. These would wake me up, and I would be absolutely shaking and sweating.'' Several doctors said such reactions are rare, and that most patients do well on Chantix. Morrison's doctor, psychiatrist Dr. Jesse Wright at the University of Louisville, said Chantix helped one of his schizophrenic patients, ''who smoked like a smokestack,'' without worsening his psychological symptoms. ''The risk-benefit ratio is still very much on the side of use of the medication,'' Williams said. ''The alternative, smoking, is extremely highly risky.'' 15% Say They Have Driven Drunk Kevin Freking, Associated Press- 4/23/2008 WASHINGTON — The upper Midwest has the worst drunken-driving rates in the country, according to a government study that says 15 percent of adult drivers nationally reported driving under the influence of alcohol. Wisconsin led the way. The federal government estimates more than a quarter of the state's adult drivers had driven under the influence. Illinois ranked 19th in the survey at 16.5 percent. Utah had the lowest incidence of drunken driving. It was the only state where fewer than 10 percent of adult motorists reported driving under the influence. Following closely behind were West Virginia, Arkansas, Kentucky and North Carolina, which all had drunken-driving rates for the prior year of less than 11 percent. The report on drunken driving relies on data obtained from the National Survey on Drug Use and Health. The survey asked 127,283 adults in 2004, 2005 and 2006 whether they had driven under the influence in the past year. Health experts say the report supports other surveys showing that residents in Northern states are more likely to engage in heavy alcohol consumption. "It's not surprising, but it means that these jurisdictions should take this data and think about how they approach public education campaigns and enforcement campaigns," said Dr. H. Westley Clark of the Substance Abuse and Mental Health Services Administration. Eric Goplerud, research professor at George Washington University Medical Center, said that religious affiliations in the Southeast often strongly discourage drinking, but that doesn't occur so much in the upper Midwest. Clark said states with the lowest rates shouldn't take comfort in the data. "Even in Utah, which reported the nation's lowest rate, nearly 1 in 10 drivers report driving under the influence of alcohol within the past year," Clark said. New Look at Kids' Divorce Trauma Bonnie Rubin, Chicago Tribune- 4/23/2008 For years, social scientists have believed that children of divorce have more behavior problems than kids growing up in two-parent homes. But the impact may not be as damaging as previously believed, according to new research to be released Friday. Instead of comparing these youngsters to those with intact families—the usual methodology—a more accurate assessment would be to evaluate them before and after the divorce, said Alan Li of the RAND Corporation. Many of the problems could be a result of pre-existing characteristics that would be a factor in emotional and behavioral issues even if parents had remained married, said Li, who will present his findings this weekend at the annual conference of the Council on Contemporary Families at the University of Illinois at Chicago. "Many studies end up comparing apples and oranges," Li said. "Personality, parenting strategies and detailed aspects of a person's biography all affect children, but researchers haven't been able to measure many of these constructs." In addition, the report said, many earlier studies failed to take into account differences among families, such as parents' socioeconomic status and education, which can affect a youngster's well-being, whether a couple stay together or not. When these variables are added to the mix, the psychological fallout is negligible, said Li, associate director of the Population Research Center for the Santa Monica-based non-profit. He drew upon a national sample of about 6,330 children ages 4 to 15, whose mothers were surveyed repeatedly from 1979 to 2002. Mothers filled out a 28-item checklist on whether their children engaged in conduct such as cheating, crying, arguing and breaking things. On average, less than half showed a one-item increase after divorce, which is not statistically significant. Stephanie Coontz, a historian who has written extensively on marriage, called the findings provocative, adding that they could reframe the national debate on divorce. The findings, suggest that staying together at all costs may not be the best solution, said Coontz, the family council's director of research. "It lets people know that there are variable outcomes . . . which will come as a relief to many people who went through divorce and raised healthy children," she said. "But there are others who will object to the idea. . . . They will see it as giving people permission to divorce." Robert Emery, a professor of psychology at the University of Virginia, takes issue with the conclusion. While Li may not have found increased negative behavior, less quantifiable is the hurt that can reverberate across a life span, he said. "For example, graduation and weddings can be turned into anxiety-ridden events for children whose parents are divorced," Emery wrote in a response to Li's findings. Closer to home, most experts agreed that it isn't the split but the discord attached to it that is so harmful. In eight years as a mediator in the domestic relations division of Cook County Circuit Court, Jeff Ginsburg has seen it all. "It never ceases to amaze me when divorcing parents cannot get past their anger with each other to decide what is in the best interest of their children," he said. Two periods of conflict surround dissolution, said Ginsburg, who is both a social worker and an attorney. "During the divorce itself, if parents litigate their case, deplete their assets and spend several years in court, what we find is that parents will almost never be able to end the high level of conflict," he said. Post-decree, minimizing conflict is still essential, he said. Kids can get through the process if parents are able to develop and maintain "a cordial or businesslike co-parenting relationship." Tim Yehl was 7 and growing up in Des Plaines when his parents ended their marriage. Now 40 and a public relations executive in Washington, he recalled it as a sad and confusing time. "All those traumatic feelings were there," Yehl said. "But I had parents who helped walk me through those feelings so I could reconcile them, grieve the divorce and move on." Diagnosis: Female Kathryn Harrison, New York Times Book Review- 4/27/2008 Mad, Bad and Sad: Women and the Mind Doctors. By Lisa Appignanesi. 535 pp. W. W. Norton & Company. $29.95. Back when Zelda Fitzgerald, her skirts wet from diving into public fountains, was accelerating from madcap toward outright madness, a Wharton School economist named George Taylor made the seemingly fey observation that hemlines rose and fell with the stock market, proposing a causal connection between two presumably separate spheres of human enterprise. Fashion, as the now familiar “hemline index” suggested, is socially determined. With prosperity come optimism and tolerance for risk; women are emboldened to show off a more daring length of leg. But what of more empirical, utilitarian domains? Surely doctors hypothesize independently of whatever forces drive style. Take, for example, the diagnosis and treatment of mental illness. Most of us trust psychiatry to remain immune to fads. And it does, doesn’t it? One of the consistently fascinating and disturbing aspects of “Mad, Bad and Sad: Women and the Mind Doctors” is Lisa Appignanesi’s assiduous tracking of the modishness of what might be mistaken for a sui generis discipline. Of course, as anyone who has visited a psychiatric hospital — or ridden the subway — can attest, crazy is what we call people who refuse to conform to accepted norms of behavior. And the definition of nonconformity must change in step with styles of conforming. “Mad, Bad and Sad” is, Appignanesi tells her readers, not only “the story of madness, badness and sadness and the ways in which we have understood them over the last 200 years,” but also a survey of the mad, bad and sad themselves, the particular women, including Zelda Fitzgerald, Lucia Joyce, Virginia Woolf and many less famous patients, who suffered “frenzies, possessions, mania, melancholy, nerves, delusions, aberrant acts, dramatic tics, passionate loves and hates, sex, visual and auditory hallucinations, fears, phobias, fantasies, disturbances of sleep, dissociations, communion with spirits and imaginary friends, addictions, self-harm, self-starvation, depression” and so on. Phew. A list like this makes a girl grateful that Freud even bothered to ask what such desperate, deluded creatures might want. No wonder the 19th century couldn’t build enough asylums to house them. It seems that as soon as society relinquished witchcraft as the crime for which to punish an overtly liberated woman, it settled on madness as the reason to incarcerate her. As Appignanesi observes, “Patients could well find themselves the victims of a doctor’s prejudice about what kind of behavior constituted sanity: this could all too easily work against women who didn’t conform to the time’s norms of sexual behavior or living habits.” That diagnoses conceived by male doctors would be subject to men’s changeable views of women — romantic, patronizing, idealistic, misogynistic: the choices are limited only by the imagination — comes as no surprise; it’s the meticulous and exhaustive account of these theories offered in “Mad, Bad and Sad” that is sobering. Victorian women who weren’t locked up for falling victim to lypemania (melancholy), monomania, homicidal monomania or “moral insanity” were at risk of neurasthenia, a “mirror image of rebellion” in which their “nervous depletion” was explained as the result of their “incursion into the masculine sphere of intellectual labor,” a strain that constitutions formed for tender sentiment couldn’t be expected to support. And then came hysteria, which “best expresses women’s distress at the clashing demands and no longer tenable restrictions placed on women in the fin de siècle.” If male doctors conspired to define madness, responding to behaviors that flouted the social conventions of their culture, female patients, in the attempt to understand themselves and their context, and maybe even to create or bolster identity, colluded with those same doctors to satisfy the changing definitions of madness. “Often enough,” Appignanesi notes, “extreme expressions of the culture’s malaise, symptoms and disorders mirrored the time’s order.” Anorexia, she writes, “is usually an illness of plenty not of famine, as depression is one of times of peace and prosperity, not of war.” Having wept, raved, trembled and hallucinated our way into the 21st century, when “the sum of information available in any given minute is larger than it has ever been in history,” we’ve conceived “a condition in which attention is at a deficit.” Among all the doctors whose diagnoses and treatments have proved provocative, none have enjoyed the tenaciously divisive stature of Sigmund Freud. Appignanesi, who (with John Forrester) documented the early years of the psychoanalytic movement in “Freud’s Women,” examines the new order ushered in by Freud’s delving “with a radical coolness which had no truck with conventional morality” into “something mysterious and perhaps threatening, constantly in need of investigation, attention or control.” That “something” was, of course, sex. To her credit, Appignanesi herself assesses Freud with a kind of radical coolness. She neither monumentalizes his influence nor engages in a perfunctory, reflexive attack on his pioneering work. Instead she tidily summarizes how Freud, having lifted the lid of consciousness off the tenebrous realm of unconscious desires, hostilities, conflicts and Oedipal struggles, begat countless intellectual heirs — his child and analysand Anna Freud, as well as Melanie Klein, Karen Horney and others — who leapt into the postwar baby boom and focused on women “in relation to their biological destiny — menstruation, pregnancy, menopause.” These female pioneers ushered in a cult of childhood and its inevitable corollary, the demonization of mothers, at whose feet piled up responsibilities for all manner of diseases and dysfunctions, from stuttering to schizophrenia, now understood to be neurochemical and decidedly outside the influence of fads. While “Mad, Bad and Sad” echoes and enlarges upon Elaine Showalter’s book “The Female Malady: Women, Madness, and English Culture, 1830-1980,” Showalter’s perspective is more exclusively feminist, arguing that psychiatry as practiced on women is a history of their subjugation and control by men. But as Appignanesi makes clear, women have had no little role in creating and fulfilling the definitions of their madness. The spreading and treatment-resistant phenomena of anorexia and bulimia are owned largely by women, who account for some 90 percent of patients with eating disorders and who are counseled and treated by an industry of specialists whose attempts to raise consciousness about these diseases have helped also to spread them, in much the same way that neurasthenia so captured the Victorian imagination. It would be hard to imagine a mental illness that better evinces the slippery interplay among fashion, delusion, diagnosis and treatment than anorexia, which announces itself with the appearance of following rather than defying social directives and which women embrace, as they did neurasthenia, as a mode of femininity, in this case to be slim rather than morbidly sensitive and enervated. Only after the obsessive pursuit of emaciation betrays a subversive refusal to play by the rules of normality does anorexia reveal itself as flagrantly unstylish, an indictment of the very norms it pretended to satisfy. “Anorectics perennially sabotage therapy,” Appignanesi writes, because it isn’t only food they refuse but “any form of intrusion,” even — perhaps especially — that of a mind doctor intent on curing them. Michael White, 59, Dies; Used Stories as Therapy Jeremy Pearce, New York Times- 4/28/2008 Michael White, a social worker and family therapist who developed an innovative and highly practical technique using storytelling to help patients of all ages deal with childhood traumas, died on April 4 in San Diego. He was 59. The cause was a heart attack, said a spokeswoman from the Dulwich Centre, a counseling service in Adelaide, Australia, where Mr. White had practiced family therapy since the early 1980s. With a colleague, David Epston, Mr. White explored the power of shaping personal accounts and memories in facing the lingering effects of childhood inadequacies and other obstacles in patients’ lives. Their technique was explained in an influential 1990 book, “Narrative Means to Therapeutic Ends,” and has since become known as narrative therapy. The technique is based in part on having a patient externalize a condition or problem — like obesity, loss of a parent or resentment of a sibling — and come up with stories and metaphors to re-evaluate the situation, usually from a more positive perspective. Narrative therapy has been used successfully to help bed-wetting children distance themselves from shame and anxiety, so they can consider their condition more objectively and not necessarily as a permanent character flaw. Some practitioners encourage patients to write stories, letters, essays or poems and to recall actual events in which they vanquished a concern or responded to a family member with cathartic satisfaction. A practitioner of narrative therapy, Dr. Gene Combs, an associate professor of psychiatry and family medicine at Loyola University in Chicago, said Mr. White emphasized the need to “elevate the person you’re working with, instead of elevating the therapist,” so that discussions with patients, alone or in family groups, can ensure that individuals are not viewed as “generic carriers of problems, or only as pathologies and not people.” The eventual goal of the technique is to help a patient recognize personal strengths and supportive relationships that can aid in surmounting a given problem, leading to what Dr. Combs termed the “preferred stories” of success and achievement in the patient’s life. Michael Kingsley White was born in Adelaide. He worked briefly as a probation and welfare officer before earning an undergraduate degree in social work from the University of South Australia in 1979. He then became a psychiatric social worker at Adelaide Children’s Hospital before starting his private practice at the Dulwich Centre. He further refined his ideas in a book published last year, “Maps of Narrative Practice.” Mr. White often traveled abroad to present case histories and refinements of narrative theory and was on a similar journey in San Diego when he died. Although narrative therapy has had relevance in treating anorexia, school-related anxiety and problems common in children and young adults, its uses continue to broaden. Beginning in the 1990s, Mr. White applied it to Aboriginal communities in New South Wales, and found that storytelling could be an incisive tool in helping tribesmen come to terms with dispossession and forced relocation from their ancestral lands. |