Re: ADHD Support Groups - Front Org. For Drug Companies??

Discussion in 'Health and medical' started by Jan, Oct 5, 2003.

  1. Jan

    Jan Guest

    Is Your ADHD Support Group a Front
    Organization for the Pharmaceutical Industry?
    By Richard DeGrandpre, Ph.D.

    On May 18, 1999, the New York Times reported that “social phobia ranks today
    as the third most prevalent psychiatric disorder in the United
    States……….affecting an estimated 19 million Americans, according to the
    Anxiety Disorders Association of America. Many are to bashful even to talk to
    therapists.” In the same week, the Boston Globe reported that
    “Epidemiological studies have found that acute social anxiety is the third
    most common psychiatric disorder in the United States………. affecting up to
    13 percent of Americans. Jerilyn Ross, president of the Anxiety Disorders
    Association of America……she hopes a publicity blitz planned
    by………..SmithKline Beecham will raise awareness of social anxiety disorder
    and lead more people to seek help, which could include psychotherapy instead of
    drugs.” Why were the Boston Globe and the New York Times both writing about
    “social phobia disorder” in the same week, and why would a drug company
    spend its money to “raise awareness” of a mental-health disorder? The
    answer: the FDA had just approved a drug for the treatment of social phobia. As
    the Boston Globe put it, SmithKline Beecham makes the drug Paxil, which was
    “the first drug approved by the FDA specifically for treating social anxiety

    Notice how, in the media reports just quoted, the drug company isn’t claiming
    that the social phobia “disorder” affects millions of people. Rather,
    it’s an organization with a professional-sounding name, and one that appears
    to have nothing to do with the pharmaceutical industry: the Anxiety Disorders
    Association of America. If these claims were presented by a drug company they
    would likely appear to the public and news organizations as self-serving and
    biased. If, however, they are presented to the public by an organization that
    seems only to have the health and welfare of the public in mind, they seem
    objective and credible. This is certainly what drug-company executives believe,
    which is why they go great lengths to create and influence what are essentially
    front organizations for the pharmaceutical industry.

    Consider the case at hand. The Anxiety Disorders Association of America, ADAA,
    receives so much funding and influence from the industry that it is misleading
    to suggest that they are not an intricate part of it. The Boston Globe and the
    New York Times both received much of their information for the above reports
    from an ADAA press release, treating it in just the manner that the industry
    would want: as objective information from an independent organization. As a
    reporter for the Chicago Sun-Times makes clear, however, the ADAA is neither
    neutral nor objective: “I recently received a press release from the Anxiety
    Disorders Association of America. It said if your child is afraid of going back
    to school, maybe it’s not normal, maybe your child needs drugs. The release
    says three children in every class have an anxiety disorder. The solution?
    Well, enclosed are details for a drug company-sponsored workshop showing the
    wonders of Paxil and similar drugs.”

    With funding coming directly from Paxil’s maker, ADAA did much more than just
    send out press releases. The summer of ‘99 also saw a barrage of advertising
    by ADAA, which asked people to imagine being “allergic to people.” A poster
    they used had a picture of a young man staring despondently into a coffee cup
    while a happy “social” couple sat at the other end of the table. The
    implication is made clear by the caption, which reads: “Over 10 million
    Americans suffer from social anxiety disorder………the good news is that
    this disorder is treatable.” In addition to a toll free number and a website
    listed, the poster indicates support, not from a drug company, as it should,
    but from three nonprofit groups: the American Psychiatric Association, the
    Anxiety Disorders Association of America and Freedom From Fear, which together
    form what is called the Social Anxiety Disorder Coalition. Like ADAA, the other
    two organizations also receive substantial funding from the pharmaceutical
    industry. “Funding for their public awareness campaign comes from a far less
    visible partner: SmithKline Beecham, the pharmaceutical giant whose flagship
    antidepressant is Paxil,” writes Michelle Cottle in The New Republic (August
    2, 1999.) Cottle also notes that the APA’s social phobia website is paid for
    by SmithKline, as is ADAA’s, and that, on July 19, 1999, ADAA would hold a
    press conference to announce the findings of a study, paid for by various drug
    makers, suggesting a huge impact of anxiety disorders on America’s
    productivity. Behind all this is ADAA’s corporate advisory board, which is
    made up of representatives from different drug companies.

    The ties between drug companies and organizations like ADAA do not end with
    public ads and education. As front organizations, they also direct the public
    toward support groups that share their two-pronged bias, that the disorder in
    question is really a legitimate medical disorder in need of medical treatment,
    and that this treatment will most likely involve psychiatric drugs. The support
    group is in many ways the most important step in the process of getting people
    on the latest pharmaceuticals, since it is the support group that will come
    into direct contact with the individual or parent. At the ADAA website
    (, for example, one finds the following description under
    “Self-Help Support Groups”: Self-help and support groups for anxiety
    disorders are a way of empowering people to help themselves, and others, on the
    path to recovery. Participation in a self-help group can end the painful
    isolation of suffering alone with a disorder that is disruptive and
    debilitating for the individual and those people around him/her. An effective
    group will help members achieve recovery through mutual support as well as
    provide them with updated information about causes and treatment, eliminating
    some of the myths about anxiety disorders. The ADAA Self-Help Support Group
    Network is available in nearly all states and various countries around the
    world. The list of support groups is provided as a service of the
    ADAA……….The ADAA is constantly listing new groups and updating
    information about current groups. Please contact-- ADAA at 301.231.9350, or by
    email at [email protected] for additional information about self-help support
    groups, including: How to start a group of your own; Adding a new group to the
    ADAA network; Notification of any changes in a group’s status or contact
    information. What the ADAA website fails to disclose is that they are there
    first and foremost to serve the interests, not of the public, but of the
    pharmaceutical industry, and that the support groups they are recommending are
    likely to be doing this as well. Consider the case of CHADD.

    CH.A.D.D., which somehow translates into “Children and Adults with
    Attention-Deficit/Hyperactivity Disorder,” asserts on its website
    ( the following: With over 22,000 members in 225 affiliates
    nationwide, CHADD is the nation’s leading non-profit organization serving
    individuals with Attention-Deficit/Hyperactivity Disorder (AD/HD). Through
    collaborative leadership, advocacy, research, education and support, CHADD
    provides science-based, evidence-based information about AD/HD to parents,
    educators, professionals, the media and the general public.

    Clearly CHADD is a powerful organization, and one that is likely to attract
    many if not most American parents confronting a possible diagnosis of
    “ADHD” in their child. What is not clear, especially to those who stray
    into the CHADD web of “support”, is what the organization is really about.
    Founded in 1987, CHADD, which estimates that 10 to 20 percent of school
    children have ADHD, organizes speaking events, publishes a monthly newsletter
    (Chadderbox) and a glossy magazine (Attention!), and operates an impressive
    website. CHADD claims that “No matter how many sources of information are out
    there, CHADD is the one you can trust.”

    This “trust” depends greatly, however, on what you want from CHADD. If you
    want an organization that has longstanding ties with pharmaceutical interests,
    and that selectively recruits only scientists proven to be pro-drug to their
    advisory board, then you can trust CHADD; if you want an organization that
    unquestionably embraces ADHD as an inherited disease for which parenting and
    culture play no role, either as causes or solutions, then you can trust CHADD;
    and if you want an organization that acts as a powerful lobby for the growing
    population of ADHD parents and children, then you can trust CHADD. If however,
    you want an honest organization that acknowledges its pro-drug and pro-disease
    agenda to its prospective (and current) members, then you cannot trust CHADD;
    and if you want an organization that carefully considers, or even considers at
    all, the findings of scientific and epidemiological studies showing that ADHD
    has strong social and cultural inputs, that psychostimulants may very will
    cause brain damage, and that psychostimulant drugs work more for parents and
    teachers than they do for children, then again you cannot trust CHADD.

    In October of 1995, the US public television network, PBS, aired a critical
    “Merrow Report” on CHADD, ADHD, and Ritalin called “Attention Deficit
    Disorder: A Dubious Diagnosis?”, anchored by John Merrow. The program
    documented in detail the deception used by the organization, including the
    concealment of its ties to the drug industry. Starting in 1988, more than $1
    million has poured into the organization from the maker of Ritalin (then
    Ciba-Geigy, now Novartis); CHADD received $748,000 for Ciba/Novartis just in
    the years 1991-1994. The Merrow Report documented this and showed how, in turn,
    CHADD did the dirty work of the drug company. They do this by policing media
    coverage on “ADHD” by propping themselves up as “the” independent,
    national support organization for “ADHD”and by lobbying the US Government,
    including the Department of Education, on behalf of Ciba/Novartis. In one
    instance, CHADD worked vigorously to have Ritalin reclassified by the US Drug
    Enforcement Administration (DEA) as a less dangerous drug. As a Schedule II
    drug, Ritalin is considered a potentially addictive drug, with restrictions
    placed on its annual production quota and with certain states monitoring who
    and how much the drug is prescribed. Getting it reclassified as a Schedule III
    drug would mean that it could be touted as being benign and could be obtained
    more easily. It would also mean that prescription refills could simply be
    called into the pharmacy, rather than requiring a new prescription each time.

    When a senior person at the US Department of Education was interviewed for this
    program by John Merrow, he was asked whether he knew CHADD received
    considerable funding from Ciba/Novartis, to which he replied that he had no
    awareness of such monies. By that time CHADD had obtained a several hundred
    thousand dollar grant from the Department to make a video about ADHD, and was
    also helping to author materials for the Department of Education. Yet the
    Department of Education had no idea of CHADD’s significant ties with the
    industry. The Department’s spokesperson was then asked if he thought he had
    been mislead by CHADD, and that the organization was doing the work of the drug
    company. Indeed he did.

    In part because of the Merrow Report, the DEA decided against softening the
    classification of Ritalin. Instead, it published a report that was highly
    critical of CHADD. Mary Eberstadt summarizes the report in her 1999 Policy
    Review article “Why Ritalin Rules: Backed by scores of footnotes and well
    over a 100 sources in the medical literature, this report amounted to a public
    excoriation of CHADD’s efforts and meticulous description, alarming for those
    who have read it, of the realities of Ritalin use and abuse. ‘Most of the
    ADHD literature prepared for public consumption and available to parents,’
    the DEA charged, ‘does not address the abuse liability or actual abuse of
    methylphenidate [Ritalin]. Instead, methylphenidate is routinely portrayed as a
    benign, mild stimulant that is not associated with abuse or serious effects. In
    reality, however, there is an abundance of scientific literature which
    indicates that methylphenidate shares the same abuse potential as other
    Schedule II stimulants.’ Ciba-Geigy, the DEA observed, ‘stands to benefit
    from a change in scheduling of methylphenidate.’ It further observed
    that……..‘abuse data indicate a growing problem among school-age
    children,’ that “adhd adults have a high incidence of substance
    disorders,” and that “with three to five percent of today’s youth being
    administered methylphenidate on a chronic basis, these issues are of great
    concern.” Eberstadt also describes how the DEA was contacted by the
    International Narcotics Control Board (INCB) of the United Nations, which
    expressed concern to them about the financial ties between CHADD and
    Ciba/Novartis. According to the DEA, the INCB charged CHADD with being a
    vehicle for marketing a controlled substance directly to the public, which is a
    isolation of the Controlled Substances Act of 1971, an international statute to
    which all signing countries, including the US, are bound.

    Despite the dubious nature of CHADD, the organization continues to have
    enormous power. In 1998, for example, the US National Institutes of Health
    (NIH) convened a Consensus Conference on whether “ADHD” was a legitimate
    disorder and whether drugs like Ritalin were effective in treating it, whatever
    it was. The Consensus Conference consists of a panel of scientists who, after
    hearing testimony from invited “experts” on the subject, assemble a report
    that is then published by the NIH. When the Conference was organized, CHADD
    played a significant role in deciding who would and would not be on the panel.
    As a result, the report was strongly biased in favor of the disease model of
    childhood, as well as the use of drugs to “cure” it. With the use of
    Ritalin and other stimulant drugs rising sharply in the 1990’s, people often
    wonder if, or believe that, drug companies are conspiring on a continual basis
    to put more and more kids on Ritalin and other drugs. The actual truth is a bit
    more complex than this. As the example of CHADD illustrates, as well as the
    case of “social phobia disorder,” drug companies have a more nuanced method
    of promoting their interests, which pay off in big dividends long after the
    money has been spent. Drug companies spend money in a targeted fashion, early
    on, planting seeds that will grow into an institutionalization of the
    “problem” and the “treatment” that they are so anxious to sell.
    Specifically, drug companies realize that they do not really need to push their
    drugs directly, knowing that once the so-called medical disorder--“ADHD” or
    “ADD”--is treated as a real medical disorder or disease, drug sales will

    As psychiatrist and historian David Healy remarks in his book, The
    Anti-Depressant Era, “When we stop by the pharmacy to pick up our Prozac, are
    we simply buying a drug? Or are we buying into a disease as well? Drug
    companies obviously make drugs, but less obviously they make views of
    illnesses.” In an early example of this, Healy describes how, in the
    1960’s, the drug company Merck, maker of the antidepressant amitriptyline,
    marketed the idea of depression by buying and distributing 50,000 copies of a
    book that encouraged the “recognition” and “treatment” of depression in
    medical settings. A more recent example is a book on obsessive-compulsiveness
    by psychiatrist Judith Rapoport called The Boy Who Couldn’t Stop Washing. The
    book was a strong seller and, as Healy points out, Rapoport was featured on
    various television shows, essentially selling the “disorder.” Rapoport, who
    was also chief of the US National Institute on Mental Health’s Child
    Psychiatry Branch, has strong ties with the drug industry. As Peter Breggin,
    M.D. points out in Talking Back to Prozac, Rapoport was receiving, via a
    private organization called The Foundation for Advanced Education in the
    Sciences, considerable funds from at least two drug companies, Eli Lilly and
    Ciba/Novartis. The method of the pharmaceutical industry madness, David Healy
    suggests, is now clear: a relatively rare psychological problem is known to
    exist (such as depression, social phobia or hyperactivity), a drug is
    “discovered” to have an effect on the problem, the problem is defined as a
    pervasive and well-defined disorder, and from that moment on, the prevalence of
    the problem and the use of the drug expand exponentially. Two examples: the
    rate of depression in the 1950’s was estimated at about 50 million, whereas
    today it is estimated at 100,000 per million; in 1975, 150,000 American
    children were said to be “ADD” (or “ADHD”), whereas today it is
    estimated at about eight million children.

    Drug companies sell psychiatric drugs by promoting the “awareness” of
    so-called mental diseases. Thus, when looking at CHADD and other support-group
    organizations, the first thing to notice is not how the pharmaceutical drugs
    are being pushed, but rather how the disorder, “ADHD,” is being sold. Few
    parents realize what exactly they are buying into when they accept a diagnosis
    of “ADD” or “ADHD”; nor do they realize that this is what CHADD-like
    organizations are asking them to do. What is obvious is that the labels of
    “ADD” and “ADHD” are applied to a diverse group of children who are
    viewed as having problems with attention, hyperactivity, and/or impulsivity (or
    are showing poor academic performance.) The label means much more, however, as
    is shown in casual statements like “my child has ADHD.” Here the label goes
    from being a loose description to a hard explanation, suggesting that
    “ADHD” is a physical thing--a problem existing within the child--that is
    the cause of the behavioral or cognitive problems. This has the effect in turn
    of isolating the problem within the child--it’s biological and thus a medical
    problem--setting the stage for the pharmaceutical solution. To be sure, this is
    exactly what organizations like CHADD mean by “ADHD,” arguing as they do
    that the problem is physiological one that can be treated but not cured.
    Notice, however, that there are no medical tests, and there is no proof there
    is anything biologically wrong with the child. All that exists are the
    so-called “symptoms,” which are as likely to be symptoms caused by the
    world of the child as they are evidence of a problem existing with his or her
    brain. Indeed, how else can we explain relative to earlier generations, why so
    many children are viewed today as being either impulsive and inattentive?

    All this boils down to the following: If you’re a parent wanting
    unconditional and uncritical support of your choice to give Ritalin or other
    drugs to your child, then a group like CHADD may be right for you. And if you
    live in the United Kingdom rather than in the United States, all you need to do
    is look for the “ADD” or “ADHD” label in the name of the organization,
    as, for example, in ADDERS, ADDISS, LADDERS, ADDCONTACT, or ADDNET. Unlike UK
    organizations like Stimulants Are Not The Answer (, OVERLOAD
    or Successful Learning, these organizations embrace the “ADD” or “ADHD”
    diagnosis. In doing so they lock themselves within the assumption that
    “ADHD” is a thing located inside the body, like a disease--a medical
    disorder--rather than realizing and acknowledging that it is really a diagnosis
    pushed by the medical and pharmaceutical industries as a means to an unjust
    economic end, the selling of powerful stimulant drugs. As such these
    organizations are best viewed as part of the institutionalization of the
    medical model, whether they know it or not, grown out from root organizations
    like CHADD, the seeds of which were planted by the pharmaceutical industry.

    If, on the other hand, you are someone who’s concerned with the future of
    your child (or grandchild), knowing that a quick-fix drug solution only masks
    the problem, then “ADD” support groups may not be for you. Trust not in
    “ADD” labels and organizations but rather in the belief that all children
    have the potential to live well-adjusted lives.

    Richard DeGrandpre, Ph.D., is a psychologist and independent science writer and
    has been published in a great variety of both professional and popular
    publications, including American Psychologist, The Sciences, Common Knowledge,
    Psychology Today, Cerebrum, and Adbusters. He is the author of RitalinNation:
    Rapid-Culture and the Transformation of Human Consciousness and Digitopia: The
    Look of The New Digital You. He is an Associate Editor of AdBusters and resides
    in Vancouver, British Columbia.

    Other articles by Richard DeGrandpre at

    Recommended website

    Permission to post this article was given by Richard DeGrandpre