A Vanishing Diagnosis?

A Powerful Identity, a Vanishing Diagnosis

From The New York Times

By CLAUDIA WALLIS
Published: November 2, 2009

It is one of the most intriguing labels in psychiatry. Children with Asperger’s syndrome, a mild form of autism, are socially awkward and often physically clumsy, but many are verbal prodigies, speaking in complex sentences at early ages, reading newspapers fluently by age 5 or 6 and acquiring expertise in some preferred topic — stegosaurs, clipper ships, Interstate highways — that will astonish adults and bore their playmates to tears.

In recent years, this once obscure diagnosis, given to more than four times as many boys as girls, has become increasingly common.

Much of the growing prevalence of autism, which now affects about 1 percent of American children, according to federal data, can be attributed to Asperger’s and other mild forms of the disorder. And Asperger’s has exploded into popular culture through books and films depicting it as the realm of brilliant nerds and savantlike geniuses.

But no sooner has Asperger consciousness awakened than the disorder seems headed for psychiatric obsolescence. Though it became an official part of the medical lexicon only in 1994, the experts who are revising psychiatry’s diagnostic manual have proposed to eliminate it from the new edition, due out in 2012.

If these experts have their way, Asperger’s syndrome and another mild form of autism, pervasive developmental disorder not otherwise specified (P.D.D.-N.O.S. for short), will be folded into a single broad diagnosis, autism spectrum disorder — a category that encompasses autism’s entire range, or spectrum, from high-functioning to profoundly disabling.

“Nobody has been able to show consistent differences between what clinicians diagnose as Asperger’s syndrome and what they diagnose as mild autistic disorder,” said Catherine Lord, director of the Autism and Communication Disorders Centers at the University of Michigan, one of 13 members of a group evaluating autism and other neurodevelopmental disorders for the manual.

“Asperger’s means a lot of different things to different people,” Dr. Lord said. “It’s confusing and not terribly useful.”

Taking Asperger’s out of the manual, known as D.S.M.-V for the fifth edition of the Diagnostic and Statistical Manual of Mental Disorders, does not mean the term will disappear. “We don’t want to say that no one can ever use this word,” Dr. Lord said, adding: “It’s not an evidence-based term. It may be something people would like to use to describe how they see themselves fitting into the spectrum.”

But the change, if approved by the manual’s editors and consultants, is likely to be controversial. The Asperger’s diagnosis is used by health insurers, researchers, state agencies and schools — not to mention people with the disorder, many of whom proudly call themselves Aspies.

Some experts worry that the loss of the label will inhibit mildly affected people from being assessed for autism. “The general public has either a neutral or fairly positive view of the term Asperger’s syndrome,” said Tony Attwood, a psychologist based in Australia who wrote “The Complete Guide to Asperger’s Syndrome” (Jessica Kingsley Publishers, 2006). But if people are told they should be evaluated for autism, he went on, “they will say: ‘No, no, no. I can talk. I have a friend. What a ridiculous suggestion!’ So we will miss the opportunity to assess people.”

The proposed changes to the autism category are part of a bigger overhaul that will largely replace the old “you have it or you don’t” model of mental illness with a more modern view — that psychiatric disorders should be seen as a continuum, with many degrees of severity. The goal is to develop “severity measures within each diagnosis,” said Dr. Darrel A. Regier, research director at the American Psychiatric Association and vice chairman of the diagnostic manual’s task force.

Another broad change is to better recognize that psychiatric patients often have many health problems affecting mind and body and that clinicians need to evaluate and treat the whole patient.

Historically, Dr. Regier said, the diagnostic manual was used to sort hospital patients based on what was judged to be their most serious problem. A patient with a primary diagnosis of major depression would not be evaluated for anxiety, for example, even though the two disorders often go hand in hand.

Similarly, a child with the autism label could not also have a diagnosis of attention deficit hyperactivity disorder, because attention problems are considered secondary to the autism. Thus, they might go untreated, or the treatment would not be covered by insurance.

The new edition, by contrast, will list not only the core issues that characterize a given diagnosis but also an array of other health problems that commonly accompany the disorder. For autism, this would most likely include anxiety, attention disorders, gastrointestinal problems, seizures and sensory differences like extreme sensitivity to noise.

Parents and advocates have been clamoring for an approach that addresses the multiple health problems that plague many children with autism. “Our kids will do much better if medical conditions like gut issues or allergies are treated,” said Lee Grossman, president of the Autism Society of America, a leading advocacy group.

The new diagnostic approach addresses another source of confusion: the current labels may change over time. “A child can look like they have P.D.D.-N.O.S., then Asperger’s, then back to autism,” Dr. Lord said. The inconsistent use of these labels has been a problem for researchers recruiting subjects for studies of autism spectrum disorder.

And it can be a problem for people seeking help. In some states, California and Texas, for example, people with traditional autistic disorder qualify for state services, while those with Asperger’s and pervasive developmental disorder do not.

A big challenge for the diagnostic manual team working on autism is how to measure severity in a condition that often causes a very uneven profile of abilities and disabilities. Mr. Grossman gives the example of a woman who serves on an advisory panel to his organization. She is nonverbal and depends on an electronic device to communicate, is prone to self-injury and relies on a personal aide. And yet “she’s absolutely brilliant, she runs a newsletter, and she’s up on all the science,” he said, adding, “Where would somebody like that come out on the rating scale?”

Recent books by people with Asperger’s give insights into the workings of some oddly beautiful minds. In “Embracing the Wide Sky” (Free Press, 2009), Daniel Tammet, a shy British math and linguistic savant, tells how he was able to learn enough Icelandic in a week to manage a television interview and how he could recite the value of pi to 22,514 decimal places by envisioning the digits “as a rolling numerical panorama” of colors, shapes and textures.

PERCEPTIONS The drawings of Daniel Tammet, above, who wrote the 2007 book “Born on a Blue Day,” about living with autism, show how he visualizes some numbers.

In “Look Me in the Eye” (Crown, 2007), John Elder Robison describes a painfully lonely childhood and an ability to look at a circuit design and imagine how it will transform sound — a talent he used to invent audio effects and exploding guitars for the rock band Kiss.

Not all people with Asperger’s have such extraordinary abilities, and some who do are so crippled by anxiety and social limitations that they cannot hold down a job or live on their own.

Dr. Susan E. Swedo, a senior investigator at the National Institute of Mental Health who heads the diagnostic manual group working on autism, acknowledges the difficulty of describing such a variable disorder. Dr. Swedo said the plan was to define autism by two core elements — impaired social communication and repetitive behaviors or fixated interests — and to score each of those elements for severity.

The trick is to “walk the tightrope of truth,” Dr. Swedo said, between providing clear, easily used diagnostic guidance to clinicians and capturing the individual variation that is relevant to treatment. “People say that in autism, everybody is a snowflake,” she said. “It’s the perfect analogy.”

The proposed elimination of autism subtypes comes at the very moment when research suggests that the disorder may have scores of varieties. Investigators have already identified more than a dozen gene patterns associated with autism, but Dr. Lord, of Michigan, said the genetic markers “don’t seem to map at all into what people currently call Asperger’s or P.D.D.”

Nor have many of these genes been linked to distinct sets of symptoms. Until research can identify reliable biological markers for autism subtypes, Dr. Lord and other experts say, it is better to have no subtypes than the wrong ones.

In interviews, people with Asperger’s and mild autism were divided on the prospect of losing the label. Temple Grandin, a Colorado State University animal scientist who is perhaps the best-known autistic American, said Asperger’s was too well established to be thrown overboard. “The Asperger community is a big vocal community,” Dr. Grandin said, “a reason in itself” to leave the diagnosis in place.

“P.D.D.-N.O.S., I’d throw in the garbage can,” she added. “But I’d keep Asperger’s.”

But some younger people involved in the growing autism self-advocacy movement see things differently.

“My identity is attached to being on the autism spectrum, not some superior Asperger’s identity,” said Ari Ne’eman, 21, an activist who founded the Autistic Self-Advocacy Network, a 15-chapter organization he has built while in college, adding, “I think the consolidation to one category of autism spectrum diagnosis will lead to better services.”

All interested parties will have an opportunity to weigh in on the proposed changes. The American Psychiatric Association is expected to post the working group’s final proposal on autism diagnostic criteria on the diagnostic manual’s Web site in January and invite comment from the public. Dr. Swedo and company are bracing for an earful.

Not sure how I feel about this. If it leads to better services for more people, then great, but as far as the “identity” side of things goes, I will be sorry to see the term “Aspie” fade from use. I wonder though, had this idea been in place many years ago, if my third son (the first to be diagnosed) would have received a more useful diagnosis entitling him to classroom assistance. He was diagnosed by a Clinical Psychologist who was very cautious about using the “new” diagnosis of Asperger’s Syndrome. Instead, he opted for the more obscure, (and totally useless) diagnosis of D.A.M.P. (Deficits of Attention, Motor and Perception) with the qualifying statement that T was very similar to a child with Asperger’s syndrome but to a lesser extent.  Although D.A.M.P. was considered to be on the autism spectrum, those magic words were never added to T’s diagnosis, so in spite of the echolalia, hand flapping, obsessions/fixations, total lack of social awareness, and a ‘zillion’ other ‘autie’ traits he didn’t qualify for any kind of assistance at school. The psychologist was very impressed with the care and support we had provided T with at home and simply wanted to know if I felt I could advocate for my child. WTF? He was basically acknowledging that ‘T’ needed help or some kind of special provisions at school but was relying on me to somehow achieve those for him without a diagnosis that the education dept would recognise. If only I knew then what I know now — sigh. Still, I did advocate for my child and gave each one of his teachers heaps of info about AS for which they were most grateful, and that info helped them to understand him better so they could appreciate and work with his strengths while being more tolerant of his shortcomings.

Things had changed by the time 4th son was diagnosed, about 8 years later, when he was given a diagnosis (by a Consultant Paediatrician) of “Mild Asperger’s Syndrome and ADHD without the Hyperactivity”, even though he was far less ‘autie’ than his older brother had been. Thankfully B did qualify for some classroom assistance (even though it is minimal because of lack of govt. funding and far less time than he needs) but I still needed to advocate for him and “educate” his teachers about AS all through primary school as well — and it’s still happening in high school too. Although he’s in a “special” class, the different teachers he has for the various subjects have not had any specific training about AS or any other issues the other students have, yet they are somehow expected to teach these kids. Our public school system needs a BIG overhaul (and more funding!) but that’s another topic.

A slight digression here — I do find it rather interesting to see the illustration above of Daniel Tammet’s drawings of numbers and his reference to being born on a “blue” day. I was born on a dark purple day. 😀 Synaesthesia is something I never knew about or realised was so much a part o AS until quite recently. I just thought that’s how all people thought — but apparently they don’t, LOL.

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5 thoughts on “A Vanishing Diagnosis?

  1. I think it’s useful for people to realize that autism is a spectrum rather than “just autism.” For people so accustomed to seeing everything as either black or white (and of course, some things are, like math), the idea of measuring autism (and who knows what else – sexual orientation?) by degrees is a helpful thing. But at the same time, the term Asperger’s Syndrome describes my specific point along the Spectrum. Yet it isn’t particularly specific. I have a bunch of the sensory issues and social cluelessness, but none of the savant-like gifts (I’m jealous!). So, maybe it could turn out to be a good thing in some ways.

    -Robin

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  2. It’s more important for people to be aware of the FRAUD and deception that has infiltrated the autism community. As in Ari Ne’eman, who is Aspergers( diagnosed in 2000 not as a child of course), and switches back and forth between the terms, as if interchangable. Then there’s the notorious Amanda Baggs (google amanda baggs controversy), a woman who took copious amounts of LSD and suffers with “factitious disorder” or “psychogenic autism”. Would make a nice TV movie of the week, actually. Then you have an old time pro at posing as autistic: the ever popular bless her heart, who really does believe she is autistic: Donna Williams, who herself admits in her book, “nobody nowhere,” she had a multiple personality disorder. So, she’s not autistic either so say many experts. Apparently, this hasn’t hit the American Psychiatry seminars, as they are totally oblivous to the factitious disorder epidemic inside the autism community. You’d think they’d get it, being shrinks and all, but I guess they forgot about groupthink, mass hysteria, etc…and that Hollywood has given all sorts of mentally imbalanced folks who need attention, a deep desire to cling to the autism diagnosis so they can get into newspapers and on CNN to tell their fake autism story. This is truly funny. It should be on the Saturday Night Live specials..everyone and their grandma now is autistic. Like it’s popular. Fun. Jump on board. Let’s ride the autism train. If you were really dealing with autism you would never ever be thinking about autism pride or activist movements. Get real. Get some Haldol

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  3. University of New Hampshire hired Amanda Baggs to speak? Is this is joke? Am I dreaming. Surely, these brilliant academics aren’t so naive and gullible as to see that Ms. Baggs is a complete con artist who should be arrested for fraud. Or, perhaps put on a psychological hold for extreme mental illness. Nope, it’s deliberate, however, so I say bring criminal charges against this woman. look into her background and discover she is not autistic. She took many drugs and was locked up and after LSD presented wtih chronic schizophrenic behavior. This woman is a disgrace and should be exposed immediately by media before she does further harm. SHAME on University of New Hampshire for being such chumps.

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