is autism just "behaving badly"? Oh what a load o

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respect
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is autism just "behaving badly"? Oh what a load o

Postby respect » Sun May 14, 2006 3:59 pm

http://www.timesonline.co.uk/article/0, ... 18,00.html


I couldnt believe what i was reading here but i have posted it for you who have healthy blood pressures. Everyone else, take caution before reading.


The Sunday Times May 14, 2006


Katie Grant: Some ‘autistic’ children aren’t ill, they’re just badly behaved


‘Autism cases soar.” The headlines this week have been dramatic, as well they might be, given a reported 600% rise in diagnosis of autistic spectrum disorder.
The statistics are alarming. In 1999 there were 114 autistic children in Scotland’s secondary schools; now there are 825. In primary schools over the same period the numbers have risen from 415 to 1,736. But while I have no doubt that Bill Welsh, the chairman of Action Against Autism, is entirely well intentioned when he labels the recent statistics a “public health crime”, he is scaremongering in the most sensational way. Look behind these stark figures and reports of an “epidemic” of autism are grossly exaggerated.



The plain fact is that autism has attained a certain notoriety, particularly after the MMR scare — and despite the fact that the study by Andrew Wakefield linking the condition with the triple vaccination for measles, mumps and rubella was so thoroughly discredited in this newspaper. Since the publication of Mark Haddon’s excellent novel The Curious Incident of the Dog in the Night-Time — whose hero is a teenager with Asperger’s syndrome — it has become even more fashionable.

To the great distress of parents whose children really are on the autistic spectrum, the condition has been adopted by many other parents on behalf of children who are not ill, just badly behaved. If a child is described as “autistic”, nobody can be angry if he or, more rarely, she throws a tantrum at school or consistently irritates the neighbours.

Children know that if they suffer from some kind of behaviour “ism”, good things result: reduced expectation, indulgence instead of punishment, safety from even the gentlest rebuke. At the first sign of a teacher’s impatience, the child can rush home and cry “abuse”. Autism, a serious condition when real, is being exploited by others for all it’s worth.

And it’s worth quite a lot. A diagnosis of some kind of behaviour “ism” might result in £80 a week disability living allowance. If a parent has to become a carer, it is worth even more. I stress again that there are families who absolutely need and deserve the state’s help with children who really do suffer from neurological disorders, but there are also families whose children are not ill and therefore deserve no such help.

Christine Grahame, the SNP MSP who has taken it upon herself to brandish the autism statistics about, needs to be careful she is not being taken for a mug. “Autism-specific inspections have been negligible,” she says. “Those pupils with autism deserve to have the right level of support in place, not just from educational staff, but also from supporting health professionals.”

Indeed they do. But we also need to understand that inspection will not be synonymous with accuracy. An inspector’s job depends on giving bad news. Create an autism-specific inspectorate and, within moments, without children being any different, the 600% increase in autism will become a 1,200% rise.

Some say that the MMR vaccine should be delayed until the child is between 18 months and two years old. However, what we should really be doing in the face of the “autism epidemic” is not showering “isms” on children, but finding out the true reasons they are doing badly at school and are unable to communicate. Nine times out of 10 it will be family breakdown, community paralysis, hopeless parenting or, perhaps more controversially, putting a child into a large nursery from the age of six weeks so that one-to-one communication is minimal from the word go. If a child cannot concentrate, why automatically blame autism? It is not autism that makes so many children fidget all the time, it is habit. Children unused to staring at anything static, or making conversation that does not consist of grunts, are bound to appear strange.

However, although some may be autistic, I doubt that most are really ill. Some may just be clever and bookish while others are simply suffering from a peculiarly modern kind of neglect and adapting their behaviour to cope.

There are no perfect parents. But it must surely be the worst kind of damage to label your child with an “ism” when there is nothing wrong except that you’ve not done a great job at child rearing. With effort, you can often remedy your own failings, but once you place your child in the hands of the “ism” authorities, who knows where they may end up? For the sake of all our children, let’s treat these “shock, horror” autism statistics with extreme care.

Mary
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Postby Mary » Sun May 14, 2006 4:51 pm

It's worth a letter to the editor. This writer clearly is just spouting off her ill-informed opinions, without benefit of any reporting, knowledge, information or insight. She's the journalistic equivalent of an aggressive driver. She's angry, she's right, get outta her way.

livsparents
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Postby livsparents » Sun May 14, 2006 9:51 pm

So the new reason for the 10 fold increase in numbers is lazy parents con-ing the system?!? This lady has some nerve. It looks like she did a LOT of research on this. She must have accessed 4...maybe even a whole half dozen websites researching all THIS data. She MAY have even INTERVIEWED one person for this. I see Pulitzer in her future. Much as I have mis-maligned the DSM-IV criterea today, I'm sure that this would catch 99% of these perpetrators. Please, all you UK posters (Kevin, even you can see the disservice in this article, no slam intended) please flood this paper with big ???? as to this person's credibility (and sanity!)
Bill

Gabesmom
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Postby Gabesmom » Mon May 15, 2006 2:09 am

If autism could be diagnosed on behavior criteria alone, I fear that 80% of U.S. kids would make the cut. Talk about an epidemic!!!!
Jennifer, Mother to Anna, 5 (NT), Gabriel, 4, Autistic

tmarthaler
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Postby tmarthaler » Mon May 15, 2006 2:52 pm

wait a second..yes this writer is off of her rocker but i would bet that if in the usa we offered $$$ for having a child with autism some people would be flocking to their doctor to have their "poorly behaved" (not autistic)children diagnosed.

respect
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Postby respect » Mon May 15, 2006 3:27 pm

Well, the ABA people should be happy with this one. Ties right in with their method and "science".

KamiO
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Postby KamiO » Mon May 15, 2006 11:47 pm

That article ticked me off.... I WISH my son was only "poorly behaved", unfortunetly he doesn't know what being bad means, if only he could understand. Nothing we do or say is going to change the mind of some people. Take Care, Kami

mouseker
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Postby mouseker » Tue May 16, 2006 5:41 am

I think Kami is probably right some people will never change thier mind no matter what you say. We do in the USA offer $$$ for having a child with Autism it is called SSI and it is closer to $150/week.

The problem that this woman has is that the things autistic kids don't learn NT kids do learn instinctively. Babies are preprogrammed to learn certain things. It is part of our makeup as a species. Babies learn from the examples of the people around them they use their senses to see and hear and taste. In kids with autism either the senses aren't working properly or the information doesn't get properly utilized in the brain all of this is still being studied.

I think that doctors who have experience with Autism can sort out the ones that are and the ones that aren't.

respect
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Joined: Mon Sep 19, 2005 3:52 am

Postby respect » Sun May 21, 2006 12:59 pm

Here is the original writers reply to a plethora of letters received about her inane article. What a maroon.


The Sunday Times May 21, 2006


Katie Grant - Autism: we need a debate
Her column last week prompted a vociferous reaction, reflected in the column and letters, at the bottom of this web page. Here Grant answers the critics




::nobreak::My views on autism last week upset many people who have autistic children. I am sorry for the pain, but not for raising the issue. My desire was — and still is — to question the reliability of the most recent statistical analysis of autism in Scotland. I believe work needs to be done to differentiate between those who have the condition and those who do not. Unfortunately, this past week I have become something of a hate figure for those who are not even prepared to concede that this matter should be debated.

I would ask those who have written attacking me to consider these words: “There is a risk of the diagnosis of autism being extended to include anyone whose odd and troublesome personality does not readily fit some other category. Such over-inclusion is likely to devalue the diagnosis to a meaningless label.” This was written by Dr Tom Berney in the British Journal of Psychiatry. He is a lead clinician and autism specialist at Northgate and Prudhoe NHS Trust in Morpeth. He was writing in 2000, when figures were far lower than they are today.

There are others within the health profession who privately share Berney’s view, perhaps reluctant to confront the wrath of a lobby group that has called into question my motives in writing the article. The fact remains that the question of autism diagnosis needs far more debate and examination. Suggestions from individuals and groups that my column should not have been published — and that the views contained should not have been expressed — are downright dangerous, not just in the context of freedom of speech, but also to those people struggling to cope with genuine cases of autism.

I support wholeheartedly all those whose children need to be helped, but autism should not be hijacked and turned into a woolly generic term. It should retain its diagnostic integrity. The condition exists and as a society we need to deal with it. But, faced with a massive statistical increase in autism, we have a duty to examine all the causes of children’s behavioural difficulties. If sceptics about official statistics are shouted down, there can be no debate.

Not everybody who disagrees with my views would have me silenced. Sophie Dow, the formidable founder of Mindroom, the charity dealing with learning difficulties, agrees a wider debate would be most welcome. Dow is against any of the different camps in this debate claiming exclusive understanding. “We need to accommodate all theories,” she says. “It is very dangerous for one group of people to claim the right to understand what learning difficulties really are.”

For a condition only identified in 1943 and only distinguished from schizophrenia in 1971, autism clearly is an evolving concept. As there is no cure, ideas and theories play a large part in both diagnosis and treatment and, as many experts, including Berney, agree, diagnosis is extremely difficult.

We need to find out more about why children develop what Berney described as “odd and troublesome personalities”, and any research must include not just the personal but also upbringing, family circumstances and other societal factors.

“Over-inclusion” — making autism a catch-all for various complaints — cannot help those children or their families whose plight is genuine. As Berney says, putting somebody on the autistic spectrum cannot become the default option, since once a label becomes meaningless, help is far less likely to be forthcoming. When figures for those on the autistic spectrum rise dramatically we must be as certain as we can be that each diagnosis not only is completely legitimate, but is recognised as such so that when help is needed, we all listen attentively.

Half a million people in Britain fall within the autistic spectrum, although it must be remembered that this figure increased when people with Asperger’s syndrome, who are often extremely clever and manage to integrate reasonably well, were included.

Last May’s BBC Horizon focussed on the controversy surrounding the triple vaccine MMR and its supposed link with autism. It found “rising awareness of autism has undoubtedly played a role in the increasing numbers,” particularly as there is “no objective test for autism and therefore the numbers diagnosed depends on the skill and experience of the medical community”.

These skills, as most would agree, have ‘improved significantly’ but when the goal posts keep changing, violent alterations in statistics are bound to follow on.

A study by Drs Jick and Kay at Boston University Medical School revealed that “as more people have been diagnosed with autism, there has been a similar decrease in other less specific diagnoses (such as ‘behaviour’ and ‘developmental’ disorders)”. Though you may disagree — and many do — that bad behaviour, as opposed to a behavioural disorder, is sometimes responsible for increases in autism diagnoses, it at least seems right to ask whether autism, by taking in other previously individualised disorders, is becoming too much of a “catch-all”.

It often seems that the MMR controversy, which still rumbles on, has hijacked any other debate about the autistic spectrum. Yet nobody has more of an interest in getting the diagnosis right, and removing from any list those who should not be on it, than those faced with autism every day.

“There is a need to define clearly what the correct numbers are to provide the appropriate statistics and then the appropriate help,” says Professor Lawrence Weaver, a consultant paediatrician at the Royal Hospital for Sick Children at Yorkhill, particularly as, so he points out, “the more you look for something, the more you find it”.

The numbers of children on the autism spectrum that he sees are growing and, by the time they reach Weaver, there is no doubt about their condition. Nevertheless, he thinks statistics must always be treated with caution, particularly statistics over diagnoses which cannot, by their nature, be completely objective. “Physicians must constantly ask themselves two questions: one about definition and one about ascertainment,” he says.

Since being on the autistic spectrum is not like having chicken-pox — there are few fail-safe physical signs like a rash, for example, and no two autistic children, just like no children, are exactly the same — great care must be taken.

We live in confusing times where mental health is concerned, and even the experts have a huge amount to learn about autism and its symptoms. Definitions of autism are not set in stone, and nor should they be. Yet this has its dangers. Berney concludes that autism can, at times, be “ indistinguishable from a dissocial personality disorder”.

Those who live with autism can only be helped by opening up the debate. Shouting down those with unpopular views will do them no favours at all.

It's not a trendy excuse

Children with a disability should not be treated as a source of ridicule, but time and again they are. For every article that is sensitively written about the difficulties families dealing with disability have to face, there are countless others — like Katie Grant’s column last week — that decried the rise in diagnoses as an “epidemic” and an excuse for children to be “badly behaved”.

What would you think if you read that nine out of 10 cases of autism were just a fashionable excuse for bad behaviour? This type of reporting is why parents move their offspring away from the “naughty” child as if they were contagious, when the child in question is simply unable to understand human interaction. Except this isn’t naughtiness we’re talking about. Autism is a lifelong disability that permanently changes families’ lives.

If I had £1 for every time someone said to me, “It’s just a stage he’s going through,” or strangers demanding, “Why can’t you control your son?” then I’d be able to retire to somewhere hot to live the “fashionable” lifestyle Grant described last week.

Grant gives the impression that the diagnosis of autism is a gravy-train to Prada whereas, in reality, parents with autistic children are battle-scarred veterans. The fight for diagnosis is just the beginning. Assuming you don’t get accused of Munchausen’s syndrome by proxy (MSBP), and can find a specialist who takes you seriously.

The disability living allowance (DLA) forms are heartbreaking. Being forced to describe just how different your child is from the norm shakes most people to the very core. Grant assumes that people can stroll in and demand DLA; it’s not true. In our support group, most parents were turned down; the vast majority only received middle or lower band after appeal. That’s worth as little as £16.50 a week.

Grant exhorts us to seek the “true reasons they (children) are doing badly at school”. This can be answered simply. With the political pressure on special schools, children have been forced into the mainstream, often with disastrous results. Teachers are ill-equipped to cope due to inadequate resources.

No parent would want a diagnosis of autism. No parent chooses to be shunned by some family and friends. No parent wants to be criticised almost every time they leave the house.

When I see my eight-year-old daughter and three-year-old son caring for their brother, I feel fiercely proud of all three. Autism isn’t about bad parenting; it’s about fantastic children.




Michaela Child is founder of ASDfriendly, an internet-based support network for parents

Increase is no surprise

KATIE GRANT’S article suggests that the increase in the number of young people diagnosed should be treated with caution. This is a reasonable point. We should note, however, that our understanding of autism has moved on over the past 10 years. We are now more informed and better able to identify autism. Similarly, there are improved systems for diagnosis, with a rise in diagnostic resources throughout the country, although long waiting lists across Scotland still prevail.

In many subject areas, improved understanding and reporting leads to increased identification of problems that have been there previously, but not dealt with appropriately. This is also the case in other social concerns such as domestic abuse. We should, therefore, not be surprised by the increased diagnosis of more young people with ASD if the system is working more efficiently.

The article suggests that there may be a queue of people aspiring to achieve the “fashionable” label of autism. This assertion is particularly unhelpful. I do not know any individuals with autism or families who have sought out a diagnosis as a trendy accessory for their lives. To suggest this is simply uninformed.

The article may well have been offensive to thousands of individuals with autism and for many parents whose children live with the disorder. The reality for many individuals and families involves considerable stress, fear and anxiety.

John McDonald, Chief Executive, the Scottish Society for Autism




SENSATIONALISM: Katie Grant’s article in last week’s Sunday Times left many people in Scotland shocked. Autism is not a consequence of poor parenting. That autistic spectrum disorders are still under-diagnosed is a given fact; that diagnostic criteria have widened over time is common knowledge.

What possible evidence does Grant have for her claim that “the condition has been adopted by many other parents on behalf of children who are not ill, just badly behaved”? When autism was first identified as a condition in the 1940s, a theory developed that parents were to blame. Such psychogenic theories were discredited 50 years ago, so it is sad to see them even hinted at again.

Worse still, we are asked to believe parents would seek this particular “ism” — the “ism” that dominates Grant’s article is nothing short of sensationalism.

Professor Aline-Wendy Dunlop, National Centre for Autism Studies, University of Strathclyde




APPALLING BEHAVIOUR: Full diagnosis of an ASD can take from 18 months to two years, with input from parents and health, social and education professionals. To accuse these people of diagnosing a child with ASD for petty behavioural issues is appalling.

Does Katie Grant believe parents would place their child under the supervision of an educational psychologist, social worker and speech therapist, be given a record of needs and placed in a special unit, in order to receive an extra £80 a week, or a free taxi to school?

Stephen Carr, Falkirk




CHEMICAL OVERLOAD: Ms Grant should consult with toxicologists, biochemists and environmental researchers about the various chemicals innundating children, which affect their behaviour, abilities and health.

For my autistic son, repeated exposures to mercury pushed him to a toxic tipping point. However, with testing and treatment he improved drastically. People such as Grant and our unresponsive governments discourage proper testing and treatment for these sad, poisoned children.

Nancy Hokkanen, Minneapolis, Minnesota, USA




NO RICH PICKINGS: I’ve been submerged in autism for five years now, day and night, with precious little financial assistance towards a condition that has already cost our family £35,000. Where are these parents who view autism as trendy and who find the “rich pickings” of benefits so irresistable? I've never come across one.

Stephanie Grabiec, Nottingham




LACK OF RESEARCH: Katie Grant is confusing autism with ASD when she suggests there could be any level of confusion between a neurotypical child with bad behaviour and a child suffering from ASD. When a child has autism there is no doubt whatsoever about their inability to behave normally. She obviously put very little research into the article.

Rebecca Hoskins, Alnwick, Northumberland


THAT’S LIFE: The 600% increase in autism is quite simply due to the fact that medical professionals (and other individuals) are becoming more aware of the condition. A lot of research has already been carried out, but more still needs to be done.

It would have been far better to have raised awareness of the condition by doing a feature on how this disability can affect people. A child in a wheelchair is given much more sympathy than a child with a mental health disorder. Unfortunately, that’s life, but articles like the one published don’t help.

Caroline Muir, Edinburgh

r's mom
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Postby r's mom » Sun May 21, 2006 3:48 pm

What really bugs me is that the DSM criteria for autistic spectrum disorders is specific in that it is marked impairment in the use of [b]multiple nonverbal behaviours ...... apparently inflexible adherence to specific, nonfunctional routines or rituals (and that is for aspergers) they now say that they are just more aware of the condition, better diagnosis blah blah blah That is saying that parents and healthcare professionals 50 years ago accepted that their kids had marked impairments in a lot of areas and I really don't buy that. That is saying that after 1000's of years the phychiatric profession today have just got smarter than everyone else and more aware. There is an epidemic and it is getting worse.

I believe that they are pulling the wool over everyones eyes and we are buying it - going back now and looking at the idiocyncracies that humans have and saying yes we have lots of traits. I like things neat must be autistic, i like math must be autistic, introvert must be autistic. I am not saying that there wasnt autism before there was but there were people who were just quirky , depressed and plain antisocial and a lot of other things. What I think is happening is that history is being reinvented to prop up the belief that there is not an epidemic and that the world is not as bad as it is.


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