It's my usual policy on this site to keep entries to below 1000 words, and ideally to about 500. You're busy people and I'm a great believer in the power of editing. This one, for all my efforts, is about 1800. I can only plead special circumstances and pledge that normal service will shortly be resumed.
The arrival of a new government seems to have raised hopes that Gary McKinnon might be spared extradition to the United States on computer hacking charges. His latest application for judicial review has been adjourned to allow the new Home Secretary, Theresa May, time to consider the latest medical evidence. It is a welcome development. McKinnon’s case has been the subject of a highly charged publicity campaign ever since he was diagnosed with Asperger’s Syndrome and fears were raised that incarceration in a foreign jail would have catastrophic consequences for his health. Sadly, publicity comes at a price, and in this case the price seems to be the abandonment of the usual standards of compassion that apply to the disabled.
The strident campaign in support of McKinnon by the Daily Mail has sparked a backlash from commentators who instinctively believe that if the Daily Mail is in favour of something, it must be wrong. These arguments are summarised concisely in a blogpost by the Labour MP Tom Harris, misleadingly titled ‘The case for McKinnon’s extradition.’ In fact Harris makes no such case; he merely sets up a row of straw men and begins firing like a hick with a blunderbuss and a bad case of hiccups. Most of the ‘arguments’ he cites in support of McKinnon simply don’t exist. Take the idea that ‘Computer hacking is not a serious crime’. It most certainly is; we have laws against it in this country. Gary McKinnon accepted that he broke those laws and admitted his guilt when interviewed. He was prepared to accept whatever punishment the court saw fit. What he wasn’t prepared for was for lawyers from another jurisdiction to sweep in and threaten to incarcerate him in a maximum security jail for a decade or longer if he didn’t co-operate.
Here’s another issue: ‘Asperger’s sufferers shouldn’t be extradited – why not?’ Again, this wilfully misunderstands the opposing view. Nobody is calling for a blanket exemption from extradition for people with AS. The contention, voiced by several medical experts including Professor Simon Baron-Cohen, is that McKinnon’s mental health would be adversely affected, possibly to the point of suicide, if he were to be extradited. It is one of the most basic principles of justice that people should not be punished or made to suffer as a result of acts committed through mental incapacity. Harris asks: ‘Would this argument be made in favour of an Asperger’s Syndrome sufferer who had committed a less “acceptable” crime, like murder or child abuse?’ The straight answer is yes, it would. It wouldn’t be a conclusive argument in itself – just as it isn’t in McKinnon’s case – but AS has been successfully used in a defence of diminished responsibility in cases such as this one about a man who killed his stepmother.
At this point we ought to leave the low-hanging fruit such as Tom Harris for the wasps and address more pertinent accusations, such as those put forward on the Socialist Unity website. It’s argued here that the threat to McKinnon’s well-being has been exaggerated to the point of hysteria by a media seeking to whip up anti-American feeling. To quote: ‘McKinnon’s spin doctors have also created an entirely fictitious narrative of him being pursued under anti-terrorism legislation, and facing 60 years in Guantanamo or a hell-hole penitentiary.’ I’m not sure where the reference to Guantanamo Bay stems from, but there were certainly concerns raised that McKinnon might wind up in a maximum security jail. And these claims were well-founded. As narrated by the Court of Appeal (an institution unconnected, as I understand it, to the Daily Mail), McKinnon was offered a plea-bargaining arrangement by US prosecutors that would see him serve six to 12 months of a four-year sentence in the States before being repatriated. If, on the other hand, he resisted: ‘no substantial remission would be 'earned': he would serve a substantial sentence in a US prison, possibly a high security prison, with, at best a 15% 'remission'.’ The ‘substantial sentence’ was described as ‘8-10 years or possibly longer’.
Like it or not, it is impossible to detach the request to extradite Gary McKinnon from the political climate in which it was made. McKinnon’s extradition was sought during the days of the Bush administration, which was strident and unapologetic in its determination to ‘get tough’ on anyone who impinged on national security. The Court of Appeal mentions a widely reported statement by a New Jersey prosecutor that the authorities wanted to see McKinnon ‘fry’. Since this was presented in court by the defence and I have been unable to find the original attribution, I am sceptical as to whether it was ever actually said, but it is typical of the kind of language that was customary in the Bush era. The Canadian Supreme Court considered a case of 89 people whose extradition was sought on mail fraud charges. The American prosecuting authority appeared on Canadian television and issued this threat to those who refused to give themselves up voluntarily: ‘I have told some of these individuals, 'Look, you can come down and you can put this behind you by serving your time in prison and making restitution to the victims, or you can wind up serving a great deal longer sentence under much more stringent conditions' and described those conditions to them.’ Pressed further on what those conditions might be, he replied: ‘You're going to be the boyfriend of a very bad man if you wait out your extradition.’
This kind of bullying rhetoric almost certainly coloured the plea bargain offered to Gary McKinnon. It doesn’t matter that, as many commentators have pointed out, he couldn’t really ‘fry’ or spend 60 years in a maximum security jail for the offences for which he was charged, or that being raped in prison is not in the gift of a state prosecutor. The message was blunt and clear: surrender to us or we will make your life hell. To someone with Asperger’s, who is prone to taking things literally, it would have been a shocking proposition. Tell a child with Asperger’s that you’ll shoot them if they don’t behave and they’ll think you mean it. Say to an adult you want them to ‘fry’ in your prison system and they’ll be similarly terrified. Professor Baron-Cohen noted that one of the things McKinnon feared most about incarceration in the US was the prospect of being raped. The threat, in his mind, was real.
What underpins many of these counter-arguments, I fear, is a suspicion that Asperger’s Syndrome is not a serious condition and that McKinnon has ‘played the Asperger’s card’ in order to get off lightly. In dismissing his appeal for judicial review*, the Court of Appeal cited the previous Home Secretary's remarks that ‘despite having had AS in childhood his condition has, so far, not necessitated any type of treatment or medical intervention. He is aged 42. He faced arrest and interview by the police, arrest on an extradition warrant, an extradition hearing, the order for his extradition, and litigation in the High Court and House of Lords, all no doubt deeply stressful events without this leading to any acute events requiring intervention.’ This seems a strange conclusion, given that McKinnon is known to have suffered depression for several years. The fact that he has not sought treatment or medical intervention for his Asperger’s does not mean that he didn’t need it or wouldn’t have benefited from it. Like many people with AS, he muddled through life for about 40 years, drifting in and out of work, filling his leisure time with strange obsessions, struggling to form friendships and relationships and assuming he was just a bit of an inadequate individual. He was coping, but he was hardly thriving.
Asperger’s Syndrome, like all forms of autism, is a lifelong condition. That applies backwards in time as well as forwards. It’s not a condition like cancer, which presents itself in a previously cancer-free individual, sometimes after decades of unblemished health. It occupies the whole space between birth and death. If the law is unable to accommodate this basic truth, the law needs to be changed. Before you’re diagnosed with Asperger’s Syndrome, you have a similar but materially different condition: undiagnosed Asperger’s Syndrome. It’s distressing, bewildering and soul-destroying, and it’s completely untreatable because nobody can tell you what you’re suffering from.
Certainly McKinnon’s case is a complicated one. There is no suggestion that he is unfit to stand trial or incapable of understanding the charges he faces. But the implication that he is seeking to avoid prosecution or belittle the seriousness of his crimes is simply false. McKinnon has admitted committing offences that were indictable in this country. He accepts that he should be punished. He is challenging extradition, not prosecution. It is a distinction that his detractors need to understand. It has not helped at all that his extradition was sought by an administration that sought to make him comply by means of grotesque and exaggerated threats. On this, at least, there is hope: the language of the US prosecuting authorities has changed dramatically in the last few years, whether because of regime change or in light of McKinnon’s diagnosis. On February 23, 2009, the US Department of Justice wrote a detailed letter to the Home Office outlining what treatment McKinnon could expect if he were to serve his sentence in the US. It is quoted at length in the Court of Appeal’s judgment and is a far cry from the earlier promises of 15 years or more in a ‘supermax’ prison.
There is a sound legal case for why Gary McKinnon should be tried in the United States: his crime was to sabotage the US military computer network. But there is also a solid legal case why he should be sentenced (not tried, if he pleads guilty as expected) in England: he committed the offences from his flat in London, and the means exist for the English courts to impose an appropriate sentence. On top of that, there are strong humanitarian grounds for not placing someone in a situation that is likely to be detrimental to their mental health. Even allowing for the benign conditions now being offered by the Americans, the effect of being removed to an alien territory by force would be alarming and distressing to someone with Asperger’s and, in McKinnon’s case, the disorienting effect could well trigger a depressive episode or worse. It is unjust and inhumane to put someone who has admitted his guilt through this kind of additional trauma unnecessarily. You have to ask, finally: if Gary McKinnon had any other kind of disability, would he be treated in this way?
* I am indebted to the estimable Jack of Kent for gathering together the links to these court documents.
My name is Gordon Darroch. My two sons have both been diagnosed with Autism Spectrum Disorder (ASD). This is a blog about raising autistic children: the highs and lows, the joys and agonies, the hopes and fears, the sheer bloody-fingernailed exasperation and the "Eureka!" moments that every breakthrough brings. I hope that through writing this blog I can in a small way improve my own and other people's understanding of this often bewildering condition.
Wednesday, 26 May 2010
Wednesday, 21 April 2010
Stage Fright or Social Frustration?
I’ve been watching Channel 4’s Young, Autistic and Stagestruck for the past couple of weeks, and despite the faux-hip title, it’s been excellent. (If you haven’t caught it, the last episode is on Monday, April 26 at 8pm). In contrast all those distressing documentaries that focus on the horror and strangeness of autism, this one makes the effort to portray the nine teenagers as individuals with distinct personalities. It underlines how no two autistic people are autistic in the same way, and yet they all share something in common. Several of them are making their first meaningful friendships within the group and it’s heartening to watch – when two of them went on a date to the cinema it seemed like a small miracle. And the parents, though present, aren’t allowed to intrude or dominate, which was the issue I had with a similar venture in the US called Autism: The Musical.
It all reinforced something I’ve observed in my own children. Autism is often portrayed as an anti-social condition, and in many ways it is, but it doesn’t follow that autistic people are inherently anti-social. Often they’re fascinated by social rules and rituals. It’s just that they don’t get them. One of the children in Young, Autistic and Stagestruck says at one point: ‘I don’t really make any friends, but I wish I could.’ And one of the breakthrough moments comes when the drama teachers stop trying to get them to ‘improvise’ and start handing out props. All of a sudden the children’s creative talents start to bloom, like flowers after a desert shower.
When Euan still went to mainstream school I used to watch him in the playground before class in the morning. At first he refused to join in, but after a few months he was bold enough to leave my side and play alongside the children from his class. He ran after them, a pace or two behind, and when they stopped, so did he. He had no idea how to start the games off and I’m not sure he even understood why they were running, but it was clear he loved being with other children, watching them and trying to join in.
How much of autism, then, comes down to what could be called social frustration? When most of us walk into a large room full of strangers, we find it daunting, but we can intuit our way through. We look for signs, little clues that people are available for conversation, and after a few minutes we’ve usually succeeded in striking up at least a superficial rapport with someone. To an autistic person, I suspect, those little cues and prompts are invisible; it’s as if they don’t exist. It’s like going fishing with a bath plug instead of a baited hook. Sooner or later you’re going to give up and go home, or start banging your head off the side of the boat in frustration. Seen in this light, my children’s behavioural quirks suddenly don’t seem so strange or alarming to me; they’re how anyone would behave in those circumstances.
It all reinforced something I’ve observed in my own children. Autism is often portrayed as an anti-social condition, and in many ways it is, but it doesn’t follow that autistic people are inherently anti-social. Often they’re fascinated by social rules and rituals. It’s just that they don’t get them. One of the children in Young, Autistic and Stagestruck says at one point: ‘I don’t really make any friends, but I wish I could.’ And one of the breakthrough moments comes when the drama teachers stop trying to get them to ‘improvise’ and start handing out props. All of a sudden the children’s creative talents start to bloom, like flowers after a desert shower.
When Euan still went to mainstream school I used to watch him in the playground before class in the morning. At first he refused to join in, but after a few months he was bold enough to leave my side and play alongside the children from his class. He ran after them, a pace or two behind, and when they stopped, so did he. He had no idea how to start the games off and I’m not sure he even understood why they were running, but it was clear he loved being with other children, watching them and trying to join in.
How much of autism, then, comes down to what could be called social frustration? When most of us walk into a large room full of strangers, we find it daunting, but we can intuit our way through. We look for signs, little clues that people are available for conversation, and after a few minutes we’ve usually succeeded in striking up at least a superficial rapport with someone. To an autistic person, I suspect, those little cues and prompts are invisible; it’s as if they don’t exist. It’s like going fishing with a bath plug instead of a baited hook. Sooner or later you’re going to give up and go home, or start banging your head off the side of the boat in frustration. Seen in this light, my children’s behavioural quirks suddenly don’t seem so strange or alarming to me; they’re how anyone would behave in those circumstances.
Wednesday, 17 February 2010
Nursery Roulette
Two good pieces of news to relate, both concerning Adam. He has a date next week for his diagnosis, and although we have a fair idea what the outcome will be, that official confirmation will still come as a huge relief. Not least because the information will feed into the crucial decision about what school he goes to when he begins in August. Because Euan's diagnosis was late, he had to go through a year of mainstream primary - something he was clearly unsuited to - and though the school jumped through hoops to accommodate him, it led to further upheaval when he transferred to a special school for his second year. With Adam our hope is that the process be smoother, easier and fairer for all concerned.
We have also secured a place for Adam in a specialist nursery where he will spend 12 weeks being closely observed by trained staff, who will then write an assessment of his progress. With three members of staff attending to half a dozen children, he will have the kind of individual attention that it's impossible to provide at a mainstream nursery. Sadly that's a problem that has been magnified by the attitude of the staff at Adam's regular nursery, who have done little to engage with his social difficulties or even acknowledge that there's a problem. When Magteld told one of the nurses to watch out for Adam hitting toys against his forehead, which he does when he's excited or overstimulated, she got the flat response: 'Oh, he doesn't do that here.' Meetings to discuss his progress were hamstrung by a perception that promoting the nursery's good practice was more important than evaluating Adam's behaviour. 'He's a good little boy, he's never any trouble, he just plays quietly by himself,' they'd say, entirely missing the point that the 'playing quietly by himself' bit was the issue we were seeking to address.
The problem stemmed, I think, from a failure to accept that Adam needed special assistance, perhaps underscored by a reluctance to seek outside help in case it was seen as an admission of failure. And we might not have been so persistent if it weren't for the fact that we already had a child with autism - which leads me to wonder how many other children in the nursery whose parents are less well informed are being denied appropriate medical intervention. Because that's what it comes down to - and while, as a parent who's been through the same cycle of denial and defensiveness, I'm aware of how hard it is to admit you don't have all the answers, my sympathy is tempered by the knowledge that doing nothing is far more damaging in the long run.
It makes me consider, too, how lucky we were with Euan, who went to a different nursery and was referred to the educational psychologist by the nursery's manager. Had it not been for her, he might well not have been diagnosed until after he started school. There is a growing body of evidence that early intervention is vital in tackling autism, but unless pre-school education is equipped with the right resources and an understanding mindset, children will continue to be diagnosed too late, or not at all.
We have also secured a place for Adam in a specialist nursery where he will spend 12 weeks being closely observed by trained staff, who will then write an assessment of his progress. With three members of staff attending to half a dozen children, he will have the kind of individual attention that it's impossible to provide at a mainstream nursery. Sadly that's a problem that has been magnified by the attitude of the staff at Adam's regular nursery, who have done little to engage with his social difficulties or even acknowledge that there's a problem. When Magteld told one of the nurses to watch out for Adam hitting toys against his forehead, which he does when he's excited or overstimulated, she got the flat response: 'Oh, he doesn't do that here.' Meetings to discuss his progress were hamstrung by a perception that promoting the nursery's good practice was more important than evaluating Adam's behaviour. 'He's a good little boy, he's never any trouble, he just plays quietly by himself,' they'd say, entirely missing the point that the 'playing quietly by himself' bit was the issue we were seeking to address.
The problem stemmed, I think, from a failure to accept that Adam needed special assistance, perhaps underscored by a reluctance to seek outside help in case it was seen as an admission of failure. And we might not have been so persistent if it weren't for the fact that we already had a child with autism - which leads me to wonder how many other children in the nursery whose parents are less well informed are being denied appropriate medical intervention. Because that's what it comes down to - and while, as a parent who's been through the same cycle of denial and defensiveness, I'm aware of how hard it is to admit you don't have all the answers, my sympathy is tempered by the knowledge that doing nothing is far more damaging in the long run.
It makes me consider, too, how lucky we were with Euan, who went to a different nursery and was referred to the educational psychologist by the nursery's manager. Had it not been for her, he might well not have been diagnosed until after he started school. There is a growing body of evidence that early intervention is vital in tackling autism, but unless pre-school education is equipped with the right resources and an understanding mindset, children will continue to be diagnosed too late, or not at all.
Friday, 18 December 2009
More on Adam
Magteld and I swithered for months about whether to have Adam assessed. There was nothing to worry about. There was something not right, but it couldn’t be autism, because he made eye contact, responded appropriately to questions and didn’t share Euan’s more extreme habits, like endlessly fidgeting or standing by the radiator singing to himself.
But the doubts kept nipping at us. As long ago as last Christmas we noticed how Adam wasn’t joining in with his nursery carol singing. We remarked on his curious habit of dragging toys across his field of vision. We registered his delayed speech and the way he froze in the presence of strangers. A playworker started coming out to see him once a week in April; it was October before she heard his voice. And then a couple of incidents happened that pretty much settled it.
A month ago Euan fractured his shoulder at school. We still don’t know how it happened: Euan’s communication is improving, to the point where a few weeks ago he was able to give me a basic run-through of his day. I never would have thought that a sentence like ‘we planted some potatoes’ could move me to the brink of tears. But relating something as complicated as a fractured shoulder remains a long way beyond his capabilities. Euan has a curious relationship with trauma: he will scream his head off if you threaten to take him away from the computer, and wail plaintively if his second slice of toast at breakfast time is a beat too late, but a really serious setback (thankfully, he’s only had a tiny number in his life) knocks him dumb. His shoulder was only noticed when a teacher saw him swinging his arm limply. When she tried to touch it, he flinched away. So Magteld took him home, thinking it was nothing more than a bruise, until he started wincing in pain in the early evening.
She took him up to the local Accident and Emergency department, with Adam in tow. I arrived soon after, straight from work. Euan was walking down a corridor wrapped in a blanket with Adam clinging to him, crying: “Euan, put your T-shirt back on” over and over again. “He’s very repetitive, isn’t he,” observed the nurse. While Euan sat quietly on the couch waiting to be examined, Adam was inconsolable. Nothing we said could assuage his sense of bewilderment. The routine was broken and he couldn’t understand why.
The week before he was about to leave nursery when one of the nurses reached into the fridge and handed him a carton of milk. The next day, at going-home time, he went to the fridge. Again he got a carton of milk. It was a classic case of kindness unwittingly being cruel. Because when, a few days later, the nurses stopped handing out the free milk, Adam was at a loss to understand why. No explanation in the world would suffice. His routine had been stopped, summarily. He howled all the way home.
How does this make him different from other children? In a word: rigidity. By the age of four, children ordinarily have a sophisticated arsenal of pestering techniques for getting what they want. All Adam can do is monotonously repeat the same demand. At times it's like watching a fly smacking its head against the same window pane again and again, oblivious to the possibility of other exits.
But the doubts kept nipping at us. As long ago as last Christmas we noticed how Adam wasn’t joining in with his nursery carol singing. We remarked on his curious habit of dragging toys across his field of vision. We registered his delayed speech and the way he froze in the presence of strangers. A playworker started coming out to see him once a week in April; it was October before she heard his voice. And then a couple of incidents happened that pretty much settled it.
A month ago Euan fractured his shoulder at school. We still don’t know how it happened: Euan’s communication is improving, to the point where a few weeks ago he was able to give me a basic run-through of his day. I never would have thought that a sentence like ‘we planted some potatoes’ could move me to the brink of tears. But relating something as complicated as a fractured shoulder remains a long way beyond his capabilities. Euan has a curious relationship with trauma: he will scream his head off if you threaten to take him away from the computer, and wail plaintively if his second slice of toast at breakfast time is a beat too late, but a really serious setback (thankfully, he’s only had a tiny number in his life) knocks him dumb. His shoulder was only noticed when a teacher saw him swinging his arm limply. When she tried to touch it, he flinched away. So Magteld took him home, thinking it was nothing more than a bruise, until he started wincing in pain in the early evening.
She took him up to the local Accident and Emergency department, with Adam in tow. I arrived soon after, straight from work. Euan was walking down a corridor wrapped in a blanket with Adam clinging to him, crying: “Euan, put your T-shirt back on” over and over again. “He’s very repetitive, isn’t he,” observed the nurse. While Euan sat quietly on the couch waiting to be examined, Adam was inconsolable. Nothing we said could assuage his sense of bewilderment. The routine was broken and he couldn’t understand why.
The week before he was about to leave nursery when one of the nurses reached into the fridge and handed him a carton of milk. The next day, at going-home time, he went to the fridge. Again he got a carton of milk. It was a classic case of kindness unwittingly being cruel. Because when, a few days later, the nurses stopped handing out the free milk, Adam was at a loss to understand why. No explanation in the world would suffice. His routine had been stopped, summarily. He howled all the way home.
How does this make him different from other children? In a word: rigidity. By the age of four, children ordinarily have a sophisticated arsenal of pestering techniques for getting what they want. All Adam can do is monotonously repeat the same demand. At times it's like watching a fly smacking its head against the same window pane again and again, oblivious to the possibility of other exits.
Wednesday, 2 December 2009
The thin line
A while ago I was minded to respond to a blog I read by the BBC reporter Mark Easton in the wake of the Baby Peter case. Since then I've read several others that touch on the same question: what can we do to spot child abuse before it's too late?
Easton is a conscientious, fair-minded journalist, and I don't mean that as an opening gambit in some kind of veiled attack. He tackles with intelligence some of the darkest, most unfathomable excesses of society, including child neglect. Like anyone with a scrap of humanity, he is concerned that an incident has to escalate, sometimes to the point of murder or serious crime, before anything is done, and investigates the possibilities of improving early intervention. But unfortunately, in doing so he unwittingly raises the spectre of Bettelheim.
In studying the case of two young brothers who carried out a series of vicious attacks in Doncaster, Easton describes an experiment in which a mother was put in a sealed room with her child and instructed not to make eye contact in the usual way. Unsurprisingly, deprived of its tried and trusted means of communication, the infant quickly became hysterical. This experiment is used to illustrate an earlier point about the two brothers: "What these children's behaviour tells us is that they lacked empathy... Without it, even very young children are capable of horrifying cruelty." In a later entry, Easton comments: "Neglect is the most common form of child abuse and it is going on in your community right now."
It's perhaps unfair of me to single out Easton's sober analysis when others who may soon have a more direct influence on public policy are making more dramatic statements (such as Iain Duncan Smith's recent proclaimation that "there are now a growing number of families who are dysfunctional".) The problem is that now and again I come across a sentence in Easton's discourse that makes me shudder, like this one: "By the age of two, these children were clearly emotionally injured - some biting and scratching other kids, others cowering in a corner."
I've seen children cower in corners, or run out of the room to flee unwanted attention. I know children who sometimes kick, head-butt, bite, scream and scratch. I can't be sure they're not being abused, but I know there's another possible explanation for their behaviour, and I know because one of the children I've just described is Euan.
In the wake of the Baby P case it was reported that social workers felt under pressure to take children into care more quickly because of the widespread criticism they received for not intervening in time. There is no argument about the horrific nature of the abuse Baby P suffered, or the fact that social services were not properly alert to the danger he was in. The problem is that it's all too easy to start "seeing" abuse everywhere and relying on a blanket safety-first approach that has as much potential for harm as a laissez-faire one.
In the 1960s the now infamous quack psychiatrist Bruno Bettelheim caused a sensation with his book The Empty Fortress, in which he identified a hidden menace to society known as the "refrigerator mother". These women, by starving their offspring of love and affection, were inducing autistic behaviour in them, sometimes without being aware of it. He related the experience of autistic children to the concentration camps (which he himself had survived) and played a key part in the mass institutionalisation of people with autism in the United States. Only after his suicide did it emerge that he had falsified his qualifications in psychiatry, and allegations surfaced that he had abused some of the people in his care. His "refrigerator mother" theory has since been entirely discredited.
Bettelheim contributed to a climate in which children who displayed autistic traits were assumed to have been abused by their parents. My concern here is that when genuinely awful cases of abuse such as that of Baby P spark mass panic about the scale of child abuse, and when even reasonable commentators such as Mark Easton write that children who are withdrawn or uncommunicative are "clearly emotionally injured", there is a real danger of history repeating itself. We understand autism better now as a society, and the support given to families who have received a diagnosis is immeasurably better than it was in Bettelheim's day, but for families at the vulnerable pre-diagnosis stage, a wrong call or a hasty one can destroy the child's life. Parents of young children with autism are hugely suggestible, as they have no idea what they are up against; Magteld and I have both remarked that if somebody in authority had told us when Euan was a toddler that we were emotionally neglecting him, we would have accepted it unquestioningly. By then we were too confused, too emotionally exhausted and too scared to understand what was really going on. The diametric opposite of the experiment in which a child that normally relies on eye contact is deprived of it is the real-life situation in which a parent is driven to despair by their child's stubborn refusal to make eye contact or offer any other kind of response.
The understandable urge to identify child abuse at the earliest stage, and the rational (and probably accurate) fear that it is more prevalent than we as a society like to admit, cannot be allowed to obscure the need to obtain a full picture of a child's circumstances. As Easton also says, we need to understand more and condemn less. When you see a mother in the supermarket shouting in exasperation at a child who seemingly can't bring himself to look at her, it's easy for the untrained eye to assume abuse and forget that the mother may be suffering too. (This isn't just true for autism - perhaps they're both victims of an abusive partner.) What we need is trained eyes, and more of them, to ensure we distinguish genuine cases of abuse from those where other forms of intervention are needed. Otherwise our efforts to save one vulnerable group risk being to the detriment of another.
Easton is a conscientious, fair-minded journalist, and I don't mean that as an opening gambit in some kind of veiled attack. He tackles with intelligence some of the darkest, most unfathomable excesses of society, including child neglect. Like anyone with a scrap of humanity, he is concerned that an incident has to escalate, sometimes to the point of murder or serious crime, before anything is done, and investigates the possibilities of improving early intervention. But unfortunately, in doing so he unwittingly raises the spectre of Bettelheim.
In studying the case of two young brothers who carried out a series of vicious attacks in Doncaster, Easton describes an experiment in which a mother was put in a sealed room with her child and instructed not to make eye contact in the usual way. Unsurprisingly, deprived of its tried and trusted means of communication, the infant quickly became hysterical. This experiment is used to illustrate an earlier point about the two brothers: "What these children's behaviour tells us is that they lacked empathy... Without it, even very young children are capable of horrifying cruelty." In a later entry, Easton comments: "Neglect is the most common form of child abuse and it is going on in your community right now."
It's perhaps unfair of me to single out Easton's sober analysis when others who may soon have a more direct influence on public policy are making more dramatic statements (such as Iain Duncan Smith's recent proclaimation that "there are now a growing number of families who are dysfunctional".) The problem is that now and again I come across a sentence in Easton's discourse that makes me shudder, like this one: "By the age of two, these children were clearly emotionally injured - some biting and scratching other kids, others cowering in a corner."
I've seen children cower in corners, or run out of the room to flee unwanted attention. I know children who sometimes kick, head-butt, bite, scream and scratch. I can't be sure they're not being abused, but I know there's another possible explanation for their behaviour, and I know because one of the children I've just described is Euan.
In the wake of the Baby P case it was reported that social workers felt under pressure to take children into care more quickly because of the widespread criticism they received for not intervening in time. There is no argument about the horrific nature of the abuse Baby P suffered, or the fact that social services were not properly alert to the danger he was in. The problem is that it's all too easy to start "seeing" abuse everywhere and relying on a blanket safety-first approach that has as much potential for harm as a laissez-faire one.
In the 1960s the now infamous quack psychiatrist Bruno Bettelheim caused a sensation with his book The Empty Fortress, in which he identified a hidden menace to society known as the "refrigerator mother". These women, by starving their offspring of love and affection, were inducing autistic behaviour in them, sometimes without being aware of it. He related the experience of autistic children to the concentration camps (which he himself had survived) and played a key part in the mass institutionalisation of people with autism in the United States. Only after his suicide did it emerge that he had falsified his qualifications in psychiatry, and allegations surfaced that he had abused some of the people in his care. His "refrigerator mother" theory has since been entirely discredited.
Bettelheim contributed to a climate in which children who displayed autistic traits were assumed to have been abused by their parents. My concern here is that when genuinely awful cases of abuse such as that of Baby P spark mass panic about the scale of child abuse, and when even reasonable commentators such as Mark Easton write that children who are withdrawn or uncommunicative are "clearly emotionally injured", there is a real danger of history repeating itself. We understand autism better now as a society, and the support given to families who have received a diagnosis is immeasurably better than it was in Bettelheim's day, but for families at the vulnerable pre-diagnosis stage, a wrong call or a hasty one can destroy the child's life. Parents of young children with autism are hugely suggestible, as they have no idea what they are up against; Magteld and I have both remarked that if somebody in authority had told us when Euan was a toddler that we were emotionally neglecting him, we would have accepted it unquestioningly. By then we were too confused, too emotionally exhausted and too scared to understand what was really going on. The diametric opposite of the experiment in which a child that normally relies on eye contact is deprived of it is the real-life situation in which a parent is driven to despair by their child's stubborn refusal to make eye contact or offer any other kind of response.
The understandable urge to identify child abuse at the earliest stage, and the rational (and probably accurate) fear that it is more prevalent than we as a society like to admit, cannot be allowed to obscure the need to obtain a full picture of a child's circumstances. As Easton also says, we need to understand more and condemn less. When you see a mother in the supermarket shouting in exasperation at a child who seemingly can't bring himself to look at her, it's easy for the untrained eye to assume abuse and forget that the mother may be suffering too. (This isn't just true for autism - perhaps they're both victims of an abusive partner.) What we need is trained eyes, and more of them, to ensure we distinguish genuine cases of abuse from those where other forms of intervention are needed. Otherwise our efforts to save one vulnerable group risk being to the detriment of another.
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