Aptos, CA psychologist: Can virtual reality technology assist young adults with autistic spectrum issues to learn social skills? Maybe…

Virtual reality technology may be useful adjunct to teaching social skills to young adults newly diagnosed with Asperger’s Syndrome, non-verbal learning disorder.

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How can young adults with autistic spectrum issues learn the social skills they need? Some are newly diagnosed for the first time. Some heard they have “non-verbal learning disability”. Others have been labeled with Asperger’s Syndrome.

There is Applied Behavioral Analysis (ABA) training. Theory of Mind training. What about virtual reality technology? Are there any virtual reality technology packages available t teach social skills?

Background
“People with autism experience profound and pervasive difficulties in the social domain. Attempts to teach social behaviours tend to adopt either a behavioural or a ‘theory of mind’ (ToM) approach. The beneficial aspects and limitations of both paradigms are summarized before an examination of how virtual reality technology may offer a way to combine the strengths from both approaches.

Methods
This is not an exhaustive review of the literature; rather, the papers are chosen as representative of the current understanding within each broad topic. Web of Science ISI, EMBASE and PsycInfo were searched for relevant articles.

Results
Behavioural and ToM approaches to social skills training achieve some success in improving specific skills or understanding. However, the failure to generalize learned behaviours to novel environments, and the unwieldy nature of some behavioural methodologies, means that there is a need for a training package that is easy to administer and successful in promoting learning across contexts.

Conclusions
Virtual reality technology may be an ideal tool for allowing participants to practise behaviours in role-play situations, whilst also providing a safe environment for rule learning and repetition of tasks. Role-play within virtual environments could promote the mental simulation of social events, potentially allowing a greater insight into minds. Practice of behaviours, both within and across contexts, could also encourage a more flexible approach to social problem solving. Virtual environments offer a new and exciting perspective on social skills training for people with autistic spectrum disorders.

Introduction
People with Asperger syndrome (AS) and other autistic spectrum disorders (ASDs) experience profound difficulties in the social domain. This can lead to social exclusion, and difficulties in maintaining and sustaining friendships and employment (Howlin 1997). There have been many attempts to help children with ASDs develop specific social and communication skills in the hope that this will improve social functioning and increase acceptance by peers (e.g. Belchic & Harris 1994). The majority of these interventions have utilized behavioural methodologies and achieved varying degrees of success in improving and maintaining specific behaviours across time and contexts (for reviews, see Pollard 1998; Hwang & Hughes 2000; Rogers 2000). Many tend to target younger children with autism in the belief that learned social behaviours might ameliorate later difficulties in the social domain. There is little doubt that targeting social difficulties at an early age can have extremely beneficial effects (for a review, see Mundy & Crowson 1997).

Very many children with autism may not get the opportunity to participate in early intervention behavioural programmes or research. Fortunately, more recent, cognitive approaches to teaching social skills to people with ASDs have included older children, and adults. These approaches tend to be based on the ‘theory of mind’ (ToM) hypothesis of autism and provide an alternative to behaviour-based techniques. The ToM hypothesis states that the social difficulties in people with ASDs arise through an inability to recognize or think about the mental states of the self and others. Higher-functioning people with autism (e.g. those with AS) have also been included in some of these studies. High-functioning individuals tend to have subtle difficulties which fall outside the scope of the basic behaviours targeted in behavioural ‘peer modelling’ paradigms (e.g. naming a toy correctly in response to a question; McGee et al. 1992).

The efficacy of teaching people with ASDs about mental states in the hope of improving social understanding is rather equivocal. Although most studies report an improvement on the specific skill or task being taught, there are frequent failures to generalize knowledge to different tasks or to real-world situations. Nevertheless, the benefit of demonstrating an increase in understanding mental states, albeit in very specific circumstances, led Howlin (1998) to state that ‘. . . even this limited success suggests that training packages specifically designed to increase the ability to “mind-read” could be an important and valuable addition to the educational curricula for many children with autism’ (p. 315). Consequently, trying to teach children to think about the mental states of others appears to be an important objective for research on social skills interventions. Surprisingly, this approach is not reflected in recent reviews on current and emerging treatments for people with autism (see the special issue of the Journal of Autism and Developmental Disorders, Volume 30, Number 5, 2000).

The main purpose of the present paper is to highlight the specific advantages which virtual reality (VR) may offer in the realm of supporting social skills amongst people with AS. The review begins with background information about autism, AS and social skills. This is followed by a summary of the effectiveness of behavioural interventions for social skills training. Next, the authors include an overview of the ToM hypothesis of autism before covering some of the research utilizing ToM principles to teach social understanding to people with ASDs. They then summarize the key strengths offered by ToM social skills training and end by outlining how VR encompasses the benefits of both the behavioural and cognitive approaches, potentially offering a powerful and flexible tool for tackling deficits in social skills for people with autism.

Background on autism and social skills
Autism is a ‘spectrum disorder’ (Wing 1996) that is diagnosed at the behavioural level according to a triad of impairments in communication, socialization and imagination (Wing & Gould 1979). The spectrum ranges from ‘classic’ Kanner-type autism with severe learning disabilities at one end of the continuum to high functioning autism (HFA) and AS at the other. Even though individuals with the same diagnosis can vary according to level of associated learning disability, a fundamental difficulty with social interactions is common to all people with an ASD.†

At the more able end of the spectrum, there is debate about the value and validity of maintaining a diagnosis of AS separately from HFA (e.g. Ozonoff et al. 1991). In the absence of firm evidence to the contrary, many authors have concluded that the diagnoses should be considered as part of the same spectrum (e.g. Tantam 1988; Gillberg 1998; Manjiviona & Prior 1999). Even very recent discussions of the topic (e.g. Ozonoff & McMahon-Griffith 2000; Volkmar & Klin 2000) admit that the evidence for considering AS and HFA as distinct diagnoses is mixed, and that more research is needed to clarify the issue. Literature relevant to both diagnoses is considered below.

Whilst typically developing children seem to learn the intricacies of social interaction almost effortlessly, the same is not true for individuals diagnosed with an ASD. Widespread impairments in the social-communicative domain are manifest in many ways. For example, people with autism often show egocentric and echolalic speech (i.e. repetition of words or phrases), inappropriate behaviours and language, limited understanding of social norms and expectations, and an overly literal interpretation of speech (Frith 1989; Baron-Cohen & Bolton 1993).

Peculiarities in behaviour may be especially problematic for people at the higher-functioning end of the spectrum. Some individuals demonstrate normal to high IQ levels, and enjoy good outcomes in terms of academic achievements and personal/life skills, but still remain significantly impaired in their social understanding (Gillberg 1998; Nordin & Gillberg 1998). This can lead to social exclusion because forming and maintaining friendships can be extremely problematic. People with AS also have the capability to reflect on the implications of their diagnosis for everyday interactions. Consequently, it is not surprising that people with AS or HFA are particularly prone to secondary psychiatric disorders, such as depression (Tantam 1988). More worryingly, Wing (1981) suggested that the incidence of suicide amongst individuals with these diagnoses may be higher than average.

Because of the social difficulties experienced by all people diagnosed with an ASD, emphasis in educational intervention has been placed on social and communicative competence (Klin & Volkmar 2000). The next section summarizes the main strengths of social skills interventions which have utilized behavioural methodologies in order to teach specific skills to young children with autism.

Behavioural methodologies for social skills training
Early behavioural methodologies for teaching social skills to (usually) pre-school children with autism focused on the application of operant conditioning principles (e.g. Lovaas 1981). In highly structured one-to-one settings, children with autism receive repetitive drilling in particular behaviours in discrete blocks of trials (e.g. imitating hand waving or completing a puzzle). This approach aims to equip children with fundamental social building blocks from which they could learn, develop and generalize to a broad range of social situations (Frankel et al. 1987). These interventions were often very effective in teaching children new behaviours or skills, but suffered from a lack of generalization in terms of transferring learned behaviours to new tasks or contexts (for discussions of the approach, see Mirenda & Donnellan 1987; Schriebman 2000). The strict discrete-trial learning approach, coupled with a decontextualized, trainer-driven ‘therapy’ environment meant that learned behaviours were context-specific and dependent on immediate reinforcement – a situation almost completely devoid of naturally occurring interactions (Frankel et al. 1987). By contrast, more recent intervention strategies have recognized the importance of embedding interventions within the child’s natural settings, such as home and school. Spontaneously occurring behaviours tend to be incorporated into the programmes, with trainers, teachers, peers or parents responding and reinforcing child-initiated interactions and behaviours. Interventions have led to improvements in behaviours such as greeting, joint attention and more general social behaviour, as well as facilitating generalization and maintenance of effects (for reviews, see Hwang & Hughes 2000; Rogers 2000).

One particularly useful strategy seems to be a script- (or prompt-) fading procedure (summarized in Krantz 2000). This involves initially providing a high level of support or prompting to the children before gradually fading the level of prompts over time. The technique led to an increase in the target behaviour (initiating interaction with a teacher) as well as promoting generalization of the behaviour to unscripted interactions (Krantz & McClannahan 1998). These procedures have also been useful in helping older children with autism to develop some functional independence, such as going shopping or buying a train ticket (Howlin & Rutter 1987).

Generally, the main behavioural principles of repetition and reinforcement seem to be effective in promoting change in specific behaviours. The techniques tend to offer greater potential for the generalization of learned behaviours if they are embedded in more naturalistic and meaningful contexts. Prompt-fading procedures are also useful for developing and sustaining new social skills. Despite such strengths, these kinds of interventions are sometimes criticized because they ‘. . . are complex in administration, data collection, and maintenance and generalization procedures, and they require trained staff and focused interventions that extend over weeks to months’ (Rogers 2000, p. 406). Klin & Volkmar (2000) and Rogers (2000) also noted that, because of the above problems, the accessibility and affordability of social skills training programmes to teachers/carers/schools/parents has been frustratingly poor. In short, the field of social skills training ‘. . . needs to develop successful and efficient intervention approaches that are manualized and packaged for dissemination to a wide variety of community settings . . .’ (Rogers 2000, p. 407).

One of the benefits of the ToM approach to teaching social skills is that the tasks are often less complex and easier to implement. Indeed, Baron-Cohen & Howlin (1998) produced a manual to help teachers and parents incorporate ‘mind reading’ tasks into educational programmes. Another advantage, as already stated above, is that more able older people with autism tend to be included in ToM interventions. Consequently, this particular approach may be more relevant to the high-functioning members of the autistic spectrum. The following section outlines the ToM hypothesis of autism before moving on to look at the value of ToM principles for social skills training.

The ‘theory of mind’ hypothesis of autism
One of the most influential approaches to explaining the triad of impairments seen in autism is based on the ToM hypothesis. The term ‘theory of mind’ comes from the work of Premack & Woodruff (1978), who used it to describe the ability to impute mental states to self and others. This ‘mentalizing’ capability supposedly underpins the essential human ability to communicate and interact in a meaningful way. In particular, it is crucial to consider the mental states of others when trying to work out their motives and predict behaviour. Extracting underlying meaning from language is central to the success of conversation. Speakers rarely say exactly what they mean, and therefore, listeners need to fill in the ‘gaps’ by appealing to the context of the conversation, and the speaker’s belief framework, to work out what was meant. People with autism find this especially difficult and are notorious for making overly literal interpretations of speech (e.g. Mitchell et al. 1997). They also have well-documented difficulties on tasks which require thinking about the mental states of themselves and others.

Many people with autism have difficulty acknowledging false belief. In the test of false belief (Wimmer & Perner 1983), a story protagonist does not witness a change in reality (e.g. some chocolate is moved from a drawer to a refrigerator without the protagonist’s knowledge), and the child participant is asked to infer where the ignorant protagonist will look for the chocolate. Normally developing children pass this task around the age of 4 years and say that the protagonist will look for the chocolate in the drawer (where the protagonist last saw it). In contrast, many children with autism, even with verbal mental ages (VMAs) greater than 4 years, fail this task by reporting that the protagonist will look for the chocolate in its present location (i.e. in the refrigerator; Baron-Cohen et al. 1985). The difficulty with the task seems to arise from the participants’ autism and not their associated learning disabilities, given that a group of individuals with similar intellectual profile but without autism typically made correct judgements of false belief. Seemingly, autism gives rise to difficulty in understanding that people can hold mental states which are different (and separate) from current reality. The failure on this task is often interpreted as an indication that children with autism have a profound mentalizing deficit, leading to social-communicative impairment. Older and higher-functioning people with autism or AS have also experienced difficulties, compared to matched control groups, on more subtle and complex ToM tasks (Happe 1994), even though they may pass different versions of the false belief task (e.g. Bowler 1992). Given this difficulty with understanding mental states, there have been some admirable attempts to teach ToM skills to people with autism in the hope that such understanding might generalize to real social situations. The following section summarizes the success and limitations of these studies.

Teaching ‘theory of mind’ to improve social understanding
One of the main paradigms for teaching people with autism about mental states is to embody a mental state (i.e. a belief) with a tangible counterpart in reality (e.g. a photograph). For example, the protagonist’s belief that the chocolate is in the drawer is shown directly as a photograph of some chocolate in the drawer. Mitchell (1997) and Saltmarsh et al. (1995) argued that this approach is effective because the belief is elevated to the same level of salience as reality, i.e. children who fail false belief tasks do so because knowledge of reality dominates their judgements, rather than because they have a conceptual deficit in understanding thoughts as representational entities (for a contrasting view, see Perner 1991). Generally, this ‘pictorial augmentation’ methodology serves to make thought concrete, which might help people with autism to consider the mental states of others and perhaps generalize this understanding to situations which require ToM understanding in the real world. Most of the following studies incorporate this approach, albeit to varying degrees, alongside the explicit teaching of ToM rules or principles (e.g. if x believes y, then x will do z).

McGregor et al. (1998a) adapted a procedure developed by Mitchell & Lacohee (1991) for use with people with autism. Participants (mean age of autistic experimental group = 17.9 years; mean VMA = 4.8 years) were instructed to post a photograph of the original location of some chocolate into the head of a mannequin doll. For example, the photograph showed a picture of some chocolate in a drawer. Compared to pre-instruction performance, people with autism were significantly better at judging false belief on being taught that the photograph could show them what the doll was thinking, i.e. they were significantly more likely to say that the protagonist thought the chocolate was in the drawer (where she/he left the chocolate). However, unlike normally developing 3-year-olds, the children with autism failed to generalize this understanding to novel false belief tasks.

In a separate study by the same authors (McGregor et al. 1998b), people with autism were helped by the ‘picture in the head’ procedure to judge correctly about false belief scenarios presented on video (participants were aged 9–39 years, with VMAs ranging from 4 to 11 years). However, in both studies, a period of repetitive teaching was necessary before any facilitation resulted, and in the latter study, only a small subset of the individuals were able to apply their understanding of the picture-in-the-head procedure to video scenarios. In other words, people with autism could be helped to pass false belief tasks, but they tended not to generalize this understanding to novel situations.

Similarly, Swettenham et al. (1996) used photographs as an analogue to mental states. The above authors emphasized the rule that seeing leads to knowing, leading to a picture-in-the-head, which can then guide behaviour. This method was successful in promoting correct predictions about the protagonist’s behaviour, but none of the children with autism (mean age = 11.6 years; mean VMA = 6.0 years) used the photographs to infer mental states. Although the children may have learned a strategy for predicting behaviour, they seemed to have no insight that this was based on a mental representation (i.e. the protagonist’s belief).

Other studies indicate that teaching ToM principles to people with autism can be successful in promoting understanding in specific tasks, but there is little sign of generalization from one context to another. Hadwin et al. (1996) devised an intervention programme in which they taught a variety of ToM tasks to children with autism (mean age = 9 years; mean VMA = 5 years) over an intensive 8-day period. The researchers taught general principles for understanding mental states (e.g. seeing leads to knowing) during a variety of tasks of increasing complexity. Children with autism were significantly helped to pass tasks on which they received teaching, but failed to demonstrate any of this understanding on tasks in which they had received no teaching. In a more ambitious 4.5-month intervention programme, Ozonoff & Miller (1995) taught five normal-IQ adolescents with autism a number of interactional and conversational skills, in addition to principles related to understanding the mental states of others. Their performance was compared to an IQ-matched group of boys with autism who received no training. Whilst the ‘treatment group’ demonstrated significant performance gains in their ability to pass false belief tasks, there was no evidence of improved social competence in the real world based on the ratings of parents and teachers.

Overall, then, it appears that people with autism can be taught to pass false belief tasks, but the benefits of this understanding are restricted to tasks on which instruction has been given. Chin & Bernard-Opitz (2000) argued that this may be because the studies have focused on specific principles or tasks rather than actual ability. Teaching rules decontextualizes knowledge and tasks; unfortunately, it does not create a situation in which the transfer of skills between taught and real contexts becomes possible. This raises the possibility that practising behaviours systematically in a role-play situation could be the ideal way to promote improvements in understanding and behaviour. Indeed, Chin & Bernard-Opitz (2000) were successful in improving the conversational skills of three children with autism (aged 5.11, 7.5 and 7.9 years) through the explicit practising of behaviours, and Mesibov (1984) also reported success in teaching greeting and interaction behaviours. This is by no means a novel suggestion. Practitioners and teachers are keen to promote the benefits of in situ social skills training (e.g. Howlin 1998), and role-playing prior to entering the real world is considered to be a good way of preparing the student for the different types of interactions which they may encounter (Mesibov 1984; Howlin & Rutter 1987; Howlin 1997; Klin & Volkmar 2000).

The main message from the ToM interventions seems to be that teaching explicit rules for understanding and behaviour can improve task-related performance. Teaching rules for social understanding is an approach often emphasized by authors for effective social skills training (e.g. Howlin & Rutter 1987; Klin & Volkmar 2000). Howlin (1997) acknowledged that teaching rules for social understanding may be a near impossible task because of the complexity of social situations and the seemingly innate ability (at least amongst people developing normally) to know how to behave in different contexts. Nevertheless, she argued that rule-based learning may be the best option for people with autism because ‘. . . without this innate understanding, rules will be all that the person with autism has to guide his or her behaviour, and, imperfect as they are, they will be crucial for acceptable social development’ (Howlin 1997, p. 77). Indeed, Carol Gray’s well-known Social Stories teaching package (Gray & Garand 1993) relies on teaching rules for social behaviour to people with autism in a friendly and supportive environment. Consequently, it is vital that social rules are clearly conveyed in any social skills teaching package. Ideally, the teaching of social rules should also utilize the strengths from the behavioural paradigm. According to Volkmar & Klin (2000), ‘. . . verbal instructions on how to interpret other people’s social behaviour are often helpful, following explicit guidelines accompanied by repeated rehearsal and practice, initially in a rote fashion and gradually moving toward variations of the initial practice situations’ (p. 354). In other words, the newly learned skill or behaviour should be practised in a safe and comfortable setting (e.g. school or home) before testing it out in different contexts in the real world in the hope of promoting generalization.

In summary, by drawing on the various strengths of both the behavioural and cognitive approaches to teaching social skills, it is possible to outline the key elements which should be included in any new social skills teaching package. Ideally, the package should allow for the following:

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repetition of the target skill or task;
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rote learning of social rules;
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fading of prompts over time;
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verbal instruction/explanation of the social skill;
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a consideration of how one’s own behaviour impacts on others (i.e. understanding other minds);
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practice of skills in realistic settings;
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the ability to practise the skill across contexts;
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role-play of target behaviours;
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accessibility and ease of use for schools and teachers; and
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affordability for home and school environments.

Moving beyond a rule-based approach
Controversy surrounds the processes of typical development in social understanding. Some accounts posit that children acquire rules and principles for working out what people think (e.g. Wimmer et al. 1988; Perner 1991; Gopnik 1993). These accounts imply that teaching rules to people with autism should be sufficient to equip them with an understanding of the mind. However, competing accounts posit that we understand other minds not by applying rules, but by imaginatively adopting other people’s conceptual perspectives (e.g. Harris 1991; Gordon 1995). In other words, we use our imagination to set aside the world as we see and know it, and then mentally simulate a counterfactual state that can then be projected onto another person as their belief. The developmental grounding of a capacity for mental simulation could be in early pretence (Harris & Kavanaugh 1993), where children have an opportunity to practise what it is like to be other people and for imagining the world to be a different kind of place, i.e. pretence gives an opportunity for role-play, which is probably an essential ingredient in the mental simulation of other minds. Note that nobody teaches children how to pretend; rather, they gain insight into other minds as a consequence of the spontaneous activity of pretence.

Children with autism have little aptitude for pretence (e.g. Lewis & Boucher 1988), thus denying them an opportunity to role-play, with the knock-on effect that they have little prospect of being able to understand other minds through mental simulation. A way to compensate for this deficiency would be to help children with autism make judgements about mental states by applying rules, and as we have already seen, this can yield limited success. However, identifying a vehicle for promoting role-play might engender even greater success, especially if it nurtures a capacity for mental simulation. In short, people with autism might be impaired in their understanding of the mind because their capacity for pretence is disrupted where this denies them opportunities for role-play. So long as opportunities for role-play via other routes can be created, this would perhaps offer the best chance for people with autism to develop insight into the mind.

Virtual reality: New potential for social skills training?
This section outlines the nature of virtual environments (VEs) and their use in the field of cognitive rehabilitation, and considers how VEs could potentially encompass all of the successful features of behavioural and cognitive paradigms in one package, including the opportunity for computer-mediated role-play.

Virtual environments allow users to interact with a three-dimensional computer-based world incorporating impressive graphics and design. Users can move through a VE in real time using a joystick or mouse. They can interact with objects in the scene and are typically represented as a humanoid ‘avatar’. Thus, VEs can look realistic, and can include representations of people as well as objects. The growing sophistication of such applications has led to their successful use in various fields of cognitive rehabilitation, such as attenuating vertigo and flying phobia (Rothbaum & Hodges 1999), and helping children with learning disabilities to develop everyday skills; for example, catching the right bus and buying food in a supermarket (Brown et al. 1999). Indeed, VR applications are currently being used for many different populations, including people with spinal cord injury (Riva 2000), and children with visual impairments (Sanchez & Lumbreras 2000).

There has been considerable discussion about the relative merits of VR technology (VRT) in the fields of education and rehabilitation for different clinical groups (e.g. Editorial 1991; Andreae 1996; Cromby et al. 1996; Wilson et al. 1997, 1998; Jones 1998; Myers & Laenger 1998; Ring 1998; Scherer 1998). Most discussions tend to concentrate on motor disabilities, severe physical handicaps or more general learning disabilities. One benefit is that people with limited mobility can engage in activities in virtual space which they would not normally be able to participate in. Some ethical concerns surround the use of fully immersive VRT (i.e. the use of head-mounted displays). Head-mounted displays can be extremely expensive and people may experience ‘cybersickness’ in the form of nausea, headaches and dizziness (Cobb et al. 1999). Desktop VEs [those shown on a standard personal computer (PC), where navigation is achieved with a joystick] tend to be much less susceptible to the problems of cybersickness (Nichols 1999). Moreover, because the software can be used on standard PCs, desktop VEs represent a more accessible and affordable approach. Indeed, a recent project at the University of Nottingham, Nottingham, UK, developed a virtual physics lab in which secondary school pupils could complete experiments which they would not be able to run in the real world; for example, those involving radioactive materials. The virtual lab (RADLAB) was widely distributed as a CD-ROM to all secondary schools in the local education authority (Crosier et al. 2002). Another concern is that target populations are not usually included in the development of an application (Korpela 1998). This may lead to applications which are not optimal for the target group. User-centred design methodologies (e.g. Brown et al. 1999) address this concern somewhat because representative users are included in product design and development from the start.

The potential usefulness of VRT for the autistic population is already being recognized. Various authors have noted the possible benefits of virtual environments for people with ASDs (e.g. Clancy 1996; Trepagnier 1999). More specifically, one advantage of VRT is that the need for ‘real world’ social interaction is minimized, thus reducing this source of anxiety for people with autism (Moore 1998; Moore et al. 2000). It is important to stress that the idea is not for the VE to minimize social interaction per se, but rather, to allow the safe and non-threatening practice of particular skills in an educational setting.

There is concern that providing a safe, non-social environment on the computer somehow ‘colludes’ with the social disability of autism. For example, Howlin (1998) suggested that an over-reliance on computer interaction could lead to obsessive behaviour and a decline in real-world interaction. Latash (1998) also commented that ‘. . . VR may become too safe and too attractive so that the patient can become a computer addict and be reluctant to re-enter the real world’ (p. 105). Whilst this is an important issue, there are two main reasons why these worries may be unfounded.

First, it is likely that the main cause of obsessive behaviour in relation to computer use is the predictability of programming, i.e. the child finds the interaction appealing because they are in control and know exactly what is going to happen next. The incorporation of more flexible, unpredictable events in VEs might go some way to overcome this problem (see below). The child would not be able to use the computer in a passive way, but would need to think about the required response in order to proceed further. Consequently, the child’s interaction with the computer would be more active, less predictable, and therefore, less obsessional.

Secondly, a VE for social skills training would best be used in collaboration with other people. The aim is not to circumvent real-world social interaction altogether, but to provide a teaching aid that would allow practice and demonstration alongside normal input from a teacher or support worker. Thus, real-world social interaction can be incorporated by the presence of teachers and parents sitting alongside the person with autism (Murray 1997), as in the use of different desktop virtual environments (Neale et al. 1999). There is certainly some encouraging evidence from normal development to suggest that interaction with another person during the use of computer-based tasks significantly improves learning outcomes. For example, Mevarech et al. (1991) found that, when children worked in pairs on computer-based tasks, they were significantly more likely to demonstrate improvements in learning compared to children who worked individually.

This collaborative set-up would ensure that instructors provide verbal explanations of the target social skills as the user worked through the programme. The inclusion of tangible representations of mental states (e.g. thought bubbles) could facilitate this process by allowing users to consider other people’s mental states directly. Encouraging evidence indicates that thought bubbles can help children with autism pass false belief tasks (Parsons & Mitchell 1999), and also help adults with AS to consider the implications of thought during conversation (Rajendran & Mitchell 2000). Allowing users to see thoughts directly could help when trying to consider how the user’s own behaviour could be perceived by others in the environment.

The computer environment offers additional advantages. It is stable, familiar and predictable, and can be adapted to suit individual needs (Swettenham 1996). The amount, type and level of particular inputs (e.g. visual, auditory) can also be controlled directly, allowing basic skills and tasks to be completed in the absence of competing and distracting cues (Wilson et al. 1998). Perhaps the most important advantage of a VE, though, over and above the benefits of normal computer-based tasks, is that the user can role-play in an environment designed to simulate real-world scenarios. Thus, responses can be practised in realistic settings in the absence of potentially threatening and frightening real-world consequences. This is of particular importance because it means that responses to different scenarios can be practised before, during or after being taught. The computer-mediated role-play might present a vital opportunity for individuals to experience different perspectives, which, in turn, might nurture more general skills in mental simulation. Perhaps it could go some way to substitute for the lack of role-play experience that stems from the autistic impairment in pretence.

A further benefit of computer-based learning is that tasks can be repeatedly presented and practised in a consistent way without the fatigue sometimes associated with task repetition by human instructors (Cromby et al. 1996). The ease of repetition of the task could facilitate the rote learning of social rules in a specific context before moving on to allow practice of the skill in a different context. The possibility of developing different VEs designed to mimic a variety of social situations is a particular strength of this approach. In addition, different types of scenario could increase in complexity as the user becomes practised at, and familiar with, a particular type of task. For example, a café environment – in which the user has to order some food and find a place to sit down – could start off with lots of empty seats, but become increasingly populated and busy as the user moves through the programme. A bus scenario could work in a similar way, with increasingly fewer choices of empty seats. An increase in complexity could also work alongside a prompt-fading sequence, in which the user is initially provided with numerous prompts when beginning the task on a more difficult level, before the prompts fade gradually over time. Text boxes, verbal instructions and flashing red areas of interaction (e.g. the lock on a bathroom door) have been used very successfully as prompts in previous training packages for people with learning disabilities (Brown et al. 1999).

The possibility of scenarios differing slightly each time that the user encounters them could promote a more flexible style of responding. For example, behaviour demonstrated on a previous occasion (e.g. walking to a particular point at the bar to order a drink) may need to be changed slightly on a subsequent trial because of a small change in the environment (the same route to the bar cannot be taken because people are standing in the way). Thus, the user has to think of different ways of solving the same problem. As noted above, this aspect of the programming could help to guard against an obsessional use of the package and an over-reliance on the technology (cf. Howlin 1998). This hierarchical approach to developing social skills within a specific environment could then be repeated in a new environment, ensuring that the same skill could be practised across different contexts.

This aspect of task presentation could improve the chances of generalizing skills across contexts. In addition, the inherent properties of VEs may facilitate the crucial transfer of understanding from the virtual to the real world because of the shared features between virtual and real environments, in the form of realistic images and scenarios. Transfer of knowledge to the real world can occur after prior training with VEs, at least amongst able-bodied adults and children with disabilities (Wilson et al. 1996, 1997; Stanton et al. 2000), and for people practising a simple sensorimotor task (Rose et al. 2000). It remains to be seen whether successful transfer can be achieved in the realm of social skills training for people with ASDs.

Generally, there seem to be good reasons for thinking that VEs might be particularly useful for people with ASDs in the context of a social skills training programme. Perhaps most crucially, though, the promotion of both intra- and intercontext flexibility within a VE training package may allow us to tackle a very specific impairment in cognitive functioning common to many people with ASDs: cognitive flexibility. The following section summarizes some research on cognitive flexibility in people with ASDs and then examines the usefulness of VEs for addressing this particular ability.

Cognitive flexibility, autism and virtual environments
Cognitive flexibility is an executive function that requires frequent shifting from one response pattern to another. ‘Executive function’ is an umbrella term covering many cognitive abilities such as interference control, inhibition, integration across space and time, set-shifting and set maintenance, planning, and working memory (Pennington & Ozonoff 1996). People with autism have shown consistent deficits in executive function tasks (e.g. Hughes & Russell 1993; Hughes et al. 1994; Ozonoff 1995), although it is important to note that participants do not seem impaired across all aspects of executive function. Ozonoff & Strayer (1997) reported that people with HFA were not impaired in their ability to inhibit responses to stimuli. The same finding in a different group of participants with HFA was reported in Ozonoff et al. (1994). Perhaps most importantly, Ozonoff et al. (1994) also reported that, whilst people with HFA were not impaired in their inhibition of responses, they were significantly impaired in their cognitive flexibility relative to control groups. Cognitive flexibility also seems to be predictive of social skills development. Berger et al. (1993) reported that 17 adolescents with HFA were given a number of assessments, including social comprehension tests and a test of cognitive flexibility (or ‘shifting’; the Wisconsin Card Sort Test, WCST; Heaton 1981). After 2 years, their social understanding was measured again and cognitive shifting was the only significant predictor of improvements in social understanding. There was a negligible and non-significant relationship between intelligence and progress in social understanding.

This impairment in flexibility could be crucial in explaining why social situations are so difficult for people with autism. Every social situation is unique, and therefore, requires flexibility of responding according to the nuances of the situation. There is a marked lack of social reciprocity in autistic social interactions. This is evident in difficulties initiating and sustaining conversations (Howlin 1997), impairments in initiating and maintaining eye-contact (Mundy et al. 1994), and often, a failure to use gaze direction as a source of information about the communicative intention of a speaker (Baron-Cohen et al. 1997). Speakers may engage in long monologues about esoteric topics without allowing input from a listener, and seemingly without any consideration of the listener’s level of interest or knowledge state. In short, thinking seems to be rigid, with a difficulty in switching attention between objects, people or topics of interest (Pennington & Ozonoff 1996).

The requirement for flexibility in social situations is where the rule-based ToM approach to teaching social skills may falter. Indeed, Berger et al. (1993) suggested that impairments in cognitive shifting may be particularly difficult to overcome because ‘. . . self-initiated flexibility . . . can hardly be taught explicitly by means of highly structured educational programs’ (p. 356). One of the specific benefits of VEs is that they allow rules for responding to be taught in one context, and also allow the practice and role-play of behaviours across different contexts. In this way, flexibility can be encouraged by providing role-play situations in which the learned rule may not apply every time. It is possible that practising flexible responding in a safe and controlled environment might reduce anxiety in people with ASDs, enabling them to plan what to do next, rather than displaying repetitive, stereotyped behaviours, which may not be helpful in achieving their goal. Additionally, the role-play might itself promote development in mental simulation abilities, which is an approach to understanding mental states that is inherently very much more flexible than a rule-bound approach (Mitchell et al. 1996; Hulme et al. 2001).

Importantly, some evidence suggests that general impairments in cognitive flexibility can be attenuated by computer-based presentation of tasks. Pascualvaca et al. (1998) reported that children with autism performed as well as controls on a computerized version of the WCST, but significantly worse than controls on the standard, non-computerized version. The authors suggested that social/motivational factors could be responsible for the effect, i.e. children with autism might prefer to receive feedback about their performance from a computer rather than the examiner. This preference could lead to reduced motivation on tasks where feedback is only available from a human examiner. Ozonoff (1995) echoed this interpretation when discussing a similar pattern of results amongst her group of children with autism. Using a different clinical population (adults with traumatic brain injury), Chen et al. (1997) also reported significant improvements in their treatment group over time on a computerized version of the WCST (as well as other cognitive tests). Overall, these findings suggest that computer presentation of set-shifting tasks can lead to reduced impairment on this measure relative to non-computer-based tasks as well as improvements in flexibility over time.

Conclusions
Overall, there seems to be an encouraging basis from which to develop a new approach to social skills training for people with autism. Virtual reality technology is an exciting tool that can accommodate the strengths of previous social skills intervention strategies, and also extend the possibilities for learning by allowing flexible responding to be practised in a safe and supportive environment. In addition, VEs may facilitate the transfer of knowledge between the virtual and the real world, a crucial consideration in any attempt to teach social skills.

Concerns that the use of computer-based technology might collude with the social disability of autism, rather than improve social understanding, are assuaged somewhat by the adoption of collaborative working practices (i.e. a teacher/parent/carer sitting alongside the person using the program) and built-in flexibility that ensures that programs remain unpredictable. In other words, VEs should be used to augment teaching practices rather than replace them.

The proliferation of new technologies is exciting because of the opportunities which they offer to different clinical groups in need of very specific kinds of help. Whilst the use of VR is not promoted as a panacea for these problems it does, nevertheless, provide a novel approach to social skills training for people with autism. Over and above the appeal of novelty, VRT allows us to target the specific realm of cognitive flexibility – an area of functioning which may not be amenable to investigation by more traditional approaches, such as story-telling and the presentation of pictures or photographs. Virtual reality technology might also offer a valuable opportunity to practise role-playing skills, which could have both practical and cognitive benefits. Only by exploring new ways of tackling the problem of social skills training for people with autism can we hope to gain further insights into what might be possible for intervention and training purposes. Virtual reality technology provides a unique viewpoint on this issue and should be welcomed, albeit with careful consideration.

Acknowledgements
This paper was supported by a grant from the Shirley Foundation. We are grateful to Anna Moore and David Moore for their comments on an earlier draft. Thanks also to the AS Interactive project team at the University of Nottingham.

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Aptos psychologist: Asperger’s or Non-Verbal Learning Disability? An example of Peter…

Nonverbal learning disability (NLD), compared to Asperger’s Disorder and PDD-NOS using a clinical example of a young man, Peter, who thinks he is neurologically defective. What is the best fit diagnosis? Most appropriate treatment?

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written by Cameron Jackson DrCameronJackson@gmail.com

Does Peter — this is a hypothetical clinical case — suffer from NLD or Asperger’s Disorder or PDD-NOS? So some combination? What is the best fit? Many of the facts are true however names and identifying information has been changed to protect privacy.

Remember the children’s verse: “Peter, Peter, pumpkin eater… had a wife and couldn’t keep her… so he put her in a pumpkin shell… there he kept her very well… ”

It certainly was socially inept of Peter to keep his wife locked in a shell….Was that the best that Peter could do?

Non-verbal learning disability (NLD) was much talked about 10 years ago. Maybe because NLD never made it into in the Diagnostic and Statistical Manual (DSM-IV) it’s only known in certain circles.

In some ways NLD is similar to 298.0 Asperger’s Disorder — which is a diagnosis in the DSM-IV.

Many people somewhat approximate the diagnosis that are in the DSM-IV. The issue is to find the best fit.

Let’s see what is the best diagnosis for Peter. A number of facts are changed to protect privacy. Let’s see whether Nonverbal Learning Disability (NLD) or Asperger’s fit as a better fit for this young man.

Peter — not his real name — is in his middle 20’s. He went to private schools in Santa Cruz County and finished at an alternative high school. Both his parents finished college and work professionally. Peter is an only child.

From his father for years he heard, “Just step up to the plate… you can do it… Try harder…” Yes, Peter has low self esteem.

Per comments from his teachers, Peter has always had problems with organization and finishing assignments. Sometimes he failed classes in high school as he did not turn in assignments. He teachers comment on his high language abilities and creativity.

Peter was never identified for special education. In 8th grade the resource teacher sent his parents a letter saying that he did not have a learning disability. As it was simply a letter sent to the home there was no one to one discussion with the school psychologist.

Had there been a school meeting, a psychologist would have noted that there was a huge, larger than 45 standard scored difference, between visual abstract reasoning ability and general academic performance. A 15 point difference is statistically significant and important. So here Peter has a 45 point standard score difference between visual abstract reasoning abilities and general performance and has no learning disability? Of course he has and did. It was not identified however in 8th grade.

Because there was no meeting of psychologist and family in 8th grade Peter’s disabilities were not identified. That Peter has extraordinary high visual abstract reasoning abilities as well as very high verbal reasoning abilities lessens the likelihood that Non-verbal Learning Disability best describes Peter’s difficulties.

Peter has heard for many years, you can do it… just step up to the plate….you’ve got great talent.

Peter is not convinced that he can do it as he flunked out of college. He had to take and pass a particular class. Having flunked it once he went back to the same instructor, the same lectures, the same assignments. How to apply certain skills to improve him portfolio was the task he flunked before. And — as you might guess — he flunked it again. And then he flunked the same class a third time. Clearly there was no academic advisor available to recommend a different strategy to getting a pass in the required class.

Peter started college at age 21. Before going to college he got some tutoring from a Santa Cruz tutoring organization. It is my understanding that this tutoring organization lacks psychologists on staff and does not use diagnosis. So, again, similiar to 8th grade, his family did not have input into Peter’s disabilities based on psychological assessment.

It does not appear that there were any accommodations put in place to assist Peter to succeed in college once he got there. Peter was across the U.S. in a different state. He had never had an IEP and he had never been identified as having developmental learning disabilities.

What is Peter good at doing? He can tell oral stories. He can write stories. He does have difficulty finishing the writing of stories. He does better with the structure of a class to finish a story.

The purpose of diagnosis — after getting the best fit diagnosis — is the suggest appropriate treatment. It looks like NLD is not the best fit diagnosis for Peter.

However, Peter has heard from one parent for many years that he has NLD. Probably based on these discussions, Peter thinks that hi is neurologically defective. One step in treatment is to change the mind set of Peter to view himself as neurologically different not neurologically defective. Web sites such as Wrong Planet.net may assist Peter to view his differences in a positve way.

Per the article included below NLD is due to traumatic brain injury of the right side.

The following was found by Google to nonverbal learning disabiliites and was written around 2000.

Success for Young Adults with NLDBy Kathy Allen

“NLD (Syndrome of Nonverbal Learning Disabilities) is a complex disorder of the brain that causes wide-ranging effects on the day-to day functioning of young adults in work and college.

The most likely cause for this disorder is a congenital or traumatic injury to the right brain. This is the location of the majority of the long, mylenated fibers which are the “highways” of the brain. The right brain takes care of many diverse functions such as planning, organization, social interaction, maintaining mood, and coordination.

Although each individual is affected differently, this disability generally impacts a young adult’s ability to organize schedules, carry through on tasks which require multi-step planning and follow-through, and deal with changes in time and place. Difficulty with subtle nonverbal cues are also common in most NLD students. NLD often causes high anxiety and impairs the fluid use of socially correct language. Double meanings, sarcasm, and polite white lies are all difficult for these young adults.

Many of these students are very bright academically, and it is easy for professionals and teachers to be confused or annoyed by the gap between their high academic skills and their poor organizational abilities. Unlike blindness or other sensory disorders, this disability is invisible. While students with cerebral palsy are routinely provided with note takers or computers,it is very difficult for college students with NLD to receive services. Frequently, these students are told they are irresponsible and should just try harder. But since NLD is a serious condition, the student is only able to achieve success when specific interventions are in place. Without help, students can become crippled by anxiety and shame, frequently dropping out of school and developing severe psychiatric problems. With these interventions, many students succeed in work and school.

The methods used are neither complex nor expensive, but they do require a radical change in perspective. First, professionals must be educated about the disability. This will lead to the understanding that right-brain injuries are real, although invisible, and pose a great challenge to the student. Counselors must be positive and affirming, and let the student know that they are a team who will work together to find strategies and support for the student. Young adults with NLD are so used to school and work authorities who are frustrated with them that even this simple change in perspective can be very powerful. Having an informed, helpful person to aid in the student’s problem-solving is crucial to student success. Given the time constraints that many professionals and teachers face, a question often asked is, “How can I achieve a basic understanding of NLD?”

There are excellent articles available at www.NLDline.com or www.NLDontheweb.org However, a model I use with students may be useful in seeing how the condition impacts day to day living.

(Here I insert the model with the island in the middle with the palm trees, and grass hut, then other concentric circles that get into the area of comfort like words about facts, predictable safe people, routine and structure. Outside of that are the circles with time and spaces that change, unpredictable people, ideas about theoretical people.)

From this model, it can be seen that the student with NLD is most at home in the world of words about unchanging, intellectual facts. Students enjoy and excel at learning the vocabulary and rules about everything from physics to computer games. This ability is a mixed blessing, as our society often defines people with large vocabularies as being very bright and capable in all areas. Instructors and counselors may be surprised and indignant when NLD students do so poorly in organization and time management, forgetting deadlines, appointments, and changes in class time. We know from experience that most students with NLD will do best in classes or jobs that have a heavy emphasis on facts, memorization, and a built-in schedule. Classes in which the bulk of work is done in class are especially successful, such as writing workshops, labs, or practicums which use special equipment. This is because the class itself provides the structure for the student.

Predictable, accepting people are also near the area of comfort, and from this we see that students/workers find it easiest to succeed if they deal mainly with these types of people. Most students with NLD suffer from a great deal of anxiety due in part to the disorder and in part from their inability to read faces and nonverbal language with ease. NLD students should have access to instructors and counselors who will be accepting of the fact that the student may need accommodations.

Just outside the comfort zone are ideas and inferences about facts. We can see that critical thinking may challenge students a little more. Drawing conclusions, solving problems that are written or presented in a different way than they were taught, and some aspects of inferential thinking may be more difficult than one would expect. Symbolism in novels, stories, and poems can be quite difficult for these students.

Moving further outside the zone of competence, we see that issues of time and space will pose challenges for the student affected by NLD. It may take anywhere from a several days to a few years for a student to navigate around the college or large work area. Support staff can help offering an escort to help point out and write down landmarks, a “script” of where to go, while some students with NLD will use a map.

It is equally difficult for our students to cope with time. Time is simply not a concrete fact that can be seen or touched, so it has little reality for these students. Regular appointments for work meetings or office hours are preferable to those which change. Use of an appointment book is very helpful. Ideally, a student will be shown several different ways to keep track of appointments, rather than only one. For important appointments, an e-mail or phone call from a counselor or coach can be a great first step. After a few weeks, the student can call the coach as a check-in that he/she remembered the appointment. It should not be assumed that the student is unmotivated based only on ability to be present at an appointment, as this is a part of the disability.

Far outside the comfort zone, (near the alligators!) we find unpredictable people and those who are ignorant of the impact that NLD has on a student. “Unpredictable people” for NLD students, are those who moods or disposition alter quite a bit from day to day, those who have a very neutral face with little expression, or those who raise their voices at unexpected times. This can be very stressful for the student. If the unpredictable person is accepting of the student, however, most students can eventually learn to cope with this type of person.

The greatest problem for students with NLD are people who are know nothing about NLD and are aggressive or hostile toward the student. Many are sure that the student has just been overprotected and needs to deal with the “real world”. While “tough love” works with some students, it rarely does with the NLD student. They misread “tough love” as meaning the employer or instructor hates them, and they rarely understand such vague concepts as “pull yourself together”, or “grow up”. Instead of making positive changes, they are flooded with anxiety.

It would be best for students to avoid this type of person if possible. If not, the student should go with an anchor person who can help with the situation. Role plays in which the student successfully explains the disability to a sympathetic listener, even by initially giving an information sheet about NLD and answering questions, should be extensively used first. This can be followed by explanations to an sympathetic adult (such as an instructor) in a real life setting. Only then should role plays toward a person with a more negative mindset begin.

NLD students have so often been told, “You ought to know that by now!” that they are very hesitant to seek help. It will help to tell the student that you will not shame her for asking “stupid” questions. After an explanation, have them explain the work assignment back to you. It’s useless to say, “Do you understand?” when a student isn’t sure what he or she might be missing.

Finally, for many students, one of the most difficult things in college or work is to make a hypothesis about the imagined behavior of people not personally known to the student. This struggle is seen in work when young adults deal with the general public, especially with frustrated customers. It’s also seen when students try to respond to questions in literature classes. Tutoring may be helpful here, as are templates for writing. In the same way, a worker should receive clear directions about how to handle people related problems. The more detail offered, the better the results will be.

Key strategies in helping the student will include:

· Understanding NLD

· Using student’s strengths in memory and rules to offset other problems

· Providing extra help in management of time and organization

· Use predictable, accepting people to problem solve solutions.

· Emphasize self-advocacy through scripts and role play

· Offers of help develop systems for student to track appointments

· Understand that the student is hesitant to ask for help.

· Offer tutoring for written assignments, especially novels or stories which involve complex characters and symbolism.

There are many other ways to help, including low and high-tech aids, but they are beyond the scope of this article. Although the focus here has been on the young person’s challenges, NLD young adults also have many wonderful traits such as persistence, reliability, honesty and a desire to succeed. Helping them to use their strengths to compensate for their problems is the key to success.

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Aptos, CA psychologist: Big change coming in how autism is defined. Asperger’s merges under autistic spectrum disorder. Are changes in diagnosis helpful?

Aspies as a clinical condition ceases to exist in the DSM-V. How do Aspies think about the proposed changes in the definition of autism? Not included in the proposed definition is the level of severity in functional abilities.

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Big changes come in 2013 with publication of a new, updated Diagnostic and Statistical Manual (DSM-V). One category which changes considerably is autism.

One wonders how Aspies view the proposed changes. Aspies by definition are not as severely afflicted. Their special category evaporates under the new diagnosis of autism. Aspies as a diagnosis will cease to be. However, their affliction will still exist.

What defines Aspies? Often they are referred to as “little professors”. They know a great deal about a few subjects. Talking for Aspies is not a conversation but more like a monologue. Aspies often are precocious at language and may appear gifted. Aspies have difficulties reading human social signals. They often have extraordinary gifts. Some people describe Aspies as perfect counterfeit bills. Their social interactions frequently are a disaster.

Whereas in DSM-IV Autistic Disorder is the most severe condition and PDD-NOS less severe followed by Aspergers, in DSM-V there will be one description titled Autistic Spectrum Disorder or Autistic Disorder.

One thing missing from the proposed definition for autism is how to quantify the degree that the person is handicapped. As the number of persons with ASD balloons, more care must occur in determining the degree of impairment.

One defining characteristic of the new definition for autism is “failure to develop.. peer relationships…” Does failure mean zero, zip, no relationships? In contrast, Aspies can and do have one way relationships and they seek relationships. Aspies have substantial difficulties making successful relationships happen.

Another characteristic of DSV-V autism is “lack of social reciprocity…” Lack means zero, zip, no social reciprocity.
Below is the proposed new definition of autism:

Autism Spectrum Disorder per the DSM-V
Must meet criteria 1, 2, and 3:

1. Clinically significant, persistent deficits in social communication and interactions, as manifest by all of the following:

a. Marked deficits in nonverbal and verbal communication used for social interaction:

b. Lack of social reciprocity;

c. Failure to develop and maintain peer relationships appropriate to developmental level

2. Restricted, repetitive patterns of behavior, interests, and activities, as manifested by at least TWO of the following:

a. Stereotyped motor or verbal behaviors, or unusual sensory behaviors

b. Excessive adherence to routines and ritualized patterns of behavior

c. Restricted, fixated interests

3. Symptoms must be present in early childhood (but may not become fully manifest until social demands exceed limited capacities)

Below is a story of an Aspie father and Aspie son…
This was published in the New York Times about ten years ago:

The Little Professor Syndrome They talk like adults and often have sky-high I.Q.’s, but their social skills are nonexistent. Can kids with Asperger’s syndrome, a recently diagnosed form of autism, harvest their strange talents in adulthood? By LAWRENCE OSBORNE
Asa Snyder at home. Around a circular classroom table, five 6-year-old boys are drawing pictures of blue whales with crayons. Mozart’s “Requiem” pipes away on a nearby cassette player; by the window, a group of sunlit bean-bag chairs looks inviting. One of the children, Asa, is turning out a waxy masterpiece with the meticulous care of a jeweler. The fins and tail of Asa’s whale, who is jumping out of the water, have been drawn with striking precision; a dialogue bubble percolates from its mouth. “Wow!” the whale is shouting.

“Look at him — he’s psyched,” the bespectacled Asa says in a curiously expressionless voice. “He’s so happy to be out of the water and turning double somersaults that he can’t stop talking.”

The teacher, Lauren Cacciabaudo, asks each boy how he has managed his day.

“How was your sitting, Henry?” she says to one boy.

“Three,” little Henry says, giving himself a grade from 1 to 3.

“Nice sitting, Henry! How about focusing, Jean Paul?”

“Three.”

“Nice focusing, Jean Paul. What about looking in the eye, Asa?”

“Three.”

“Nice eye contact, Asa!”

More Information on Asperger’s
Online Asperger Syndrome Information & Support

Yale Child Study Center

New York Autism Network

Further Information from The Center for Study of Autism
These sites are not part of The New York Times on the Web, and The Times has no control over their content or availability.

Glued onto the surface of the classroom table are pairs of cut-out handprints. Frequently, Cacciabaudo asks the boys to put their hands on these prints and keep them still. For there is a flitting energy of restless birds about these boys, even though not one of them looks up to inspect the stranger sitting in their midst. Instead, they fixate on a colorful pencil I have just bought at the Guggenheim gift shop. Bright green, it sports an elephant’s head with felt ears on a mountable spring. The boys are mesmerized.

“Where did you get that?”

“How old is that elephant?”

They bounce the elephant’s head back and forth, sticking their fingers into its grasping mouth.

“It’s prehensile!” Asa coos.

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Lawrence Osborne is a frequent contributor to the magazine. He last wrote about bacteriophages.

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At first glance, this brightly decorated room is no different from that of any other elementary school. Shelves are filled with storybooks; on the chalkboard, a vertical line of words reads “prudence,” “pretzel,” “prairie,” “purple.” But the nervous agitation of the boys’ hands, punctuated by occasional odd flapping gestures, betrays the fact that something is off kilter. There is also a curious poster on one of the walls with a circle of human faces annotated with words like “sad,” “proud” and “lonely.” When I ask Cacciabaudo about it, she explains that her students do not know how to read the basic expressions of the human face. Instead, they must learn them by rote.

he boys in this Manhattan classroom, part of a special education school run in association with the New York League for Early Learning, all have a mysterious condition known as Asperger’s syndrome — a neurological disorder that disproportionately affects males and is often connected to a striking precosity with language. The Learning Disabilities Association of America defines Asperger’s syndrome as “a severe developmental disorder characterized by major difficulties in social interaction and restricted and unusual patterns of interest and behavior.” Although sufferers display behaviors associated with autism — monotonic speech, social isolation, a paucity of empathy — they are not mute or incapacitated. Indeed, the outsize vocabularies of children with Asperger’s often make them seem less disabled than gifted. In the United States, the syndrome was only made official among psychologists by entry into the D.S.M.-IV, or Diagnostic and Statistical Manual of Mental Disorders, in 1994.

Asa Snyder, Henry Goldsmith and Jean Paul Stiller doing their best to pay attention at school.
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The precise relationship between Asperger’s and autism remains to be untangled. Dr. Richard Perry, a child psychiatrist at N.Y.U. Medical Center, argues that Asperger’s syndrome shares a basic triad of dysfunctions with autism: problems with social interaction, with communication and with play. Both types of children, he says, have perplexing difficulties in “reading” human social signals like facial expressions and dealing with the nuanced to-and-fro of ordinary conversations. “For some reason we don’t yet fully understand,” he explains, “Asperger’s kids cannot decipher basic visual social signals. This leads people to see them as emotionally disturbed.”

Or brilliant. For the flip side of this somber picture is a recognition that Asperger’s sufferers may also have extraordinary gifts. Consider Glenn Gould. The eccentric Canadian pianist, who died in 1982 and who retired from the concert circuit at age 31, was notorious for his bizarre behavior: he had a phobia about shaking hands, ate nothing but scrambled eggs and arrowroot biscuits and rocked incessantly at the keyboard. At the same time, Gould’s obsessive focus and prodigious memory helped give his legendary renderings of Bach their burning intensity. Might Gould have been an Asperger’s sufferer? Timothy Maloney, a musicologist who manages the Gould archives, suggested precisely that at a recent academic conference.

Others scholars have retroactively applied the Asperger’s label to oddball intellectuals ranging from Vladimir Nabokov to Béla Bartok to Ludwig Wittgenstein. Nabokov’s hypertrophied vocabulary and obsession with butterflies, some say, may qualify him for the disorder (though an equally focused obsession with nymphs seems somewhat less incriminating). Such claims may be dubious, and probably infuriating to lepidopterists, but the argument is seductive to many: could the very qualities that make Asperger’s people so strange lie at the root of their peculiar talents?

This sense of potential explains why kids with Asperger’s are being grouped together in special-ed classrooms. “If you look at these children, you can see at once that they don’t have classical autism,” says Jeanne Angus, director of the New York League school, who stops by Cacciabaudo’s class for a visit. “They’re normal in so many ways. They’re often very sweet. And they’re often amazingly precocious, with sky-high I.Q.’s. But look closer and you’ll see cracks. Many of them have had appalling difficulties in the regular school system.”

Scholars have retroactively applied the Asperger’s label to oddball intellectuals ranging from Glenn Gould to Vladimir Nabokov.

Those difficulties include temper tantrums and erratic behavior that can unnerve the most strong-willed teacher. Angus nods toward Asa. “When he first came here, he would roll around the floor all the time, just to get a feel for its texture.” The boy had no idea that this was inappropriate. “The thing is,” she goes on, “everything has to be taught to them — everything. When you ask them at first, ‘How do you do?’ they will say something like, ‘Why do you want to know?’ They simply don’t understand social games.”

It is an impression of anarchic solitude that is often reinforced by the tendency of Asperger’s children to have obsessional interests. Angus tells me that Michael, one of the boys in the class, had a fixation with tornados when he first arrived at the school. “He knew everything about them. The statistics, the G forces, the wind velocities. He was like a videocassette about tornados, which he could rewind and play over and over. He was using technical terms I’ve never even heard of. And he was 5!” Michael also behaved like a tornado, whirling round the room and tearing everything up.

Other children have sometimes bizarre fixations. They will memorize entire TV shows and recite them over and over (an ability known as perseverative scripting). Other times, they specialize in memorizing everything there is to know about the oddest things: deep-fat fryers, telephone cable insulating companies, the passengers on the Titanic, exotic species of cicadas, the provincial capitals of Brazil. In one documented case, a child memorized the birthdays of every member of Congress.

Needless to say, these obsessions are deeply unsettling to parents. “Just imagine,” says Fred Volkmar, a child psychiatrist at the Yale Child Study Center, which is conducting the nation’s largest research project on Asperger’s syndrome. “You walk into a hamburger joint and your 5-year-old suddenly points at the fryer machine and cries, ‘That’s a Sigma Model 3000!’ What do you say?” It is a confusion that is compounded by the linguistic precosity of Asperger’s children. “Up to the age of 3,” Richard Perry says, “Asperger’s syndrome and autism are very similar. But then the former begin to talk. And how!”

Unlike the linguistically impaired autistics of the type depicted in the movie “Rain Man,” Asperger’s children talk like little professors. “They seem brilliant because they have this language,” Volkmar says. “But in reality, it’s fact-obsessed, fact-oriented. It’s rigid and insular. It’s not a social brilliance. Usually, their social interactions are a disaster.”

And according to Perry, this has been precisely the predicament of Asperger’s children in the past. “Frequently,” he says, “they have been misdiagnosed because they’re almost normal. They almost blend in, but not quite. That’s their tragedy.”

“They are,” says one parent at the Manhattan school, “perfect counterfeit bills.”

This baffling syndrome was originally diagnosed a half-century ago by the Austrian pediatrician Hans Asperger. In 1944, Asperger published his postgraduate thesis, “Autistic Psychopathy’ in Childhood,” which described many of the symptoms of the syndrome and ascribed a genetic basis for them. But Asperger refused to label children with a heavy psychiatric hand. Autism, he argued, was not a straightforward fate; the condition could be ameliorated through “pedagogical methods.”

Working in Nazi Vienna, Asperger was surely aware of the prospect of many autistic children being sent to concentration camps after being labeled mentally retarded. Thus, he ended up creating a more optimistic picture of the disorder than the vision of crippling disability that the psychiatrist Leo Kanner had described in his groundbreaking analyses of classical autism, first published in 1943. Asperger and Kanner mapped out two different ends in the spectrum of autism: the Asperger end was distinctly sunnier, with the possibility that such “high end” autistic children could thrive and even be gifted in their way.

After World War II, Asperger’s subtle contributions were temporarily lost as the center of gravity in child psychology moved from the German-speaking to the English-speaking world. Only in the 1970’s was Asperger’s research revived by a British researcher named Lorna Wing at the Medical Research Council in London. Along with her collaborator, Judith Gould, Wing set out to study autistic children in the London borough of Camberwell.

After a few months, Gould and Wing began to realize that the social problems of autism could be manifested in highly divergent ways. “For example,” Wing says, “instead of being socially aloof and indifferent, the classic autistic picture, some children made active social approaches to others, but in a nave, hopelessly inappropriate way.” Instead of having no language or stunted language development, some children had perfect grammar and a huge vocabulary. “Even so,” she continues, “they used this to talk on and on in a monotonous way about pet subjects.”

Asa with his parents, Lise Varrette and Philip Snyder. The elder Snyder was recently told that he, too, has Asperger’s.

Wing began to see a link between the children she was studying and the symptoms described by Asperger back in 1944. But unlike Asperger, who had believed in a clean distinction between autism and “his” syndrome, Wing saw the two as shading into each other. “We developed the idea of a very wide spectrum of autistic disorders, of which Asperger’s was only a part.” Wing published her findings in 1981 in the journal Psychological Medicine. At last, Asperger’s syndrome, the hyperverbal realm of autistic experience, had entered the realm of official psychiatry. “I felt,” Wing recalls, “like Pandora opening the box.”

Currently, the Yale Child Study Center is working with 900 families nationwide to produce the first empirical diagnostic for Asperger’s syndrome. One of its directors, Ami Klin, says that it was only seven years ago that Yale researchers began tracking socially isolated children who did not fit the profile for classic autism. “Cognitively, they were quite good,” he says. “But socially, they were disabled. They fell between the cracks.”

Asperger’s children, Klin feels, are unique. “Classic autistic people,” he says, “are bad at language, good at images; with Asperger’s people, it’s exactly the opposite.” Yet efforts to produce a cast-iron definition of Asperger’s has been difficult. Scientists involved in the Yale study are mapping out chemical reactions in the brain as it tries to decode faces and exploring abnormalities in “eye tracking” — the reaction of the human eye to social signals. This research may provide a way of pinpointing Asperger’s suffers. “But it will take time,” Klim cautions.

This diagnostic uncertainty makes it extremely hard to know exactly how many people suffer from Asperger’s. A 1993 study reported a prevalence of 36 per 10,000 children, while a 1999 paper reported a rate between 2 and 5 per 10,000. (The male to female ratio is at least 5 to 1.) Since Asperger’s entered the D.S.M., the number of students in U.S. elementary schools found to have some form of autism has soared by 154 percent to around 35,000, an increase attributable in part to Asperger’s awareness. Indeed, Asperger’s advocates tout figures as high as 1 per 250 of the general population, though this is most likely an exaggeration. Yet because Asperger’s sufferers usually manage to get by in the world, it is indeed possible that someone we know — someone previously dismissed as a bookish outcast — might suffer from it.

lightly built, with closely cropped black hair, glasses and a jittery manner, Philip Snyder is a 36-year-old aspiring actor who grew up in Berkeley, Calif. Only recently told by doctors that he suffers from Asperger’s, Snyder has spent his entire life in a state of bemused noncommunication with the rest of the world.

“I studied acting at Harvard,” he says resignedly, “but they threw me out because I was so rude to the other students. Of course, I had no idea that I was being rude. I thought I was actually being nice. But that’s the story of my life: one long non sequitur.”

Phil is the father of Asa, the boy who admired my elephant pencil. We are sitting in Starbucks on East 87th Street with Asa and Phil’s wife, Lise, from whom he is separated. Asa and Phil are telling each other about their nightmares.

“I saw my room collapsing,” Phil says.

“That’s cool,” says Asa. “Were you scared?”

“Very.”

“Do you have a lot of nightmares?” I ask Asa.

“I can’t sleep much,” he replies. “My mind doesn’t stop.”

Phil met Lise while they were both waiting on tables at the Vienna Cafe in Los Angeles. “I always knew he was a little odd,” Lise laughs. “But I was drawn to that very quality.” Their relationship soon grew troubled, however, and she left him while pregnant with Asa. “Phil and Asa,” she adds affectionately, “are very similar. They can tell you how to get to the moon, but not to their own rooms. I think Phil would agree with that.”

“Oh, yes,” Phil sighs. “It’s pretty bad.”

With his round-frame glasses and high voice, Asa is adorable enough to draw attention from doting granny-types around us. “I like Mary Poppins and Roger Rabbit!” he cries to one of our neighbors. “I’m going to be a director and a dentist.”

“And what do you like about Mary Poppins?” she says.

“Supercalifragelisticexpialidocious,” comes the reply.

“Ah.”

Asa was always verbally adroit, his parents recall; he spoke his first words at 7 months. At the same time, however, potty training and learning to get dressed were arduous chores. Asa also suffered from a common Asperger’s affliction known as auditory hyperactivity, meaning an inability to tolerate noise; he used to sit through entire movies with his hands over his ears. Asa also suffered from irrational fears, scared even by the popping of soap bubbles.

“Almost from the beginning,” Lise admits, “I knew that Asa was different. My conversations with him aren’t like normal adult-child ones. Instead, Asa fires off research questions. He never goes in for small talk of any kind. There’s no reciprocity or bantering trivia. He’s too focused. With him, talking is not really a conversation.”

Asa was always rather philosophical, too, Phil adds. “During his second birthday party, he came up to me and said, ‘I’ll never be 2 again.’ It reminded me so much of myself. Sometimes he would say simply, ‘I feel so alone.”‘

Tellingly, Phil identifies closely with Glenn Gould. He listens to his recordings constantly. I wonder, indeed, if Gould has not become something of a hero among Asperger’s sufferers, proof that the diagnosis is a blessing as much as a burden. Phil sees much of Gould in Asa, as well. Asa has also taken a shine to Gould and his music, although he oddly insists on referring to the pianist as “Mr. Ratburn” (a cartoon character on one of Asa’s favorite TV shows).

Asa also has an imaginary friend called Ehe, who is a brilliant inventor. Ehe, in short, shares Asa’s consuming interest in all things scientific. Ehe “shows” Asa how to draw diagrams of atoms so precise that they include neutron clusters and orbiting electrons. Asa’s own insights are sometimes worthy of Ehe: the previous night, says Phil, his son calmly informed him that written numbers were fast, whereas spoken ones were slow. Asa is similarly fascinated with black holes and likes to say that a human entering one would be “stretched like spaghetti.”

Inspired by the example of Gould, Phil clearly regards Asa as having his own Asperger’s intellectual vector, one that should be respected. “If you ride a wild elephant,” he is fond of saying, “you go where the wild elephant goes.” Indeed, he feels that the ability of an Asperger’s person to synthesize information in novel ways will eventually work to Asa’s advantage. “Society,” he says hyperbolically, “will actually become more and more dependent on people with Asperger’s to usher it through the difficulties ahead.”

Nevertheless, Asa has had his share of problems in the regular school system. He started out at P.S. 198 on the Upper East Side, until those problems became too much. “At first,” Lise confesses, “I didn’t want to admit to myself that he might be ill.” One telltale difficulty was Asa’s refusal to do the school fire drill. “He simply couldn’t grasp the concept behind it, that you had to pretend there was a fire when there wasn’t one. He’d say, ‘Is there a fire or isn’t there?”‘ Asa’s stubborn refusal to follow the imaginary logic of fire drills earned him time out. “It was a blow he never got over,” Lise says.

Perplexed, school officials suggested that he needed therapy. But what kind? Since Asa had not received a diagnosis of any official disorder and because he was not obviously abnormal, the school simply allocated him a posse of specialists: a communication therapist, a socialization therapist, a physical therapist and a speech coach. The quartet followed Asa around during his school day. “Needless to say,” Phil says, “they made him feel 10 times more abnormal than he had before.” Asa himself called them “the shadows.”

Eventually, Phil and Lise rebelled; they argued that Asa was gifted, a special case rather than a problem child. The school disagreed. “We were told,” Lise says, “that he couldn’t get into the program for gifted children because he was ‘quiet.’ Quiet? Since when is a kid singled out for being introspective?”

Only at the private New York League school, Lise adds, has Asa really flourished. The school’s STAR program (Social-Emotional Training and Academic Readiness) aims not to drum every Asperger’s characteristic out of the children’s heads but simply to help them control the more outwardly disadvantageous ones, enabling them to survive in the social jungle. Jeanne Angus explains that in the regular school system the emphasis is on “inclusion” — that is, lumping Asperger’s children with everyone else and hoping for the best. “It doesn’t work,” she says. “We feel that we need to get to the Asperger’s children as early as possible in order to get through to them.” They are, she goes on, usually unhappy and isolated in normal school, whereas in the tiny classes provided by a specialty school like hers, they are among peers who share their problems. “When we teach them the facial expression charts here, they are all learning the same thing,” she says. “When we make them focus and maintain eye contact, they all have to do it. It doesn’t make them feel abnormal.” The school recognizes that, with patience, Asperger’s children can at least learn to imitate social behavior that other kids learn intuitively. “We take it slowly, rather than forcing them to conform to what neurotypical children can do,” Angus says.

The school day is broken down into small periods in which socializing is strongly emphasized; even lunch breaks have structured conversations. Angus has seen Asa’s progress firsthand. “When he first came to this school,” she remembers, “he would clasp his hands together and jump up and down all the time. It’s typical self-stimulation that we see in a lot of Asperger’s boys. But he’s calmed down a lot.”

Asa’s experience is one that most Asperger’s parents can easily sympathize with. Echo Fling, the president of the Asperger’s Syndrome Coalition of the United States, is also the mother of an Asperger’s child. Her new book, “Eating an Artichoke,” chronicles the struggles of getting her son Jim’s ailment correctly diagnosed and then him eased onto the right pedagogic path.

“Because it wasn’t on the books until 1994, even getting diagnosed was a nightmare,” she says. “And Jim always seemed very precocious. But then he’d use memorized dialogue from movies to converse with people, and if you didn’t know the movie, you’d find it awfully strange! And he was so stoic, so seemingly emotionless. Give him an umbrella and a cigar, and he’d be a perfect mini-Winston Churchill. He had to be taught what a smile means.”

Recalls Phil: “I was always the cleverest kid in English, but I practically flunked college. I was always inventing personae for myself. One month I’d be Groucho Marx; then I’d be Sherlock Holmes. I was trying to find a character who people would like, but it never worked. Eventually they called me Mr. Peabody, that pedantic little talking dog!”

“What about Mr. Ratburn?” Asa pipes up, eyes twinkling behind his rather professorial wire frames.

“Yes, he’s a great character, isn’t he?”

“Personally, I’d rather be Roger Rabbit,” Asa says matter-of-factly. “Roger Rabbit can dance.”

urious about the kind of adults that Asperger’s children eventually become, I decide one night to drop in on the monthly Asperger’s parents’ meeting held in a social-services center on West 65th Street. Although most of the people here are frustrated parents of children who cannot find affordable targeted schooling, there is also a smattering of Asperger’s adults who show up to offer solidarity or to meet one another. I am not sure, however, quite what to expect.

I recall a haunting passage I have read recently in the American Journal of Psychiatry in which a 11-year-old Asperger’s boy tries to describe himself. He writes: “I am an intelligent, unsociable but adaptable person. I would like to dispel any untrue rumors about me. I am not edible. I cannot fly. I cannot use telekinesis. My brain is not large enough to destroy the entire world when unfolded. I did not teach my long-haired guinea pig Chronos to eat everything in sight (that is the nature of the long-haired guinea pig).”

Asperger’s kids often memorize everything there is to know about the oddest things: deep-fat fryers, telephone cable insulating companies, exotic species of cicadas.

With this unnerving prospect in mind, I fall in with the Asperger’s adult group, which is sitting somewhat to one side by itself. One of them is Mark Romoser, a Yale graduate in his mid-30’s. Unlike Phil, Mark has a more pronounced aversion to eye contact and seems to observe any interlocutor slightly sideways. Now a research assistant at Columbia University, he once hoped to enter graduate school in psychology but “had trouble obtaining recommendations from professors.” Mark is dry and droll, with a seductive, slightly effeminate drawl; after telling me that many Asperger’s people are huge Monty Python fans because it conforms to their actual rather absurd experience of the world, he asks me point-blank if I find him normal.

“Perfectly,” I say.

“Mahalo nui loa,” he fires back.

“Excuse me?”

He leans forward and says quietly: “Hawaiian. I must tell you, I hate living on the mainland.”

The “mainland,” for Mark, seems to be the realm of a suspect normality filled with what Asperger’s people often call “typicals” — those who are neurotypical or, to use the outlawed word, normal. Instead, he calls himself an “ex-pat waiting to happen” who has made Hawaii the object of his impassioned interest. Indeed, the full-time Manhattan resident now writes a regular column for an online magazine called enewshawaii.com.

But why, I ask, Hawaii?

“My mother thought it would be a good idea for me to swim with dolphins. So I found a woman in west Oahu who takes autistic people out for swims. She calls us ‘unique beings.’ That was that. I was hooked. After all, we’re supposed to be gripped by obsessions, aren’t we?”

He winks. I ask him about romantic relationships, and he shakes his head. He hasn’t had a girlfriend in years.

“That’s a tough one. I’d say the only place I could be considered popular on the mainland was college. But girlfriends. . . .” He shrugs. “You know, I was a big Deadhead at college. But I must have been the only one ever to leave a Dead concert completely alone.”

This inability to form close sexual bonds is widespread (though, as Phil shows, it is by no means universal). Fred Volkmar, the Yale professor, shared with me the example of one 18-year-old Asperger’s patient who simply stared at girls in his college cafeteria. When the unlucky object of this attention came up to him and asked him what he wanted, he would simply blurt out the carnal truth. Needless to say, the police were called on several occasions.

“When I was at school,” Mark says, “I was doing too well to be called mentally retarded. So they called me ’emotionally disturbed’ instead. That was the trendy label at the time. I’ve often wondered if it was accurate. I wouldn’t say disturbed, though. Dislocated more like.” Then he adds, “Except when I’m in Hawaii, of course.”

Says Judy Rivkin, the executive vice president of the Asperger’s Syndrome Coalition: “People forget that autistic and Asperger’s children grow up. They don’t just vanish into thin air. But we have to remember that you can often get by masking a disability, passing for something that you’re not. Many Asperger’s people seem gifted and normal, and maybe they are in some regards. But that doesn’t mean that they don’t have to face profound problems.”

In the end, perhaps Asperger’s sufferers perpetually swing between brilliance and isolation, between originality and awkwardness. Lise, for her part, recognizes that Asa alternates between wildly differing psychological states. “When I walk him from home to school,” she says, “I see him stepping from one state into the other. He puts on his ‘school face’ and goes from being lively and relaxed to being locked into a kind of monotone. It’s a startling transformation. But then, that’s the Asperger’s world in a nutshell.”

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How well does the ADOS assess for autism in adults? How might Obama perform on an ADOS?

The ADOS Manual recommends users to regular video tape ADOS assessments to prevent “drift” in scoring. The ADOS cut off score does not include coding of category 3 behaviors which is a necessary component for a diagnosis of Autistic Disorder. Post is a hypothetical exam of how President Obama might perform.

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How might Obama perform on an ADOS test for autistic spectrum disorders?

Let’s imagine what might happen were President Obama given an ADOS assessment. An ADOS is administered one-to-one — not done here.

What the ADOS is:
The ADOS assesses for autistic spectrum disorders. Adolescents or adults assessed with an ADOS are asked to do various tasks including: 1) play interactively with the person who is assessing; 2) demonstrate how to do an activity; and 3) tell a story based on a picture book which has no words.

One ADOS task is engaging in interactive play that involves joint attention and ability to change based on what the other person does. President Obama seems to engage in a lot of “my way or no way” behavior which is not interactive. When President Obama got the stimulus bill signed he immediately turned it over to Speaker of the House Nancy Pelosi to figure out how to distribute the “pork”. President Obama did not wield his mighty pen and interactively “cut” out pork. Overall global assessment: As Obama’s abilities to interactively “play” appear low, he gets a score of 2 for the joint interactive task.

A second task on the ADOS: The person must demonstrate both verbally and non-verbally how to do something in daily life. Getting bills such as ObamaCare passed has been part of President Obama’s daily life. Can you imagine President Obama — without a teleprompter — explaining with use of gesture and words how he got ObamaCare passed? On the demonstrate a Daily Activity task Obama scores another 2. The total score is now 4 points.

A third task on the ADOS: The person assessed must tell a story based on a picture book that has no words. So, imagine a picture book showing the Tea Party movement at various rallies. How might Obama tell that story? Can Obama see a series of pictures and make a coherent story about a major political event, i.e. the Tea Party movement? Doubtful. Hence, on the Tell a Story task President Obama gets another score of 2.

On just three ADOS tasks Obama is already up to a total score of 6. There are about 12 or so tasks on the ADOS.

Let’s hypothetically assume that President Obama can meet the ADOS cutoff score for a possible diagnosis of an autistic spectrum disorder. More information is necessary to assign a diagnosis of autism or some variation.

The foregoing gives you an idea of the kind of tasks persons must perform during an ADOS assessment.

For each ADOS task a rater gives one global overall rating. O = no impairment. Various numbers can be assigned.

How subjective is ADOS? Relatively, the ADOS test is substantially more subjective compared to a Wechsler IQ test. Assigning one overall value to how well a task has been performed is a subjective act. How accurate are subjective ratings? In California the Board of Psychology finally stopped requiring Oral Exams for licensure because the subjective ratings over time varied so much.

What does the ADOS Manual say? The ADOS manual (i.e., the manual that comes with tapes) states that persons using the ADOS should regularly videotape. That way the videotape can be examined by others.

When litigation arises are videotapes of the ADOS routinely provided as evidence? Per what I hear and in my experience, taping is not typically done. .Should videotapes be routinely done of the ADOS when litigation may be involved? Yes.

The ADOS manual states that it is important to routinely get supervision.
Videotaping, comparing to test tapes and regular outside supervision are important to prevent “drift” as to how global ratings are assigned.

Of importance, in contrast to the ADOS, Manuals for I.Q tests do not suggest or recommend that videotaping and on-going supervision are necessary for accuracy in scoring an intelligence test.

To get a diagnosis of 299.0 Autistic Disorder an adult — such as President Obama — must be substantially impaired in a number of areas.

How might President Obama do given the above hypothetical performance on the ADOS combined with additional background information and interview data?

Diagnostic criteria for 299.00 Autistic Disorder: A total of six with at least two from Category 1 and at least one from Categories 2 and 3.

Category 1: Qualitative impairment in social interaction, as manifested by at least two of the following.
a. Marked impairment in multiple nonverbal behaviors such as eye to eye gaze, facial expression, body postures and gestures.

Might the teleprompter which Obama routinely uses show marked impairment in eye to eye gaze with the general public? Notice that Obama typically has his chin tilted to the left or right when speaking? Notice that on television Obama rarely makes direct eye contact? Of importance, Obama does not readily “read” non-verbal clues directed to him from the American public. Thus, Obama gets an X in this category.

b. Failure to develop peer relationships appropriate to age.
Obama has peer relations appropriate to his age and development.

c. A lack of spontaneous seeking to share enjoyment, interests or achievements with other people.
Both before and after the 2010 election, did President Obama share his enjoyment and achievements with the American public? No. He did not talk about his achievements (ObamaCare, the stimulus bill, the bailouts) and he immediately left the county for ten days. On his most recent birthday, President Obama went by himself to Chicago. His wife and child went to Spain for a separate holiday. Obama scores an X in this category.

For Category 1, Obama meets the criteria of two different areas. He must get one in Category 2 and one in Category 3 and a total of six. Can he meet criteria for a diagnosis of 299.0 Autistic Disorder? Let’s see….

d. Lack of social or emotional reciprocity
Obama is frequently described as aloof, cold, distant. First visiting the gulf after the oil disaster he chastised the governor as soon as he got off the plane. That Obama was largely interested in how he was viewed and perceived rather than how were the people in the gulf doing says a lot. In various situations, Obama’s social and emotional reciprocity is low — but not lacking entirely. So, no X here.

Category 2: Quantitative impairments in communication as manifested by at least one of the following:

a. Delay in or total lack of development of spoken language .in individuals with adequate speech not accompanied by alternative modes, e.g., gesture, mime.

There is no information in President Obama’s two autobiographies about his early development. Insufficient information known. No rating given.

b. In individuals with adequate speech, marked impairment in the ability to initiate or sustain a conversation with others

President Obama says that most Americans do support his policies but that there has been a “communication problem”. Obama says it is a PR problem and that he must do a better job explaining his policies to the public. Does Obama’s comments on the election results show an inability to “sustain a conversation” with the American public? Is Obama merely tone deaf? A conversation entails the ability to “hear” what others are saying and understand what is said from their perspective. Obama is not hearing what the public said per the 2010 elections. Hence, Obama gets an X rating for Category 2 b.
c. Stereotyped and repetitive use of language or idiosyncratic language.
Obama engages considerable repetitive use of language. How many hundreds of times has Obama said, “you can keep your health care… you can keep your health care….health care costs will not rise…. taxes on the middle class will not rise… Hence, Obama gets an X in this category.

d. Lack of varied spontaneous make believe play or social imitative play appropriate to developmental level.
President Obama engages in considerable make believe play and there is a knee jerk reaction rather than spontaneity in how he does it. For example, it is make believe play to print billions of funny money and say to the public that this will “grow the economy”. But there is no “lack…” Thus, no rating of an X.
Category 3: Restricted repetitive and stereotyped patterns of behavior, interests, and activities as manifested by at least one of the following:
a. Encompassing preoccupation with one or more stereotyped and restricted patterns of interest that is abnormal either in intensity or focus

President Obama clearly was preoccupied in pushing his agenda through congress. ObamaCare will pass whether the public likes it or not. The intensity of focus to achieve his goals was apparent to the American public. Was his preoccupation abnormal either in intensity or focus? That is hard to estimate. The American public said no more and voted Democrats out of office who were pro-Obama policies. It was not only what he did but how President Obama went about it. There was no listening to l the Republicans. No inclusion of others. Overall, an X here.

b. Apparently inflexible adherence to specific, nonfunctional routines or rituals.
No information. No rating made.

c. Stereotyped and repetitive motor mannerisms.
None observed or reported. Head bobbing because of teleprompter has been coded already.

d. Persistent preoccupation with parts of objects.
Not observed or reported. No rating made.

Overall, using the above scoring — an adult such as President Obama does not meet criteria for a diagnosis of 299.0 Autistic Disorder. However, he may meet a criteria for PDD-NOS or Asperger’s Disorder. More information is necessary….

Yes this is done tongue in cheek. This is an imaginary exercise.

Conclusions: The ADOS is a test that is subjective and “drift” in scoring can readily occur. When used in litigation the entire ADOS tape should be provided in evidence for others to examine.

In actuality I do not think President Obama suffers from an autistic disorder. But he is “tone-deaf”. And he seems convinced that he knows best for America. Probably, narcissistic is a better description of many of his behaviors.

So what say you? Is President Obama “out of it”? Tone deaf? Narcissistic? Sort of autistic?

written by Cameron Jackson DrCameronJackson@gmail.com

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Aptos psychologist: perhaps an enzyme sprinkled on food can help autistic children to absorb proteins better?

autistic children often are picky eaters
Lots of children with autism are picky eaters. Frequently these children prefer pasta and carbs and reject various categories of food. So, maybe autistic children’s brains are not getting the proper nutrients? How to feed starving brains is a theory worth exploring. The company Curemark has an enzyme that may help autistic children to absorb the nutrients they need.

“Researchers are kicking off a clinical trial to test whether certain children with autism can benefit from regular doses of an enzyme to help them digest proteins, which may in turn improve their brain function and ease some symptoms of their disease.

It’s one of several treatments being explored that could address the root causes of autism – an incurable set of developmental problems that affects socialization, language and behavior – instead of just the symptoms of the disease. But the theory behind the enzyme is controversial, because there is little solid research demonstrating that the missing enzyme, or digestion problems in general, is a direct cause of autism.

Some studies have shown that autistic children are more likely than healthy children to have gastrointestinal problems, and that a certain subgroup of autistic kids have enzyme deficiencies. But whether those problems cause autism or are just another symptom of the disease isn’t known for sure.

Still, some researchers say that even if there’s no clear connection between the missing enzyme and autism, it’s a treatment worth exploring.

“I think every avenue, every potential hypothesis, should be investigated in autism,” said Dr. Antonio Hardan, a pediatric psychiatrist and an autism researcher at Lucile Packard Children’s Hospital who is not involved in the enzyme trial. “This is one of them, and regardless what the results show, it will be helpful to look at what they find.”

The trial is being paid for by Curemark, the New York-based drug company that developed the enzyme. UCSF is one of 15 sites around the country participating in the trial, which will involve 170 children ages 3 to 8. UCSF is planning to recruit up to 10 children.The trial is double-blind, meaning that children will be randomly assigned to receive either the enzyme or a placebo, and the patients, their parents and the researchers will not know who is getting the treatment and who isn’t.

Children will eat the enzyme three times a day – they sprinkle the tasteless powder over their food – for 90 days. After that time period, parents can opt to give their children the enzyme for up to a year, whether they were in the treatment group or the placebo group.

Researchers will use interviews with parents and other behavioral tests to assess whether there are any changes in the children’s symptoms.

“The treatment is enormously simple, but finding it out wasn’t simple at all,” said Joan Fallon, chief executive of Curemark, who is a pediatric chiropractor who works with autistic children. “Is it theoretical? Yes. But we hope the trials will give some benefit to a subgroup of children. And we hope our trials will make other researchers look at the physiology of the disorder.”

Carb heavy
Fallon took an interest in enzyme replacement when she saw that many autistic children had diets heavy in carbohydrates – french fries and pastas and breads – but hardly any protein. These kids may avoid protein because they’re missing the enzyme to help them digest it.

That enzyme helps the body break down proteins in a process that produces certain amino acids, which are important for brain development and communication between brain cells. So some autistic kids aren’t eating enough protein to begin with, and what protein they do eat isn’t being digested properly. The idea is that those missing amino acids may be a cause of autism.

At least anecdotally, doctors seem to agree that gastrointestinal problems are common among autistic children. And many parents have reported – again, anecdotally – that dietary changes help improve symptoms of autism.

So it’s possible that giving the enzyme to children who are missing it will help some autistic kids, doctors say. At the very least, it’s worth testing, especially since the enzyme itself is unlikely to have any side effects, some researchers say.

“I do think there is a subgroup of kids who have these gastrointestinal symptoms or some difficulty digesting proteins, who may have that relate somewhat to autism,” said Dr. Robert Hendren, director of child and adolescent psychiatry at UCSF. “We’re always thinking about what else we can try. What else we can do that might help these kids. We have a responsibility to leave no stone unturned.”

Much of the research into treatments for autism is based on anecdotal evidence, Hardan said. Doctors often hear of reports from parents who try one trick or another to help ease symptoms in their children, and if something sounds promising, they’ll test the treatment in a scientific study.

“I meet with a lot of parents, and they support our research. But some of them, they want something this afternoon, not tomorrow,” Hardan said. “And I understand that, it’s very frustrating. But that’s science. It takes time.”

What is autism?
Autism, which usually appears before age 3, is one of a group of developmental problems that generally affect three key areas: social interaction, language and behavior. While there is no cure, early treatment can make a difference.

Causes: Autism has no single, known cause and probably has many. These may include genetic problems that can make a child more susceptible to the disorder or worsen symptoms. Environmental factors may also contribute.

Symptoms: Children with autism show unique patterns of behavior, but common symptoms include delayed development, poor eye contact, failure to hear others, resistance to close contact and unawareness of others’ feelings.

Source: Mayo Clinic

E-mail Erin Allday at eallday@sfchronicle.com.

Read more: http://www.sfgate.com/cgi-bin/article.cgi?f=/c/a/2010/11/07/MNLJ1G7T0C.DTL#ixzz14uCMFWHQ

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Aptos, CA psychologist: How best to measure autism? Caveats about use of the ADOS? What happened to the toddler version of the ADOS? Is there a way to accurately used standardized scores when measuring autism?

Cameron Jackson DrCameronJackson@gmail.com

Some caveats concerning the use of the ADOS in the assessment of autism.

One caveat: The ADOS measures autistic spectrum disorders but does not distinguish between the severity of autistic symptoms. That is, it does not distinguish between 299.0 Autistic Disorder (most severe), PDD-NOS (less severe) and Asperger’s Disorder (normal IQ and normal adaptive functioning).

A second caveat: The ADOS only picks up information between the interaction of an adult (psychologist, therapist) with a child. Unfortunately, there is no sampling of the child’s behaviors with same age peers. And, needless to say, how a child interacts with same age peers is crucial information. Frequently persons with an autistic spectrum disorder (ASD) do fine with persons older or younger. How the ASD functions in relation to persons fairly close in age is highly important. Why? In America, we educate children that are the same age. In many states, including California, once a child has been held back one time they cannot be held back again. So if a child cannot readily function with same age peers that is highly significant for that child’s educational experience.

The ADOS, a measure of autistic spectrum disorders, is a very different kind of measure compared to measures of intelligence.

We have lots of measures of intelligence and they all do a fairly good job. Most of the well known measures of intelligence result in standard scores and persons can be classified in a range: Average range, Superior range, Deficient range. A person who scores in the Average range on one measure typically and usually will score in the Average range on other measures of intelligence. For example, the Test of Nonverbal Intelligence (TONI) will give a standard score in the Average range that is fairly close to the Performance I.Q. of a Wechsler IQ test.

In contrast to measures of intelligence (I.Q.), the measurement of autistic spectrum disorders with an ADOS does not result in a standard scores. Scores are not spread out along the bell curve. Thus it is mot possible to talk about Average range, Superior range, Deficient range.

Hence, because there are no standard scores there is no way to compare performance on the ADOS with all the hundreds of tests that exist which use standard scores.

Instead of providing standard score information, the ADOS has a “cut-off” score. If the person scores above then they supposedly have an autistic spectrum disorder. The ADOS does include Category 3 (repetitive behaviors, unusually strong, limited interests) items in determining the overall scores.

So what happened to the ADOS for toddlers that was coming soon — but not here yet?

How did the new ADOS Module T perform?

1.The sensitivity of the ADOS Toddler module was 91%. That is, the test was able to correctly identify 91% of the cases of ASD (based on a cut off score of 12).

2.The specificity of the ADOS-Module T when tested against non-ASD disorders was also 91%. This means that only in 9% of the cases, the test suggested a diagnosis when the child had been previously identified as not having an ASD.

3.The specificity of the ADOS-Module T when tested against typically developing cases was 94%. That is, only in 6% of the cases, the test suggested a diagnosis in children who were actually typically developing kids.
What happened to the ADOS Toddler Module? Not happening?

One of the authors writes:

“These are actually excellent numbers and indicate that the ADOS Toddler Module has excellent sensitivity and specificity. However, the authors also described some general concerns and limitations.

The ADOS, although it is the most reliable and valid diagnostic instrument available, it is still only a clinical tool that must be used in the context of a comprehensive clinical evaluation and it is subservient to clinical judgment.

Specifically, a diagnosis of autism is provided only when the person meets the DSM-IV diagnostic criteria. Therefore, clinicians must use their judgments in interpreting and applying the results from the ADOS. There will be cases when the ADOS suggests a diagnosis but the clinician will not provide the diagnosis because the child doesn’t meet full diagnostic criteria based on the DSM-IV.

So you may ask, what is the point? Why do we have the ADOS if all a clinician has to do is go down the list of the DSM-IV criteria and add up the check marks? The ADOS provides for a reliable and valid tool to assess for the specific symptoms included in the DSM-IV criteria and it helps the clinician interpret the child’s clinical presentation as it applies to the DSM-IV criteria. The ADOS standardizes this process so that diagnoses are less dependent upon other factors, such as biases in parental reporting of symptoms, or the skills or training of the clinician in properly indentifying such symptoms. Therefore, the ADOS greatly improves the validity and accuracy of our ‘clinical judgment’.

On a personal note and disclaimer. Dr. Luyster (lead author of the study), Dr. Richler, and Dr. Oti were all my classmates in graduate school and I congratulate them for their wonderful work. In addition Dr. Lord, creator of the ADOS and founder of the University of Michigan Autism and Communication Disorders Clinic, will be my collague this Fall when I join the University of Michigan faculty.

The Reference: Luyster, R., Gotham, K., Guthrie, W., Coffing, M., Petrak, R., Pierce, K., Bishop, S., Esler, A., Hus, V., Oti, R., Richler, J., Risi, S., & Lord, C. (2009). The Autism Diagnostic Observation Schedule—Toddler Module: A New Module of a Standardized Diagnostic Measure for Autism Spectrum Disorders Journal of Autism and Developmental Disorders DOI: 10.1007/s10803-009-0746-z

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Aptos psychologist: Yes there are ways to reduce early signs of autism. Figure out ways so, unprompted, your infant gazes at you. Pay attention most to the non-verbal clues.

DrCameronJackson@gmail.com

A family has one  child  diagnosed with autism.  Then they have a second child.  Siblings of autistic children have a 25 times greater  likelihood than average also developing autism.

Can parents reduce likelihood of autism in child #2? Possibly and certainly worth the try. One avenue: what are ways to increase gaze between parent and child which is unprompted?

DSM IV 299.0 Autistic Disorder is characterized by three kinds of difficulties: the hardest to “fix” are the non-verbal social communication problems (poor eye contact, not ‘reading’ facial clues, low social and emotional reciprocity).

It is possible to identify children at risk of autism quite early. Interestingly, when and to whom a child gazes is an early marker. To me that suggests why not figure out all sorts of ways that babies can do something to prompt adults for gaze. The baby is not seeking gaze but by doing something they in fact increase gaze.

Might it not be the total gazing and human interactions that gaze provides that assists children to learn all sorts of non-verbal clues?

 Per article below, at six months, siblings do less gazing at parents when not prompted than children who do not have a autistic sibling.

So what might be some ways to encourage siblings of autistics to increase non-prompted gazing at parents and caregivers? Below are some ideas and why not share your ideas? Continue reading “Aptos psychologist: Yes there are ways to reduce early signs of autism. Figure out ways so, unprompted, your infant gazes at you. Pay attention most to the non-verbal clues.”

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