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First Published Friday, 27 March 2009


Alone

By Rick Nauert, Ph.D.
Senior News Editor

Reviewed by John M. Grohol, Psy.D. on September 9, 2008

Friday, Sep 5 (Psych Central) —


Feeling a connection to others is a critical component of a person’s mental and physical health.


New studies show that a sense of rejection or isolation disrupts not only will power and perseverance, but also key cellular processes deep within the human body.


Chronic loneliness belongs among health risk factors such as smoking, obesity or lack of exercise.


Feeling connected to others is vital to a person’s mental well-being, as well as physical health, research at the University of Chicago shows.


The studies, reported in a new book, Loneliness: Human Nature and the Need for Social Connection, show that a sense of rejection or isolation disrupts not only abilities, will power and perseverance, but also key cellular processes deep within the human body.


The findings suggest that chronic loneliness belongs among health risk factors such as smoking, obesity or lack of exercise, according to lead author John Cacioppo, the Tiffany & Margaret Blake Distinguished Service Professor in Psychology at the University.


“Loneliness not only alters behavior, but loneliness is related to greater resistance to blood flow through your cardiovascular system,” Cacioppo said.


“Loneliness leads to higher rises in morning levels of the stress hormone cortisol, altered gene expression in immune cells, poorer immune function, higher blood pressure and an increased level of depression.


Loneliness also is related to difficulty getting a deep sleep and a faster progression of Alzheimer’s disease, said Cacioppo.


One of the founders of a new discipline called social neuroscience, Cacioppo used functional Magnetic Resonance Imaging (fMRI) brain scans and advanced scientific techniques to document the roles of loneliness and social connection as central regulatory mechanisms in human physiology and behavior.


The authors traced the need for connection to its evolutionary roots. In order to survive, humans needed to bond to rear their children. In order to flourish, they needed to extend their altruistic and cooperative impulses beyond narrow self-interest and immediate kin. But in the environment of evolutionary adaptation, the only real safety was in numbers.


Just as physical pain is a prompt to change behavior (such as moving a finger away from the fire), loneliness evolved as a prompt to action, signaling an ancestral need to repair the social bonds. Feelings of loneliness take a variety of forms, Cacioppo said.


“There are three core dimensions to feeling lonely—intimate isolation, which comes from not having anyone in your life you feel affirms who you are; relational isolation, which comes from not having face-to-face contacts that are rewarding; and collective isolation, which comes from not feeling that you’re part of a group or collective beyond individual existence,” he said.


It is not solitude or physical isolation itself, but rather the subjective sense of isolation that Cacioppo’s work shows to be so profoundly disruptive. Yet, outward circumstances such as moving to a new community or losing an intimate partner can trigger loneliness. And as the authors make clear, today’s culture is not always conducive to promoting strong social bonds.


The problem of social isolation will likely grow as conventional societal structures fade. The average household size is decreasing, and by 2010, 31 million Americans—roughly 10 percent of the population—will live alone. Sociologists also have found that people report significantly fewer close friends and confidants than those a generation ago.


Cacioppo and Patrick also demonstrate how loneliness creates a feedback loop that reinforces social anxiety, fear and other negative feelings. By learning more about what underlies this experience, then learning to reframe their response, lonely individuals can reverse the feedback loop, overcome fear and find ways to reconnect.


“We try to offer some help for those who’ve become stuck,” said Patrick. “The process begins in rediscovering those positive, physiological sensations that come during the simplest moments of human contact. But that means overcoming the fear and reaching out.”


“Lonely people feel a hunger,” Cacioppo added. “The key is to realize that the solution lies not in being fed, but in cooking for and enjoying a meal with others.”


Source: University of Chicago




First Published Friday, 27 March 2009


Anorexia Hurts

According to a leading expert, severe cases of anorexia may be the result of undetected autism in women.


Professor Christopher Gillberg, of the University of Strathclyde, says that autism, characterised by defects in communication and social interaction, also makes many anorexic patients unresponsive to traditional treatments and may be responsible for anorexia’s low recovery rates.


Professor Gillberg believes that although autism is thought to be predominately a male problem, affecting up to four times more boys than girls, the disorder has been overlooked in women because their autistic traits present themselves differently.


For example an obsession with counting calories may be an outward sign of autism.


He says their research has shown that a small but important minority of all teenage girls, with anorexia nervosa in the general population, meet the diagnostic criteria for autistic disorder, Asperger syndrome or atypical autism.


He has apparently seen quite a number of cases where the anorexia has become completely entrenched because people have not understood that underlying the eating disorder is autism.


Professor Gillberg says anorexic patients with autism tend to be severe cases because traditional treatment for eating disorders proved ineffective.


A good example is family therapy, a popular psychotherapy in which family members discuss eating with the sufferer which is all but useless for autistic patients.


People with an autism spectrum disorder have great difficulty even understanding basic concepts about other people’s thoughts and feelings, which means that anything said in a family-therapy session is likely to be misconstrued by the affected individual who will not grasp what is going on in that particular context.


They need far more concrete, one-to-one interventions.


A spokesman for the Eating Disorder Association welcomed the research and said it could help develop more effective treatments for eating disorders.


About 5 per cent of anorexic patients die from complications of the disorder and only 40 per cent make a full recovery.


Ten per cent of the 1.1 million reported anorexia cases in the UK are in men, and Professor Gillberg says autism is behind the majority of male anorexia cases.


He says his clinical impression over the past 30 years has been that males struck by anorexia nervosa very often have autism spectrum disorders.


Judith Gould, director of the National Autistic Society’s Diagnostic Centre, agrees with the study’s findings, and feels autism in girls is being missed because it often manifests itself in females in different ways.


She agrees that anorexia, which is predominantly diagnosed in girls, could be linked to autism in an unknown proportion of cases.


About 500,000 people in the UK are thought to have some form of autism.


Source:   http://www.opposingviews.com/articles/research-undetected-autism-in-women-manifests-as-anorexia-nervosa


anorexia

Psychiatric Disorders Are Common In Adults Who Have Had Anorexia


ScienceDaily (Mar. 26, 2009) — The study was initiated in 1985. A total of 51 teenagers with anorexia nervosa were studied, together with an equally large control group of healthy persons. The groups have been investigated and compared several times as the years have passed.


“This study is unique in an international perspective. It is the only study in the world that reflects the natural course of anorexia nervosa in the population”, says Elisabet Wentz, Associate Professor in Child and Adolescent Psychiatry at the Sahlgrenska Academy.


The research group has published new results from the study in two scientific journals: the British Journal of Psychiatry and the International Journal of Eating Disorders.


Three women have still not recovered from anorexia, 18 years after the start of the study. Thirteen people, or around 25%, are on disability benefit or have been signed off sick for more than six months due to an eating disorder or other psychiatric disorder.. Thirty-nine percent have at least one other psychiatric disorder, in addition to the eating disorder. The most common of these is obsessive compulsive disorder.


But the results also contain some positive surprises.


“Previous studies have shown that anorexia is a diagnosis with a very poor prognosis, with as many as one in five patients dying as a result of the disease. In contrast, we have not had a single death among the subjects of our study”, says Elisabet Wentz.


Other studies have also shown that infertility is a common complication for adult women who have had anorexia, as are increased risks of giving birth prematurely and of post-natal depression. The women in the two groups in this study have had essentially the same number of children, but the women who have had anorexia were younger when they had their first child. Such children had a lower birth weight than children of women in the control group.


“None of the women who had had children still suffered from an eating disorder, but it is still more common that they worry about whether their babies are putting on weight”, says Elisabet Wentz.


Brief Facts: Anorexia Nervosa


Anorexia nervosa is one of the most common psychiatric disorders among young women, and 1% of all teenage girls suffer from the condition. The figure for boys is 0.1%. The most common age range for being diagnosed with anorexia is 14-17 years, and the condition can continue for a very long time.


Journal references:


  1. 1. Wentz E, Gillberg IC, Anckarsäter H, Gillberg C, Råstam M. Adolescent-onset anorexia nervosa: 18-year outcome. The British Journal of Psychiatry, 2009; 194 (2): 168 DOI: 10.1192/bjp.bp.107.048686
  2. 2. Wentz et al. Reproduction and offspring status 18 years after teenage-onset anorexia nervosa-A controlled community-based study. International Journal of Eating Disorders, 2009; DOI: 10.1002/eat.20664

Source:  http://www.sciencedaily.com/releases/2009/03/090326134012.htm

New Family Approach Uses Milkshakes for Anorexia


By Rick Nauert, Ph.D.
Senior News Editor

Reviewed by John M. Grohol, Psy.D. on April 3, 2009

Friday, Apr 3 (Psych Central) —


Getting your teenager to drink a chocolate milkshake isn’t something most parents need to worry about. But this is just the approach used in one treatment for anorexia nervosa.


The technique, known as Behavioral Family Therapy, or the Maudsley Approach, calls for parents to supervise the eating habits of their anorexic child, feeding them high-calorie meals like milkshakes and macaroni and cheese until they regain a healthy weight.


For the first time, the Maudsley Approach is being compared with a more established treatment known as Family Systems Therapy as part of an ongoing National Institutes of Health (NIH)-funded treatment study at New York-Presbyterian Hospital/Westchester Division and five other centers nationally. Both are outpatient therapies for adolescents, aged 12 to 18.


“Anorexia is a life-threatening condition. Treating it early is very important since it is during the teenage years that this disorder usually takes hold,” says Dr. Katherine Halmi, founder of the Eating Disorders Program at New York-Presbyterian Hospital/Westchester Division and professor of psychiatry at Weill Cornell Medical College.


“Traditionally, patients with anorexia have been treated in a hospital setting or through one-on-one outpatient therapy. While inpatient treatment is still appropriate in acute cases, we have increasingly seen the value of family-oriented outpatient therapy for adolescents.”


The current study is designed to compare two different therapeutic approaches that involve the family — one is a behavioral therapy initially focused on weight gain, and the other examines various underlying issues in the family dynamic.


In the Maudsley Approach, named after the hospital in London where it was developed in the 1980s, the anorexic teenager attends therapy sessions together with parents and siblings. Parents work with the Maudsley therapist to develop ways in which they can monitor their child’s intake, choosing the amounts and types of foods necessary for them to regain to a healthy weight.


Siblings are encouraged to act as a support system for their sister or brother. Once patients achieve a healthy weight, they graduate toward taking more responsibility for their intake. At this point, family and developmental issues relevant to the patient maintaining a healthy weight are addressed.


In Family Systems Therapy, families also attend regular therapy sessions, but discussions do not necessarily focus on eating. Instead, family members are free to broadly explore and challenge any problematic communication patterns or stressors within the family unit.


“In Maudsley, food is medicine that restores the body and mind. When the body is starving, the mind also weakens, becoming more susceptible to anorexia’s rigid, often obsessive logic. Supervised feeding helps to break this vicious cycle. With the anorexia in charge, the adolescent really cannot regain the weight on his or her own. Nutritional rehabilitation gives the brain the nutrition it needs to re-establish healthy eating habits,” says Dr. Dara Bellace, a clinical psychologist at New York-Presbyterian Hospital/Westchester Division and an instructor of psychology in psychiatry at Weill Cornell Medical College.


“This approach does not blame parents, but rather calls on their ability to nurse their child back to health. It requires a strong commitment to be with them for every meal — something that can mean rearranging schedules and taking a tag-team approach to sharing the responsibility,” adds Dr. Bellace.


“The adolescent must also dedicate themselves to the therapy, understanding that, until they regain the weight, their parents will be feeding them much as they did when they were younger, deciding what and how much they eat and making sure they finish.”


Previous research has shown the Maudsley Approach successfully prevented hospitalization and helped adolescents recover their normal weights, with at least 75 percent of patients maintaining their recovery after five years.


A total of 240 adolescents aged 12 to 18 are being recruited for the study at six centers: New York-Presbyterian/Westchester; Stanford University in Palo Alto, Calif.; Sheppard Pratt in Baltimore, Md.; University of California at San Diego; University of Toronto; and Washington University in St. Louis.


Those eligible must be medically stable individuals ages 12 to 18 with a body weight between 75 percent and 87 percent of its healthy range. Families are randomized to receive either the Maudsley Approach or Family Systems Therapy. In each family treatment, they attend 16 one-hour sessions over the course of nine months. Sessions are held weekly for the first seven to eight weeks, bimonthly for the next six sessions, and monthly for the remaining sessions.


Anorexia nervosa is an eating disorder characterized by extreme low body weight and body image distortion with an obsessive fear of gaining weight. The condition largely affects adolescent females, who make up more than 40 percent of all cases. As much as 3 percent of American girls and women are anorexic. Contributing causes may include genetics, personality type, hormones, stress and societal pressures.


Anorexia carries the highest mortality rate of any psychiatric condition. Previous research by Dr. Halmi found that 7 percent of affected women died within 10 years. In a Swedish study that followed patients for 30 years, 18 percent to 20 percent of the women died. Even when anorexia is not fatal, it can cause long-term complications, including damage to the heart and bones.


For more information, eligible participants can e-mail the study coordinator, Samantha Berthod, at sab2024@med.cornell.edu.


Source:Cornell University


http://psychcentral.com/news/2009/04/03/new-family-approach-uses-milkshakes-for-anorexia/5139.html


Related Stories




First Published Sunday, 29 March 2009


Bichon Frise

ACTRESS and model Emma Noble knew her little boy would be overwhelmed by his new pet, but even she did not expect such an emotional response.


For as young Harry opened the front door and saw his mum sitting on the stairs with his gift on her lap, his mouth opened in shock — then seconds later tears began to fall and his little body began to shudder.


After what seemed like an eternity, the eight-year-old blurted out: “Put him on the floor, Mummy.”


Seconds later he was hugging the little bundle of fluff and declaring: “I love you, Shoeshine,” while the pup jumped all over his new owner.


It was the beginning of a very special friendship and one which has helped Harry — who has autism — on many levels.


Since Shoeshine — a bichon frisé — moved in with Emma and Harry just before Christmas, the isolated world which the youngster inhabited has opened up hugely.


Today he is happy to leave the house, will chat contentedly to strangers and is learning to empathise with others — none of which was even a vague possibility before.


Autism is a life-long developmental disability which affects social skills. It is thought that dogs have a special affinity with autistic children and help them because they provide a constant in a world which the child can otherwise find confusing.


In the US it is well established that dogs can help autistic children out of their isolation, but the theory is still relatively new in Britain.


In fact, the idea to get a puppy came entirely from Harry, whose dad James — son of ex-PM John Major — was divorced from Emma in 2003.


Years ago Harry started to develop a phobia of dogs, even insisting on crossing the road if he saw one, so Emma started taking him to her parents’ neighbours to see their little pet.


With regular visits, Harry soon forgot his fear and developed a real love for dogs.


Emma says: “One day he asked me out of the blue, ‘What would it be like if I had a friend, Mummy?”


“It broke my heart because Harry doesn’t have many friends. His family are his friends. But there he was, thinking of a dog in terms of a friend.”


From then on, Harry started avidly reading books on dogs, watched every documentary and film he could find to do with them, and talked non-stop about how much he wanted one as a little friend.


Toys


Emma, 37, says: “I also had a phobia of dogs after getting badly bitten on the back of my legs as a little girl, so the idea of having a dog in the house certainly wasn’t what I had in mind.


“But Harry kept on about how much he would really love a little friend, so slowly I started to come round to the idea.”


Harry first started showing classic signs of autism when he was two and a half.


He lost all the language he had learned, started to leave food that had touched other food on his plate, would line up his toys for hours on end and withdrew into his own little world, hardly responding when Emma tried to communicate.


Just a couple of months later Harry was diagnosed with the condition. At around the same time, Emma broke up with husband James.


Now, thanks to Emma’s determination, Harry is a little chatterbox, although he is still struggling to deal with many other aspects of autism.


But Shoeshine is definitely helping him to cope.


Emma says: “He is such a good dog, he is so affectionate and Harry adores him.


“Shoeshine looks like a teddy bear, he has such a lovely, smiley face that I’m sure his unthreatening look is part of why Harry feels safe with him.


Love


“Play with Shoeshine is very simple. It’s repetitive, throwing a ball or stick for him over and over.


“And Harry loves that he can easily change the agenda.


“Unlike with other children, who might object, Shoeshine is happy to go along with whatever Harry wants.


“His love for Shoeshine is also helping him to empathise — something he would never have done before.


“Harry understands that Shoeshine needs to eat and get exercise, so he’s learning to appreciate the needs of others.


“When Shoeshine has been ill, Harry gets very upset.


“I was amazed one day when Harry said, ‘Poor Shoeshine’.


“It may sound like such a simple thing but for Harry that is massive — for him to be concerned about someone else.


“Before, if I’d told him I was poorly he would understand it but wouldn’t worry. Now I’m hoping that might begin to change.”


Another major change for animal-mad Harry is that he is a lot happier going outside.


Emma, who lives near Cambridge, says: “Home is his sanctuary.


“He knows where everything is here, but outside he suffers with sensory overload and becomes very anxious.


“Now Harry understands that Shoeshine needs his daily walk — it’s in the puppy rules that mustn’t be broken.”


And once outside Emma has been delighted to see Harry interact with strangers — something he would never have done before.


Again, the link is Shoeshine. Before, if someone approached Emma and Harry for a chat he would avoid eye contact and discussion.


But now, inevitably, the conversation turns to Shoeshine, who Harry is more than happy to chatter about.


Emma says: “Harry is so proud of his dog. He always introduces him as his friend.


“He has come on so far and I have no doubt that Shoeshine is a big part of his development.


“I recently went to his school where he read me a book — of course, it was about dogs — but that was such a major milestone for us.”


Emma is asking Sun readers to “stand up for autism” on April 2 to mark UN World Autism Awareness Day and help increase understanding of the condition.


To find out more, visit waad.org.uk. For information and advice on autism, visit the National Autistic Society’s website at autism.org.uk.


Source:   http://www.thesun.co.uk/sol/homepage/woman/real_life/article2346343.ece



First Published Monday, 30 March 2009


REBECCA McQUILLAN


SAFE HAVEN: Brian Rafferty feels secure in his Broughton Street bookshop.
SAFE HAVEN: Brian Rafferty feels secure in his Broughton Street bookshop.

Brian Rafferty’s secondhand bookshop feels like a sanctuary. Painted claret red and lined with the colourful spines of several thousand volumes, its quiet, compact interior is the sort of place you could happily while away your lunch break. Open just a few months, it is already a popular fixture on Edinburgh’s cafe-lined Broughton Street.


Brian, 21, runs the shop from behind a desk in a back corner and is happy to give his customers the space and time to make their choices, though with his precise knowledge of the stock, he’s also able to help them find a particular volume in seconds. Temperamentally, he appears to be ideally suited to the work of a second-hand bookseller – a job which has given him fresh hope.


“I like the interaction with the customers,” he says, laying down his own book, Sharon Osbourne’s autobiography. “I like it when there are several people in at once.”


But he also loves the calm. “I get things done when it’s quiet, like moving the books around and sweeping up. It’s relaxing.”


For any 21-year-old to be running his own shop would be an achievement, but for Brian it is doubly so, because he has Asperger’s syndrome, a condition on the milder end of the autism spectrum. He did well at school and college, but struggled to find a full-time job afterwards.


“When he was looking for employment in banks, and in IT, he found it really difficult because he was coming up against people who were, in inverted commas, normal’,” says Brian’s stepfather Kevin, a police officer, who has popped in from the family home around the corner. “He was getting up at midday, and had no purpose. Now he’s up first thing in the morning.”


How does he feel about life now? “I’m really happy that I’ve managed to get more employment.”


Brian has a leaflet that he hands out to customers explaining what Asperger’s is and that he intends to donate a percentage of profits each year to the National Autistic Society.


The bookshop was the suggestion of a family friend, who owns the premises, and has been trading since before Christmas. But it was opened officially earlier this month by the entrepreneur Sir Tom Farmer, who paid tribute to Brian’s “can-do attitude”. The stock is donated.


Kevin, and Brian’s mum Sandra, who works in the pharmaceuticals industry, have been deeply touched by how local traders have taken Brian to their hearts. “Broughton Street is a small community. He feels safe here. This is now his home environment, which is fantastic,” says Kevin. “I see such a difference in him. Prior to this, you’d ask him what his day had been like and he’d say fine’. Now, when he goes for a pint, he’ll talk about the shop. It’s something to talk about.”


Brian’s experience underlines how people with certain forms of autism can participate fully in society and the economy. But loneliness and social isolation are widespread among people on the autism spectrum, and are a cause of deep unhappiness.


Autism and Asperger’s are characterised by difficulties in communication, interaction and social imagination. At one end of the spectrum are high functioning people with Asperger’s whose social difficulties may not be very noticeable, while at the other are those with severe autism who may not be able to communicate through speech at all.


“From childhood right through to adulthood, their experience is often of being bullied for being different, or ignored,” says Carol Evans, Scottish director of the National Autistic Society. “Often they want to make friends, but find it very hard.”


One-third of adults with autism develop severe mental health problems like depression or anxiety disorders. Many people with autism spectrum disorders, particularly severe autism, therefore remain at home. “If there was ever a condition that breaks up families, it’s this one,” says Evans. “We find an awful lot of families split because they can’t cope with the sense of stigma. Because autism often results in inappropriate behaviour, people start avoiding the general public. They go to Tesco at midnight instead of midday.”


In a bid to tackle this, 19 autism charities have come together to open people’s eyes to autism on World Autism Awareness Day on Wednesday. The theme is Stand Up For Autism, and a procession of celebrities such as Jane Asher and Patrick Kielty have recorded short videos of themselves doing just that. The aim, says Evans, is to end the litany of tuts and mutterings that autistic people and their families often encounter.


“Our message is: be more tolerant,” says Evans. “Don’t assume the child on the shop floor screaming or waving their arms about is badly behaved. That is their way of trying to convey they’re in trouble. If people were more tolerant, a more normal family life might be possible rather than fearing to leave the house.”


Maureen Rocks from Paisley has two sons with mild Asperger’s syndrome. Her son, Oliver, was diagnosed aged 10. Maureen says: “He was shy and didn’t like to go anywhere. He liked collecting things and doing the same things repetitively, and found it difficult to mix with other children.”


Oliver didn’t like going to school. His teachers noticed him becoming isolated in the playground. One lunchtime, the bell rang and he refused to go in. “The headteacher was brilliant,” says Maureen. “She went out to speak to him and I think she saw in him similarities with another child. She suggested speaking to a psychologist. It was a bit of a relief because I was thinking I was doing something wrong.”


After being diagnosed, Oliver became much happier at school, like Brian,he was picked on by other children. But having a talent for both drumming and playing the guitar, he had a focus and is now studying music performance at college. Oliver’s younger brother Harry was diagnosed with Asperger’s aged five because his behaviour was more challenging, but his character is completely different. “I’d say his social skills are very good,” says Maureen. “He left primary school with lots of friends and won an award for creativity.”


Now the two boys and their brother Jack, 10, who does not have Asperger’s, support one another. Maureen says: “I’m very lucky, my boys have very mild autism. The boys all have an interest and we all get on really well.”


Evans points out that often after leaving the education system, people with autism spectrum disorders get little formal support, because their condition falls between learning disability and mental health problem. Greater public understanding can make a difference.


Maureen’s message is simple: “Learn more about it, be more aware and if you come across someone whose behaviour is negative or difficult, try to be sympathetic and understand why they are behaving that way.”


  • Broughton Street Book Shop, 44 Broughton Street, Edinburgh. Donations gratefully received. Call 07960 015499 or visit www.nas.org.uk

  • Autism: the facts
    Autism spectrum disorders affect 50,000 Scots, one in 100 people, though some scientists believe the rate is rising.


  • *Autism is more prevalent among males than females.

  • *Many adults with autism have not been formally diagnosed, as the condition is usually picked up in school.

  • *Genetic factors are thought to be responsible for some forms of autism, though environmental factors have an influence.

  • People with autism have difficulties in three areas:
    Social communication
    Difficulty understanding facial expressions or tone of voice; body language; jokes, sarcasm and metaphor. Some people with autism may not speak; others will have good language skills.


    Social interaction
    Difficulty understanding unwritten social rules like how close to stand to another person; may become withdrawn or behave in what might seem an inappropriate way.


    Social imagination
    People with autism have imagination and many are very creative. But social imagination – understanding or guessing another person’s thoughts and feelings – is more difficult.


  • *People with autism like routines, and may have sensory sensitivity.

  • Source:   http://www.theherald.co.uk/features/features/display.var.2498557.0.Treatment_by_the_book.ph



    First Published Monday, 30 March 2009


    Playing action video games can boost an aspect of adult vision previously thought to be fixed, a US study shows.


    Researchers found playing the games improved the ability to notice even very small changes in shades of grey against a uniform background.


    “Contrast sensitivity” is important in situations such as driving at night, or in conditions of poor visibility.


    The Nature Neuroscience study raises the possibility of using a video game training regime to improve vision.


    Contrast sensitivity is often one of the first aspects of vision to be affected by ageing.


    There is some evidence that the visual system can learn
    John Sloper
    Moorfields Eye Hospital

    It can also be affected by conditions such as amblyopia, known as “lazy eye”.


    Improving contrast sensitivity usually requires physical changes in eye optics, through eye surgery, glasses or contact lenses.


    A team from the University of Rochester studied expert video game players playing games involving aiming and shooting at virtual targets.


    They found that they had better contrast sensitivity when compared with players who played non-action video games.


    These results were not because people with better contrast sensitivity were more likely to be action video game players – giving non-video game players intensive daily practice in video game playing improved this group’s performance on tests of contrast sensitivity.


    Crucially, the improvements in this study were sustained for months or even years in some cases, suggesting that time spent in front of a computer screen is not necessarily harmful for vision, as has sometimes been suggested.


    Unpredictable events


    Lead researcher Dr Daphne Bavelier said it was likely that several aspects of playing video games combined to produce the beneficial effect.


    The games immersed players in an environment where they had to be constantly ready to react to unpredictable events, and where visual information had to be responded to instantly in very precise physical ways.


    In addition, the mere fact that the games were stimulating and rewarding should not be overlooked.


    Dr Bavelier hopes to make use of the discovery to develop new ways to treat amblyopia.


    The hope is that by using video games researchers can encourage the two eyes to work together, and restore the stereo vision which is lacking in people with a lazy eye.


    Professor Gary Rubin, of the University College London Institute of Ophthalmology, said he was surprised by the findings.


    He said other work had shown that it was possible to train people to improve some aspects of their vision – for instance, to widen the visual field.


    But he said: “Contrast sensitivity is a very basic visual function, and usually they are more difficult to alter in adulthood.


    “This is a small study, showing a small effect, but it was carefully done, and merits further investigation.”


    John Sloper, a consultant at Moorfields Eye Hospital in London, said other researchers were also examining the potential for using video games to treat amblyopia.


    He said: “There is some evidence that the visual system can learn.”


    Source:   http://news.bbc.co.uk/2/hi/health/7967381.stm



    First Published Monday, 30 March 2009


    The new edition of Scientific American Mind is out an it has an excellent cover article on the psychological effects of humour and laughter.


    It’s a remarkably wide-ranging article, covering everything from the effect on the immune system, to laughter’s pain killing properties to its beneficial effect on mental health.


    There’s also an interesting aside on the role of humour in attraction:


    In 2006 psychologists Eric R. Bressler of Westfield State College and Sigal Balshine of McMaster University in Ontario reported that women are more likely to consider a man in a photograph a desirable relationship partner if the picture is accompanied by a funny quote attributed to the man. In fact, the women preferred the funny men despite rating them, on average, less intelligent and less trustworthy.


    Although the men in Bressler and Balshine’s study did not prefer witty women as partners, other research indicates that both men and women value a “sense of humor” when choosing a partner. Either way, males do seem to like ladies who laugh at their jokes. A 1990 study suggests that when women and men chat, the amount of laughing by the woman indicates both her interest in dating the man and her sexual appeal to the man. (The man’s laughter did not relate to attraction in either direction.)


    The issue also has freely available online articles on ‘brain training’, the psychological effect of architecture and personality disorder with many more in the print edition.



    Link to April’s SciAmMind.


    Source:   http://www.mindhacks.com/blog/2009/03/the_attractions_of_h.html


    By John M. Grohol, Psy.D.
    March 22, 2009

    Contrary to popular opinion, it appears that romance doesn’t have to die a natural death in a long-term relationship. In a meta-analysis review of 25 studies with 6,070 individuals in short- and long-term relationships published last week, researchers set out to find out whether romantic love is associated with greater relationship satisfaction.


    The findings?


    The researchers found that those who reported greater romantic love were more satisfied in both the short- and long-term relationships.


    Perhaps not surprising, those who reported greater passionate love in their relationships were more satisfied in the short term compared to the long term. Companion-like love, on the other hand, was only moderately associated with satisfaction in both short- and long-term relationships.


    What’s the secret?


    “These people are often very relationship focused,” Acevedo told LiveScience. “Their relationship is something that is very central to their lives, something they spend time on, work on, really care about. They seem to resolve conflicts relatively efficiently and smoothly.”


    Other studies on building strong, romantic relationships also suggest the following may help:


    • *Continue exploring and engaging in new activities and opportunities with one another.
    • *Resolve conflicts as they occur, respectfully; don’t let conflicts simmer and build into something bigger over time.
    • *Find something challenging to do together; a shared challenge can help bring you closer together if you work as a team.
    • *Feeling that your partner is “there for you” is invaluable for a good relationship.
    • *Guard against insecurity, as it can lead to spark relationship problems that otherwise wouldn’t exist.

    Romance doesn’t have to turn into pure friendship over time, nor does it have to die a natural death in long-term relationships. Strive to keep the romance alive in your long-term relationship — it’s not as impossible as it may seem.


    Read the full article: Romance Can Be Maintained in Long-term Relationships.



    Married women lonelier than men


    Stephen Lunn, Social affairs writer | March 19, 2009


    MEN benefit more from being married than women, at least in the emotional stakes, as new research shows married women are lonelier than married men.


    The study finds single, separated and widowed men are considerably lonelier than their female counterparts, but the reverse is true for married or de facto couples.


    Overall, more than 30 per cent of Australians rate themselves as lonely, the latest Australian Unity Wellbeing Index shows, although men’s emotional welfare is harder hit by this loneliness.


    “While the proportion of females reporting loneliness is similar, the wellbeing loss associated with loneliness is most pronounced for males,” says the report, due for release today.


    “Men who have never been married, who are separated or who are widowed are significantly lonelier than females in the same circumstances. Curiously, married and de facto females record higher levels of loneliness than married or de facto men. In this respect, therefore, marriage benefits males more than females.”


    The Wellbeing Index had 2000 people rate their level of loneliness on a scale of 0 to 100. More than 30 per cent of people put their loneliness above 40.


    Report author Bob Cummins said a rating of more than 30 put emotional wellbeing at risk. He said the different emotional make-up of men and women might explain why single men were lonelier than single women.


    In addition to relying more on their relationship for emotional sustenance, men also relied on money to stave off loneliness more so than women.


    “Men from households with an income less than $60,000 are significantly lonelier than men with a household income between $100,000 and $250,000,” the report says.


    Source:   http://www.theaustralian.news.com.au/story/0,25197,25208448-23289,00.html


    By Therese J. Borchard
    March 22, 2009

    A few readers asked if I would write out the content of my videos in accompanying text. Here you go:


    Friendships are a lot like marriages in that some are healthy and some are toxic, or unhealthy. But you sound pretty ridiculous explaining to people why you are sad: “Man, I just broke up with a friend, and it’s really painful.” But that is, in essence, what you are doing, and it needs to be treated the same way as a romantic relationship or marriage ending: with a lot of support and nurturing. As friendships develop and evolve, some don’t have all the right ingredients to last. So it’s right and natural that some break. But that period after the split is so awkward, for both people: the breaker-upper, or the breaker-uppee. I’ve sat in both seats.

    I love the way Anne Morrow Lindbergh talks about friendships in her classic, “Gift from the Sea.” She writes:


    I shall ask into my shell only those friends with whom I can be completely honest. I find I am shedding hypocrisy in human relationships. What a rest that will be! The most exhausting thing in life, I have discovered, is being insincere.


    I love that. Because I’m trying to be more sincere in my relationships. And as I do that I’m finding that some aren’t as healthy as I thought. The only requirement lately that I’ve been asking myself is this: Do I feel empowered by this relationship? Or do I feel deflated? After having coffee or lunch with this person, do I feel better about myself? Does this person build me up? Or do I feel worse about myself? Does this person in some way take away from me?


    When I ask that question it reveals to me whether the relationship is toxic or healthy.


    Yesterday I was having a discussion with one of my friends about a friendship with which I’m frustrated, and she made a point that helped me understand why some of my relationships can’t be healthy. She said, “It’s hard to be in a true, loving, mutual friendship with a person who is so wounded that they can’t reciprocate the love and the support.”


    Understood in that perspective, I feel less jaded, less hurt, by the person. I just know that she or he is so wounded that they can’t act in any other way. It’s not possible for them to be in a mutual loving relationship. Their wounds get in the way.


    I’m going to close by reading Anne Morrow Lindbergh’s excerpt again, because I find it so empowering:


    I shall ask into my shell only those friends with whom I can be completely honest. I find I am shedding hypocrisy in human relationships. What a rest that will be! The most exhausting thing in life, I have discovered, is being insincere.


    Source(Includes Video 3:12):  http://psychcentral.com/blog/archives/2009/03/22/video-when-a-friendship-ends/


    Further evidence explains ‘broken heart syndrome’


    By Crystal Phend, Staff Writer, MedPage Today


    PROVIDENCE, R.I., March 27 — More evidence emerged that stress cardiomyopathy, popularly known as “broken heart syndrome,” is not a classic heart attack.


    The long-term effects of the syndrome’s heart attack-like symptoms, brought on by sudden emotional or physical trauma, appeared almost fully reversible, Richard A. Regnante, MD, of the Miriam Hospital and Brown University here, and colleagues found.


    More…

    © 2004-2009 MedPage Today, LLC. All Rights Reserved.



    First Published Tuesday, 3 February 2009


    Communication

    According to research, almost 50% of AS children are late in their development of speech, but they are usually fluent talkers by the age of five (Eisenmajer et al. 1996). Although pronunciation and grammar (phonology and syntax) tend to be on a par with your average neurotypical child, differences tend to occur in the areas of pragmatics(ie how language is used in a social context); semantics (ie not recognising there may be several meanings); and prosody (ie an unusual pitch, stress or rhythm).


    A proportion of children who are now widely accepted to have Asperger’s Syndrome, but showed the classic signs of autism in their pre-school years have been known to show significant improvement in communication and abilities later. “This improvement can be remarkably rapid and occur just prior to the age of five.” (Shah, 1988). The experts aren’t sure whether this is a natural progression for some children or a tribute to early intervention programmes; probably both.


    As A Matter of Interest …

    Albert Einstein

    Einstein himself was well past 2 years of age before making any attempt at language. His most memorable utterance was at two and a half years of age when his sister, Maja, was born. Apparently expecting some kind of a toy, he demanded to know why she didn’t have any wheels! Until the age of seven, he had a habit of repeating softly to himself every sentence he uttered.


    Albert with his sister, Maja

    In an interview later in her life, his mother, Pauline, ascribed the success of her household to discipline – patient, persevering, warm but practical. Music played quite an enormous role in their lives. His typical playmates were chickens and pigeons in his temperamental youth …


    It is approximated that around 90% of children on the spectrum develop speech by the age of nine years, and some, well beyond this. (Reference for this statistic: C. Lord, S. Risi, A. Pickles, “Trajectory of language development in autism spectrum disorders” in Developmental Language Disorders: From Phenotypes to Etiologies, edited by Mabel L. Rice and Steven F. Warren (Laurence Erlbaum Associates, 2004).


    There are speech pathologists who will admit that in their studies, they found that the object was far too often to force speech at all costs, even if one of the costs was communication.


    A very wise lady I know of, who is minus speech, once wrote that ‘communication is way more important than speech. Be sure that whatever you are teaching your child focuses on communication, not just speech. Some people aren’t cut out for speech even if they’re capable of making all the sounds and seem “promising”. Go with whatever communication method (or methods) works best for your child expressing himself, not with what communication method is the most normal.”


    Antique phone

    The following article is courtesy of NAS Communication Magazine, Autumn 2008 Edition.


    Practical Advice – Speech and Language Therapy


    Speech and language therapy is vital for anyone with a diagnosis on the autism spectrum. Here, speech and language therapists (SALTs), working with autistic children at NAS schools across the UK, have gathered to tell us exactly why it’s so important.


    From early diagnosis and intervention with young children to help for those with a late diagnosis and complex needs, a SALT can help access appropriate support for the individual’s communication needs. The type of work the SALT undertakes will depend on many complex factors. Whether the individual is non-verbal or has varying degrees of language, a SALT will be needed to advise on:


    • *communication strengths and needs
    • *the training of other staff
    • *intervention strategies
    • *the use of visual aids to enhance understanding and communication. These can be objects, photos, symbols or written words
    • *the use of specific symbols or written words
    • *the use of specific systems for communication – such as signing, picture exchange, pointing systems, voice output and communication aids
    • *promoting social interaction
    • *how to develop understanding of language
    • *how to develop expressive language

    Generally, most SALTs work within the person’s environment, whether that is in class, at home or in a residential setting. Generalising skills (transferring them from one setting to another) is often a problem for people on the autism spectrum.


    Imagine being in a world where everyone speaks a language you can’t understand


    Tips for Helping Communication


    If you can imagine being in a world where everyone speaks a language you can’t understand, you will have a fleeting glimpse of the world inhabited by a person on the autism spectrum. Unlike the person with an ASD, however, you would still be able to interpret clues like facial expression, body language and tone of voice.


    To make communication easier, here are some general points which can help many people on the autism spectrum, although each individual requires a SALT to assess their particular situation.


    • *Ensure you’ve got the person’s attention before presenting information to them.
    • *Allow lots of time for processing.
    • *Present information visually where possible. Use objects, photos, symbols, drawings or write it down, depending on the person’s ability level.
    • *Use a visual timetable to show what’s happening now, next and later.
    • *When presenting information orally, try shortening sentences or just use one or two key words. Find out what the individual needs.
    • *Use areas of special interest to motivate the person.
    • *Watch for symptoms of stress and reduce demands, accordingly.
    • *Don’t use idioms like ‘raining cats and dogs’ or ‘pull your socks up’ unless you’re confident that the person won’t take them literally!
    • *Provide specific information on social rules at the level of understanding the person has: don’t expect the person will learn them automatically.
    • *If choosing between options is a problem for the person, reduce the number of options.

    By the SALT team, working across all six NAS schools: Faye Coles, Frances Edmonds, Karen Kerr, Joanne Neill, Katie Newton, Lilias Nicholls, Teresa Povey, Karen Reeves and Linda Robinson.


    Further Information


    Useful information sheets, available from the NAS Autism Helpline(0845 070 4004), on this and related subjects, include:


    • *Speech and language therapy
    • *Social skills in young children

    http://www.autism.org.uk/a-z


    PECS

    Other Resources


    Speech therapy activities http://www.speechtx.com/


    The Makaton charity Call 01276 606760 or visit http://www.makaton.org/


    Picture communications symbol clipart http://www.setbc.org/pictureset/


    Picture sets and communication resources http://www.do2learn.com/


    Picture exchange communication system (PECS) Call 01273 609555 or visit http://www.pecs.org.uk/


    The Royal College of Speech and Language Therapists Call 020 7378 1200 or visit http://www.rcslt.org/


    The Association of Speech and Language Therapists in Independent Practice Call 01494 488306 or visit http://www.helpwithtalking.com/


    ICAN – children’s communication charity Call 0845 225 4071 or visit http://www.ican.org.uk/


    Afasic – charity representing children and adults with communication impairments Call 0845 355 5577 or visit http://www.afasic.org.uk/


    Talking Point – for information about speech and language development in children http://www.ican.org.uk/TalkingPoint/Home.aspx


    Readers’ Advice


    Buzz and Woody

    My autistic son is four. He is on the waiting list for speech and language therapy. What can I be doing in the meantime to encourage him to talk?


    “We also have an autistic son who is four. Though he is very vocal, he has little discernible speech and we use Signalong/Makaton. This happened by accident when he was watching Something Special (pictured below) on CBeebies and made the sign for ‘eating’. We sat and watched all episodes of Something Special, and learnt the signs for basic things, such as toilet, eating, various foods, transport and colours. Our son now has a small repertoire of signs that he uses to convey what he wants and for us [to use] to communicate a little better with him, which lessens his frustration.


    Other methods for helping your son are the Picture Exchange Communication System (PECS) which has pictures for your child to use when he finds difficulty in expressing himself and his needs. Our daughter, who is six, speaks fluently on a very superficial level. However, she needs pictures to sequence events and constant reassurance that her needs will not be ignored and are understood. Our daughter can’t read or write, yet when she sees signs and pictorial representations she can generally grasp the meaning of what information is being conveyed.


    Finally, higher-level language is often the most cause for concern for children, as they fail to grasp the implied meanings in social settings and communication exchanges, as well as gestures, idioms and facial expressions.


    Try and help your son by showing him pictures and gauging his understanding of events in the picture – for example, potentially dangerous situations, children being excluded and more everyday situations, like roads, cars and traffic, and what would happen if he ran into the road.


    We wish you and your son all the best. Enjoy the journey – you will learn things you never thought you would!” Jeanette and Don Pearson


    CBeebies logo

    Something Special is a BBC CBeebies programme and website, aimed at children with learning difficulties. For more information, visit http://www.bbc.co.uk/cbeebies/somethingspecial/


    Echolalia


    Echolalia is meaningful communication and easily translated if you look at the total context in which echolalic statements are uttered, rather than taking them at face value and perceiving them to be meaningless. Many echolalic utterances will be about safety and security from the autistic person’s perspective.


    laptop

    A few more sites…can never have too many:) ~ either specifically for PECS or speech related:


    Nonverbal Communication Pages:


    http://trainland.tripod.com/pecs.htm


    Widget Software:


    http://www.widgit.com/


    Special Education Technology – British Colombia – Assistive Techology for K-12 Students:


    http://www.setbc.org/#top


    Speaking of Speech:


    http://www.speakingofspeech.com/


    Speech Fun:


    http://www.speechfun.com/


    Use Visual Strategies:


    http://www.usevisualstrategies.com


    Special Reports


    Support for Augmentative and Alternative Communication


    Children with little or no speech (augmentative and alternative communication) can now be supported by a wide range of communication aids, but much still depends on funding


    Augmentative and Alternative Communication (AAC) is the umbrella term used to describe the full range of communication methods that can be used to supplement or substitute for ‘normal’ speech or writing when these are impaired or absent. The term encompasses everything from gestures and signing, to aids, which can be low-tech (such as picture boards) or high-tech (employing the latest technology). Impaired communication or speech loss can result from a range of conditions, including Down’s syndrome, autistic spectrum disorders (ASD), acquired brain injury, cerebral palsies, hearing impairment and learning disability.


    While exact numbers of people who need AAC are not known, research carried out in 2007 by Scope as part of its No Voice, No Choice campaign estimated that 600,000 people in the UK would benefit from it, including 106,000 young people aged between five and 18. However, as the researchers note: ‘Whilst these figures give an indication of the overall level of need; there are no national statistics on what proportion of this population are getting their communication needs met.’


    So what solutions are available and what do we know about current provision? Communication aids are usually split into two broad groups: unaided and aided, with the aids sub-divided into low-tech and high-tech. There is an obvious risk in labelling aided AAC systems in this way, in that it could suggest that some are better than others. This is not the case: as with much technology, there is no point in using high-tech solutions if low-tech resources will do the job. Most of us have learnt this lesson the hard way when a high-tech device has let us down in a situation where the low-tech solution would have been more than adequate.


    Deciding which form of AAC a child needs requires a full and ongoing assessment, as the child’s needs are likely to be complex and may change over time. Assessment should involve family members as well as teaching and support staff, as the system chosen is likely to be used at home as well as in school. If the child’s needs are complex, it is best if a qualified and experienced professional carries out the assessment.


    Where the child’s communication needs are not so severe it may be that an unaided or low-tech system to complement ‘normal’ speech will suffice. Many mainstream schools with units catering for children with speech, language and communication needs support spoken English with either one of the established signing systems (of which more later), or a system of objects, pictures or symbols. For example, a range of objects might be used to indicate what is going to happen next, such as a paintbrush to signify art or a triangle for music. These are sometimes referred to as ‘objects of reference’. Photographs are used instead of real objects in some instances, such as to show the items on a lunchtime menu. Sometimes line drawings or symbols might replace images, as they do in everyday life where it is critical that everyone understands what is being said, as in the warning signs we see on the roads.


    Signs
    British Sign Language (BSL) is probably the best known of the established signing systems. Although BSL is now familiar to most people through its use in signed performances and on television, its widespread adoption and development are relatively recent. The British Deaf Association’s Dictionary of British Sign Language was not published until 1992 and BSL was not recognised as an official British language until 2003. The exact number of people in the UK who use BSL as their first language is not known and common estimates range between 30,000 and 70,000.


    BSL is different from other national sign languages because it is a visual-gestural language with its own grammar, syntax and dialects. Other signing systems draw on BSL, but they do not have the status or structure of a language. While BSL is used almost exclusively within some sections of the deaf community, it is these other signing systems that are used to complement spoken English in many schools where children’s speech, language and communication needs are due to causes other than deafness. There are four main signing systems that you are likely to come across.


    • Signed English

    Signed English, based on BSL, emerged in the 1980s in response to pressure for the use of sign in the education of deaf children. It follows the word order of spoken English and uses additional signs and finger spelling to convey what is being said. Originally developed for use within schools for deaf children, it is now also used with children and adults who have impaired speech and language. Signed English has a sign for every word and is regulated by the Working Party on Signed English.


    • Makaton

    Makaton was first developed in 1972 in Surrey as a project to teach sign language to deaf adults with learning disabilities and is now especially popular in early years settings, where it is used with children with delayed speech. Today it is an internationally recognised communication system, used in more than 40 countries. Makaton uses signs and symbols to support spoken and written English. Based on BSL, it uses a carefully selected core vocabulary (approximately 450 words/signs) structured into graded stages of increasing complexity. This core vocabulary can be combined to form short phrases and sentences and can be used in combination with other alternative communication tools.


    • Paget Gorman Signed Speech

    Paget Gorman Signed Speech was originated by Sir Richard Paget in the 1930s and developed by Grace Paget and Dr Pierre Gorman after Sir Richard’s death in 1955. It consists of a large vocabulary of approximately 4,000 words/signs, extended through the use of affixes to more than 50,000 words. Wherever possible, words are grouped together around a series of Basic Signs. Each word in a group uses the Basic Sign with a gesture that identifies the specific word. Signs are presented in the same sequence as the words in the spoken phrase or sentence. Paget Gorman is primarily used for people with specific speech disorders not related to learning disabilities. A simplified version is used with young children.


    • Signalong

    Signalong emerged in the 1980s when a group of practitioners wanted a signing system that was more flexible than Makaton. Signalong is a sign-supporting system: it requires you to speak as you sign. Signalong uses unaltered BSL signs wherever possible and is loosely modelled on the structure of the Derbyshire Language Scheme. Phase 1 of Signalong was first published in April 1992. Since then the authors have added to the core vocabulary, now available in four manuals, and published additional resources covering educational and vocational topics. Signalong is now widely used in the UK and Europe.


    Symbols
    Many AAC systems use symbols as well as signs. Some are specific to a particular signing system, such as Makaton, while others have been developed independently. At an elementary level, symbols can be used to reinforce speech or signs, or to supplement written text.


    A small number of symbol systems besides Makaton are now well established and widely used. These include Widgit Literacy Symbols (previously known as Rebus) and Picture Communication Symbols (PCS: also referred to as Boardmaker Symbols and not to be confused with PECS, the Picture Exchange Communication System). Signalong doesn’t have its own symbol set but is working closely with Widgit to match its signs to WLS. As Signalong explained earlier this year: ‘We have always been clear that our core expertise is in sign-supported communication. While we strongly promote the Total Communication approach [an approach to deaf education that aims to make use of a number of modes of communication, depending on the particular needs and abilities of the child], we have always preferred to work with others who have special skills in other formats rather than introduce unnecessary competition.’


    WLS and PCS have much larger vocabularies than other symbol systems and include a range of grammatical elements. This means they are inherently more flexible and symbols can be combined to form sentences and phrases. WLS, for instance, consists of 7,000 images in colour and black-and-white, covering a vocabulary of over 20,000 words.


    Symbol systems have long been an important tool for aiding communication but it is computers that have really transformed their use. Bespoke and mainstream software programs have simplified the creation of symbols-based resources and made the translation of text into symbols and vice versa far easier.


    Boardmaker from the American company Mayer-Johnson is among the best known software package for creating printed symbol-based resources. The program features more than 4,500 Picture Communication Symbols in colour and black-and-white, sample boards and templates. A new feature of the latest version of Boardmaker is the Symbolate button, which automatically inserts symbols alongside text as the user types. Boardmaker Plus builds on these features by allowing the user to create on-screen activities such as audio, animations and video.


    Widgit produces another popular range of symbol-based software, which includes Writing with Symbols 2000, a talking word processor that also automatically inserts symbols as you type. Other features include the generation of grids to make teaching and communication resources, and the on-screen grids to be used as an aid to writing. Widgit’s other products include the Communicate suite, which consists of a desktop publishing program (Communicate: In Print, now available as Communicate: In Print 2), a program for generating early learning activities (Communicate: By Choice) and, most recently, a word and symbol processor for emergent writers (Communicate: SymWriter).


    Although a number of symbol-based systems exist, the differences are subtle and there is extensive collaboration between the producers. In 2007 Widgit Software and Mayer-Johnson announced they were teaming up to bring both companies’ products to one another’s home markets.


    Widgit says its own system (WLS) is designed to support literacy and written information, while Picture Communication Symbols are designed for face-to-face communication, as in communication aids for people with no speech. In the UK, both systems are also available through Inclusive Technology. Makaton is also now compatible with Communicate in Print, Symwriter (version 1.1.6444) and Writing with Symbols. As well as the established symbol sets, users of both WLS and PCS can import their own drawings and photographs. PCS can also be used in the Clicker software produced by Crick Software, which is popular in both mainstream and special schools.


    High-tech aids
    Children who have little or no speech might benefit from using a dedicated Voice Output Communication Aid (VOCA) as well as sign and symbol systems. These enable the child to communicate in a setting where signing or the use of symbols is not an option,  extending the child’s independence.


    VOCAs range from single-message devices to those capable of storing thousands of messages. Understandably, the more complex the device the higher the price, which is why at this level, above all others, professional assessment is essential. Factors to be considered in choosing a VOCA include the setting in which it will be used, the cognitive ability of the user, how the device will be accessed, appropriate mounting, whether the device will use symbols or text (or both), the type of display (static or dynamic), training, support and, of course, cost.


    Scope’s No Voice, No Choice campaign produces a useful Communication Aids Journey Map, which shows the varied — and at times tortuous — routes to acquiring a VOCA. It can be downloaded from www.timetogetequal.org.uk. Help in choosing an appropriate device can be provided by a number of centres, including the ACE Advisory Trust, the ACE Centre North, CENMAC, AbilityNet and the CALL Centre in Edinburgh. Most centres have a loan bank of equipment, which means children can try out devices before deciding which one to opt for. With the rapid changes in technology it is no surprise that the choice of communication devices has mushroomed in recent years. ACE North’s database of VOCAs includes more than 120 devices although, thankfully, there are relatively few key suppliers. Major names include DynaVox (Mayer Johnson’s sister company), Liberator (part of the Prentke Romich group), AMDi, AbleNet, Attainment Company, Toby Churchill and Techcess.


    All VOCAs work by allowing the user to trigger pre-recorded messages, either directly — by touching the relevant text, image or symbol — or indirectly, through scanning and the use of switches. Devices that offer more stored messages than can be reasonably accommodated on the screen do so by storing them in ‘levels’. AMDi’s Smart/128, for example, has a maximum of 128 messages per level and six levels, which means it can store up to 768 messages of 2.25 seconds in length. Optional interchangeable keyguards on a system like this mean that a single user can choose between 4, 8, 16, 32 and 128 ‘buttons’ by grouping locations together. This means the device’s set-up can be changed depending on the user’s ability or the context in which it is being used. On some multi-level VOCAs, it is necessary to change the overlay to access a different level, while on those with ‘dynamic’ pages the level can be changed by pressing a button.


    While dedicated aids simply provide speech output non-dedicated or ‘open’ devices combine speech output with other features. These might include wi-fi connectivity giving access to the typical features of a laptop computer, including email and the internet, or environmental control systems (ECS) that allow the user to turn on the lights or draw the curtains.


    Funding
    While technical advances in communication aids have created impressive new opportunities for their users, they have also highlighted a paradox all too familiar to those who work in the field of special educational needs. While everyone will happily subscribe to the view that society should do all it can help individuals realise their potential, there is a cost associated with making each opportunity a reality. Scope’s 2007 Communication Aids Survey found that the average cost of a high-tech aid was £5,800, with 47 per cent of respondents’ aids costing over £5,000. As the survey report noted:
    ‘The prohibitively high cost of AAC equipment, not including the ongoing costs of insuring, servicing and repairing equipment, means that disabled people on low incomes who cannot get equipment funded by statutory sources are often left without a voice. Significant numbers of people are still told by statutory agencies to ask charities to fund AAC equipment that should be provided
    as of right.’


    Rectifying this situation is at the heart of the campaigning efforts of Scope and other organisations concerned about provision for those with speech, language and communication needs (SLCN). Between 2002 and 2005-06, the Department for Education and Skills provided £5m a year through the Communication Aids Project (CAP) to help meet some of the demand for communication aids.


    During this time, equipment was provided for more than 4,100 children and young people whose needs had not been met locally. Following CAP’s closure, campaigners lobbied for replacement funding.


    Understandably, many organisations and individuals raised this issue in the course of the recent Bercow Review. In its final report, the review panel recommended ‘appropriate commissioning, guidance and inspection arrangements should be in place by April 2010 with funding streams identified and mandated across government, including the Department of Health and the Department for Children, Schools and Families’. It also proposed an immediate injection of capital for purchasing, monitoring and measuring the supply of equipment and services, and of revenue funding to avoid the imminent closure of both the ACE Centres. The government’s long-awaited Child Health Strategy, due to be published in the autumn, is expected to contain detailed proposals relating to this.


    Meanwhile, Scope launched the second phase of its research project in August, ‘aiming to find out the true scale of the current crisis affecting communication equipment users’.


    Its new survey is targeted at professionals and statutory agents, such as speech and language therapists, as well as people involved in the commissioning, assessment, provision and support of AAC services.


    Ruth Scott, head of policy at Scope, said: ‘The UK is facing a real communication aid crisis — thousands of disabled people are being denied their right to communicate because they cannot get access to the equipment and support they need. It is essential that professionals and statutory agents are given the opportunity to discuss their experiences of providing AAC services and suggest ways of improving the current situation. This will help us achieve our goal of ensuring that those with communication impairments are able to speak for themselves.’


    Scope is calling for any professionals who are concerned with disabled people’s use of AAC, including those working for statutory agencies, to get involved in the research project.


    For more details go to www.timetogetequal.org.uk

    Links


    General
    1 Voice
    Afasic
    Bercow Review
    Communication Matters
    ICAN
    Scope’s No Voice, No Choice campaign


    Assessment

    ACE Centre Advisory Trust
    ACE Centre North
    AbilityNet
    CALL Centre
    CENMAC


    Signing
    BSL
    Makaton
    Paget Gorman
    Signalong
    Signed English


    Symbols
    Makaton
    PCS
    WLS



    Source:   http://www.teachingexpertise.com/articles/support-augmentative-and-alternative-communication-4968



    Pragmatics – The Art Of Conversation


    Carol Gray developed a technique entitled Comic Strip Conversations as a pictorial representation of the different levels of communication that occur on a conversation. Stick figures, speech and thought ‘bubbles’, symbols and colour are used to enable the child to see aspects they may not have been aware of.


    Take the skill of learning how to interrupt a conversation without causing offence or disruption, for example. It’s quite complex and difficult to explain, but a picture is worth a thousand words. The technique of using drawings of stick figures and speech bubbles may be applied to a wide range of situations that are proving challenging conversation and social skills wise. Speech bubbles may be drawn in a variety of ways to convey emotion – for example, sharp edges may be used to indicate anger or wavy lines may be used to indicate anxiety. Colours may also be useful in conveying happy or positive statements. These may be written in green, for example, while unpleasant thoughts may be written in red. In developing a colour chart, embarrassed comments may be written in pink marker, while sad feelings are written in blue. These may then be translated into relevant aspects of the person’s tone of voice or body language.


    Comic Strip Conversations are a wonderful tool in allowing children to analyse and understand the range of messages and meanings that are a natural part of conversation or play. While children may become naturally confused and upset by teasing or sarcasm, speech and thought bubbles in conjunction with colour choice, can illustrate the hidden messages.


    Carol Gray learned that children on the spectrum often assume that the other person is thinking exactly what they are thinking or they assume the other person was thinking exactly what they said and nothing else. Comic Strip Conversations can be beneficial in showing that each person may have very different thoughts and feelings in the same situation. An added advantage is that they may be used to represent the sequence of events in a conversation , as well, illustrate the effects of a range of alternative comments or actions for different scenarios.


    My Social Stories Book

    Carol Gray

    http://www.jkp.com/catalogue/book/9781853029509


    Revealing the Hidden Social Code: Social Stories TM for People with Autistic Spectrum Disorders

    Marie Howley and Eileen Arnold

    Foreword by Carol Gray

    http://www.jkp.com/catalogue/book/9781843102229


    Acting Antics: A Theatrical Approach to Teaching Social Understanding to Kids and Teens with Asperger Syndrome

    Cindy B. Schneider

    http://www.jkp.com/catalogue/book/9781843108450


    Getting IT: Using information technology to empower people with communication difficulties

    Dinah Murray and Ann Aspinall

    http://www.jkp.com/catalogue/book/9781843103752


    Baj and the Word Launcher: Space Age Asperger Adventures in Communication

    Pamela Victor

    http://www.jkp.com/catalogue/book/9781843108306


    Brief Summary of Strategies for Language


    Pragmatics


    Learn:


    appropriate opening comments


    to seek clarification or assistance when confused


    Encourage confidence to admit ‘I don’t know’


    Teach the cues of when to reply, interrupt or change the topic


    Model sympathetic comments


    Whisper in the child’s ear what to say to the other person


    Use speech and drama activities on the art of conversation


    Use Social Stories and Comic Strip Conversations as a verbal or pictorial representation of the different levels of communication


    Literal Interpretation


    Think how your comment or instruction could be misinterpreted


    Explain metaphors and figures of speech


    Prosody


    Teach how to modify stress, rhythm and pitch to emphasise key words and associated emotions


    Pedantic Speech


    Avoid abstractions and lack of precision


    Idiosyncratic Words


    A genuinely creative aspect of Asperger’s Syndrome to be encouraged


    Vocalising Thoughts


    Encourage whispering and ‘think it, don’t say it’ when near other people


    Auditory Discrimination and Distortion


    Encourage asking for the instruction to be repeated, simplified, put into other words or written down


    Pause between instructions


    Verbal Fluency


    Anxiety may inhibit speech and require treatment


    Both children and adults on the autism spectrum are prone to stuttering when anxious. Language skills in this case tend not to be the issue, but rather, the effect of emotion on the ability to speak. There are a range of strategies that may assist in coping with anxiety should stuttering become an issue. For further information …


    “Autism Spectrum Disorders and Stuttering”
    http://www.stutteringhelp.org/Default.aspx?tabid=625


    [Being lost for words, or even being mute may certainly be due to high levels of anxiety. Prolonged periods of severe anxiety can lead to a secondary psychiatric condition such as Obsessive Compulsive Disorder.]


    Articles


    “Communicating with Children Via Fragrance”:
    http://aspie-editorial.blog-city.com/communicating_with_children_via_fragrance.htm


    Selective Mutism “Big Rise in Children Left Mute Outside the Home”:
    http://aspie-editorial.blog-city.com/selective_mutism_big_rise_in_children_left_mute_outside_the.htm


    “Benefit of Early Detection of Developmental Language Disorders Cannot Be Proven Due to Lack of Data”:
    http://aspie-editorial.blog-city.com/benefit_of_early_detection_of_developmental_language_disorde.htm


    “Speech & Language Issues in Children”:
    http://aspie-editorial.blog-city.com/speech__language_issues_in_children.htm


    USA TODAY “iPhone Applications Help The Autistic”:
    http://aspie-editorial.blog-city.com/usa_today_iphone_applications_help_the_autistic.htm


    “Assistive Technologies eSchool News: Five Key Trends In Assistive Technology/Talking Head Baldi Now An iPhone App”:
    http://aspie-editorial.blog-city.com/assistive_technologies_eschool_news_five_key_trends_in_assi.htm


    “Communication: Voice4u iPod Touch iPhone App”:http://aspie-editorial.blog-city.com/communication_voice4u_ipod_touch_iphone_app.htm


    “A Crucial Tool In English Language Development: Reading To Our Children”:http://aspie-editorial.blog-city.com/acrucial_tool_in_english_language_development_reading_to_ou.htm



    First Published Wednesday, 4 February 2009


    Sensory Room

    An interactive sensory room is helping Rosehill School, St Ann’s Nottingham, pupils to learn


    PUPILS at a St Ann’s special school are embarking on global adventures and can even control the weather.


    It’s made possible in the Multi Interactive Learning Environment (MILE) recently installed at Rosehill School.


    Virtual worlds can be created inside the £35,000 facility.


    Scenarios can range from windy days to snowy evenings, underwater diving missions to mountain climbs, even journeys to erupting volcanos or treks in the South American rainforest.


    Sights, sounds and textures create a sensory experience which calms pupils, helps them to put scenarios into context and learn about the world around them.


    Click here!Wind, smoke and snow machines and state-of-the-art technology work together in the MILE and even smells can be generated to give authenticity.

    Rosehill teaches around 90 pupils, from five to 19, who all have varying degrees of autism and Aspergers syndrome.


    Deputy head Andy Sloan said: “Our pupils have autism, which is a spectrum disorder.


    “It means they are affected in different ways. Some pupils are very sensitive to smells so our staff don’t wear perfume or aftershave that is too strong. Others crave noise, for example, and like to stimulate their senses.


    “Sensory impairment can affect different people in different ways and the MILE helps to regulate their experience and the sensory input.


    “Our children absolutely love the MILE and their parents do, too.


    “It makes them [pupils] so calm and relaxed and if they are calm they learn more effectively.


    “The MILE helps them understand concepts and scenarios which they may not be able to imagine as easily as other pupils.”


    Classes use the equipment twice a week.


    As more such areas are installed at other schools, it is hoped that programmed scenarios can be shared and best practice created to get the most out of the innovative learning resource.


    Mike Anderton, who is a sensory advisor at Experia, a designer and manufacturer of equipment for special schools and adults, helped Rosehill staff create the scenarios in the MILE.


    Mr Anderton said: “There are 30 MILEs in various guises and sizes in the UK.


    “Rosehill School’s is currently the only fully operational MILE in Nottingham and Notts schools and is one of our largest MILEs that exists.


    “It is a very flexible space and provides very valuable and meaningful learning.


    “Its a key MILE also as other schools visit Rosehill School to see how effective it is.”


    The MILE was paid for using a donation from British and Irish Rugby charity Wooden Spoon.


    It uses donations to support mentally and physically disadvantaged children.


    michael.greenwell@nottinghameveningpost.co.uk


    Source:   http://www.thisisnottingham.co.uk/homenews/Technology-sets-school-MILEs-apart/article-660360-detail/article.html



    First Published Wednesday, 4 February 2009


    A headshot of Jacobus tenBroek from the left side.

    Jacobus ten Broek was a founder of the National Federation for the Blind — one of the first organizations of people with disabilities to insist that those with disabilities sit on the board and direct the organization.


    When : April 17, 2009
    Where: The National Federation of the Blind
    Jernigan Institute
    1800 Johnson Street
    Baltimore, MD 21230


    View the Agenda (Word
    file)<http://www.nfb. org/images/ nfb/Agenda% 202009%20symposi um.doc>


    Registration :


    Registration Fee . . . . . . . $150.00
    Student . . . . . . . . . . . . . $20.00


    A limited number of scholarships to cover the registration fee will be
    available to individuals with demonstrated financial need.


    To register online<https://www. nfb.org/Forms. asp?MODE= NEW&SnID= 2021426860& Forms_FormTypeID =-129>,
    payment must be made by credit card at the time of registration.


    To register by mail or fax, *download the registration form (Word
    file)<http://www.nfb. org/images/ nfb/2009% 20symposium% 20registration% 20form.doc>
    *. Completed registration forms with credit card information may be faxed
    to Lou Ann Blake at (410) 659-5129. Mail forms giving credit card
    information or enclosing check made payable to the National Federation of
    the Blind to:


    Lou Ann Blake
    National Federation of the Blind
    1800 Johnson Street
    Baltimore, MD 21230


    Hotel Information :


    A block of rooms has been reserved for law symposium participants at the
    Holiday Inn Inner Harbor, located at 301 West Lombard Street, Baltimore,
    Maryland 21201. Rooms may be reserved for April 16 and 17, 2009, at the
    rate of $157.00 per night, plus applicable taxes and surcharges, by calling
    the hotel directly at (410) 685-3500 and requesting the National Federation
    of the Blind block, group number 373400. Reservations must be made by 3:00
    p.m., March 26, 2009. The NFB will provide a free morning and evening
    shuttle between the hotel and Jernigan Institute. Participants who will be
    staying at the Holiday Inn and who require accessible transportation should
    contact Lou Ann Blake by April 1, 2009.


    Accommodations : Symposium materials will be provided in print, large
    print, and Braille. Participants who require other accommodations should
    contact Lou Ann Blake by April 1, 2009.


    For More Information Contact: Lou Ann Blake, Law Symposium Coordinator
    Phone: (410) 659-9314, extension
    2221
    E-mail: lblake@nfb.org


    “The right of access to public accommodations and common carriers is a
    civil right. It is a basic right indispensable to participation in the
    community, a substantive right to which all are fully and equally
    entitled.” Jacobus tenBroek, The Right to Live in the World: The Disabled
    in the Law of Torts, 54 CAL. L. REV. 841, 858 (1966).
    About the Symposium


    Jacobus tenBroek founded the National Federation of the Blind in 1940 and
    served as its president until his death in 1968. He was a constitutional law
    scholar, a blind professor at Berkeley, and an author of treatises on the
    Fourteenth Amendment and social welfare. Dr. tenBroek created the concept
    that civil rights should apply to disabled Americans, [image: Jacobus
    tenBroek works at his desk.]and he published extensively regarding the
    variables involved in the application of the law to those with
    disabilities. That blind and other disabled people have been able to gain a
    substantial measure of participation in American life is largely due to Dr.
    tenBroek’s thought and energy.


    To carry forward the work of Dr. tenBroek in assuring that all citizens may
    have the opportunity for full participation in the society in which we live,
    the National Federation of the Blind is hosting the Jacobus tenBroek
    Disability Law Symposium. The 2009 symposium, “New Perspectives on
    Disability Law: Advancing the Right to Live in the World,” will examine the
    new perspectives on disability law both in the United States, brought about
    by the election of a new administration and the signing of the ADA
    Amendments Act, and internationally, as a result of the ratification of the
    United Nations Convention on the Rights of Persons with Disabilities. The
    symposium will consist of five panels of distinguished law professors,
    practitioners, and advocates, who will discuss various aspects of both
    United States and international disability law. Invitations to present have
    already been accepted by Samuel Bagenstos, Professor of Law at Washington
    University School of Law and Visiting Professor at the University of
    Michigan School of Law; Gerard Quinn, Professor of Law at the National
    University of Ireland, Galway; and Peter Blanck, University Professor and
    Chair of the Burton Blatt Institute at Syracuse University. We have also
    extended invitations to officials of the Obama administration including the
    United States Attorney General and the White House advisor on disability
    policy. *Ari Ne’eman, president of The Autistic Self-Advocacy Network, will
    give the luncheon keynote address.


    —
    Ari Ne’eman
    President
    The Autistic Self Advocacy Network
    1660 L Street, NW, Suite 700
    Washington, DC 20036
    http://www.autistic advocacy. org
    732.763.5530



    First Published Wednesday, 4 February 2009


    Mitchell Library, Glasgow

    Autistic adults from across Scotland have highlighted their own experiences of living with the condition by producing artwork and poetry, which is being shown in an unique exhibition running at the Mitchell Library, Glasgow from 10-16 February.


    The pieces in the exhibition, entitled ‘My life with autism or Asperger syndrome’ were entries in The National Autistic Society’s recent creativity competition, and provide fascinating individual perspectives of autism through poetry and prose, 2D art and photography.


    The competition is part of our ongoing I Exist campaign, launched in 2008, which highlights the lack of support available for adults living with autism. Based on the largest ever survey in Scotland on the experiences of adults with autism and their families, the campaign revealed for the first time the daily reality for many thousands of adults who feel isolated, ignored and unable to access the required support.


    Carol Evans, National Director of NAS Scotland and Northern Ireland, said: “There are 50,000 people in Scotland with autism - that’s 1 in 100 – and many adults with autism from across Scotland tell us how important art and creativity are to their well-being.

    “We believe this exhibition is an exciting and rewarding way of showing how a person with autism expresses themselves and it allows us to share their unique experiences and creativity. We hope that the works in this exhibition will bring home to the general public just some of the realities faced by adults living with autism across Scotland today.”


    The exhibition can be seen at the Mitchell Library, Glasgow, from Tuesday 10th February until Friday 16th February 2009, from 9am to 8pm.

    For more information about the I Exist campaign and how you can get involved, visit www.think-differently.org.uk


    Related resources



    External links


    Source:  http://www.nas.org.uk/nas/jsp/polopoly.jsp?d=253&a=18695



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