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petition about Autism Speaks

by mfasp @ 27/03/2008 - 11:36:47

The Autism Speaks: Don't Speak For Me petition

www.autism-hub.co.uk/autism-speaks-dont-speak-for-me/index.php

We, the undersigned:

  • Utterly repudiate the notion of murder being an acceptable response to disability
  • Vehemently deny that most parents of autistic — or otherwise disabled — children harbour thoughts of murder
  • Testify that the false 'reality' concocted by Autism Speaks film 'Autism Every Day' is not a true reflection of the reality of parenting an autistic child
  • Call for a public apology from Lauren Thierry for increasing ignorance regarding autism

 
 

Midnight In Chicago: podcast on bullying

by mfasp @ 16/03/2008 - 18:31:57

Midnight In Chicago is an international culture and tourism initiative raising awareness and funds for autism and for underrecognised artists. It is co-run by Thomas Taylor who is also a valuably active opponent of Aspies For Freedom.

Autism and Bullying: Part One

www.mic.mypodcast.com/

This is part one of a two-part podcast on the issue of bullying as
it relates to children on the autism spectrum.

A clear definition of bullying, identifying bullies, the causes for
bullying and more are examined in the first part of this podcast.

This FREE 16 minute audio podcast is offered by Midnight In Chicago
to the the listening public.

Please spread the word, and feel free to link to all the Midnight In
Chicago autism spectrum podcasts.

Thomas and Raven

15 Mar 2008

Autism and Bullying: Part II Podcast Now Available

Midnight In Chicago is pleased to announce the public posting of Part II of our Autism and Bullying Podcast.

Both Part I and Part II of the Autism and Bullying Podcast are of interest to people with ASDs, as well as parents, siblings, relatives, friends, teachers, physicians, and caregivers of those on the autistic spectrum.

Like ALL of our Midnight In Chicago Podcasts, Autism and Bullying Parts I & II are FREE to the general public.

Go here to download:

www.mic.mypodcast.com/

And please be sure to tell your friends and whomever else might be interested in hearing them.

To learn more about the Midnight In Chicago project which seeks to raise funds and awareness for autism, be sure to visit www.midnightinchicago.com. The purchase of Midnight In Chicago products helps to pay for the production of these podcasts.

Many thanks to those who have supported us.

Thomas and Elyse

7 Apr 2008

Youtube group for exposing Wikipedia

by mfasp @ 02/03/2008 - 16:23:49

Site: Nadir Ali Rahman, one of thousands who have experienced the corruption of power and aggressiveness at the core of Wikipedia's admin system, has circulated a notice of a project to spread the alert against Wikipedia through Youtube. His heading, on the page linked to, contains an anti-Zionist personal view, but the resistance to Wikipedia should be nothing to do with whether you support Zionism or not.

youtube.com/group/stopwikipedia

Get a youtube account and select the link where it says join this group.

If you find any anti-Wikipedia videos you can just add it to our group page for everyone to see.
All the best & hope you & your friends join.

david cunningham on simon baron-cohen

by mfasp @ 22/12/2007 - 12:12:43

Site: David Cunningham, the angry parent in Fife, perceives Simon Baron-Cohen to be too pro-government in his writing in the Times, 15 Dec 2007, and asked for his grounds for saying that to be circulated.

PM Brown is my MP and although he has ignored and dumped my son due to the embarrassment of his party's policies in Scotland he knows that my son is typical of the bulk of people with Autism where my son has received no quality, competent Education for nearly 4 years, locked in the house with only his parents for support.

In the last 18 months, after fighting Gordon Brown's Fife Social Services for over 10 years they gave my son 16 hours per week of support. The fact that my son's Psychiatrist Dr Rosemary Logan, son's Senior Social Work Mangers Janice McCrimmond, Dave Lister, Donald Ramsay and Senior Social Worker Arlene Honeyman have all stated that my son's needs are 24 hour 7 day has had no impact on a system that is now bankrupt.

On Friday the 14th December 2007 (my son's adult birthday) my son was totally dumped by the PM's Constituency for Xmas and New Year. All professionals in the PMs constituency know the situation and despite the fact that the 16 hour per week funding ran out on the 16th October 2007 I received a communication from Senior Managers within the Prime Minister's Constituency that the Social Service Committee set up and reporting to Mr Stephen Moore Director of Prime Ministers Fife Social Services had again rejected the package for my son. BUT IT IS WORSE THAN THAT. SENIOR SOCIAL WORK MANAGERS JANICE MCCRIMMOND, AND DAVE LISTER HAVE ASSESSED MY SON AS REQUIRING 24 HOUR 7 DAY PER WEEK SERVICES. YET THEY HAVE BEEN TOLD BY THEIR BOSS'S TO ONLY APPLY FOR 33% OF 24/7. SO MR STEPHEN MOORE DIRECTOR OF FIFE SOCIAL SERVICES NOT ONLY KNOW'S THAT 66% OF MY SON'S NEEDS WERE REMOVED BUT WORSE MR MOORE EVEN REFUSED TO APPROVE THE 33%.

SO SINCE THE 14TH OF OCTOBER 2007 ALL FUNDING FOR MY SON RAN OUT. BUT IN A DESPERATE EFFORT TO COVER UP MR MOORE KNOWS THAT ONE OF HIS MANAGERS MR JIM BURKE IS REFUSING TO HAND OVER £7,803-40p OF FUNDING THAT HAS ALREADY BEEN SPENT. THE CORRUPT PM'S CONSTITUENCY WANT TO MAKE OUT THAT FUNDING IS STILL LEFT EVEN ALTHOUGH THE SERVICE PROVIDERS HAVE ALREADY SPENT THE MONEY PRE 14TH OCTOBER 2007. SO PROFESSOR BARON-COHEN THIS IS THE REALITY THROUGHOUT THE COUNTRY PUBLIC SERVICES ARE LYING THROUGH THEIR BACK TEETH TO PAINT A LOVELY XMAS SCENE. ...

NHS Fife have also refused to support the bulk of my son’s needs over the last 4 years Professor James McGoldrick and Dr Francis Elliot have stolen over £27k of my son's health budget. A budget that instead had to be fund raised through Car Boot Sales and Jumble Sales. Dr Elliot Director of NHS Fife Services has also personally intervened with our GP.

So in conlusion please will the 2400 on my distribution list pass this e-mail round the world.

How your autistic brothers and sisters are being treated

by mfasp @ 28/10/2007 - 15:38:53

Read the parts that are bolded.

Tom Taylor
28 Oct 2007

women.timesonline.co.uk/tol/life_and_style/women/families/article2732991.ece

Shock tactics

Hundreds of children no other school wants — from the autistic to the merely troubled — attend a centre in America where electric shocks are administered for even the smallest misdemeanour. Forced to wear 10lb backpacks with electrodes attached to their skin, they never know when their teachers will deliver this `behaviour-modification' therapy. Why hasn't the school been closed down?

Rob Santana awoke terrified. He'd had that dream again, the one where silver wires ran under his shirt and into his pants, connecting to electrodes attached to his limbs and torso. Adults armed with surveillance cameras and remote-control activators watched his every move. One press of a button, and there was no telling where the shock would hit – his arm or leg or, worse, his stomach. All Rob knew was that the pain would be intense. Every time he woke from this dream, it took him a few moments to remember that he was in his own bed, that there weren't electrodes locked to his skin, that he wasn't about to be shocked. It was no mystery to him where this recurring nightmare came from – not A Clockwork Orange or 1984, but the years he spent confined in America's most controversial "behaviour-modification" institution.

In 1999, when Rob was 13, his parents sent him to the Judge Rotenberg Educational Center, in Massachusetts, 20 miles outside Boston. The institution, which calls itself a "special-needs school", takes in all kinds of troubled kids – autistic, mentally retarded, schizophrenic, bipolar, emotionally disturbed – and attempts to change their behaviour with a complex system of rewards and punishments, including painful electric shocks to the torso and limbs. Of the 230 residents, about half are wired to receive shocks. Eight states send students to this institution, with New York providing the most. The price tag for a year there is $220,000; states and school districts pick up the tab.

The Judge Rotenberg Educational Center is the only institution in the US that disciplines students by giving them electric shocks, a form of punishment not inflicted on serial killers or child molesters, or any of more than 2.2m inmates in US jails and prisons. Over its 36-year history, there have been numerous lawsuits and government investigations. Last year, New York-state investigators filed a blistering report that made the place sound like a high-school version of Abu Ghraib. Yet the programme continues to thrive – in large part because nobody, except desperate parents and a few legislators, seems to care about what happens to the hundreds of kids who pass through its gates.

In Rob Santana's case, he freely admits he was an out-of-control kid with "serious behavioural problems". At birth he was abandoned at the hospital, traces of cocaine, heroin and alcohol in his body. A middle-class couple adopted him when he was 11 months old, but his troubles continued. He started fires; he got kicked out of preschool for opening the back door of a moving school bus; he cut himself with a razor when he was six. His mother took him to specialists, who diagnosed him with a slew of psychiatric problems: ADHD, post-traumatic stress disorder, bipolar disorder, obsessive-compulsive disorder.

Rob remained at the Rotenberg Center for about 3 1/2 years. From the start, he cursed, hollered and fought with employees. Eventually the staff obtained permission from his mother and a court to use electric shock. Rob was forced to wear a backpack containing five 2lb battery-operated devices, each connected to an electrode attached to his skin. "I felt humiliated," he says. "You have a bunch of wires coming out of your shirt and pants."

Rob remained hooked up to the apparatus 24 hours a day. He wore it while jogging on the treadmill and playing basketball, though it wasn't easy to sink a jump-shot with a 10lb backpack on. At night, he slept with the backpack next to him, under the gaze of a surveillance camera.

Employees shocked him for aggressive behaviour, he says, but also for minor misdeeds, like yelling or cursing. Each shock lasts two seconds. "It hurts like hell," Rob says. (The school's staff claims it is no more painful than a bee sting; when I tried the shock, it felt like a horde of wasps attacking me all at once. Two seconds never felt so long.)

On several occasions, Rob was tied face down to a four-point restraint board and shocked again and again by a person he could not see. The constant threat of being zapped did persuade him to act less aggressively, but at a high cost.

"I thought of killing myself a few times," he says.

Rob's mother, Jo-Anne deLeon, had sent him to the Rotenberg Center at the suggestion of his school district in New York, which, she says, told her that the programme had everything that Rob needed. She believed he would receive regular psychiatric counselling – though the school does not provide this. As the months passed, Rob's mother became increasingly unhappy. "My whole dispute with them was, `When is he going to get psychiatric treatment?' " she says. "I think they had to get to the root of his problems – like why was he so angry?"

She didn't think the shocks were helping, and in 2002 she sent a furious fax demanding that Rob's electrodes be removed before she came up for parents' day. She says she got a call the next day from the executive director, Matthew Israel, who told her: "You don't want to stick with our treatment plan? Pick him up." (Israel says he doesn't remember this conversation, but adds:

"If a parent doesn't want the use of the skin shock and wants psychiatric treatment, this isn't the right programme for them.")

After Rob left the centre he moved back in with his parents. At first glance, he seems like any other 21-year-old: baggy jeans, black T-shirt, powder-blue Nikes. But when asked to recount his years at the Rotenberg Center, he speaks for nearly two hours in astonishing detail, recalling names and specific events from seven or eight years earlier. When he describes his recurring nightmares, he rubs his forehead with his palms.

Despite spending more than three years at this behaviour-modification institution, Rob still has problems controlling his actions. In 2005 he was arrested for attempted assault and sent to jail. (This year he was arrested again, for drugs and assault.) Being locked up gave him plenty of time to reflect on his childhood, and he has gained a new perspective on the Rotenberg Center.

"It's worse than jail," he told me. "That place is the worst place on Earth."

The story of the Rotenberg Center is in many ways a tale of 2 schools. Slightly more than half the residents are what the school calls "high functioning": kids like Rob and Antwone, who have diagnoses like attention-deficit disorder (ADD), bipolar disorder, and post-traumatic stress disorder. The other group is even more troubled. Referred to as "low functioning", it includes kids with severe autism and mental retardation: most cannot speak or have very limited verbal abilities. Some have behaviours so extreme they can be life-threatening – chomping on their hands, running into walls, nearly blinding themselves by banging their head on the floor again and again.

The Rotenberg Center has long been known as the school of last resort – a place that will take any kid, no matter how extreme his or her problems are. Residents range in age from as young as 9 or 10 up to their forties. For desperate parents, the institution can seem like a godsend. Just ask Louisa Goldberg, the mother of 25-year-old Andrew, who has severe mental retardation. Andrew's last residential school kicked him out after he kept assaulting staff members; the Rotenberg Center was the only place willing to accept him. According to Louisa, Andrew's quality of life has improved dramatically since 2000, when he was hooked up to the shock device known as the graduated electronic decelerator (GED).

Louisa and many other parents like the Rotenberg Center's policy of not giving psychiatric drugs to students. At Andrew's last school, Louisa says: "He had so many medicines in him he'd take a two-hour nap in the morning, he'd take a two-hour nap in the afternoon. They'd have him in bed at eight o'clock at night. He was sleeping his life away." These days, Louisa says she is no longer afraid when her son comes home to visit. "[For him] to have an electrode on and to receive a GED is to me a much more favourable way of dealing with this," she says. "He's not sending people to the hospital [with injuries]."

Marguerite Famolare brought her son Michael to the Rotenberg Center 6 years ago, after he attacked her so aggressively she had to call the police and, in a separate incident, flipped over the kitchen table onto a tutor. Michael, now 19, suffers from mental retardation and severe autism. These days, when he comes home for a visit, Marguerite carries his shock activator in her purse. All she has to do, she says, is show it to him: "He'll automatically comply to whatever my signal command may be, whether it is `Put on your seat belt' or `Sit appropriately and eat your food.' It's made him a civilised human being."

State officials have twice tried to shut down the Rotenberg Center – in the 80s and again in the 90s. Both times parents rallied to its defence, and both times it prevailed in court. The name of the centre ensures nobody forgets these victories; it was Judge Ernest Rotenberg who, in the mid-1980s, ruled that the institution could continue using "aversives" – painful punishments designed to change behaviour – so long as it obtained authorisation from a local court in each student's case. These days, the court rarely, if ever, bars the Rotenberg Center from adding shock to a student's treatment plan.

Whenever the Rotenberg Center faces criticism, it relies on the testimonials of parents like Louisa Goldberg and Marguerite Famolare to defend itself. Not surprisingly, the most vocal parent-supporters tend to be those with the sickest children, since they are the ones with the fewest options. But at the Rotenberg Center, the same methods of "behaviour modification" are applied to all kids, no matter what their behaviour problems. And so, while Rob would seem to have little in common with mentally retarded students like Michael and Andrew, they all shared a similar fate once their parents placed them under the care of the same psychologist: a radical behaviourist known as Dr Israel.

In 1950, Matt Israel was a freshman at Harvard looking to fill his science requirement. He knew little about B F Skinner when he signed up for his course, Human Behaviour. But he became fascinated with Skinner's scientific approach to the study of behaviour, and he picked up Walden Two, Skinner's controversial novel about an experimental community based on the principles of behaviourism. The book changed Israel's life. "I decided my mission was to start a utopian community," he says.

Israel got a PhD in psychology in 1960 from Harvard, and started two communal houses outside Boston. In one of these houses, Israel lived with a three-year-old named Andrea, the daughter of a roommate. He recalls she was out of control: "Wild and screaming… When company would come over, she would walk around with a toy broom and whack people over the head." Through experiments with rats and pigeons, Skinner had demonstrated how animals learn from the consequences of their actions. With permission from Andrea's mother, Israel decided to try out Skinner's ideas. When Andrea was well behaved, Israel took her for walks. When she misbehaved, he snapped his finger against her cheek. Israel says his methods worked: "Instead of being an annoyance, she became a charming addition to the house."

Israel's success with Andrea convinced him to start a school. In 1971, he founded the Behavior Research Institute, an institution that would later become known as the Rotenberg Center. Israel took in the children nobody else wanted – severely autistic and mentally retarded kids who did dangerous things to themselves and others. To change their behaviour, he developed a large repertoire of punishments: spraying kids in the face with water, shoving ammonia under their noses, pinching the soles of their feet, smacking them with a spatula, forcing them to wear a "white-noise helmet" that assaulted them with static. After nearly 20 years, Israel began to move away from these methods and towards another one: electric shock. From his perspective, shock offered many advantages: "To give a spank, a muscle squeeze or a pinch, you had to control the student physically, and that could lead to a struggle. A lot of injuries were occurring." By using electric shock, which requires just pushing a button, he could eliminate the need for employees to wrestle a kid to the ground.

Israel purchased a shock device then on the market known as Sibis – Self-Injurious Behavior Inhibiting System – that had been invented by the parents of an autistic girl. It delivered a mild, two-second shock. Between 1988 and 1990, Israel used Sibis on 29 students, including one of his most challenging, Brandon, then 12, who would bite off chunks of his tongue, regurgitate entire meals, and pound himself on the head. At times Brandon was required to keep his hands on a paddle; if he removed them, he'd get shocks, one per second. One infamous day, Brandon received more than 5000 shocks. "You have to realise," Israel says, "I thought his life was in the balance. He was vomiting, losing weight. He was down to 52lb. I knew it was risky to use the shock in large numbers, but if I persevered that day, I thought maybe it would eventually work."

This day was a turning point in the history of Israel's operation: that's when he decided to ratchet up the pain. The problem, he decided, was that the shock Sibis emitted was not strong enough. "So we had to redesign the device ourselves," he says. He created his own, much more powerful shock device: the GED.

30 years earlier, O Ivar Lovaas, a psychology professor at the University of California at Los Angeles (UCLA), had pioneered the use of electric jolts to try to normalise the behaviour of autistic children. But eventually Lovaas abandoned these methods, telling a reporter in 1993 that shock was "only a temporary suppression" because patients become inured to the pain. "These people are so used to pain that they can adapt to almost any kind of aversive you give them," he said. Israel encountered this same sort of adaptation in his students, but his solution was markedly different: he decided to increase the pain once again. Today, there are two shock devices in use at the Rotenberg Center: the GED and the GED-4. They both administer a two-second shock, but the GED-4 is nearly three times more powerful – and the pain it inflicts is much more severe.

The Rotenberg Center is a bit like a carnival fun house, I found, during a two-day visit last autumn. Giant silver stars dangle from the lobby ceiling; the walls and chairs in the front offices are turquoise, lime green and lavender. Israel, 74, still holds the title of executive director, and when he first greets me, he appears utterly unimposing: short and slender with soft hands, rounded shoulders, curly white hair, paisley tie. Then he sits down beside me and, unprompted, starts talking about shocking children. "The treatment is so powerful it's hard not to use if you have seen how effective it is," he says. "It's brief. It's painful. But there are no side effects. It's two seconds of discomfort." His tone is neither defensive nor apologetic: it's calm. It's the sort of demeanour a mother might find comforting if she were about to hand over her child.

Before we set off on our tour of the institution, there's something Israel wants me to see: Before & After, a home-made movie featuring six of his most severe cases. He has been using some of the same grainy footage for more than two decades, showing it to parents of prospective students as well as reporters. It shows how in 1977, an 11-year-old girl, Caroline, arrives at the school strapped on a stretcher, her head encased in a helmet. Next, free from restraints, she tries to smash her helmeted head against the floor. In 1981 it shows Janine, also 11, who shrieks and slams her head against the ground, a table, the door. Bald spots testify to the severity of her troubles; she's yanked out so much hair it's half gone. Compared with these scenes, the "after" footage looks almost unbelievable: Janine splashes in a pool; Caroline grins as she sits in a chair at a beauty salon.

"These are children for whom positive-only procedures did not work, drugs did not work," says Israel. "And if it wasn't for this treatment, some of these people would not be alive." The video is very persuasive: the girls' self-abuse is so violent and so frightening it almost makes me want to grab a GED remote and push the button myself. Of course, this is precisely the point.

Considering how compelling the after-footage is, I am surprised to learn that 5 of the 6 children featured in it are still here. "This is Caroline," one of my escorts says later as we walk down a corridor. Without an introduction, I would not have known. Caroline, 39, slumps forward in a wheelchair, her fists balled up, head covered by a red helmet. "Blow me a kiss, Caroline," Israel says. She doesn't respond.

A few minutes later, I meet 36-year-old Janine, who appears in much better shape. She's not wearing a helmet and has a full head of black hair. She's also got a backpack on her shoulders and canvas straps hanging from her legs, the telltale sign that electrodes are attached to both calves. For 16 years – nearly half her life – Janine has been hooked up to Israel's shock device. A few years ago, when the shocks began to lose their effect, the staff switched the devices inside her backpack to the much more painful GED-4.

In 1994, Israel had just 64 students. Today he has 230. This astonishing rate of growth is largely the result of a dramatic change in the types of students he takes in. Until recently, nearly all were "low functioning" autistic and mentally retarded people. But today slightly more than 50% are "high functioning", with diagnoses like ADD, ADHD, and bipolar disorder. New York supplies most of these students, many of whom grew up in the poorest parts of New York City. Yet despite this change in his population, Israel's methods have remained essentially the same.

Students spend their days in classrooms, staring at a computer screen, their backs to the teacher. An elaborate system of rewards and punishments governs all interactions. Teachers and aides watch them all day, tallying their misbehaviours. Well-behaved kids can watch TV, go for a pizza, play basketball. Among the most prized rewards is a visit to the Big Reward Store, an arcade with pinball machines, video games, and flat-screen TVs hooked up to Xbox 360s. Each time a student curses or yells or disobeys the rules, a staffer marks it down on the student's "recording sheet". Staff then use the sheet to calculate what level of punishment is required – when to just say no and when to shock. They carry students' shock activators at all times, hooked on to their belts. Each activator is contained in a plastic case, or "sled", and each sled has a photo on it to ensure employees don't zap the wrong kid.

Employees shock students for a wide range of behaviours, from violent actions to less serious offences, like getting out of their seats without permission. Every time they shock a child, they are encouraged to use the element of surprise. "Attempt to be as discreet as possible and hold the transmitter out of view of the student," states the employee manual. This way, students cannot do anything to minimise the pain, like flipping over their electrodes or tensing their muscles. "We hear the sound of [a staffer] picking up a sled," says Isabel Cedeno, a former student. "Then we see the person jump out of their seat."

When they talk about why they use the shock device, Israel and his employees like to use the word "treatment", but it might be more accurate to use words like "convenience" or "control". "The GED – it's two seconds and it's done," says Patricia Rivera, a psychologist who serves as assistant director of clinical services. "Then it's right back to work." By contrast, it can take eight or 10 employees half an hour or more to restrain a strong male student: to pin him to the floor, wait for him to stop struggling, then move his body onto a restraint board and tie down each limb.

Even with the GED, the stories both students and employees tell make the place sound at times like a war zone: a teenage boy sliced the gym teacher across the face with a CD; a girl stabbed a staffer in the stomach with a pencil. While staff have been contending with injuries since Israel opened his institution, the recent influx of high-functioning students, some with criminal backgrounds, has brought a new fear: that students will join forces and riot. Tellingly, among high-functioning kids most of the violence is directed at the staff, not each other.

Rotenberg staff place the more troubled (or troublesome) residents on one-to-one status, meaning that an aide monitors them everywhere they go. For extremely violent students, the ratio is two to one. Before I set off on my tour, a small crowd gathered: it seemed that almost the entire hierarchy of the Rotenberg Center was going to follow me. That's when I realised that I'd been put on 5 to 1. As I roamed the school with my escorts, my every move monitored by surveillance cameras, I realised that it would be impossible to have a private talk with any student.

In the world of the Rotenberg Center, Katie Spartichino is a star. A former student, she left the institution in 2006 and now attends community college in Boston. Around noon, a staff member brings her back to the institution to talk to me. We sit at an outdoor table away from the surveillance cameras, but there's no privacy: Israel and Karen LaChance, the assistant to the executive director for admissions, sit with us. Katie, 19, tells me she overdosed on pills at 9, spent her early adolescence in and out of psychiatric wards, was hooked up to the GED at 16, and stayed on the device for 2 years. "This is a great place," she says. "It took me off all my medicine. I was close to 200lb and I'm 160 now." But when she first had to wear the electrodes, she says: "I cried. I kind of felt like I was walking on eggshells; I had to watch everything I said. Sometimes a curse word would just come out of my mouth. So being on the GEDs and knowing that swearing was a targeted behaviour where I'd receive a [GED] application, it really got me to think twice before I said something rude."

As Katie speaks, LaChance runs her fingers through Katie's hair again and again. The gesture is so deliberate it draws my attention. I wonder if it's just an expression of affection – or something more, like a reward.

"Do you swear any more?" I ask.

"Oh, God, all the time," Katie says. "I've learnt to control it, but I'm not going to lie. When I'm on the phone, curse words come out." The hair-stroking stops. LaChance turns to Katie. "I hope you're not going to tell me you're aggressive."

"Oh, no, that's gone," Katie says. "No, no, no. The worst thing I do sometimes is me and my mom get into little arguments."

For Israel, of course, one drawback of having so many high-functioning students is that he cannot control everything they say. One afternoon, when I walk into a classroom, a 15-year-old girl catches my eye, smiles, and holds up a sheet of paper with a message written in pink marker: "Help us." She shuffles it into her stack of papers before anyone else sees. When I move closer, she tells me her name is Raquel, she is from the Bronx, and she wants to go home.

My escorts allow me to interview Raquel while 2 of them sit nearby. Raquel is not hooked up to the GED, but she has many complaints, including that she has just witnessed one of her housemates get shocked. "She was screaming," Raquel says. "They told her to step up to be searched; she didn't want to, so they gave her one." After 20 minutes, my escorts cut us off.

Faculties Not Gifts

by mfasp @ 18/10/2007 - 13:04:33


www.scottishautismnetwork.org.uk/FacultiesNotGifts.doc

A write-up against homework + on how ASD has finally totally discredited the gifted children movement.

Adders: a new cull

by mfasp @ 09/07/2007 - 11:06:31

Site: A report of yet more purges on the Adders ADHD site has been added to the post of March 1 titled "Adders again", which may be found below, as it is a natural extension of it and continuation of the argument around it.

7 Jul 2007.

David Cunningham: Gordon Brown's Constituency - NHS Fife Break Health and Safety Legislation To Maximise Systematic Abuse

by mfasp @ 27/04/2007 - 15:48:20

Site: Passed on at his invitation.

Senior NHS Management in Gordon Brown's Constituency of Fife have for the last 3 1/2 years maximised the systematic abuse on a severely Autistic boy by playing politics with his health while breaking Health & Safety Legislation.

Nearly 3 1/2 years ago a severely disabled, vulnerable Autistic boy was identified by his Psychiatrist Dr Rosemary Logan as in desperate need of support for his "health and Well Being". The Clinical Advisory Panel (CAP) in Fife approved the health package as being desperate and indeed not to deliver it was agreed by all in CAP as breeching Health and Safety Legislation.

But what followed next highlighted just how bad things are in Gordon Brown's Constituency.

Dr Francis Elliot stated that while the service was going to have a significant impact on quote "the Autistic boy's health and well being" it was not within NHS Fife's competency remit to deliver the service because it was not what she called (Dr Elliot is now Director of health services Fife) "Direct Health Services". So she with the full support of Mr Brechin Senior Finance Manager and Professor James McGoldrick Chairman NHS Fife refused to release the funding to the service providers used by the parents. Instead CAP said it would only be paid when Fife Council delivered it. The reality was that Fife Council did not have the competence or the service to deliver so the the parents and family were forced to pay for the Service. The parents had no choice to pay for the service because for them not to would in the words of CAP and the Psychiatrist severely damage the child's health.

Please pass this round.

GORDON BROWN'S CONSTITUENCY OF NHS FIFE ARE PLAYING POLITICS WITH DISABLED , VULNERABLE PEOPLE WITH AUTISM WHILE FORCING FAMILIES AND FRIENDS TO BUY IN HEALTH SERVICES BECAUSE OF THE CHANCELLOR'S AND JACK MCCONNELL'S POLICIES THAT ALMOST GUARANTEE THE SYSTEMATIC ABUSE OF PEOPLE WITH AUTISM. WHILE NHS FIFE HAVE STARTED TO PAY SOME OF THE FUNDING IN THE LAST 2 OR 3 MONTHS THEY STILL REFUSE TO PAY IT TO THE PARENTS WHO ARE STILL EMPLOYING AND PAYING FOR THE SERVICE. THEY ARE ALSO REFUSING TO PAY THE PARENTS FOR THE 3 PLUS YEARS THAT THE PARENTS WERE LEFT TO PAY FOR THE SERVICE, EVIL OR WHAT!

WHEN WILL GORDON BROWN'S LABOUR PARTY START DELIVERING THE BILLION'S OF POUNDS REQUIRED. FOR TOO LONG THIS UNCARING IMMORAL PARTY HAS DELIBERATELY TARGETED AND SYSTEMATICALLY ABUSED PEOPLE WITH AUTISM.

THE ABUSE HAS GOT TO STOP.

FROM AN ARTICLE IN THE LOCAL PAPERS GORDON BROWN'S LAST VISIT TO AN AUTISTIC CENTRE IN HIS CONSTITUENCY RESULTED IN HIM SAYING THAT "THE USE OF REDUNDANT NCB COAL BUILDINGS WERE AN EXCELLENT USE IN A SOCIALLY DEPRIVED AREA". HE TOTALLY MISSED THE POINT THAT THE REASON THE DISABLED AND VULNERABLE ARE FORCED TO USE OLD RUN DOWN BUILDINGS WAS BECAUSE THE LABOUR PARTY HAD SLASHED YEAR ON YEAR THE AVERAGE ANNUAL SPEND ON A PERSON WITH AUTISM.

Dave Cunningham who's severely Autistic son has and still is being Systematically abused by Gordon Brown's Labour Party.
25 Apr 2007

David Cunningham on "systematic abuse of the disabled"

by mfasp @ 23/02/2007 - 16:12:50

Site: Passed on at his invitation.

Firstly a big Welcome to those 'Decision Makers' who have joined my 1700 distribution list. As a reminder the primary aim is to highlight the Labour Party's systematic abuse Of the disabled, particularly people with autism. Gordon Brown is my MP but with Ming Campbell also being in Fife you will get first hand how their constituency Of Fife is equal to if not worse than any other area of the country in perfecting the systematic abuse Of the disabled, particularly people with autism.

Back to the farce of the so called £25 million for carers. The facts are:

1. Education. The Labour Party gave teachers £2 billion in Scotland and not one penny was to improve services to normal children far less the disabled and people with autism. In addition Gordon Brown and Ming Campbell's Education Authority like the rest of the country get rewarded whether they deliver one second of education or not. Take my severely autistic son the Labour Party and Executive has allowed Fife education to effectively steal over £200k of my son's education funding for doing nothing. This is because like the £25 million proposed for carers there are no measures or requirements to prove that the money gets to the child. Indeed it is estimated that in Scotland alone that at least £75 million pounds per annum that was supposedly identified for disabled/special needs children is routinely stolen by the councils because there is no requirement for any of the country's councils to prove that they spent the money on the disabled/people with autism. SO THERE ARE LITTLE GUARANTEES THAT ANY OF THE £25 MILLION WILL GO ON CARERS.

2. Social Services. An Independent Review identified that over 90% of disabled/people with autism had NOT got an approved Social Services assessment report. Similar situation for carers assessment. Again Gordon Brown and Ming Campbell's Constituency seems to have perfected the act of avoiding this. Indeed for several years Fife Social Services has totally refused to agree to issue an accurate report. The Informed Parents of Scotland and others believe that the reason for this is simple. Like education there is no requirement for councils in the country to prove where that they are spending the funding on disabled/people with autism. But by not issuing assessment details or reports then even if the incompetent Labour Party or Executive asked then this makes it easier for Gordon Brown and Ming Campbell's constituency to effectively steal the social services money as well.

3. NHS. NHS is the same. The incompetent Labour Party gave doctors hundreds of millions of pounds for effectively reducing the standard of care to patients. But specifically take Professor James McGoldrick (Chairman NHS Fife) and Dr Francis Elliot (Director of Health Services NHS Fife) they deliberately blocked payment for my severely autistic son's health care for over 3 years by trying to tie it into a so called Integrated package with the immoral and incompetent Fife education and Fife social services. Yet for the 3 years having starved my son of his healthcare and knowing full well that I and relatives had to borrow they finally caved in to the fact that they were breaking Health and Safety Legislation but refused to reimburse us for the previous 3 years.

Conclusion

The services for disabled and people with autism were described by the Children’s Commissioner as a national disgrace. UNICEF has also highlighted that Scotland and the UK as a whole is one of the worse places to bring up children. BUT THE BIGGEST LIE THAT THE CHANCELLOR OF THE EXCHEQUER CAN DUMP ON THE DISABLED/PEOPLE WITH AUTISM IS THE FARCE OF CREATING 'SMOKE AND MIRRORS' THAT THE MONEY GETS TO THE DISABLED/PEOPLE WITH AUTISM AND THEIR FAMILY CARERS. SO NOT ONLY ARE HUNDREDS OF MILLIONS OF POUNDS BEING EFFECTIVELY STOLEN BY THE COUNCILS ALL OVER THE COUNTRY BUT IT IS A NATIONAL DISGRACE THAT THE EVIL IMMORAL LABOUR PARTY IN SCOTLAND SHUT DOWN THE CROSS PARTY GROUP FOR AUTISM, WIPED THE WEBSITE BUT WORSE SLASHED THE AVERAGE ANNUAL SPEND FOR A PERSON WITH AUTISM.

FOR THE SAKE OF OUR CHILDREN'S HEALTH, WELFARE AND DEVELOPMENT DON'T EVER VOTE FOR THE IMMORAL INCOMPETENT LABOUR PARTY AT THE NEXT ELECTIONS.

FINALLY CAN ENGLAND NOT TAKE SCOTLAND'S INCOMPETENT EDUCATION AND SOCIAL SERVICES MINISTER HUGH HENRY WHO PRIDES HIMSELF IN NOT LISTENING TO THE INFORMED PARENTS OF SCOTLAND? NO DOUBT HE'LL DO HIS USUAL STICK HIS FINGERS IN HIS EAR, SING LA LA LA, DELETE THIS EMAIL AND WITH A SMILE ON HIS WARPED FACE GET ON WITH IMPLEMENTING A SYSTEM THAT CONTINUES THE SYSTEMATIC ABUSE OF PEOPLE WITH AUTISM.

PLEASE PASS THIS EMAIL ON.

Dave Cunningham Parent whose severely autistic son like thousands of others is being systematically abused by Labour. No education for over 3 Years. No social services for longer and basic healthcare. The legacy of the incompetent, uncaring and immoral Labour Party
22 Feb 2007

Zyprexa Files Not Secret But Lilly Targets MindFreedom website

by mfasp @ 15/01/2007 - 16:18:00

MindFreedom News - 15 January 2007

Nonviolent Revolution in Mental Health

The New York Times reports today that Eli Lilly's files on the
psychiatric drug Zyprexa are no longer secret, and are still
available on the Internet. Yet, as the Times also reports, Lilly
continues to target the MindFreedom web site for censorship with a
Temporary Restraining Order.

MindFreedom's Ted Chabasinski is one of the attorneys arguing against Eli Lilly and for free speech tomorrow, 16 January 2007, in US District Court in Brooklyn, New York.

British Medical Journal, journalist Evelyn Pringle and other media
are covering the controversy. Why is mass publicity of the exposed
files about Zyprexa a threat to Eli Lilly?

For all this news, analysis and more see MindFreedom News Update #26
published 15 January 2007:

www.mindfreedom.org/know/psych-drug-corp/eli-lilly-secrets/

or: tinyurl.com/yx6k9x

ACTIONS:
STOP THE CENSORSHIP!

Please redistribute this news to all appropriate places on and off
the Internet.

See the alert about how you can contact you Attorney General and ask
for criminal prosecution of Eli Lilly execuives.

For more info on MindFreedom see the newly redesigned web site at
www.MindFreedom.org

Adders again

by mfasp @ 03/01/2007 - 13:39:18

Adders.org are at it again, this time trying to shut up a member who
has criticised (not nastily) a member of admin (sounds familiar).
Suddenly her posts get locked, admin starts to make sarky remarks...people are allowed to make unpleasant remarks about her... again familiar. Perhaps this time they've learnt a lesson, as they've not banned her, perhaps free speech will finally be allowed on adders.org? I particularly liked it when one member of admin commented that they'd never ban anyone for having an opinion because seems to me that's exactly what keeps happening, specially if that opinion is about a member of admin doing something out of order e.g. Exfactor with Adrian and now this person with Dr Billy.

Think power of being admin is a bit much for some people hmmm. They get to lock posts whenever they feel like it and to boot off anyone they don't like.

Unimpressed
30 Dec 2006.

Site: All sites discussed have a right of reply. Hence here are some comments copied into the main article, for the sake of even-handedness of prominence for them. But it is not "comment behind people's backs" for Unimpressed to post here, as it is done openly for anyone to read, and nobody can reasonably be asked to "put up or shut up" on a site where they find intimidatory group dynamics being allowed, can they?

Now they've banned her completely!!!!!!!!!!!!!!!!!!!!!! Why not just call it a support site FOR ADMIN??????????????????????

Unimpressed, March 10

I have made enquiries to ascertain the validity of your statement and find that it is untrue. Nobody has been banned. Perhaps you should ensure you have all the facts and that they are correct before making misleading and incorrect statements.

Unimpressed2, March 16

As with all people calling names they never have there facts right. Too much in a rush to open there mouths and say something without checking first

there was no ban the person requested to leave for reasons of there own.

If the person writing this finds it such an issue why not say so publicly on the site instead of comments behind people's backs
or is it a case of they will find that the support they enjoy at the moment wont be there for them when the truth about things are reveiled.

And the other members will not find this kind of helpful to a site they feel comfortable with.

Perhaps its time to put up or shut up.

Angry Person, March 16

July 7 !
Now there's been another cull!

Darky, Chrissie, FeeinLeeds
The site has gone riiiiiiggggghht down the pan.

Even their posts saying bye were deleted. As always admin were allowed to make negative comments about Samantha's SENDIST tribunal with JM saying she couldn't see the point but then when people objected posts were locked and when people said bye we're leaving and mentioned it their posts were deleted. someone needs to ask Caroline what's going on, such rubbish to say that everyone's entitled to there opinions and then to delete messages which express opinions about other peoples opinions Not a support site anymore, not at all.

Themostunimpressedofalltheunimpressed

dangerous psychiatrist wants to return to unmitigated school atrocities

by mfasp @ 01/12/2006 - 17:02:00

This Sunday Mirrror item - that's a tabloid paper, remember - www.sundaymirror.co.uk/news/tm_headline=naughty-kids-need-discipline-not-drugs-&method=full&objectid=18109811&siteid=94762-name_page.html

is exploiting the well-funded fear of overpushed drugs for ADHD, to call for a return to belief in discipline instead of in the reality of ADHD at all.

This when evidence up to a generation old, of serious life-wrecking abuses committed by schools in the name of discipline, are still being systematically suppressed from public awareness. They are neither getting published nor covered in the media - how work pressure and teachers deciding they know best a child's abilities can make a child's life impossible. Resulting in a clash that can even be called life-threatening if running away or suicide are the child's only escape options, otherwise results in descent into the social service/mental health underworld.

Growth in understanding of the neurodiverse or autistic spectrum, whichever you prefer to call it, is the only major gain that has been achieved in the direction of overturning the wall of silence around teachers' atrocities. A silence there has been a unanimous criminal consensus in the media and politics to maintain. Only the crime of that silence is served when a psychiatrist comes along and says to the tabloid press, okay I'll back you, dictatorial power for teachers is right and the autistic spectrum isn't real.

Quoting: "Consultant child psychiatrist Dr Sami Timimi argues that medicalisation of childhood problems is due to a search for "an easy cure that fits in with our fast lifestyles and gives us a quick answer".

Consultant child psychiatrist. A profession with an overwhelming history, familiar to many spectrumites, of siding with persecution of us and with medical crimes seeking to destroy us. Do you see how Orwellian is the inversion of reality this sinister whitecoat Timimi is trying to pull? Under a cloak of opposing the medical crimes that involve drugs, he is promoting a wider agenda of medical crimes to be perpetrated through sheer authoritarian bullying. He is medicalising us by opposing accepting our reality! A politics of group destruction..

(link to a comment on Aspergian island.)

A worldwide emergency alert by the ASD scene is important.

Maurice Frank, 1 Dec 2006.

Patients' Association

by mfasp @ 22/11/2006 - 17:21:32

The Patients' Association, certainly its Scottish branch, is ruthless, self-interested, + not interested a damn in the patients in whose name it exists.

When it is approached concerning corrupt warping of the procedures in the NHS complaints and Ombudsman systems,

the Patients' Association's chair will just say, sorry can't help, you have tried all possibilties, nothing we can do. When she knows there is something she can do, she can expose what is going on. This can be done both on the Patients' Association's website and in all the representational material it produces at a general level on NHS patients' behalf. But the PA's response to being told this, + told it has an AUTOMATIC duty to do it or else is itself criminally culpable towards many people, is just to ignore it.

When an "advance statement" under the 2003 Mental Health Act is presented to the NHS, and contains declared information affecting every other person either presenting such a statement or using mental health systems, the information must be acted on. It is not enought just to file away the advance statement in the personal files of the person who wrote it. Because it is potentially evidence in every mental health case, it is a legal corruption of the case of everyone in the system unless that is done, which makes it an automatic duty. This is a description of the case the PA's assistance in was applied for. Its reaction is a deliberate siding with suppression of facts. It is a criminal act towards all users of the mental health system.

Everyone thinking of trying the Patients' Association, for anything, instead tell it you know of this + enquire as to how it explains a claim to be entitled to say not he exposing any, that's any, corruption in health service procedures !!!

more David Cunningham anger with the Labour Party

by mfasp @ 20/09/2006 - 18:54:22

(his politics are personal, of course)

This e-mail has been sent to over 600 of those influential people who in Scotland who claim an interest in Autism

Question

-------------
1. Why is it when every Labour MSP know's that report after report has demonstrated that things are worse for Scotland's People With Autism that they have starved Scotland's Disabled People With Autism of funding while Westminster MP's are now going to significantly and quite rightly increase funding in England (reference the attached web link to the BBC article

news.bbc.co.uk/1/hi/education/5352262.stm

BBC Headline
More funding could be found for teaching autistic youngsters in England, a minister has said.

Quote:

The pledge for action came after the children's commissioner for England described existing provisions as "shocking and appalling".

Unquote

PLEASE PASS THIS E-MAIL ON TO WORLD. SCOTLAND'S EVIL, UNCARING, INCOMPETENT REGIME CALLED THE LABOUR PARTY HAS DEVELOPED A MISSION AND STRATEGY TO MAKE SCOTLAND A SECOND CLASS COUNTRY BY SYSTEMATICALLY DESTROYING SCOTLAND'S DISABLED PEOPLE WITH AUTISM.

EVERY DAY (YES DAILY) NEARLY £400 MILLION POUND OF OIL, GAS AND GOLD REVENUES GO DOWN TO ENGLAND FROM SCOTLAND WHILE SCOTLAND IS TREATED LIKE SCUM.

YES SCOTLAND GIVES ENGLAND NEARLY £142 BILLION POUNDS PER ANNUM FROM OIL, GAS AND GOLD FROM ONSHORE AND OFFSHORE.

IT IS NO WONDER THAT THE BULK OF SCOTTISH PEOPLE HATE LABOUR MSP'S WITH EVERY FIBRE IN THEIR BODY AND WHY THEY ARE TELLING ALL SCOTTISH LABOUR MSP'S TO FCUK OFF OUT OF SCOTLAND AND GO AND LIVE IN ENGLAND. THE SCOTTISH PEOPLE DON'T WANT YOU AND TRUTH BE KNOWN IF YOUR FAMILIES AND FRIENDS KNEW WHAT YOUR WERE DOING THEY WOULD DISOWN YOU TO.

Dave Cunningham Fife parent of a severely disabled Autistic Boy who's Labour Stronghold of Fife have chosen to be one of the best examples of Labours lack of caring and delivery by refusing to deliver any Education for 3 years and who have stated in writing for 6 years that it is the lack of funding that stop's them delivering David's Social Services needs.

David Cunningham 18 Sep 2006

an undoing of police public order powers, passports + tickets

by mfasp @ 19/09/2006 - 15:52:19

Police forces are being required statutorily to compile "diversity policies" to make sure they are operating with understanding of minorities with any type of limitations or disability, however you like to class these things. The Elas AS society in Edinburgh has been invited to contribute to this for the Lothian/Borders police area.

It is fortuitous how AS includes a genuine reliance on having the full explicit logic in any situation expressed openly. It means we can't be expected to guess, culturally or from the state of politics, what will or won't be counted as acceptable. As many abuses are made possible by expecting folks to guess, everyone, the folks without AS too, are better off if because we exist nobody can be expected to guess. AS's existence excludes the option of deciding the public should be expected to accept regular situations of challenge on a basis of unannounced rules culturally assumed by police officers to exist.

Because we can't be distinguished on sight from the neurotypical population, our existence makes this apply to everyone! The state's duty not to commit population-scale abuses on any section of population, exists at a supraparliamentary international level regardless of what domestic laws on public order are in force at any time. It defines in human rights law the state's own validity, this is the principle all the supranational trials for population crimes have established. So AS's existence imposes on the police everywhere - a duty never to enforce on any person any rule that has never been specifically enacted, under generally worded laws of public order giving the police situational powers of interpretation.

This annuls every generally or discretionarily worded power that can ever be enacted, from the medieval English/Scottish law of "breach of the peace" to the modern powers created since 911, from being used to impose any rule that has no separate specific enacted existence. This is a massive thing to say, an advance in democracy, a constitutional and supranational fundamental in the relation of law enforcers and public. It now stands irreversibly recorded as police notified, creating a formal (we'll see about what really happens) entitlement for all to expect it will be followed. It's in Scotland but it's by reasoning that is not confined to here, so it's everywhere. This is simply thanks to an anti-discrimination duty given to them because the spectrum exists.

The AS scene worldwide should record this for citation + use in all police situations + all liaisons with governments, + all other civil liberty groups should seize on it too. Notify your politicians of it too.

  • Note the parallel with the Dalgety Bay library case. It and this stand separately, don't depend on each other, but each can be quoted in pursuit of the other. It is a timely example, that though every incidence of unclear or improperly discretionary rulemaking is worth fighting, the position you fight from is stronger when you know you have made a review of anti-discrimination standards at state level answerable to the AS case against this type of rulemaking.
  • It also meant an opportunity to suggest to police, in a situation of their formal duty to have an answer to it, though not of addressing the right force area, so this is just a marker for when other force areas do their "diversity policies" - that to be seen as non-discriminatory in their response to AS means having to take up the stalking issues around AFF and the offence committed against SF by Schlund-1and1.
  • What advances in democracy can be proved from other conditions, in the same way?

ADHD and dyspraxia, for a start, each prove it a minority persecution for anyone ever to be judged by their bearing of any physical document. This is simply because all physical documents are losable. Because you can't tell by sight who has ADHD, this applies to everyone too. The fact of human fallibility that any physical document can be lost or stolen, may no longer be conflicted with by allowing such loss or theft to result in a disastrous situation. Spread the word on this, make it widely known as fast as possible, to force recognition of it. You can bet the system will be reluctant to concede this if it's not widely known, they prefer it to be possible for anyone's life to be devastated in an instant + by chance as you move through the day. It's absolutely fundamental to personal safety in moving around, that the loss or theft of a physical document which may not be your fault should never place you stranded at the mercy of any official who can hold you responsible for it not to have happened.

This would overturn and prevent identity cards!!! Including the identity cards already used to govern international travel - passports!!! Regardless of the effect on how public transport shall be paid for, it would force an end to the use of losable tickets!!! Thanks to ASDs! and I report this being notified to 3 MEPs, that's for each non-Labour party - MEPs in order to claim for EU-wide synchrony on it.

Can you beat the importance that people-action like this should abolish tickets? It's funny how we don't even have an equivalent of how in Victorian times anyone without money in any place had a right to admit themself to the workhouse for a night. You can have any view you like on how transport should be paid for, but you can't argue it's practical that whenever you are distant from home there is an ever-present danger of your life being devastated in an instant by loss or theft of a little scrap of paper or of money, which may not be your fault. This removes, deliberately don't you think, a position of security from existing when you are moving around, so that there isn’t really free movement.

Once these advances are made, think how barbaric the present situation we have accepted as normal for 200 years will seem in memory! For now, it's a question of persistence in spreading the word.

Sep 28: Update on 2 MEPs' responses. Elspeth Attwooll (LD) has promised a response to follow her acknowledgement. This never came - these promises are often just a way of shutting you up until time has moved on and they can pretend to foregt about it. Struan Stevenson (Tory) has responded to the identity cards issue only, expressing his opposition to them and the mass surveillance trends under Labour and "interest" in the angle of using AS and ADHD against identity cards. Oct 19: the third one, Alyn Smith (SNP), has obviously ignored it. How does that contrast with the recent SNP conference going on about winning public confidence, with a Scottish election on in 7 months?

Dec 1: Following a letter in the Metro that mentioned how on the commuter trains into Glasgow, the operators are refusing to bother to sell tickets on trains, instead making passengers queue to get them at the ticket barriers when they each the city, + this can take over 5 minutes, adding unfairly to journmey times + resulting in avoidable latenesses for work. I wrote today to British Transport Police in follow-up to the Lothian police item, to point out that it is now a proven consequence of disability discrimination that there can no longer be such thing as train tickets. Consequently, it is criminal false imprisonment to keep passengers stuck at these ticket barriers, + hence the police are now obliged to back the passengers' right to proceed without tickets.

2007 election: Mark Ballard, Green transport spokesman until he lost his seat, ignored a lobby about this issue., Nor even about more ordinary dumb behaviour by the giant transport company First which operates some bus and train services in duplication between the same places but without interchangeable fares, as if they were competing services. Not wanting to make any fight about that is a disgusting depth of cycnicism for the party most popularly associated with public transport as a cause. Ballard wouldn't make any election campaign comment on either issue. His behaviour is too bad for his own candidates: the Green council candidate for "Almond" (west Edinburgh) gave a private answer in support of renationalising most transport in order that multimodal fares could be introduced mostly in the good form of wideranging travel passes. But there was still no comment on not having