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By Jennifer Lebovich and Kathleen McGrory | Miami Herald

Three boys were charged Wednesday in the sexual assault of an 11-year-old autistic girl in an elementary school restroom.
One of the boys, also 11, followed the girl into a restroom at Norland Elementary School in Miami Gardens earlier this month and forced her to perform oral sex on him, authorities said.

He is charged with sexual battery on a child under 12 and with false imprisonment.
The two others, ages 13 and 11, acted as lookouts outside the restroom, the arrest report said.
The Miami Herald is not identifying the youths because of their ages.

“It’s a terrible, unfortunate incident,’ said Miami-Dade Schools Police Chief Charles Hurley. “I don’t know where youngsters are learning some of these things. These are acquired behaviors.
The girl’s mother said she did not find out about the attack until two days later, when she got a call from the school. She said, though, that family members noticed a change in the girl’s behavior right away.

“She wouldn’t hold her head up, she wasn’t the same,’ said the girl’s mother.
The girl has Asperger’s syndrome, a mild form of autism, and is in a special education class at Norland Elementary, 19340 NW Eighth Ct.

The girl’s mother and attorneys hired by the family called for more security to prevent such incidents in schools.
“Two places your children should be safe: home and school,’ the mother said. “That should be a safe haven for them.’

The attorneys said they had not ruled out taking legal action.
A schools spokesman said the alleged assailants had been suspended and would be recommended for expulsion. The three, who were charged as juveniles, were not physically taken into police custody. Instead, the department filed the charges directly with the Miami-Dade state attorney’s office.

Police said the assault took place about noon March 3. The girl had been in a class preparing students for the FCAT, the attorneys said.

She was in a restroom when one of the boys came in and locked the door.
The boy “told the victim to get on her knees and he unzipped his pants,’ the arrest report said. He then made her perform a sex act .

The two other boys were outside the bathroom acting as lookouts, the report said. They were charged with false imprisonment and as accessories to sexual battery.
Hurley, the schools police chief, said his department approached the case “with an extreme amount of caution, care and sensitivity.’

“Instead of just making a quick arrest, we tried to gather as much information as we could,’ he said.
School administrators said they were reviewing procedures at the school.
Hurley said schools remain a safe place for children.
“We open our doors every day to 340,000 kids,’ he said. (more…)

Support for parents with Autistic children – Autism Parents Club

(Joanne Rathe, Globe Staff Photo, photo taken from http://signposts-au.org/)

Family health insurance is important if you are looking for secure future.

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The Autism News English, English Aimee Mury, autism, autistic, Eliza Mury, film

Eliza Mury was only one year old when she said her first word — ”doggie” — and a few more words followed. But soon her parents noticed that her vocabulary seemed frozen. Speech therapy didn’t help.

Eliza’s mother, Aimee Mury, took her daughter to doctors and specialists, but none diagnosed anything more serious than a hearing deficiency. Friends and relatives, though, had gently begun to suggest that Eliza might be autistic. Aimee Mury was so fearful of the condition, she could barely say the word.

After repeated exams by specialists, Eliza was diagnosed with autism when she was 2 1/2, in the spring of 2007. Aimee Mury read everything she could about the condition. But as she learned about traits and treatment, she had a hard time seeing what an autistic child looked like.

”It’s very hard initially to meet other people and kids,” Mury said. ”I was on YouTube and I was trying to search for autism. And I found there was very little out there.”

Nearly three years after Eliza’s diagnosis, Aimee Mury has helped create a movie about her daughter and their struggle to get her diagnosed called ”Eliza, My Songbird.” The movie, produced and directed by Mury’s neighbor, Zadi Zokou, will have its first public showing Sunday at Natick’s Morse Institute Library.

Mury, 42, saw the movie as a chance to help other families with autistic children get diagnosed more quickly than Eliza. But Eliza also plays a prominent role in the movie. Mury and her husband, John, pastor of Natick’s Beacon Community Church, hope that making autistic children more visible will help diminish the stigma of the neurological disorder.

”I think it’s a wonderful tribute that she is willing to do this,” said Kelly Gryglewicz, a member of the board of directors of the Autism Alliance of MetroWest, and a friend of Mury’s. ”A lot of people are not willing to disclose the diagnosis.”

Getting Eliza diagnosed with autism was a long and frustrating process that began when the girl was 18 months old. Appointments with specialists took months to book, and in the beginning, none of them believed Eliza was autistic. Girls are less likely than boys to be autistic. And while many autistic children shy away from social contact, Eliza was very social — even though she was indiscriminate, trying to sit on a stranger’s lap, for instance.

”That’s what I was quickly learning was that even within the professional group, there’s a lot of misunderstanding of what a child with autism can look like,” Aimee Mury said. (more…)

“Beading to Beat Autism”

The Autism News | English

By Fox 41 | Louisville News

Michala Riggle is taking her “Beading to Beat Autism” project to prison. Wednesday the 13-year-old from Louisville spoke to nearly two dozen inmates at the Kentucky Correctional Institution for Women. The women have volunteered to bead bracelets to be sold on her website.

KCIW Warden Janet Conover explains, “I think the inmates get a sense of giving back to the community. You know they’ve committed some crimes, been convicted by a court, and this is their way of giving back to society in a positive way.”

Jail officials say more than thirty inmates signed up, but only 23 are participating. The program’s goal is to help in raising $300 million to build the most comprehensive autism research and treatment center in the world. (more…)

Daily challenges of raising a child with autism

The Autism News | English

Published by Trumpeter Books

Given the daily challenges of raising a child with autism, it’s easy for parents to lose themselves and for their overall quality of life to plummet.

The Autism Mom’s Survival Guide contains many parents’ stories and ideas (including my own) on handling feelings of despair and hopelessness, caring for your marriage, enjoying your life as an adult — not just as a parent — having fun with your kids, finding a good balance between accepting your child and seeking new treatments, dealing with the rest of the world’s attitudes towards your child, looking toward your child’s adulthood, letting go, and allowing yourself to find your own joy even in the midst of great struggle. (more…)

National disability insurance scheme

By Mike Steketee | The Australian

Voters are being asked to back only parties that promise a national disability insurance scheme

IN the 1976 movie Network, Peter Finch in his role as a television broadcaster urges people to go to their windows, stick their heads out and shout: “I’m as mad as hell and I’m not gonna take this any more.” Windows are thrown open and the words echo around the country.

Australians with disability and their supporters are hoping for something similar from the campaign they are launching via their “australiansmadashell” website. As it says, “we are not going to take it any more — and there are millions of us”.

They are asking people to take a pledge to vote in state and federal elections only for parties that promise to introduce a national disability insurance scheme. The responses will be compiled and candidates, particularly in marginal seats, will be told of the number of pledges in their electorate.

An insurance scheme, rather than paying a welfare benefit or damages, as with motor vehicle or workers’ compensation schemes, would provide the essential services and facilities to the disabled and increase their prospects of a meaningful life, including a job. It would constitute a landmark economic and social reform and, while costly in the short term, would pay for itself in the long run, according to its proponents.

The insurance concept is based on the fact that all Australians are at risk in life’s lottery, whether they are among the one in 160 born with autism, one in 400 with cerebral palsy, are blind or deaf, have Down syndrome, suffer severe intellectual disability, fall from a skateboard and suffer brain damage, or dive into the surf and end up as a quadriplegic. As Sue O’Reilly, one of the campaign organisers, puts it: “This is not something that happens to Martians on another planet.”

People decide how to vote for all sorts of different reasons and there are any number of issues jostling for a place on the political agenda. But grey power helped elevate the concerns of older Australians up the scale of political priorities and the Women’s Electoral Lobby succeeded in putting issues such as child care on the agenda.

The Australian Institute of Health and Welfare estimates there are 1.5 million people with a severe disability and that will grow to 2.3 million by 2030. Including parents and other primary carers, extended family members, disability support workers, health professionals and specialist teachers, organisers say their campaign could influence more than 2 million voters, people for whom disability is not just one of many issues but central to their lives.

For years, the disabled and those supporting them mostly have accepted their lot, often consumed by the daily struggle to survive. Now, something is definitely stirring. O’Reilly says they hit on their theme because they kept hearing people saying, “I’m just so angry, just so fed up.” Under her maiden name, Corrigan, she wrote an article last year for The Weekend Australian Magazine that told of parents who, at the point of collapse, resorted to abandoning their children in emergency respite centres. She wrote of her experiences raising a son with cerebral palsy, how the lack of support drove her family to live in England, where there is a legal right to vital equipment and services, including a residential secondary school.

The death of her husband prompted her to return to Australia, to be confronted all the more starkly with the lack of services here. Her article prompted one of the biggest reader responses the magazine has received. (more…)