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Archive for November, 2009

Mall program helps autistic children visit Santa Claus

November 30th, 2009

The Autism News | English


Bright lights, loud noise too much for many with disorder

By Kristin Harty Barkley | Cumberland Times-News

LAVALE — Until last year, Debbie Lashbaugh’s grandson couldn’t visit Santa.

The mall was just too much for him.

“You cannot take him to Walmart, you cannot take him to the mall, because he melts down,” Lashbaugh said of her grandson Chase, 5, who is autistic.

“He cries and has a fit. … Most autistic children have sensory disorder. To go somewhere where there is bright lights and loud noise is too much stimulation.”

Then last year, a mall near Chase’s home in Dayton, Ohio, offered a special time for autistic children to visit Santa.

“All the other stores were closed,” Lashbaugh said. “The music was just barely audible, just barely. They did not have all the overhead lights on. It was a very serene environment.”

This year, Country Club Mall in LaVale is offering a similar program. “Sensitive Santa” is scheduled for 9:30 to 11:30 a.m. Dec. 6 — before the mall opens to the public.

The event is only open to families of children with autism. For more information, call Lashbaugh at (301) 707-0139.

Source: http://www.times-news.com/local/local_story_333230622.html

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Autism Treatments, Pregnancy & Drugs

November 30th, 2009

The Autism News | English


By Dr. Sapna Parikh | My FOX New York

AUTISM EARLY TREATMENT: New research suggests that early treatment of autism in babies as young as 18 months could improve their symptoms. It found that kids who underwent intensive early behavioral treatment for 2 years showed better social interaction, a higher increase in IQ and better language skills. There were only 48 children in this small study at the University of Washington but the researchers say the results were so encouraging they are now expanding the study.

PREGNANCY AND DRUGS: A new report finds that many pregnant women are taking drugs that could be harmful to their baby, but they may not even know it. The Canadian researchers looked at prescriptions filled by just over 100,000 pregnant women and about 6-percent of the women got a medication that is known to be risky for the fetus. They say doctors and young women should review all medications together before a planned pregnancy or as soon as an unplanned pregnancy is recognized.

THERAPY & HAPPINESS: If you think the key to happiness is more money- think again. This new report says go see a therapist instead. It found that therapy could be as much as 32 times more cost effective when it comes to improving your well-being. The researchers say it would take a pay raise of about $40,000 to equal the happiness boost that was achieved by a course of therapy costing just over a thousand dollars.

Source: http://www.myfoxny.com/dpp/good_day_ny/091130-autism-treatments-pregnancy-drugs

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Trial begins of accused teacher’s aide

November 30th, 2009

The Autism News | English

By Emily Lenihan | WIVB

BUFFALO, N.Y. – A non-jury trial of a Buffalo teacher’s aide, accused of sexually abusing a kindergarten student, is scheduled to begin Monday.

John Colazzi, 61, is charged with felony sexual abuse.

A teacher at the Discovery School reported seeing Colazzi fondling a child with autism, in a restroom in 2007.

Source: http://www.wivb.com/dpp/news/local/Trial-begins-of-accused-teachers-aide

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Autism treatment works in kids as young as 18 months

November 30th, 2009

The Autism News | English


(getty Images)

By Lindsey Tanner | The Associated Press

CHICAGO — The first rigorous study of behavior treatment in autistic children as young as 18 months found two years of therapy can vastly improve symptoms, often resulting in a milder diagnosis.

The study was small — just 48 children evaluated at the University of Washington — but the results were so encouraging it has been expanded to several other sites, said Geraldine Dawson, chief science officer of the advocacy group Autism Speaks. Dawson, a former University of Washington professor, led the research team.

Early autism treatment has been getting more attention, but it remains controversial because there’s scant rigorous evidence showing it really works. The study is thus “a landmark of great import,” said Tony Charman, an autism education specialist at the Institute of Education in London.

There’s also a growing emphasis on diagnosing autism at the earliest possible age, and the study shows that can pay off with early, effective treatment, said Laura Schreibman, an autism researcher at the University of California at San Diego.

The National Institute of Mental Health funded the study, which was published online Monday in Pediatrics.

Children aged 18 months to 30 months were randomly assigned to receive behavior treatment called the Early Start Denver model from therapists and parents, or they were referred to others for less comprehensive care.

The therapy is similar to other types of autism behavior treatment. It focused on social interaction and communication — which are both difficult for many autistic children. For example, therapists or parents would repeatedly hold a toy near a child’s face to encourage the child to have eye contact — a common problem in autism. Or they’d reward children when they used words to ask for toys.

Children in the specialized group had four hours of therapist-led treatment five days a week, plus at least five hours weekly from parents.

After two years, IQ increased an average of almost 18 points in the specialized group, versus seven points in the others. Language skills also improved more in the specialized group. Almost 30 percent in the specialized group were re-diagnosed with a less severe form of autism after two years, versus 5 percent of the others. No children were considered “cured.”

Ashton Faller of Everett, Wash., got specialized treatment, starting at age 2.

“He had no verbal speech whatsoever, no eye contact, he was very withdrawn,” recalled his mother, Lisa Faller.

Within two years, Ashton had made “amazing” gains, she said. Now almost 6, he’s in a normal kindergarten class, and though he still has mild delays in social skills, people have a hard time believing he is autistic, Faller said.

The treatment is expensive; participants didn’t pay, but it can cost $50,000 a year, Dawson said. Some states require insurers to cover such costs, and Autism Speaks is working to expand those laws.

Source: The Associated Press

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For students with disabilities, it’s all in the plan

November 28th, 2009

The Autism News | English


Mike Blood (left) and Derrick Pendilla (lower right) go for a fist bump as students talk about Boy Scouts and after-school activites while they wait for the bell to ring and Keene Middle School to let out. Other students in the picture, from left to right: Jake Borden, Nick Champney, Tyler Fish, Michael Frazier and Terrell Peterson.

A fair shake

For students with disabilities, it’s all in the plan

By Sarah Palermo | Sentinel Source

Derrick Pendilla is 12 years old, loves sports, cartoons, his dog and his little sister. All of his classes — he’s in 6th-grade at Keene Middle School — are his favorite.

He wants to be a zookeeper when he grows up, and if asked about his favorite animals, he questions if you mean his favorite mammal or reptile, because he has one of each.

This past summer, he caught a snapping turtle one day while out fishing.

In many ways, Derrick is unique among the 5,000 students in the Keene School District.

In one big way, he’s not.

He’s one of the hundreds of children in local schools who lives every day with a disability.

When Derrick was only a few months old, his mom, Shannon, and dad, Darrell, noticed he wasn’t crawling, sitting up, or starting to move the way they were told he would.

At his first-year checkup, his pediatrician started the ball rolling on tests and specialists, and Derrick was eventually diagnosed with spastic quadriplegic cerebral palsy. The disease causes rigid muscles that Derrick can’t move easily, leading to trouble with motor skills, cognitive processes, mobility and speaking.

Through the years that diagnosis has meant a lot of things to the Pendilla family.

Often, it’s meant Derrick is the center of attention, a position he doesn’t mind much at all.

One day this past fall, a group of adults spent several hours focused on Derrick, learning how to use a special chair designed to help get him out of the school quickly in case of an emergency.

Surrounded by teachers, therapists, his parents and his aide, Derrick said he felt “like a superstar.”

He also got the star treatment during the scavenger hunt, designed to help the 6th-graders learn the layout of the school, and learn vocabulary to help them read maps.

To get around the three floors, Derrick got to use the school’s elevator, which on one level is located inside a classroom.

A few students watched as Derrick and “Mr. B.,” his aide, marched in and out of the elevator doors, on a mission to meet up with the rest of their team and find the clues.

“Mr. B.” is Christian Battaglia, Derrick’s one-on-one aide. He helps Derrick get around the school and take notes, because holding a pencil can be tough.

Having a one-on-one aide is something that’s in Derrick’s “individual education plan,” or IEP.

The plan was written in a meeting between his parents and school staff members at the beginning of the year.

According to the Individuals with Disabilities in Education Act, commonly called IDEA, each plan is written to provide an equal playing field to students with disabilities, so they can access the curriculum and prepare for adult life.

Everything that’s in a student’s education plan is something the school is legally obligated to provide, whether it’s an aide like Battaglia, or the freedom for a child with autism to leave an overwhelming class for a few minutes of quiet time in another room.

Derrick’s first plan was written when he turned 3, the year federal laws say school districts must begin helping kids diagnosed with a disability.

Children who are diagnosed with a disability before age 3, like Derrick, get support until their third birthday from a state program called Early Supports and Services. After age 3, the responsibility shifts to the schools.

Derrick attended Keene’s preschool — which mixes students with disabilities with typical kids their age. With all the paperwork involved in shifting duties to the school district, staff members start early, evaluating and assessing a toddler with disabilities when he or she is about 21/2, said Catherine L. Reeves, director of special education for N.H. School Administrative Unit 29.

Unit 29 provides top-level administration to the Chesterfield, Harrisville, Keene, Marlow, Marlborough, Nelson and Westmoreland school districts.

For every child in the special education system, whether they’re diagnosed with cerebral palsy as a baby or attention deficit disorder in high school, the path starts with a referral.

In cases where a toddler is already receiving early support services, the referral is a technicality, because educators communicate often about children who are soon turning 3, Reeves said.

But for other students, like Charlie Gurney, a referral would be the first step toward getting help.

Finding the cause of a child’s troubles

Charlie Gurney is the son of Keene’s co-superintendent, William B. Gurney.

Now attending college at a military academy, Charlie received a diagnosis of Attention Deficit/Hyperactivity Disorder when he was in high school.

There had been signs for a few years, seen more easily now in hindsight, like the day Charlie forgot about the hammer.

Bill Gurney was doing housework up on a ladder fixing the eaves of their Dublin home. Charlie, then in elementary school, was playing in the yard nearby, and when Bill needed a hammer, he sent his son to the garage for it.

“Ten minutes pass, 15 minutes pass. And I’m up on a ladder, like 21/2 stories up, and there’s still no Charlie, and I’m starting to get mad. I go down and he’s standing there in the garage,” Gurney said.

His son had forgotten what he was sent to fetch, and stood staring at the tool bench. The incident inspired Bill and his wife to get some tests done.

Attention Deficit/Hyperactivity Disorder is recognized when a person tests positive for at least nine of 18 markers — things like chronic inattention, hyperactivity and impulsivity. The tests showed Charlie might have some issues, but not enough to make the family seek further testing, or qualify Charlie for special education.

Then high school came. Charlie went to boarding school, a tradition in his mother’s family. His first two years, he did fine, his father said.

But in 11th-grade teachers started sending notes home that he wasn’t turning in his work.

“We were frustrated — we made a commitment to send him to that school … We thought at first he was just being lazy. As much as you love your kid, if you think they’re being lazy, you get on them,” Gurney said.

“He would come home and sleep all weekend. He’d say ‘I’m exhausted; I’m tired.’ ”

At first, Charlie’s parents thought maybe he was taking drugs. Then they decided to get another test done.

The second round of test results showed Charlie tested positive for 16 of the 18 markers for ADHD.

“It made us feel a little guilty,” Bill Gurney said. “We were riding him pretty hard. I wouldn’t make him run a race with a broken leg, but we were saying ‘Why can’t you keep up?’ when there was a real physical issue behind it.

“It’s a relief when you know that your kid is doing their best.”

The public school special education system can work in much the same way: A parent notices something is wrong, and the student is tested. But, often the wheels of support start turning early.

Teachers, counselors, aunts, uncles, grandparents — anyone can make a referral, recommending that a child be evaluated for a learning disability or other issue.

Once that referral is made, the school district calls together a team of people, called the IEP team — which stands for the “individual education plan” team.

Every team includes the parents, a special education teacher and regular classroom teacher, and anyone else the parents or district officials think should be there, such as counselors, evaluators or volunteer advocates.

The team tries to answer three questions to determine whether the child should receive special education services.

First, is there a disability?

While it might seem simple, this question, like most about special education, isn’t.

The federal government lists which disabilities qualify for special education services, but each state defines those disabilities, and each school district sets its own threshold for what it means.

If a child is diagnosed with a disability, the team poses another question: Does it have an adverse effect on the child’s ability to learn?

There are some children who have a disability, but can still learn and keep up with their peers. In those cases, no special services are allocated.

The third question asks if the child is in need of specialized instruction.

If the answer to all three questions is “yes,” the parents and school staff members sit down to draft the student’s IEP.

Each plan describes how the child is performing, and how that’s affected by his or her disability.

The plan also outlines goals that should be achieved during the coming school year, and what services and supports will be provided to help the child achieve them.

The team also decides the least restrictive environment where the child’s plan can be put into action. For most students, that’s the regular classroom with some support from the special education teacher for certain periods of the day.

Others might need to spend most of their time in a smaller class, or in a program with staff members who are specifically trained to help students with a particular disability.

Students with even more severe disabilities might be placed at facilities like Crotched Mountain Rehabilitation Center, Perkins School for the Blind or Kendall Farm, a program in Vermont for children with disruptive behavioral problems.

Every year, the IEP team meets to review the child’s progress, and whether the plan still addresses his or her needs.

Educators have a bigger plan in mind than just assuring a student makes it through the next school year, Reeves said.

“The goal is to put ourselves out of business” by giving students strategies to cope with their disabilities, she said.

“If we’re doing a good job, we are helping children to advocate for themselves … because their disability in all likelihood isn’t going to go away. People with a learning disability will have it forever. We try and figure out what strategies will they need to employ in order to be successful in college or in the world of work.”


Derrick Pendilla raises his hand to answer a question in health class. Pendilla needs assistance to take notes and write answers but loves participating in class. To his left is his one-on-one aide, Christian Battaglia. Others in the class, from center to right: teacher Deb Thompson, Justin Johnson, Tyler Fish, John Bisson and Lexi Riley in the foreground.

Source: http://sentinelsource.com/articles/2009/11/28/news/special_reports/special_education/id_378037.txt

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Autistic boy, 10, drowns in neighbor’s pool

November 28th, 2009

The Autism News | English

By Austin L. Miller | Ocala

A 10-year-old boy who was autistic and non-verbal wandered from his northwest Marion County home sometime Friday morning and drowned in a neighbor’s murky swimming pool, according to officials.

Bernard C. Latimore’s body was found in the deep end of an enclosed, in-ground swimming pool at 5920 N.W. 57th Court, just across the street from his family’s home at 5951 N.W. 57th Court.

The homes are in the Ocala Park Estates subdivision, which is west of Northwest 44th Avenue, north of U.S. 27 and south of County Road 326.

The boy’s mother, Katese Richardson, gathered at the drowning scene with the boy’s father and other family members and friends. She asked to see her son’s body before it was taken away by the Medical Examiner’s Office.

The wish was granted. After seeing her son, Richardson was so overcome with grief that she had to be taken home. Within minutes, an ambulance took her to West Marion Regional Medical Center for observation.

Sheriff’s deputies said they received a call from Richardson at 10:12 a.m. saying her son was missing. Officials say the woman was at work, and her 16-year-old son was caring for Bernard.

The older boy, according to deputies, had been asleep. He woke, noticed his brother was missing, then called his mother.

With assistance from the Air Unit and canines, deputies searched the area and looked for Bernard. They also activated a reverse 911 system, which alerted all neighbors and asked them to help locate the boy.

Officials expanded the search by contacting the Department of Corrections for their bloodhound dogs. The dogs sniffed the boy’s backpack and sneakers to get a scent.

At approximately 11:30 a.m., Katie Wyns, who lives at 5920 N.W. 57th Court, came home and told deputies she noticed a pink pillow in her pool.

Authorities say Bernard was known to carry around the pink pillow. They immediately searched the pool, where they found him in the deep end.

Deputies said the pool, which was covered with algae, was roughly 7 feet to 8 feet deep.

Authorities do not suspect foul play, and believe the child left his home and went to the neighbor’s home.

“He was a real smart boy who loved to play,” said Virgil Moore, one of the boy’s uncles.

Moore said he received the call about his nephew’s disappearance around 10 a.m. and joined the search. He said they looked in the nearby wooded area and along the streets.

Another relative, Lillie Sams, Bernard’s cousin, said “nobody was a stranger” to Bernard.

Sams said he joined the search, hoping they would find him playing somewhere.

“He liked to hug you. He was just a friendly little boy,” she said.

Sams and Moore said Bernard loved music and going to church.

They say he attended Roslyn Murray Home Day Care.

The relatives said Bernard normally had a pillow or a toy with him.

Beverly Standridge, a crisis-intervention specialist for the Sheriff’s Office, said the support the family received for searching for Bernard “was amazing.” She said the neighborhood came out in droves, looking for Bernard.

Department of Children and Families officials came to the scene and took a report.

Source: http://www.ocala.com/article/20091128/ARTICLES/911281010/1402/NEWS

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N.Y. Band Members Live With Blindness, Autism, Down Syndrome

November 27th, 2009

The Autism News | English

flame


Click to view Flame on Good Morning America

Flame’s Members Say Disabilities Won’t Stop Band From Making Music

By MARY PFLUM and SUZAN CLARKE | Good Morning America

Many start-up bands dream of achieving worldwide fame one day.

That the band Flame achieved the dream is remarkable in and of itself. But the band is extraordinary in another respect: Each musician has a physical or mental disability.

Indeed, Flame is the only touring band in the world to be wholly composed of disabled members.

The upstate New York band’s members live with conditions that include Down syndrome, cognitive delays, autism, cerebral palsy and blindness.

Band member David LaGrange is blind and mentally disabled. He grew up in an institution and had a passion for rock ‘n’ roll.

“The Iron Butterfly, Led Zeppelin, sometimes I listen to AC/DC,” LaGrange, Flame’s drummer, said.

LaGrange studied music and earned a master’s degree, but he was told to give up his dreams of becoming a rock star.

He persevered, and for him, the band’s success is a dream come true.

Band Has Changed Woman’s Life

Flame was formed six years ago in Gloversville, N.Y., after an area talent contest for the mentally disabled turned up several accomplished musicians.

“Flame is a group of musicians that produce unbelievably great music who just happen to have a disability,” Paul Nigra, the band’s manager, said.

What started out as an experiment has quickly blossomed. The band had T-shirts, CDs and a tour bus, and has played to cheering crowds.

They’ve already been on world tour, including to Athens to play at the Parthenon. They performed at Eunice Kennedy Shriver’s funeral this summer, drawing compliments from talk show host and media mogul Oprah Winfrey.

Mary King said Flame has been a lifesaver for her daughter, lead singer Michelle King.

King’s daughter is autistic and used to be incapable of taking care of herself. Her mother says involvement in the group has changed her daughter’s life.

“Oh gosh, they have done, I just don’t know how to explain, so much that they have done for her, brought her out so much,” King added.

More Than Just a Band

LaGrange and other band members live in a group home in Gloversville, upstate New York. He said Flame has given him the kind of family he never had.

“It’s fantastic, being able to meet new people, make new friends,” he said.

The musicians’ goal is have their music played on radio stations everywhere and to demonstrate what the disabled can do if they’re given the opportunity.

“Our disability will not stop us,” LaGrange said. “We keep going and the more we keep going, we want more people to see what we do.”


Members of Flame, an upstate New York band that is comprised entirely of physically or mentally disabled musicians. (Courtesy of Flame)

Visit the official site of Flame The Band: www.flametheband.com

Source: http://www.abcnews.go.com/GMA/disabled-musicians-make-band-flame/story?id=9184434

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After fire, boy with autism on road to recovery and rebuilding

November 27th, 2009

The Autism News | English

By Kara Finnstrom | CNN

Sylmar, California (CNN) — One year ago Jonathan Reyes wrote a letter to give his parents on Thanksgiving, telling them “I’m thankful for my house which is blue and keeps me safe.”

Today, as his mother, Jan Reyes, shows the letter she is in tears. “When he brought it home we cried a lot, of all things for a 7-year-old to be grateful for!” She cried because weeks before Jonathan’s letter came home, that blue house and their entire neighborhood were destroyed by a massive wildfire. She cried because as difficult as losing a home would be for any child, it’s a different kind of stress for Jonathan. He is autistic.

Children with autism thrive on familiarity and routine and his life had been turned upside down.

The Reyes family’s plight came to light during the fire’s immediate aftermath as a bewildered and frightened Jonathan sifted through the rubble. The family was meticulously searching the charred debris for anything that survived.

Jonathan’s father, Augustine Reyes, says objects and belongings are especially important to children with autism. And everything Jonathan had loved was gone, from the cherished blanket he clutched to sleep, to his fixation — more than 500 Hot Wheels cars. Jonathan could calm himself by lining them up, counting and playing with them. The family was hoping at least one of Jonathan’s metal cars would somehow be intact, but found only charred parts.

“Augie and I didn’t know how to deal with it,” Jan Reyes says, “let alone how to deal with Jonathan and help him deal with it.”

The huge toll of the fire on Jonathan soon became clear. “He started to have frequent meltdowns,” Jan says, and “if he hears a helicopter he still wants to make sure it isn’t a fire helicopter. He runs outside to make sure there’s no smoke or no flames.”

Jonathan also began suffering from night terrors.

Augustine Reyes says his son would wake up screaming. “I distinctly remember going into his room and going to the bed trying to comfort him,” the father said. “The night of the fire we woke him up. It was pitch dark. We only had the two flashlights, so to take him out of that room in that circumstance. … He relived it for quite a while really, the emotional fear.”

Reyes says he and his wife grew frustrated. “We know he has these feelings inside but we can’t get him to discuss them.”

At Herrick Avenue Elementary School, the school psychologist and Jonathan’s special education teachers also saw changes.

“He was very nervous and very scared,” says teacher Maribel Orozco. “He doesn’t know how to express himself, so for him it’s his behavior where we can tell something is going on. He’s crying, shaking. He starts peeling at his hands.”

Jonathan’s teachers say they had to halt mainstreaming him with other students for a while and began keeping a joint communication log with his parents, tracking behaviors day and night. “Really the autism kind of overtook him,” Augustine Reyes says. “No matter what kind of serenity or help we gave him, it just didn’t help.”

But then, slowly, over months, the positive changes began. Jonathan started responding to therapy, opening up and sharing his feelings.

A few weeks ago as he spoke to a TV camera, he was able to express his fears. “I am worried about another fire,” he said.

Jonathan’s tantrums and his night terrors have now largely subsided. At the same time, his parents say, they have all been buoyed by a tremendous outpouring of support from hundreds of people touched by Jonathan’s story. “The response we received as a family and for Jonathan was just absolutely outrageous,” Augustine says. “It changed my wife and I in a lot of ways. We saw how people really opened their hearts to us.”

Part of that overwhelming response: Other children with autism mailed postcards; a parent who had lost a son to cancer sent his child’s Hot Wheels collection to Jonathan; Hot Wheels’ maker, Mattel, responded with a huge shipment of the exact cars Jonathan had lost, and more cars came from American soldiers who’d seen Jonathan’s story in Iraq.

“They decided to send me some Hot Wheels and then Mommy and Daddy started to cry,” Jonathan says. Adds Jan: “We were just so touched. Here they were fighting for us, and here they took the time out … a whole troop who saw Jonathan in Iraq.”

And now, one year later, the Reyeses are receiving another incredible gift: a long-awaited return home.

They have rebuilt back in Oakridge Mobile Home park, and will be one of the first families to bring the community back from ashes. This week, Jonathan and his father loaded the moving truck at what has been their temporary apartment. “Are you ready to go home? How long have you been waiting for it?” Augustine asks his son. “Every day,” says Jonathan.

At their freshly painted home, Jonathan can’t wait to show off his room and those beloved Hot Wheels.

“Those are some of my favorite cars,” he says. “And here’s some of my Hot Wheels that you are going to want to see.”

This Thanksgiving Jonathan has another gift for his parents. He’s drawn a bright, happy picture of their new home. “He’s just like a little bird spreading his wings all over again,” Augustine Reyes says. “He’s Jonathan again. He came back.”

Source: http://www.cnn.com/2009/HEALTH/11/26/reyes.autism.fire/

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Exercises tailored for kids with autism

November 26th, 2009

The Autism News | English


Seneca Valley School District physical education teachers Eric Grove and Michael Serventi demonstrate fitness techniques during a presentation by Eric Chessen, left, founder of Autism Fitness. (Pam Panchak/Post-Gazette)

By Mark Roth | Pittsburgh Post-Gazette

Like most parents, those who have children with autism want them to be physically active and healthy.

And like other parents, their first option is often Little League or soccer, says Elliot Frank, chairman of ABOARD, a local autism advocacy and educational group.

“For some of our kids, though, running around a field kicking a ball to put up a point on some abstract scoreboard doesn’t track very well,” Mr. Frank said.

In addition, many children with autism have mild physical disabilities, from toe walking to lack of coordination, that make it difficult for them to succeed in regular team sports.

Or, as autism fitness expert Eric Chessen says, “if kids fail at something over and over, they no longer will want to do it.”

Mr. Chessen, who says he is one of the few people in the nation focusing exclusively on autism and physical fitness, spoke at a conference sponsored by ABOARD Friday at the Regional Learning Alliance in Cranberry.

“You have to be physically fit to participate in sports,” he said, “but you don’t have to participate in sports to be physically fit.” Besides, he said, “there’s a big difference between kids who want to play sports and parents who want their kids to play sports.”

Building on that philosophy, Mr. Chessen, founder of Autism Fitness, a Long Island business, has built a phys ed program for children on the autism spectrum that focuses on five basic movements: pushing, pulling, rotation, squatting and locomotion.

Using volunteers from the physical education staff at the Seneca Valley schools, he demonstrated all five motions, using simple equipment like pouches filled with sand and giant rubber bands.

For pushing, one volunteer lay on his back and threw a sand ball to someone standing over him. For pulling, two people pulled in opposite directions on the oversized rubber band, and a third man pulled back on the center, turning it into a slingshot.

For rotation, two men stood back to back and then swiveled to pass the sand bag to each other; for squatting they stood back to back and passed the sand ball between their legs; and for locomotion, one of them put the rubber band around his waist and tried to run forward while another pulled back on it like a leash.

By teaching such basic movements and then building them into a chain of activities, Mr. Chessen said, “we work to maintain their strengths, overcome their deficits and move on from there.”

Mr. Chessen, 29, got his bachelor’s degree in forensic psychology, but then became a fitness trainer and earned a master’s in exercise physiology at California University of Pennsylvania.

One summer, a friend asked him to develop a fitness program for teenagers with autism in New York City, and “I was fascinated by it, and I thought, this is something really worthwhile for them and also worthwhile professionally for me.”

Brimming with energy and pacing constantly on the stage at the Regional Learning Alliance, Mr. Chessen emphasized how important it is to make sure fitness activities also enhance the children’s emotional control and thinking ability.

Children with autism often have distinctive repetitive behaviors, and “if I’ve got a child who usually jumps up and down and makes a loud vocalization and then runs across the room, and I can substitute working with a medicine ball or moving around like an animal, that gives him a larger repertoire of things to do that are functional that are going to enhance his life overall, and will eradicate some of those maladaptive behaviors.”

The animal movements are a major part of his toolkit, he said, and he made sure that many of the 170 people registered for the conference experienced it firsthand.

After asking everyone to move to the back of the room, he demonstrated a bear crawl, and then asked everybody to use it to get back to their chairs. The movement involved people getting on their feet and hands and kicking their legs upward toward their rear ends as they moved forward, many of them huffing and giggling along the way.

“You can devise an entire fitness program based on animal movements,” Mr. Chessen said, “and my kids especially like the bear crawl, because they love the fact they can kick their own butts.”

The fitness exercises can easily add an educational component, he said. One example is having children jump from one large letter on the floor to another to spell a certain word.

And they enhance education in another way, he said, because study after study has shown that regular exercise helps children think more clearly and have longer attention spans.

In the end, he wants to give the children fitness habits that can last a lifetime. And in the process, he hopes they avoid the maladies that afflict many people later in life.

“These kids already face a lot of challenges,” he said. “To add certain cancers or type 2 diabetes to that would be a real disservice to the population as a whole.”

Source: http://www.post-gazette.com/pg/09329/1016099-114.stm

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Trained guide dog soothes autistic children in the classroom

November 26th, 2009

The Autism News | English

By WKOW TV

WAUNAKEE (WKOW) — Can a dog make a difference in a classroom? You’ve probably heard of autism, a disorder affecting the ability to interact and communicate.

There is no cure yet, but the cliche that a dog is man’s best friend is fact in a local special education classroom.

The students in Katie Hauge’s class at Waunakee Middle School have a variety of special needs. Most of them have some degree of autism, which affects one out of every 100 Wisconsin children.

Eighth-grader Nick Lutz has a high-functioning form of autism called Asperger’s syndrome. His language and intellectual skills develop like his fellow students, but he has a tough time with communication and social interaction, so fitting in is hard.

For an hour every Tuesday, a special friend visits the class: Arya, a trained guide dog.

“She acts kind of like a confidant; they can talk to her, they can read to her, they can discuss things and not really feel weird about it,” said Patrick Schwigen, a teacher’s aide in the classroom.

And for these kids, a friend is exactly what they need.

“You don’t worry about being rejected, and you don’t have to worry about doing or saying the right thing,” said Hauge. “She’s kind of an unconditional partner.”

It doesn’t take much – just a wag of her tail – but the teachers say her presence alone makes a big difference.

“If it’s a rough day for some of the kids – maybe they’re not having the best time at school – they have an opportunity to just sit back and relax and not really think about that. They get to play with a dog for part of the day; who wouldn’t want to do that?” said Schwigen.

“Maybe sometimes if I have a stressful day, [Arya] will calm me down,” said Nick Lutz.

A 2008 Canadian study found service dogs act as a “sentinel of safety” for autistic children. In the study, kids felt more comfortable and confident with the dog around.

Still, autism experts want to see more research before they endorse this as a viable therapy for the disorder.

“Parents and teachers should be cautious about their generalizations from this instance of anecdotal information to their own child who has autism,” said Wendy Machalicek, professor of behavioral disorders at UW-Madison. “This could turn out to be a great therapy for individuals who have autism, but the case is still out.”

But in Hauge’s classroom, there’s a big difference when Arya is in the room.

“Temper can be an issue, but whenever the dog comes in, it’s always a highlight of the day, and they know that if they want to be able to spend time with Arya, they have to be on their best behavior,” said Schwigen.

Sometimes all it takes is a calming touch that only a dog can provide.

“She’s nice and soft and fluffy, like a cloud,” said Lutz. “When I told my parents about this, they were really excited, and they were thinking about getting me a dog.”

The students aren’t the only ones enjoying the visits; Arya does, too. Her owner, Ruth Meese of Waunakee, says Arya sees this visit as a call to duty, and one she’s happy to answer.

“She enjoys it. She looks forward to it. You can tell when she’s coming into the building. When she’s at home and gets her vest on and she knows she’s off to go working, she’s ready,” said Meese.

Meese says Arya was born to serve, and she takes her job seriously.

“If she can help lower the stress level for the kids and help them focus, and even 10 minutes out of the week, make learning fun for them, then she’s done her job,” said Meese.

Judging by the looks on the kids’ faces, it’s a job well done.

“She’s so calm, and I mean, look at her. Isn’t she the sweetest thing you’ve ever seen?” said Lutz.

27 News Reporter Jamie Hersch spent some time with Arya and her students to see what a difference she really makes in the classroom.

Source: http://www.wkowtv.com/Global/story.asp?S=11557022

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