Thursday, August 16, 2007

Autism News Articles for August 10th - 16th URGENT

Autism News Articles

August 9th- August 16, 2007

We appreciate your patience for these mailings
Delays are expected due to vacation

Thank you.
Trish

Minister of Children and Youth Services to make an important announcement regarding services and support for children with autism and their families

TORONTO, Aug. 16 /CNW/ - Minister of Children and Youth Services Mary
Anne Chambers will make an important announcement about additional services
and supports for children and youth with autism and their families.

<<
DATE: Friday, August 17, 2007

TIME: 10 a.m.

LOCATION: Surrey Place Centre
2 Surrey Place
(across from Women's College Hospital, west of Bay St.,
north of College St.)
Toronto

Disponible en français

http://www.children.gov.on.ca
>>



For further information: Tricia Edgar, Minister's Office, (416)
212-7161, (416) 571-7247 (cell); Anne Machowski-Smith; Ministry of Children
and Youth Services, (416) 325-5156

From A Listmate
GUEST BOOK FOR SHELLEY MARTEL.

As many already know Shelley Martel who has been one of the most vocal Canadian politicians for the equal rights for people with Autism is retiring this fall after 20 years in politics.

For over half a decade she has gone beyond the call of duty in helping
families with children who have autism bring serious issues to the forefront of Government, media and the general population at large.

FEAT of Ontario has added a guest book on it's site for Shelley Martel. We hope to have all the names with their comments presented to Shelley at her retirement event coming up next week.

We hope that all organizations, professionals and most importantly families will take a few minutes of their time to visit www.featontario. org to let this amazing person know what her time and effort have meant to you. I"m hoping to have Nancy Morrison present it to her.

Please feel free to pass along this email to all your contacts. Shelley has
done so much for us, let's show her it has been appreciated.

Best Regards,
Norrah Whitney
E.D. FEAT of Ontario
www.featontario. org

ps. there is a link on the main page for it



Michelle Robinson
President
Autism Ontario - North Bay
www.autismontario.com





>From: "Karyn Dumble"
>To:
>Subject: FOR DISTRIBUTION: Weekly News
>Date: Thu, 9 Aug 2007 11:48:35 -0400
>
>This message has been sent to all Chapter Presidents and Staff.
>
>Please distribute to your members.
>
>
>
>
>
>Autism Ontario is creating a Public Service Announcement (PSA)
>
>Looking for males with autism for PSA
>
>This fall, Autism Ontario is producing a public service announcement
for
>broadcast on radio and television. We are looking for three males
>between the ages of 5 and 35 to participate. Production will take
place
>in and around Toronto on one day in the fall. Specifically, we are
>looking for individuals with autism whose symptoms would be similar to
>an individual in the middle of the spectrum with some visibly typical
>physical behaviours.
>
>
>
>Interested participants should email a picture, contact information
and
>short introduction to Jeff Dobbin of Parashoot Productions Inc. (
>jdobbin@parashoot.ca) by Friday September 7, 2007.
>
>
>
>
>
>Funds are still available for one-to-one workers to accompany children
>and youth to summer camp.
>
>
>
>Autism Ontario received funds from the Ministry of Children and Youth
>Services to provide workers for at least 500 children or youth with
the
>diagnosis of an Autism Spectrum Disorder. To find out how your family
>can access these funds, check out our website at www.autismontario.com
> .
>
>
>
>Questions can be directed to Ginny Kontosic, Summer Camp Subsidies
>Coordinator. Her phone number is 416-246-9592 x225 and her email is
>ginny@autismontario.com.
>
>The application form and FAQs are easily accessed on our website at
>www.autismontario.com .
>
>
>
>Realize Community Potential Program Update
>
>From Marilyn Thompson, Program Manager
>
>
>
>I want to take this opportunity to thank those Chapters that have met
>and forwarded Social Learning Opportunity ideas. Information about the
>Social Learning Opportunities is now posted on our website at
>www.autismontario.com/rcp.
>
>
>
>There is still time to submit more ideas. We've extended the deadline
>for submissions to August 13, 2007.
>
>
>
>Thank you to the many volunteers that are continuously supporting the
>program in a variety of ways. Your participation in attending meetings
>to review planning processes, contributing to creating documents,
>emailing and identifying needs to address for the future, and
submitting
>the social learning opportunity ideas helps to shape the program and
>ensure that it continues to meet the needs of families. We value your
>contribution!
>
>
>
>
>
>Disclaimer: It is important to do your own research and make your own
>informed decisions. Please note Autism Ontario does not endorse any
>specific therapy, product, treatment, strategy, opinions, service, or
>individual. We do, however, endorse your right to information.


Pickering respite program growing, seeks volunteers
Friday, August 10, 2007 -- Michelle Strutzenberger
After a slow start, a respite program in Pickering is growing, bringing with it a need for more volunteers.
Footprints is a non-profit organization started in 2004 to provide respite for families who have children with autism spectrum disorders.
Corrine Brook-Allred, chair of the organization’s steering committee, says when the program first began, there was a surprising lack of interest from families.
“We thought the door would be knocked down by families wanting to get in,” says Brook-Allred.
Knowing that about one in every 150 children is affected by autism spectrum disorder, the founding group had determined the need for respite would be high.
In the Durham region, only one other respite program exists, and its location in Oshawa makes it difficult for many Pickering and Ajax families to access.
With funding from the local United Way, Footprints hired a consultant to determine what would make the program more attractive to families.
“With those ideas, we tweaked a few things, lowered the price and extended our Saturday to five hours instead of just the three hours,” says Brook-Allred.
Numbers have since increased and the program now has a waiting list.
“Now we’re just trying to make sure we stay ahead and have enough volunteers,” says Brook-Allred.
The program is offered under the supervision of a trained and qualified part-time co-ordinator. All the children are partnered with a volunteer who has been trained in crisis prevention and intervention and First Aid.
Every Saturday parents can bring their children for a few hours of activities tailored to the child’s interests and skills. The program is also offered Friday evenings.
Last October Footprints received a multi-year grant of over $130,000 from the Ontario Trillium Foundation. The grant will be used to facilitate the development of Footprint’s five-year strategic plan, which includes expansion to accommodate the increased number of clients and bringing in more volunteers.
Footprints was started when the pastor of Dunbar Heights United Church, Glenn Brown, visited a family with a child with autism spectrum disorder and saw firsthand how the parents would need time for rest or just to do other things.
“He couldn’t get over how busy the child was,” says Brook-Allred, who took on the task of researching the feasibility of a respite program.
Footprints is offered as an outreach of the church, though it operates as a separate entity, looking after its own finances and making its own decisions.
For more information, see www.footprints4autism.org

Ask Lindsay Moir:
The decision of a child's "school readiness"
Friday, August 10, 2007
Question:
I am a family support worker who works with preschool families of children with special needs. Over the past two years I have heard a familiar story at "Team Meetings":
"we will allow the student to come to school in September for a couple of weeks to assess their "school readiness," then we will decide if they can come to Junior kindergarten, or remain in preschool."
To be honest, our association has gone along with this for years, and many of the students we work with have been sent back to preschool until Grade 1.
This year, I have a new colleague who says that this is not legal. Is it?
The most common reasons given by the school for a child not being "school ready" are:
- not toilet-trained
- needs 1:1 support
- cannot ride the big yellow bus without support
Can a school set-up a trial placement, then refuse to educate a student on these grounds??
Answer:
Other than age and residence (and religion of the parent in Separate schools), children do NOT need to qualify to attend schools in Ontario.
That means that there is no such thing as a "Trial Placement to determine school Readiness"!
The purpose of the Team Meeting should be to to deterimine "the pupil's apparent needs" so that the appropriate program is provided in the Fall until such time as an IPRC can be held.
In Regulation 181/98,The Ministry of Education gives clear and strong direction to school Boards:
Reg 181/98 Section 9:
(1) in accordance with the requirements under the Eduaction Act, no pupil is to be denied an education program pending a meeting or decision under this Regulation.
(2) Where an education program is provided to a pupil pending a meeting or decision under this Regulation,
(a) the program must be appropriate to the pupil's apparent strengths and needs;
(c) appropriate educational services must be provided to meet the pupil's apparent needs.
In their "determination of school readiness" the school has done a great job of identifying the "pupil's apparent needs" — now the discussion is HOW WILL THEY PROVIDE THE "APPROPRIATE EDUCATION SERVICES" (REG 181 9:2(c) above)
In law the word "must" is a very strong one — it creates a legal obligation — Section 9: 2(a) and 2(c) above make the illegality of this situation very clear. Since this an ongoing issue, perhaps rather than dealing with each case individually, your association should meet with the Director of Education and ask for a clarifying memo to be sent to all principals.
In the matter of "toiletting," just a reminder that this is no longer a Duty of a Pupil in the Education Act — it is not grounds for refusing entry — it is just a need that must be addressed through a Toiletting program!
It is 100% a parental decision whether or not to send a pupil to JK and/or SK. Once they reach the appropriate age, they have a right to attend. Where there is an appropriate preschool program, a parent can consider whether to stay in preschool or send their child to school. "School Readiness" is not something that the educators determine!
Lindsay Moir retired from the Ministry of Education in 1997 and has been assisting agencies, associations and parents in obtaining appropriate special education services for exceptional pupils.
Family Net welcomes your questions about special education in Ontario.
E-mail Lindsay at ask.questions@yahoo.ca He will answer as many questions as possible.



>From: "Karyn Dumble"
>To:
>Subject: FOR DISTRIBUTION: Weekly News
>Date: Thu, 9 Aug 2007 11:48:35 -0400
>
>This message has been sent to all Chapter Presidents and Staff.
>
>Please distribute to your members.
>
>
>
>
>
>Autism Ontario is creating a Public Service Announcement (PSA)
>
>Looking for males with autism for PSA
>
>This fall, Autism Ontario is producing a public service announcement
for
>broadcast on radio and television. We are looking for three males
>between the ages of 5 and 35 to participate. Production will take
place
>in and around Toronto on one day in the fall. Specifically, we are
>looking for individuals with autism whose symptoms would be similar to
>an individual in the middle of the spectrum with some visibly typical
>physical behaviours.
>
>
>
>Interested participants should email a picture, contact information
and
>short introduction to Jeff Dobbin of Parashoot Productions Inc. (
>jdobbin@parashoot.ca) by Friday September 7, 2007.
>
>
>
>
>
>Funds are still available for one-to-one workers to accompany children
>and youth to summer camp.
>
>
>
>Autism Ontario received funds from the Ministry of Children and Youth
>Services to provide workers for at least 500 children or youth with
the
>diagnosis of an Autism Spectrum Disorder. To find out how your family
>can access these funds, check out our website at www.autismontario.com
> .
>
>
>
>Questions can be directed to Ginny Kontosic, Summer Camp Subsidies
>Coordinator. Her phone number is 416-246-9592 x225 and her email is
>ginny@autismontario.com.
>
>The application form and FAQs are easily accessed on our website at
>www.autismontario.com .
>
>
>
>Realize Community Potential Program Update
>
>From Marilyn Thompson, Program Manager
>
>
>
>I want to take this opportunity to thank those Chapters that have met
>and forwarded Social Learning Opportunity ideas. Information about the
>Social Learning Opportunities is now posted on our website at
>www.autismontario.com/rcp.
>
>
>
>There is still time to submit more ideas. We've extended the deadline
>for submissions to August 13, 2007.
>
>
>
>Thank you to the many volunteers that are continuously supporting the
>program in a variety of ways. Your participation in attending meetings
>to review planning processes, contributing to creating documents,
>emailing and identifying needs to address for the future, and
submitting
>the social learning opportunity ideas helps to shape the program and
>ensure that it continues to meet the needs of families. We value your
>contribution!
>
>
>
>
>
>Disclaimer: It is important to do your own research and make your own
>informed decisions. Please note Autism Ontario does not endorse any
>specific therapy, product, treatment, strategy, opinions, service, or
>individual. We do, however, endorse your right to information.


From another List:
MP requesting your stories


Notice about an MP wanting to hear our stories:

Summer is a time when MPs have some time off but parents and other
caregivers actually work harder than ever.

Luckily there are some MPs who are noticing the value of care work and
wanting to bring more attention to it.

MP Lynne Yelich, parliamentary secretary for Human Resources and Development
has advised that there will be a debate this fall in the House of Commons on
the topic of care of children. She is urging people to send along a brief
personal note about how present policy affects their ability to provide
care.

The personal stories will be cited in the House but people need not be
named. Deadline September 1 2007. Keep your stories brief and she'll contact
you for more info if needed. Yelich's office is documenting as many case
histories as possible in its move to find fair and equitable tax policy for
all care styles. I do urge people to contribute. Send a brief summary of
your experience ( at-home parent, grandparent, tag-team, home-school, nanny,
dayhome, daycare or other circumstance) to Toni Chasmar, her assistant.
Mention if you wish how lack of or amount of maternity, parental, child
allowance, pension or tax policy has affected your struggles.

kenastonmp@sasktel. net

1-306-252-6100

Sincerely Beverley Smith

editor

Recent Research on Caregiving

403-283-2400


from: "Ontario Autism Coalition"


----- Original Message -----
From: "Ontario Autism Coalition"
Sent: Tuesday, August 14, 2007 9:23 AM
Subject: [news] OAC Media Release


Please distribute to any of your media or contact lists:

Media Release
August 13, 2007
For immediate release

The Ontario Autism Coalition ('OAC') is a grassroots organization with
over 600 active members throughout the Province of Ontario. Our members
are connected to thousands of families and supporters affected by
autism. The OAC is determined to ensure the delivery of services and
supports to families and individuals with Autism in the Province of
Ontario. As political parties in the Province of Ontario prepare for a
Provincial election in October 2007, the OAC seeks commitment from all
Provincial parties to the following platform planks, which will improve
the quality of life for over 10,000 pre-school and school age children
and their families:

1) Allow IBI instructor therapists currently working within the AIP
entry into the school system so that scientifically valid, supervised
ABA can be implemented. Children receiving intensive ABA through the
AIP and students attending school should receive the same quality of
ABA services.

2) Eliminate the waitlist in the AIP and fully fund services for all
children with Autism--from the mild to severe end of the Autism
Spectrum.

3) Develop a formal credentialing system and a proper training and
recruitment system for the implementation of ABA to ensure
accountability and capacity within the system.

"Under the current Liberal government, funding for Autism programs has
gone unspent, waitlists have ballooned, school-age children were denied
scientifically valid ABA models and Autism-related court cases have
dragged on at taxpayer expense, says Susan Fentie, one of the OAC
co-founders. "Parents of pre-school children with Autism continue to go
broke paying for treatment out of their own pocket while their children
sit indefinitely on the waitlist. Parents of school-aged children
encounter institutional road blocks as they try to secure an
appropriate education for their children, and services for teens and
adults on the Autism spectrum are either non-existent or inconsistent
in terms of quality," she added.

"Today we seek commitment from all political parties to the OAC
platform to address Autism issues. The OAC will be pressing all of the
Provincial political Parties for their commitment to these planks now,
and monitoring the performance of the parties after the election to
ensure they live up to their commitments, as the current Liberal
Government and all of its predecessors have consistently failed to do."

The OAC will be issuing further statements, hosting press conferences
and organizing events during the election campaign to draw attention to
these important issues. To find out more, media may contact any members
of our leadership team for interviews or comments at the numbers listed
below:

-30-

For further information:
GTA
Laura & Bruce McIntosh
416-315-7939
905-761-5226
tosh555@hotmail.com

Toronto
Malcolm Stanley
416 275-3562
amstanley@rogers.com

York Region
Sharon Gabison
647 892-4418
shar.gabison@utoronto.ca

Windsor
Mary Beth Rocheleau
519 734-6387
grocheleau6@hotmail.com

Western Ontario
Susan & Dan Fentie
519-869-4198
autism@coolgoose.com

Ottawa
Sam Yassine
613-841-3886
Sam_yassine@rogers.co


From a Listmate
Natural Learning Concepts
School is approaching
To all the special people who work with children on the autism spectrum, find out just how highly we think of you. http://www.nlconcepts.com/autism-approval.htm

Basic & Abstract Concepts
Matching Identical & Non-identical Items, Fill-ins and Reversals and Abstract Categories are now just $48. That’s a $12 savings on 252 cards. This back to school offer is available for a limited time only. http://www.nlconcepts.com/index.htm
http://www.nlconcepts.com

From a Listmate
TV Ontario's TVOParents.com is looking for four families with autistic children or children on the autism spectrum to participate in a roundtable discussion on Thursday, August 30th at 7 pm in the TV Ontario studios (2180 Yonge St., Toronto).

The discussion will focus on the early days of worry, doubt and then diagnosis. What is discussed will help other parents at this stage in their journey to gain the knowledge they need to move forward towards diagnosis and treatment.

The roundtable discussion will be recorded in audio format only and will be posted on the TVOParents.com site. Participants must also be willing to have a camera crew film their stories for a series of mini documentaries that will also be placed on the site. (Please note: only one member from each family will participate in the roundtable discussion.)

If you are interested or have any questions, please contact the producer Sarah Michaelis ( smichaelis@tvo.org or 416-484-2600 x2100). Sarah also welcomes the input from families with ideas about other autism-related stories.

If you, or a family you know, is interested in making a difference by sharing your/their journey, please contact Sarah. Sarah also welcomes input from families with ideas for other autism-related stories.
Sarah Michaelis
Producer, TVO Parents.com
416-484-2600 x2100
www.tvoparents.com
smichaelis@tvontario.org

in partnership with
Kelli & Michael Pallett
Parents Listen
519-942-3738
www.pallettcorner.net
parentslisten@gmail.com


Check out Your Voice every Tuesday at 1 pm on TVOParents.com!
++++++++++++++++++++
Here is a FlashCard website:
http://www.flashcardexchange.com/
+++++++++++++++++++++
Two research studies have been approved by the Queen's University Ethics Board.
Participation by families, children and/or adults is invited.
More studies will begin in September, when I will let you know more.

1. Social Cognitive Skill in Young Children with Autism and Toddlers at Risk for Autism
We are looking for:
. high-functioning children (under 4 years) or lower-functioning children
(under 7 years) with a diagnosed ASD;
. children (under 30 months) who have an older sibling with a diagnosed
ASD of any age;
. children with a developmental delay (under 7 years) and their younger
siblings (under 30 months)
The study involves a number of play-like tasks and participation will require one to two visits that will be between 45 minutes to one hour long. Parents will also be asked to fill out two short surveys and participate in a short interview over the phone. You will be reimbursed $10.00 for transportation costs, and your child will receive a small toy and certificate of appreciation.
See contact note below.

2. Action Observation and Eye Gaze
We are looking for high- or low-functioning adults over 18 years of age with a diagnosed ASD who can follow simple instructions and repeat them back This study consists of multiple parts. These may include watching another person performing a task, watching a video, completing hands-on tasks and/or answering a series of questions. During some of the tasks, your eye movements will be recorded using an eye movement tracker. The study will involve between one to three visits that will be 45 minutes to an hour in duration. Please do not feel obligated to participate in all of the visits. You will be reimbursed $10 for every visit made to the lab.

In addition, ASD Studies is in the process of initiating new research projects for participants of all ages. Check out: http://psyc. queensu.ca/ asdstudies
For more information regarding this study as well as others, please contact us at:
613-533-2841 OR
asd.studies@ queensu.ca
Dr Elizabeth Kelley
ASD Studies Group
Queen's University
Department of Psychology
62 Arch St.
Kingston, ON. K7L 3N6

============ ========= ========= ==
Read more on the OAARSN site at http://www.ont- autism.uoguelph. ca
Please note the Search feature on the Main Page.
See our archive of past OAARSN news bulletins.

OAARSN welcomes discussion of ideas and topics related to adults with autism.
We support freedom of information and expression and encourage everyone
to try to see all sides of issues and to understand the viewpoints of others.
We do not endorse all opinions or interventions that we may report in this bulletin.
++++++++++++++++++++++++++++++++++++++++
Jock Doubleday, director of the California non-profit corporation Natural Woman, Natural Man, Inc., has offered $75,000 to the first medical doctor or pharmaceutical company CEO who publicly drinks a mixture of standard vaccine additives.

The additives would be the same as those contained in the vaccines recommended for a 6-year-old according to U.S. Centers for Disease Control and Prevention (CDC) guidelines, and the dose would be body-weight calibrated. It would include, but not be limited to:
• Thimerosal (a mercury derivative)
• Ethylene glycol (antifreeze)
• Phenol (a disinfectant dye)
• Aluminum
• Benzethonium chloride (a disinfectant)
• Formaldehyde (a preservative and disinfectant)
On August 1, 2007, if no one has taken the challenge, the offer will be increased to $90,000 and will increase at a rate of $5,000 per month until an M.D. or pharmaceutical company CEO, or any of the 14 relevant members of the ACIP (see below), agree to drink a body-weight calibrated dose of the poisonous vaccine additives that M.D.s routinely inject into children in the name of health.

This offer, dated April 25, 2007, has no expiration date unless superceded by a similar offer of higher remuneration.
Jock Doubleday
Director
Natural Woman, Natural Man, Inc.
A California 501(c)3 Nonprofit Corporation
http://gentlebirth.org/nwnm.org/nwnm_org.html
++++++++++++++++++++++++++++++
+++++++++++++++++++++++++++++++++++++++++++++++++++++++++++
KS: What inspired you to write this song?
Initially, the inspiration for this song came from our brother with special needs; he has Prader Willie Syndrome (as a side note, he was once actually thought to have autism). The whole concept for this song stemmed from our experiences with him and the pre-conceived notions that a lot of people still have surrounding people with special needs.
KS: So what is the core concept behind the song?
The core concept that we wanted to share through this song was acceptance. We wanted to show that no matter what our differences (physical, mental or any thing else) we're all still connected, and that through education and patience all people can come to accept other people that are different.
KS: What do you hope to accomplish by sharing it?
The goal that we have in mind is to show people that no matter how we are on the outside, we're all the same on the inside.
KS: What are you doing with the funds that you raise with this song?
A portion of the proceeds is being donated to The KEEN Foundation. The KEEN Foundation supplies resources and education tools for free to those whom care for some one with special needs but can't afford the information and services that are available. That said, we are also open to helping other organizations use this music as a fundraiser if they wish to do so (Please email shane@livingillusion.com for fundraising opportunities).
KS: Who do you hope gets to hear this song?
Our brother obviously :) But, on the larger scale we want every one to hear this song, especially those that know the experiences of working with, living with, or hanging out with some one whom has special needs... and also those who don't. I find that to often people assume so much just based on a first glance of others, through this song we hope to raise awareness, and shine some light on the stars that these wonderful people are. It's time to put an end to people looking at the glass as half empty.
Listen to the song: http://www.autismtoday.com/livingillusion.htm
++++++++++++++++++++++++++++++
Autistic savants are very hard to come by, as the savant syndrome itself is very uncommon. There are less than 50 savants alive today. The memories of savants are likely unlike anything you will ever know or experience. Savants can recite, both forward and backward, a book that they have just read, yet some can barely speak. Their memories are specific and complete however there is little emotion in them. Studies describe savants as human tape recorders.
The term savant originated in Europe in the late 19th century when a small group of people in asylums was discovered to have astonishing and mysterious talent.
Neuroscientists are discovering the difference between a "normal" person and the astonishing skills of savants is that the savants are able to tap into areas of the mind that function like supercomputers. These supercomputers that we call our mind are accumulating immense amounts of information from the senses to create a working model of the world, which could only make sense to them. One researcher believes that "average" people are blind because of what we know and see. He feels that if we could shut off our theoretical mind, we could literally for one moment see the real world that surrounds us.
These children come into the world with deep artistic talents and their minds will continue to be a fascination to all researchers. As one researcher is quoted in "The Key to Genius," "By finding out how savants work, we learn how we work."
http://www.wired.com/wired/archive/11.12/genius_pr.html
************************************************
L.A.Times Staff Writer

July 30, 2007

Women who live near California farm fields sprayed with
organochlorine pesticides may be more likely to give birth to
children with autism, according to a study by state health officials
to be published today.

The rate of autism among the children of 29 women who lived near the
fields was extremely high (6 X higher) , suggesting that exposure to the
insecticides in the womb might have played a role. The study is the
first to report a link between pesticides and the neurological
disorder. .. For most pesticides, no unusual numbers of autism cases were found,
but the exception was a class of compounds called organochlorines.
Most, including DDT, were banned in the United States several
decades ago because they were building up in the environment. Only
dicofol and endosulfan remain.
+++++++++++++++++++++++++++++
**********************************************
Click here: Fun Way to Increase Your Brain Fitness - Articles
http://articles.mercola.com/sites/articles/archive/2007/06/06/fun-way-to-increase-your-brain-fitness.aspx
++++++++++++++++++
Brain-Injured Man Speaks After Six Years!
(AP) - He was beaten and left for dead one night in a robbery while walking home in 1999. His skull was crushed and his brain severely damaged. The doctor said if he pulled through at all, he'd be a vegetable for the rest of his life. Deep Brain Stimulation (DBS) leads were implanted in his brain to stimulate areas critical for specific skills ... like speaking. For six years, the man could not speak or eat.On occasion he showed signs of awareness, and he moved his eyes or a thumb to communicate. His arms were useless. He was fed through a tube. But researchers chose him for an experimental attempt to rev up his brain by placing electrodes in it. And here's how his mother describes the change in her son, now 38:
"My son can now eat, speak, watch a movie without falling asleep," she said Wednesday while choking back tears during a telephone news conference. "He can drink from a cup. He can express pain. He can cry and he can laugh. The most important part is he can say, `Mommy' and `Pop.' He can say, `I love you, Mommy' ... I still cry every time I see my son, but it's tears of joy."
Experts called the results encouraging but cautioned that the experimental treatment must be tried in more patients before its value can be assessed. The researchers are already proceeding with a larger study. Before the electrodes were implanted, the man was in what doctors call a "minimally conscious state." That means he showed only occasional awareness of himself and his environment. In a coma or vegetative state, by contrast, patients show no outward signs of awareness.
There are no reliable statistics on how many Americans are in a minimally conscious state, but one estimate suggests 112,000 to 280,000. Doctors may try medications to improve their condition but no drugs have been firmly established as helpful.The experimental treatment is called deep brain stimulation. It has been used for years in treating Parkinson's disease, although in this case the electrodes were implanted in slightly different places. The goal of the stimulation was to provide "drive" to areas of the brain that are critical for specific skills like speaking.Similar stories of partial recovery from brain damage occasionally grab headlines, whether the improvement came from treatment or just out of the blue.
Terry Wallis of Arkansas lingered in a minimally conscious state for almost 20 years before he suddenly regained some ability to speak and move in 2003. In 2005, a former firefighter in Buffalo, N.Y., turned from being barely aware and almost mute for nearly a decade into a virtual chatterbox for 14 hours. His doctor had been trying a cocktail of drugs.The man described in the Nature paper, despite his improvements, remains severely disabled in a rehabilitation facility for brain injury on the East Coast. (To preserve the man's anonymity, the researchers would not identify the facility or even reveal which state it is in).
He can't walk. While he has regained the ability to chew and swallow, he must be spoon-fed. He can demonstrate the motion of brushing his teeth, for example, but he can't actually do it. That's because tendons in his arms contracted after years of immobility, said study lead author Dr. Nicholas Schiff of Weill Cornell Medical College in New York.
The man doesn't initiate conversation but can reply to others, generally with one to three words, said Dr. Joseph Giacino, a co-lead author of the Nature study.Several weeks ago, he recited the first half of the Pledge of Allegiance without assistance, said Giacino, of the JFK Johnson Rehabilitation Institute in Edison, N.J.
The man's electrodes are left on for 12 hours a day. He has continued to improve since the experiment formally ended in February 2006, the doctors said. After the research was over, doctors started giving him the drug amantadine, which has shown some potential for treating people in a minimally conscious state. It's not clear whether amantadine can boost the effects of deep brain stimulation or vice versa, Giacino said. Dr. James Bernat, a professor of neurology at Dartmouth Medical School who didn't participate in the new research, called the Nature report exciting and important. Further study is needed to sort out how many patients would respond and how to identify the minimally conscious patients with the best chance of being helped, he said.He noted that a similar treatment did not help Terri Schiavo, the Florida woman in a vegetative state whose care triggered national controversy before her death in 2005. That's the typical outcome for electrical brain stimulation in vegetative states, he said. Dr. Ross Zafonte of the University of Pittsburgh, who also was familiar with the study results, agreed that "we need to know more." He said the approach is "very interesting and holds great promise."
+++++++++++++++++++++++++++++++++++++++
IF we need to care for our children in the long run, let’s all take care of ourselves now.
A dose of caring.
Half a teaspoon of cinnamon a day significantly reduces blood sugar levels in people with type 2 diabetes, and it can also reduces triglyceride, LDL cholesterol, and total cholesterol levels. Herbs such as oregano, dill, garden thyme, rosemary and peppermint are packed full of antioxidants, and garlic can help boost your immune system.
Some of my favorite spices are the hot spices. So I think it’s great news that cayenne pepper in particular is such a healthy food. The active ingredient in cayenne pepper, called capsaicin, has been found to reverse Type 1 diabetes in mice, for example -- an astounding breakthrough that the medical community keeps quiet about. Jamaican healers use it to treat diabetes, although I don't believe it should be relied upon for primary control. Capsaicin also has cancer-fighting benefits.
A substance found in a popular spice that is responsible for turning curry and mustard yellow, might also help with treating the deadly disease, cystic fibrosis. In a study of mice afflicted with cystic fibrosis, researchers found that deaths were reduced significantly after the mice consumed large amounts of the substance found in the spice turmeric. Results from this study initiated the Cystic Fibrosis Foundation to allocate monies for a study on turmeric and its effects on patients. The same compound in turmeric was also found to be useful in fighting multiple sclerosis.
In spite of the many benefits of turmeric and its component curcumin, you really do want to honor what your body tells you. If any food or spice does not taste good or "feel right," stay away from it -- no matter who is telling you how good it is for you. Your body is a far better judge of that than anything you will ever read.
Eliminating sugar and grains from your child’s diet and giving your child fish oil or cod liver oil for the valuable omega-3 is a good bet with any of these diseases.
Cinnamon’s other benefits include:
• Supports digestive function
• Constricts and tones tissues
• Relieves congestion
• Relieves pain and stiffness of muscles and joints
• Relieves menstrual discomfort
• Blood-thinning compounds that stimulate circulation
• Anti-inflammatory compounds that may relieve arthritis
• Helps prevent urinary tract infections, tooth decay and gum disease
• It’s a powerful anti-microbial agent that can kill E. coli and other bacteria
Nutmeg
Nutmeg is another spice that has a variety of healing properties and can be used in a wide range of dishes during the holidays and all year long. It is useful for:
• Insomnia (nutmeg can produce drowsiness so it should be taken when you have a chance to relax or sleep)
• Anxiety
• Calming muscle spasms
• Nausea and vomiting
• Indigestion
• Diarrhea
• Joint pain and gout
• Lowering blood pressure
• Male infertility and impotence
• Improving concentration
• Increasing circulation
• Lowering cholesterol
• Toothaches (nutmeg oil)
** Please note that taking too much nutmeg (one to three nuts or less) can cause side effects such as nausea, hallucinations, swelling and shock.
Clove
Cloves have a potent, sweet and spicy, aromatic flavor that makes a great complement to many foods. They have been consumed in some areas, such as Asia, for more than 2,000 years. Among the clove’s most well-known healing properties is its ability to relieve tooth and gum pain, but it has many benefits beyond that. These include:
• Anti-inflammatory, anti-bacterial and antioxidant properties
• Relief from respiratory ailments such as asthma and bronchitis
• Relief from muscle pains from injuries or arthritis and rheumatism
• Eliminates intestinal parasites, fungi and bacteria
• May encourage creativity and mental focus
Ginger
Ginger is another spice with a potent flavor that is great for warming your body and adding kick to foods. It’s medicinal properties include:
• Soothes nausea, motion sickness and other stomach upset
• Relieves morning sickness
• Anti-inflammatory properties
• Eliminates intestinal gas
• Relaxes and soothes the intestinal tract
• Antioxidant properties
• Relieves dizziness
• Boosts the immune system
• Protects against bacteria and fungi
• Encourages bile flow
• Promotes cardiovascular health
Peppermint
The therapeutic effects of fresh peppermint leaves have been known since ancient times and its aromatic aroma has come to symbolize hospitality in many cultures. Its healing properties include:
• Soothing to the digestive tract
• Relieves symptoms of irritable bowel syndrome
• May protect against cancer
• Inhibits the growth of bacteria and fungus
• Relieves the symptoms of allergies and asthma
While there are many benefits to be had by adding spices to your diet, don't forget that these foods should not be taken every day or you run the risk of developing an allergy to them. Spices should not be looked at as a "cure" for your health problems, only by addressing the underlying causes of illness with a healthy diet and lifestyle will you be able to achieve optimum health.
Please use care when choosing your spices, as in the United States over 65 million pounds of spices, herbs and dry ingredients are irradiated each year. Fortunately, in the United States and Canada irradiated spices have to be labeled with the international symbol for irradiated foods, the "radura" symbol. However, processed foods that contain irradiated spices do not have to be labeled in the United States. So before you purchase a spice be sure to check the label to ensure that it has not been irradiated--organic varieties are your best bet.
But don’t let this discourage you from taking advantage of all that spices have to offer. Spices used with the above advice in mind are indeed an excellent way to add flavor and healing properties to your diet.
+++++++++++++++
My daughter will be holding her 2nd Annual Lemonade Sale for Autism Awareness this Sunday August 19th, 2007.
Details are below. All proceeds will be donated to Autism Ontario – Toronto Chapter.
Martha Veliz
mjveliz@rogers.com
2nd Annual Lemonade Sale
For Autism Awareness


When: Sunday, August 19th, 2007
Time: 2 – 5 pm
Where: 6 Chiswick Ave, Toronto
(closest intersections: Jane St and Trethewey Dr)
Cost: only 25 cents per glass

Autism Facts:
Autism is a developmental disability that begins by 2 years of age and is a life-long disability.
Autism impacts the normal development of the brain in the areas of social interaction and communication skills.
Children with autism look the same as typical children.
1 of every 165 Canadians is affected by Autism Spectrum Disorders (ASDs).
Autism is 4-5 times more prevalent in boys than girls
Autism is not a mental illness.

All proceeds will be donated to: Autism Ontario – Toronto Chapter



From NEWSWEEK
The Puzzle of Hidden Ability
By Sharon Begley
Newsweek
Aug. 20-27, 2007 issue - Even their parents struggle to draw the tiniest hint of emotion or social connection from autistic children, so imagine what happens when a stranger sits with the child for hours to get through the standard IQ test. For 10 of the test's 12 sections, the child must listen and respond to spoken questions. Since for many autistics it is torture to try to engage with someone even on this impersonal level, it's no wonder so many wind up with IQ scores just above a carrot's (I wish I were exaggerating; 20s are not unknown). More precisely, fully three quarters of autistics are classified as having below-normal intelligence, with many deemed mentally retarded.
It's finally dawning on scientists that there's a problem here. Testing autistic kids' intelligence in a way that requires them to engage with a stranger "is like giving a blind person an intelligence test that requires him to process visual information," says Michelle Dawson of Rivière-des-Prairies Hospital in Montreal. She and colleagues therefore tried a different IQ test, one that requires no social interaction. As they report in the journal Psychological Science, autistic children's scores came out starkly different than on the oral, interactive IQ test—suggesting a burning intelligence inside these kids that educators are failing to uncover.
That failure has lifelong implications. "If we label these children as below-normal in intelligence, that is how they're treated," says Laurent Mottron, who led the study. The disparity between scores on the two IQ tests also makes you wonder who else the tests, which are used for everything from screening military recruits to filling "gifted" classes, are mislabeling.
For the study, children took two IQ tests. In the more widely used Wechsler, they tried to arrange and complete pictures, do simple arithmetic, demonstrate vocabulary comprehension and answer questions such as what to do if you find a wallet on the street—almost all in response to a stranger's questions. In the Raven's Progressive Matrices test, they got brief instructions, then went off on their own to analyze three-by-three arrays of geometric designs, with one missing, and choose (from six or eight possibilities) the design that belonged in the empty place. The disparity in scores was striking. One autistic child's Wechsler result meant he was mentally retarded (an IQ below 70); his Raven's put him in the 94th percentile. Overall, the autistics (all had full-blown autism, not Asperger's) scored around the 30th percentile on the Wechsler, which corresponds to "low average" IQ. But they averaged in the 56th percentile on the Raven's. Not a single autistic child scored in the "high intelligence" range on the Wechsler; on the Raven's, one third did. Healthy children showed no such disparity.
The Wechsler measures "crystallized intelligence"—what you've learned. The Raven's measures "fluid intelligence"—the ability to learn, process information, ignore distractions, solve problems and reason—and so is arguably a truer measure of intelligence, says psychologist Steven Stemler of Wesleyan University.
That presents a puzzle. If many autistics are more intelligent than an IQ test shows, why haven't their parents noticed? Partly because many parents welcome a low score, which brings their child more special services from schools and public agencies, says one scientist who has an autistic son (and who fears that being named would antagonize the close-knit autism community). But another force is at work. "We often think of intelligence as what you can show, such as by speaking fluently," says psychologist Morton Ann Gernsbacher of the University of Wisconsin. "Parents as well as professionals might be biased to look at that" rather than dig for the hidden intellectual spark.
The challenge is to coax that spark into the kind of intelligence that manifests itself in practice. That is something autism researchers are far from doing. Worse, much of the expert advice might be counterproductive. Many experts dismiss autistics' exceptional reading, artistic or other abilities as side effects of abnormal brain function, "not a reflection of genuine human intelligence, which it is likely to be," says Mottron. They advise parents to steer their child away from what he excels at and obsesses over, such as letters and words and details, and toward what he struggles with, such as faces and the big picture. Dawson, who is autistic, thinks that's a prescription for intellectual failure; autistics should be encouraged to build on their strengths, as everyone else is. The problem of a lurking intelligence that won't be coaxed out by the usual education and parenting methods is not necessarily unique to autistics. It makes you wonder how many other children, whose intellectual potential we're too blind to see, we've also given up on.

From A listmate
Backgrounder

Next Steps In Funding Formula Changes
Since coming to office, the McGuinty government has made significant changes to the education funding formula and increased its investment in Ontario's publicly funded education system by $3.7 billion — an increase of $2,156 per pupil or 29 per cent.
The new investment of $182 million for the 2007-08 school year announced today, combined with an additional $127 million in 2008-09, will support further improvements to the education funding formula through a variety of ways.
For 2007-08, the changes announced today include:
• $41 million to fund 300 more vice-principals and ensure funding better matches actual staffing costs
• $20 million to fund 240 more teachers to reduce class size in primary grades
• Investment to ensure funding better matches actual costs
o $21 million for professionals and para-professionals
o $19 million for supply teachers
o $20 million for education assistants and special education
o $12 million for secretaries
o $20 million for school operations
o $12 million for student transportation
o $12 million for rural schools, including funding for over 100 additional schools through our Supported Schools Allocation
o $5 million to deliver an additional $1,000 per school for school office supplies.
For 2008-09, additional changes announced today include further investments to ensure that funding better matches actual costs:
• $50 million for non-salary compensation
• $10 million for Special Education staffing and costs
• $10 million for school operations
• $10 million for student transportation
• $10 million for English-as-a-Second-Language and Perfectionnement du français
• $10 million for the operation of small boards
• $10 million to expand local education priorities through the Program Enhancement Grant
• $10 million in funding to support the construction of $140 million worth of schools in areas of local growth
• $6.5 million for Continuing Education and Adult English-as-a-Second-Language and Perfectionnement du français.
Minister Chambers will be making an Announcement

(Re: More IBI spots and Respite Plan for Autism)

FRI AUG 17th
Surrey Place Centre
2 Surrey Place
10AM


Regards,
Lillian Wagman

From ONTABA
http://www.ontaba.org/consumers.htm
Consumer's Corner

I remember attending a conference in Toronto a few years ago and listening to the keynote speaker say in her speech: “Often parents, teachers, and other individuals involved in Autism, advocate for ABA without really understanding what IT is”. I did not realize at the time just how pertinent Dr. Patricia Krantz’s words of wisdom were but I do now.

On February 23, 2007, the Ministry of Education made an elaborate announcement that they will be providing ABA in the schools in September for Ontario students with Autism. What joy and relief this brought to families like mine who have been advocating for this for many years. The public assumed that the Premier had finally followed through on his pre-election promise from four years ago and we all looked forward to learning more about this in the weeks ahead.

Days after the announcement, the Deputy Minister of Education sent a memo to all School Boards in Ontario attempting to clarify the message they felt had resonated not so accurately through the media. The memo stated: “The focus of this PPM will be ABA teaching practices and not Intensive Behavioral Intervention (IBI) that is used by the Ministry of Children and Youth Service’s Autism Intervention Program.” This statement made it clear that the mutual exclusivity issue between IBI and Education would continue despite the fact that an inclusion component can have such a significant impact on a child’s achievement. The memo further stated: “ABA is a relatively common practice now in schools…” which gave us reason to question what the Ministry had in mind for ABA in the schools.

It may not be too difficult to trace back our steps to see exactly where, when, and by whom the concrete wall was placed between ABA and IBI. The difference between the two as used by the Ontario Government and the School Boards is completely arbitrary. IBI is the intensive application of ABA-based techniques. The real discussion should be on how to determine what the parameters are of the teaching interactions that need to occur for a child with autism to master appropriate IEP goals and objectives, and to hopefully make the transition to a less restrictive environment. In order to accomplish this, the question that should be asked is: “What does the child NEED to learn?” When the Ministry asks the right question and then holds local School Boards accountable for implementation of effective teaching for children with Autism, then we will be on the right track. Until then, the children with Autism in Ontario will continue to be sadly neglected.

On May 17, 2007, the Ministry of Education released PPM 140, a direction to the School Boards as to how to provide ABA in the schools, an incredibly vague memo with no mention of qualified behaviour analysts whatsoever. Its vagueness was a stark contrast to the systematic and detailed direction of programs and services for the Deaf, Blind, and both Deaf-Blind in PPM 76C and gave us more reason to question what ABA in the schools would look like in September.

The Ministry of Education and a Toronto-based Agency providing services for Autism made presentations to School Boards on PPM 140 and ABA in the schools last month. During the presentation, they stated: “(IBI) is delivered by trained therapists, supervised by Behaviour Analysts and overseen by a behavioural psychologist.” However for ABA, they stated: “With training in ABA parents, teachers, and interventionists all make use of behavioural teaching practices”. Now our concerns developed into solid fear for what the Ministry would implement for our children in the fall.

Sure, I’ve realized for many years how some service providers who claim to offer ABA and IBI services are not qualified and families have been taken advantage of as a result but to have our Government and School Boards jump on that bandwagon also was not something I had expected.

ONTABA has much work to do. Not only do we still not have formal credentialing of qualified behaviour analysts in Ontario (and we are in the 8th year of a $130M publicly funded IBI initiative), but it has also recently become clear that the ABA the Ministry plans to implement in the schools for this September is not ABA at all. This is of grave concern to the families, but it should also be of concern to the qualified behaviour analysts being moved to the side as a result and the taxpayers in our province who are obviously being fooled. Finally, this is an insult to the science that ABA truly is and calls for the attention of ABA International.

Who decides what ABA is? What protection do Ontario families have against organizations, Government, and School Boards who claim to be providing ABA when they’re really not? I had always walked into every discussion on this issue with the Autism SIG Guidelines for ABA Consumers in hand and am now hanging on to these guidelines more than ever before and try at every opportunity to educate other families to do the same.

Dr. Krantz’ wise words will be a test for every parent advocating for ABA and IBI during this crucial time in our province’s history of developing infrastructure. If ABA is not overseen by qualified behaviour analysts, IT is not ABA.
Regards
Taline Sagharian

Autism issues front, centre

SHARON GABISON: Concord teacher to help make autism funding an election issue.
MORE STORIES
Vaughan
Aug 15, 2007 10:57 PM

By: Michael Power
A Vaughan resident has become one of four new members of the Ontario Autism Coalition’s executive committee.

Sharon Gabison of Concord recently joined the organization in its campaign to raise awareness of autism issues before the Oct. 10 provincial election.

“We’re putting autism issues front and centre,†Ms Gabison said. “We want to make sure the government follows through with three main things. They’ve made a lot of promises in the past but with very little follow through.â€

The Ontario Autism Coalition was co-founded by Vaughan residents Bruce and Laura McIntosh in 2005 and now boasts more than 600 members. It organizes rallies and has met with dozens of politicians and government officials to raise awareness of the need for publicly funded autism programs.

Specifically, the coalition will pressure the government to:

• allow specialized therapists to work with children with autism within schools;

• eliminate wait lists and fully fund children with autism, from the mild to the severe end of the autism spectrum;

• develop a formal system of credentials and a training and recruitment system for autism therapy and treatment.

Ms Gabison’s 10-year-old son, Eric Segal, is autistic and has benefited from five years of applied behavior analysis, a form of autism treatment.

“I’ve seen the remarkable things it’s done for him,†she said.

Ms Gabison is also a physiotherapist and teaches in Seneca College’s autism and behavioural science program and physiotherapy at the University of Toronto.

For more information on the Ontario Autism Coalition, visit www.ontarioautism.com
From a listmate

Jump start for autistic kids at August skills camps

Whitchurch-Stouffville
Aug 15, 2007 10:02 PM
If your child has autism, the Back to School Social Skills Summer Camp run by Making Small Talk can help them get back into the school routine ahead of time.

Courses run from Aug. 20 to 24 for children nine to 12 and from Aug. 27 to 31 for children five to eight. They are run by the TLC Sensory Leisure Centre.

The focus of the week-long courses is on preparing children for going back to school. They will be reminded of school and classroom rules, friendships, conversations, self-awareness and recess activities. This will be done through teaching, stories, play, role playing, games and crafts.

Spaces are limited since a maximum of six children are accepted for each session.

Classes run from 9 a.m. to noon at St. Paul’s United Church on Sunset Beach Road in Richmond Hill.

The cost is $300 per child.

E-mail smalltalk@sensoryleisure.com or call Linda Hurren at 647-519-6739.Log on to www.makingsmalltalk.com for more information. For more information and help with autism-related issues, check out the latest newsletter of the York Region chapter of Autism Ontario at autismontario.com/york


From a Listmate

Significance of NYC v. Tom F.
In New York City Bd of Ed. v. Tom F., the Supreme Court will determine if a child will be forced to "try" an inappropriate placement before the parents can remove the child to an appropriate placement and seek reimbursement.

If the Supreme Court affirms the decision by the Second Circuit, parents will have the right to obtain reimbursement from the public school even if the child was never enrolled in a public school special education program.
Parents will still be required to show that the district's proposed program was inappropriate and that the private special education program they chose is appropriate, consistent with the established tuition reimbursement remedy authorized by the IDEA and the Supreme Court's decisions in Florence County School District Four v. Shannon Carter, 510 U.S. 7 (1993) and School Committee of Burlington, Mass v. Department of Education, 471 U.S. 359 (1985).

If the Supreme Court reverses the Second Circuit, parents will have two choices:
they can place their child in an appropriate private program and forfeit any chance to obtain reimbursement, or they can place their child into an inappropriate public school program so they can later remove the child from that program and seek reimbursement.
The message is ready to be sent with the following file or link attachments:
Shortcut to: http://www.wrightslaw.com/news/07/nyc.tomf.htm

Note: To protect against computer viruses, e-mail programs may prevent sending or receiving certain types of file attachments. Check your e-mail security settings to determine how attachments are handled.

End of Mailing for August 10-16th 2007

Thursday, August 9, 2007

Autism News Articles for July 31st - August 9th, 2007

Autism News Articles

July 31st to August 9th

We appreciate your patience for these mailings
Delays are expected due to vacation

Thank you.
Trish


FROM:
http://www.standard-freeholder.com/webapp/sitepages/content.asp?contentid=635144&catname=Local+News&classif=

Novel therapy for autism; Snoezelen Room has city families all smiles

Elisabeth Johns

Wednesday, August 01, 2007 - 08:00

Local News - Giggling and laughing, Paskale Pilon waves at himself in the mirror.

His parents, Nyree and Serge, watch as he then dives under a blanket full of plastic balls and declares that "it's like a cave" in there. The 11-year-old has only been coming to this therapy room, called the Snoezelen Room, for about a month, but he already knows he loves it.

"Do you like coming to the Snoezelen Room?" his dad asks.

"Uh-huh," Paskale replies. "Because I love it. It's so cool."

Paskale was diagnosed as autistic when he was three years old.

The Snoezelen (pronounced snooz-e-len) Room is a type of multisensory room designed to stimulate a child (or adult) who has autism or developmental disabilities.

Since Paskale has been going to the Snoezelen Room over the past month, his parents have noticed the normally energetic, smiley talkative boy co-operates more and looks forward to going to the therapy room.

It also provides mom and dad with a much needed break as Paskale is quite a handful: from the moment he gets up at 6 a.m., his dad said, to the time he falls asleep he chatters non-stop.

"He requires 24-7 care," Serge said. "It gives us a chance to do other things, like stuff around the house, errands, while he is in here."

Nyree added that they both knew about the concept before the room was built in Cornwall and couldn't wait to see how Paskale would react when he made his first visit.

Created by two Dutch psychiatrists, the belief is that the different sensations in the room - sound, smell, touch, sight - provide a soothing environment, which can help to reduce agitation or make people relax.

It's a small room in a building located at 126 Gloucester St., maybe big enough to fit a child's bed, desk and drawers. Being in the room can be very therapeutic, said Debbie Keillar, the local chapter president of Autism Ontario, but it's not necessarily meant to be educational.

Although, she added, depending on the individual, there can be educational benefits, like learning about different colours, to count and about cause and effect.

"A lot of people with autism need (the stimulation)," she explained. "The way they process their environment is different. Someone who you might think is unresponsive - you'd be amazed what responses this will bring out of them."

A common myth about autistic individuals is that they have no emotion: a myth Keillar said she's seen debunked by the Snoezelen Room's sensory therapy approach.

"If an individual is non-verbal, they may be able more clearly communicate in here," she said, adding that parents have seen their seemingly unemotional children smile and laugh while exploring the Snoezelen Room's environment.

But not every child reacts positively to the room, added Bernadette van Gurp, a supervisor with S, D and G Developmental Services.

"We had one girl who wanted nothing to do with it," van Gurp said. "But most often, the reaction is positive."

Different types of lights, from the tiny bead lights in the "milky-way" carpet to lava lamp style lights that can be projected on the wall.

There are blankets filled with plastic balls, which Keillar said a child might lay under - the heavy blanket could provide an enjoyable "deep pressure" feeling - funhouse-type mirrors and 30 different aromatherapy scents.

Children and adults alike can watch bubbles rise and fall in a water tube, crinkle a blanket filled with foil or just fall asleep to soft nature music.

Heidi Penning, the former local chapter president of Autism Ontario, is credited with writing the grant to secure the $25,000 in funding from the Ronald McDonald Children's Charities of Canada.

Another $6,000 was donated by the Upper Canada chapter of Autism Ontario. The money was required to purchase all the equipment and train staff, Keillar said. The room was officially opened last November.
********************


FROM a Listmate

The New Haven Learning centre is currently expanding it’s enrolment across all age groups for the upcoming 2007-2008 school year. Interested families should contact Tracey Lacka, Executive Assistant at 416-259-4445 x 0 or Newhaven@bellnet.ca for more information.


New Haven Learning Centre
301 Lanor Avenue, Etobicoke, ON M8W 2R1
p 416.259.4445
f 416.259.2023
www.newhavenlearningcentre.com


From The Wall Street Journal
http://online.wsj.com/article/SB118584776380882977.html?mod=googlenews_wsj

For Parents of Children with Special Needs, Public School Offers No Relief
Word Count: 717
As the father of a mildly autistic first-grade boy I would like to say thanks for your series of articles that have brought the challenges of special education to light. When I tell family or friends the things we have had to endure they think I am exaggerating. Your articles, and this one in particular ("Staying the Course: Schools Beat Back Demands for Special-Ed Services," Page One, July 24), make me want to plead and beg all the more for real school choice and vouchers.
The public-school system in this country is broken. Union thugs and overpaid fat-cat administrators don't ...
• THE FULL WSJ.com ARTICLE IS ONLY AVAILABLE TO SUBSCRIBERS.
• IF YOU ARE ALREADY A SUBSCRIBER, PLEASE LOG IN AT THE TOP RIGHT OF THE PAGE.




SYMTREND= A social Skills software program available on the market.

Minna Levine
President
SymTrend, Inc.
89 Bay State Rd.
Belmont, MA 02478
617-484-7510 (phone)
617-484-1430 (fax)

Thank you for your inquiry. We don't have an actual device. What we
have is software to run on a regular Palm computer that you can buy in an
electronics store or online.

Our software, which works on a handheld computer and on the web at our
site (www.symtrend.com) lets the user record information about
behaviors, feelings, stresses, and physical symptoms, as well as gives the user
guidance about things to do in challenging situations.

Applications for Asperger Syndrome, a form of autism, and applications for lower functioning autistic persons who cannot respond adequately or read adequately for themselves. Then the parent or teacher records about him/her.

If you want to learn more about applications for Asperger persons, go
to http://www.youtube.com and search for SymTrend. We have a video there
you can watch.

If you'd like to discuss what your child needs with one of our
clinicians, call us (toll-free) at 866-796-8736.

I look forward to working with you to help your child.

=====================
Welcome toSymTrend®“Testing out the tips and writing down how it went has made the reminders stick more than usual…I used to feel anxious, about what to talk about, how to say it….”-Arthur, East Bridgewater, MAUse a handheld computer and SymTrend software to:-Monitor someone’s feelings or have him self-monitor-Understand what triggers problems-Improve interactions & behavior


VIDEOS AVAILABLE
FROM A LISTMATE

From: "Julie Coulter"
>To:
>Subject: NEW Sibling Autism and Asperger Sydrome DVDs
>Date: Tue, 26 Jun 2007 14:52:37 -0400
>
>
>
>Hi,
>
>We're letting our customers know about a new DVD Coulter Video is releasing
>today titled, "Understanding Brothers and Sisters on the Autism Spectrum."
>
>This video is designed for siblings who have brothers and sisters diagnosed
>with autism. The video deals with a range of autistic conditions, with the
>exception of Asperger Syndrome. We'll be releasing a similar video for
>siblings of brothers and sisters diagnosed with Asperger Syndrome within
>the
>next few months.
>
>Each DVD (the autism version and the Asperger Syndrome version) contains
>four programs; three for siblings of different ages and developmental
>levels, and one for their parents. The sibling programs are for children
>ages 4-7, ages 7-12 and ages 12 to adult. While the two DVDs have a similar
>format, each is unique. For example, we interviewed families dealing with
>an autism diagnosis for the autism DVD and families dealing with an
>Asperger
>Syndrome diagnosis for the Asperger Syndrome DVD.
>
>These videos show siblings that other kids are facing the same challenges
>they face, and explores a range of ways the kids interviewed have learned
>to
>get along with and enjoy their brothers and sisters. The videos also can
>help parents understand the special needs of their neurotypical children.
>The segments for siblings ages 4-7 feature puppets and the segments for
>older siblings feature interviews with brother and sisters. We interviewed
>mothers and fathers for the parent segments.
>
>Overall, we interviewed members of 24 families with children on the autism
>spectrum to create these two videos. After viewing these programs,
>siblings
>should have a better understanding that their brothers and sisters aren't
>trying to be difficult, and should be more willing to treat them with
>tolerance, caring and respect.
>
>Again, "Understanding Brothers and Sisters on the Autism Spectrum" is
>available now. "Understanding Brothers and Sisters with Asperger Syndrome"
>is scheduled for release in August, 2007. Here's the Internet address to
>view more information about the video on our website:
>
>http://home.att.net/~coultervideo/understandautas.htm
>
>We hope these videos can be a helpful resource for families.
>
>Sincerely,
>
>Julie and Dan Coulter
>
>COULTER VIDEO
>1428 Pinecroft Drive
>Winston-Salem, NC 27104
>tele. & fax: 336 794 0298
>www.coultervideo.com


OFF TOPIC
Not autism related but your child might have these toys on recall
http://www.service.mattel.com/us/recall/39054_IVR.asp?prod


From a Listmate:

Ask Lindsay Moir:
More on provincial campaign questions
Friday, August 03, 2007
In last week's column I asked parents to send me ideas for questions to be directed to candidates and parties in the upcoming provincial election — thank you for the great response! Here are three questions constructed out of several concurrent responses.
Background: (Based on five emails)
Parents of special education students are generally pleased with new initiatives such as funding for ABA in education, Special Education Transformation, Special Education Funding reform, new resource documents, changes in the Safe Schools Act etc. These initiatives seem to have all-party support, so this is a non-partisan issue. HOWEVER it is the impression of many parents that the Ministry of Education continues to roll out excellent changes, but there is little or no monitoring of implementation. There does not appear to be consequences for boards or educators who ignore Ministry initiatives, or contravene the Act.
Question 1:
Several excellent Special Education initiatives which have all-party support have been announced by the current government. In order to implement these reforms, it is my belief that the Ministry must invest significantly in training and close monitoring of school board implementation. Significant sanctions need to be put in place for educators and school boards who ignore provincially-mandated policy direction. Where do you stand on the mandatory training of school boards, mandatory external monitoring and sanctions of boards who fail to implement provincial policy?
Background: (based on three emails)
We believe strongly in integration (inclusion) and public education. We are seeing an increase in the number of parents of special needs children who are contacting associations and support groups for information on private schools and homeschooling. Major issues for these parents are the resistance to change by the school board bureacracy, failure to deal with staffing or training issues, timeliness of decision making, a perception that staff issues and desires supercede student needs. and negative attitudes towards families who speak out.
Question #2:
Given a perceived exodus of exceptional students and their families from the publically-funded school system, what are you and your party prepared to do to investigate this perception and if it is correct, respond to these families?
Background:(based on 3 emails)
There has been considerable discussion in this campaign about funding "faith-based" education. Many parents of special needs have "faith" in a particular technique or instructional approach. These strategies are widely-used in other jurisdictions, but some schools or boards in Ontario often refuse to implement them. (Some examples from the emails are an IBI-based school program, Direct-Teaching, DTT, phonics-based Reading, Sign Language).
Question #3:
Where parents and community professionals can demonstrate that an unusual teaching approach can be used to the benefit of an exceptional student, and that research can document that it is pedagogically-sound, and training is available, would you support legislation that would make the the timely provision of such an approach, mandatory?
Lindsay Moir retired from the Ministry of Education in 1997 and has been assisting agencies, associations and parents in obtaining appropriate special education services for exceptional pupils.
Family Net welcomes your questions about special education in Ontario.
E-mail Lindsay at ask.questions@yahoo.ca He will answer as many questions as possible.
• Events & Opportunities
View upcoming events and available job openings.
• Family Net
Helping families through shared experiences. Featuring "Ask Lindsay Moir"
• News
Keep up-to-date with our infomative news articles.


From a Listmate


Reception to honour Shelley Martel:


There will be a reception to honour Shelley Martel and celebrate Shelley's twenty years of outstanding parlimentary and community service.

Wednesday, August 22nd

5:30 to 7:30 pm
Stop 33, Sutton Place Hotel
955 Bay Street, Toronto

Must RSVP for tickets to Shirley Darling 416-535-2031 or shirley.darling@sympatico.ca


PRESS RELEASE
From a Listmate:

O N T A R I O A U T I S M C O A L I T I O N (“O.A.C.”)
www.ontarioautism.com

Media advisory
August 3, 2007

The Ontario Autism Coalition, a grassroots advocacy group, is pleased to welcome several new activists to leadership positions within the organization.

• Malcolm Stanley ( Toronto ) is the father of a three-year old girl with Autism and an active “blogger” on autism related topics. You can view his blog at www.soaringhorse.com.

• Sharon Gabison ( Concord ) is a mother of two (including a 10-year old son with Autism), a physiotherapist, entrepreneur and college professor.

• Sam Yassine ( Ottawa ) is a father of a seven-year old son with Autism, an M.D. and a strong activist for autism.

• Mary Beth Rocheleau ( Windsor ) is the mother of a 6-year old son with Autism, and a Registered Nurse.

These enthusiastic new members have joined forces with co-founders Bruce & Laura McIntosh and Dan & Susan Fentie to move this organization into their next phase of lobbying for improved services for children with Autism in Ontario .

Founded in 2005, The Ontario Autism Coalition has grown into a province-wide organization with over 600 members. Over the past two years, the OAC has organized over 20 rallies and drawn public attention to the need for publicly funded programs that effectively meet the needs of individuals in the Autism community. They have also met with dozens of government Policy Advisors, senior provincial Cabinet Ministers and Members of Provincial Parliament to make their case.

The OAC is committed to placing autism issues front and centre in the upcoming 2007 provincial election campaign. The OAC is dedicated to ensuring that politicians from all political parties are aware of concerns facing the Autism community through organized events and press releases.

Media may contact any members of our leadership team for interviews or comments:

GTA Laura & Bruce McIntosh 905-761-5226 tosh555@hotmail.com
Richmond Hill Sharon Gabison 647 892-4418 shar.gabison@utoronto.ca
Sarnia Dan & Susan Fentie 519-869-4198 autism@coolgoose.com
GTA Malcolm Stanley 416 275-3562 amstanley@rogers.com
Windsor Mary Beth Rocheleau 519 734-6387 grocheleau6@hotmail.com
Ottawa Sam Yassine 613-841-3886 Sam_yassine@rogers.com


from a listmate:




> Hi Everyone,
> Please pass this information on to anyone you think
> might be interested in learning how to teach children
> with autism using a blend of ABA and Montessori.
>
> I am teaching two new courses at Sheridan (Oakville
> Campus) in the Fall.
>
> 1. Autism-Montessori Approaches in the Home. This
> course is for parents and caregivers of children with
> autism, teaching strategies of our program in a home
> setting. It begins Sept 12 (Wednesday) and runs one
> evening a week for twelve weeks. The course code is
> SOCS78000.
>
> 2. Autism-A Montessori Approach. This course is for
> already certified Montessori teachers who want to
> learn how to do our program either in a regular
> Montessori classroom (integration) or develop their
> own clinic room. This course begins Sept 10 (Monday)
> and runs one evening a week for 11 weeks. The course
> code is SOCS78001.
>
> You can go online to register for the courses or
> contact Sheridan College directly.
>
> Their website is the following:
>
http://sculptor.sheridanc.on.ca/webapp/wcs/stores/servlet/TopCategoriesDisplay?storeId=10051&catalogId=10051
>
> If anyone has any questions about this email please
> feel free to contact me.
>
> Kind regards,
> Michelle
>
> K. Michelle Lane B. A., A.M.S., (M.A.A.A.)
> President/Founder
> The Lane Montessori School for Autism
> Not for Profit Organization
> (formerly The Toronto Montessori School for Autism)
> t. 416.435.2460
> f. 416.483.8613
> e. montessoriautism@yahoo.com
> w. http://www.montessoriautism.com
>


From a Listmate:

From the New York Times
August 5, 2007
A Faith’s Embrace Leaves No One on the Outside
By JOSEPH BERGER
NEW ROCHELLE
JEWISH mothers fret about that spotlight moment when their child is called to the Torah for the first time, but few have the sorts of worries that Jackie Saril had before her daughter, Jami, was bat mitzvahed.
Jami is autistic, which means she lacks a whole quiver of intellectual and social skills and might create some awkward moments by whining or jumping up and down on the bimah, the stage where the Torah is read.
“I was worried about her having a meltdown, refusing to get on stage, to stay on the stage, to get off the stage,” Ms. Saril said. “Jami wore leggings because she doesn’t understand how to cross your legs when you sit with a dress. She wore flat shoes so she could climb the bimah without tripping.”
Ms. Saril wanted her daughter to follow the blessings with a hand-shaped pointer, like other children do, but the pointer had a chain and Ms. Saril anticipated that Jami would fiddle with it instead of reciting her blessings. So she and Erik Contzius, the cantor at Temple Israel of New Rochelle , taped the chain to the pointer. She made sure to have Jami listen to a CD during parts of the service when she was not on stage. Music would calm her.
While the synagogue normally schedules bar and bat mitzvahs outside the sluggish summer, Ms. Saril intentionally scheduled Jami’s on July 21, two days after her 13th birthday, because she knew the audience would not be teeming with unfamiliar faces that might rattle her.
“It was all about Jami having this wonderful milestone in life with the people who helped get her there,” Ms. Saril said.
Such milestones probably would not have been observed in any religion just a few generations ago. Children with autism and Down syndrome were often institutionalized, hidden from the daily ebb and flow. “It was a shanda and nobody spoke about it,” said Ms. Saril, using the Yiddish word for shame. Now such children are raised at home and communities are bringing them into the fold. At this reporter’s synagogue, a teenager with Down syndrome is one of the Hebrew Torah readers.
“These families wanted to be part of Jewish life, but they were either uncomfortable or Jewish life had shut them out,” said Deena Spindler, director of community programs for Matan, the special-needs agency housed at the Jewish Community Center of Mid-Westchester. “Many families say, ‘We come to synagogue and everyone looks at our child,’ but Judaism teaches every person is important, and that demands embracing everybody.”
Ms. Saril, a product of an Orthodox yeshiva in Brooklyn, though Temple Israel is Reform, wanted her daughter to connect with Jewish traditions, even if she didn’t quite understand what God meant — a hard concept for anybody. Matan taught Jami biblical stories and Jewish values and had her make Passover plates like other Hebrew school children.
“I never wanted her to be the kid looking out the window while everyone else is playing,” Ms. Saril said.
Mr. Contzius, who has a son with a form of autism known as Asperger’s syndrome, first proposed having a bat mitzvah for Jami. He taught her the blessings, and he and Ms. Saril worked out a minute-by-minute schedule (autistic children thrive on schedules). It read in part: “1. Cantor C calls me to the Beema. 2. I go up to the Beema. 3. I sit quietly and keep my feet still while the curtain opens. 4. I carry the Torah carefully to the podium.”
On a radiant day, Temple Israel’s stained-glass sanctuary was lined with the people who had helped Jami reach this moment: her mother and stepfather; her 4-year-old sister, Dani; her stepbrother, Matt, 24; two sets of grandparents; four nannies, and therapists and educators from New Rochelle and from her current school, Devereux Millwood Learning Center in Millwood. Somewhat sadly, there were no friends Jami’s age.
“Jami doesn’t have friends,” Ms. Saril said.
Jami spent the first half-hour listening to music from “Hannah Montana.” When the ark was opened, she scampered up the stage without tripping and, with the cantor standing protectively alongside, carried the Torah to the podium. Announced by her Hebrew name as Chana Bracha bat Yocheved Devora, she read the same blessing every Jew reads, if perhaps not as clearly as some. Her mother chanted the Torah passage. Jami pronounced the second blessing and then recited her speech, reading headline-size words with a scanning device that allows her to focus one line at a time.
The speech was just 10 sentences long, but every one was resonant.
“Today is my bat mitzvah,” it began. “Becoming a bat mitzvah means that I have to be a good person every day.” It closed with a pledge that stirred more than a few tears: “I promise to be the best Jami I can be.”
After she finished, she skipped once around the stage and let out a soft whoop of pleasure. No one minded.
E-mail: joeberg@nytimes.com
From a Listmate

http://www.nytimes.com/2007/08/05/magazine/05autism-t.html?_r=1&oref=slogin

August 5, 2007
What Autistic Girls Are Made Of
By EMILY BAZELON
Caitlyn & Marguerite sat knee to knee in a sunny room at the Hawks Camp in Park City , Utah . On one wall was a white board with these questions: What’s your favorite vacation and why? What’s your favorite thing about yourself? If you could have any superpower, what would it be?
Caitlyn, who is 13, and Marguerite, who is 16 (I’ve used only their first names to protect their privacy), held yellow sheets of paper on which they had written their answers. It was the third day of the weeklong camp, late for icebreakers. But the Hawks are kids with autistic disorders accompanied by a normal or high I.Q. And so the main goal of the camp, run on a 26-acre ranch by a Utah nonprofit organization called the National Ability Center, is to nudge them toward the sort of back and forth — “What’s your favorite video game?” — that comes easily to most kids.
Along with Caitlyn and Marguerite, there were nine boys in the camp between the ages of 10 and 18. They also sat across from one another in pairs, with the exception of one 18-year-old who was arguing with a counselor. “All I require is a purple marker,” the boy said over and over again, refusing to write with the black marker he had been given. A few feet away, an 11-year-old was yipping and grunting while his partner read his answers in a monotone, eyes trained on his yellow paper. Another counselor hurried over to them.
Marguerite was also reading her answers without eye contact or inflection. “My favorite vacations were to India and Thailand my favorite thing about myself is that I’m nice to people if I could choose any superpower I’d be invisible,” she said in an unbroken stream. She looked up from her paper and past Caitlyn, smoothing her turquoise halter top over the waist of a pair of baggy cotton pants. Caitlyn was also staring into the middle distance. She has gold-streaked hair, which was bunched on top, and wore a black T-shirt with a sunburst on the front and canvas sneakers with skulls on the tops. The girls didn’t look uncomfortable, just unplugged.
A counselor noticed their marooned silence and prodded Caitlyn to take her turn. At first, she ran quickly through her answers, too. But Caitlyn loves fantasy — she is an avid writer of “fan fiction,” spinning new story lines for familiar characters from “Pokémon” and “Harry Potter” — and the superpower question grabbed her. She looked at Marguerite. “If I could have any power, I’d want to be able to transform into an animal like a tiger,” she said, smiling and putting her hands in front of her face, fingers tensed as if they were claws. Marguerite smiled and tentatively mirrored the claw gesture. Caitlyn smiled back. “I like tigers,” she said, her eyes bright behind her glasses. “Do you?”
It was a small, casual encounter and also an exceedingly rare one — a taste of teenage patter shared by two autistic girls.
Autism is often thought of as a boys’ affliction. Boys are three or four times as likely as girls to have classic autism (autism with mental retardation, which is now often referred to as cognitive impairment). The sex ratio is even more imbalanced for diagnoses that include normal intelligence along with the features of autism — social and communication impairments and restricted interests; this is called Asperger’s syndrome (when there is no speech delay) or high-functioning autism or, more generally, being “on the autistic spectrum.” Among kids in this category, referral rates are in the range of 10 boys for every girl.
According to the Centers for Disease Control, there are about 560,000 people under the age of 21 with autism in the United States . (Adults aren’t included because there is no good data on their numbers.) If 1 in 4 are female, the girls number about 140,000. The C.D.C. estimates that about 42 percent of them are of normal intelligence, putting their total at roughly 58,000 (with the caveat that these numbers are, at best, estimates).
Because there are so many fewer females with autism, they are “research orphans,” as Ami Klin, a psychology and psychiatry professor who directs Yale’s autism program, puts it. Scientists have tended to cull girls from studies because it is difficult to find sufficiently large numbers of them. Some of the drugs, for example, commonly used to treat symptoms of autism like anxiety and hyperactivity have rarely been tested on autistic girls.
The scant data make it impossible to draw firm conclusions about why their numbers are small and how autistic girls and boys with normal intelligence may differ. But a few researchers are trying to establish whether and how the disorder may vary by sex. This research and the observations of some clinicians who work with autistic girls suggest that because of biology and experience, and the interaction between the two, autism may express itself differently in girls. And that may have implications for their well-being.
The typical image of the autistic child is a boy who is lost in his own world and indifferent to other people. It is hard to generalize about autistic kids, boys or girls, but some clinicians who work with high-functioning autistic children say they often see girls who care a great deal about what their peers think. These girls want to connect with people outside their families, says Janet Lainhart, a professor of psychiatry and pediatrics at the University of Utah who treats Caitlyn and Marguerite. But often they can’t. Lainhart says that this thwarted desire may trigger severe anxiety and depression.
Other specialists are not sure that girls struggle more in these ways. “This is a profile of both boys and girls,” Klin says of the wish to connect that some people with autism have. But he agrees with Lainhart that it is easier for Asperger’s boys to find other boys — either on or off the autistic spectrum — who want to spend hours on their Game Boys or in a realm of Internet fantasy. Klin and Lainhart also say they think that the world is a more forgiving place for boys with the quirks of Asperger’s because, like it or not, awkwardness is a more acceptable male trait.
This gender dynamic doesn’t necessarily affect girls with Asperger’s when they are very young; if anything, they often fare better than boys at an early age because they tend to be less disruptive. In 1993, Catherine Lord, a veteran autism researcher, published a study of 21 boys and 21 girls. She found that when the children were between the ages of 3 and 5, parents more frequently described the girls as imitating typical kids and seeking out social contacts. Yet by age 10, none of the girls had reciprocal friendships while some of the boys did. “The girls often have the potential to really develop relationships,’ says Lord, a psychology and psychiatry professor and director of the Autism and Communication Disorders Center at the University of Michigan. “But by middle school, a subset of them is literally dumbstruck by anxiety. They do things like bursting into tears or lashing out in school, which make them very conspicuous. Their behavior really doesn’t jibe with what’s expected of girls. And that makes their lives very hard.”
No doubt part of the problem for autistic girls is the rising level of social interaction that comes in middle school. Girls’ networks become intricate and demanding, and friendships often hinge on attention to feelings and lots of rapid and nuanced communication — in person, by cellphone or Instant Messenger. No matter how much they want to connect, autistic girls are not good at empathy and conversation, and they find themselves locked out, seemingly even more than boys do. At the University of Texas Medical School, Katherine Loveland, a psychiatry professor, recently compared 700 autistic boys and 300 autistic girls and found that while the boys’ “abnormal communications” decreased as I.Q. scores rose, the girls’ did not. “Girls will have more trouble with social networks if they’re having greater difficulty with communication and language,” she says.
And so girls with autism and normal intelligence may end up at a particular disadvantage. In a new study published in May, a group of German researchers compared 23 high-functioning autistic girls with 23 high-functioning boys between the ages of 5 and 20, matching them for age, I.Q. and autism diagnosis. Parents reported more problems for girls involving peer relations, maturity, social independence and attention.
The difficulty may continue into adulthood. While some men with Asperger’s marry and have families, women almost never do, psychiatrists observe. A 2004 study by two prominent British researchers, Michael Rutter and Patricia Howlin, followed 68 high-functioning autistics over more than two decades. The group included only seven women, too small a sample to reach solid conclusions about gender differences, Rutter and Howlin caution. But 15 men — 22 percent of the sample — rated “good” or “very good” for educational attainment, employment, relationships and independent living, while no women did. Two women rated “fair,” compared with 11 men, and the other five women were counted as “poor” or “very poor.” None had gone to college. None reported having friends or living on their own. Only one had a job. Undermined by anxiety and depression, women with autism appear to be more often confined to the small world of their families.
When Caitlyn started kindergarten and didn’t play normally with other kids, her mother, Juli, thought it was because she hadn’t gone to preschool. The first warning of real trouble came from the first-grade gym teacher, who told Juli that Caitlyn exposed herself to the class. Caitlyn is overweight, and she has always been private about her body. Juli couldn’t imagine her daughter taking off her clothes in public, and when she asked what had happened, Caitlyn said another girl had pulled down her pants. “Caitlyn stood there mortified,” Juli says. “But she couldn’t express that to the teacher.”
Caitlyn lives with her mother, her older sister, the girls’ great-grandparents and a pair of poodles in Farmington , outside of Salt Lake City . (Her father died before she was 2.) Until second grade, Caitlyn had a neighborhood friend with whom she went to school. Other than that, she was often alone in class. Her teachers were frequently frustrated with her inability to work and play in groups. But she connected with a few adults — in fifth grade, one class aide took her horseback riding, and the school librarian gave Caitlyn her own copy of “Spindle’s End,” a retelling of “Sleeping Beauty,” “because she said I helped her so much,” Caitlyn remembers.
Contrary to the Asperger’s stereotype, Caitlyn struggles in math but tests in the highly gifted range in reading and writing. This is another sex difference that Lord sees among her patients. “I don’t have any real data, but a lot of high-functioning girls are real readers — not great on subtleties, but they like fantasies and the ‘Baby-Sitters’ series,” she says. “The boys are much less so.”
In elementary school, Caitlyn went to special-education classes for math and social skills. At 11, as other girls began to slip out of reach, Asperger’s was diagnosed. The shift a year later to junior high for seventh grade was a jolt. By the second week of school, a few boys were mocking Caitlyn’s weight and calling her weird while other kids laughed. “No one would sit by me at lunch,” Caitlyn says. Girls told her that they didn’t want her to be in their reading group. Caitlyn did her homework, but she was too anxious to walk to the front of the room to turn it in. At home, her neighborhood friend no longer came out to play.
In the winter, Caitlyn switched from a special-education math class into a mainstream one, and the kids in her new class made her miserable. For days she refused to go to school. She told Lainhart: “No one likes me at lunch. I’m very sad.” (With Juli’s and Caitlyn’s permission, I read Lainhart’s notes on Caitlyn’s treatment.) After a huge outburst of anger at home, Caitlyn told her mother that she wanted to die. At her next appointment with Lainhart, she said: “I listen to people’s conversations during free time in science. They talk about live games, R-rated movies, outfits. I feel left out.” Caitlyn told Lainhart about two dreams. In one, her school had a bridge running through it, and she kept falling off. In the second, she was in the lunchroom throwing a party; no one came. Lainhart says that while boys are aware of rejection and bullying, in her experience they are not hurt by it to the extent that some girls are. “I have rarely had a male patient with autism become suicidal or express such intense emotional pain,” she says.
Caitlyn has never hit another child. But at school, her retorts to her peers — “I yelled at a . . . little bimbo. They yelled at me,” she told Lainhart during one appointment — pushed them further away. With Lainhart’s help, Juli persuaded the school to let her daughter eat lunch in a classroom rather than in the cafeteria. Still, Caitlyn’s grades dropped from A’s and B’s to D’s and F’s. Her anxiety level spiked, and her sadness bloomed into depression.
Lainhart has seen the same blend of anxiety and depression in other female patients. Like Caitlyn, Marguerite’s serious problems date from middle school. In sixth grade, she moved to Salt Lake City and away from a couple of strong friendships, and she couldn’t replace them. “She found it increasingly difficult to do the things necessary to maintain friendships with ‘normal’ kids,” her father says. Last fall, at 15, she withdrew further. An olive-skinned girl with thick brown hair — she was adopted from Guatemala as a baby — Marguerite has always liked to go shopping and wear pretty things (not a typical trait for a girl with autism, though not unique either). But she stopped dressing herself, washing her hair and going to school. For months, Marguerite spiraled into one of the worst bouts of depression Lainhart has ever seen.
Since 1990, when she was recruited to work with autistic children by Susan Folstein, a prominent Johns Hopkins researcher, Lainhart has been interested in the relationship between autism and depression. In a 1994 paper, Lainhart and Folstein pointed out that despite the 4-to-1 male-female ratio for autism, females made up half the autistic patients with mood disorders described in the medical literature. The case reports may not represent the population as a whole; still, the overrepresentation is suggestive. Lainhart is currently looking at the relationship between autism and depression in boys and girls and the potential link to depression in their parents and siblings. “We know that anxiety and depression are co-morbid,” meaning that they occur together, Lainhart says. “And we know that depression is worse for women in the general population. But what’s the link to autism? And is it worse for girls?”
Social anxiety affects Lainhart’s female patients into adulthood. Liz Lee, who is 43, is studying for her master’s degree in electrical engineering, yet she cannot cope with going to lunch with the other graduate students at the lab where she works. Ash Baxter, who is 22, spends hours making art, sewing dolls with wild yarn hair and macramé-edged suits; she created an extraordinary blue-and-gold octopus mask out of a three-foot gourd she found in the garage. She is talented and would like to attend art school, but Baxter can’t master her anxiety well enough to learn to drive or live in a dorm, so college art classes remain out of reach. Another patient, Charlotte (she asked that I not use her last name) is 23 and goes to a social-skills class that Lainhart runs for her patients in their late teens and early 20s. Because of the dearth of females, the class is mostly male, and Charlotte often leaves in the middle saying she’s “stressed out.” “She can only take so much,” her mother told me. Lainhart says, “You see these incredible areas of anxiety in Liz and Charlotte and Marguerite that don’t seem to have a parallel in the boys and men.”
There is preliminary evidence that girls and women also vary from the male Asperger’s profile in terms of their interests, as Catherine Lord suggests. David Skuse, a psychiatry professor at the Institute of Child Health at University College London, has analyzed data from 1,000 children, 700 of them on the autistic spectrum. “Girls with autism are rarely fascinated with numbers and rarely have stores of arcane knowledge, and this is reflected in the interests of females in the general population,” Skuse explains. “The girls are strikingly different from the boys in this respect.”
With her high aptitude for reading and writing and her difficulties with math, Caitlyn fits Skuse’s model. Even as she was failing school last year, she kept up her fan fiction, posting stories she had written on the Web site Gaia Online. On the 40-mile drive home from camp, she told me about her plan to write an original eight-book fantasy series about a werewolf, to be called “Midnight Wind.”
One of the best-known theorists on sex difference and autism, Simon Baron-Cohen, comes at these questions from another angle. A psychology professor and director of the Autism Research Centre at Cambridge University, Baron-Cohen has characterized autism as a condition of the “extreme male brain.” His research shows that in the general population men are more likely than women to score low on a test of empathy and high on a test of recognizing rules and patterns, or “systemizing.” High systemizing together with low empathy correlates with social and communication deficits and, at the extreme end of the scale, with autism. Baron-Cohen is currently studying whether elevated levels of fetal testosterone — a prime driver of masculinity — are linked to autistic traits.
Baron-Cohen says that he believes that autistic girls are strong systemizers. That quality may manifest itself in letters rather than numbers. But in his view, the thought processes for Asperger’s girls mirror those of boys. He explains, “These females often feel more compatibility with typical males simply because typical males may be more willing to adhere to the linear, step-by-step form of thinking and conversation — more like debating or playing chess or doing logic.”
To Lainhart, Baron-Cohen’s extreme-male-brain theory is an apt description for a subset of her female patients, for example Liz Lee, who in pursuing electrical engineering is training for a classic Asperger’s profession. Lee is socially aloof: she usually sits on the floor with her back to Lainhart during their sessions, twirling the propeller of a toy helicopter. Eye contact makes Lee angry, and she says she would like to live alone in the desert.
But based on their clinical experience, Lainhart and also Skuse see autism as a heterogeneous disorder. Its profile may change and expand as more is understood about girls, whose autism, they worry, often goes undiagnosed. That is partly, Skuse posits, because girls’ general aptitude for communication and their social competence helps some Asperger’s girls “pass” — they pick up on their difference and carefully mask it by mimicking other girls’ speech and manner and dress. In a sense, their femaleness allows some girls to seem less autistic. It is as if they start off with a social advantage — Skuse sees this as a 20-point bonus on a scale of 100 — that helps counter the disorder. This idea isn’t necessarily at odds with the findings that show girls to be more seriously affected by autism, Skuse says, because the girls who succeed in masking their deficit wouldn’t be included in studies. And so they are missing from the picture. “There is no doubt in my mind that the way we have defined autism currently biases our assessments strongly in the direction of identifying a male stereotype,” he says. The C.D.C. agrees and says that as a result the estimate for the number of girls with autism and normal intelligence may be low.
Why would autism express itself differently depending on sex? The short answer is that no one knows. Genetic researchers, however, have just begun to hint at possibilities. In the last two years, new data-pooling efforts have yielded two major genetic-linkage studies — attempts to link autism to specific chromosomes — that suggest that some of the genes underlying autism may be different in males and females. By isolating sex as a variable, scientists are seeing potential genetic hot spots for autism. “By comparing males and females, we will have a much better chance of discovering the causes of autism,” says Geraldine Dawson, a psychology professor and director of the University of Washington Autism Center, who was a co-author of one of the studies.
Studies that use the latest brain-scanning tools — magnetic resonance imaging and diffusion tensor imaging — generally focus on boys. But a single study of M.R.I.’s of both boys and girls found differences in their brain anatomy. Published in April in The Journal of the American Academy of Child and Adolescent Psychiatry, the study compared nine girls and 27 boys who were matched for age, I.Q. and severity of autism. Other research has established some correlation between abnormally large brain size and autism; the April paper reported that the brain volume of the autistic girls deviated from the norm more than the volume of the autistic boys. Lainhart, who is a member of the University of Utah ’s Brain Institute, has measured head circumference as a proxy for brain volume. (The two are linked.) In a 1997 paper, she reported that the mean head circumference of eight autistic girls at birth was significantly greater than the norm, whereas the mean head size of 37 autistic boys was not.
These are small and preliminary studies, but their findings may relate to a puzzle of autism: while overall, there are more mentally retarded autistic boys than girls, a greater proportion of autistic girls are retarded — 58 percent compared with 42 percent for boys, according to the C.D.C. As for Asperger’s girls, Lainhart, who continues to conduct brain research, says she hopes eventually to shed light on the deficits of girls like Caitlyn and Marguerite and suggest new treatments for them. “In children with dyslexia, scientists identified where the basic cognitive deficits were,” she says. “Then they intervened to go after those deficits, and they saw the brain change in those areas.”
In the meantime, girls with autism and normal I.Q.’s pose a particular challenge for schools. Though mainstreaming has its benefits, autistic kids risk becoming outcasts in a regular classroom. Yet if girls go to a special-education program or a separate school, they are often swimming in a sea of boys. Lord pointed to this as a factor in girls’ lack of friendships in her 1993 study. When the girls in her sample were shifted to specialized programs, “their opportunities to meet girls and women with some common interests were even more limited than those of the boys and men,” she wrote.
The Harbour School in Baltimore has tried to address this predicament. The school has 120 students, all with learning disabilities, speech impairments, attention-deficit disorders and autistic-spectrum disorders. Only 19 of them are girls, which leaves one or two in each class from first to 12th grade. (More boys than girls are also diagnosed with the hyperactive form of A.D.D. and some learning disabilities.) Along with the playful Baltimore street scenes that decorate the walls of the hallways at Harbour, the predominance of gangly male bodies and loud voices was the first thing I noticed on a recent visit. The school felt like a haven — for boys.
And so I wondered whether the girls would feel overwhelmed, as Charlotte often is at her mostly male social-skills class. In the school auditorium at about 9 a.m., there were 13 sixth graders — 12 boys and a single girl, Krissy, whose clinical designation is pervasive developmental disorder on the autistic spectrum. She was sitting on the floor playing Connect Four with one of the boys. She won her game, smiled without looking at her opponent, then got up and walked across the room to another of her classmates.
“Hi, Michael,” she said. He didn’t look up. Krissy sat down next to him and watched him play on his Game Boy. They talked quietly about his progress; she knew the game. A few minutes later, she found her Connect Four partner again, and they decided to play Operation. They talked about the rules, but when Krissy tripped the buzzer, he let her finish taking out the body parts she was maneuvering. Krissy declared victory and moved on again, this time to lie on the floor next to a boy who was building with metal rods and blue glass balls.
“Do you need help?” she asked him.
“No,” he answered.
“Can I at least play with you?” Krissy persisted. The boy grunted. Without talking more, they each built a structure.
Krissy has been at Harbour since first grade, and the small size of her class means that she knows the boys well. Her teachers say she is at ease with them because she shares their Game Boy enthusiasm and watches the same movies. But sometimes Krissy’s interests seem entirely girlish. She was excited about straightening her hair and then styling it into corkscrew curls for her interview with me and showed off pictures she had drawn of princesses, covered with hearts.
Harbour makes a concerted effort to give its girls the chance to develop relationships with one another. The girls’ lunch periods coincide to give them time together. A social worker, Kelli Remmel, runs a regular “girls club” for a group of about half a dozen. “There are some things the girls don’t want to discuss in front of their male peers,” she says. “It’s a chance for them to talk about boys, how to handle hormonal changes, other girls, their bodies, dating.”
Krissy seems to be getting the social opportunities and support that Lord and Lainhart want for the girls they treat. Salt Lake City has good schools for kids with Asperger’s, Lainhart says, but the catch is money. School districts in Maryland , Washington and Virginia pay Harbour’s tuition for more than 95 percent of the students. But districts in many parts of the country — including Utah — don’t pay for private-school placements for kids with Asperger’s. Caitlyn doesn’t go to a school like Harbour because her family can’t afford it; her experience, not Krissy’s, is typical.
Lord and Lainhart try to help by setting up social-skills groups for their patients. But families must pay for the classes out of pocket because medical insurers generally don’t pay for treatment and services that focus on autism — a terrible problem for her patients, Lainhart says. So the groups tend to meet only a couple of times a month for a few hours. Charlotte doesn’t know the boys in her group the way Krissy knows her classmates. At the University of Michigan , Lord runs co-ed groups for younger children and then tries to put together groups of older girls that mix autistic and nonautistic kids. As the girls get older, it is harder to find normally developing girls who want to participate. Twenty years ago, as a clinical psychologist in Canada , Lord started a group of four Asperger’s girls who stayed in touch into adulthood. They called themselves the highest-functioning autistic women in Canada , she remembers, and treasured their solidarity. “It’s striking how much girls with autism can care about each other and other people and develop friendships that are really a source of joy for them,” Lord says. “But when I think of the teenage girls I know, many of them have no shot at forming those relationships.”
At the Hawks Camp in Utah , Caitlyn and Marguerite didn’t become friends. A week earlier, Marguerite and Lainhart had made a list of conversation starters, but Marguerite didn’t really use them. Caitlyn didn’t try to talk to her much, either. The camp lasted only a week; for these girls, not long enough for bonding. Still, Caitlyn said it was the best week of her year. One day after lunch, the Hawks campers drove in two minivans to a nearby lakefront to go tubing and Jet Skiing. Caitlyn changed into her bathing suit, then wrapped herself in a towel despite the strong hot sun. “Do I look O.K.?” she asked a counselor. “It’s just that there are so many people.”
But the other kids were paying Caitlyn no mind. This wasn’t a group that Caitlyn had to fear. She balled her hands into fists, visibly holding her anxiety at bay. “Sometimes I feel like I’m weird and ugly,” she said, “but I’m not going to today. I’m confident!” She strode out to Jet Ski and later returned with a description that she planned to use in a future story: “It was like riding a dragon through the storm.”
Back at camp, the Hawks poured onto the playground. During the school year, Caitlyn had been excused from gym class because she was so nervous about changing her clothes and running around in front of her classmates. As she sat on a swing and watched kids play tag, a counselor named Claire came over. As she and Caitlyn talked, Caitlyn did all the tiny things that people do to engage one another, smiling, laughing, gesturing, looking Claire in the eye. Claire urged her to join the game and called out, “Caitlyn’s playing!” Caitlyn protested. But Claire persisted, and finally Caitlyn yelled, “O.K., where’s the base?” A teenage boy pointed to the monkey bars, and Caitlyn ran for it. Her glasses slipped off her nose, and her shorts slipped a bit, too. She hiked them up and kept running, surrounded by other kids. Sweating and laughing, she yelled, “Safe!”
Emily Bazelon is an editor of the online publication Slate. Her last article for the magazine was about the grass-roots pro-life movement.

ION Kids
A way to keep your EYE on your KIDS

Trish K ordered a kit and will keep you posted on how she likes it

http://www.ion-kids.com/


kptv.com

Family Claims Airline Put Autistic Son In Harm's Way
POSTED: 8:28 am PDT August 7, 2007
UPDATED: 8:38 am PDT August 7, 2007

The parents of a 22-year-old man claimed their son was kicked off a non-stop Southwest Airlines flight to Chicago because he has autism.
Nick Andrews said he was removed from a non-stop Southwest Airlines flight from Portland to Chicago after explaining the mechanics of jet planes to nearby passengers.
“Just told me, ‘Sir, we’re going to need you to step off the plane,’” said Andrews. “I think they may have been scared of me.”
Because of Andrews’ autism, he fixates on things such as airplanes and loves to talk about them.
“I focus on lots of things like carpet cleaners, power engines and jetliners,” Andrews said.
The family claimed that after they put Andrews on the plane to Chicago and made sure he was safe, employees removed him and placed him on connecting flights from Portland to Oakland to Ontario to Phoenix, and finally to Chicago.
A flight that was supposed to take a few hours took 12.
“We had no idea for several hours where he was. He could’ve ended up anywhere in America,” said Andrews’ dad, Dixon.
Southwest Airlines issued a statement, saying, “We deeply regret the inconvenience Nicholas suffered. It appears our flight attendants and employees working at the departure gate were unaware that Nicholas has autism. Without knowing the reason for Nicholas' behavior, our employees had no choice except to make the best decision possible with the information available.”
The family said they are asking for a formal apology from the airlines.

http://www.kptv.com/news/13838990/detail.html


From a Listmate

Web is new battleground for fall provincial vote
Aug 06, 2007 04:30 AM
Ian Urquhart
This fall's provincial election will be fought not only the old-fashioned way – over the airwaves and on the ground; effectively for the first time in Ontario, the battle will also take place on the Internet.
All the parties have websites and are putting increasing emphasis on them. And there is a plethora of interest groups with websites, ranging from property taxpayers to parents of autistic children, as well as individual bloggers and postings on YouTube and Facebook. Combined, they are reaching hundreds of thousands of voters.
Credit – or blame – Joe Trippi. He's the guy who managed Howard Dean's presidential campaign in 2003-04 and used the Internet to take his candidate from also-ran status to frontrunner within a matter of months.
Trippi was in town last week to give advice to the provincial Green party, among others.
The Internet provides "a big opportunity" for non-establishment parties like the Greens, said Trippi in an interview. For example, they can take advantage of YouTube as a substitute for television ads, which are out of their financial reach.
"You can put a really powerful video on YouTube and hundreds of thousands of Canadians can watch it, (but) it doesn't cost you a penny," said Trippi.
"The same tool set exists for the Conservatives and Liberals, but they have money to do it another way, so they're not as adept at levering these new tools."
Maybe so, but Liberal and Conservative operatives have read Trippi's book (The Revolution Will Not Be Televised) and are applying some of his principles to their own Internet campaigns.
In the book, Trippi refers to the power of "concentric circles," or "the idea that you could spread a candidate or a cause or any issue like a virus – starting with a small, key group of people and letting them run wild for you."
Accordingly, the Dean website became interactive, with links to other sites, like meetup.com, and interest in the candidate started to snowball.
"The Internet was like concentric circles on steroids," writes Trippi.
Both the Conservatives and Liberals have adopted some of Trippi's thinking in their websites.
The Conservative site – www.leadershipmatters.ca – includes a blog by party leader John Tory and an invitation to visitors to offer their own commentary. Even negative comments are posted.
"You can't get people engaged if you're not prepared to allow for political discourse," explains a party spokesperson.
The Liberal site (www.dalton.ca) is full of YouTube-style videos in which Premier Dalton McGuinty talks about himself and frankly addresses his broken promises.
In launching the site, the Liberals reached out to about 20 bloggers to encourage them to provide links to dalton.ca. It seems to have worked, as the Liberals claim more than 30,000 people have visited the site since it was launched a month ago.
The New Democrats also plan to launch an edgy new website shortly. It will likely include a blog by their leader, Howard Hampton.
But all this effort may pale in comparison to what the Americans call a "macaca moment" – where an amateur video capturing a candidate in an unguarded moment is posted on YouTube and effectively destroys the campaign.
This is a reference to George Allen, a Republican senator whose re-election campaign was torpedoed last year by a YouTube video showing him calling somebody a "macaca."
"That moment is going to happen here," said Trippi last week. "It's just a matter of time."
McGuinty, Tory and Hampton can only hope it's after the Oct. 10 vote.

From a Listmate

Holy Name community raised plenty to fight autism in spring
By Bill Rea

The community of Holy Name Catholic School in King City spent a week in the spring raising funds in their Toonies for Autism drive.
And the amount raised was well in excess of the $1,800 mark
The effort was spearheaded by two education assistants at the school, Kim Parcells and Kristy McCague.
McCague said this was the second year the school has run such a campaign, and Parcells was quick to add things have gone a lot better this time. They raised about $850 last year.
The events started on the Monday with the showing of a video from the Autism Society of Ontario. The Tuesday saw the sale of hot dogs at the school, and the Wednesday it was ice cream sandwiches. All those food items were donated from the community, they added. the Thursday saw showing of a couple of movies, with students buying tickets and popcorn. They saw Flushed Away and Pursuit of Happiness. The Friday featured a silent auction for staff, while students bought pieces of a jigsaw puzzle (the symbol for autism) in lieu of raffle tickets for a host of donated prizes that were available.
Principal Beverley Coles said there was "tremendous outpouring from the community in terms of donating."
"It really brought us together as a community," she added.
McCague said the effort was inspired by the fact there are several autistic children in the school community.
"It's near and dear to our hearts," Parcells added.


Coming to Kitchener Ontario (near Niagra Falls) Sept 29

For parents, care givers, educators and practitioners

Presented by Great Plains Laboratory

A comprehensive bimedical treatment approach for Autism, PDD, and behavior disorders.

Read about the very wonderful speakers and take advantage of the Earlybird Registration Special at:

http://autismtoday.com/kitchener.html

Remaining seats are going fast.

Autism Today

1425 Broadway
#444
Seattle, WA
98122
US




And Finally
Shared by a listmate, a book dedicated to her (the listmates) two boys on the spectrum....
. “I have committed all the money collected from the sale of my book Missing Pieces to the Autism Spectrum Disorders Society of Ontario,” she added.
Book helps survivor process memories
By CYNTHIA GASNER, Special to The CJN
Thursday, 09 August 2007
Many children who survived the Holocaust have never had the opportunity to piece together the fragments of their horrific memories.
Their loved ones tried to shelter them, feeling that children were too young to understand what they experienced. As a result, they carried with them painful, unanswered questions.
“When I was seven years old, my world came tumbling down, and throughout my life, the smallest thing triggers my anxiety and depression and leaves me helpless and paralyzed with fear,” said 71-year-old, Hungarian-born Olga Verrall.
Her 244-page book, Missing Pieces: My Life as a Child Survivor of the Holocaust, was published recently by the University of Calgary Press’ Legacies Shared series.
Her suppressed memories of the loss of her home, the loss of her most loved possession, the loss of her confidence that her parents could protect her, the vicious rape of her mother by a high-ranking SS officer, the suicide of her Jewish friend’s family, and her transfer of fear from the Nazis to the Communists, all deeply affected her life in Canada.
Despite the love that she found in this country, the ghosts of Verrall’s childhood manifested themselves in bouts of psychiatric depression and hospitalization.
Missing Pieces is her search for validation. She describes the pain she experienced here, as well as her courage to try to understand the source of her emptiness juxtaposed with feelings of joy and optimism.
Verrall was born in 1936 in the small town of Szarvas, the fourth child after three boys, to Laszlo and Mariska Berger. Her father was a successful grain merchant, and her early years were idyllic and free of anti-Semitism.
“In 1944, we heard from people who escaped the Nazis what was happening, but for some time, my parents, grandparents and others could not believe it was happening,” she said.
The day the Nazis came to remove the Bergers from their home was a pivotal experience in Verrall’s life, and it shook her so badly that it still haunts her to this day, she said.
“I remember clearly that the German soldiers were waiting for us at the gate of our house. We could take only one possession, and I was carrying my doll Pani, who was always with me. I believe that my mother told me to go back to the house to get a jacket, as it was getting cold and I wanted to get something to cover my Pani,” Verrall said.
“I placed Pani on a table at the gate and when I returned, Pani was gone and the soldiers were laughing. I broke down crying and screaming and said I wanted to die. At the age of eight, it was a most significant loss which affected my entire life.”
Her family was taken to a ghetto in the spring of 1944. They were interned in the Auspitz labour camp.
“Our lives were saved when an acquaintance of my grandfather whispered into his ear that if the Germans asked if anyone had any skills, he should raise his hand,” Verrall said. “My grandfather obeyed this man’s instructions and subsequently, this definitely prolonged the lives of my family.”
Her grandfather later died of starvation.
After they were liberated on April 13, 1945, the Berger family returned to Szarvas and later moved to Budapest. Under Communist rule, the family changed its name to Barsony to deflect attention from the fact they were Jews. She describes this part of her life as another time of persecution.
In 1957, she immigrated to Winnipeg, where other members of her family had already settled. Soon after, she met and married Orland Verrall, the cantor at Rosh Pina Synagogue. She said it was love at first sight.
Being the wife of a clergyman, the birth of their two daughters, Judy and Lesley, and an active communal life brought some contentment and security, but deep inside, insecurity and emptiness would erupt from time to time.
When her husband retired from the synagogue, the Verralls moved to Toronto. In 1992, her husband died and Olga again faced emotional trauma and felt a need to search for meaning and an understanding of her troubled childhood.
She took courses, organized a widows’ and widowers’ group at Beth Tzedec Congregation, and began doing volunteer work at Baycrest that she has continued.
Her search for understanding took her back to Hungary three times. On her third visit, she decided to begin documenting her childhood memories and their effect on her life.
For six years, Verrall painstakingly wrote the book by hand, chapter by chapter, as she looked for the missing pieces of her childhood.
She told The CJN that her early years have given her a deep sensitivity for children who suffer. “I have committed all the money collected from the sale of my book Missing Pieces to the Autism Spectrum Disorders Society of Ontario,” she added.
From the smile on her face, it’s hard to believe that Verrall lived a life of anguish.
“My life purpose is to smile. It makes people smile back. And I have learned that life is the greatest miracle.”

End of Mailing for August 9th, 2007