Articles from a month ago, Taline's email

York Region News Group

Better stop stalling, start helping autistic children

Letters to the Editor
Mar 16, 2008
Re: Autistic kids deserve better treatment, editorial, Feb. 21.

An important factor for children with autism is early diagnosis.

Services are required for prompt diagnosis and referral.

Resources must be sufficient and accessible to all families. Time is critical for these children.

A growing body of literature suggests early and intensive intervention may greatly enhance outcomes for children with autism.

Evidence-based research shows early specialized and appropriate intervention can help these children thrive in their families and our community.

We need our government to work in partnership with families to enable children with autism to reach their full potential.

We need to stop wasting time and instead invest in these children now.

Pat DiVecchia
Richmond Hill

-------------------------------------------------------------------------------------------------------


York Region News Group

Let's give help to those who need it most

Letters to the Editor
Mar 16, 2008
Re: Autistic kids deserve better treatment, editorial, Feb. 21.

I agree with your editorial on the subject of the Dalton McGuinty government’s poor treatment of children with autism and their families.

On Feb. 11, I attended proceedings at the Ontario Court of Appeal, where a three-judge panel was asked to decide if a class-action lawsuit could go ahead on behalf of autistic children seeking treatment within the Ontario public school system.

I was there to show my strong support for these parents whose own Liberal MPP had refused to attend.

This government’s continued discrimination against children with autism is a deplorable breach of trust. Children with other special needs receive education and therapy within the public school system, whereas autistic children in need of intensive behavioural intervention (IBI) and applied behaviour analysis (ABA) therapies are forced to seek treatment elsewhere.

Only two children in the entire province receive IBI therapy while attending school full-time.

Ontario is the only North American jurisdiction that does not deliver IBI treatment within the public education system.

A March 2007 memorandum written by the deputy minister of education stated the focus of a policy memorandum on autism spectrum disorders would be the use of ABA teaching practices and not IBI.

By not permitting IBI treatment within schools, the McGuinty government is forcing the parents of autistic children to choose between education and therapy.

Just like any other child in Ontario, autistic children are entitled to an education and do not deserve to be treated as second-class citizens.

We need a comprehensive educational strategy that addresses the unique needs of all Ontario children, including those with autism.

What we don’t need is a government that chooses political expediency over even-handed assistance to all Ontarians, notably to those needing it most and least able to stand up for themselves.

Peter Shurman
MPP, Thornhill


----------------------------------------------------------------------------------------------


Our lawyer for the lawsuit, David Baker, represented the Justin Clark case mentioned in this article 25 years ago. There's a quote from David in the article and also a couple of blurbs about autism.


Star

Disabled leave the shadows and their mark

After 25 years of activism, the emphasis is finally on ability – not disability
Mar 15, 2008
Helen Henderson
Living Reporter


Justin Hines has had two songs on the charts from his debut album, a career poised to explode and a message to the world: Follow your passion.

He is the future of a culture emerging from the shadow, a generation of young people who transcend wheelchairs and labels. In the 25 years he has been on this planet, the pace of change has gone from eons to nanoseconds. For those who move or communicate or process information differently from the majority, progress takes many forms.

The spectrum of disability today stretches all the way from a mother accused of giving into frustration and drowning her 4-year-old autistic daughter to Ontario's latest lieutenant-governor, a man who has brought leg braces and an electric scooter into the chambers of power.

Twenty-five years ago, another young guy named Justin had to take on his parents in court to get permission to leave the institution he had lived in since age 2. Justin Clark used a wheelchair and did not communicate verbally. When he won the right to make his own decisions and moved into a house in Ottawa with three other people at age 20, he made history.

Where is the disability community today and where is it going? Hines' story could be the face of the future.

Justin Hines' mother started singing to him when it looked as if he wasn't going to make it in the first fragile years of his life.

Until he was 5, he and his mom, Carol, lived at what is now Bloorview Kids Rehab while his father and grandmother looked after his brother at their home in Unionville.

Through surgery after surgery to fuse bones that would otherwise repeatedly dislocate, "Justin never lost his smile," his mother says. Nor did he lose the music.

At age 6, enrolled in a mainstream school, Hines started singing lessons, partly to help with persistent breathing problems, partly because he says his grandmother believed in his voice.

"I was very nurtured," he says.

Eight years later, he won a contest to do the national anthem at a Raptors' game. Then Wal-Mart picked his haunting song "Wish You Well" to advertise its Walk for Miracles on television and his voice captivated viewers. His first album, Sides, came out last year.

Through high school, he says, it was his music career, as much as his disability, that made him feel different. These days, with music evocative of the best of the folk era ballads, he says: "My vision is to connect with as many people as possible."

Twenty-five years ago, a young musician in a wheelchair might have been little more than a curiosity, a performer barred from many venues by a shortage of ramps and an oversupply of closed minds. Today, Hines has toured from London to Dubai with no problem. Check it out at www.justinhines.com/downloads.php.

Of his record label, Orange, part of Universal Music Studios, he says: "They have been great: they haven't tried to exploit the disability or hide it."

Hines speaks to the world through the music he makes but many others with disabilities are communicating equally strong messages.

FINDING A VOICE

As more people with disabilities make their case, their message is being heard, advocates say.

"The rank and file and their families are speaking out – which is every disability advocate's dream and every government's nightmare," says legal activist David Lepofsky.

"Self advocacy means the individual voice is gaining credibility and power," adds Keith Powell, executive director of Community Living Ontario.

"We have a voice at the policy table," says Catherine Frazee, co- director of Ryerson University's school of disability studies. "It hasn't yet achieved results but we have a place of belonging and respect, a recognition of citizenship."

Public sympathy for Robert Latimer, who killed his 12-year-old daughter Tracy, who had cerebral palsy, "was a very profound wake-up call, bringing the disability community together," says Frazee.

Still, many advances in disability rights have not translated into practical changes. A decade ago, the Supreme Court ruled that hospitals across the country should provide free sign language interpretation for anyone who is deaf.

"It was a big court breakthrough but the impact has been weak because governments have never lived up to their obligations," says Lepofsky.

"In Europe and the U.S., they look at some of our wins in court as state of the art but in terms of actual access, we are still the pits," says David Baker, the lawyer who acted for Justin Clark.

Baker has continued to be a central player in some of the most significant disability rights cases, including a Supreme Court decision last year ordering VIA Rail to make its passenger trains wheelchair accessible.

POVERTY'S TOLL

Adults with disabilities who cannot find jobs must exist on support payments that top out at just over $900 a month. Most get much less.

Families caring for a child with a disability too often pay dearly, advocates note.

Most rely on one income because one parent becomes the full-time caregiver. They also face extra expenses for disability-related goods and services not covered by governments.

"Living on the Ontario Disability Support Program means living below the poverty level and poverty is a huge barrier," says Powell.

"The problems of poverty are becoming more and more entrenched," adds Frazee.

"Support is profoundly inadequate. We need a radical rethinking of social policy."

As Marie White, chair of the Council of Canadians with Disabilities, puts it: "Social policy is homeless in this government."

GAINING ALLIES

Bit by bit, the message is getting out.

"Our issues have gone mainstream," says Lepofsky. "Queen's Park politicians have started thinking of voters with disabilities. The fact that disability issues really have to be included in policy strategy proves that."

"There's a sea change in acknowledging disabilities," says Melanie Panitch, director of Ryerson's school of disability studies. "We're seeing activism through broad-based groups and coalitions looking at poverty."

Globally, last year's United Nations agreement on the rights and dignities of people with disabilities is "very significant" in adding weight to the movement," she adds.

STILL A LONG WAY TO GO

"We're stalled for lack of federal leadership," says Marcia Rioux, head of York University's school of critical disability studies, currently spending some time in Australia as a "Distinguished Fellow" at LaTrobe University in Melbourne.

Australia, by contrast, "is back on board," she says. "During the good times, when the economy was strong, we should have got further. There's no trickle-down for people with disabilities."

HOW TO GET THERE

"Attitudes will change only when people are seen out in the community," says motivational speaker Judith Snow, another leader in the move out of institutions.

"It took 12 years of fighting. "I was physically and emotionally dying in a nursing home," says Snow, who put together a "circle of friends" to help look out for her welfare.

Today, she laments moves to place young people in nursing homes where enough community support isn't available. As Lepofsky says: "Twenty-five years ago, we said, `The biggest problem is attitudes. We need to educate the public.'

"But once people raised awareness, they didn't know where to put it. Attitudes don't change behaviour. Behaviour changes attitudes. That's why you have to make people do things."

MILESTONES IN A QUARTER-CENTURY OF ACTIVISM

Twenty-five years in the disability movement – here are just a few of the many markers along the way:

* 1983: Justin Clark, 20, who has cerebral palsy, moves from the institution in which he has lived for 18 years to a house in Ottawa. The groundwork for the was laid the year before, after disability rights were included in the Constitution, when Clark won an important court battle allowing him to make his own decisions.

* 1985: Rick Hansen embarks on his epic Man In Motion 40,000-kilometre journey around the world, changing the way Canadians look at people in wheelchairs.

* 1987: Ontario promises to develop community living supports, saying it plans to close all large institutions for people with developmental disabilities in 25 years. (Twenty years later, with community resources still lacking, relatively young adults find themselves moved not to the community but to other institutions, such as nursing homes.)

* 1990: Gary Malkowsk becomes the first deaf person to address the Ontario Legislature as an elected MPP.

* 1993: At age 12, Tracy Latimer, who has cerebral palsy, is killed by her father. After a number of trials and appeals, Robert Latimer is convicted of murder. He begins his sentence in 2001 and is granted day parole in 2008.

* February 1994: Toronto's Metro Hall becomes home to the Terry Fox Hall of Fame, honouring people with physical disabilities who have made a difference.

* September 1994: Ontario premier Bob Rae's government passes employment equity legislation, fulfilling a prominent plank in the platform that catapulted his New Democratic Party to a surprise victory in the 1990 election.

* 1995: The Conservative government of premier Mike Harris repeals the Employment Equity Act.

* 1997: The Supreme Court Of Canada rules that all hospitals must provide free sign language interpretation services to deaf patients.

* 2001: The Ontario Human Rights Commission orders Famous Players to make three landmark theatres in Toronto wheelchair accessible. The ruling finds the lack of full access violates the rights of the complainants, including Toronto Star reporter Barbara Turnbull.

* 2003: 29 Ontario families launch a $100 million lawsuit against the province because their autistic children are being denied costly intensive behaviour therapy after age 6.

* June 2004: Winnipeg Conservative Steven Fletcher becomes the first quadriplegic to win a seat in the House of Commons.

* April 2005: The Ontario Superior Court rules the province violated the rights of children with autism by denying them intensive behaviour therapy on the basis of age. The province appeals the decision and wins in 2006.

* May 2005: The Ontario Court of Appeal strikes down part of a law that allows employers to deny severance packages to disabled workers who can no longer continue in their jobs. The court says the legislation violates the Charter rights of people with disabilities.

* June 2005: After a decade-long battle by blind lawyer David Lepofsky, the Ontario Human Rights Tribunal rules the TTC must order drivers to call out all stops on streetcars and buses. (It will be another two years before Lepofsky wins the same for subway stops.)

* June 2005: Queen's Park passes legislation ordering equal access for people with disabilities and promising tougher standards to make Ontario barrier-free in 20 years.

* November 2005: Sam Sullivan, a quadriplegic after a skiing accident, is elected mayor of Vancouver. (The next year he will capture world attention in Turin when he takes the flag for Vancouver's 2010 Olympics for a spin in his wheelchair.)

* November 2006: A proposed $700 million class-action lawsuit on behalf of thousands of families with severely disabled children collapses when a court rules Ontario has no legal duty to provide special funding for their treatment. The families allege they are forced to hand their children over to Children's Aid Societies to get the care and treatment they need.

* November 2006: More than 300 people from disability groups across the country gather on Parliament Hill to discuss a national action plan for building an inclusive and accessible Canada. The EndExclusion movement is born.

* December 2006: The provincial government uses closure to pass a bill that overhauls the Ontario Human Rights Commission. Starting in July 2008, those with human rights complaints must go directly to an adjudication tribunal rather than first taking their complaint to the commission to investigate.

* December 2006: Canada is among countries signing a landmark United Nations agreement protecting the rights of people with disabilities. It is expected to take effect this year.

* March 2007: The federal budget introduces a registered disability savings plan to help families plan for the future of children with disabilities.

* March 2007: After an epic seven-year battle, the Supreme Court orders VIA Rail to make passenger cars wheelchair accessible, underscoring the Charter rights of people with disabilities to barrier-free transportation.

* August 2007: Ontario pledges $12 million to provide special treatment and support for autistic children and their families.

* September 2007: David Onley, a former Citytv journalist, who had polio as a child and uses an electric scooter, becomes Lieutenant- Governor of Ontario.

* January 2008: The Canadian Transportation Agency rules that Canadians with severe disabilities who need to travel with a caregiver or require more than one seat on a plane will no longer face the charge of an extra fare from domestic airlines.

- With files from the Star library
-----------------------------------------------------------------------------------------------


York Region News Group

Treatment of autistic children shameful

Letters to the Editor
Mar 02, 2008
Re: Autistic kids deserve better treatment, editorial, Feb. 21.

I applaud the author of this article.

Children with autism deserve the same education and medical treatment as any other child; with or without special needs.

How dare the government put stipulations on the needs and welfare of these young children, shame on them.

Children with autism and their families deal with stresses and burdens just as other children and families with other special needs, so why wouldn’t the government treat them the same?

Who are they to say one child is entitled to public education and treatment and the other is not?

I agree that helping children with autism now, when they are young, will better their lives and in turn, will better our society in the future. What the government is doing is totally unacceptable.

Again and again, they are failing our young children who represent our future. It is time for a change. Wake up, Ontario, and join Alberta and British Columbia in covering the costs for these autistic children.

Rose Granato
Thornhill

--------------------------------------------------------------------------------------------


Mississauge News

By: Sharon Anderson

February 26, 2008

Dear Editor:
As the mother of a 15-year-old daughter with autism, I agree it's unfair children cannot have their therapists accompany them to school.
Through my Masters program in Disabiity Studies at York University, I have learned accommodations are allowed for every other disability.
For example, brain-injured students can have note-takers and extra time for tests, and ramps are provided for those in wheelchairs.
My daughter attended a special needs class at Ashgrove for Grade 3, and I know there are good teachers there. However, they are not trained in autism and behavior therapy, and one would think the board would welcome any help they could get.
I recently completed the course work in the graduate program in Autism and Behavioral Science and was told behavior therapists were in demand and would be quickly hired. However, school boards don't seem willing to spend their money to hire therapists to work with these children.
Let's hope the government earmarks some of the money they are promising to hire behavior therapists for autistic students.