Monte Python’s Cheese Shop: Canadian Edition

It’s another day, with another story published about Canadian children with autism being denied therapy for their condition. In the land of a vaunted health-care system which is held up as the defining characteristic of Canadian nationhood, in the largest, most prosperous province of Ontario, children with autism are:
• excluded from the health care system and
• can wait on a social services waiting list for early intervention services for four to six years!

No, that’s not a typo.

When a child is fortunate enough to be diagnosed early at two years of age, which is almost a miracle in itself in a thoroughly dysfunctional system, the government offers the child easy access to a waiting list for treatment, with full knowledge that the child will age out before his turn comes up. We all know it is critical to start at two years of age when the child’s development window is great, but apparently that is does not keep Ontario bureaucrats up at night.

Monty Python’s parody on the dysfunctional British society of the 1970s could have been written for children with autism in Canada. Unfortunately, children with autism need quality therapy, and they need it when they are diagnosed!

When the fox guards the chicken coop: A review of the film "Medicare's Orphans"

Now that the new documentary film about Canada’s abject failure in autism health care has been released, I’d like to share some thoughts about the precedent setting film in the world of autism advocacy: Medicare’s Orphans.

Many films about autism understandably focus in on the miserable lives of children with autism. This can sometimes be hard to watch.
Medicare’s Orphans is not that kind of film.

The documentary chronicles the protracted battle to include children with autism in the Canadian health care system. It’s a strange juxtaposition to watch since in the United States, the debate lately has been about creating a health care system where everyone is covered. In contrast, Canada already has a supposed
universal health care system, yet this is a story about the systematic exclusion of the one group that is shut out of health care -- children afflicted with autism.

How strange! There is a group of Canadians who don’t get health care coverage for their core health need -- autism! I guess that’s what happens when the fox guards the chicken coop, when the health care system and the government are one in the same. When government is the health insurance provider, it apparently does a lousy job of holding itself to account where a lack of autism treatment coverage is concerned.

The film describes the amazing lengths to which Canadian parents have gone to right this wrong. It shows the important successes in the courts, and the failure of the legal system at the highest level -- the Supreme Court of Canada. The filmmakers take us on a journey from coast to coast, meeting courageous parents and their children with autism. We are introduced to one parent who actually walked 286 miles in the harsh Canadian winter to Ottawa to plead his case and raise awareness of this horrendous injustice.

We are heartened by the successes of children who were fortunate enough to receive treatment because, in some cases, their parents forfeited everything to fund the treatment. In one case, we meet a woman who has rented out every room in her home to pay for autism treatment. We are also angered and disgusted by the complete failure of the Canadian health care system, which lands one child in the psychiatric unit of an Ontario hospital.

Through all this, the message is clear. The film acts as a call to action!

Those who live in the United States need to wake up every morning and appreciate the fact that in the U.S., children with autism enjoy the protection of the
Americans with Disability Act, the Individuals with Disability Education Act, the Mental Health Parity Act and the States’ Autism Mandates that are being passed daily, the most recent one in the State of New York, marking the 29th state that now legally requires insurance companies to cover the cost of effective autism treatment.

Let’s hope that
Medicare’s Orphans will so thoroughly embarrass the Canadian government that it finally does something about its hypocrisy. Canada claims to be a light unto nations where universal health coverage is concerned, yet it does precisely the opposite by excluding a whole class of its citizens from healthcare - kids with autism.

Visit their website to learn more about the
Medicare for Autism Now! movement.

Hypocrisy, thy name is Canada

"The war that our own government is waging against our children is not over..."

Jean Lewis,
“Medicare’s Orphans”

have previously discussed the important Canadian documentary film produced by the autism treatment advocacy organization, Medicare For Autism Now! In the most recent trailer released, Jean Lewis and David Marley, co-founders of Medicare for Autism Now!, discuss the long-running autism wars in British Columbia; they lay Canada bare. Read more...

Persons with Disabilities Need Good Laws, Not Good Intentions

From time to time, news reports are full of horrible stories regarding the mistreatment of people with autism. Unfortunately, news from Canada suggests the abuse seems to be more entrenched than previously thought, as the blog Facing Autism in New Brunswick lays out. From the prairie province of Alberta to the maritime province of New Brunswick, in Canada, abuse is indeed evident from sea to shining sea. Read more...