Sunday, October 07, 2007

Ontario Election Autism Poll

The "official" Facing Autism in New Brunswick" Ontario Election 2007 autism poll is now closed. The final results:

Who Should Ontario Autism Parents Trust On Autism Issues?



Dalton McGuinty, Liberal 11 (22%)
Howard Hampton, NDP 17 (34%)
John Tory, Conservative 18 (36%)
Frank de Jong, Green 4 (8%)

Assuming votes were cast sincerely, (obviously a big assumption), I am not sure why any one voted for the Green Party leader on Autism Issues. To my knowledge the Green Party took no position on autism issues.

Saturday, October 06, 2007

Autism Biting

Those that glorify autism, that try to deny that autism is a disorder, never mention some of the more serious even dangerous behavioral problems that can occur with autism. There is probably no single behavior that is any more serious and dangerous than biting; self biting and biting others. My son Conor is profoundly autistic. When frustrated, or overwhelmed, he will sometimes bite himself. There are times when he bites others. I have been bitten while holding Conor to get his hair cut. I do not blame him for that behavior but as his father I have to try and teach him not to bite. Conor's biting has subsided considerably but not completely.

In Lab Worker Charged With Biting Boy Arrested Yahoo News reports the story of a former hospital lab technician, Anne McGlorthon, 53, who is charged with biting an autistic boy while holding him as a colleague drew blood from his arm. The lab tech stated that the boy had bitten her first and that she bit him to get him to release the bite on her arm. The boy was left with bite marks on his shoulder and had to take anti-biotics. I do not defend the lab tech, who lost her job as a result of the incident and who now faces criminal charges but her story is not unfamiliar to many parents with severely autistic children - except for the return bite.

Such incidents are part of the realities facing many families with children with Autism Disorder. Such incidents are part of the reason I get nauseous when I read ridiculous Neurodiversity accounts of autism as being nothing more than a trait or personality type.

The CIHR's Autism Agenda - What Is It?

Amongst the many criticisms of the CIHR' s secretive National Autism Symposium is the fact that there is still, one month before the chosen ones gather behind closed doors at the Toronto Airport, no publicly available agenda, no list of speakers, and no list of names of the chosen ones.

In this exercise in "community building above all" who will be representing the autism community in New Brunswick? What questions will they be asking on behalf of my 11 1/2 year old profoundly autistic son? What subjects will they be discussing which might affect my son's future?

The speakers must have been confirmed for weeks now and the subjects on which they will be speaking at this Star Chamber proceeding must be known to Ms Beckett, Mr. Quiron and Mr Harper. Why not at least tell potential members of this community that you plan to build what the CIHR, and your hand picked "community" representatives, will be discussing on our behalf?

Public invited to attend international autism conference

No, the title of this comment is not a reference to the Harper government/CIHR National Autism Symposium scheduled for November in Toronto. Harper and the CIHR have shamed themselves in bypassing provincial Autism Societies and FEAT organizations and handpicking "community" representatives to attend what is billed as "above all" an exercise in community building. In the US, by contrast, those staging conferences actually seek real public input.

In Public invited to attend international autism conference the Hometown News reports on the 2 day conference scheduled for October 18 and 19 at the Florida Institute of Technology and the Holy Trinity Episcopal Academy. The conference is desribed by Mary Beth Kenkle, dean and professor at Florida Tech's college of psychology and liberal arts as part of an mission to be a resource to the community. Professor Kenkle had some interesting observations about Applied Behavior Analysis:

"applied behavior analysts have made headway in techniques to treat children with the developmental disorder, ... There are a lot of treatments for autism out there that don't have empirical support, ... We will be using applied behavior analysis-one of the treatments shown to be most effective."


Autistic Adults Lack Vital Services

When people think of adults with autism they tend to think of Dustin Hoffman's role in "Rain Man", or real people like Temple Grandin Ph. D. one of the most accomplished autistic adults in the world. Others might think of anti-ABA crusader Michelle Dawson who has appeared before the Supreme Court of Canada and the Canadian Standing Senate Committee on Social Affairs, Science and Technology as part of her ongoing campaign to prevent Canadian governments from funding Applied Behavior Analysis interventions for autistic children. Here in New Brunswick many people would think of Jason Oldford who has long been involved in efforts to help autistic children and adults in New Brunswick. Mr Oldford also appeared before the Canadian Senate Committee and offered a positive voice in support of efforts to assist autistic children with ABA intervention.

When thinking of autistic adults most people will not think of the 50 year old autistic woman who can not speak or convey emotions or pain and who was repeatedly battered and beaten by employees at the PLUS Group Home Inc. residential care facility in Long Island. This sad case is not an isolated event. In Reopen the institutions? Advocates Reverse Stand as "Community" Tragedy Unfolds (1997) Bernard Rimland exposed the horrors that resulted from closing down institutions that provided residential care and treatment for autistic adults and other persons with developmental and mental impairments. Rimland cited the 1993 report by US Congressman Ron Wyden which noted that:

"the private sector residential facilities for the mentally retarded have become an $11 billion-a-year business.. Millions of Americans with these life-long handicaps are at risk for poor quality care, questionable and even criminal management practices by service providers, and lackluster monitoring by public health and welfare agencies."


Rimland cited a disturbing pattern of abuse, neglect, and mismanagement and some terrifying statistics:

"A disturbing pattern of abuse, neglect, and fiscal mismanagement has emerged:

  • "Employees at small community based facilities are often under-trained, poorly paid, and inadequately screened. As one New York State official put it: 'some consumers leave institutional programs where staff have received 100 hours of training, and move to homes where staff do not even know first aid.'

  • "Former employees of one facility reported that prescribed medications for residents are routinely discarded."

  • Dr. Cindy Ochs, of Livonia, Michigan, who cares for mentally retarded residents at about forty metro Detroit homes, stated, "They're hiring people off the street for five or six dollars an hour to care for patients who have complicated seizure disorders, feeding tubes, all kinds of problems."

Under these conditions, it should surprise no one that death rates have risen to horrifying proportions. As we recently reported (ARRI 10/4, 1996), a study by David Strauss and Theodore Kastner, based on 18,000 adults who were "clients" of the Department of Developmental Services in California from 1980 to 1992, found the death rate to be 72% higher in group homes than in asylums. A more recent study of nearly 1,900 California patients transferred to group homes from asylums in 1993-1994 showed an 82% higher death rate in group homes. In both studies, the "institution" and "community" patients had been carefully matched on all known risk factors.

Death can come quickly to those removed from institutions. Ten patients died after being discharged from the Porterville Developmental Center into group homes. "Most were middle-age and had lived much of their lives in state centers," the San Francisco Chronicle reported on February 25, 1997. "Their average life span after leaving Porterville: just 62 days."

As Strauss points out, "deaths are but the tip of the iceberg. Where there's an excessive number of deaths, there's an excess of other types of medical problems. for every death, there are many emergency hospitalizations." And, obviously, for every emergency hospitalization, there are a multitude of untold and unrecorded tales of hunger, neglect, and abuse of every imaginable kind. The situation is so clearly monstrous that even the most vocal advocates of the "close the institutions" school of thought (actually non-thought) have been forced to change their tune.

In Australia both government and opposition parties have recently announced funding packages to provide early intervention for autistic children, a critically important service. Autism advocates and service providers though remain concerned that the needs of adolescent and adult autistic persons, most of whom would not have benefited from receipt of ABA intervention, remain neglected. Ken Baker, chief executive of National Disability Services, said the Government's plans were a strong foundation that the:

"challenge now is to ensure that services for people with autism, where required, are also readily available later in life," Mr Baker said.

In Canada, in the current Ontario election campaign, debate has taken place around the provision of Intensive Behavior Intervention services to school age children and the removal of waiting lists for autistic children to receive services. There has been very little mention, if any, of the needs of autistic adults; of the residential care and treatments needs of our most vulnerable autistic adults.

Here, in New Brunswick there is a lack of information available concerning actual conditions facing autistic youths and adults living in group homes. My own experience as an autism advocate and discussion with other advocates indicates that staff in New Brunswick group homes lack autism specific training. As a province, as a society, we have failed our more severely autistic youths and adults by failing to provide appropriate residential care and treatment. In New Brunswick our more severely autistic youths and adults have been sent out of province to other provinces and in some cases to the United States to receive treatment. In one instance an autistic youth who had been charged with no criminal offence was sent to reside on the grounds of a youth correctional facility because that was the only accommodation available for him while he awaited treatment at the Spurwink facility in Maine.

We have to do more for our autistic youths and adults. We have to ensure that residential accommodations suitable for autistic people are available for them, accommodations in which they can maintain ties with their families and friends in safe, hygienic settings. We also need institutional care facilities for the most severely autistic; facilities at which they can receive proper care and treatment.

It is time we stopped pretending that privately run group homes operated by poorly, or untrained, staff are a fix all solution to the very serious residential and treatment needs of autistic youths and adults. It is time we started talking about autistic adults and their needs.

Thursday, October 04, 2007

Autism Society Canada Letter to Health Minister Clement re CIHR Autism Symposium
















October 3rd, 2007

Honorable Tony Clement

House of Commons
Ottawa, Ontario
K1A 0A6


cc: Rémi Quirion, PhD
Scientific Director
CIHR Institute of Neurosciences, Mental Health and Addiction

cc: Barbara Beckett, PhD
Assistant Director
CIHR Institute of Neurosciences, Mental Health and Addiction


Dear Honorable Tony Clement,

Autism Society Canada (ASC) recently received an invitation to send a representative to the
previously cancelled (June 2007) Canadian Institutes of Health Research Autism Symposium now taking place on November 8th-9th, 2007 in Toronto. The CIHR is hosting this event in collaboration with Health Canada and the Public Health Agency of Canada.


The symposium was described in our invitation as “part of a package of federal initiatives that the Honourable Tony Clement, the federal Minister of Health, announced in November 2006 to
improve knowledge and research on autism spectrum disorders (ASD) and to help address the
challenges facing individuals with ASD and their families.”

The symposium goals stated in the original March 2007 letter were as follows:

Provide latest research results for families, health care professionals and other service providers, policy makers & administrators. Provide researchers with perspectives of families and service providers regarding what types of interventions are perceived as most effective and need to be further investigated .

Provide families, service providers, researchers, and policy makers & administrators with information about what is being done in Canada and abroad, to identify best practices in intervention and service delivery.


The revised goals outlined in this new invitation are as follows:

To inform service providers, policy makers, and those with autism and their families about the scientific evidence base on autism. To assist the research community in planning further research.

We are deeply concerned by what seems like a redirection of this meeting. ASC hosted the first
Canadian Autism Research Workshop in Toronto in 2002, with lead sponsors: the Canadian
Institutes of Health Research (CIHR) and the National Alliance for Autism Research (NAAR) in the U.S.

While we appreciate and welcome this opportunity to participate in moving the autism
research agenda forward, we do have concerns about what appears to be dwindling community
input into this process as well as how exactly this event will “address the challenges facing
individuals with ASD and their families.”

We would like to know if this research symposium is meant to replace the broader stakeholder
symposium you announced last November – an ASD stakeholder symposium in 2007 to further
the development of ASD knowledge and dissemination among health care professionals,
researchers, community groups, teachers, individuals and family members? There is great
community concern that your department has chosen to respond only to the research components of both your 2006 promises and the Senate recommendations of May 2007.

In its final report entitled, PAY NOW OR PAY LATER: Autism Families in Crisis, the Senate
Committee made many important recommendations to the federal government, prioritizing the
following:

an autism strategy to address the complex needs of our community – one that would be inclusive of all stakeholders, including those with ASD;

to convene a federal/provincial/territorial ministerial conference to look at innovative funding arrangements for the purpose of financing autism therapy in order to establish an “appropriate level of funding by the federal government”; and,

creation of an Autism Research Network with substantial new funding through CIHR.

While the research component is important, there are currently glaring gaps in the availability of fully funded treatment for children with Autism Spectrum Disorders, as well as damaging service gaps for adults and youth with ASD. Autism Society Canada strongly believes that federal leadership is needed to develop and commit to a comprehensive National Autism Strategy. The lifespan needs facing our community are complex. The treatment, training, service and accommodation needs across the ASD spectrum are multi-faceted. Families and people with ASD are tired of waiting.

As you are aware, ASC represents a federation of Canada-wide provincial and territorial autism
societies whose collective memberships include a very large community of individuals with ASD
and their families in Canada. We have carefully outlined our concerns regarding the process by
which this research symposium has come about in our letter to you of August 6th, 2007 letter to
Hon. Tony Clement . Some of the concerns centered on the last-minute notice for representatives with ASD who need time to make plans and prepare. We have yet to receive a reply to this letter.

We are being asked by many members of our community, including researchers, whether CIHR has ensured fair regional representation at this closed meeting. Our members provide direct services to the ASD community. They are very well-positioned to provide comprehensive regional input by identifying the practical needs and realities for children and adults with ASD in their respective areas. They feel this input should inform the planning of future research initiatives. They have requested that CIHR, if it has not already done so, ensure that each member society of ASC is invited to put forward a representative of their choosing to this research symposium.

Quite a number of people have made enquiries of CIHR about representation and have been told by CIHR that this is a complex scientific meeting – the implication being that community
representatives will find the content somehow confounding. CIHR staff should be aware that when they are speaking with ASD parents, people with ASD and community representatives, they are in fact, speaking with “experts in the field”. In the invitation letter, CIHR has referred to the research symposium as being, above all…… an opportunity for knowledge exchange, networking, and community-building. Can a closed research meeting with a private invitation list and no available genda, help to build community?

Finally we would like to remind the Minister that expecting people with ASD and their families,
who are already shouldering serious financial burdens, to front the costs for attending this meeting in advance was unrealistic and actually sets up a barrier to participation. We are sure this is not what you or CIHR intended.


ASC looks forward to working with you and CIHR to further the ASD research agenda. We also
look forward to addressing the other key National ASD Strategy issues brought forward in your
November, 2006 announcement and especially in the 2007 Senate Report. October is Autism
Awareness Month, let’s work together to ensure that all Canadians with ASD will one day be able to reach their full potential.

Sincerely,

Christine Dade, President,


On behalf of ASC’s Board of Directors:

Michael Lewis, First Vice-President, (representing British Columbia)

Vic Douse, Director, Second Vice-President, (representing Prince Edward Island)

Nancy Adams, CA, Treasurer, (Chair, Finance Committee)

David Jardine (representing Alberta)

Sandra McKay, Director, (representing Manitoba)

Brian Rimpilainen, Director, (representing New Brunswick)

Doreen Stryde, Director, (representing Newfoundland)

Lynn Elkin, Director, (representing Northwest Territories)

Vicki Harvey, Director (representing Nova Scotia)

Ginny Pearce, Director, (representing Ontario)

Lynn Verklan, Director, (representing Saskatchewan)

Lisa Rawlings, Director, (representing Yukon Territory)

Dr. Jeanette Holden, Director, (Queen’s University: ASD-Canadian-American Research Consortium)

Kristian Hooker, Director, (Chair, Advisory Committee of Adults with ASD)

Elizabeth Oliver, Director (Director-at-Large)

Autistic Boy One of 11 Molested, Raped In Ontario Group Home

From Barrie, Ontario, the Toronto Sun reports the conviction of Joseph Cross, 37, for molesting and raping 11 children in in group homes run by the Barrie and District Association for People with Special Needs. One of the victims was an autistic boy whose mother was heart broken when she had to leave the boy in a group home and who was crushed when she found out later that he was sexually molested at the home. Sentencing is scheduled for December 10.

This story and others should be a wake up call for the people in the Neurodiversity movement who argue on the internet, publish books and establish "acceptance projects" proclaiming that autism is not a disability, that we should find joy in autism. These people pontificate on such important issues as whether the puzzle piece image is offensive as a symbol for autism and whether it is more appropriate to refer to someone with an autism disorder as an autistic person or as a person with autism. Some Neurodiversity ideologues talk about the superiority of autistic intelligence and attack anyone who advocates a theory of autism, or autism cause or treatment inconsistent with their ideology. And almost all like to downplay some of the harsher realities of life confronting the many severely autistic persons who lack the ability to engage in internet debates. Truth talking parents like those in the Autism Every Day video are vilified by these ideologues.

But each day the news brings us back to reality - an autistic child is sexually molested in a group home in Barrie, Ontario, an autistic boy is killed by a motor vehicle after he snuck out of his home clad in pyjamas to run in traffic in New Zealand, a middle aged autistic woman with no communication ability is repeatedly assaulted by attendants in a Long Island residential care facility, an autistic boy is left locked on a hot school bus for hours in Kansas.

These are ugly realities but they are realities that parents and other caregivers of severely autistic children and adults can not, should not, must not ignore.

Autistic Boy Left on Locked, Hot Bus for Hours

In Leavenworth, Kansas an autistic boy was left locked on a hot school bus for hours after the other students were dropped off at their elementary school on Monday. The KCTV5.com story indicates that there were 2 adult supervisors on the bus. The Leavenworth School District supervisor didn't answer questions about procedures for checking buses.

I think I can, all the way up here in Fredericton, New Brunswick, Canada, answer the KCTC5 news team questions on that one. There either are no procedures for checking the school buses in the Leavenworth School District or they exist only on paper. It is beyond comprehension that an autistic child could have been left on that locked bus by any competent, conscious and conscientious adult. The article indicates that the bus company employees were at work the NEXT day on a different route.

With the wonders of the internet you never know who will read your blog. If the 2 "supervisors" on that bus ever Stumble Upon, Digg, Google, or otherwise come across this comment I have some words of advice for them:

Find a different line of work. One where vulnerable children are not entrusted to your care.
If that is too harsh for you, if you continue your employment as supervisors then - SUPERVISE, earn your pay checks, fulfill your responsibilities.

Wednesday, October 03, 2007

Maternal Flu Response Causes Autism, Schizophrenia?


Researchers Discover Link Between Schizophrenia, Autism and Maternal Flu from PhysOrg.com

A team of California Institute of Technology researchers has found an unexpected link connecting schizophrenia and autism to the importance of covering your mouth whenever you sneeze.

[...]



Autism Awareness Month - 1 in 150

In Canada, October is Autism Awareness Month.

Since October 2006 there have been many important developments in autism awareness. The Autism Knowledge Revolution has picked up steam with almost each new day bringing news of an important new scientific study on the causes of, or potential treatments for, autism. A Unified Autism Theory was advanced. There is a renewed focus on the study and development of bio-medical treatments. The CDC estimate of 1 in 166 persons having an autism disorder which had stood since 2004 was replaced in February 2007 by a prevalence rate of 1 in 150.

The 1 in 150 estimate by the CDC in the US is not necessarily the end of the story. In the UK the generally accepted estimate is 1 in 100. Debates continue to rage, as all debates on autism issues seem to do, over whether the newer prevalence rates actually reflect increases in autism cases, changes in diagnostic criteria and public awareness or some combination of these factors.

At the end of the day though the reality remains that autism specific services are needed in great number. Many autistic children pre-school or school age, require Applied Behavior Analysis intervention as a health treatment and as an educational interventions. And many autistic adults are not capable of living independent lives. SOME require residential care and treatment and some require full institutional care.

These are hard realities that many would rather avoid. We do so at peril, not to ourselves, but to the autistic persons we care about. During Autism Awareness month we should celebrate the joy that our autistic loved ones being to our lives but, if we truly care,we should also help them face the challenges ahead. We must ensure that autism specific services are available for them across the life span.

Tuesday, October 02, 2007

Shining A Light on Autism in Barrie, Ontario

Parents of autistic children, siblings, friends and neighbours held a sunset vigil outside the office of Barrie MPP Joe Tascona's constituency office to "remind themselves to be vigilant in the fight to equip their children to shine." The six year age limit on government funded Intensive Behavioural Intervention has been lifted in Ontario - theoretically. Practically, waiting lists for services have grown longer and more children are on the waiting lists than 4 years ago. Parents will undoubtedly have to remain vigilant to ensure that promises are kept, and waiting lists are eliminated. Bitter experience has already taught them that. The vigil is a good reminder.

Monday, October 01, 2007

11 Year Old Autistic Boy In Zealand Killed In Traffic

I felt a real jolt when I saw this story from New Zealand on Hawke's Bay Today of an 11 year old autistic boy killed running alongside an expressway after sneaking out of his home clad only in his pyjamas. Police said Andrew had managed to flee his home in Spriggs Avenue despite his family doing all they could to ensure he stayed safely inside.

A few years ago Conor snuck out of the house without me noticing while I was engaged in a long business call. He crossed a parking lot in front of a busy drinking establishment and was crossing a busy main street when a good Samaritan stopped and took him to safety in a nearby service station convenience store.

Conor is alive and well, unlike Andrew Seong Nam Chan of Hawke's Bay, New Zealand, because of good luck and a good Samaritan. I have never in my life felt such intense fear, and intense guilt, as I did after realizing Conor had left the house. To this day, neither feeling is ever too far from my conscious mind. My thoughts are very much with Andrew's family.


Peer Reviewed Study Claiming to Confirm Mercury-Autism Connection Published

David A. Geir and Dr. Mark R. Geir have published a new study, “A Prospective Study of Mercury Toxicity Biomarkers in Autistic Spectrum Disorders” in the Journal of Toxicology and Environmental Health, Part A (volume 70, issue 20, pgs 1723-1730). The Press Release issued by Coalition for Mercury-free Drugs (CoMeD) claims that the study "confirms that many children with autistic spectrum disorders (ASDs) suffer from mercury poisoning."

The Press Release also goes on to claim that:

This study utilized urinary porphyrin profile analysis (UPPA) to assess body-burden and physiological effects of mercury in children diagnosed with ASDs.

Using UPPA, Geier and Geier (2007) examined 71 children diagnosed with ASDs, 9 neurotypical siblings, and 5 general population controls. The researchers studied urinary porphyrin patterns using results reported both by the US Laboratory Corporation of America (LabCorp) and the French Laboratoire Philippe Auguste.

Their findings demonstrated that:

• Only the non-chelated patients diagnosed with ASDs had porphyrin patterns indicative of clinical mercury toxicity.

• Treating ASD diagnosed patients with chelating agents resulted in lower mercury-specific urinary porphyrins.

• The UPPA patterns reported were consistent between the two labs used.

The results of the present study confirm and extend previous observations by Nataf et al. (2006) and Geier and Geier (2006) on the use of UPPA profiling to establish the causal role for mercury in ASDs. Additionally, the current findings are consistent with those observed by many other physicians who treat patients diagnosed with both ASDs and mercury toxicity.

Given the ferocity of the debate over a possible mercury autism connection this latest study will give rise to still more heated debate. Hopefully professionals on all sides of this issue will look as this study calmly and objectively and provide the critical analysis that any such study should receive.

Autism In Ontario Election 2007

Autism appears to be an impact issue in the current Ontario election campaign. On the first day of October, which is the Autism Awareness month in Canada, the Globe and Mail has an article on autism in the campaign which also highlights NDP candidate and autism mother Nancy Morrison. Ms. Morrison is the mother to whom Ontario Liberal Leader Dalton McGuinty promised help for autistic children in the 2003 campaign before breaking the promise and fighting parents of autistic children in court.

"Mr. McGuinty promised in the letter to end the previous Progressive Conservative government's "unfair and discriminatory" practice of cutting off funding when children turned 6. "These children need - and deserve - our help and support," the letter says.

The problem for Mr. McGuinty is that Ms. Morrison kept her end of the bargain and he didn't."

- Karen Howlett, Globe and Mail, Plight of Autistic Children Resonates in Campaign

It would be great if the NDP or Conservative Parties formed the government, or held the balance of power in a minority government. A lot could change in the week and a half left in the election campgain. Right now though it is looking like another McGuinty Majority. And that would mean 4 years of keeping the pressure on Dalton McGuinty to provide real help for autistic children. If that happens then, hopefully, Nancy Morrison will be sitting as an MPP in the Ontario Legislature to see to it that Mr. McGuinty provides real help to autistic children.

Facing Autism in New Brunswick Hesitant Ontario Election Prediction - 4 More years of McGuinty and more broken autism promises.

Hopeful Note - I also picked Bob Rae to win the Liberal Party nomination, Ottawa to beat Anaheim in the Stanley Cup finals last spring, and France to beat Italy for the World Cup.

Sunday, September 30, 2007

Jenny McCarthy Knocks Over Neurodiversity Hornet's Nest

As expected, Jenny McCarthy’s appearance on Oprah has stirred up the Internet’s Neurodiversity bloggers. During the past week they buzzed about in a paroxysm of sarcastic rage over Ms McCarthy's audacity in speaking out about autism. Some of the Neurodiversity commentary has been mean and snide. Some of it has been outright offensive.

Following is a list of Neurodiversity Hub bloggers who fell over themselves taking cheap shots at Ms. McCarthy and her views on the nature of autism, autism causes and cures. Some, like Mike Stanton, Educator, and Kristina Chew, Educator, Ph.D., felt compelled to belittle her more than once. Ms Chew in fact featured Ms McCarthy in no less than 7 of her commentaries over the past week. What will the Neurodiversity Hub bloggers ever do with themselves until the next autism appearance by Ms McCarthy?

Mike Stanton
Respectful Insolence
Autism Street
Left Brain/Right Brain (Kevin Leitch)
Natural Variation (Joseph)
Autism Diva
One Dad’s Opinion
Autism Vox

Although I do not share her views on autism cause and cure, I respect Ms. McCarthy for speaking up. As noted previously she may yet be proven right, and I may be proven wrong on our differing autism opinions. I have not subscribed to the dietary interventions for autism. But yesterday the Autism Canada conference focused on biomedical interventions with Dr. Derrick MacFabe of the UWO team that reported a gut-brain autism link, and Dr. Martha Herbert of Harvard Medical School. The conference also featured Dr. Wendy Edwards, a paediatrician and mother of an autistic child, who advocates the use of various biomedical treatments including dietary interventions. The Neurodiversity ideologues will have to come up with different ad hominem attacks to use against Dr. Edwards.

Trail Walking with Conor
























Today was another perfect day in Fredericton.


This afternoon Conor did some Nashwaaksis trail walking with Dad.

Dr. Wendy Edwards, Pediatrician and Autism Mother, Advocates Treating Autism as a Whole Body Medical Illness

The Times Colonist has an article on yesterday's Autism Canada conference and its focus on treating autism as a whole body medical illness. Speakers included Dr. Derrick MacFabe of the UWO team which recently released its findings on proprionic acid and Dr. Martha Herbert of the Harvard Medical School. Much of the article though focused on Dr. Wendy Edwards, a Southern Ontario pediatrician whose son was diagnosed with autism at age 3. The message at the conference as summarized by the Times Colonist is that autism is a full body illness and is not limited to the brain.

Dr. Edwards advocates the use of biomedical treatments in addition to applied behaviour analysis in treating autism. She recommends diets aimed at eliminating toxins and reducing digestive tract inflammation and describes some elements of such diets including melatonin, antioxidants and the GF-CF free diet. Dr. Edwards acknowledges that her biomedical recommendations are not supported by scientific study but questions whether parents should wait while the studies are done:

"Why not do what we feel is working while we wait for the study to prove or disprove it? If we're not out there doing all these things and telling the researchers 'What about this?' the research won't get done."

There are good arguments against the use of experimental treatments for autism or any other medical condition. Financial resources are not unlimited, special diets can often add expense to a family budget already stretched tight particularly if the family is already strapped by the expense of paying for ABA, which although not curing autism, is an evidence based effective health and education intervention. Experimental treatments can also waste time and morale both of which are valuable to a family trying to help their child. Further, some seemingly innocuous interventions might in fact have unforeseen and possibly harmful effects on a child.

Still, if a family can afford the interventions, consults with physicians and does not get their hopes too high, it is difficult to see why they shouldn't try interventions backed by anecdotal evidence of other parents some of whom like Dr. Edwards are also pediatricians themselves. Especially if they do not forgo evidence based interventions in order to try experimental approaches. The UWO Proprionic Acid study grew out of parental observations. Although all parents are not also medical professionals like Dr. Edwards, they are the front line observers of their children's condition.

Yes, Autism Should Be Cured

Autism should be cured.

Most parents of severely autistic children will answer that question as I have just done. There are some high functioning autistic persons who argue that autism should not be cured. There are some parents of high functioning autistic persons and professionals who work with them who argue that autism should not be cured. Some simply ask whether we should seek to cure autism. The answer to any such question is yes, yes, yes, we should.

We should seek to cure autism so that severely autistic people can be cured and their lives enhanced. That is really all there is to it. This is not to suggest that the higher functioning autistic people who push their views on the internet should be forced to be cured. Absolutely not. But for severely autistic children, whose parents, legally, morally and practically speak for them, the answer is yes they should be given the chance to be cured. What other medical condition do we not seek to cure, or at least to give people the choice of being cured if they are capable of making the choice; or of having their care givers or guardians make the choice if they are not capable?

My son Conor is 11 1/2 and did not have access to 40 hours of ABA between the ages of 2 and 5. He has received ABA as much as possible though particularly since trained UNB-CEL Autism Training Intervention Program began graduating Autism Support Workers; some of whom now work in the school system. With ABA we are able to communicate at a basic level with Conor and he has learned some reading, writing and math skills. (He loves Dr. Seuss and Pinky Dinky Doo) We have also been able to moderate his self aggressive behaviour using ABA and knowledge of what environmental factors are likely to prompt frustration and self aggression.

Would we accept a cure for Conor if one were available and did not involve serious risk to his safety? Yes, if I could cure Conor's autism with the wave of my hand I would stop typing this commentary and do it now before finishing this sentence. I know that Conor is more than his autism; that his personality, his identity, are not dictated by his autism, that Conor would still be Conor. With one major difference. His opportunities to experience and enjoy life would be enhanced immeasurably.

The high functioning autistic persons who oppose curing autism have every right to decide not to be cured of their autism - for themselves. They have absolutely no right to do so for my son and other severely autistic children. They can argue until the sun ceases to shine but they will never convince me, nor most parents of severely autisic children, that we should not cure our children of their autism, that we should not enhance our childrens' lives as parents have strived to do since the beginning of human existence.

Yes, autism should be cured. And the Autism Knowledge Revolution which jumps almost daily onto our internet pages holds out great promise of doing exactly that.

Saturday, September 29, 2007

A Perfect Day



Today was a perfect day in Fredericton. A clear blue sky, a beautiful sunny day with a comfortable fall breeze.











Conor enjoyed the cool breeze ... and the McDonald's Hash Browns.





























A visitor also enjoying the breeze ... and showing us some flying techniques.














The view from the picnic bench.

FEAT-BC - Fund-raiser at CAPONES & Bill Good Show








FEAT-BC continues its relentless campaign to ensure that all Canadians with autism receive full Medicare coverage for the costs associated with the treatment of their often devastating medical condition.

Today, Saturday, September 29th, FEAT-BC welcomes a full house of parents and supporters to a fund-raiser at CAPONES, in Yaletown. The evening promises lots of fun, a silent auction featuring a truly incredible array of donated items [ie. a three day stay in a deluxe Whistler condo; a Vancouver Canucks' jersey, signed by the entire team; a case of Burrowing Owl merlot; etc.], and the opportunity to play an important part in the early stages of what is going to be a successful campaign! We're told that CBC-TV's "National" news team intends to cover the event, as part of their plan for a possible mini-documentary on "autism activism".

On Tuesday, October 2nd, for one half-hour beginning at 11:30am, FEAT-BC founding director Jean Lewis and moi will be guests on CKNW's Bill Good Show. We'll be discussing the launch of the "FEAT-BC goes coastal" campaign. If you are able, tune in AM980 and listen to the programme. Call in, if you're moved to do so.

North America is experiencing an autism epidemic of staggering proportions and, unlike the situation with our neighbours to the south, Canada's national government is doing absolutely nothing to address it. This is both morally reprehensible and economically stupid.

The upcoming federal election offers the best chance to put right this wrong. FEAT-BC intends to lead the campaign, from the Pacific to the Atlantic, in search of justice for some of Canada's most vulnerable citizens. You can help in many ways: donate some money [always the easiest thing to do]; volunteer some time to serve as a "FEAT soldier" in your community; e-mail, telephone or otherwise contact your family, neighbours, work associates and others in your circle of acquaintance, encouraging them to vote for a candidate who will support Medicare coverage for the treatment of autism; write letters to newspaper editors and MPs demanding urgent action; or any combination of this list.

David O. Marley
Tel. 604-970-1258 / Fax 604-926-8994

"A nation of sheep begets a government of wolves."
- Edward R. Murrow