No Stereotypes Here

In Ontario, the Social Assistance programs are under review.  The Commission involved is in charge of “examining social assistance in Ontario through engagement, research and analysis to provide the government with a concrete action plan to improve the system for the people who need it.”

There are comment and response forms for people to reply and contribute, found on the Commission for the Review of Social Assistance in Ontario website.  

Being a recipient of ODSP, I contributed my own comments, as seen below:

When determining social assistance rates, the cost of living needs to be considered.  Depending on location and the fluctuation of the economy, the cost of living changes.  In such cases such as the present, when the cost of living rises, so should the rates in order to ensure that recipients are able to afford necessary items such as food, clothing, rent (which for any higher quality of life is much higher than the amount given for rent with ODSP), as well as be able to pay the bills. 

As a recipient of ODSP, I find it a challenge to find work that makes it worth the deductions from social assistance.  Part of the problem is that it seems that the deductions are taken off with the assumption that any income we make in the previous month will be used for the next month.  I can tell you that it is not.  Often, because ODSP does not adequately cover all the costs of living, recipients who are working use income in the same month that they earn it.  This means that there is no saving for the month ahead, and the deductions actually serve to create a cycle of debt and poverty that is increasingly harder to break.

Also, with the current economy and job market, it is extremely difficult for persons with and without disabilities to get a job that would lead to coming off of social assistance.  The amount paid by most jobs available are not sufficient to take the place of the deductions in a person’s social assistance and so there is a constant need to find a better job, leading to an inconsistent history of employment, as well as an increased risk of a person burning out and becoming depression and/or further disabled mentally. 

By the time a person is able to find a decent paying job that does not cost a huge amount of emotional stress and is able to gradually have social assistance withdrawn, the person is in quite a bit of debt due to the cycle created by earning deductions in social assistance. In such a situation, it is near impossible for a person to save for the future, either for needed items for a new job, or items to enhance quality of life, or to put towards miscellaneous costs such as over the counter flu and cold medications as well as other medical costs that are not covered by benefits, or towards retirement in old age.

The Registered Disability Saving Plan is an attempt to allow persons with disabilities to save towards their old age, however, there are some concerns about being able to get accounts registered.  For accounts to be registered, a person must have the Disability Tax Credit, which has a different definition and set of requirements than ODSP.  What is puzzling is the mix of seemingly specific yet vague criteria needed on the applications.  What is needed is a standardized definition of disability so that ODSP recipients applying for the tax credit in order to register their RDSP is able to be approved and thus be granted financial security for the future by saving what they can afford from jobs, especially if they are able to get jobs that just barely gets them off social assistance but not improve their quality of life.

What is also problematic is how education is handled by ODSP.  ODSP is suppose to not deduct earnings if a recipient is taking post-secondary education classes.  However, there are times in which earnings are deducted despite the recipient informing and even providing documentation of their student status.  This is especially the case during the summer months, when there are also classes available for students. 

Between being unable to save for the future, and being unable to save for post-secondary education that may especially prove to lead to higher-paying employment, ODSP often hinders the efforts of recipients to gain adequate employment to no longer require social assistance and be able to improve one’s quality of life.  Rather than aiding people, social assistance as it currently operates perpetuates and increases poverty conditions for low-income persons, families and disabled people.


Whew!! Things have been busy for me this summer!

I’m currently working on an essay on violence and disability for school, an article on functioning labels for AWN, and a piece on self-definitions of recovery for here.  Some of them, just when I think I have all the materials I need to finish them, someone mentions some very good resources that make me rethink some of my points or what to include more information. 

However, I’m also getting ready for Autistics Speaking Day 2011.  It was an overwhelming success last year, with such a small amount of planning and advertisement.  I’m excited to see the results of this year.  I’ve read some of the responses to ASDay last year, and it’s been incredible!! I am still blown away and amazed at people’s responses. 

So we’re doing it again!!! We’re a little bit more organized this year, got our Facebook event up in advance, and Kathryn and I have started an official blog so that we can compile everyone’s contributions in one spot.  It’s still under some work, but it’s up and running!

We’re also going to be looking for people to help us out.  Last year, we were a little overwhelmed by the flow of blogs.  Kathryn was incredible being able to keep on track of everything on Facebook, and I had my hands full on Twitter.  We’d like someone who is fairly familiar with social networking sites to help us out.  But more on that later. 

Yay!!!  Our blog is up!!

To Yeti

Posted on: August 2, 2011

If you see my twitter and Facebook being flooded with pictures of a little white cat, it is because today Yeti is being put down.

Mom and dad say that she wasn’t feeling well, not eating or drinking. They took her to the vet. Turns out all her organs are shutting down and she’s dying. The vet can only make it happen painlessly and quick.

So afterwards, we’re bringing her back home and laying her to rest amongst the roses she loved so much, by the house.

I remember bring Yeti home for the first time. It was after Lunamus died, we had gotten used to being a two-cat house. And we wanted a cat that would mentally stay young. So mom called all the pet stores and requested to be put on the notification list for simease- cross kittens.

I was walking home from high school, in my kilt and rowing jacket, when mom and Loren pulled up. “we’re picking up Loren’s cat,” they said, and I got in. We were the first to respond, so we had the pick of the litter. And so we got the prettiest, more playful girl there.

She would climb up curtains and furniture, so Loren named her Yeti. Since I had Nibbles, an older cat that didn’t like the young kitten, Yeti stayed in Loren’s room for the night until Nibbles got used to her. At Christmas, she’d climb up the Christmas tree and sit in fake branches. As she got older, she loved to curl up under the tree and in boxes and corners.

Lately, she took to curling up at the foot of my paintings, which I found funny. I had used her temperament as inspiration for my character Kithara, and her colouring for another character, Joshi, both of Amhelaki Misadventures. The painting she liked was of those two characters.

She liked going outside and exploring, constantly getting into places where she shouldn’t be. I’ve caught her sneaking downstairs into the basement, where the cats aren’t allowed because of the sewing machines and because we keep it free of cat hair for guests with allergies. It was also routine to check a couple times a day where she was, especially at night. Once or twice, she did let locked outside for the night, but in the morning, she’ll be on the porch, sitting on the rockers, waiting.

She loved sitting on the patio furniture, or in the flowerbeds by the house when she wasn’t exploring the yard. She hunted birds, catching one last june, and bugs. When the neighborhood cats came by, she’d chase them off, but never got into fights.

She liked people, loved having attention and being petted, although only when she wanted it. She and dad had a routine; he would sit down to put on his shoes for work on the stairs, and she would circle around him, purring and then crawl into his lap. They would sit there for a while until she would jump off and he would go to work.

For everyone else, if she rubbed your leg and purred in the kitchen, you could pick her up and cuddle with her, but she fully expected food afterwards. Elsewhere, she’s walk away and expect you to follow her to where she curled up. There you could pet and comb her, but not pick her up. She would just wiggle out of your grip, and jump down, or else walk down your back and jump.

She liked exploring too, would get into the neighbor’s yards and then run back when she heard our door opening. Couldn’t keep her on a leash or collar; she was double jointed and very flexible, would just slip through it. But we didn’t worry, once we found that she knew the boundaries and didn’t go near the road. She liked to go out the front door, and then circle around the house to the back to be let in.

The two times she stayed on her leash was when we took her for walks. Once, to the lemoint point conservation area. She’d walk for a bit, then stop to check out things off the path. Some times we’d carry her, when it looked like she was tired. Second time, we took her on a walk to the convience store for milk. She was doing the same for that, but the way back she walked the entire way, in the lead.

Even though she’d wander the longer she was outside, she always came home.

So yeah, both Glenn and Ted haven’t responded to me.  However, I’m going ahead in my plans.  I started a petition on!!!!   You can find it and sign it here!

I need to come up with an image, but I don’t know whether  I can do it until I can get back to my very old version of Photoshop.  Which won’t be until after my DST 501 Rethinking Disability course ends, next Saturday.

With the concerns about the Canadian Autism Bills, and the lack of response from Glenn Thibeault, I have decided to contact my own MP and address the issue with him.  The following email was sent Ted Hsu, MP for Kingston and the Islands, on the morning of July 5th, 2011:

Dear Ted Hsu,
First of all, I want to congratulate you on your appointment to Member of Parliament for Kingston and the Islands.  I am very pleased to be represented by such an upstanding representative, and hope that together, much good will come of it.
However, I need to come to the main reason as to why I am writing to you.  Recently, Glenn Thibeault has re-introduced two Private member’s Bills, Bill C-219 and C-218, that has me concerned on many levels.  Before I get started, I do need to disclose to you that I am a person diagnosed with Asperger Syndrome, and consider myself an Autistic individual, as Autism is a part of who I am, how I think and interact with the world.   It is because of my identity as such that has me especially interested in these legislations. 
Bill C-219 is the National Strategy for Autism Spectrum Disorders.  To be honest, I am not sure what to make of it, since it seems a little vague.  I am worried about the potential misuse of a national surveillance program, especially with the ongoing research into pre-natal testing for Autism.  However, I am also hopeful for “the provincial government in providing education, professional training and other required supports for Canadians with Autism Spectrum Disorders”.  I do hope that this includes adults and students, as a university student myself finding it difficult to both work and attend courses on social assistance. 
What really has me and other Autistics worried is Bill C-218, the amendment to the Canada Health Act to include Applied Behavioural Analysis (ABA) and Intensive Behavioural Intervention (IBI) as services “medically necessary or required… for persons suffering from Autism Spectrum Disorders”.  In fact, given the language and potential negative consequences of the Bill, I strongly oppose it. 
As an Autistic individual, I can tell you that I do not suffer from Autism.  Both my-self and many other Autistic people will tell you that what we suffer from is a society and environment that is inaccessible, and unable to understand and accommodate our needs so that we can flourish as active and contributing members of society.  Part of this is the fact that often Autistic individuals are not included in local, provincial and national discussions about Autism, thus silencing our voices in matters that effect us and future generations.  In correction of this error, I hope that you will work with us to make sure that Autistic voices are being heard within our communities, with our social services and organizations, and in our government. 
The second part of language that I object to is the term “medically necessary”.  I understand that the term is a legislative term, apparently used to ensure “that such services cannot be withheld by any province or territory” (Glenn Thibeault, email Wed June 29, 2011 at 11:59am to myself).  However, it has the implications that Autism is a disease that is contagious and/or full of suffering and misery.  This re-enforces harmful negative stigma and stereotypes about Autism, and can hinder Autistics from gaining meaningful education, employment and involvement within our own communities.  This also gives a false impression as to the reality of our existence and our lives, making us out to be living lives full of tragedy, suffering and misery.  In some cases, because we are “diseased” and because we are disabled, we are seen as sub-human, and this justifies abuse, discrimination and even murder of Autistic people, usually in the case of relieving us of our “suffering” or else in plain cruelty towards perceived inferior individuals.  Thus, such language as “suffering” and “medically necessary” poses negative consequences on the lives of Autistic individuals and creates barriers for us to be a part of society and our country, if not outright threatening our lives.
And then there is the matter of ABA and IBI in terms of the legislation and in of itself. Glenn has tried to assure me that no one will be forced into ABA and IBI treatment, but both are early intervention treatments that focus on children, as young as possible.  This means that recipients of ABA/IBI are not always given a choice, or even an informed choice, about whether they receive treatment.  In the cases where they do object to the treatment, it is often taken as more proof that the child requires treatment.  This leads to a situation where the child’s wants are not being met, in favour for the wants and perhaps ease of the parents, and even for the benefit of ABA/IBI providers. 
There is a large community of Autistic individuals who object to ABA/IBI, because of how it traditionally treats Autistics, its philosophy and methods, and the possible failure for it to equip Autistics for life in the long-term. 
Applied Behavioural Analysis and Intensive Behavioural Intervention is often toted as an effective treatment for Autistic children, usually citing studies where treatment has been found to successfully render children “indistinguishable from their peers”, which is the whole aim of ABA/IBI.  However, such treatments suppress the natural coping strategies and communication styles of Autistic people, leaving them unable to cope with everyday stresses and situations.  Individuals then experience a melt-down when entering adult-hood and are unable to cope with being independent, a valued ability in our society.  This, combined with some of the dog-obedience-school like training of ABA/IBI treatment, leaves Autistic individuals completely dependent on caregivers.  It should also be noted that this leaves them vulnerable to various abuses at the hands of caregivers and strangers alike, including potential sexual predators.  It is noted that disabled people, men and women, are more likely to be sexually assaulted than non-disabled people.
There is also the issue of quality of life of a child undergoing ABA/IBI treatment.  Most treatments call for up to 40 hours a week of sessions, on top of a child’s regular schooling and possible other therapies such as occupational, physical and speech therapy (depending on the needs of the child).  Given the other stresses in a child’s daily life, 40 hours is a lot of work for a child.  It is comparable to a 40 hour job for an adult, and leaves very little time for a child to engage in other developmental activities such as one’s regular routines to de-stress, plus a child’s natural desire to play and simply be a kid.  Myself and other Autistic individuals consider this amount of time in ABA/IBI to be child labour, and is an inexcusable stress on a child’s life.
A counter-argument to the one I just presented is that ABA/IBI is worth it if it is effective in diminishing disabling aspects of Autism in the long-term.  First, I would question what would be considered disabling aspects of Autism, and whether it is really something that is disabling a person, or whether it is society’s inaccessibility that is really the disabling aspect.  In such a case, such arguments is then victim-blaming the disabled instead of working towards becoming more accessible and accepting of human diversity. 
Second, I question the actual sources of their success rates.  As noted by researchers such as Michelle Dawson, a lot of the studies concerning Autism do not meet quality standards required by other studies.  Plus data from such studies do not always meet the conclusions made about it and represent false impressions as to the long-term effects of treatments for Autism, including ABA/IBI.  I highly recommend Michelle Dawson’s work, as an Autistic individual herself with highly informative research at the University of Montreal, plus her experiences at the Supreme Court.  Her work can be accessed at her website No Autistics Allowed.
Looking into the studies, it can be seen that when comparing treatments for Autism, ABA/IBI scores no higher than any other treatment.  Even then, the treatments are not entirely clear as to the efficiency and success in the long-term, compared to no treatment at all.  There are even some suggestions that treatments for some Autistics are unnecessary, due to the fact that Autism is a developmental disorder, meaning that development may progress in an unique manner, but does occur.  It should be noted that this does not mean that Autistics do not require accommodations and supports in the classroom as disabled students, but rather that treatments to improve developmental milestones may be misguided. 
There is one study that does highly suggest success for ABA/IBI treatment, and this is often the study that all other studies reference or depend on for proof of success.  However, that study was done when ABA was developed, and uses the original methods designed by Lovaas in the late 1950s.  Studies to replicate the results are impossible, since the original Lovaas method included aversives such as electric shock, physical restraint, yelling and hitting, purpose exposure to unpleasant physical stimuli such as loud noises, smells, and various forms of pain. These techniques were used on children and teenagers in treatment for Autism (in most cases, ironically, to reduce self-injury behaviour) and homosexuality.  Since such techniques are now illegal, current studies are unable to replicate results, and thus prove that ABA/IBI is in any way effective or superior to other treatments. 
I will repeat, the goal of such treatments is to render children to be as indistinguishable from their peers as possible by suppressing Autistic behaviours, coping strategies and interests.  Given the long-term negative effects of such treatment, many Autistic people oppose ABA/IBI due to their own experiences upon reaching adulthood.  Also given the many advances in art and technology that Autistic people have provided, I wonder whether such disabling treatments are necessary, especially if our society is striving to become more accessible, accepting and inclusive of disabled persons. 
If our society is truly striving to be more inclusive of disabled persons, including Autistic individuals, then such legislation as Bill C-218 is a grave error.  While attempting to improve the lives of Autistic people, it servers to re-enforce negative stigma and stereotypes that creates barriers to accessibility and inclusion, if not outright threatening our lives.  I think that the Autistic people in Canada would be better served if we were included in discussions and conversations that ultimately concern us in our communities and on a national scale.  There are many alternatives to Bill C-218 that would benefit Autistics more than this very flawed and limited source to a particular treatment. 
Instead of treatments such as ABA/IBI, which are extremely costly with questionable benefits, Canadian Autistics would be better served with more teachers educated in teaching methods for an inclusive classroom, access to Alternative Augmentative Communication devices and assistive technology, education in inclusive classrooms that are designed to assist students to learning everyday living skills such as cooking and nutrition.  Post-secondary students and adults could benefit from workshops to learn living skills, support groups and more opportunities to funding for post-secondary education, professional training and employment that suits their abilities and meeting their needs.  There is a lack of supports for Autistic women in particular, in support groups, self-advocacy workshops and in women’s shelters.  Often Autistic women do not know whether shelters can support them, and will remain in abusive situations. 
This is just a brief list, limited in that it is only me thinking of alternatives.  But if there were more Autistic persons involved, I am sure that a more complete list of ways that Autistics can be better served by our government will be created.  I am proud to be Canadian, but I think that Canada can do better, and that Autistics deserve better than legislation such as Bill C-218.  To us, Bill C-218 does not properly serve our needs, and I hope that you will part of including Autistic Canadians to create an accessible and inclusive Canada, and help us to oppose this bill. 
Thank you for your time,
Corina Lynn Becker

Here’s hoping for a good response!

As you might have known from my previous post, there are two Private member bills being re-introduced that concern Autism, and I have been attempting to have a discussion with Glenn Thibeault, the MP who is doing the re-introduction.  Alas, his replies have been…. less than assuring….

Here’s the discussion, so far:

June 24
To Glenn

Hi, I would like to have more information on the autism spectrum disorder bills, especially on what the national strategy would entail and the reasoning for ABA/IBI, especially when there is very little good evidence that demonstrates that it is effective and beneficial for individuals with autism spectrum disorder.  In fact, many adults with ASD strongly disagree with ABA methods and traditional philosophy.  It would be beneficial for all people, children, teens and adults, if autistic people are included in the creation of legislation that ultimately affect them.

~Corina Becker

 To Corina


I can assure you that I spent a great deal of time liaising with autism groups before bringing these bills forward, and I have personal experience working with individuals with autism as prior to being elected to Parliament, I graduated from the Developmental Service Workers program at Cambrian College in Sudbury and I worked as a behavioural consultation in Vancouver.

Neither of these bills would force individuals to use ABA/IBI; they would simply ensure that no individual who wished to have access to the treatments could be refused by their provincial health service.

The two bills can be found online at:


All the best,


June 28

To Glenn

Hello Glenn, it’s very nice of you to provide links to the Bills. 

I am aware of your time as manager of Residential Programs for Youth and Adults with Disabilities.  It is conceivable that you had contact with some Autistic individuals there.  However, there is quite a spectrum of individuals and autism groups.  It would be beneficial to know which autism groups you have liaised with, as to be fully aware of your specific experiences.   This is especially important given the rather offensive wording in Bill C-218. 

Far from assuring me, you have deepened my concerns, and have not answered my questions.  So I will ask again, as an Autistic individual and voting citizen.  Upon which scientific studies and knowledge did you base your decision to make ABA/IBI as “medically necessary”, despite the numerous scientific studies that prove it to be no more effective than other teaching methods?  Why did you single out ABA/IBI specifically, even though the majority of the Autistic community is strongly opposed to its methods and philosophy? 

Why is it that you are not paying attention to the vast amount of Autistic citizens who oppose this bill, and persist to pass C-218? Especially when your own National Strategy for Autism Spectrum Disorders renders C-218 to be useless should ABA/IBI be an appropriate and safe method of teaching an Autistic individual? 

I would appreciate more specific answers.


June 29

To Corina

Thank you for your continued correspondence. I have worked with a number of autism groups – both provincial and national – over the past three years while I have been in Parliament regarding these bills. ‘Medically necessary’ is a legislative term used in the Canada Health Act to mean that such services cannot be withheld by any province or territory. It has no influence on whether an individual should or should not have any specific treatment. While I understand your criticism of ABA and IBA, Bill C-218 would simply assure that individuals who wish to received these treatments have equal access to them, and this was an issue that numerous groups brought to my attention and asked for legislative chances to rectify.
All the best,


July 1

To Glenn

Dear Glenn,
You have still failed to answer my questions sufficiently enough to address my concerns and fears. As such, I feel as though my voice as a voting Canadian citizen is not being heard. 
I ask again, which autism organizations in specific have you worked with? 
This is so that I can have a better understanding as to the scope of your autism experience.  Some Autism organizations, for example, do not represent my concerns and needs as an Autistic adult. 

Also, which scientific studies do you base your decisions that ABA/IBI is deemed to be more effective than other teaching methods to warrant it being singled out for Bill C-218? 
This is despite the increasingly large amount of data that suggests that it is no more effective than other means of teaching, and various accounts that it might actually be harmful to individuals, as it suppresses their natural coping mechanisms and renders them unable to adjust to the realities of adulthood and independence.  Which then leads them to be vulnerable to being dependent on service providers, some of which take advantage of their state.  

I highly recommend reading the work of Michelle Dawson, an Autistic researcher at the University of Montreal who has covered numerous studies on Autism and has been involved with cases at the Supreme Court about ABA/IBI.  You can see her work at her website No Autistics Allowed

Plus, ABA/IBI are early intervention therapies; they are directed to young children who are often not given a choice about whether or not they receive these treatments.  When they do try to object, the manner in which they do so are often taken as more reasoning on why the children need treatment. 

Furthermore, why do you use the term “suffering”  in Bill C-218?  This is problematic because I can tell you that numerous Autistic individuals, myself included, do not suffer from Autism; we suffer from society and autism organizations not being able to meet our needs, and misrepresenting us in our communities and in our governments. 

Also, in terms of ” medically necessary”, while a legislative term, it suggests to the general public that Autism is a disease.  While medically, it suits the definition, Autism is not a contagious disease, which is implied by the “medically necessary”  and “suffering” terms.  It may not be your intention, but the connotations of these words matter a lot.  The connotations of these words support the negative stigma and stereotypes about Autistic individuals, that our existence is a tragedy full of misery and suffering.  At best, these stereotypes make it difficult for us to gain meaningful education, employment and interaction within our communities; at worse, these stereotypes justify the discrimination, abuse and even murders of Autistic individuals, as we are seen as sub-human and our lives so full of suffering that it is a mercy to put us out of our misery. 

With these connotations in mind, I ask that you rethink the terms that you use to create legislation, and not degrade the lives and experiences of Autistic people.   I would also ask that you be more specific with your answers, as to reassure me. 

Thank you for your continued correspondence,

~ Corina

Glenn hasn’t responded to me yet.  It could be the long weekend that has him busy, but I’m not entirely sure.  I wonder whether I will get a reply, or rather, having patted me on the head, he has dismissed the contents of my emails entirely.  Time will only tell. 

So I was on twitter yesterday, and a link in a tweet caught my eye. It was a link to this piece.

Curious and worried, I emailed Glenn Thibeault:

Hi, I would like to have more information on the autism spectrum disorder bills, especially on what the national strategy would entail and the reasoning for ABA/IBI, especially when there is very little good evidence that demonstrates that it is effective and beneficial for individuals with autism spectrum disorder.  In fact, many adults with ASD strongly disagree with ABA methods and traditional philosophy.  It would be beneficial for all people, children, teens and adults, if autistic people are included in the creation of legislation that ultimately affect them. (my signature)  

And he responded:


I can assure you that I spent a great deal of time liaising with autism groups before bringing these bills forward, and I have personal experience working with individuals with autism as prior to being elected to Parliament, I graduated from the Developmental Service Workers program at Cambrian College in Sudbury and I worked as a behavioural consultation in Vancouver.

Neither of these bills would force individuals to use ABA/IBI; they would simply ensure that no individual who wished to have access to the treatments could be refused by their provincial health service.

The two bills can be found online at:



All the best,


Now, as I’m not at home right now and am using my iPod, and it takes me a while to sort through and process what I’m reading on a bigger screen, I was wondering whether anyone had any more information on this? Or even thoughts and feelings about these two bills?


  • None
  • Corina Becker: Hi Anonymous person who apparently doesn't feel like giving me a name to address, and thus hides behind anonymity!!! I never said the federal gov
  • Anonymous: I think that it is about time something is being done federally to help those with ASD to get much needed therapies for their disability and YES I do
  • Corina Becker: Hi Janine! Melody reads here? Awesome. I honestly had no idea she was aware of this blog.And thank you so much, I'm glad both of you like the bl